Int Manual EU28
Int Manual EU28
Int Manual EU28
The Interpretation Manual of European Union Habitats - EUR28 is a scientific reference document. It is based on the version for EUR15, which was adopted by the Habitats Committee on 4. October 1999 and consolidated with the new and amended habitat types for the 10 accession countries as adopted by the Habitats Committee on 14 March 2002. A small amendment to habitat type 91D0 was adopted by the Habitats Committee in its meeting on 14th October 2003. The Habitats Committee at its meeting on 13 April 2007 adopted additional changes for the accession of Bulgaria and Romania, and for the marine habitats, followed the descriptions given in Guidelines for the establishment of the Natura 2000 network in the marine environment. Application of the Habitats and Birds Directives published in May 2007 by the Commission services. Amendments for the accession of Croatia were adopted by the Habitats Committee on 4 October, 2012. The April 2013 version consolidates the changes for Croatia in the text and corrects the references to EUNIS codes for three marine habitat types.
TABLE OF CONTENTS
WHY THIS MANUAL? HISTORICAL REVIEW THE MANUAL THE EUR15 VERSION THE EUR25 VERSION THE EUR27 VERSION THE EUR28 VERSION EXPLANATORY NOTES COASTAL AND HALOPHYTIC HABITATS COASTAL AND HALOPHYTIC HABITATS OPEN SEA AND TIDAL AREAS SEA CLIFFS AND SHINGLE OR STONY BEACHES ATLANTIC AND CONTINENTAL SALT MARSHES AND SALT MEADOWS MEDITERRANEAN AND THERMO-ATLANTIC SALTMARSHES AND SALT MEADOWS SALT AND GYPSUM INLAND STEPPES BOREAL BALTIC ARCHIPELAGO, COASTAL AND LANDUPHEAVAL AREAS COASTAL SAND DUNES AND INLAND DUNES SEA DUNES OF THE ATLANTIC, NORTH SEA AND BALTIC COASTS SEA DUNES OF THE MEDITERRANEAN COAST INLAND DUNES, OLD AND DECALCIFIED FRESHWATER HABITATS STANDING WATER RUNNING WATER TEMPERATE HEATH AND SCRUB SCLEROPHYLLOUS SCRUB (MATORRAL) SUB-MEDITERRANEAN AND TEMPERATE SCRUB MEDITERRANEAN ARBORESCENT MATORRAL THERMO-MEDITERRANEAN AND PRE-STEPPE BRUSH PHRYGANA NATURAL AND SEMI-NATURAL GRASSLAND FORMATIONS NATURAL GRASSLANDS SEMI-NATURAL DRY GRASSLANDS AND SCRUBLAND FACIES SCLEROPHILLOUS GRAZED FORESTS (DEHESAS) SEMI-NATURAL TALL-HERB HUMID MEADOWS MESOPHILE GRASSLANDS
Interpretation Manual - EUR28
3 3 4 5 5 6 6 7 7 8 8 17 20 22 24 26 29 29 35 37 38 38 44 48 58 58 60 61 63 65 65 70 78 78 82
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RAISED BOGS AND MIRES AND FENS SPHAGNUM ACID BOGS CALCAREOUS FENS BOREAL MIRES ROCKY HABITATS AND CAVES SCREE ROCKY SLOPES WITH CHASMOPHYTIC VEGETATION OTHER ROCKY HABITATS FORESTS FORESTS OF BOREAL EUROPE FORESTS OF TEMPERATE EUROPE MEDITERRANEAN DECIDUOUS FORESTS MEDITERRANEAN SCLEROPHYLLOUS FORESTS TEMPERATE MOUNTAINOUS CONIFEROUS FORESTS MEDITERRANEAN AND MACARONESIAN MOUNTAINOUS CONIFEROUS FORESTS
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Historical review
The "Habitats" Directive1 is a Community legislative instrument in the field of nature conservation that establishes a common framework for the conservation of wild animal and plant species and natural habitats of Community importance; it provides for the creation of a network of special areas of conservation, called Natura 2000, to "maintain and restore, at favourable conservation status, natural habitats and species of wild fauna and flora of Community interest". Animal and plant species names are clearly presented in the Directive and, despite minor misspellings or use of synonyms, no major additional work needs to be done to allow a correct interpretation of Annex II. In contrast, the development of a common agreed definition appeared to be essential for the different habitat types of Annex I. Annex I lists today 233 European natural habitat types, including 71 priority (i.e. habitat types in danger of disappearance and whose natural range mainly falls within the territory of the European Union). Annex I was initially based on the hierarchical classification of European habitats developed by the CORINE Biotopes project 2 since that was the only existing classification at European level. A draft list of habitat types for Annex I was therefore drawn up on the basis of this classification by Professor A. Noirfalise and submitted to the national experts preparing the Directive as a working document in August 1989. Numerous discussions with the national experts then took place between 1989 and 1991, culminating in the version of Annex I published in the Official Journal in May 1992. In December 1991, while the Directive was being adopted, a thorough revision of the CORINE classification was published 3. This revision introduced numerous changes within codes and habitat types, in particular involving the division of the latter into sub-types. Definitions had been prepared for the various categories. Consequently, the Annex I codes no longer corresponded fully to the codes and descriptive content of the various categories of CORINE, resulting in considerable ambiguities in the interpretation of Annex I on the basis of the CORINE classification. The Task Force/European Environment Agency thus produced a paper establishing the correspondence between the habitat codes of Annex I and those of the 1991 version of the CORINE classification 4. This paper also included the description proposed in the 1991 CORINE version for the various habitat types of Annex I.
1 2 3 4
Council Directive 92/43/EEC of 21 May 1992 on the conservation of natural habitats and of wild fauna and flora, O.J. L206, 22.07.92 CORINE Biotopes - Technical Handbook, volume 1, p. 73-109, Corine/Biotopes/89-2.2, 19 May 1988, partially updated 14 February 1989. CORINE Biotopes manual, Habitats of the European Community. EUR 12587/3, Office for Official Publications of the European Communities, 1991. Relation between the Directive 92/43/EEC Annex I habitats and the CORINE habitat list 1991 (EUR 12587/3). Version 1 - Draft, November 1992. CEC-DG XI, Task Force Agency (EEA-TF).
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The manual
Having in mind all these difficulties of classification, the Scientific Working Group, set up by the Habitats Committee (established by Directive 92/43/EEC), expressed in May 1992 the need to prepare a manual for the interpretation of Annex I. Following a call for proposals the Commission charged Professor Thanghe from the Universit Libre de Bruxelles to prepare a draft manual 5. Following several meetings of the Scientific Working Group, the Commission agreed the two following points with the national experts: (1) The interpretation work on Annex I should primarily focus on the priority habitat types. (2) The CORINE classification (1991 version) provides a basis for a description of the Annex I habitat types; where the experts feel that it is not suitable, an operational scientific description should be produced from the contributions of the national experts. In September 1993 the Universit Libre de Bruxelles finalised the study relating to the interpretation of Annex I priority habitat types. This study focused on the drafting of an eight field descriptive sheet drawn up on the basis of written and oral scientific contributions from the national experts. Each sheet gathers the information on national and regional particularities, as well as types of associated habitats. The manual for the interpretation of Annex I priority habitat types of the Council Directive 92/43/EEC was compiled by the Commission (DG XI), based on the study of the Universit Libre de Bruxelles, the contributions of the national experts, and the CORINE classification (1991 version); this document was approved by the Habitats Committee in February 1994 (Doc. HABITATS 94/3 FINAL). Following the adoption of the priority habitats manual, the experts identified a set of 36 non priority habitat types also causing interpretation problems. An interpretation document was drafted by the Universit Libre de Bruxelles, discussed in a meeting of the Scientific Working Group (December 1994) and revised accordingly 6 . On April 1995 the Habitats Committee approved the EUR12 version of the Interpretation Manual of European Union Habitats7, which incorporated: i) the descriptive sheets for priority habitats8, which establish clear, operational scientific definitions of habitat types, using pragmatic descriptive elements (e.g. characteristic plants), and taking into consideration regional variation; the descriptive sheets of 36 non priority habitats similar to those used for priority habitats; the CORINE Biotopes definitions for the remaining non priority habitats; these definitions should be considered 'a minimal interpretation', not exclusive; some CORINE definitions do not take account of sub-types, regional varieties and/or do not cover all the geographical range of an habitat type - this fact should be recognised, thus allowing a certain flexibility in the interpretation of these Annex I habitat types.
ii) iii)
The contents of the manual did not take into account the accession of Austria, Finland and Sweden, which has resulted in the inclusion of a new biogeographical region (the Boreal region) in the Directive. These new Member States have asked for the introduction in Annex I of several priority habitat types that are restricted or only apply to them. In order not to delay the distribution of the manual, the Commission has decided to
5 6 7 8
tude relative au projet de manuel technique d'interprtation de l'Annexe I de la Directive habitats 92/43/CEE. Rapport final, September 1993. Universit Libre de Bruxelles (contrat n 4-3040(92)15504). tude relative au projet de manuel technique d'interprtation de l'Annexe I de la Directive habitats 92/43/CEE - Types d'habitats non prioritaires. Rapport final, Janvier 1995. Universit Libre de Bruxelles (contrat n B4-3040/94/000212/MAR/B2). Also available in French under the title 'Manuel d'interpretation des habitat de l'Union europenne' From Doc. HABITATS 94/3 FINAL
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publish that first version (EUR12) and envisaged the preparation of a second version (EUR15) in order to incorporate new information (mainly on distribution and regional sub-types).
Accession Act of Austria, Finland and Sweden (OJ L1,1.1.1995, p.135) Devillers, P. & Devillers-Terschuren, J. (1993). A classification of Palaearctic habitats. Strasbourg: Council of Europe 11 Institut Royal des Sciences Naturelles de Belgique 12 Council Directive 97/62/EC of 27 October 1997 adapting to technical and scientific progress Directive 92/43/EC on the conservation of natural habitats and of wild fauna and flora, O.J. L305, 8.11.1997.
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Explanatory Notes
The habitat types are grouped and sorted according to Annex I of the Directive.
Name of the habitat type; an asterisk (*) indicates a priority habitat Natura 2000 code; this is the four digit code given in the Natura 2000 standard data-entry form (Appendix B)
2140 * Decalcified fixed dunes with Empetrum nigrum
PAL.CLASS.: 16.23
Code(s) based on "A classification of Palaearctic habitats" 1995 version Definition - general description of the vegetation, syntaxa, abiotic features, origin Characteristic animal and plant species, including details of their occurrence in Annex II and IV (*=priority, #=nonpriority from Annex II/IV, +=Annex IV only)
1) Decalcified dunes colonised by Empetrum nigrum heaths of the coasts. Syntaxa associated to this habitat type: Empetrion nigri, Calluno Genistion pilosae p., Ericion tetralicis p. The term "fixed" should be taken to mean the opposite of "shifting". The psychrophilic coastal association Carici trinervis-Callunetum vulgaris de Foucault & Gehu 78 may be included here. 2) Plants: Carex arenaria, Empetrum nigrum, Genista tinctoria, Pyrola rotundifolia. 3) Corresponding categories United Kingdom classification: "H11b Calluna vulgaris-Carex arenaria heath community, Empetrum nigrum ssp. nigrum sub-community". German classification : "100401 Krhenbeer-Heide der Ksten".In Germany highly endangered coastal Empetrum nigrum heathland on the Geest are included. Nordic classification: "4143 Calluna vulgaris-Empetrum nigrum-Carex arenaria-typ". 4) Humid dune slacks (16.3), grey dunes (16.22), wooded dunes (16.22, 16.25). 5) Mc.Manus, D. (1988). Plant community dynamics on sand dunes at Murlough National Nature Reserve, Dundrum, Co. Down, Northern Ireland. M.Phil. Thesis, University of Ulster. Olsson, H. (1993). Dry coastal ecosystems of southern Sweden. In: van der Maarel, E. (ed.) Ecosystems of the world 2A. Dry coastal ecosystems, polar regions and Europe. Elsevier, Amsterdam. pp. 131143.
Corresponding categories, sub-types, regional varieties, correspondence with other classification systems, typical sites Habitat types generally associated in the field (phytodynamic successions, zonations or mosaics)
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1110
Sandbanks which are slightly covered by sea water all the time
Sandbanks are elevated, elongated, rounded or irregular topographic features, permanently submerged and predominantly surrounded by deeper water. They consist mainly of sandy sediments, but larger grain sizes, including boulders and cobbles, or smaller grain sizes including mud may also be present on a sandbank. Banks where sandy sediments occur in a layer over hard substrata are classed as sandbanks if the associated biota are dependent on the sand rather than on the underlying hard substrata. Slightly covered by sea water all the time means that above a sandbank the water depth is seldom more than 20 m below chart datum. Sandbanks can, however, extend beneath 20 m below chart datum. It can, therefore, be appropriate to include in designations such areas where they are part of the feature and host its biological assemblages. Plants: North Atlantic including North Sea - Zostera sp., free living species of the Corallinaceae family. On many sandbanks macrophytes do not occur. Central Atlantic Islands (Macaronesian Islands) - Cymodocea nodosa and Zostera noltii. On many sandbanks free living species of Corallinaceae are conspicuous elements of biotic assemblages, with relevant role as feeding and nursery grounds for invertebrates and fish. On many sandbanks macrophytes do not occur. Baltic Sea - Zostera sp., Potamogeton spp., Ruppia spp., Tolypella nidifica, Zannichellia spp., carophytes. On many sandbanks macrophytes do not occur. Mediterranean - The marine Angiosperm Cymodocea nodosa, together with photophilic species of algae living on the leaves (more than 15 species, mainly small red algae of the Ceramiaceae family), associated with Posidonia beds. On many sandbanks macrophytes do not occur. Animals: North Atlantic including North Sea - Invertebrate and demersal fish communities of sandy sublittoral (e.g. polychaete worms, crustacea, anthozoans, burrowing bivalves and echinoderms, Ammodytes spp., Callionymus spp., Pomatoschistus spp., Echiichtys vipera, Pleuronectes platessa, Limanda limanda). Central Atlantic Islands (Macaronesian Islands) - Fish, crustacean, polychaeta, hydrozoan, burrowing bivalves, irregular echinoderms. Baltic Sea - Invertebrate and demersal fish communities of sandy sublittoral (fine and medium grained sands, coarse sands, gravely sands), e.g. polychaetes: Scoloplus armiger, Pygospio elegans, Nereis diversicolor, Travisia sp., e.g. bivalves: Macoma balthica, Mya arenaria, Cerastoderma sp., e.g. crustaceans: Crangon crangon, Saduria entomon, e.g. fish species: Platichthys flesus, Nerophis ophidion, Pomatoschistus spp., Ammodytes tobianus. Mediterranean - Invertebrate communities of sandy sublittoral (e.g. polychaetes). Banks are often highly important as feeding, resting or nursery grounds for sea birds, fish or marine mammals. Corresponding categories French classification: ZNIEFF-MER: Biocnose des sables fins de haut niveau, Biocnose des sables fins bien calibrs. German classification: Sandbank der Ostsee (stndig wasserbedeckt)(040202a), Sandbank der Nordsee (stndig wasserbedeckt)(030202a).
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1)
2)
3)
Barcelona Convention: Biocenosis of fine sands in very shallow waters (III. 2. 1.) with facies with Lentidium mediterraneum (III. 2. 1. 1.), Biocenosis of well sorted fine sands (III. 2. 2.) with associations with Cymodocea nodosa on well sorted fine sands (III. 2. 2. 1.) and with Holophila stipulacela (III. 2. 2. 2), the latter considered determinant habitat in C. B., Biocenosis of coarse sands and fine gravels mixed by the waves (III. 3. 1.) with association with rhodolithes (III. 3. 1. 1), considered determinant habitat in the C. B., Biocenosis of coarse sands and fine gravels under the influence of bottom currents (also found in the Circalittoral) (III. 3. 2.). It is possible to find a facies and an association which are determinant habitats for C. B.: the marl facies (= Association with Lithothamnion corallioides and Phymatoliton calcareum), also found as facies of the biocenosis of coastal detritic (III. 3. 2. 1), and the association with rhodolithes (III. 3. 2. 2.), Biocenosis of infralittoral pebbles (III. 4. 1.) with facies with Gouania wildenowi (III. 4. 1. 1.), small teleostean which lives among pebbles. Vegetationstyper i Norden (Phlsson (ed.) 1994): Zostera marina-typ (4.4.1.1), Ruppia maritimatyp (4.4.1.2), Chara-typ (6.3.3.1), Potamogeton pectinatus (6.3.2.2). Kustbiotoper i Norden (Nordiska Ministerrdet 2001): Sandbottnar (7.7.1.2; 7.8.1.2; 7.8.4.2; 7.8.5.2; 7.8.6.7; 7.8.6.8; 7.8.6.9; 7.8.7.9; 7.8.7.10; 7.8.7.11; 7.9.1.1.; 7.9.2.1; 7.9.3.1; 7.9.4.1). HELCOM classification: Sublittoral gravel bottoms. Banks with or without macrophyte vegetation (2.4.2.3), Sublittoral sandy bottoms. Banks with or without macrophyte vegetation (2.5.2.4). The National Marine Habitat Classification for Britain and Ireland Version 03.02: Relevant types within Sublittoral coarse sediments (SCS), Sublittoral sands (SSA) and Sublittoral macrophytes communities (SMP). EUNIS classification: Relevant types within A5.1 Sublittoral coarse sediment, A5.2 Sublittoral sand, A5.4 Sublittoral mixed sediments, A5.5 Sublittoral macrophyte-dominated sediment. 4) Sandbanks can be found in association with mudflats and sandflats not covered by seawater at low tide (1140), with Posidonia beds (1120) and reefs (1170). Sandbanks may also be a component part of habitat 1130 Estuaries and habitat 1160 Large shallow inlets and bays. Augier H. (1982). Inventaire et classification des biocnoses marines benthiques de la Mditerrane. Publication du Conseil de l Europe, Coll. Sauvegarde de la Nature, 25, 59 pages. Dyer Kr & Huntley Da (1999). The origin, classification and modelling of sand banks and ridges. Continental Shelf Research 19 1285-1330 Connor, D.W., Allen, J.H., Golding, N., Lieberknecht, L.M., Northen, K.O. & Reker, J.B. (2003). The National Marine Habitat Classification for Britain and Ireland Version 03.02. Internet version. Joint Nature Conservation Committee, Peterborough. (www.jncc.gov.uk/marine/biotopes/default.htm) Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X) Ericson, L. & Wallentinus, H.-G. (1979). Sea-shore vegetation around the Gulf of Bothnia. Guide for the International Society for Vegetation Science, July-August 1977. Wahlenbergia 5:1 142. European Environment Agency (2002). EUNIS habitat classification. Version 2.3. Copenhagen, EEA (Internet publication: http://eunis.eea.europa.eu/habitats.jsp ) Haroun, R.J., Gil-Rodrguez, M.C., Daz De Castro, J. & Prudhomme Van Reine, W.F. (2002). A check-list of the marine plants from the Canary Islands (Central Eastern Atlantic Ocean). Botanica Marina. 45: 139-169. Helcom (1998). Red List of Biotopes and Biotope Complexes of the Baltic Sea, the Belt Sea and the Kattegat. Baltic Sea Environment Proceedings No. 75.: 126pp. Kautsky, N. (1974). Quantitative investigations of the red algae belt in the Ask area, Northern Baltic proper. Contrib. Ask Lab. Univ. Stockholm 3: 1-29. Lappalainen, A., Hllfors, G. & Kangas, P. (1977). Littoral benthos of the northern Baltic Sea. IV. Pattern and dynamics of macrobenthos in a sandy bottom Zostera marina community in Tvrminne.
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Nordheim, H. Von, Norden Andersen, O. & Thissen, J. (Eds.) (1996). Red Lists of Biotopes, Flora and Fauna of the Trilateral Wadden Sea Area 1995. Helgol. Meeresuntersuchungen. 50 (suppl.): 136 pp. Nordiska Ministerrdet (2001). Kustbiotoper i Norden. Hotade och representativa biotoper. TemaNord 2001: 536. 345 pp. Oulasvirta, P., Leinikki, J. & Reitalu, T. (2001). Underwater biotopes in Vinameri and Kpu area, Western Estonia. The Finnish Environment 497. Pavn-Salas, N., Herrera, R., Hernndez-Guerra, A. & Haroun R. (2000). Distributional pattern of sea grasses in the Canary Islands (Central-East Atlantic Ocean). J. Coastal Research, 16: 329-335. Phlsson, L. (Ed.) (1994). Vegetationstyper i Norden. TemaNord 1994: 665. 627 pp. Pers J. M. & Picard J. (1964). Nouveau manuel de bionomie benthique de la mer Mditerrane. Rec. Trav. St. Mar. Endoume 31 (47): 5-137. Ravanko, O. (1968). Macroscopic Green, Brown And Red Algae In The South-Western Archipelago Of Finland. Acta Bot. Fennica 79: 1-50. Riecken, U., Ries, U. & Ssymank, A. (1994). Rote Liste der gefhrdeten Biotoptypen der Bundesrepublik Deutschland - Schriftenreihe fr Landschaftspflege und Naturschutz. 41: 184 pp.
1120
PAL.CLASS.: 11.34
1)
2)
5)
1130
PAL.CLASS.: 13.2, 11.2
Estuaries
Downstream part of a river valley, subject to the tide and extending from the limit of brackish waters. River estuaries are coastal inlets where, unlike 'large shallow inlets and bays' there is generally a substantial freshwater influence. The mixing of freshwater and sea water and the reduced current flows in the shelter of the estuary lead to deposition of fine sediments, often forming extensive intertidal sand and mud flats. Where the tidal currents are faster than flood tides, most sediments deposit to form a delta at the mouth of the estuary. Baltic river mouths, considered as an estuary subtype, have brackish water and no tide, with large wetland vegetation (helophytic) and luxurious aquatic vegetation in shallow water areas. Plants: Benthic algal communities, Zostera beds e.g. Zostera noltii (Zosteretea) or vegetation of brackish water: Ruppia maritima (= R. rostellata (Ruppietea)); Spartina maritima (Spartinetea); Sarcocornia perennis (Arthrocnemetea). Both species of fresh water and brackish water can be
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2)
found in Baltic river mouths (Carex spp., Myriophyllum spp., Phragmites australis, Potamogeton spp., Scirpus spp.). Animals: Invertebrate benthic communities; important feeding areas for many birds. 3) Corresponding categories German classification : "D2a stuare (Fliegewssermndungen mit Brackwassereinflu u./od. Tidenhub eingeschlossen werden", "050105 Brackwasserwatt des stuare an der Nordsee", "050106 Swasserwatt im Tideeinflu des Nordsee". An estuary forms an ecological unit with the surrounding terrestrial coastal habitat types. In terms of nature conservation, these different habitat types should not be separated, and this reality must be taken into account during the selection of sites. Brunet, R. et al. Les mots de la gographie-dictionnaire critique. Ed. Reclus. Gillner, W. (1960). Vegetations- und Standortsuntersuchungen in den Strandwiesen der schwedischen Westkste. Acta Phytogeogr. Suec. 43:1-198.
4)
5)
1140
PAL.CLASS.: 14
1)
1150
PAL.CLASS.: 21
* Coastal lagoons
Lagoons are expanses of shallow coastal salt water, of varying salinity and water volume, wholly or partially separated from the sea by sand banks or shingle, or, less frequently, by rocks. Salinity may vary from brackish water to hypersalinity depending on rainfall, evaporation and through the addition of fresh seawater from storms, temporary flooding of the sea in winter or tidal exchange. With or without vegetation from Ruppietea maritimae, Potametea, Zosteretea or Charetea (CORINE 91: 23.21 or 23.22). - Flads and gloes, considered a Baltic variety of lagoons, are small, usually shallow, more or less delimited water bodies still connected to the sea or have been cut off from the sea very recently by land upheaval. Characterised by well-developed reedbeds and luxuriant submerged vegetation and having several morphological and botanical development stages in the process whereby sea becomes land. - Salt basins and salt ponds may also be considered as lagoons, providing they had their origin on a transformed natural old lagoon or on a saltmarsh, and are characterised by a minor impact from exploitation.
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Plants: Callitriche spp., Chara canescens, C. baltica, C. connivens, Eleocharis parvula, Lamprothamnion papulosum, Potamogeton pectinatus, Ranunculus baudotii, Ruppia maritima, Tolypella n. nidifica. In flads and gloes also Chara ssp.(Chara tomentosa), Lemna trisulca, Najas marina, Phragmites australis, Potamogeton ssp., Stratiotes aloides, Typha spp. Animals: Cnidaria- Edwardsia ivelli; Polychaeta- Armandia cirrhosa; Bryozoa- Victorella pavida; Rotifera - Brachionus sp.; Molluscs- Abra sp., Murex sp.; Crustaceans- Artema sp.; Fish- Cyprinus sp., Mullus barbatus; Reptiles- Testudo sp.; Amphibians- Hyla sp. Corresponding categories German classification : "0906 Strandsee", "240601 Brackwassersee im Ostseekstenbereich". Saltmarshes form part of this complex. Bamber et al. (1992). On the ecology of brackish lagoons in Great Britain. Aquatic conservation: marine and freshwater ecosystems, 2, 65-94. Barnes, R.S.K. (1988). The faunas of landlocked lagoons: chance differences and problems of dispersal. Estuarine and Coastal Shelf Science, 26, 309 - 18. Munsterhjelm, R. (1995). The aquatic macrophyte vegetation of flads and gloes, S coast of Finland. Acta Bot. Fennica (in print). Palmer, M.A., Bell, S.L., Butterfield, I. (1992). A botanical classification of standing waters: Applications for conservation and monitoring. Aquatic conservation: marine and freshwater ecosystems, 2, 125-143.
3)
4) 5)
1160
PAL.CLASS.: 12
1)
2)
3)
5)
13
National experts consider inappropriate to fix a maximum water depth, since the term 'shallow' may have different ecological interpretations according to the physiographic type considered and geographical location.
