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2014, Encyclopedia of Global Archaeology
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6 pages
1 file
Basic Species Information The olive (Olea europea L.) tree is a subtropical evergreen plant that was indigenous to the Mediterranean Basin, confined by its intolerance of frost. It has adapted to long summer droughts and a semiarid temperate climate, well-drained soils, moderate-to-low pH (below 8.5), and mild soil salinity (Terral et al. 2004: 64; Doveri & Baldoni 2007: 254-5). The genus Olea, belonging to the family Oleaceae, currently consists of more than 20 species found in tropical and subtropical areas over five continents. Recent revisions of the taxonomy surrounding O. europea suggest that this species should be divided into six subspecies based on morphology and geographical distribution including: (1) subsp. europea with two botanical varieties europea (cultivated olive) and sylvestris (wild olive), which is widely distributed throughout the Mediterranean Basin; (2) subsp. cuspidate distributed from SE Asia to SW China as well as the Arabian peninsula through East and South Africa; (3) subsp. laperrinei is restricted to the Sahara region; (4) subsp maroccana, which is restricted to Morocco; (5) subsp cerasiformis restricted to the island of Madeira; and, (6) subsp guanchica which is restricted to the Canary Islands.
TAG Theoretical and Applied Genetics, 2002
Tandem repeats belonging to three DNA sequence families (OeTaq80, OeTaq178, and OeGEM86) were isolated from the nuclear DNA of Olea europaea cv. Carolea and dot-hybridized to the genomic DNA of 14 hypothetically different Olea species, 78 olive cultivars, and 14 wild olives. The copy number per unreplicated haploid genome of OeTaq80-and OeTaq178-related sequences was in the 10 7 -10 6 range and that of OeGEM86-related sequences was in the 10 5 range in cultivars, wild olives and some Olea species. A large variation in the frequency of repeats belonging to each sequence family was observed within each group of plants. Positive correlations existed in each genome between the frequencies of repeats belonging to each family, and their overall frequency was positively correlated to the genome size. Duncan grouping showed that the frequency variation of tandem repeats within each group of plants was not continuous. Two main groups and several subgroups of genotypes could be separated within both the olive cultivars and the wild olives. Discrete areas in the Mediterranean Basin could be delimited by the geographic distribution of cultivated olives with different genotypes and the wild plants were associated with the cultivars in these areas according to genotypic similarity. The Olea species could be divided into four genotypic groups. Three of these, comprising accessions from Asia and North Africa, showed similarity with the genotypes of cultivars and wild olives. These results suggest a polyphyletic origin of cultivated olives from different wild Olea forms distributed throughout the Mediterranean Basin.
Vegetation History and Archaeobotany, 2005
The remains of Olea europaea in archaeological contexts in the southern Iberian Peninsula have been found in the Epipalaeolithic levels of Cueva de Nerja (10860±160 b.p.). The abundant appearance of charcoal and some seed remains from the Copper Age (3rd millennium b.c.) in the coastal zones of the southeast indicate that this species formed part of the vegetation of the Thermo-mediterranean zone and that its fruits were collected during these periods. However, Olea did not appear in the Meso-mediterranean zone until the Roman period, when olive cultivation was introduced there. The presence of charcoal and olive stones from the 1st century a.d. onwards is abundant, together with remains of structures for oil pressing.
Plants
Oleaster (Olea europaea L. subsp. europaea var. sylvestris) is the ancestor of cultivated olive (Olea europaea L. subsp. europaea var. europaea) and it is spread through the whole Mediterranean Basin, showing an overlapping distribution with cultivated olive trees. Climate change and new emerging diseases are expected to severely affect the cultivations of olive in the future. Oleaster presents a higher genetic variability compared to the cultivated olive and some wild trees were found adapted to particularly harsh conditions; therefore, the role of oleaster in the future of olive cultivation may be crucial. Despite the great potential, only recently the need to deeply characterize and adequately preserve the wild olive resources drew the attention of researchers. In this review, we summarized the most important morphological and genetic studies performed on oleaster trees collected in different countries of the Mediterranean Basin. Moreover, we reviewed the strategies introduced so...
XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010): Olive Trends Symposium - From the Olive Tree to Olive Oil: New Trends and Future Challenges, 2011
Plants
A prospecting campaign in the Maltese Islands has ensured the survival of several ancient olive trees (Olea europaea L.), genetically distant from known cultivars. Most of these plants were abandoned or partially cultivated. A two-year evaluation of fruit characteristics and compositions was performed on samples collected from the main representatives of these indigenous genotypes. Analyses were carried out using Gas Chromatography, High-Performance Liquid Chromatography and Near Infrared Spectrometry. Among the fruit samples, a wide range of variations was observed. Some of the genotypes showed fruit traits suitable for table olive production. This is the case of samples with a pulp/pit ratio higher than four, such as 1Wardija, 1Caritas, 1Plattini, 1Bingemma Malta and 3Loretu, whilst 1Bidni, 1Mellieha, 2Qnotta, 3Loretu, 1Bingemma Malta and 1Caritas were suitable for dual purpose. The total phenol content ranged from 6.3 (1Wardija) to 117.9 (2Mtarfa) g/kg of fresh pulp. The average ...
Exploration on wild olive diversity carried out during the period 2000-2011, recorded a number of 27 wild forms. Morphological marker based analysis were performed for olive identity characterization, to determine their localization, usage limits as well as to build in -situ & ex-situ collection of 27 wild olive forms. Morphological description (Rezgen) was don e for each olive genotype, in total of 49 characters; of tree, leaf, inflorescence, fruit and endocarp were measured during the study. . Information was gathered for 27 forms with local designations, which represent 7 populations. Basing on the endocarp characteristics, as an important morphological marker, wild olive forms have been modelled and analysed (PCA), are clustered in two groups. (i) Olea europaea L. subsp. oleaster (Hoffmgg. & Link) 6 Varity, (ii) O lea europaea L. subsp. sylvestris (Mill.) 1 Varity. According to the oil content, genotypes are clustered in two main groups in: (i) low oil content (>14%), (ii) me...
Todos os direitos autorais reservados pela TOTVS S.A. Proibida a reprodução total ou parcial, bem como a armazenagem em sistema de recuperação e a transmissão, de qualquer modo ou por qualquer outro meio, seja este eletrônico, mecânico, de fotocópia, de gravação, ou outros, sem prévia autorização por escrito da proprietária. O desrespeito a essa proibição configura em apropriação indevida dos direitos autorais e patrimoniais da TOTVS. Conforme artigos 122 e 130 da LEI no. 5.988 de 14 de Dezembro de 1973. MRP Protheus-Versão 12
Sistemi Intelligenti, 2024
Recently, a part of research in pragmatics has been focused on neurolinguistics and neuropragmatics. Since it is believed that Autism Spectrum Disorder (ASD) and schizophrenia represent the most vital core of neuropragmatics and clinical pragmatics research (Cummings, 2009; 2017; Bambini, 2010), we will review and discuss the neuropragmatic literature on these clinical cases. Therefore, the philosophical implications of the recent debate on the role of temporo-parietal junction in Theory of Mind (ToM) will be discussed. Some scholars hypothesized that humans usually exercise a sort of mental state integration through inferential processes that are specific for mental phenomena (Saxe, Baron Cohen, 2006) and that probably this ability is damaged in patients with ASD (Charman, Baron-Cohen, 1992; Leslie, Thaiss, 1992; Pennisi, 2016b) and schizophrenia (Lee et al., 2011). Trough the discussion of studies on theory of mind we will try to show how psychopathology contributes to enriching the knowledge of the problems raised by neuropragmatics. Specifically, for example, ASD seems to negatively impact the linguistic integration of the context in the disambiguation of meaning, but not the intuition of the other’s intention. Although neurolinguistics and/or neuropragmatic studies seem to show that the schizophrenic subject is incapable of understanding and using irony, sarcasm and generally has difficulty in figurative language – as we will try to show in this essay – the letters written by the patients or their poetic productions show a different reality. Probably, in psychotic language cases, the problem is to consider schizophrenia without its delusional-hallucinatory context. So, it seems necessary that neuropragmatics and clinical pragmatics should better consider the schizophrenic communicative context: therefore, also that of delusion and hallucinations. Keywords: neurolinguistics, neuropragmatics, ASD, schizophrenic speech, delusional-hallucinatory context.
Editing the Greek Psalter, 2024
The secondary literature frequently references purported Jewish Greek Psalter adaptations from the early modern period, often citing Codex Vaticanus gr. 343 (dated to 1450) as the earliest example and a printed edition from 