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1170
PAL.CLASS.: 11.24, 11.25
Reefs
Reefs can be either biogenic concretions or of geogenic origin. They are hard compact substrata on solid and soft bottoms, which arise from the sea floor in the sublittoral and littoral zone. Reefs may support a zonation of benthic communities of algae and animal species as well as concretions and corallogenic concretions. Clarifications: - Hard compact substrata are: rocks (including soft rock, e.g. chalk), boulders and cobbles (generally >64 mm in diameter). - Biogenic concretions are defined as: concretions, encrustations, corallogenic concretions and bivalve mussel beds originating from dead or living animals, i.e. biogenic hard bottoms which supply habitats for epibiotic species. - Geogenic origin means: reefs formed by non biogenic substrata. - Arise from the sea floor" means: the reef is topographically distinct from the surrounding seafloor. - Sublittoral and littoral zone means: the reefs may extend from the sublittoral uninterrupted into the intertidal (littoral) zone or may only occur in the sublittoral zone, including deep water areas such as the bathyal. - Such hard substrata that are covered by a thin and mobile veneer of sediment are classed as reefs if the associated biota are dependent on the hard substratum rather than the overlying sediment. - Where an uninterrupted zonation of sublittoral and littoral communities exist, the integrity of the ecological unit should be respected in the selection of sites. - A variety of subtidal topographic features are included in this habitat complex such as: Hydrothermal vent habitats, sea mounts, vertical rock walls, horizontal ledges, overhangs, pinnacles, gullies, ridges, sloping or flat bed rock, broken rock and boulder and cobble fields. Plants: North Atlantic including North Sea and Baltic Sea: - A large variety of red, brown and green algae (some living on the leaves of other algae). Atlantic (Cantabric Sea, Bay of Biscay): - Gelidium sesquipedale communities associated with brown algae (Fucus, Laminaria, Cystoseira), and red algae (Corallinaceae, Ceramiceae, Rhodomelaceae). Central Atlantic Islands (Macaronesian Islands) and Mediterranean: - Cystoseira/Sargassum beds with a mixture of other red algae (Gelidiales, Ceramiales), brown algae (Dictyotales) and green algae (Siphonales, Siphonacladales). Animals - reef forming species: North Atlantic including North Sea: - Polychaetes (e.g. Sabellaria spinulosa, Sabellaria alveolata, Serpula vermicularis), bivalves (e.g. Modiolus modiolus, Mytilus sp.) and cold water corals (e.g. Lophelia pertusa). Atlantic (Gulf of Cdiz): - Madreporarians communities: Dendrophyllia ramea community (banks), Dendrophyllia cornigera community (banks); white corals communities (banks), (Madrepora oculata and Lophelia pertusa community (banks). Solenosmilia variabilis community (banks). Gorgonians communities: Facies of Isidella elongata and Callogorgia verticillata and Viminella flagellum; Facies of Leptogorgia spp.; Facies of Elisella paraplexauroides; Facies of Acanthogorgia spp. and Paramuricea spp. Filigrana implexa formations. Central Atlantic Islands (Macaronesian Islands): - Warm water corals (Dendrophilia, Anthiphates), serpulids, polychaetes, sponges, hydrozoan and briozoan species together with bivalve molluscs (Sphondillus, Pinna). Baltic Sea: - Bivalves (e.g. Modiolus modiolus, Mytilus sp., Dreissena polymorpha). Mediterranean: - Serpulid polychaetes, bivalve molluscs (e.g. Modiolus sp. Mytilus sp. and oysters) Polychaetes (e.g. Sabellaria alveolata). South-West Mediterranean: - Dendropoma petraeum reefs (forming boulders) or in relation with the red calcareous algae Spongites spp or Litophyllum lichenoides. Filigrana implexa formations. Gorgonians communities: Facies of holoaxonia gorgonians (Paramuricea clavata forest, Eunicella
1)
2)
Page 13
singularis forest), mixed facies of gorgonians (Eunicella spp, P. clavata, E. paraplexauroides, Leptogorgia spp). Facies of Isidella elongata and Callogorgia verticillata; Facies of scleroaxonia gorgonians (Corallium rubrum). Madreporarians communities: Cladocora caespitosa reefs, Astroides calycularis facies. Madreporarians communities: Dendrophyllia ramea community (banks); Dendrophyllia cornigera community (banks); white corals communities (banks): Madrepora oculata and Lophelia pertusa community (banks). West Mediterranean: - Polychaetes (exclusively Sabellaria alveolata). Animals - non reef forming: North Atlantic including North Sea: - In general sessile invertebrates specialized on hard marine substrates such as sponges, anthozoa or cnidaria, bryozoans, polychaetes, hydroids, ascidians, molluscs and cirripedia (barnacles) as well as diverse mobile species of crustaceans and fish. Central Atlantic Islands (Macaronesian Islands): - Gorgonians, hydrozoans, bryozoan and sponges, as well as diverse mobile species of crustacean, molluscs (cephalopoda) and fish. Baltic Sea: - Distribution and abundance of invertebrate species settling on hard substrates are limited by the salinity gradient from west to east. Typical groups are: hydroids, ascidians, cirripedia (barnacles), bryozoans and molluscs as well as diverse mobile species of crustaceans and fish. Mediterranean: - Cirripedia (barnacles), hydroids, bryozoans, ascidians, sponges, gorgonians and polychaetes as well as diverse mobile species of crustaceans and fish. 3) Corresponding categories German classification : Benthal der Nordsee mit Hartsubstrat (010204), Riffe der Nordsee (010204a), Benthal der Flachwasserzone der Nordsee mit Hartsubstrat, makrophytenarm (030204), Benthal der Flachwasserzone der Nordsee mit Hartsubstrat, makrophytenreich (030206), Miesmuschelbank des Sublitorals der Nordsee (030207), Austernbank des Sublitorals der Nordsee (030208), Sabellaria-Riff des Sublitorals der Nordsee (030209), Felswatt der Nordsee (050104), Miesmuschelbank des Eulitorals der Nordsee (050107); Benthal der Ostsee mit Hartsubstrat (020204), Riffe der Ostsee (020204a), Benthal der Flachwasserzone der Ostsee mit Hartsubstrat, makrophytenarm (040204), Benthal der Flachwasserzone der Ostsee mit Kies- und Hartsubstrat, makrophytenreich (040206), Miesmuschelbank des Sublitorals der Ostsee (040207), Vegetationsreiches Windwatt mit Hartsubstrat (060203) (Ostsee). Barcelona Convention: Biocenosis of supralittoral rock (I.4.1.), Biocenosis of the upper mediolittoral rock (II.4.1.), Biocenosis of the lower mediolittoral rock (II.4.2.), Biocenosis of infralittoral algae (III.6.1.), Coralligenous (IV.3.1.), Biocenosis of shelf-edge rock (IV.3.3 ), Biocenosis of deep sea corals present in the Mediterranean bathyal (V.3.1.). The National Marine Habitat Classification for Britain and Ireland (Version 03.02): Littoral rock and other hard substrata (biotopes beginning with LR), Infralittoral rock and other hard substrata (biotopes beginning with IR), Circalittoral rock and other hard substrata (biotopes beginning with CR), Littoral biogenic reefs (biotopes beginning with LBR) and Sublittoral biogenic reefs (biotopes beginning with SBR). EUNIS classification: Relevant types within A1 Littoral rock and other hard substrata, A2.7 Littoral biogenic reefs, A3 Infralittoral rock and other hard substrata, A4 Circalittoral rock and other hard substrata, A5.6 Sublittoral biogenic reefs, A6.1 Deep-sea rock and artificial hard substrata, A6.6 Deep-sea bioherms, A6.7 Raised features of the deep-sea bed HELCOM classification: Sublittoral soft rock reefs of the photic zone with little or no macrophyte vegetation (2.1.1.2.3), Hydrolittoral soft rock reefs with or without macrophyte vegetation (2.1.1.3.3), Sublittoral solid rock reefs of the photic zone with or without macrophyte vegetation (2.1.2.2.3), Hydrolittoral solid rock reefs with or without macrophyte vegetation (2.1.2.3.3), Sublittoral stony reefs of the photic zone with or without macrophyte vegetation (2.2.2.3), Stony reefs of the hydrolittoral zone with or without macrophyte vegetation (2.2.3.3). Trilateral Wadden Sea Classification (von Nordheim et al. 1996): Sublittoral (old) blue mussel beds (03.02.07), Sublittoral oyster reefs (03.02.08), Sublittoral sabellaria reefs (03.02.09), Eulittoral (old) blue mussel beds (05.01.07), Benthic zone, stony and hard bottoms, rich in macrophytes, incl. artificial substrates (03.02.06), Benthic zone, stony and hard bottoms, few macrophytes (03.02.04).
Page 14
Nordic classification (Kustbiotoper i Norden, Nordiska Ministerrdet 2001): Klippbottnar (7.7.1.3; 7.7.2.3; 7.7.3.3; 7.7.4.3; 7.7.5.3; 7.8.1.3; 7.8.2.3; 7.8.3.4; 7.8.4.3; 7.8.5.3; 7.8.6.13; 7.8.7.16), Sublittorale samfund p sten- och klippebund (7.9.1.2), Sublittorale samfund p stenbund (7.9.2.2; 7.9.3.2). 4) Reefs can be found in association with vegetated sea cliffs (habitats 1230, 1240 and 1250) sandbanks which are covered by sea water all the time (1110) and sea caves (habitat 8830). Reefs may also be a component part of habitat 1130 estuaries and habitat 1160 large shallow inlets and bays Augier H. (1982). Inventaire et classification des biocnoses marines benthiques de la Mditerrane. Publication du Conseil de l Europe, Coll. Sauvegarde de la Nature, 25, 59 pages. Ballesteros E. (1988). Estructura de la comunitad de Cystoseira mediterranea Sauvageau en el Mediterraneo noroccidental. Inv. Pesq. 52 (3): 313-334. Ballesteros E. (1990). Structure and dynamics of the Cystoseira caespitosa (Fucales, Phaeophyceae) community in the North-Western Mediterranean. Scient. Mar. 54 (2): 155-168. Bellan-Santini D. (1985). The Mediterranean benthos: reflections and problems raised by a classification of the benthic assemblages. In: J.E. Treherne (Ed.) Mediterranean Marine Ecosystems pp. 19-48. Bianchi, C.N., Haroun, R., Morri, C. & Wirtz, P. (2000). The subtidal epibenthic communities off Puerto del Carmen (Lanzarote, Canary Islands). Arquiplago, Sup.2 (Part A): 145-155. Borja, A., Aguirrezabalaga, F., Martnez, J., Sola, J.C., GarcaArberas, L., & Gorostiaga (2003). Benthic communities, biogeography and resources management. In: Borja, A. & Collins, M. (Ed.). Ocenaography and Marine Environment of the Basque Country, Elsevier Oceanography Series n. 70: 27-50. Boudouresque C.F. (1969). Etude qualitative et quantitative dun peuplement algal Cystoseira mediterranea dans la rgion de Banyuls sur Mer. Vie Milieu 20: 437-452. Connor, D.W., Allen, J.H., Golding, N., Lieberknecht, L.M., Northen, K.O. & Reker, J.B. (2003). The National Marine Habitat Classification for Britain and Ireland Version 03.02. Internet version. Joint Nature Conservation Committee, Peterborough. (www.jncc.gov.uk/marine/biotopes/default.htm) European Environment Agency (2002). EUNIS habitat classification. Version 2.3. Copenhagen, EEA (Internet publication: http://mrw.wallonie.be/dgrne/sibw/EUNIS/home.html) Giaccone G. & Bruni A. (1972-1973). Le Cistoseire e la vegetazione sommersa del Mediterraneo. Atti dell Instituto Veneto de Scienze 81: 59-103. Gil-Rodrguez, M.C. & Haroun R.J. (2004). Litoral y Fondos Marinos del Parque Nacional de Timanfaya. En: Parques Nacionales Espaoles. MMA/Ed. Canseco, Madrid (en prensa). Haroun, R. Y Herrera R. (2001). Diversidad Taxonmica Marina En: J.M. Fernndez-Palacios y J.L. Martn Esquivel (Eds.), Naturaleza de las Islas Canarias. Ecologa y Conservacin, Ed. Turquesa, S/C de Tenerife, pp. 127-131. Helcom (1998). Red List of Biotopes and Biotope Complexes of the Baltic Sea, the Belt Sea and the Kattegat. Baltic Sea Environment Proceedings No. 75.: 126pp. Holt, T.J., Rees, E.I., Hawkins, S.J. & Seed, R. (1998). Biogenic Reefs (volume IX). An overview of dynamic and sensitivity characteristics for conservation management of marine SACs. Scottish Association for Marine Science (UK Marine SACs Project), 170 pp. (www.ukmarinesac.org.uk/biogenic-reefs.htm) Kautsky, N. (1974). Quantitative investigations of the red algae belt in the Ask area, Northern Baltic proper. Contrib. Ask Lab. Univ. Stockholm 3: 1-29. Montesanto B. & Panayotidis P. (2000). The Cystoseira spp. communities from the upper the Aegean Sea. J. mar. biol. Ass., U.K. 80:357-358. Von Nordheim, H., Norden Andersen, O. & Thissen, J. (Eds.) (1996). Red Lists of Biotopes, Flora and Fauna of the Trilateral Wadden Sea Area 1995. Helgol. Meeresuntersuchungen. 50 (suppl.): 136 pp. Nordiska Ministerrdet (2001). Kustbiotoper i Norden. Hotade och representativa biotoper. TemaNord 2001: 536. 345 pp.
5)
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Medina, M., Haroun, R.J. Y Wildpret, W., (1995). Phytosociological study of the Cystoseira abies-marina community in the Canarian Archipelago. Bull. Museu Mun. Funchal, Sup. 4: 433439. Panayotidis P., Diapoulis A., Varkitzi I. & Montesanto B. (2001). Cystoseira spp. used for the typology of the NATURA-2000 code 1170 (reefs) at the Aegean Sea (NE Mediterranean). Proceedings of the first Mediterranean Symposium on Marine Vegetation. Ajaccio 3-4 October 2000, pages 168-172. Pers J. M. & Picard J. (1964). Nouveau manuel de bionomie benthique de la mer Mditerrane. Rec. Trav. St. Mar. Endoume 31 (47): 5-137. Ravanko, O. (1968). Macroscopic green, brown and red algae in the south-western archipelago of Finland. Acta Bot. Fennica 79: 1-50. Riecken, U., Ries, U. & Ssymank, A. (1994). Rote Liste Der Gefhrdeten Biotoptypen Der Bundesrepublik Deutschland - Schriftenreihe fr Landschaftspflege und Naturschutz. 41: 184 pp
1180
PAL.CLASS.: 11.24
1)
2)
3)
4) 5)
Page 16
Hansen, J.M. (1988). Koraller i Kattegat, kortlgning. Miljministeriets, Skov- og Naturstyrelsen. Hovland M. & Judd A.G. (1988). Seabed Pockmarks and seepages: Impact on Geology, Biology and the Marine Environment. Graham & Trotman, London. 245pp. Jensen, P. et al. (1992). Bubbling reefs in the Kattegat: submarine landscapes of carbonatecemented rocks support a diverse ecosystem at methane seeps. Mar. Ecol. Prog. Ser., vol. 83:103112. Johnston, C. J., Turnbull, C. G. & Tasker, M. L. (2002). Natura 2000 in UK Offshore Waters: Advice to support the implementation of the EC Habitats and Birds Directives in UK offshores waters. JNCC Report 325. Jrgensen, N.O. et al (1989). Holocene methane-derived dolomite-cemented sandstone pillars from Kattegat, Denmark. Mar. Geol., vol. 88: 71-81. Jrgensen, N.O. at al (1990). Shallow hydrocarbon gas in the nothern Jutland-Kattegat region, Denmark. Bull. Geol. Soc., vol. 38: 69-76. Laier, T. et al. (1991). Kalksjler og gasudslip i Kattegat, seismisk kortlgning af omrdet nordvest for Hirsholmene. Miljministeriet, Danmarks Geologiske Undersgelse
1210
PAL.CLASS.: 17.2
1)
2)
3)
4)
5)
Page 17
1220
PAL.CLASS.: 17.3
1)
2)
3)
5)
Page 18
1230
PAL.CLASS.: 18.21
1)
2)
3)
5)
1240
PAL.CLASS.: 18.22
Vegetated sea cliffs of the Mediterranean coasts with endemic Limonium spp.
Vegetated cliffs and rocky shores of the Mediterranean, of the Mediterraneo-temperate eastern Atlantic (south-western Iberia) and of the Black Sea. Crithmo-Limonietalia Plants: Crithmum maritimum, Plantago subulata, Silene sedoides, Sedum litoreum, Limonium spp., Armeria spp., Euphorbia spp., Daucus spp., Asteriscus maritimus. Many Limonium species, in particular, are endemics of extremely local occurrence.
1) 2)
Page 19
1250
PAL.CLASS.: 18.23 and 18.24
1)
2)
1310
PAL.CLASS.: 15.1
1)
2)
Page 20
3)
Corresponding categories United Kingdom classification: "SM7 Arthrocnemum perenne stands", "SM8 Annual Salicornia saltmarsh", "SM9 Suaeda maritima saltmarsh" and "SM27 Ephemeral saltmarsh vegetation with Sagina maritima". Nordic classification: 15.11 - "4233 Salicornia strictissima-typ", "4252 Salicornia europaea-typ", "4253 Spergularia salina-typ". Ericson, L. & Wallentinus, H.-G. (1979). Sea-shore vegetation around the Gulf of Bothnia. Guide for the International Society for Vegetation Science, July-August 1977. Wahlenbergia 5:1-142. Sanda V. & Popescu A. (1991). La cnotaxonomie des phytocnoses halophyles (PuccinellioSalicornietrea Topa, 39) de Roumanie. (II). Rev.Roum de Biol., Sr.Bot.,
5)
1320
PAL.CLASS.: 15.2
1)
2) 3)
1330
PAL.CLASS.: 15.3
1) 2)
3)
Page 21
"SM17 Artemisia maritima community", "SM18 Juncus maritimus community", "SM19 Blysmus rufus saltmarsh community" and "SM20 Eleocharis uniglumis community". Nordic classification : 15.32 - "4231 Puccinellia maritima-typ", 15.33 - "422 vre landstrandens vegetation". 5) Burd, F. (1989). The saltmarsh survey of Great Britain. Peterborough, Nature Conservancy Council. Research and survey in nature conservation, no. 17. Johansson, D., Ekstam, U. & Forshed, N. (1986). Havstrandngar. LTs frslag, Stockholm, 96 pp.
1340
PAL.CLASS.: 15.4
1)
2)
3)
4)
1410
PAL.CLASS.: 15.5
1)
15.55 - halophilous marshes along the coast and the coastal lagoons (Puccinellion festuciformis) 15.57 - humid halophilous moors with the shrubby stratum dominated by Artemisia coerulescens (Agropyro-Artemision coerulescentis). Cyprus subtypes14 - Halophytic vegetation periodically inundated by saline or bracking water 2) Plants : Juncus maritimus, J. acutus, Carex extensa, Aster tripolium, Plantago cornuti, Scorzonera parviflora, Merendera sobolifera, Taraxacum bessarabicum, Samolus valerandi (15.51); Hordeum nodosum, H. maritimum Trifolium squamosum, T. michelianum, Alopecurus bulbosus, Carex divisa, Ranunculus ophioglossifolius, *Linum maritimum (15.52); Plantago crassifolia, Blackstonia imperfoliata, Centaurium tenuiflorum, Orchis coriophora ssp. fragans (15.53); Puccinellia fasciculata, Aeluropus littoralis, Juncus gerardii (15.54); Puccinellia festuciformis (15.55); Artemisia coerulescens (15.57). Eleocharis palustris, Puccinellia gigantea, Arthrocnemum macrostachyum, Aeluropus littoralis, Centaurium spicatum, Cressa cretica, Crypsis factorofskyi, Crypsis schoenoides, Glinus lotoides, Limonium echioides, Parapholis marginata, Schoenoplectus litoralis, Spergularia marina (= S. salina), Sphenopus divaricatus, Suaeda vera (Cyprus) Sanda, V., Popescu, A. (1992). Contribuii la cunoaterea structurii fitocenozelor de pe grindurile din Delta Dunrii. Ocrot. nat. med. nconj., 36(2): 129-136.
5)
1420
PAL.CLASS.: 15.6
1)
2)
3)
1430
PAL.CLASS.: 15.72
1)
14
A revised version of the Palaeartic classification which will include a better coverage of Cyprus is expected to be available in December 2001, this section may then need amending. Page 23
2)
Plants: Peganum harmala, Artemisia herba-alba, Lycium intricatum, Capparis ovata, Salsola vermiculata, S. genistoides, S. oppositifolia, Suaeda pruinosa, Atriplex halimus, A. glauca, Camphorosma monspeliaca, Haloxylum articulatum.
1510
PAL.CLASS.: 15.8
1)
2) 5)
1520
PAL.CLASS.: 15.9
1)
2)
1530
Page 24
1)
Pannonic and Ponto-Sarmatic salt steppes, salt pans, salt marshes and shallow salt lakes, which are highly influenced by a pannonic climate with extreme temperatures and aridity in summer. The enrichment of salt in the soil is due to high evaporation of ground water during summer. These habitat types are partly of natural origin and partly under a distinct influence of cattle grazing. The halophytic vegetation consists of plant communities on dry saltpans and steppes, humid salt meadows and annual plant communities of periodically flooded salt lakes with typical zonation. Plants: Artemisia santonicum, Suaeda corniculata, S. pannonica, Lepidium crassifolium, Puccinellia peisonis, Aster tripolium, Salicornia prostata, Camphorosma annua, Plantago tenuiflora, Juncus gerardii, Plantago maritima, Cyperus pannonicus, Pholiurus pannonicus, Festuca pseudovina,. Achillea collina, Artemisia pontica, Puccinellia limosa, Scorzonera cana, Petrosimonia triandra, Peucedanum officinale, Halocnemum strobilaceum, Frankenia hirsuta, Aeluropus littoralis, Limonium meyeri, Limonium gmelini, Nitraria shoberi, Carex distans, C. divisa, Taraxacum bessarabicum, Beckmannia eruciformis, Zingeria pisidica, Trifolium fragiferum, Cynodon dactylon, Ranunculus sardous, Agropyron elongatum, Halimione verrucifera (syn Obione verrucifera),. Lepidium latifolium, Leuzea altaica (syn L. salina), Iris halofila, Triglochin maritima, Hordeum hystrix, Aster sedifolius. Scorzonera austriaca var. mucronata, Kochia laniflora, Festuca arundinacea ssp. orientalis Animals: Molluscs- *Helicopsis striata austriaca; Insects- *Callimorpha quadripunctaria, #Lycaena dispar; Mammals- +Microtus oeconomus mehelyi, #Spermophilus citellus; Birds- Botaurus stellatus, Platalea leucorodia, Porzana parva, Ixobrychus minutus, Acrocephalus melanopogon, Aythya nyroca, Ardea purpurea, Panurus biarmicus. Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X) Mucina, L., Grabherr, G., Ellmauer,T. (1993). Die Pflanzengesellschaften sterreichs, Teil 1. Pop, I. (2002). Vegetaia solurilor srturoase din Romnia. Contrib. Bot., Cluj-Napoca, XXXV(2), 19992000: 285332. Soo, R. (1957). Systematische bersicht pannonischer Pflanzengesellschaften, Acta Bot. Acad. Sci. Hung., Budapest, 3:317-373. Wendelberger, G. (1954). Steppen, Trockenrasen und Wlder des pannonischen Raumes. Angew. Pflanzensoziol., Wien, Festschrift Aichinger: 573-634.
2)
5)
Page 25
PAL.CLASS.: 11.22, 11.23, 11.27, 11.28, 11.29, 16.122, 16.13, 16.132, 16.133, 17.21, 17.31, 19, 42C51 (1997 version)
1)
2)
4)
5)
1620
1)
2)
acre, Sedum telephium, Silene viscosa, Viola tricolor. Algae: Ceramium tenuicorne, Chorda filum, Cladophora glomerata, Cladophora rupestris, Fucus vesiculosus, Furcellaria lumbricalis, Pilayella littoralis. Animals:. Mammals- Halichoerus grypus, Phoca hispida; Birds- Alca torda, Arenaria interpres, Cepphus grylle, Larus fuscus, Stercorarius parasiticus, Sterna caspia, Uria aalge; CrustaceansBalanus improvisus, Idothea sp; Molluscs- Mytilus edulis 4) Often associated with the habitat type: Reefs (1170) and Perennial vegetation of stony banks (1220). 5) Eklund, O. (1931). -ber Ursachen der Regionalen Verteilung der Schrenflora SdwestFinnlands. Acta Botanica Fennica 8: 5-133. Hllfors, G. (1976).- The plant cover of some littoral biotopes at Krunnit (NE Bothnian Bay). Acta Univ. Oul. A, 42: 87-95. Luther, H. (1961).- Vernderungen in der Gefsspflanzenflora der Meeresfelsen von Tvrminne. Acta Botanica Fennica, 62: 1-100. Vartiainen, T. (1980).- Succession of island vegetation in the land uplift area of the northernmost Gulf of Bothnia, Finland. Acta Botanica Fennica, 115: 1-105. Waern, M. (1952)- Rocky-shore algae in the regrund archipelago. Acta Phytogeogr.Suecica 30: 1-298.
1630
1)
2)
5)
Siira, J. (1970).- Studies in the ecology of the sea-shore meadows at the Bothnian Bay with special reference to the Liminka area. Aquilo Ser. Bot. 9. Siira, j. (1984).- The vegetation and ecology of the primary saline soils of the Bothnian Bay. Aquilo Ser. Bot. 20.
Page 27
1640
1)
2)
3)
4)
5)
1650
PAL.CLASS.: 12.51 (1997 version)
1)
2)
4)
Page 28
5)
Lindholm, T. (1991).- Frn havsvik till insj. Miljfrlaget. bo, 160 pp. Luther, H. (1951).- Verbreitung und kologie der hheren Wasserpflanzen im Brackwasser der Ekens-Gegend in Sd-Finnland. I. Allgemeiner Teil. Acta Bot. Fennici, 49:1-232. & II. Specieller Teil. Acta Bot. Fennici, 50:1-370. Mathiessen, H. & Mathiessen, L. (1992).- Floristic aspects of one coastal inlet inre Verkviken, northern land. Acta Phytogeogr. Suecic., 78: 101-110. Niemi, . (1978).- Ecology of phytoplankton in the Tvrminne area, SW coast of Finland. III. Environmental conditions and primary production in Pojoviken in the 1970s. Acta Bot. Fennici, 106:1-28.
COASTAL SAND DUNES AND INLAND DUNES Sea dunes of the Atlantic, North Sea and Baltic coasts
2110
PAL.CLASS.: 16.211
1) 2)
3)
5)
2120
PAL.CLASS.: 16.212
Shifting dunes along the shoreline with Ammophila arenaria (white dunes)
Mobile dunes forming the seaward cordon or cordons of dune systems of the coasts (16.2121, 16.2122 and 16.2123). Ammophilion arenariae, Zygophyllion fontanesii. Plants: 16.2121- Ammophila arenaria, Eryngium maritimum, Euphorbia paralias, Calystegia soldanella, Otanthus maritimus, Leymus arenarius; 16.2122 - Ammophila arenaria, Echinophora spinosa, Eryngium maritimum, Euphorbia paralias, Cutandia maritima, Medicago marina, Anthemis maritima; 16.2123 - Zygophyllum fontanesii, Euphorbia paralias, Polycarpaea nivea, Cyperus capitatus, Ononis natrix, *Convolvulus caput-medusae, Polygonum maritimum, *Androcymbium psammophilum. Corresponding categories United Kingdom classification: " SD6 Ammophila arenaria mobile dune community".
1) 2)
Page 29
Nordic classification : 16.2121 - "4131 Ammophila arenaria-Leymus arenarius-typ". 5) Willers, T. (1988). Die Vegetation der finnischen Kstendnen. Norden 6:41-88.
2130
1)
2)
Plants: Aira spp., Anacamptis pyramidalis, Bromus hordeaceus, Carex arenaria, Cerastium spp., Corynephorus canescens, Erodium glutinosum, E. lebelii, Galium verum, Gentiana campestris, G. cruciata, Koeleria spp., Milium scabrum, Myosotis ramosissima, Ononis repens, Phleum arenarium, Polygala vulgaris var. dunensis, Silene conica, S. otites, Trifolium scabrum, Tuberaria guttata, Viola curtisii, V. rupestris var. arenaria; Mosses- Tortula ruraliformis; Lichens- Cladonia spp. Corresponding categories United Kingdom classification: 16.221 -"SD12 Carex arenaria-Festuca ovina-Agrostis capillaris grassland", "SD8 Festuca rubra-Galium verum fixed dune grassland", "SD7 Ammophila arenaria-Festuca rubra semi-fixed dune community" and "SD11 Carex arenariaCornicularia aculeata dune community". 16.226 - "SD9b Ammophila arenariaArrhenatherum elatius dune grassland Geranium sanguineum sub-community". 16.227 Page 30
3)
most likely, certain sub-communities of the type "SD7 Ammophila arenaria-Festuca rubra semi-fixed dune community" and "SD11 Carex arenaria-Cornicularia aculeata dune community". German classification: "1003 Dnenrasen (Graudne)", "1003a Dnenpionierrasen mit einjhr. Vegetation (Thero-Airion)", "1003b Dnenrasen mit geschlossener Narbe u. berwieg. ausdauernden Arten (Graudne)". Nordic classification: "4141 Corynephorus canescens-typ" and "4142 Festuca rubra-Hieracium umbellatum-typ". 4) There is a transition towards communities of Mesobromion (34.31 - 34) in the following cases: old mesophile grasslands of dune slacks and inner dunes (Anthyllido Thesietum), frequently in mosaic with communities of Salix repens and particularly developed on the west face of the dunes; grasslands with Himantoglossum hircinum of the dunes in the De Haan area. Dune scrubs (16.25) and humid dune slacks (16.3) with distinct vegetation form closely knit complexes with grey dunes devoid of ligneous vegetation. Andersson, D. (1950). The Scanian sand vegetation - a survey. Bot. Not. 1950:145-172. Curtis, T.G.F. (1991). The flora and vegetation of sand dunes in Ireland. In: A Guide to the Sand Dunes of Ireland (M.B. Quigley, Ed.). 42-46. European Union for Dune Conservation and Coastal Management. Dargie, T.C.D. (1993). Sand dune vegetation survey of Great Britain. Part II Scotland. JNCC, Peterborough. Doody, J.P. (1991). Sand Dune Inventory of Europe. JNCC, Peterborough and EUCC. Meshinev, T, V. Velchev, A. Petrova, I. Apostolova, P. Vassilev,1994. Flora and vegetation of the dunes in the Sunny Beach Resort. Sofia, 59 pp. Rivas-Martnez, S., Lous, M., Daz, T.E., Fernndez-Gonzlez, F. & Costa, J.C. (1990). La vegetacin del sur de Portugal (Sado, Alentejo y Algarve). Itinera Geobot. 3. 5 - 126. Tzonev, R., M. Dimitrov, V. Roussakova, 2005. Dune vegetation on the Bulgarian Black sea coast. Hacquetia, 4/1:7-32.
5)
2140
PAL.CLASS.: 16.23
1)
2) 3)
4) 5)
Page 31
Olsson, H. (1993). Dry coastal ecosystems of southern Sweden. In: van der Maarel, E. (ed.) Ecosystems of the world 2A. Dry coastal ecosystems, polar regions and Europe. Elsevier, Amsterdam. pp. 131-143.
2150
PAL.CLASS.: 16.24
1)
2) 3)
4)
2160
PAL.CLASS.: 16.251
1) 2)
2170
PAL.CLASS.: 16.26
1)
2) 3)
Page 32
4)
This habitat forms mosaics with other dune slack vegetation containing Salix arenaria but which is rich in bryophytes and referable to the Caricion davallianae (16.33), as well as mosaics with dune grasslands and with thickets with Rosa pimpinellifolia. This habitat is often invaded by Hippophae rhamnoides and Ligustrum vulgare. Anon. (1977). A study of the Raven, Co. Wexford. An Foras Forbartha/Forest and Wildlife Service, Dublin. Cotton, J. (1974). Pyrola rotundifolia L. in Co. Wexford (H12). Ir. Nat. J. 18, 44-46. Olsson, H. (1993). Dry coastal ecosystems of southern Sweden. In: van der Maarel, E. (ed.) Ecosystems of the world 2A. Dry coastal ecosystems, polar regions and Europe. Elsevier, Amsterdam, pp. 131-143.
5)
2180
1)
PAL.CLASS.: 16.29
2) 3)
4)
5)
2190
PAL.CLASS.: 16.3 = 16.31 to 16.35
1)
Page 33
Sub-types : 16.31 - Dune-slack pools (Charetum tomentosae, Elodeetum canadense, Hippuridetum vulgaris, Hottonietum palustris, Potametum pectinati): fresh-water aquatic communities (cf. 22.4) of permanent dune-slack water bodies. 16.32 - Dune-slack pioneer swards (Juncenion bufonii p.: Gentiano-Erythraeetum littoralis, Hydrocotylo-Baldellion): pioneer formations of humid sands and dune pool fringes, on soils with low salinity. 16.33 - Dune-slack fens: calcareous and, occasionally, acidic fen formations (cf. 54.2, 54.4, in particular 54.21, 54.2H, 54.49), often invaded by creeping willow, occupying the wettest parts of dune-slacks. 16.34 - Dune-slack grasslands: humid grasslands and rushbeds (see 37.31, 37.4) of dune-slacks, also often with creeping willows (Salix rosmarinifolia, S. arenaria). 16.35 - Dune-slack reedbeds, sedgebeds and canebeds: reedbeds, tall-sedge communities and canebeds (cf. 53.1, 53.2, 53.3) of dune-slacks. 3) Corresponding categories United Kingdom classification: "SD13 Salix repens-Bryum pseudotriquetrum dune slack community", "SD14 Salix repens-Campylium stellatum dune slack community", "SD15 Salix repens-Calliergon cuspidatum dune slack community", "SD16 Salix repens-Holcus lanatus dune slack community" and "SD17 Potentilla anserina-Carex nigra dune slack community". Olsson, H. (1993). Dry coastal ecosystems of southern Sweden. In: van der Maarel, E. (ed.) Ecosystems of the world 2A. Dry coastal ecosystems, polar regions and Europe. Elsevier, Amsterdam, pp. 131-143.
5)
21A0
PAL.CLASS.: 1A
Machairs ( * in Ireland)
Complex habitat comprised of a sandy coastal plain resulting partially from grazing and/or rotational cultivation, in an oceanic location with a cool, moist climate. The wind blown sand has a significant percentage of shell derived material, forming a lime rich soil with pH values normally greater than 7. Vegetation is herbaceous, with a low frequency of sand binding species. Plants: Cochlearia scotica, Dactylorhiza fuchsii ssp. hebridensis, Euphrasia marshallii, Festuca rubra, Galium verum, Lotus corniculatus, Plantago lanceolata, Poa pratensis, Trifolium repens. Lakes (ponds and small lakes in Scotland) of widely varying salinity, pH and chemical composition, transitions to saltmarsh and blanket bog are associated habitats. In the United Kingdom, twelve different types of vegetation under the National Vegetation Classification can be identified. Bassett, A. & Curtis, T.G.F. (1985). The nature and occurrence of sand-dune machair in Ireland. Proceedings of the Royal Irish Academy. 85B: 1 - 20. Curtis, T.G.F. (1991). The flora and vegetation of sand dunes in Ireland. In: A Guide to the Sand Dunes of Ireland (M.B. Quigley, Ed.). 42-46. European Union for Dune Conservation and Coastal Management. Ritchie, W. (1975). The meaning and definition of machair. Transactions of the Botanical Society of Edinburgh, 42, 431-440.
1)
2) 4)
5)
Page 34
2210
PAL.CLASS.: 16.223
1) 2)
2220
PAL.CLASS.: 16.224
1) 2)
2230
PAL.CLASS.: 16.228
1)
2)
2240
PAL.CLASS.: 16.229
1)
2)
Page 35
2250
PAL.CLASS.: 16.27 and 64.613
1)
2) 4)
5)
2260
PAL.CLASS.: 16.28
1)
2270
PAL.CLASS.: 16.29 x 42.8
1)
2) 4)
Page 36
2310
PAL.CLASS.: 64.1 x 31.223
1)
2) 3) 5)
2320
PAL.CLASS.: 64.1 x 31.227
1) 2) 3) 5)
2330
PAL.CLASS.: (64.11 or 64.12) x 35.2
1)
2) 3)
Page 37
United Kingdom classification : "SD11 Carex arenaria-Cornicularia aculeata dune community p.p." and "SD12 Carex arenaria-Festuca ovina-Agrostis capillaris grassland p.p.". Nordic classification : "4141 Corynephorus canescens-typ". 5) Olsson, H. (1974). Studies on South Swedish sand vegetation. Acta Phytogeogr. Suec. 60:1-170.
2340
PAL.CLASS.: 64.71
1)
2)
3) 4) 5)
3110
PAL.CLASS.: 22.11 x 22.31
Oligotrophic waters containing very few minerals of sandy plains (Littorelletalia uniflorae)
Shallow oligotrophic waters with few minerals and base poor, with an aquatic to amphibious low perennial vegetation belonging to the Littorelletalia uniflorae order, on oligotrophic soils of lake and pond banks (sometimes on peaty soils). This vegetation consists of one or more zones, dominated by Littorella, Lobelia dortmana or Isoetes, although not all zones may not be found at a given site. Plants: Isoetes lacustris, I. echinospora, Littorella uniflora, Lobelia dortmanna, Deschampsia setacea, Subularia aquatica, Juncus bulbosus, Pilularia globulifera, #Luronium natans, Potamogeton polygonifolius; in the Boreal region also Myriophyllum alterniflorum, Drepanocladus spp., Warnstorfia spp. and Fontinalis spp.
1)
2)
Page 38
3)
Corresponding categories German classification : "24020201 kalkarmer, oligotropher See des Tief- und Hgellands", "24020301 kalkarmes, oligotrophes, sich selbst berlassenes Abbaugewsser". Nordic classification: "6413 Lobelia dortmanna-Isoetes spp.typ", "6414 Littorella uniflora-Lobelia dortmanna-typ". In the Boreal region this habitat is particularly found on glacio fluvial soil and with usually dense isoetid vegetation, sparse reedbeds, helophytic vegetation and carpets of submerged bryophytes. This habitat is found in association with heath (31.1) and Nanocyperion (22.32) communities. In France and Ireland this habitat occurs, in particular, in heathland of sandy plains on podzols, where the water table occurs at the surface Mkirinta, U. (1978). Die Pflanzensoziologische Gliederung der Wasservegetation im See Kukkia, Sdfinnland. Acta Univ. Ouluensis Ser. A. Scientiae Rerum Naturalium Nr. 75, biologica Nr.5. Thunmark, S. (1931). Der See Fiolen und seine Vegetation. Acta Phytogeogr. Suecica. II:1-198.
4)
5)
3120
Oligotrophic waters containing very few minerals generally on sandy soils of the West Mediterranean with Isoetes spp.
Dwarf amphibious vegetation of oligotrophic waters with few minerals, mostly on sandy soils of the Mediterranean region and some irradiations in the thermo-Atlantic sector, and belonging to the IsoetoNano-Juncetea. Short grasslands of temporary ponds (the Annex I priority habitat type 3170) is a particular subtype (temporary and very shallow waters). Plant species: high level - Isoetes velata, I. setacea, Pilularia minuta, #Marsilea strigosa; low level Isoetes histrix, I. durieui, Serapias spp. (Serapion). Correspondances: In the Azores the corresponding association is Anthemido-Menthetum pulegii Lp., with Anthemis nobilis, Mentha pulegium, Juncus bulbosos, Hypericum humifusum, Scirpus setacea, Peplis portula, Isoetes azorica
1)
2)
3)
3130
Oligotrophic to mesotrophic standing waters with vegetation of the Littorelletea uniflorae and/or IsoetoNanojuncetea
22.12 x 22.31 - aquatic to amphibious short perennial vegetation, oligotrophic to mesotrophic, of lake, pond and pool banks and water-land interfaces belonging to the Littorelletalia uniflorae order. 22.12 x 22.32 - amphibious short annual vegetation, pioneer of land interface zones of lakes, pools and ponds with nutrient poor soils, or which grows during periodic drying of these standing waters: IsoetoNanojuncetea class. These two units can grow together in close association or separately. Characteristic plant species are generally small ephemerophytes.
Page 39
1)
2)
Plants: 22.12 x 22.31: Littorella uniflora, #Luronium natans, Potamogeton polygonifolius, Pilularia globulifera, Juncus bulbosus ssp. bulbosus, Eleocharis acicularis, Sparganium minimum. 22.12 X 22.32 : #Lindernia procumbens, Elatine spp., Eleocharis ovata, Juncus tenageia, Cyperus fuscus, C.flavescens, C.michelianus, Limosella aquatica, Schoenoplectus supinus, Scirpus setaceus, Juncus bufonius, Centaurium pulchellum, Centunculus minimus, Cicendia filiformis. Corresponding categories German classification : "240301 mesotropher See (Bleisee) (mit Zwergbinsenfluren -wechselnass-, P143)", "240306 meso- bis eutrophes, sich selbst berlassenes Abbaugewsser (mit Zwergbinsenfluren -wechselnass-, P143)". Nordic classification : "6411 Eleocharis acicularis-typ", "6412 Ranunculus reptans-Subularia aquatica-typ". in the Azores the corresponding association is Isoetetum azorica Lp. This habitat type could also develop in wet dune slacks (see 16.32 in 2190, included in Annex I). In the Atlantic region, such lakes can shelter glacial relict species, e.g. fish such as Selvelinus alpinus. Areas with a variable hydrological system, periodically lacking vegetation due to trampling, should not be included. Jenssen, S. (1979). Classification of lakes in southern Sweden on the basis of their macrophyte composition by means of multivariate methods. Vegetatio 39:129-146.
3)
4)
5)
3140
1)
2) 3)
5)
3150
Page 40
1)
Lakes and ponds with mostly dirty grey to blue-green, more or less turbid, waters, particularly rich in dissolved bases (pH usually > 7), with free-floating surface communities of the Hydrocharition or, in deep, open waters, with associations of large pondweeds (Magnopotamion). Plants: Hydrocharition - Lemna spp., Spirodela spp., Wolffia spp., Hydrocharis morsus-ranae, Stratiotes aloides, Utricularia australis, U. vulgaris, #Aldrovanda vesiculosa, Ferns (Azolla), Liverworts (Riccia spp., Ricciocarpus spp.); Magnopotamion - Potamogeton lucens, P. praelongus, P. zizii, P. perfoliatus. Corresponding categories Nordic classification : "632 Potamogeton spp.-huvudtyp", "6511 Lemna minor-Spirodela polyrrhiza-typ". Dahl, E., Kalliola, R., Marker, E. & Persson, . (1971). Nordisk vegetationsklassificering fr kartlggning. In: IBP i Norden 7. Universitetsforlaget, Oslo, pp. 3-12.
2)
3)
5)
3160
PAL.CLASS.: 22.14
1)
2)
3)
3170
PAL.CLASS.: 22.34
1)
2)
Page 41
batardae, #M. strigosa, Mentha cervina, Ranunculus dichotomiflorus, R. lateriflorus, Serapias lingua, S. neglecta, S. vomeracea. 3) Corresponding categories In the Azores the corresponding association is Anthemido-Menthetum pulegii Lp., with Anthemis nobilis, Mentha pulegium, Juncus bulbosos, Hypericum humifusum, Scirpus setacea, Peplis portula, Isoetes azorica.
3180
PAL.CLASS.: 22.5
* Turloughs
Temporary lakes principally filled by subterranean waters and particular to karstic limestone areas. Most flood in the autumn and then dry up between April and July. However, some may flood at any time of the year after heavy rainfall and dry out again in a few days; others, close to the sea, may be affected by the tide in summer. These lakes fill and empty at particular places. The soils are quite variable, including limestone bedrock, marls, peat, clay and humus, while aquatic conditions range from ultra oligotrophic to eutrophic. The vegetation mainly belongs to the alliance Lolio-Potentillion anserinae Tx. 1947, but also to the Caricion davallianae Klika 1934. Plants: Cinclidotus fontinaloides, Fontinalis antipyretica (Bryophyta). Animals: Tanymastix stagnalis (wet phase) and the beetles Agonum lugens, A. livens, Badister meridionalis, Blethisa multipunctata and Pelophila borealis (dry phase) 15. Coxon, C.E. (1986). A study of the hydrology and geomorphology of turloughs. Ph.D. Thesis, Trinity College, Dublin. Coxon, C.E. (1987). The spatial distribution of turloughs. Irish Geography. 20: 11 - 23. Goodwillie, R. (1992). Turloughs over 10 ha: vegetation survey and evaluation. A report for the National Parks and Wildlife Service of the Office of Public Works (unpublished). Macgowran, B. (1985). Phytosociological and ecological studies on turloughs in the west of Ireland. Ph.D. Thesis, National University of Ireland, Dublin. Praeger, R.L. (1932). The flora of turloughs: a preliminary note. Proceedings of the Royal Irish Academy. 41B: 37 - 45. Sykora, K.V. (1982). Lolio-Potentillion Communities in Ireland. Acta Botanica Neerlandica. 31(3): 185 - 199.
1)
2)
5)
3190
PAL.CLASS.: 22.12p
1)
15
The animals listed should not be regarded as characteristic in any strict sense; both fauna and flora of turloughs are characteristic of intermittently flooded zones.
Page 42
2)
Plants: Lemna trisulca, Chara globularis, Chara contraria, Warnstorfia exannulata, Ceratophyllum demersum, Potamogeton pectinatus, Potamogeton lucens, Schoenoplectus lacustris, Sparganium erectum These lakes are similar in some respects to 3180 Turloughs but that habitat is found in limestone not gypsum areas and does not support mats of green and purple bacteria
4)
31A0
PAL.CLASS.: 22.43113
*Transylvanian
1) 2)
Formations of Nymphaea lotus of geo-thermal waters (unit 66.94) of Petea Lake, western Romania. Plants Nymphaea lotus, Ceratophyllum demersum, Sparganium erectum ssp neglectum, Butomus umbellatus, Alisma plantago-aquatica, Phragmites australis. Animals: Molluscs (Gastropoda) Melanopsis parreyss, Fish Scardinius erythrophalmus racovitzae. Bnrescu, P. (1964). Fauna RPR. Pisces- Osteichthyes. Edit. Acad. RPR. XIII:355-356. Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X) Olteanu-Cozma, C. (1959). Biologia si ecologia plantei Nymphaea lotus L. var.thermalis (DC.)Tusz. de la Baile 1 Mai - Oradea. Ocr.Nat., 4 Hungarian examples (e.g. Budapest) are introductions.
5)
6)
Running water
Sections of water courses with natural or semi-natural dynamics (minor, average and major beds) where the water quality shows no significant deterioration
3210
PAL.CLASS.: -
1)
2)
Page 43
Petromyzon marinus, # Lampetra fluviatilis, Thymallus thymallus, # Cottus gobio s. lat., C. poecilobus, Leuciscus leuciscus, Phoxinus aphya
5)
Ericsson, S. (1985).- lvens miljer. In: lvboken . Fltbiologerna. Nilsson, Ch. (1978).- Vegetationens verlevnadsekologi p Gardikens regleringsstrnder - en problemorientering. Svensk Bot. Tidskr., 72: 227. Nilsson, Ch. (1979). - Florafrndringar vid kraftverksutbyggnad. Ibid. 73: 266. Nilsson, Ch. (1979). - Vegetationfrhllanden i kraftverkslvar. Ibid. 73: 257. Sjrs, H. (1973). - Om botaniska skyddsvrden vid lvarna. Rapport till SNV fr Utredningen rrande vattenkraftsutbyggnader i sdra Norrland och norra Svealand. Vxtbiol.inst.Uppsala.
3220
PAL.CLASS.: 24.221 and 24.222
1)
2)
3)
3230
PAL.CLASS.: 24.223 x 44.111
1)
2)
Page 44
3)
3240
PAL.CLASS.: 24.224 x 44.112
1)
2)
Page 45
3250
PAL.CLASS.: 24.225
1) 2)
3260
Water courses of plain to montane levels with the Ranunculion fluitantis and Callitricho-Batrachion vegetation
Water courses of plain to montane levels, with submerged or floating vegetation of the Ranunculion fluitantis and Callitricho-Batrachion (low water level during summer) or aquatic mosses. Plants: Ranunculus saniculifolius, R. trichophyllus, R. fluitans, R. peltatus, R. penicillatus ssp. penicillatus, R. penicillatus ssp. pseudofluitantis, R. aquatilis, Myriophyllum spp., Callitriche spp., Sium erectum, Zannichellia palustris, Potamogeton spp., Fontinalis antipyretica. Corresponding categories German classification : "23010101 naturnahes, kalkreiches Epi-/Metarhithral", "23010201 naturnahes, kalkarmes Epi-/Metarhithral", "23010301 naturnahes, kalkreiches Hyporhithral", "23010401 naturnahes, kalkarmes Hyporhithral", "23020101 naturnahes Epipotamal", "23010201 naturnahes Metapotamal", "23010301 naturnahes Hypopotamal" (mit flutenden Macrophyten, P138). Nordic classification : "6621 Myriophyllum alterniflorum-Potamogeton alpinus-Fontinalis antipyretica-typ". This habitat is sometimes associated with Butomus umbellatus bank communities. It is important to take this point into account in the process of site selection. Sjrs, H. (1967). Nordisk vxtgeografi. 2 uppl. Svenska Bokfrlaget Bonniers, Stockholm, 240 pp.
PAL.CLASS.: 24.4
1)
2)
3)
4)
5)
3270
PAL.CLASS.: 24.52
Rivers with muddy banks with Chenopodion rubri p.p. and Bidention p.p. vegetation
Muddy river banks of plain to submontane levels, with annual pioneer nitrophilous vegetation of the Chenopodion rubri p.p. and the Bidention p.p. alliances. During the spring and at the beginning of the summer, sites look like muddy banks without any vegetation (developes later in the year). If the conditions are not favourable, this vegetation has a weak development or could be completely absent.
Page 46
1)
2) 3)
Plants: Chenopodium rubrum, Bidens frondosa, Xanthium sp., Polygonum lapathifolium. Corresponding categories German classification : "230605 zeitweilig trockenfallende Schlammflche an flieenden Gewssern (krautreich, P026)", "230605 zeitweilig trockenfallende Schlammflche an flieenden Gewssern (krautreich, P026)". This habitat is found in close association with dense populations of the genus Bidens or of neophitic species. In order to support the conservation of these communities, with a late or irregular annual development, it is important to take into account bank widths of 50 to 100 m and even parts without vegetation (24.51).
4)
3280
Constantly flowing Mediterranean rivers with PaspaloAgrostidion species and hanging curtains of Salix and Populus alba
Nitrophilous annual and perennial grass and sedge formations of the alluvial banks of large Mediterranean rivers, with Paspalum paspaloides, P. vaginatum, Polypogon viridis (= Agrostis semiverticillata), Cyperus fuscus, and hanging curtains of Salix spp and Populus alba. Plants: Paspalum paspaloides, P. vaginatum, Polypogon viridis (= Agrostis semiverticillata), Cyperus fuscus, Salix spp., Populus alba.
PAL.CLASS.: 24.53
1)
2)
3290
PAL.CLASS.: 24.16 and 24.53
1)
2)
32A0
PAL.CLASS.: 24.423
1)
Page 47
2)
Plants: Eucladium verticillatum, Didymion tophaceus, D. bosniacus, Cinclidotus aquaticus, C. riparius, Bryum bentricosum, Fontinalis antipyretica, Cratoneuron commutatum, Platyhypnidium rusciforme, Aneura pinguis, Pellia fabbronianas. Animals: Polycelis cornuta, Planaria gonocephala, Ancylus fluviatilis, Propanus volki, Rivulogammarus balcanicus, Fontogammarus dalmatinus, Wilhelmia salopiensis. Corresponding categories Croatian classification: "A.3.5 Sedrotvorne rijene zajednice" and A.3.6 Sedrotvorna vegetacija na slapovima". Similar vegetation can also occur with habitat type 7220 *Petrifying springs with tufa formation (Cratoneurion) but that habitat type is associated with springs not rivers. Horvat, I., Glavac, V. & Ellenberg, H. (1974). Vegetation Sd-Osteuropas. Stuttgart, pp. 768. Dravni zavod za zatitu prirode (2009). Nacionalna klasifikacija stanita Republike Hrvatske (III. dopunjena verzija) http://www.dzzp.hr/dokumenti_upload/20100527/dzzp201005271405280.pdf
3)
4)
5)
4010
PAL.CLASS.: 31.11
1) 2) 3)
4020
PAL.CLASS.: 31.12
* Temperate Atlantic wet heaths with Erica ciliaris and Erica tetralix
Hygrophilous heaths of areas with a temperate oceanic climate, on semi-peaty or dried-out soils, with surface minerals in the case of peaty soils (hydromor), with vegetation of the alliances Genistion micrantho-anglicae and Ulicion minoris: Ulici minoris-Ericetum ciliaris, Ulici gallii-Ericetum mackaianae, Ulici minoris-Ericetum tetralicis (Schwickerath 33 Tuxen 37), Cirsio filipenduli-Ericetum ciliaris. Plants: Centaurea uliginosa, Erica ciliaris, E. mackaiana, E. tetralix, Euphorbia polygaliphylla, Genista anglica, G. carpetana, G. micrantha, Sphagnum spp., Ulex minor var. lusitanicus.
Page 48
1)
2)
3)
Corresponding categories United Kingdom classification: "H3 Ulex minor-Agrostis heath", "H4 Ulex galli-Agrostis heath" and "M16 Erica tetralix-Sphagnum compactum" where these contain Erica ciliaris.
4030
PAL.CLASS.: 31.2
1)
2)
3)
Page 49
4040
PAL.CLASS.: 31.234
1) 2) 3)
4050
PAL.CLASS.: 31.3
1)
2)
4) 5)
4060
PAL.CLASS.: 31.4
1)
Page 50
31.43 - Mountain dwarf juniper scrub. Juniperion nanae, Pino-Juniperion sabinae p., PinoCytision purgantis p. Usually dense formations of prostrate junipers of the higher levels of southern Palaearctic mountains. 31.44 - High mountain Empetrum-Vaccinium heaths. Empetro-Vaccinietum uliginosi. Dwarf heaths dominated by Empetrum hermaphroditum, Vaccinium uliginosum, with Arctostaphylos alpina, Vaccinium myrtillus, Vaccinium vitis-idaea and lycopodes (Huperzia selago, Diphasiastrum alpinum), mosses (Barbilophozia lycopodioides, Hylocomium splendens, Pleurozium schreberi, Rhythidiadelphus triquetrus) and lichens (Cetraria islandica, Cladonia arbuscula, Cladonia rangiferina, Cladonia stellaris, Cladonia gracilis, Peltigera aphthosa) of the sub-alpine belt of the Alps, the Carpathians, the Pyrenees, the Central Massif, the Jura, the Northern Apennines, characteristic of relatively windswept, snow-free stations, in frostexposure situations that are, however, less extreme than those prevailing where communities of 31.41 dominate. Unlike the formations of 31.41, those of 31.44 are clearly two-layered. 31.45 - Boreo-alpine heaths Alpine heaths of the highlands and islands of Scotland, alpine and lowland boreal heaths of Iceland, alpine heaths of boreal mountains, in particular of the mountains of Scandinavia, of the Urals, of the mountains of Siberia, alpine heaths of Far Eastern mountains at, or just south of, the limits of the boreal zone, with Juniperus nana, Loiseleuria procumbens, Empetrum hermaphroditum, Arctostaphylos uva-ursi, Arctostaphylos alpina and elements of Alpine flora. 31.46 - Bruckenthalia heaths. 31.47 - Alpide bearberry heaths. Mugo-Rhodoretum hirsuti p., Juniperion nanae p., i.a. Mats of Arctostaphylos uva-ursi or Arctostaphylos alpina of the alpine, sub-alpine and locally, montane, belts of the Alps, the Pyrenees, the northern and central Apennines, the Dinarids, the Carpathians, the Balkan Range, the Rhodopides (south to the Slavianka-Orvilos, the Menikion, the Pangeon, the Falakron and the Rhodopi), the Moeso-Macedonian mountains (including Athos), the Pelagonides (south to the Greek Macedonian border ranges Tzena, Pinovon and Kajmakchalan) and Olympus, in the Thessalian mountains, mostly on calcareous substrates. 31.48 - Hairy alpenrose-erica heaths. Mugo-Rhodoretum hirsuti p. Forest substitution heaths, treeline fringe formations and alpine heaths or mats of calcareous soils in the Alps and the Dinarides, with Rhododendron hirsutum, Rhododendron intermedium, Rhodothamnus chamaecistus and Erica herbacea, often accompanied by Clematis alpina, Daphne striata, Daphne mezereum, Globularia cordifolia, Arctostaphylos uva-ursi. Rhododendron hirsutum and, mostly in the Austrian Alps, Erica herbacea are the most frequent dominants; other shrubs can locally play that role. Arctostaphylos spp.-dominated facies have, however, been included in 31.47. 31.49 - Mountain avens mats Dwarf heaths formed by mats of the woody Dryas octopetala in high Palaearctic mountains, in boreal regions and in isolated Atlantic coastal outposts. 31.4A - High mountain dwarf bilberry heaths Vaccinium-dominated dwarf heaths of the sub-alpine belt of southern mountains, in particular, of the northern and central Apennines, the Balkan Range, the Helenides, the Pontic Range and the Caucasus, with Vaccinium myrtillus, Vaccinium uliginosum s.l., Vaccinium vitis-idaea and, locally, Empetrum nigrum. They are richer in grassland species than the communities of 31.44 and often take the appearance of alpine grassland with dwarf shrubs. Vaccinium myrtillus also plays a much more dominant role, in lieu of Vaccinium uliginosum and Empetrum hermaphroditum. 31.4B - High mountain greenweed heaths Low Genista spp. or Chamaecytisus spp. heaths of the sub-alpine, low alpine or montane belts of high southern nemoral mountains, in particular of the southern Alps, the Apennines, the Dinarides, the southern Carpathians, the Balkan Range, the Moeso-Macedonian mountains, the Pelagonides, the northern Pindus, the Rhodopides, the Thessalian mountains. 2) Plants: 31.41 - Loiseleuria procumbens, Vaccinium spp.; 31.42 - Rhododendron ferrugineum; 31.44 - Empetrum hermaphroditum, Vaccinium uliginosum; 31.45 - Juniperus nana, Loiseleuria procumbens, Empetrum hermaphroditum, Arctostaphylos uva-ursi, Arctostaphylos alpina; in Fennoscandia also Betula nana, Cassiope tetragona, Cornus suecica, Juniperus communis,
Page 51
Phyllodoce caerulea, Vaccinium myrtillus and Cladonia alpestris; 31.47 - Arctostaphylos uva-ursi, Arctostaphylos alpina; 31.48 - Rhododendron hirsutum, Rhododendron intermedium, Rhodothamnus chamaecistus and Erica herbacea; 31.49 - Dryas octopetala; 31.4A - Vaccinium myrtillus, Vaccinium uliginosum s.l., Vaccinium vitis-idaea; 31.4B - Genista radiata, G. holopetala, G. hassertiana, Chamaecytisus eriocarpus, C. absinthioides. 3) Corresponding categories United Kingdom classification: "H13 Calluna vulgaris-Cladonia arbuscula heath", "H14 Calluna vulgaris-Racomitrium lanuginosum heath", "H15 Calluna vulgaris-Juniperus communis ssp. nana heath", "H17 Calluna vulgaris Arctostaphylos alpinus heath", "H19 Vaccinium myrtillus-Cladonia arbuscula heath", "H20 Vaccinium myrtillus-Racomitrium lanuginosum heath" and "H22 Vaccinium myrtillus-Rubus chamaemorus heath". Nordic classification: "11 Snfria vindhedar", "121 Hedvegetation p fattigt underlag", "122 Hedvegetation p rikt/kalkrikt underlag", "1311 Cassiope hypnoides-Salix herbacea typ", "1321 Salix polaris typ". Haapasaari, M. (1988). The oligotrophic heath vegetation of northern Fennoscandia and its zonation. Acta Bot. Fennica 135:1-219. Oksanen, L. & Virtanen, R. (1995). Topographic, altitudinal and regional patterns in continental and suboceanic heath vegetation of northern Fennoscandia. Acta Bot. Fennica 153:1-80.
5)
4070
PAL.CLASS.: 31.5
1)
2) 3) 5)
4080
1)
31.6214 - Pyreneo-Cantabric willow brush Subalpine, alpine and occasionally montane Salix dominated brushes and low scrubs of the Pyrenees and the Cordillera Cantabrica. 31.6215 - Hercynio-Carpathian willow brush Subalpine, alpine and occasionally montane Salix dominated brushes and low scrubs of the Carpathians and the eastern Hercynian ranges of the Sudeten (Salicetum lapponum, Salici silesiacae-Betuletum carpaticae [p.], Piceo-Salicetum silesiacae [i.a.]). 31.622 - Boreo-Alpine willow brush Subarctic willow formations of the Highlands of Scotland, of the mountains of Iceland and of the boreal mountains of Scandinavia. 2) 3) Plants: Salix lapponum, S. lanata, S. arbuscula, S. myrsinites, S. glauca, S. helvetica, S. bicolor. Corresponding categories United Kingdom classification: "W20 Salix lapponum-Luzula sylvatica scrub". Nordic classification: "127 Videvegetation".
4090
PAL.CLASS.: 31.7
1)
Page 53
Lava-colonising formations with cushions of Astragalus granatensis ssp. siculus, Berberis aetnensis, Juniperus hemisphaerica, Genista aetnensis, Adenocarpus bivonae, Viola aethnensis. 31.77 - Madonie and Apennine hedgehog-heaths Hedgehog-heaths formed by Astragalus spp. or Genista spp., of the mountains of the southern Italian peninsula and Sicily, except Etna. 31.78 - Helleno-Balkanic sylvatic Astragalus hedgehog-heaths Hedgehog-heaths occupying situations peripheral to the main range of the alti- and oroMediterranean hedgehog-heath communities of high Hellenic mountains (31.79 and 31.7A), mostly dominated by Astragalus angustifolius, characteristic, in particular, of zoogenous clearings within the forest belt of southern Greek mountains and of regions of irradiation of Mediterranean communities within the hills and mountains of the Moesian zone. 31.79 - Hellenic oro-Mediterranean hedgehog-heaths. Daphno-Festucetea: Eryngio-Bromion p. Hedgehog-heaths developed on relatively humus-rich rendziniform soils at or above treeline, in the 1700-2200 m altitudinal range of high Greek mountains; hedgehog-heath facies of associated grasslands; similar, impoverished formations descending into the forest belts of the same mountains, with the exception of those of the Peloponnese, where they are replaced by distinctive formations, listed under 31.78. 31.7A - Hellenic alti-Mediterranean hedgehog-heaths. Daphno-Festucetea: Astragalo-Seslerion Shrubby formations of the high mountains of the Peloponnese, of the southern mainland Greek mountains and of the Thessalian Olympus system, colonising the altitudinal range immediately above that occupied by the communities of 31.79, as well as stony slopes with shallow soil, loose screes and humus-deficient soils within the main 1700-2200 m range of these communities. Included are true spiny hedgehog-heaths, cushiony formations of dwarf suffrutescents and bush-dominated facies of stripped grasslands. Astragalus angustifolius, Acantholimon androsaceum, Astragalus lacteus, Convolvulus cochlearis, Rindera graeca, Aster alpinus, Globularia stygia, Minuartia stellata, Erysimum pusillum, Thymus teucrioides, Alyssum kionae, Paronychia kapela, Thymus hirsutus, Anthyllis aurea, Achillea ageratifolia, Sideritis scardica, Linum flavum, Thymus boissieri, Sesleria caerulans are characteristic. 31.7B - Cretan hedgehog-heaths. Saturejetea spinosae Hedgehog-heaths of high mountains of Crete, in the 1500-2500 m altitudinal range, with Astragalus creticus ssp. creticus, A. angustifolius, Acantholimon androsaceum, Atraphaxis billardieri, Berberis cretica, Chamaecytisus creticus, Daphne oleoides, Prunus prostrata, Euphorbia acanthothamnos, Verbascum spinosum, Sideritis syriaca, Satureja spinosa, Asperula idaea, Rhamnus prunifolius, Pimpinella tragium, Acinos alpinus. 31.7C - Aegean summital hedgehog-heaths Isolated, endemic-rich, mostly summital hedgehog-heaths of calcareous mountains of Aegean islands and Mount Athos. 31.7D - Southern Hellenic Genista acanthoclada hedgehog-heaths Formations dominated by hemispherical shrubs of Genista acanthoclada of the middle levels (about 800 - 1200 m) of mountains and plateaux of the Peloponnese. 31.7E - Astragalus sempervirens hedgehog-heaths Astragalus sempervirens ssp. sempervirens, ssp. muticus, ssp. cephalonicus formations of the southern Alps, the eastern Pyrenees, Iberia, the Apennines and Greece, transitional between the alpine and sub-alpine heaths of 31.4 and the true Mediterranean hedgehog-heaths of 31.7. 31.7F - Canarian cushion-heaths. Spartocytision nubigeni Open formations dominated by broom-like plants of the montane zone (above 1900 m) of the Canary Islands, with many endemic species. 2) Plants: 31.71 - Echinospartum horridum; 31.72 - Echinospartum lusitanicum ssp. barnadesii, E. ibericum ssp. pulviniformis; 31.73 - Erinacea anthyllis, Vella spinosa, Astragalus sempervirens ssp. nevadensis, A. granatensis ssp. granatensis (A. boissieri), Ptilotrichum spinosum, Bupleurum spinosum, Genista baetica; 31.74 - Erinacea anthyllis, Vella spinosa, Andryala agardhii, Convolvulus boissieri, Hippocrepis squamata ssp. eriocarpa, Pterocephalus spathulatus, Thymus granatensis; 31.75 - Astragalus sirinicus ssp. genargenteus, Rosa seraphini, Anthyllis hermanniae, Thymus herba-barona, Cerastium boissieri, Genista salzmannii, G. corsica, Berberis aetnensis, Prunus prostrata, Daphne oleoides; 31.76 - Astragalus granatensis ssp. siculus, Berberis aetnensis, Juniperus hemisphaerica, Genista aetnensis, Adenocarpus bivonae, Viola aethnensis;
Page 54
31.77 - Astragalus granatensis ssp. nebrodensis, A. parnassi ssp. calabrus, A. sirinicus ssp. sirinicus, Genista cupanii, G. sylvestris ssp. dalmatica; 31.78 - Astragalus angustifolius; 31.79 Astragalus creticus ssp. rumelicus, A. parnassi, A. angustifolius; 31.7A - Astragalus angustifolius, Minuartia stellata; 31.7B - Astragalus creticus ssp. creticus, A. angustifolius, Chamaecytisus creticus; 31.7C - Astragalus creticus var. samius, A. pilodes, A. trojanus var. chius, A. parnassi, A. p. var. samothracius, A. monachorum; 31.7D - Genista acanthoclada; 31.7E - Astragalus sempervirens ssp. sempervirens, A. s. ssp. muticus, A. s. ssp. cephalonicus; 31.7F - Spartocytisus supranubius, Adenocarpus viscosus var. spartioides.
40A0
1)
2)
Plants: Amygdalus nana (syn Prunus tenella), Cerasus fruticosa, C. mahaleb, Spiraea media, Rosa spinosissima, R. gallica, R. pimpinellifolia, Amelanchier ovalis, Cornus mas, Crataegus monogyna, Acer tataricum, Cotoneaster integerrimus, C. tomentosus, C. matrensis, C. niger, Allium sphaerocephalon, Anemone sylvestris, Asparagus officinalis, Buglossoides purpurcaerulea, Geranium sanguineum, Peucedaunum carvifolia, Teucrium chamaedrys, Aster linosyris, Inula ensifolia, Inula hirta, Melica picta, Nepeta pannonica, Peucedanum cervaria, Phlomis tuberosa, Jurinea mollis, Vinca herbacea, Verbascum austriacum, Salvia austriaca, Stipa dasyphylla, Aconitum anthora, Chrysanthemum corymbosum, Vincetoxicum hirundinaria, Waldsteinia geoides, Syringa vulgaris, Euonymus verrucosus, Viburnum lantana, Spiraea chamaedryfolia, S. crenata, Fraxinus ornus, Paliurus spina-christi, Jasminum fruticans, Syringa josikaea, Genista radiata, Sorbus dacica, Sorbus aria, Sorbus cretica, Paeonia peregrina, Teucrium polium, Asplenium rutamuraria, Ceterach officinarum. Corresponding categories
Page 55
3)
Hungarian classification: continental deciduous steppe thickets (identification code: M6), continental deciduous rock thickets (identification code: M7), white-oak shrub woodlands (identification code: M1) 5) Borhidi, A. & Snta, A. (eds.) (1999). Vrs Knyv Magyarorszg nvnytrsulsairl. 1-2. (Red Book of Hungarian Plant Communities.Vols. 1-2). TermszetBVR Kiad, Budapest, pp. 768 (in Hungarian) Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X) Raiu O. & Gergely I. (1979). Caracterizarea sinecologic a principalelor fitocenoze lemnoase din Tara Oaului (jud. Satu Mare). Contrib. Bot., Cluj-Napoca, 85118. Zlyomi, B. (ed.) (1967). Guide der Exkursionen des Internationalen Geobotanischen Symposium. Ungarn. Eger-Vcrtt, 95p.
40B0
PAL.CLASS.: 31.636
1)
2)
5)
40C0
PAL.CLASS.: 31.8B7
1)
2)
5)
Page 56
5110
PAL.CLASS.: 31.82
Stable xerothermophilous formations with Buxus sempervirens on rock slopes (Berberidion p.p.)
Stable xerothermophilous and calcicolous scrubs dominated by Buxus sempervirens, of hill and montane levels. These formations correspond to xerothermophilous Buxus thickets with their fringe associations of the Geranion sanguinei alliance on calcareous or siliceous substratum. They also constitute the natural woodland edge of calcareous dry forests rich with Buxus. In the euro-siberian region, the more open formations are rich in submediterranean plant species. Syntaxa: Berberidion p.p., Amelanchiero-Buxion Plants: Buxus sempervirens, Prunus spinosa, Prunus mahaleb, Cornus mas, Crataegus spp., Berberis vulgaris, Ligustrum vulgare, Viburnum lantana, Amelanchier ovalis, Geranium sanguineum, Dictamnus albus. Corresponding categories German classification : "410103 Gebsch trocken-warmer Standorte (Berberitzen-, Felsenmispel-, Felsenbirnen-, Sanddorngebsch etc) (mit Buxus sempervirens, P036b). Succession phase of calcareous grasslands toward mixed deciduous forests, for example with Quercus pubescens or continental pine forests with Pinus sylvestris (the word "stable" concerns those formations which are practically at climax stage, but on very superficial soils where natural succession towards forest can not take place). These communities are associated with calcareous grasslands, mixed oak or Quercus pubescens groves, beech groves rich in orchid species or with Pinus nigra and Pinus leucodermis (e.g. in Greece).
1)
2)
3)
4)
5120
PAL.CLASS.: 31.842
1)
2)
Page 57
5130
PAL.CLASS.: 31.88
1)
2)
3)
5)
5140
PAL.CLASS.: 32.2B
1) 2)
5)
Page 58
5210
PAL.CLASS.: 32.131 to 32.136
1)
2)
5220
PAL.CLASS.: 32.17
1)
2)
5)
16 17
42.A5 - Syrian juniper woods : Juniperus drupacea woods of the northern slopes of Mount Parnon and of the Karlik mountain in Thrace, Greece. Part of the formation takes the appearance of an arborescent matorral, listed under 32.135. 42.A2 - Spanish juniper woods (Juniperion thuriferae) : Forest formations dominated by Juniperus thuriferae of Spain, southern France and Corsica and North Africa. Many communities may be better described as arborescent matorrals, and listed under 32.136; geographical divisions can nevertheless be retained by appending the suffixes of 42.A2 to 32.136.
Page 59
Peinado, M., Acaraz, F. & Martnez Parras, J.M. (1992). Vegetation of South-eastern Spain. Flora et Vegetatio Mundi. 10: 1 - 487.
5230
PAL.CLASS.: 32.18
1) 2)
3)
5310
PAL.CLASS.: 32.216
1)
2)
5320
PAL.CLASS.: 32.217
1)
2)
Page 60
5330
1)
18
Communities dominated by hummocks of very tall stands of Lotus tree Zyziphius lotus, are included in the Annex I priority habitat 'Matorral with Zyziphius' (32.17). Page 61
West Mediterranean formations dominated by retamas (Lygos spp.) or by large, non-spiny thermo-Mediterranean brooms of genera Cytisus and Genista, limited to the Iberian peninsula, the Balearics, Mediterranean North Africa, Sicily and its associated islands, the Cilento coast of Campania. 32.441p - Spiny spurge garrigues Euphorbia melitensis garrigues of Malta 2) Plants: 31.21G - G. fasselata; 31.8B5p - Crataegus azarolus var. aronia; 32.22 - Euphorbia dendroides; 32.23 - Ampelodesmos mauritanica; 32.24 - Chamaerops humilis; 32.25 - Ziziphus lotus, Maytenus senegalensis var. europaeus, Periploca laevigata ssp. angustifolia, Salsola webbii, Sideretis foetens, Ulex argentatus ssp. erinaceus, Genista umbellata; 32.26 - Lygos sphaerocarpa, L. monosperma, L. raetam ssp. gussonei, Genista cinerea ssp. speciosa, G. valentina, G. spartioides ssp. retamoides, G. s. ssp. pseudoretamoides, G. haenseleri, G. ramosissima, G. ephedroides, G. dorycnifolia, Cytisus aeolicus. 32.441 Euphorbia melitensis.
Phrygana 19
5410
PAL.CLASS.: 33.1
1)
2)
5420
PAL.CLASS.: 33.3
1)
2)
19
Cushion-forming thermo-Mediterranean sclerophyllous formations, often thorny and summer deciduous. They are best developed in the eastern Mediterranean, where they may occupy considerable surfaces in coastal areas and occasionally inland. They also include a few rare, relict associations of the west Mediterranean, mostly characteristic of the edge of seashores and of maritime cliffs, where they constitute an often narrow belt between the cliff communities and thermoMediterranean brushes, incorporating, in addition to characteristic, often endemic or very rare, hemispherical cushionforming species, an admixture of species belonging to these two vegetation complexes.
Page 62
Ononis spinosa, Helichrysum italicum ssp. microphyllum, Helichrysum italicum ssp. italicum, Phagnalion graecum.
5430
PAL.CLASS.: 33.4 to 33.A
1)
2)
Page 63
6110
PAL.CLASS.: 34.11
1)
2) 3)
4)
6120
PAL.CLASS.: 34.12
1) 2)
3)
4) 5)
6130
PAL.CLASS.: 34.2, 36.44
Page 64
1)
Generally open natural or semi-natural grasslands 1) on natural rock outcrops, rich in heavy metals (e.g. zinc, lead), 2) river gravels and shingles, 3) on old terrils or spoil heaps around mines. These open grasslands are characterised by a highly specialised flora, with subspecies and ecotypes adapted to heavy metals. The threatened endemic taxa are generally absent from the pioneer vegetation of younger terrils. This pioneer vegetation is not considered to be a priority. Plants: Viola calaminaria and metallophyte races of Thlaspi caerulescens, Armeria maritima, Minuartia verna, Silene vulgaris, Festuca ophioliticola, Cochleria alpina sensu lato. Corresponding categories German classification : "3405a natrliche und halbnatrliche Schwermetallrasen". United Kingdom classification: "OV37 Festuca ovina-Minuartia verna community". Seminatural sites are to be taken into account mainly if natural sites are very rare or absent from a region or, if these sites shelter characteristic or outstanding plant species. Birse E.L. (1982). Plant communities on serpentine in Scotland. Vegetatio, 49 141-162.
2)
3)
4)
5)
6140
PAL.CLASS.: 36.314
1)
2)
6150
1)
2) 3)
5)
Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X)
6160
PAL.CLASS.: 36.361
1)
2)
6170
1)
Page 66
36.44 - Alpine heavy metal communities: included in habitat 6130 'Calaminarian grasslands (Violetalia calaminariae)', 36.37 - Oro-Corsican grasslands Grasslands of the subalpine (oro-Mediterranean) and alpine levels of the highest mountains of Corsica. 36.38 - Oro-Apennine closed grasslands Mesophile, closed, short turfs of the subalpine and alpine levels of the southern and central Apennines, developed locally above treeline, on calcareous substrates. 2) Plants: 36.41 to 36.43 - Dryas octopetala, Gentiana nivalis, Gentiana campestris, Alchemilla hoppeana, Alchemilla conjuncta, Alchemilla flabellata, Anthyllis vulneraria, Astragalus alpinus, Aster alpinus, Draba aizoides, Globularia nudicaulis, Helianthemum nummularium ssp. grandiflorum, Helianthemum oelandicum ssp. alpestre, Pulsatilla alpina ssp. alpina, Phyteuma orbiculare, Astrantia major, Polygala alpestris; 36.37 - Plantago subulata ssp. insularis, Sagina pilifera, Armeria multiceps, Paronychia polygonifolia, Bellardiochloa violacea, Phleum brachysrachyum, Geum montanum, Sibbaldia procumbens, Veronica alpina; 36.38 - Festuca violacea ssp. macrathera, Trifolium thalii. Corresponding categories United Kingdom classification: "CG12 Festuca ovina-Alchemilla alpina-Silene acaulis dwarf-herb heath", "CG13 Dryas octopetala-Carex flacca heath", "CG14 Dryas octopetala-Silene acaulis ledge community". Nordic classification: "123 Lgrtvegetation p rikt/kalkrikt underlag". Romanian classification: "R3401-Pajiti sud-est carpatice de Asperula capitata i Sesleria rigida", "R3402-Pajiti sud-est carpatice de Helictotrichon decorum", "R3601-Pajiti sud-est carpatice de rogoz pitic (Kobresia myosuroides) i Oxytropis carpatica", "R3605-Pajiti sud-est carpatice de piu cu coli (Festuca versicolor) i Sesleria rigida ssp. haynaldiana", "R3606-Pajiti sud-est carpatice de piu de stnci (Festuca saxatilis) ", "R3607-Pajiti sud-est carpatice de Festuca amethystina i Dianthus tenuifolius", "R3611Pajiti sud-est carpatice de coada iepurelui (Sesleria rigida ssp. haynaldiana) i rogoz (Carex sempervirens) ", "R3612-Pajiti sud-est carpatice de rogoz (Carex sempervirens) i coarn mare (Sesleria bielzii) ", "R3613-Pajiti sud-est carpatice de Carduus kerneri, Festuca carpatica i Trisetum fuscum", "R3614-Pajiti sud-est carpatice de Festuca xanthina" Bringer, K.-G. (1961). Den lgalpina Dryas-hedens differentiering och stndortsekologi inom Tornetrsk-omrdet. 1-2. Sven. Bot. Tidskr. 55:349-375, 551-584. Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X)
3)
5)
6180
PAL.CLASS.: 38.5
1) 2)
Page 67
6190
PAL.CLASS.: 34.35
1)
2)
Plants: Festuca pallens, Bromus pannonicus, Stipa eriocaulis, S. joannis, S. pulcherrima, Carex humilis, Chrysopogon gryllus, Iris pumila, Pulsatilla grandis, Alyssum montanum, Helianthemum nummularium agg., Globularia punctata, Anacamptis pyramidalis. Seseli leucospermum, Linum dolomiticum, Vincetoxicum pannonicum, Draba lasiocarpa, Dianthus regis-stephani, Biscutella laevigata agg., Polygala amara, Daphne cneorum, Paronychia cephalotes, Sesleria sadleriana, Festuca amethystina Corresponding categories Hungarian classification: Calcareous open rock grasslands (identification code: G2)", "Acidophilous open rock grasslands (identification code: G3)", "Closed rock grasslands (identification code: H1)". Dolomitic grasslands are stable associations preserving many relict species, which may persist for several thousand years. They are in contact with karst shrub (Cotino-Quercetum pubescentis) and karstic beech woods (Orno-Fagetum). During primary succession the limestone and siliceous rock grasslands become closed and form transition to slope steppe vegetation (Festucion rupicolae), then rock shrub vegetation (Spiraeion mediae) and thermophile oak woods (Corno-Quercetum) and rock forests (Tilio-Fraxinetum). Borhidi, A. & Snta, A. (eds.) (1999). Vrs Knyv Magyarorszg nvnytrsulsairl. 1-2. (Red Book of Hungarian Plant Communities.Vols. 1-2. TermszetBVR Kiad, Budapest, pp. 768 (in Hungarian) Zlyomi, B. (1966). Neue Klassifikation der Felsenvegetation im pannonischen Raum und angrentenden Gebiete. Bot. Kzlem.53. 49-54
3)
4)
5)
Page 68
6210
Semi-natural dry grasslands and scrubland facies on calcareous substrates(Festuco-Brometalia) ( * important orchid sites)
Dry to semi-dry calcareous grasslands of the Festuco-Brometea. This habitat is formed on the one hand by steppic or subcontinental grasslands (Festucetalia valesiacae) and, on the other, by the grasslands of more oceanic and sub-Mediterranean regions (Brometalia erecti); in the latter case, a distinction is made between primary Xerobromion grasslands and secondary (semi-natural) Mesobromion grasslands with Bromus erectus; the latter are characterised by their rich orchid flora. Abandonment results in thermophile scrub with an intermediate stage of thermophile fringe vegetation (Trifolio-Geranietea). Important orchid sites should be interpreted as sites that are important on the basis of one or more of the following three criteria: (a) the site hosts a rich suite of orchid species (b) the site hosts an important population of at least one orchid species considered not very common on the national territory (c) the site hosts one or several orchid species considered to be rare, very rare or exceptional on the national territory. Plants: Mesobromion - Anthyllis vulneraria, Arabis hirsuta, Brachypodium pinnatum, Bromus inermis, Campanula glomerata, Carex caryophyllea, Carlina vulgaris, Centaurea scabiosa, Dianthus carthusianorum, Eryngium campestre, Koeleria pyramidata, Leontodon hispidus, Medicago sativa ssp. falcata, Ophrys apifera, O. insectifera, Orchis mascula, O. militaris, O. morio, O. purpurea, O. ustulata, O. mascula, Polygala comosa, Primula veris, Sanguisorba minor, Scabiosa columbaria, Veronica prostrata, V. teucrium. Xerobromion - Bromus erectus, Fumana procumbens, Globularia elongata, Hippocrepis comosa. Festucetalia valesiacae: Adonis vernalis, Euphorbia seguierana, Festuca valesiaca, Silene otites, Stipa capillata, S. joannis. Animals: Papilio machaon, Iphiclides podalirius (Lepidoptera); Libelloides spp., Mantis religiosa (Neuroptera). Corresponding categories United Kingdom classification : "CG1 Festuca ovina-Carlina vulgaris grassland", "CG2 Festuca ovina-Avenula pratensis grassland", "CG3 Bromus erectus grassland", CG4 Brachypodium pinnatum grassland", "CG5 Bromus erectus-Brachypodium pinnatum grassland", "CG6 Avenula pubescens grassland", " CG7 Festuca ovina-Hieracium pilosella-Thymus praecox/pulegioides grassland", "CG8 Sesleria albicans-Scabiosa columbaria grassland", "CG9 Sesleria albicans-Galium sterneri grassland". In France the following sub-types are found: 34.31 - Subcontinental (Euro-Siberian and eastern) grasslands of the inner Alps stretching perhaps to Alsace (Stipo capillatae-Festucenea valesiacae Gaultier 89 prov.); 34.32 - Sub-Atlantic xerocline calcicolous grasslands [Mesobromenalia erecti Royer 87 (IX 212: Brometalia erecti Br-Bl. 36)]; 34.33 Sub-Atlantic xerophile calcicolous grasslands (Xerobromenalia erecti Royer 87); 34.34 Central European calcareo-siliceous grasslands generally established on hyperxerothermophile sands, partly denuded (Koelerio macranthae-Phleion phloeidis Korneck 74 (Koelerio macranthae-Phleenalia phloeidis (Korneck 74) Royer 87. German classification: "340101 submediterraner Trockenrasen auf karbonatischem Unterground", "34020301 subkontinentaler Halbtrockenrasen auf karbonatischem Boden, gemht", "34020102 submediterraner Halbtrockenrasen auf karbonatischem Boden, beweidet Mhweide", "34020103 submediterraner Halbtrockenrasen auf karbonatischem Boden, brachgefallen", "340103 subkontinentaler Trockenrasen auf karbonatischem Untergrund",
1)
2)
3)
Page 69
"34020101 submediterraner Halbtrockenrasen auf karbonatischem Boden, gemht", "34020302 subkontinentaler Halbtrockenrasen auf karbonatischem Boden, beweidet Mhweide", "34020303 subkontinentaler Halbtrockenrasen auf karbonatischem Boden, brachgefallen", "3403 natrlicher Steppenrasen (kontinental, auf tiefgrndigem Boden)". Nordic classification: Avenula pratensis-Artemisia oelandica-variant of "5213 Avenula pratensisFragaria viridis-Filipendula vulgaris-typ" 4) 5) Often in association with scrubland and thermophile forests and with dry pioneer Sedum meadows (Sedo-Scleranthea). Albertsson, N. (1950). Das grosse sdliche Alvar der Insel land. Eine Pflanzensoziologische bersicht. Sven. Bot. Tidskr. 44:269-331.
6220
PAL.CLASS.: 34.5
1)
2)
6230
* Species-rich Nardus grasslands, on siliceous substrates in mountain areas (and submountain areas, in Continental Europe)
Closed, dry or mesophile, perennial Nardus grasslands occupying siliceous soils in Atlantic or sub-Atlantic or boreal lowland, hill and montane regions. Vegetation highly varied, but the variation is characterised by continuity. Nardetalia: 35.1-Violo-Nardion (Nardo-Galion saxatilis, Violion caninae); 36.31- Nardion. Species-rich sites should be intrepreted as sites with are remarkable for a high number of species. In general, the habitats which have become irreversibly degraded through overgrazing should be excluded. Plants: Antennaria dioica, Arnica montana, Campanula barbata, Carex ericetorum, C. pallescens, C. panicea, Festuca ovina, Galium saxatile, Gentiana pneumonanthe, Hypericum maculatum, Hypochoeris maculata, Lathyrus montanus, Leontodon helveticus, Leucorchis albida, Meum
1)
2)
Page 70
athamanticum, Nardus stricta, Pedicularis sylvatica, Platanthera bifolia, Polygala vulgaris, Potentilla aurea, P. erecta, Veronica officinalis, Viola canina. Animals: Miramella alpina. 3) Corresponding categories The habitat sub-types belonging to the Nardion alliance shows a strong regional differentiation: Alps and Pyrenees - Geo-montani-Nardetum, Black Forest - Leontodonto-Nardetum, Harz Pulsatillo micranthae-Nardetum, Bayerischer Wald - Lycopodio-Nardetum. In the United Kingdom, the habitat covers the most species-rich sites of the types "CG10 Festuca ovina-Agrostis capillaris-Thymus praecox" and "CG11 Festuca ovina-Agrostis capillaris-Alchemilla alpina grass heath". German classification : "34060101 gemhter Borstgrasrasen der planaren bis submontanen Stufe", "34060102 beweideter Borstgrasrasen der planaren bis submontanen Stufe (incl. Mhweide)", "34060103 brachgefallener Borstgrasrasen der planaren bis submontanen Stufe", "34060201 gemhter Borstgrasrasen der montanen bis hochmontanen Stufe", "34060202 beweideter Borstgrasrasen der montanen bis hochmontanen Stufe (incl. Mhweide)", "34060203 brachgefallener Borstgrasrasen der montanen bis hochmontanen Stufe". Nordic classification : "5133 Nardus stricta-typ" and "5233a Carex nigra-Carex panicea-Nardus stricta-variant". Sjrs, H. (1967). Nordisk vxtgeografi. 2 uppl. Svenska Bokfrlaget Bonniers, Stockholm, 240 pp.
5)
6240
PAL.CLASS.: 34.315
1)
2)
3)
5)
6250
PAL.CLASS.: 34.91
Page 71
1)
Grassland communities rich in perennial grasses and herbs on loess deposits. Originally covering large areas, nowadays restricted to specific land forms like loess ridges formed by fluviatile erosion and accumulation. Plants: Artyemisia pontica, Astragalus vesicarius, A. austriacus, A. onobrychis, Crambe tataria, Nonea pulla, Salvia nemorosa, Ornithogalum pannonicum, Agropyron pectinatum, Phlomis tuberosa, Bromus inermis, Festuca rupicola, Falcaria vulgaris, Peucedanum alsaticum, Elymus hispidus, Chamaecytisus supinus, Achillea pannonica.. Corresponding categories Syntaxa for Austria: Astragalo excapi-Crambetum tatarici. Mucina, L., Grabherr, G., Ellmauer, T. (1993). Die Pflanzengesellschaften sterreichs, Teil 1. Anthropogene Vegetation. Gustav Fischer, Jena.Stuttgart. New York. pp 578.
2)
3) 5)
6260
PAL.CLASS.: 34.A1, 34.A2
1)
2)
3)
5)
Page 72
6270
1)
2)
3)
6280
1)
2)
3)
Corresponding categories Nordic vegetation types: 5151 Sedum album-Tortella spp. -type, 5152 Festuca ovina-Tortella spp. -type and 5213c Avenula pratensis-Artemisia oelandica -variant Albertson, N. (1950).- Das grosse sdliche Alvar der Insel land. Svensk Bot. Tidskrift, 44: 269331. Pettersson, B. (1958).- Dynamik och konstans i Gotlands flora och vegetation. Acta Phytogeogr. Suec. 40. Rosn, E.L (1982).- Vegetation development and sheep grazing in limestone grassland of south land, Sweden. Acta Phytogeogr. Suec., nr 72.
5)
62A0
1)
PAL.CLASS.: 34.75
2)
62B0
PAL.CLASS.:
1)
2)
Page 74
62C0
PAL.CLASS.: 34.92
*Ponto-Sarmatic steppes
Steppes of the plains, plateau and hills of the western Black Sea, west of the Dniester and the basins, including those of the lower Danube, of Transylvania and of northern Thrace, of the southern edge and valleys of the Podolian plateau, of the Central Russian plateau, of the Volga plateau, of Orenburg and of Bachkiria, with grasses such as Stipa capillata, S. lessingiana, Kochia prostrata, Koeleria lobata (Koeleria degeni), Festuca valesiaca, Dichanthium ischaemum (syn Bothriochloa ischaemum). Includes vegetation in the alliances Festucion valesiacae, Stipion lessingianae, Agropyro-Kochion and Pimpinello-Thymion zygoidi Plants: Festucion valesiacae: Poa angustifolia, Festuca valesiaca, Chrysopogon gryllus, Alyssum saxatile, Agropyron pectiniformae, Koeleria macrantha, Dichanthium ischaemum, Stipa capillata, Stipa ucrainica, Elymus hispidus; Stipion lessingianae: Stipa lessingiana,S. pulcherrima, S. joannis, Vinca herbacea, Salvia nutans, Cephalaria uralensis, Teucrium polium, Iris pumila, Bromus barcensis, Euphorbia dobrogensis, Crambe tataria; Artemisio-Kochion: Kochia prostrata; Pimpinello-Thymion zygioidi: Agropyron brandzae, Thymus zygioides, Artemisia caucasica, Artemesia pedemontana, Koeleria lobata, Artemisia lerchiana, Festuca callieri, Sedum hillebrandtii, Polythricum piliferum, Melica ciliata, Dianthus nardiformis, Dianthus pseudarmeria, Satureja coerulea, Pimpinella tragium ssp. lithophila. Sometimes in association with 40C0 Ponto-Sarmatic deciduous thickets (31.8B7) and 91AA Eastern white oak woods (41.73) Sanda, V.& Arcus, M., 1999- Sintaxonomia gruparilor vegetale din Dobrogea i Delta Dunarii, Ed. Cultura, Pitesti. Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X)
1)
2)
4)
5)
62D0
PAL.CLASS.: 36.39
1)
Page 75
2)
Plants : Festuca airoides, Festuca balcanica, Festuca nigrescens, Festuca paniculata, F. riloensis, Festuca valida, Bellardiochloa violacea, Calamagrostis arundinacea, Sesleria comosa, Aquilegia aurea, Lilium jankae, Gentiana lutea, Gentiana punctata, Viola rhodopaea, Primula deorum, Carex bulgarica Bondev, I. 1991. The vegetation of Bulgaria. Map 1:600000 with explanatory text. St. Kliment Ohridski University Press, Sofia : 183p. (in Bulgarian) Meshinev, T., Apostolova, I., Kachaunova, E., Velchev, V. & I. Bondev, 2000. Flora and plant communirties. In: Popov, A., Meshinev, T. (eds) High mountain treeless zone of the Central Balkan National Park. Biological diversity and problems of its conservation. Sofia, BSBCP : 1337.. Rousakova, V. 2000. Vegetation alpine et sous alpine superiore de la montagne de Rila (Bulgarie). Braun-Blanquetia, 25: 132
5)
6310
PAL.CLASS.: 32.11 x 91.2
1)
2)
6410
PAL.CLASS.: 37.31
1)
Page 76
2)
Plants: 37.311 - Molinia caerulea, Dianthus superbus, Selinum carvifolia, Cirsium tuberosum, Colchicum autumnale, Inula salicina, Silaum silaus, Sanguisorba officinalis, Serratula tinctoria, Tetragonolobus maritimus; 37.312 - Viola persiciflora, V. palustris, Galium uliginosum, Cirsium dissectum, Crepis paludosa, Luzula multiflora, Juncus conglomeratus, Ophioglossum vulgatum, Inula britannica, Lotus uliginosus, Dianthus deltoides, Potentilla erecta, P. anglica, Carex pallescens. Corresponding categories United Kingdom classification: "M26 - Molinia caerulea-Crepis paludosa fen meadow" and "M24 Molinia caerula-Cirisum dissectum fen meadow type" ("M23 - Juncus effusus/acutiflorusGalium palustre rush pasture" and "M25 - Molinia caerulea-Potentilla erecta mire" are excluded). German classification: "35020102 Pfeifengraswiese auf kalkreichen Standort". Nordic classification: "5233 Carex nigra-Carex panicea-Molinea caerulea-typ", "5234 Carex flacca-Primula farinosa-Orchis spp.-typ" and "5235 Molinia caerulea-typ". In some regions, these grasslands are in close contact with Nardetalia communities. For the Molinia meadows of river valleys, a transition toward Cnidion dubii alliance is observed. Ekstam, U., Aronsson, N. & Forshed, N. (1988). ngar. Om naturliga slttermarker i ngslandskapet. LTs frlag, Stockholm, 209 pp.
3)
4)
5)
6420
PAL.CLASS.: 37.4
1) 2)
Page 77
6430
PAL.CLASS.: 37.7 and 37.8
Hydrophilous tall herb fringe communities of plains and of the montane to alpine levels
37.7 - Wet and nitrophilous tall herb edge communities, along water courses and woodland borders belonging to the Glechometalia hederaceae and the Convolvuletalia sepium orders (Senecion fluviatilis, Aegopodion podagrariae, Convolvulion sepium, Filipendulion). 37.8 - Hygrophilous perennial tall herb communities of montane to alpine levels of the BetuloAdenostyletea class. Plants: 37.7 - Glechoma hederacea, Epilobium hirsutum, Senecio fluviatilis, Filipendula ulmaria, Angelica archangelica, Petasites hybridus, Cirsium oleraceum, Chaerophyllum hirsutum, Aegopodium podagraria, Alliaria petiolata, Geranium robertianum, Silene dioica, Lamium album, Lysimachia punctata, Lythrum salicaria, Crepis paludosa; 37.8 - Aconitum lycoctonum (A. vulparia), A. napellus, Geranium sylvaticum, Trollius europaeus, Adenostyles alliariae, Peucedanum ostruthium, Cicerbita alpina, Digitalis grandiflora, Calamagrostis arundinacea, Cirsium helenioides. Corresponding categories United Kingdom classification: "U17 - Luzula sylvatica-Geum rivale tall herb community". German classification: "390101 krautiger Ufersaum an besonnten Gewssern", "39050101 feuchter Staudensaum der planaren bis submontanen Stufe", "390102 krautiger Ufersaum an beschatteten Gewsern (z.B. mit Cardamine amara, Bitteres Schaumkraut)", "35020203 nhrstoffreiche, Feucht- bzw. Nagrnlandbrache der planaren bis submontanen Stufe", "35020303 nhrstoffreiche, Feucht- bzw. Nagrnlandbrache der planaren bis hochmontanen Stufe", "39050201 montane bis hochmontane Hochstaudenflur", "39050202 montane bis hochmontane Hochgrasflur (Calamagrostion arundinaceae)", "6701 subalpine bzw. alpine Hochstaudenflur (Alpen)". Nordic classification: "126 Hgrtngsvegetation". Similar communities to 37.8, with a weak development, occur at lower altitude along rivers and forest borders (in Wallonia -Belgium for example). Nitrophilous edge communities comprising only basal, common species in the region have no conservation priority. These tall herb communities could also develop in wet meadows, let lie fallow, without any cutting. Large areas of wet meadows let lie fallow and neophyte communities with Helianthus tuberosus, Impatiens glandulifera, should not be taken into account. Dahl, E. (1987). Alpine-subalpine plant communities of South Scandinavia. Phytocoenologia 15:455-484. Larsson, A. (1976). Den sydsvenska fuktngen. Vegetation, dynamic och sktsel. Medd. Avd. Ekol. Bot. Lund 31.
1)
2)
3)
4)
5)
6440
PAL.CLASS.: 37.23
1)
Page 78
2)
Plants: Cnidium dubium (C. venosum), Viola persicifolia, Scutellaria hastifolia, Allium angulosum Oenanthe lachenalii, Gratifolia officinalis, Carex praecox var. suzae, Juncus atratus, Lythrum virgatum. Corresponding categories German classification : "35020201 nrrstoffreiche, extensive Feucht- bzw. Nawiese der planaren bis submontanen Stufe", "35020202 nrrstoffreiche, extensive Feucht- bzw. Nawiese der planaren bis submontanen Stufe (incl. Mhweide)", "350204 Flutrasen". This is a transition habitat between wet and dry meadows and which cover small areas. This point has to taken into account during site selection.
3)
4)
6450
PAL.CLASS.: -
1)
2)
4)
5)
6460
PAL.CLASS.:
1)
Page 79
and Poa pratensis, and by a few endemic species occuring only at the high altitude damp places in the Troodos mountains 3) Plants:. Calamagrostis epigejeos, Juncus littoralis, Poa pratensis, Polypogon semiverticillatus, Ornithogalum chionopilum, Pteridium aquilinum, Viola siechiana, Alyssum cypricum, Brachypodium firmifolium, Hypericum perforatum, Scirpoides holoschoenus, Crocus cyprius (proposed for Annex II and IV), Schoenus nigrigans, Carex divulsa, Carex distans, Taraxacum holmboei.
Mesophile grasslands
6510
PAL.CLASS.: 38.2
1)
2)
3)
4) 5)
Page 80
6520
PAL.CLASS.: 38.31
1)
2)
3)
5)
6530
PAL.CLASS.: -
1)
2)
5)
Hggstrm, C.-A. (1988).- Protection of wooded meadows in land - problems, methods and perspectives. Oulanka Reports, 8:88-95.
6540
PAL.CLASS.: 37.63
1)
2)
3)
5)
7110
PAL.CLASS.: 51.1
1)
2)
Chamaedaphne calyculata, Calluna vulgaris, Ledum palustre and Sphagnum angustifolium. Scheuchzerietalia palustris p., Utricularietalia intermedio-minoris p., Caricetalia fuscae p.- Carex fusca, C. limosa, Drosera anglica, D. intermedia, Eriophorum gracile, Rhynchospora alba, R. fusca, Scheuchzeria palustris, Utricularia intermedia, U. minor, U. ochroleuca; in the Boreal region also Sphagnum balticum and S. majus. Animals: Dragonflies- Leucorrhinia dubia, Aeshna subartica, A. caerulea, A. juncea, Somatochlora arctica, S. alpestris; Butterflies- Colias palaeno, Boloria aquilonaris, Coenonympha tullia, Vacciniina optilete, Hypenodes turfosalis, Eugraphe subrosea; Spiders- Pardosa sphagnicola, Glyphesis cottonae; Ants- Formica transkaucassia; Cricket/Grasshopper- Metrioptera brachyptera, Stethophyma grossum. 3) Corresponding categories United Kingdom classification: "M1 Sphagnum auriculatum bog pool community", "M3 Eriophorum angustifolium bog pool community", "M18 Erica tetralix-Sphagum papillosum raised and blanket mire", "M20a Eriophorum vaginatum blanket and mixed mire - species poor sub community". German classification: "360101 Hochmoor der planaren bis submontanen Stufe", "360102 Hochmoor der montanen bis hochmontanen Stufe". Nordic classification: "312 Ristuvvegetation", "313 Fastmattevegetation", "314 Mjukmatte-och lsbottenvegetation" and "311 Skogmossvegetation" when comprising a part of the mire complexe. In order to support the conservation of this ecosystem over its geographic range and its genetic diversity, marginal areas of lower quality as a result of damage or degradation which abut active raised bogs may need to be included, protected and, where practicable, regenerated. There are very few intact or near-intact raised bogs in Europe, except in Finland and Sweden where active raised bogs are the predominant mire complex type in hemiboreal and southern boreal regions. Curtis, J.R. (in press). The raised bogs of Ireland: their ecology, status and conservation. Government Publications, Dublin. Eurola, S., Hicks, S. & Kaakinen, E. (1984). Key to Finnish Mire Types. Moore, J.J. (1968). A classification of the bogs and wet heaths of northern Europe (Oxycocco-Sphagnetea Br.-Bl. et Tx. 1943). In: Pflanzensoziologische Systematik. Bericht ber das internationale Symposium in Stolzenau/Weser 1964 der Internationale Vereinigung fr Vegetationskunde (R.Tuxen, Ed.). Junk, Den Haag. 306 - 320. Nature Conservation Council (1989). Guidelines for the selection of biological SSSI's. Nature Conservation Council , Peterborough. Oswald, H. (1923). Die Vegetation des Hochmoores Komosse. Sv. Vxtsociol. Sllsk. Handl. 1:1436. Schouten, M.C.G. (1984). Some aspects of the ecogeographical gradient in Irish ombrotrophic bogs. Peat Congress, Dublin. 1: 414 - 432. Tuxen, R., Miyawaki, A. & Fujiwara, K. (1972). Eine erweiterte Gliederung der Oxycocco-Sphagnetea. In: Grundfragen und Methoden in der Pflanzensoziologie. (R.Tuxen, Ed.). Junk, Den Haag. 500 - 520.
4)
5)
7120
PAL.CLASS.: 51.2
1)
capable of natural regeneration will include those areas where the hydrology can be repaired and where, with appropriate rehabilitation management, there is a reasonable expectation of reestablishing vegetation with peat-forming capability within 30 years. Sites unlikely to qualify as SACs are those that consist largely of bare peat, that are dominated by agricultural grasses or other crops, or where components of bog vegetation have been eradicated by closed canopy woodlands. 5) Malmer, N. (1965). The southern mires. Acta Phytogeogr. Suec. 50:149-158.
7130
PAL.CLASS.: 52.1 and 52.2
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2)
3)
4)
5)
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Moore, J.J. (1968). A classification of the bogs and wet heaths of northern Europe (Oxycocco-Sphagnetea Br.-Bl. et Tx. 1943). In: Pflanzensoziologische Systematik. Bericht ber das internationale Symposium in Stolzenau/Weser 1964 der Internationale Vereinigung fr Vegetationskunde (R.Tuxen, Ed.). Junk, Den Haag. 306 - 320. Nature Conservation Council (1989). Guidelines for the selection of biological SSSI's. Nature Conservation Council , Peterborough. Tuxen, R., Miyawaki, A. & Fujiwara, K. (1972). Eine erweiterte Gliederung der Oxycocco-Sphagnetea. In: Grundfragen und Methoden in der Pflanzensoziologie. (R.Tuxen, Ed.). Junk, Den Haag. 500 - 520.
7140
PAL.CLASS.: 54.5
1)
2)
3)
4) 5)
Page 85
7150
PAL.CLASS.: 54.6
1)
2)
Page 86
7160
PAL.CLASS.: 54.11(1997 version)
1)
2)
3)
5)
Calcareous fens
7210
PAL.CLASS.: 53.3
*Calcareous fens with Cladium mariscus and species of the Caricion davallianae
Cladium mariscus beds of the emergent-plant zones of lakes, fallow lands or succession stage of extensively farmed wet meadows in contact with the vegetation of the Caricion davallianae or other Phragmition species [Cladietum marisci (Allorge 1922) Zobrist 1935]. Plants: Cladium mariscus, #Kostelezkia pentacarpos. Corresponding categories United Kingdom classification: "S2 Cladietum marisci", "S24 Peucedano-Phragmitetum australis", "S25 Phragmites australis-Eupatorium cannabinum fen", "M9 Carex rostrata- Calliergon spp. mire", "M13 Schoenus nigricans-Juncus subnodulosus mire", "M14 Schoenus nigricans-Narthecium ossifragum mire", "M24 Molinia caerulea-Cirsium dissectum fen
1)
2) 3)
Page 87
meadow", "SD14 Salix repens-Campylium stellatum dune slack" and "SD 15 Salix repens-Calliergon cuspidatum dune slack". German classification: "3804 Schneidenrhricht". Nordic classification: "3441a Cladium mariscus-variant". 4) 5) In contact with calcareous fens (7230), but also with acid fens, extensive wet meadows, other reed beds and tall sedge communities. Sterner, R. (1926). lands vxtvrld. Sdra Kalmar ln III. Hjalmar Appeltoffts Bokhandel, Kalmar, 237 pp.
7220
PAL.CLASS.: 54.12
1)
2)
3)
4)
5)
7230
PAL.CLASS.: 54.2
Alkaline fens
Wetlands mostly or largely occupied by peat- or tufa-producing small sedge and brown moss communities developed on soils permanently waterlogged, with a soligenous or topogenous baserich, often calcareous water supply, and with the water table at, or slightly above or below, the substratum. Peat formation, when it occurs, is infra-aquatic. Calciphile small sedges and other Cyperaceae usually dominate the mire communities, which belong to the Caricion davallianae, characterised by a usually prominent "brown moss" carpet formed by Campylium stellatum,
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Drepanocladus intermedius, D. revolvens, Cratoneuron commutatum, Acrocladium cuspidatum, Ctenidium molluscum, Fissidens adianthoides, Bryum pseudotriquetrum and others, a grasslike growth of Schoenus nigricans, S. ferrugineus, Eriophorum latifolium, Carex davalliana, C. flava, C. lepidocarpa, C. hostiana, C. panicea, Juncus subnodulosus, Scirpus cespitosus, Eleocharis quinqueflora, and a very rich herbaceous flora including Tofieldia calyculata, Dactylorhiza incarnata, D. traunsteineri, D. traunsteinerioides, D. russowii, D. majalis ssp.brevifolia, D. cruenta, #Liparis loeselii, Herminium monorchis, Epipactis palustris, Pinguicula vulgaris, Pedicularis sceptrum-carolinum, Primula farinosa, Swertia perennis. Wet grasslands (Molinietalia caerulaea, e.g. Juncetum subnodulosi & Cirsietum rivularis, 37), tall sedge beds (Magnocaricion, 53.2), reed formations (Phragmition, 53.1), fen sedge beds (Cladietum mariscae, 53.3), may form part of the fen system, with communities related to transition mires (54.5, 54.6) and amphibious or aquatic vegetation (22.3, 22.4) or spring communities (54.1) developing in depressions. The subunits below, which can, alone or in combination, and together with codes selected from the categories just mentioned, describe the composition of the fen, are understood to include the mire communities sensu stricto (Caricion davallianae), their transition to the Molinion, and assemblages that, although they may be phytosociologically referable to alkaline Molinion associations, contain a large representation of the Caricion davallianae species listed, in addition to being integrated in the fen system; this somewhat parallels the definition of an integrated class Molinio-Caricetalia davallianae in Rameau et al., 1989. Outside of rich fen systems, fen communities can occur as small areas in dune slack systems (16.3), in transition mires (54.5), in wet grasslands (37), on tufa cones (54.121) and in a few other situations. The codes below can be used, in conjunction with the relevant principal code, to signal their presence. Rich fens are exceptionally endowed with spectacular, specialised, strictly restricted species. They are among the habitats that have undergone the most serious decline. They are essentially extinct in several regions and gravely endangered in most. 2) 3) 5) Plants: Schoenus nigricans, S. ferrugineus, Carex spp., Eriophorum latifolium, Cinclidium stygium, Tomentypnum nitens. Corresponding categories Nordic classification : 34 Rikkrrvegetation-typ", "352 Rik kllkrrvegetation". Sjrs, H. (1948). Myrvegetation i Bergslagen. Acta Phytogeogr. Suec. 21:1-299.
7240
PAL.CLASS.: 54.3
1)
2)
3)
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Corresponding category of the Nordic vegetation types: "3422 Carex atrofusca-Drepanocladus revolvens-typ" and "3423 Carex saxatilis-Drepanocladus revolvens-typ". 4) 5) Associated with humid meadows managed extensively, but also with communities of Caricion davallianae. Persson, . (1965). Mountain mires. Acta Phytogeogr. Suec. 50:249-256.
Boreal mires
7310
PAL.CLASS.: 54.8
* Aapa mires
Mire complexes in southern, middle and northern boreal zones characterised by minerotrophic fen vegetation in the central parts of the complexes. Hydro-topographical mire-units are: mixed mires, string-fens, flark-fens, unraised Sphagum fuscum-bogs, unpatterned topogenous or soligenous lawn-, carpet or mud-bottom fens. Poor Sphagum fens are the most common vegetation types whilst brown moss fens can be common in some regions. In prealpine areas in Sweden and in hill regions of Kainuu and Kuusamo in eastern Finland, sloping fens (>5 grades) are typical variants of aapa mires. They occur rarely also in the Suomenselk water divide region in western Finland as well in Lapland. In the mire margins, pine mires and spruce swamps and mires on thin peat of different types dominate. In some limited areas with calcareous bedrock rich fens dominate in the complexes. Plants: Chamaedaphne calyculata, Empetrum nigrum (s.lato), Betula nana, Thricophorum cespitosum, Eriophorum vaginatum, E. russeolum, Carex rostrata, C. lasiocarpa, C. rotundata, C. chordorriza, C. livida, Scheuchzeria palustris, Molinia caerulea, Rubus chamaemorus, Saxifraga hirculus, Dactylorhiza incarnata; Mosses- Sphagnum papillosum, S. jensenii, S. lindbergii, S. majus, S. aongstroemii, S. subsecundum, S. subfulvum, S. pulchrum, Warnstorfia exannulata (Drepanocladus exannulatus), Limprichtia revolvens (Drepanocladus revolvens), Drepanocladus (s.lato) spp., Scorpidium scorpioides. Animals: Butterflies - Pyrgus centaureae, Erebia disa; Moths: Syngrapha diasema, Apamea maillardi, Nola karelica, Hypoxyxtis pluviaria. Eurola, S., Hicks, S. & Kaakinen, E. (1984). Key to Finnish mire types. In: Moore, P.D. (ed). European mires, 11-117. Academic Press, London. Ruuhijrvi, R. (1983). The Finnish mire types and their regional distribution. In: Gore, A.J.P. (ed.). Ecosystems of the world. 4B. Mires: Swamp, bog, fen and moor. Regional studies, 47-97. Elsevier, Amsterdam.
1)
2)
5)
7320
PAL.CLASS.: 54.9
* Palsa mires
Mire complexes in the northern boreal, orohemiarctic and alpine regions, where the climate is slightly continental and the mean annual temperature is below -1. The mires are mainly minerotrophic, excluding the palsas, which are peat mounds with sporadic permafrost. The palsas are usually 2-4 metres high, but up to 7 metres high palsas have been found in Finland and Sweden.
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Plants: Eriophorum russeolum, Carex rotundata, C. saxatilis, Empetrum nigrum ssp. hermaphroditum, Ledum palustre, Betula nana, Vaccinium microcarpum; Mosses- Dicranum elongatum; Lichens: Ochrolechia spp., Cladonia spp., Cladina spp. Eurola, S., Hicks, S. & Kaakinen, E. (1984). Key to Finnish mire types. In: Moore, P.D. (ed). European mires, 11-117. Academic Press, London. Ruuhijrvi, R. (1983). The Finnish mire types and their regional distribution. In: Gore, A.J.P. (ed.). Ecosystems of the world. 4B. Mires: Swamp, bog, fen and moor. Regional studies, 47-97. Elsevier, Amsterdam.
5)
8110
PAL.CLASS.: 61.1
Siliceous scree of the montane to snow levels (Androsacetalia alpinae and Galeopsetalia ladani)
This habitat consist of: a) communities of siliceous scree of the upper montane level to the permanent snow level, growing on more or less moving "cryoclastic systems" with variable granulometry and belonging to the order Androsacetalia alpinae. b) vegetation of the montane level of the west and centre of Europe growing on screes sometimes of artificial origin (extraction of materials). It consists of alpine communities often rich in bryophytes, lichens and sometimes in ferns (Cryptogramma crispa), belonging to the order Galeopsietalia. Plants: a) Androsacetalia alpinae: Androsacae alpina, Achillea nana, Oxyria digyna, Geum reptans, Saxifraga bryoides, Ranunculus glacialis, Linaria alpina, Cerastium uniflorum, Doronicum clusii, D. grandiflorum, Poa laxa, Viola valderia, Luzula alpinopilosa, Cryptogramma crispa; Veronica baumgartenii, Saxifraga carpatica, Senecio carniolicus, Poa contracta, Festuca picta, Saxifraga pedemontana ssp. cymosa, Silene acaulis, Androsace chamaejasme b) Galeopsietalia ladani: Galeopsis ladanum ssp. ladanum, Anarrhinum bellidiflorum, Cryptogramma crispa, Athyrium alpestre (A.. distentifolium). Corresponding categories United Kingdom classification: "U21 Cryptogramma crispa-Deschampsia flexuosa community" and "U18 Cryptogramma crispa-Athyrium distentifolium snow bed". German classification: "6304 Silikatschutthalde der Alpen". Nordic classification: "1251a Cryptogramma crispa-variant", "7141 Veronica fruticans -typ" and "7142 Veronica fruticans-Juniperus communis -typ". This habitat is generally in close association with the chasmophytic vegetation on siliceous rocky slopes (8220). In Ireland and the United Kingdom, sites sheltering rare arctic-alpine plants (post glacial remnants) have a high conservation value.
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2)
3)
4)
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Bringer, K.-G. (1965). Plant cover of the alpine regions. Chionophobous plant communities. Acta Phytogeogr. Suec. 50:257-262. Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X).
8120
Calcareous and calcshist screes of the montane to alpine levels (Thlaspietea rotundifolii)
Calcshist, calcareous, or marl screes of the montane to alpine levels under cold climates, with the associations respectively of Drabion hoppeanae, Thlaspion rotundifolii , Petasition paradoxi. Plants: Drabion hoppeanae (calcschist screes) : Draba hoppeana, Artemisia genipi, Campanula cenisia, Saxifraga biflora, Herniaria alpina, Trisetum spicatum ssp. ovatipaniculatum; Thlaspion rotundifolii (calcareous scree): Thlaspi rotundifolium, Hutchinsia alpina, Papaver rhaeticum, Galium villarsi, Berardia subacaulis, Viola cenisia, Arabis alpina; Acinos alpinus, Cerastium arvense ssp. calcicolum, Saxifraga moschata, Cardaminopsis neglecta, Papaver corona-sanctistephani, Rumex scutatus, Doronicum carpaticum, Cerastium lerchenfeldianum, C. transsilvanicum, Galium anisophyllon, Thymus comosus. Petasition paradoxi (marl screes): Morina persica, Sideritis scardica Petasites paradoxus, Gypsophila repens, Valeriana montana, Leontodon hyoseroides. Corresponding categories United Kingdom classification: "OV38 - Gymnocarpium robertianum-Arrhenatherum elatius community". German classification: "6302 Kalkschutthalde der Alpen". Nordic classification: "7143 Arenaria norvegica-typ". In Ireland and United Kingdom preference should be given to sites sheltering rare arctic-alpine plants (post glacial remnants). Bringer, K.-G. (1965). Plant cover of the alpine regions. Chionophobous plant communities. Acta Phytogeogr. Suec. 50:257-262. Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X).
PAL.CLASS.: 61.2
1) 2)
3)
4) 5)
8130
PAL.CLASS.: 61.3
1)
61.33 - Pyreneo-Alpine thermo-siliceous screes. Senecion leucophyllae, Taraxacion pyrenaici. Siliceous screes of warm slopes of the sub-alpine level of the Alps and of the alpine and subalpine levels of the Pyrenees, usually composed largely of big stones or boulders, with Senecio leucophyllus, Taraxacum pyrenaicum, Galeopsis pyrenaica, Xatartia scabra, Armeria alpina. 61.34 - Pyrenean calcareous screes. Iberidion spathulatae. Calcareous screes of the Pyrenees. 61.35 - Oro-Cantabrian calcareous screes. Linarion filicaulis, Saxifragion praetermissae. Basiphile screes of the Cordillera Cantabrica. 61.36 - Oro-Cantabrian siliceous screes. Linarion filicaulis p., Linario-Senecion carpetani p. Siliceous screes of the Cordillera Cantabrica; floristically rich formations of the "dark" screes of the Cordillera are related to those of 61.351, though somewhat intermediate towards 61.38; other more species-poor ones, characterised by Trisetum hispidum and Rumex suffruticosus, belong to the latter. 61.37 - Iberian fern screes. Dryopteridion oreadis, Dryopteridion submontanae. Fern-dominated chaotic, boulder fields of siliceous and calcareous Iberian mountains. 61.38 - Carpetano-Iberian siliceous screes. Linario-Senecion carpetani. Screes of the Cordillera Central, the Iberian Range, the Leonese mountains, with Linaria saxatilis, L. alpina, Digitalis purpurea var. carpetana, Senecio pyrenaicus ssp. carpetanus, Rumex suffruticosus, Santolina oblongifolia, Conopodium butinioides, Reseda gredensis. 61.39 - Nevadan siliceous screes. Holcion caespitosae. Siliceous screes of the high levels of the Sierra Nevada, very rich in endemics. 61.3A - Southern Iberian calcareous screes. Platycapno-Iberidion granatensis, Scrophularion sciaphilae Screes of the calcareous Baetic mountains of southern and south-eastern Iberia. 61.3B - Central Mediterranean screes Screes of the Italian peninsula and of the large Mediterranean islands. 2) Plants: 61.31 - Achnatherum calamagrostis, Galeopsis angustifolia, Gymnocarpium robertianum, Lentodon hyoseroides, Sisymbrium supinum, Linaria supina; 61.32 - Gouffeia arenarioides,Ptychotis heterophylla, Centranthus ruber, Crucianella latifolia; 61.33 - Senecio leucophyllus, Taraxacum pyrenaicum, Xatartia scabra, Armeria alpina; 61.34 - Iberis spathulata, Papaver suaveolens, Galium cometerhizon, Plantago monosperma, Viola lapeyrousiana, Campanula jaubertiana, Crepis pygmaea, Doronicum grandiflorum, Campanula cochleariaefolia, Carduus carlinoides, Galium cespitosum, Festuca glacialis, Androsace ciliata, Saxifraga oppositifolia, Hutchinsia alpina, Galium pyrenaicum, Minuartia cerastiifolia, Saxifraga praetermissa, S. aizoides, Epilobium anagallidifolium, Veronica alpina, Taraxacum alpinum, Crepis pygmaea; 64.35 - Linaria filicaulis, Arabis cantabrica, Iberis lereschiana, Ranunculus parnassifolius ssp. favargeri, Crepis pygmaea, Iberis aperta, Rumex scutatus, Epilobium anagallidifolium, Doronicum grandiflorum ssp. braunblanquetii, Campanula arvatica, Saxifraga praetermissa, Arabis cantabrica, Ranunculus alpestris ssp. leroyi, Salix breviserrata, Galium pyrenaicum; 61.38 - Linaria saxatilis, L. alpina, Digitalis purpurea var. carpetana, Senecio pyrenaicus ssp. carpetanus, Rumex suffruticosus, Santolina oblongifolia, Conopodium butinioides, Reseda gredensis; 61.39 - Senecio tournefortii var. granatensis, Digitalis purpurea var. nevadensis, Cirsium gregarium, Solidago virgaurea var. alpestris, Holcus caespitosus, Crepis oporinoides, Eryngium glaciale, Linaria aeruginea var. nevadensis, Viola crassiuscula, Linaria glacialis, Rhynchosinapis cheiranthos ssp. nevadensis,Ranunculus glacialis, R. parnassifolius, Saxifraga oppositifolia, Papaver suaveolens, Holcus caespitosus, Crepis oporinoides.
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8140
PAL.CLASS.: 61.4, 61.5
1)
2)
3) 5)
8150
PAL.CLASS.: 61.12
1)
2)
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8160
PAL.CLASS.: 61.313
1)
2) 3)
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8210
PAL.CLASS.: 62.1
1)
2)
3)
4)
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In Ireland and the United Kingdom: sites sheltering relict arctic-alpine flora and important bryophyte and/or lichen assemblages. 5) Brullo S. &Marceno C. (1979). Dianthion rupicolae nouvelle alliance sud-Tyrienne des Asplenietalia glandulosi. Doc. Phytosoc., N.S. 6: 131-146. Biondi E. & Ballelli (1982). La vgtation des gorges calcaires des Apennins de l'Ombrie et des Marches. Guide-itinraire Exc. Int. Phytosoc. en Italie centrale (2-11/7/1982): 189-201. Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X). Karlsson, L. (1973). Autecology of cliff and scree plants in Sarek National Park, northern Sweden. Vxtekol. Stud. 4:1-203. Syrinki, N. & Saari, V. (1980). Die Flora von Oulanka Nationalpark, Nordfinnland. Acta Flor. Fennica 154.
8220
PAL.CLASS.: 62.2
1) 2)
3)
4)
This habitat type is found in close association with siliceous scree (8110) and pioneer grassland (8230). In Ireland and the United Kingdom: sites sheltering relict arctic-alpine flora and important bryophyte and/or lichen assemblages.
5)
Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X). Jalas, J. (1961). Regionale Zge in der Felsenvegetation und flora Ostfennoscandiens. Arch. Soc. Vanamo, 16 Suppl.:38-49. Kallio, P. (1954). Zge aus der flora un vegetation der rapakivifelsen im sudstlichen teil des rapakivigebietes von Laitila in Sdwestfinnland. Ann. Univ. Turkuensis A XVII:1-64.
8230
PAL.CLASS.: 62.42
Siliceous rock with pioneer vegetation of the SedoScleranthion or of the Sedo albi-Veronicion dillenii
Pioneer communities of the Sedo-Scleranthion or the Sedo albi-Veronicion dillenii alliances, colonising superficial soils of siliceous rock surfaces. As a consequence of drought, this open vegetation is characterised by mosses, lichens and Crassulacea. Plants: Sedo-Scleranthion: Sempervivum arachnoideum, Sempervivum montanum, Sedum annuum, Silene rupestris, Veronica fruticans; Sedo albi-Veronicion dillenii: Veronica verna, Veronica dillenii, Gagea bohemica, Gagea saxatiles, Riccia ciliifera; Plant species belonging to the two syntaxa: Allium montanum, Sedum acre, Sedum album, Sedum reflexum, Sedum sexangulare, Scleranthus perennis, Rumex acetosella. Mosses- Polytrichum piliferum, Ceratodon purpureus. Corresponding categories German classification : "320102 natrlicher Silikatfels (ohne Serpentinit) (lckige Vegetation, P002)". Nordic classification : partly "711 Klippvegetation p fattiga bergarter" and "5211 Sedum spp.Viola tricolor-Aira praecox-typ". This habitat is associated with the 8220 type, and corresponds to the vegetation colonising siliceous rocks. The vegetation colonising calcareous rocks is included under 6110 " Rupicolous calcareous or basophilic grasslands of the Alysso-Sedion albi)" and 8240 "Limestone pavements. Hallberg, H. P. & Ivarsson, R. (1965). Vegetation of coastal Bohusln. Acta Phytogeogr. Suec. 50:111-122.
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8240
PAL.CLASS.: 62.3
* Limestone pavements
Regular blocks of limestone known as "clints" with loose flags separated by a network of vertical fissures known as "grykes" or "shattered pavements", containing more loose limestone rubble. The rock surface is almost devoid of overlying soils (considerably less than 50% cover) except for some patches of shallow skeletal or loessic soils, although more extensive areas of deeper soil occasionally occur; sometimes there is encroachment of peat. This morphology offers a variety of microclimates allowing the establishment of complex vegetation consisting of a mosaic of different communities. The fissures provide a cold humid microclimate where shade-tolerant vascular plants such as Geranium robertianum and Ceterach officinale occur, as well as formations of herbaceous species typical of calcareous woodland; the small pockets of soil are occupied by communities of Mesobromion (e.g. Seslerio-Mesobromenion); heath and scrub also occur (e.g. Corylo-Fraxinetum). Apart from areas of species rich scrub (generally Prunetalia spinosae), the ecosystem is maintained by grazing in some regions; this, combined with severe winds, means that isolated shrubs can only survive in prostrate growth form (e.g. Dryas octopetala); at the margins of ungrazed sites Geranium sanguineum occurs. In Sweden, limestone blocks are larger and cracks are smaller. The species composition reflects a more continental, dryer and cooler climate. The pavements are mostly exposed with scattered cushions of bryophytes, more seldom covered by a thin layer of soil. The surface is covered by Sedum album, Cerastium pumilum, C. semidecandrum, lichens (Aspicilia calcarea, Thamnolia vermicularis, Verrucaria nigrescens) and bryophytes (Tortella tortuosa, Grimmia pulvinata). The vegetation in the cracks contains Gymnocarpium robertianum, Asplenium ruta-muraria, A. trichomanes ssp. quadrivalens and, occasionally, bushes of Prunus spinosa, Fraxinus excelsior, Cotoneaster spp., Rosa spp. Some sites in Ireland host an open Taxus-Juniperus scrub of major interest; certain arctic alpine species such as Gentiana verna and Dryas octopetala are characteristic and in The Burren, these species occur with Atlantic-Mediterranean species such as Neotinea maculata. Plants: Britain and Ireland - Asplenium spp., Ceterach officinale, Cystopteris fragilis, Dryas octopetala, Dryopteris villarii, Epipactis atrorubens, Gentiana verna, Polygonatum odoratum, Ribes spicatum. Sweden - Sedum album, Cerastium pumilum, C. semidecandrum, Aspicilia calcarea, Thamnolia vermicularis, Verrucaria nigrescens, Tortella tortuosa, Grimmia pulvinata, Gymnocarpium robertianum, Asplenium ruta-muraria, A. trichomanes ssp. quadrivalens. Corresponding categories United Kingdom classification : "W8 Fraxinus excelsior-Acer campestre-Mercurialis perennis woodland" and "W9 Fraxinus excelsior-Sorbus aucuparia-Mercurialis perennis woodland". Very locally in the United Kingdom, ancient woodland containing Tilia cordata occurs which is of great conservation importance. Nordic classification: "5151b Asplenium ruta-muraria-Asplenium trichomanes-Homalothecium sericeum-variant" variant of "5151 Sedum album-Tortella spp. typ". Bobe, B. (1991). Gefsspflanzenvegetation und Mikroklima der Karstspalten des Grossen Alvars auf land, Schweden. Unpubl. diploma work, Mnchen. Etherington, J.R. (1981). Limestone heaths in south-west Britain: their soils and the maintenance of their calcicole-calcifuge mixtures. Kelly, D. & Kirby, E.N. (1982). Irish native woodlands over limestone. J, Life Sci. R. Dubl. Soc. 3, 181-198. O' Sullivan, A.M. (1982). The lowland grasslands of Ireland. J. Life Sci. R. Dubl. Soc. 3, 131-142. Ward,S.D. & Evans,D.F.(1976).Conservation assessment of British limestone pavements based upon floristic criteria. Biological Conservation, 9, 217-233.
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8310
PAL.CLASS.: 65
1)
2)
3)
5)
8320
PAL.CLASS.: 66.1 to 66.6
1)
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Caves formed by hollow basaltic tubes resulting from the cooling of the surface of lava flows whose molten interior continued to flow. The very large tube created by the volcano La Corona of Lanzarote harbours unique communities of invertebrates, in particular, the decapode crustacean Munidopsis polymorpha, endemic to that locality, and several crustaceans of the genus Speleonectes. 66.6 - Fumaroles Orifices in volcanic areas through which escape hot gases and vapours. Their very extreme environment is colonised by paucispecific but highly distinct communities. 2) Plants: Viola cheiranthifolia, Silene nocteolens, Argyranthemum teneriffae; Lichens: Stereocaulon vesubianum. Animals: crustaceans: Munidopsis polymorpha, Speleonectes spp.
8330
PAL.CLASS.: 12.7, 11.26, 11.294
1)
8340
PAL.CLASS.: 63.2 and 63.3
Permanent glaciers
Rock and true glaciers.
1)
FORESTS
(Sub)natural woodland vegetation comprising native species forming forests of tall trees, with typical undergrowth, and meeting the following criteria: rare or residual, and / or hosting species of Community interest 20
9010
* Western Taga
20
For forest habitat types the following additional criteria were accepted by the Scientific Working Group (21-22 June 1993): - forests of native species; - forests with a high degree of naturalness; - forests of tall trees and high forest; - presence of old and dead trees; - forests with a substantial area; - forests having benefited from continuous sustainable management over a significant period.
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Natural old forests as well as those young forest stages naturally developing after fire. Natural old forests represent climax or late succession stages with slight human impact or without any human impact. Present natural old forests are only minor remnants of those originally occurring in Fennoscandia. With intensive forestry, which is carried out practically throughout this region, the main features of natural old forests disappear, i.e. the considerable amount of dead and rotten wood, the great variation in tree age and length and species composition, the trees from previous generations, the more stable microclimate. Old natural forests are habitats of many threatened species, especially bryophytes, lichens, fungi, and invertebrates (mostly beetles). Some of the present old natural forests have human impact, but in spite of that they maintain many characteristics of the natural forests. Because of the important role of fire, burned forest areas, and their young succession stages, have been naturally common in the boreal region. Nowadays they are extremely rare because of efficient fire protection and forestry. Natural recently burned forest areas are very important habitats for many endangered species. Typical of natural burned areas is a great amount of dead burned wood and a varying density of living trees which greatly conditions the regeneration of the forest. The character of the forests vary with the different boreal zones (hemi-, southern, middle, northern) and different site types. The following sub-types are distinguished, according to the main tree species and site type variation: - natural old spruce forests - natural old pine forests - natural old mixed forests - natural old deciduous forests - recently burnt areas - younger forests naturally developed after fire Plants: Pine forests - Pinus sylvestris, Vaccinium vitis-idaea, Calluna vulgaris, Empetrum nigrum, Pleurozium schreberi, Cladonia spp.; Spruce and mixed forests - Picea abies, Pinus sylvestris, Betula spp., Vaccinium myrtillus, Deschampsia flexuosa, Maianthenum bifolium, Oxalis acetosella, Trientalis europea, Dicranum spp., Pleurozum schreberi, Hylocomium splendens; Deciduous forests - Betula spp., Populus tremula, Deschampsia flexuosa, Vaccinium myrtillus, Agrostis capillaris, Equisetum sylvaticum. Lichens - Evernia divaricata, Lobaria pulmonaria. Fungi Amylocystis lapponica, Gloiodon strigosum, Fomitopsis populicola, Skeletocutis odora, S. stellae, Phlebia centrifuga, Haploporus odorus, Aporpium cargae, Gelatoporia pannocincata, Phellinus populicola. Animals: Mammals - *Pteromys volans, Myopus schisticolor, Sorex minutus; Birds - Picoides tridactylus, Perisoreus infaustus, Dendrocopos leucotos, D. minor; Beetles - Tragosoma depsarium, Pytho kolwensis, P. abieticola, #Cucujus cinnaberinus, Peltis grossa, *Osmoderma eremita. Originally natural old forests were found in the whole boreal and hemiboreal zones, except in the oro-hemiarctic treeless zone. In Finland nowadays most of the natural old forests are found in eastern and northern parts, in southern and western parts of the country only remnants of these forests remain. In Sweden most of the old natural forests are in the north and only some of them in the south. Kalela, A. (1961). Waldvegetationszonen Finnlands und ihre klimatischen paralelltypen. Arch. Soc. zool. bot. fenn. Vanamo 16 Suppl.:65-83. Kalliola, R. (1973). Suomen kas vimaantiede. Wsoy, Porvoo. 308 pp. Kielland-Lund, J. (1967). Zur systematik der Kiefenfelder Fennoscandiens. Mitt. flor.-soz. ArbGemein. 11/12:127-141. Kielland-Lund, J. (1981). Die Waldgesellschaften SO-Norwegens. Phytocoenolog. 9:53-250. Kujala, V. (1981). Suomen metstyypit. Commun. Inst. For. Fenn., 92(8):1-45. Kuusinen, M. (1994). Epiphytic lichen diversity on Salix caprea in old-growth southern and middle boreal forests of Finland. Ann. Bot. Fennici, 31:77-92. Phlsson, L. et al. (1995). Vegetationstyper I Norden. Nordiska Ministerrdet Tema Nord 1994:665 pp.
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Tanninen, T., Storrank, B., Haugen, I., Moller, P.F., Lfgren, R. Thorsteinsson, I. & Ragnarsson, H. (1994). Naturskogar i Norden. Nord 1994:7. Virkkala, R., Alanko, T., Laine, T. & Tiainen, J. (1993). Population contraction of the whitebacked woodpecker Dendrocopos leucotos in Finland as a consequence of habitat alteration. Biological Conservation 66:47-53.
9020
* Fennoscandian hemiboreal natural old broad-leaved deciduous forests (Quercus, Tilia, Acer, Fraxinus or Ulmus) rich in epiphytes
The hemiboreal natural old broad-leaved deciduous forest forms a transition between the Western Taiga and the nemoral forests. The most common tree species are Quercus robur, Ulmus spp., Fraxinus excelsior, Tilia cordata or Acer platanoides. There is typically a considerable amount of dead wood and a long continuity of woodland cover on the sites. The species-diversity of lichens, fungi, insects and soil-organisms is high. In many cases the forests have previously been used for grazing or mowing. Plants : Allium ursinum, Anemone nemorosa, Corylus avellana, Dentaria bulbifera, Hepatica nobilis, Lathyrus vernus, Mercurialis perennis, Milium effusum, Poa nemoralis, Polygonatum multiflorum; Bryophytes- Antitrichia curtipendula, Homalia trichomanoides, Orthotrichum spp., Porella platyphylla, Zygodon spp.; Fungi- Auricularia mesenterica, Ganoderma lipsiense, Eichomitus campestris, Mycena galericulata, Tricholoma album, T. sulphureum; LichensArthonia vinosa, Biatorella monasteriensis, Cliostomum corrugatum, Gyalecta flotowi, Lobaria pulmonaria, Phlyctis agelaea Corresponding categories Nordic classification: 2233 Ulmus glabra type , 2234 Fraxinus excelsior type , 2235 Tilia cordata type and 2236 Quercus robur-Ulmus glabra-Tilia cordata type. Almgren, G. (1984).- dellvskog - ekologi och sktsel. Skogsstyrelsen. Jnkping. Kielland-Lund, J. (1973).- A classification of Scandinavian forest vegetation for mapping purposes. In: IBP i Norden, No 11. Universitetsforl. Oslo. Pettersson, B. & Fiskesj, A. (1991).- Lvnaturskogens flora och fauna. Naturvrdsverket Rapport 3991. Samuelsson, J. & Ingelf, T. (1996).- Den levande dda veden. Bevarande och nyskapande i naturen. ArtDatabanken. Uppsala.
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the shrub layer. Grasses are abundant. Further inland the influence of the sea is weakened, the soils are often poor in nutrients and coniferous forests are typical. Pine, and often also spruce, dominates the tree layer and dwarf shrubs dominate in the field layer. In the ground layer mosses are common, but in many areas lichens are abundant. 3) Corresponding categories Nordic classification: 2215 Betula pendula-Vaccinium myrtillus-Deschampsia flexuosa type, 2216 Betula pubescens-Molina caerulea-Sphagnum spp. type, coastal variants, 7213 Hippopha rhamnoides-type . Many other units have unclassified and undescribed variants occurring in land upheaval areas. Havas, P. (1967).- Zur kologie der Laubwelder, insbesondere der Grauerlenwlder, an der Kuste der Bottenwiek. Aquilo, Ser. Bot., 6: 314-346. Vartiainen, T. (1980).- Succession of island vegetation in the land uplift area of the northernmost Gulf of Bothnia, Finland. Acta Botanica Fennica, 115: 1-105
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9040
PAL.CLASS.: 41.B72 (1997 version)
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9050
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This type occurs in areas of brown forest soils with mull, often in low-lying areas, ravines and slopes with fine sediment and a favourable water regime. The succession of this vegetation type normally leads to the dominance of spruce in the tree layer, although the broad-leaved trees often comprise a significant element. Tall herbs and ferns dominate, but the species composition varies greatly between northern, southern and western Fennoscandia. The forests are characterized by distinct layers of vegetation. The bottom layer is covered unevenly by bryophytes, the field layer is dominated by herbs and grasses, the bush and tree layers are well developed including a variety of species. Several vegetation types have been described, the main groups being dry, mesic and moist grass-herb forests. Sometimes ground water is flowing near the ground surface, which give rise to a specific species rich wet-forest flora and invertebrate fauna. Plants : Actaea spicata, A. erythrocarpa, Botrychium virginianum, Calypso bulbosa, Carex remota, Cicerbita alpina, Crepis paludosa, # Cypripedium calceolus, Diplazium sibiricum, Epipogium aphyllum, Geranium sylvaticum, Impatiens noli-tangere, Matteuccia struthiopteris, Melica nutans, Milium effusum, Paris quadrifolia, Viola selkirkii; Mosses- Brachythecium spp., Cirriphyllum piliferum, Eurhynchium spp., Plagiomnium spp. Corresponding categories Nordic classification: 2124 Picea abies-Oxalis acetosella-Melica nutans -type, 2125 Picea abiesDryopteris spp.-type and 2126 Picea abies-Geranium sylvaticum-Aconitum lycoctonumtype . Mkirinta, U. (1968).- Haintypenuntersuchungen im mitteleren Sd-Hme, Sd-Finnland. Ann. ot. Fenn.,5: 34-64. Koponen, T. (1967).- On the dynamics of vegetation and flora in Karkali Nature Reserve, Southern Finland. Ann. Bot. Fenn., 4:121-218.
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9060
PAL.CLASS.: -
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Stands of esker forests on sunny slopes are often characterized by a relatively open tree structure and in addition the undergrowth often consists of species of warmer climate (e.g. Carex pediformis, Pulsatilla patens, P. vernalis, Gypsophila fastigiata) and some endangered butterfly species. About six different forest site types of eskers have been described, representing a gradient from xeric lichen rich forests to humid herb-rich forests. Heikkinen, R.K. (1991) - Multivariate analysis of esker vegetation in southern Hme, S Finland. Ann. Bot. Fenn. 28: 201-224. Jalas, J. (1961) - Besondere Zge der Vegetation und Flora auf der Osen. Arch. Soc. Zool. Bot. Fenn. Vanamo, 16 Suppl. 25-33. Rajakorpi, A. (1987) - Topographic, microclimatic and edaphic control of the vegetation in the central part of the Hmeenkangas esker complex, western Finland. Acta Bot. Fennica, 134: 1-70. Uotila, P. (1969) - Ecology and area of Pulsatilla patens (L.) Mill. in Finland. Ann. Bot. Fenn.. 6:105-111.
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9070
PAL.CLASS.: -
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9080
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very thin. Ash (Fraxinus excelsior) in the hemiboreal zone and black alder (Alnus glutinosa) reaching the middle boreal zone are typical tree species. Gray alder (Alnus incana), silver birch (Betula pubescens) and willows (Salix spp.) are also common. A mosaic of patches with different water level and vegetation is typical for the type. Around the tree stems are small hummocks, but wet flooded surfaces are dominant. Deciduous swamp woods are most common in Finland in the southwestern archipelago and other coastal areas. On the mainland they are rare. In Sweden they are common throughout the whole region. 2) Plants : Carex caespitosa, C. diandra, C. disperma, C. elongata, C. loliacea, C. rhynchospora, C. tenuiflora, Calamagrostis canescens, C. chalybea, C. stricta, Calla palustris, Glyceria lithuanica, Iris pseudacorus, Lycopus europaeus, Lysimachia thyrsiflora, Lythrum salicaria, Solanum dulcamara, Thelypteris palustris; Mosses- Calliergon cordifolium, Helodium blandowii, Pseudobryum cinclidioides, Spagnum squarrosum, S. teres, S. fimbriatum, S. riparium Corresponding categories Nordic classification : 2241 Alnus incana -type, 2242 Alnus glutinosa - Lycopus europaeus type, 2243 Alnus spp. - Filipendula ulmaria - Carex elongata -type, 3413 Alnus spp. Betula pubescens - Salix spp. - Filipendula ulmaria -type. Associated with the habitat type: Residual alluvial forests (91E0) Ruuhijrvi, R. (1983).- The Finnish mire types and their regional distribution. In: Gore, A.J.P. (ed.) Ecosystems of the World 4B. Mires: Swamp, bog, fen and moor. Regional studies, 4767. Elsevier, Amsterdam. Eurola, S. & Kaakinen, E. (1984).- Key to Finnish mire types. In: Moore, P.D. (ed.). European mires, 11-117. Academic Press, London
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9110
PAL.CLASS.: 41.11
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Corresponding categories Nordic classification: "2221 Fagus sylvatica-Deschampsia flexuosa-Vaccinium myrtillus-typ" Lindgren, L. (1970). Beech forest vegetation in Sweden - a survey. Bot. Notiser 123:401-421.
9120
Atlantic acidophilous beech forests with Ilex and sometimes also Taxus in the shrublayer (Quercinion robori-petraeae or Ilici-Fagenion)
Beech forests with Ilex, growing on acid soils, of the plain to montane levels under humid Atlantic climate. The acid substrate corresponds to alterations of acid rocks or to silt with flints more or less degraded or, to old alluvial deposits. The soils are of acid brown type, leaching or with an evolution towards podsol type. The humus is of moder to dysmoder type. These beech forests present different varieties: a) subatlantic beech-oak forests of the plains and hill levels with Ilex aquifolium b) hyper-Atlantic beech-oak forests of the plains and hill levels with Ilex and Taxus, rich in epiphytes c) pure beech forests or acidophilous beech-fir forests of the montane level, with Ilex aquifolium in the field layer. Plants: Ilex aquifolium, Taxus baccata, Ruscus aculeatus, Deschampsia flexuosa, Hieracium sabaudum, H. umbellatum, Pteridium aquilinum, Vaccinium myrtillus, Lonicera periclymenum, Melampyrum pratense, Teucrium scorodonia, Holcus mollis. Corresponding categories United Kingdom classification: "W14 Fagus sylvatica-Rubus fruticosus woodland" pp and "W15 Fagus sylvatica-Deschampsia flexuosa woodland p.p.". German classification: "43070502 bodensaurer Buchenwald der planaren Stufe". Oak may dominate in some of these forests due to the coppice-with-standards regime of the past centuries. If the intensity of the management decreases beech and also Ilex often regenerate spontaneously.
PAL.CLASS.: 41.12
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9130
PAL.CLASS.: 41.13
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Neutrocline or basicline Fagus sylvatica and Fagus sylvatica-Quercus petraea-Quercus robur forests of hills, low mountains and plateaux of the Hercynian arc and its peripheral regions, of the Jura, Lorraine, the Paris basin, Burgundy, the Alpine piedmont, the Carpathians and a few localities of the North Sea-Baltic plain. 41.132 - Atlantic neutrophile beech forests Atlantic beech and beech-oak forests with Hyacinthoides non-scripta, of southern England, the Boulonnais, Picardy, the Oise, Lys and Schelde basins. 41.133 - Medio-European montane neutrophilous beech forests Neutrophile forests of Fagus sylvatica, Fagus sylvatica and Abies alba, Fagus sylvatica and Picea abies, or Fagus sylvatica, Abies alba and Picea abies of the montane and high-montane levels of the Jura, the northern and eastern Alps, the western Carpathians and the great Hercynian ranges. 41.134 - Bohemian lime-beech forests Fagus sylvatica or Fagus sylvatica-Abies alba forests rich in Tilia spp., of the Bohemian basin. 41.135 - Pannonic neutrophilme beech forests Neutrophilous beech forests of medio-European affinities of the hills of the Pannonic plain and its western periphery. 2) 3) Plants: Fagus sylvatica, Abies alba, Picea abies, Anemone nemorosa, Lamiastrum (Lamium) galeobdolon, Galium odoratum, Melica uniflora, Dentaria spp. Corresponding categories United Kingdom classification: "W12 Fagus sylvatica-Mercurialis perennis woodland p.p." and "W14 Fagus sylvatica-Rubus fruticosus woodland p.p.". Nordic classification: "2222 Fagus sylvatica-Lamiastrum galeobdolon-Melica uniflora-typ" and "2223 Fagus sylvatica-Mercurialis perennis-Allium ursinum-typ". Romanian classification: R4118 Pduri dacice de fag (Fagus sylvatica) i carpen (Carpinus betulus) cu Dentaria bulbifera, R4119 Pduri dacice de fag (Fagus sylvatica) i carpen (Carpinsu betulus) cu Carex pilosa,R4120 Pduri moldave mixte de fag (Fagus sylvatica) i tei argintiu (Tilia tomentosa) cu Carex brevicolis" Relict stands of collinar neutrophilous beech forests of the Macin Mountains of Dobrogea, Romania are the priority habitat 91X0*Dobrogean Beech forests Bergendorff, C., larsson, A. & Nihlgrd, B. (1979). Sydliga lvskogsbestnd i Sverige. Statens naturvrdsverk. Rapport. SNV PM 1278, Solna, 68 pp.
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9140
PAL.CLASS.: 41.15
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9150
PAL.CLASS.: 41.16
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9160
PAL.CLASS.: 41.24
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Not to be confused with forests of Quercus robur arising from the management of beech-oak forests as coppice or coppice-with-standards on well drained soils. Diekmann, M. (1994). Decidious forest vegetation in Boreo-nemoral Scandinavia. Acta Phytogeogr. Suec. 80:1-112.
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9170
PAL.CLASS.: 41.261, 41.262
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9180
PAL.CLASS.: 41.4
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Slight changes in the conditions of the substrate (especially "consolidated" substrate) or humidity produce a transition towards beech forests (Cephalanthero-Fagenion, Luzulo-Fagenion) or towards thermophile oak forests. Bergendorff, C., Larsson, A. & Nihlgrd, B. (1979). Sydliga lvskogsbestnd i Sverige. Statens naturvrdsverk. Rapport. SNV PM 1278, Solna, 68 pp.
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9190
PAL.CLASS.: 41.51 and 41.54
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91A0
PAL.CLASS.: 41.53
Old sessile oak woods with Ilex and Blechnum in the British Isles
Acidophilous Quercus petraea woods, with low, low-branched, trees, with many ferns, mosses, lichens and evergreen bushes. Sub-types : 41.531 - Irish sessile oak woods Quercus petraea woods of Ireland, particulary rich in evergreen bushes, including Arbutus unedo. 41.532 - British sessile oak woods Acidophilous Quercus petraea woods of western Britain, mostly found in Scotland, Wales, Northern England and South Western England. Plants: Quercus petraea, Ilex aquifolium, Blechnum ssp. Corresponding categories
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United Kingdom classification: "W10 Quercus spp.-Pteridium aquilinum-Rubus fruticosus woodland p.p.", "W11 Quercus petraea-Betula pubescens-Oxalis acetosella woodland p.p." and "W17 Quercus petraea-Betula pubescens-Dicranum majus woodland p.p.".
91B0
PAL.CLASS.: 41.86
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91C0
PAL.CLASS.: 42.51
* Caledonian forest
Relict, indigenous pine forests of Pinus sylvestris var. scotica, endemic in the central and north eastern Grampians and the northern and western Highlands of Scotland and associated Betula and Juniperus woodlands of northern character within this area. They are mostly open and have a ground layer rich in ericaceous species and bryophytes, in particular Hylocomium splendens, and often harbouring abundant Deschampsia flexuosa, Goodyera repens, Listera cordata, Corallorhiza trifida, Linnaea borealis, Trientalis europaea, Pyrola minor, Moneses uniflora, Orthilia secunda. The dominant trees are: Sorbus aucuparia, Betula pubescens, B. pendula, Juniperus communis, Ilex aquifolium, Populus tremula. Plants: Corallorhiza trifida, Deschampsia flexuosa, Goodyera repens, Linnaea borealis, Listera cordata, Moneses uniflora, Orthilia secunda, Pinus sylvestris var. scotica, Pyrola minor, Trientalis europaea. Bryophytes- Hylocomium splendens, Pleurozium schreberi. Corresponding categories United Kingdom classification: the majority of Caledonian forests belong to "W18 Pinus sylvestris-Hylocomium splendens woodland"; however, not all of these forests are semi-natural. Stands dominated by Juniperus belong to the category "W19 Juniperus communis ssp. communis-Oxalis acetosella woodland".
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91D0
PAL.CLASS.: 44.A1 to 44.A4
* Bog woodland
Coniferous and broad-leaved forests on a humid to wet peaty substrate, with the water level permanently high and even higher than the surrounding water table. The water is always very poor in nutrients (raised bogs and acid fens). These communities are generally dominated by Betula pubescens, Frangula alnus, Pinus sylvestris, Pinus rotundata and Picea abies, with species specific to bogland or, more generally, to oligotrophic environments, such as Vaccinium spp., Sphagnum spp.,
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Carex spp. [Vaccinio-Piceetea: Piceo-Vaccinienion uliginosi (Betulion pubescentis, Ledo-Pinion) i.a.]. In the Boreal region, also spruce swamp woods, which are minerotrophic mire sites along margins of different mire complexes, as well as in separate strips in valleys and along brooks. Sub-types : 44.A1 - Sphagnum birch woods 44.A2 - Scots pine mire woods 44.A3 - Mountain pine bog woods 44.A4 - Mire spruce woods 2) Plants: Agrostis canina, Betula pubescens, B. carpatica, Carex canescens, C. echinata, C. nigra, C. rostrata, Eriophorum vaginatum, Frangula alnus, Juncus acutiflorus, Molinia caerulea, Trientalis europaea, Picea abies, Pinus rotundata, P. sylvestris, P. mugo, Sphagnum spp., Vaccinium oxycoccus, V. uliginosum, Viola palustris; in spruce swamp woods also: Carex disperma, C. tenuiflora, Diplazium sibiricum, Hylocomium umbratum and Rhytidiadelphus triquetrus. 3) Corresponding categories United Kingdom classification : "W4 Betula pubescens-Molinia caerulea woodland". German classification: "430101 Birken-Moorwald", "440104 Latschen-Moorwald", "440101 FichtenMoorwald", "440103 Spirken-Moorwald", "440102 Waldkiefern-Moorwald". Nordic classification: "311 Skogsmossevegetation", "321 Skogs-och krattkrrvegetation". Romanian classification: R3106 Tufriuri sud-est Carpatice de jneapn (Pinus Mugo) n mlatini oligotrofe de Sphagnum, R4412 Raristi sud-est carpatice de molid (Picea abies) si/sau pin silvestru (Pinus sylvestris) de tinoave, R4414 Tufriuri sud-est carpatice de mlatini de mesteacn pufos (Betula pubescens). 4) Forests on the edge of upland bogs or transition mires may form a transition towards swamp forests (Alnetea glutinosa, Alno-Ulmion pp.). Where bog woodland has colonized former non-woodland bog because of human impacts (bog degradation), the bog woodland may be removed in order to restore favourable conservation status of the former bog (types 7110, 7130 and 7140). Such secondary bog woodland is included in the definition of type 91D0, but generally has lower conservation priority than restoration of the original bog type. Dierssen, B. & Dierssen, K. (1982). Kiefernreiche Phytocoenosen oligotropher Moore im mittleren und nordwestlichen Europa. berlegungen zur Problematik ihrer Zuordnung zu hheren syn systematischen Einheiten. In:Dierschke, H. (ed.) Struktur und Dynamic von Wldern. Ber. Intern. Symp. IVV 1982, pp. 299-331.
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91E0
PAL.CLASS.: 44.3, 44.2 and 44.13
* Alluvial forests with Alnus glutinosa and Fraxinus excelsior (Alno-Padion, Alnion incanae, Salicion albae)
Riparian forests of Fraxinus excelsior and Alnus glutinosa, of temperate and Boreal Europe lowland and hill watercourses (44.3: Alno-Padion); riparian woods of Alnus incanae of montane and sub-montane rivers of the Alps and the northern Apennines (44.2: Alnion incanae); arborescent galleries of tall Salix alba, S. fragilis and Populus nigra, along medio-European lowland, hill or sub-montane rivers (44.13: Salicion albae). All types occur on heavy soils (generally rich in alluvial deposits) periodically inundated by the annual rise of the river (or brook) level, but otherwise well-drained and aerated during low-water. The herbaceous layer invariably includes many large species (Filipendula ulmaria, Angelica sylvestris, Cardamine spp., Rumex sanguineus, Carex spp., Cirsium oleraceum) and various vernal geophytes can occur, such as Ranunculus ficaria, Anemone nemorosa, A. ranunculoides, Corydalis solida. This habitat includes several sub-types: ash-alder woods of springs and their rivers (44.31 - Carici remotae-Fraxinetum); ash-alder woods of fast-flowing rivers (44.32 - Stellario-Alnetum glutinosae); ash-alder woods of slow-flowing rivers (44.33 - Pruno-Fraxinetum, Ulmo-Fraxinetum); montane grey alder galleries (44.21 - Calamagrosti variae-Alnetum incanae Moor 58); sub-montane grey alder galleries (44.22 - Equiseto hyemalis-Alnetum incanae Moor 58); white willow gallery forests (44.13 Salicion albae). The Spanish types belong to the alliance Osmundo-Alnion (Cantabric atlantic and southeast Iberia peninsula). Plants: Tree layer - Alnus glutinosa, Alnus incanae, Fraxinus excelsior; Populus nigra, Salix alba, S. fragilis; Betula pubescens, Ulmus glabra; Herb layer - Angelica sylvestris, Cardamine amara, C. pratensis, Carex acutiformis, C. pendula, C. remota, C. strigosa, C. sylvatica, Cirsium oleraceum, Equisetum telmateia, Equisetum spp., Filipendula ulmaria, Geranium sylvaticum, Geum rivale, Lycopus europaeus, Lysimachia nemorum, Rumex sanguineus, Stellaria nemorum, Urtica dioica. Corresponding categories United Kingdom classification: "W5 Alnus glutinosa-Carex paniculata woodland", "W6 Alnus glutinosa-Urtica dioica woodland)" and "W7 Alnus glutinosa-Fraxinus excelsior-Lysimachia nemorum woodland". German classification: "43040401 Weichholzauenwald mit weitgehend ungertrter berflutungsdynamik", "43040402 Weichholzauenwald ohne berflutung", "430403 Schwarzerlenwald (an Fliegewssern)", "430402 Eschenwald (an Fliegewssern)", "430401 Grauerlenauenwald (montan, Alpenvorland, Alpen). Nordic classification: "2234 Fraxinus excelsior-typ" and "224 Alskog". Most of these forests are in contact with humid meadows or ravine forests (Tilio-Acerion). A succession towards Carpinion (Primulo-Carpinetum) can be observed. Brunet, J. (1991). Vegetation i Sknes alm- och askskogar. Sven. Bot. Tidskr. 85:377-384.
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91F0
Riparian mixed forests of Quercus robur, Ulmus laevis and Ulmus minor, Fraxinus excelsior or Fraxinus angustifolia, along the great rivers (Ulmenion minoris)
Forests of hardwood trees of the major part of the river bed, liable to flooding during regular rising of water level or, of low areas liable to flooding following the raising of the water table. These forests develop on recent alluvial deposits. The soil may be well drained between inondations or remain wet. Following the hydric regime, the woody dominated species belong to Fraxinus, Ulmus or Quercus genus. The undergrowth is well developed. Plants: Quercus robur, Ulmus laevis, U. minor, U.glabra, Fraxinus excelsior, Fraxinus angustifolia, Populus nigra, P. canescens, P. tremula, Alnus glutinosa, Prunus padus, Humulus lupulus, Vitis vinifera ssp. sylvestris, Tamus communis, Hedera helix, Phalaris arundinacea, Corydalis solida, Gagea lutea, Ribes rubrum. Corresponding categories German classification: "43040501 Hartholzauenwald mit weitehend ungestrter berflutungsdynamik", "43040502 Hartholzauenwald ohne berflutung". Nordic classification: "2223 Ulmus glabra-typ", "2236 Quercus robur-Ulmus glabra-Tilia cordata typ". These forests form mosaics with pioneer or stable forests of soft wood trees, in low areas of the river bed; they may develop also from alluvial forests of hard wood trees. This habitat type often occurs in conjunction with alder-ash woodlands (44.3).
PAL.CLASS.: 44.4
1)
2)
3)
4)
91G0
PAL.CLASS.: 41.2B, 41.266, 41.267
1)
2)
4) 5)
Borhidi, A. & Kevey, B. (1996). An annotated checklist of the Hungarian plant communities. II. The forest vegetation. In: Borhidi, A. (ed.): Critical Revision of the Hungarian Plant Communities. Janus Pannonius Univ. Pcs, 95-138. Csapody, I. (1967). Eichen-Hainbuchenwlder Ungarns. Feddes Repert. 77: 245-269. Mucina, L., Grabherr, G., Wallnfer, S. (1993). Die Pflanzengesellschaften sterreichs. Teil III, S. 199. Neuhusl U. Neuhuslova-Novotna (1968). bersicht der Carpinion-Gesellschaften der Tschechoslowakei.
91H0
PAL.CLASS.: 41.7373, 41.7374
1)
2)
4)
91I0
PAL.CLASS.: 41.7A
1)
2)
4)
Page 117
91J0
PAL.CLASS.: 42.A71
1)
2) 3)
91K0
PAL.CLASS.: 41.1C
1)
2)
5)
Page 118
91L0
PAL.CLASS.: 41.2A
1)
2)
5)
91M0
PAL.CLASS.: 41.76
1)
2)
Primula acaulis ssp rubra, Epimedium pubigerum, Cyclamen coum, Nectaroscordum siculum, Galanthus plicatus. 5) Bondev I. (1991).The vegetation of Bulgaria. Map 1: 600 000 with explanatory text. St. Kl. Ohridsky Univ. Press, Sofia .(in Bulgarian) Borhidi, A. (1996). A critical revision of the Hungarian plant communities. Janus Pannonius University, Pcs, 138 pp. Borhidi A. and Snta A. (eds.) (1999). Vrs Knyv Magyarorszg nvnytrsulsairl. 1-2. ktet. (Red Book of Hungarian plant communities. Vol. 1-2.) - TermszetBVR Alaptvny Kiad, Budapest. 768 pp. (in Hungarian). Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X) Hornszky, A. (1964). Die Wlder des Szentendre-Visegrder Gebirges. - Akadmiai Kiad, Budapest. Pcs, T., Domokos, ., Pcs-Gelencsr, I. & Vida, G. (1958): Vegetationsstudien in rsg (Ungarisches Ostalpenvorland). - Akadmiai Kiad, Budapest. Jordanov, D., (1939). The vegetation of the Bulgarian part of the Stranja Mts.Proceed. of Sofia Univ., Faculty of Physics and Matematics, 34.3:409-476; 35, 3:1-90. .(in Bulgarian) Simon, T. (1979). Vegetationsuntersuchungen im Zemplner Gebirge. - Akadmiai Kiad, Budapest.
91N0
PAL.CLASS.: 41.87
1)
2)
5)
Page 120
91P0
PAL.CLASS.: 42.134
1)
2)
91Q0
PAL.CLASS.: 42.542, 42.5C8
1)
2)
3)
5)
91R0
PAL.CLASS.: 42.5C52
1)
2)
Page 121
91S0
PAL.CLASS.: 41.1E1
1)
2)
5)
91T0
PAL.CLASS.: 42.52112, 61.15p
1)
2)
4)
91U0
PAL.CLASS.: 42.5232
Page 122
1)
Xerophilous Scots pine woods of the Sarmatic region of western Eurasia and of areas with an extremely continental micro climate in northeastern Central and Eastern Europe. Towards its western limit this habitat is restricted to well drained habitats such as inland dunes and cliffs. There are many relict species of continental origin. Syntaxa included are the Anemono-Picetum sylvestris, Peucedano-Pinetum, Koelerio glaucae-Pinetum sylvestris, Caragano-Pinetum, Pyrolo-Pinetum sylvestris (p.) & Corynephoro-Pinetum sylvestris. Plants: Pinus sylvestris, Vaccinium myrtillus, Pyrola minor, Orthilia minor, Chimaphilla umbellata, Ophrys insectifera, Coronilla vaginalis, Globularia punctata, Brachypodium pinnatum. Corresponding categories Czech classification: L8.2 Lesostepn bory
2) 3)
91V0
PAL.CLASS.: 41.1D2
1) Fagus sylvatica, Fagus sylvatica-Abies alba, Fagus sylvatica-Abies alba-Picea abies and Fagus sylvatica-Carpinus betula forests of the Romanian, Ukrainian and eastern Serbian Carpathian mountains and pre-Carpathian hills of the alliance Symphyto cordati-Fagion, with typical Fagetalia species, developed on neutral, basicline and sometimes acidocline substrates. 2) Plants:. Symphytum cordatum, Cardamine glanduligera (syn Dentaria glandulosa), Hepatica transsilvanica, Pulmonaria rubra, Leucanthemum waldsteinii, Silene heuffelii, Ranunculus carpaticus, Euphorbia carniolica, Aconitum moldavicum, Saxifraga rotundifolia ssp. heuffelii, Primula elatior ssp. leucophylla, Hieracium rotundatum, Galium kitaibelianum, Moehringia pendula, Festuca drymeja Coldea G.H. (1991). Prodrome des associations vegetales des Carpates du sud-est (Carpates Roumaines). Documents Phytosociologiques, Camerino Doni, N., Popescu, A., Pauc-Comnescu, M., Mihilescu, S., Biri, I.A. (2005). Habitatele din Romnia. Edit. Tehnic Silvic, Bucureti, 500 p. (ISBN 973-96001-4-X)
5)
91W0
PAL.CLASS.: 41.19
1)
2)
Page 123
5)
Bondev, I.. (1991). The vegetation of Bulgaria. Map 1:600000 with explanatory text. St. Kliment Ohridski University Press, Sofia : 183p. (in Bulgarian) Horvat, I., Glavac, H. & H. Ellenberg. (1974). Vegetation Sudosteuropas. Gustav Fisher Verl. Jena : 767p. Michalik, S. (1990) Plant communities in the Boatin biosphere reserve on the northern slopes of the Stara Planina mountains. Ochrony przyrody 47 9-36
91X0
PAL.CLASS.: 41.1F
1)
2)
5)
91Y0
PAL.CLASS.: 41.2C
1)
2)
5)
Page 124
91Z0
PAL.CLASS.: 41.841
1)
2) 5)
91AA
PAL.CLASS.: 41.7371, 41.7372
1)
2) 5)
Page 125
91BA
PAL.CLASS.: 42.16
1)
2) 5)
Plants: Abies alba, Fagus sylvatica, Picea abies, Pinus sylvestris Bondev, I. 1991. The vegetation of Bulgaria. Map 1:600000 with explanatory text. St. Kliment Ohridski University Press, Sofia : 183p. (in Bulgarian) Horvat, I., Glavac, H. & H. Ellenberg, 1974. Vegetation Sudosteuropas. Gustav Fisher Verl. Jena : 767p.
91CA
PAL.CLASS.: 42.5C2, 42.5C3
1)
2) 5)
Plants: Pinus sylvestris, Calamagrostis arundinacea, Brachypodium pinnatum, Sesleria latifolia, Luzula sylvatica, Pteridium aquilinum. Bondev, I. 1991. The vegetation of Bulgaria. Map 1:600000 with explanatory text. St. Kliment Ohridski University Press, Sofia : 183p. (in Bulgarian) Horvat, I., Glavac, H. & H. Ellenberg, 1974. Vegetation Sudosteuropas. Gustav Fisher Verl. Jena : 767p.
Page 126
9210
1)
2)
9220
PAL.CLASS.: 41.186 and 41.187
* Apennine beech forests with Abies alba and beech forests with Abies nebrodensis
Beech forests of the hill level, on sites colder than those of 41.181, highly fragmented and harbouring many endemics, with Abies alba and Abies nebrodensis (Geranio nodosi-Fagion, Geranio striati-Fagion). Relict beech forests of the Madonie, Nebrodi and, very locally, the monti Peloritani, with Ilex aquifolium, Daphne laureola, Crataegus monogyna and Prunus spinosa (41.186); isolated beech forests of Mount Etna, at the southern limit of the range of the species (41.187). Plants: Abies alba, *A. nebrodensis, Fagus sylvatica.
1)
2)
9230
PAL.CLASS.: 41.6
1)
Page 127
41.63 - Maestrazgan Quercus pyrenaica forests Cephalanthero rubrae-Quercetum pyrenaicae Quercus pyrenaica forests of the sub-Mediterranean siliceous enclaves of the Maestrazgo and eastern Catalonian ranges, reduced to a very few relicts in the Penagolosa and Prades massifs. 41.64 - Baetic Quercus pyrenaica forests Adenocarpo decorticantis- Quercetum pyrenaicae Quercus pyrenaica forests of siliceous supra-Mediterranean areas with sub-humid climate of the western Sierra Nevada, the Sierra de Alfacar, the northern flanks of the Sierra de Cazulas and the Sierra Tejeda; in more humid locations Fraxinus angustifolius and Acer granatense accompany Q. pyrenaica. 41.65 - French Quercus pyrenaica forests Betulo-Quercetum pyrenaica i. a. Quercus pyrenaica forests of south-western France north to the Sologne where they constitute relatively extensive formations on poor soils, with Betula pendula, Lonicera periclymenum, Deschampsia flexuosa, Holcus mollis, Molinia caerulea, Teucrium scorodonia. 2) Plants: Quercus pyrenaica, Q. robur.
9240 woods
PAL.CLASS.: 41.77
1)
Forests and woods dominated by Quercus faginea, Quercus canariensis or Quercus afares. The humid formations of south-western Iberia (41.772 and 41.773) are forest types of unique character in Europe and of extreme biological importance. Sub-types : 41.771- Spanish Quercus faginea forests Spiraeo obovatae-Quercetum fagineae, Cephalanthero longifoliae-Quercetum fagineae, Violo wilkommii-Quercetum fagineae, Daphno latifoliae-Aceretum granatensis, Fraxino orniQuercetum fagineae Xero-mesophile Quercus faginea formations of slopes and plateaux of middle elevations of the Spanish Meseta and associated ranges. 41.772 - Portuguese Quercus faginea forests Arisaro-Quercetum fagineae Humid, epiphyte-clad, dense, relict Quercus faginea forests of Portugal, restricted to a very few isolated localities. 41.773 -Andalusian Quercus canariensis forests Rusco hypophylli-Quercetum canariensis Humid and hyper-humid, luxuriant Quercus canariensis forests of the sierras of extreme southern Spain, limited to the Aljibe and a very few localities in the Serrania de Ronda. 41.774 - Catalonian Quercus canariensis stands Carici depressae-Quercetum canariensis Formations of Catalonia rich in Quercus canariensis. 41.775 - Balearic Quercus faginea woods Aceri-Quercetum fagineae p. Relict formations of Mallorca dominated by, or rich in, Quercus faginea. Plants: Quercus faginea, Q. canariensis.
2)
Page 128
9250
PAL.CLASS.: 41.78
1)
2)
9260
PAL.CLASS.: 41.9
1) 2)
9270
PAL.CLASS.: 41.1A
1)
2)
9280
PAL.CLASS.: 41.1B
1)
2)
Page 129
9290
PAL.CLASS.: 42.A1
1) 2)
92A0
1)
2)
92B0
Riparian formations on intermittent Mediterranean water courses with Rhododendron ponticum, Salix and others
Distinctive, relict thermo- and meso-Mediterranean alder galleries of deep, steep-sided valleys, with Rhododendron ponticum ssp. baeticum, Frangula alnus ssp. baetica, Arisarum proboscideum and a rich fern community including Pteris incompleta, Diplazium caudatum, #Culcita macrocarpa (44.52). Relict Betula parvibracteata riparian galleries. The dominant species, an extremely local endemic, is accompanied by Myrica gale, Frangula alnus, Salix atrocinerea, Galium broterianum, Scilla ramburei (44.54). Plants: Rhododendron ponticum ssp. baeticum, Frangula alnus ssp. baetica, Arisarum proboscideum, Betula parvibracteata. The Rhododendron-alder galleries are often in contact with humid to hyper-humid Quercus canariensis forests (41.773) and with Salix pedicellata formations (44.1271).
1)
2) 4)
Page 130
92C0
PAL.CLASS.: 44.71 and 44.72
1)
Page 131
areas. This forest constitutes the only European formation of this species and harbours the unique, concentrated aggregation of Jersey Tiger Moths, Panaxia quadripunctaria. 2) Plants: Platanus orientalis, Liquidambar orientalis.
92D0
PAL.CLASS.: 44.81 to 44.84
1)
2)
Plants: Nerium oleander, Vitex agnus-castus, Tamarix spp., Securinega tinctoria, Prunus lusitanica, Viburnum tinus.
9310
PAL.CLASS.: 41.735
1) 2)
9320
PAL.CLASS.: 45.1
1)
45.12 - Carob woodland Ceratonia siliqua - dominated formations, often with Olea europaea ssp. sylvestris and Pistacia lentiscus. The most developed examples, some truly forest-like, are to be found in Tunisia, on the slopes of the Djebel, where they constitute carob-dominated facies of the wild olive woodlands (45.11), in Mallorca (Cneoro tricocci-Ceratonietum siliquae), in eastern Sardinia, in south-eastern Sicily, in Puglia, in Crete. 45.13 - Canarian olive woodland Olea europaea ssp. cerasiformis and Pistacia atlantica formations of the Canary Islands. 2) Plants: Olea europaea ssp. sylvestris, Ceratonia siliqua, Pistacia lentiscus, Myrtus communis, Olea europaea ssp. cerasiformis, Pistacia atlantica.
9330
PAL.CLASS.: 45.2
1)
2)
9340
PAL.CLASS.: 45.3
1)
Page 133
Isolated Quercus ilex-dominated stands occurring as a facies of dunal pine-holm oak forests. 45.34 - Quercus rotundifolia woodland Iberian forest communities formed by Q. rotundifolia. Generally, even in mature state, less tall, less luxuriant and drier than the fully developed forests that can be constituted by the closely related Q. ilex, they are, moreover, most often degraded into open woodland or even arborescent matorral. Species characteristic of the undergrowth are Arbutus unedo, Phillyrea angustifolia, Rhamnus alaternus, Pistacia terebinthus, Rubia peregrina, Jasminum fruticans, Smilax aspera, Lonicera etrusca, L. implexa. 2) Plants: Quercus ilex, Q. rotundifolia.
9350
PAL.CLASS.: 41.79
1)
2)
9360
PAL.CLASS.: 45.61 to 45.63
1)
Page 134
2)
Plants: Apollonias barbujana, Ardisia bahamensis, Asparagus fallax, Canarina canariensis, Carex canariensis, C. eregrina, Clethra arborea, Convolvulus canariensis, Cryptotaenia elegans, Erica arborea, Euphorbia melifera, #E. stygiana, #Frangula azorica, Geranium canariensis, Heberdenia excelsa, Hedera canariensis, Ilex canariensis, I. perado ssp. azorica, I. perado ssp. perado, Isolexis canariensis, Ixanthus viscosus, Juniperus brevifolia, Laurus azorica, Myrica faya, Ocotea foetens, Persea indica, #Picconia azorica, P. excelsa, *Pittosporum coriaceum, Pleiomeris canariensis (=Myrsine canariensis), Prunus lusitanica, #P. l. ssp. azorica, P. l. ssp. hixa, Rubia peregrina, Rubus bollei, Ruscus streptophyllus, Sambucus lanceolata, *S. palmensis, Semele androgyna, Senecio auritus (=S. maderensis), Sideretis canariensis, S. macrostachys, Smilax aspera, S. canariensis, S. divaricata, Sonchus fruticosus, Tamus edulis, Teline maderensis (=Cytisus maderensis), Vaccinium cylindraceum, V. padifolium, Viburnum tinus ssp. subcordatum, Visnea mocanera. Animals: Columba bollei, C. junionae, C. trocaz, Fringilla coelebs ssp. ombriosa, F. teydea, F. t. ssp. polatzeki.
9370
PAL.CLASS.: 45.7
1)
2)
9380
PAL.CLASS.: 45.8
1)
Communities dominated by arborescent Ilex aquifolium, relict of various forests with a field layer rich in Ilex and sometimes with Taxus (42.A7), of the supra-Mediterranean level on various substrates. These woods correspond to the senescence stage of a forest with a undergrowth with Taxus and Ilex (belonging among others to the Ilici-Quercetum ilicis), after the fading of the tree layer. They generally form patches inside or outside forests.
Page 135
9390
PAL.CLASS.: 45.48
1)
2)
93A0
1)
2)
4)
9410
1)
42.22 - Inner range montane spruce forests. Piceetum montanum. Picea abies forests of the montane level of the inner Alps, characteristic of regions climatically unfavourable to both beech and fir. Analogous Picea abies forests of the montane and collinar levels of the inner basin of the Slovakian Carpathians subjected to a climate of high continentality. 42.23 - Hercynian sub-alpine spruce forests Sub-alpine Picea abies forests of high Hercynian ranges 21. 42.24 Southern European Norway spruce forests Outlying Picea abies formations of the Apennines, the southern Dinarides, the Balkan Range and the Rhodopides, at the southern limit of the range of the species and mostly south of its continuous range. 42.25 - Peri-Alpine spruce forests Spontaneous Picea abies formations occupying outlying altitudinal or edaphic enclaves within the range of more predominant vegetation types of the montane levels of the outer Alps, the Carpathians, the Dinarides, the Jura, the Hercynian ranges, the subalpine levels of the Jura, the western Hercynian ranges and the Dinarides 2) Plants: Picea abies, Vaccinium spp.
9420
1)
2)
21
9430
PAL.CLASS.: 42.4
1)
2)
4)
9510
PAL.CLASS.: 42.15
1) 2)
9520
PAL.CLASS.: 42.19
1) 2)
Page 138
9530
PAL.CLASS.: 42.61 to 42.66
1)
2)
9540
PAL.CLASS.: 42.8
1)
Page 139
42.824 - Corsican mesogean pine forests Pinetum pinastri, Erico-Arbutetum p., Galio-Pinetum p. Pinus pinaster-dominated forests of the meso- and supra-Mediterranean levels of Corsica, mostly on granitic substrates; they are very developed, accompanied by a maquis-like understory, in the meso-Mediterranean zone, mostly in its upper levels; they occur locally within the supra-Mediterranean zone, on adrets and at lower altitudes, as facies of laricio pine forests. 42.825 - Sardinian mesogean pine forests Pinus pinaster formations on granitic substrates of northern Sardinia, with Arbutus unedo, Quercus ilex, Rosmarinus officinalis, Erica arborea, Genista corsica, Lavandula stoechas, Rubia peregrina, Calicotome spinosa, Pistacia lentiscus, Teucrium marum. 42.826 - Pantellerian mesogean pine forests Pinus pinaster woods of Pantelleria. 42.83 - Stone pine forests Mediterranean forests and old naturalised plantations of Pinus pinea. Old introductions in many areas often makes the distinction between self sown forests and long-established formations of artificial origin difficult. These are thus included here, while recent, obviously artificial groves are not. 42.831 - Iberian stone pine forests Pinus pinea forests of the Iberian peninsula, where they reach their greatest development. 42.832 - Balearic stone pine woods Pinus pinea formations of the Balearic Islands, native only on Ibiza and Formentera. 42.833 - Provence stone pine woods Pinus pinea formations of Provence, possibly spontaneous on coastal sands and in the Maures area. 42.834 - Corsican stone pine woods Pinus pinea formations of the littoral of Corsica, some of which may be of natural origin, in particular on old dunes of the east coast. 42.835 - Sardinian stone pine forests Pinus pinea formations of Sardinia. 42.836 - Sicilian stone pine forests Pinus pinea formations of the Monti Peloritani, north-western Sicily, of probable native origin. 42.837 - Peninsular Italian stone pine forests Large, ancient, Pinus pinea plantations of the Tyrennian, and locally, Adriatic coasts of the Italian peninsula, in Liguria, Toscany, Latium, Campania, Emilia-Romana (Ravenna) and Friuli-Venetia Giulia (Grado). 42.838 - Greek stone pine forests Pinus pinea woods of the littoral and coastal hills of the Peloponnese, Chalcidice, Crete and Aegean islands, rather local but probably in part, at least, spontaneous; a splendid example exists, in particular, on Skiathos. 42.84 - Aleppo pine forests Woods of Pinus halepensis, a frequent colonist of thermo- and calcicolous meso-Mediterranean scrubs. The distinction between spontaneous forests and long-established formations of artificial origin is often difficult. The latter are thus included here, while recent, obviously artificial groves are not. 42.841 - Iberian Aleppo pine forests Pinus halepensis forests of Spain, considered native for at least two-thirds of their considerable expanse; they are mostly restricted to eastern regions on the Mediterranean slope of the Catalonian mountains, the Maestrazgo, the pre-Baetic ranges of the upper Guadalquivir basin, the southern Andalusian mountains; they penetrate farther inland in the Ebro basin and around the headwaters of the Tagus and Guadalquivir systems. 42.842 - Balearic Aleppo pine forests Pinus halepensis formations of the Balearics, present and probably native on all the major islands. 42.843 - Proveno-Ligurian Aleppo pine forests
Page 140
Mostly lower meso-Mediterranean Pinus halepensis forests of Provence and of the lower slopes and coastlines of the Maritime and Ligurian Alps, extensive and undoubtedly native. 42.844 - Corsican Aleppo pine woods Rare and local Pinus halepensis woods of the Corsican coasts, some, at least, possibly natural. 42.845 - Sardinian Aleppo pine woods Pinus halepensis formations of Sardinia, where certainly native woods occur on Isola di San Pietro and the Sulcis coast of Iglesiente. 42.846 - Sicilian Aleppo pine woods Pinus halepensis formations of Sicily and peripheral islands (Egadi, Lampedusa, Pantelleria). 42.847 - Peninsular Italian Aleppo pine forests Pinus halepensis formations of the Italian peninsula; extensive, probably at least partially native ones are individualised in the subdivisions below. 42.848 - Greek Aleppo pine forests Pinus halepensis formations of Greece, where the species is relatively widespread, particularly in Attica, Thessaly, the coasts of the Peloponnese and of central continental Greece, the Ionian islands, Chalcidici, the northern Sporades, Euboea and Skiros. 42.85 - Aegean pine forests Pinus brutia forests of Crete and eastern Aegean islands. Eastern vicariants of Aleppo pine forests (42.84), they comprise, however, taller, more luxuriant, and often extensive, formations. Disjunct formations of this pine or of related species, described from Crimea and the Caucasian region (Pinus pityusa, Pinus stankewiczii, Pinus eldarica) have been included.. 42.851 - Aegean pine forests of Crete Pinus brutia-dominated forests of Crete and its satellite islands Gavdos and Gaidaronisi, pure or mixed with Cupressus sempervirens; they are widespread in particular in the White Mountains, the Psiloriti range, the Dikti range and, locally, in the Sitia mountains and the Asterousia mountains. 42.852 - Aegean pine forests of Lesbos Extensive Pinus brutia forests of Lesbos, occupying Mount Olympus and surrounding hills in the south-eastern quadrant of the island, as well as parts of the Kuratsonas range in the north-west; these forests harbour the only European population of the nuthatch Sitta krueperi and the most significant one of the orchid Comperia comperiana. 42.853 - Aegean pine forests of Samos Pinus brutia forests covering large expanses of Samos, in particular in the Ambelos range, the Kerki mountains, the southern hills and the north-eastern peninsula. 42.854 - Aegean pine woods of Chios Remnant forests of Chios with a composition and stratification similar to those of the forests of Samos. 42.855 - Aegean pine forests of Thasos Broad Pinus brutia belt on the lower reaches of Thasos, up to about 400 to 500 metres, mixed with Pinus pallasiana in the higher areas. 42.856 - Aegean pine woods of Samothrace Mostly sparse Pinus brutia formations of the lowlands of Samothrace. 42.857 - Aegean pine forests of Rhodes Remnant Pinus brutia forests of Rhodes, still represented by some relatively natural formations with rich scrub undergrowth. 42.858 - Aegean pine forests of Karpathos Fairly extensive Pinus brutia forests of Karpathos, distributed, in particular, in the northern coastal area, the southern interior and the middle elevation of Kali Limni. 42.859 - Aegean pine forests of the Dodecanese Pinus brutia formations of the islands of Simi, Kos, Leros and Ikaria. 2) Plants: Pinus pinaster ssp. atlantica, Pinus pinaster ssp. pinaster (=Pinus mesogeensis), Pinus pinea, Pinus halepensis, Pinus brutia.
Page 141
9550
PAL.CLASS.: 42.9
1)
2)
9560
PAL.CLASS.: 42.A2 to 42.A5 and 42.A8
1)
Luna, with Juniperus nana, J. sabina, Berberis vulgaris ssp. cantabrica, Rhamnus alpinus, Viburnum lantana; gypsiferous soils of the Ebro basin, with Rhamnus lycioides; clay soils of the Campo de Montiel; Sierra Taibilla), southern France (Montagne de Rie); warm calcareous supra-Mediterranean slopes of the south-western Alps, in Drme, Hautes-Alpes and Alpes-de-Haute-Provence, between 700 and 1200 metres; warm calcareous supra-Mediterranean slopes of the Isre valley, in the western Alps, between 300 and 500 metres; valleys in the interior of Corsica -Pinnera, Rudda, Pruniccia - sometimes mixed with Pinus laricio; 42.A3 - Grecian juniper woods (Juniperetum excelsae) - forest formations dominated by Juniperus excelsa, of the Ostryo-Carpinion zone of the mountains of northern Greece (up to 900-1000m, around lake Prespa); 42.A4 - Stinking juniper woods - forest formations dominated by Juniperus foetidissima on adrets of the upper supra-Mediterranean level in Greece; 42.A5 - Syrian juniper woods - Juniperus drupacea woods of the northern slopes of Mount Parnon, Greece; 42.A8 - Macaronesian juniper woods - Juniperus cedrus formations of the high altitudes in Tenerife, La Palma, Gomera, Gran Canaria, restricted to steep rocky slopes; Juniperus phoenicea formations of Tenerife, La Palma, Hierro, Gran Canaria, La Gomera (Maytenio-Juniperion phoeniceae p.); endemic Juniperus brevifolia formations of the Azores (Juniperion brevifoliae p.). 2) 4) Plants: Juniperus brevifolia, J. cedrus, J. drupacea, J. excelsa, J. foetidissima, J. oxycedrus, J. phoenicea, J. thurifera. The arborescent matorrals of Juniperus thurifera (32.136), Juniperus excelsa and J. foetidissima (32.133), Juniperus drupacea (32.135) and the ericoid-dominated facies of the Macaronesian Juniperus formations (31.3) are generally associated in the field, but they should not be included in this habitat type.
9570
PAL.CLASS.: 42.A6
1)
2)
9580
PAL.CLASS.: 42.A72 and 42.A73
1)
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42.A73 - Sardinian yew woods - Taxus baccata and Ilex aquifolium woods of the Catena del Marghine and the Mount Limbara system. In the north and centre of Portugal there are Taxus baccata relicts, sometimes in small isolated formations (Serras do Gers and Estrela), that may be included in this habitat type. 2) Plants: Buxus sempervirens, Ilex aquifolium, Mercurialis perennis, Sorbus aria, Taxus baccata.
9590
PAL.CLASS.: 42.B2
1) 2)
95A0
PAL.CLASS.: 42.7
1)
2)
5)
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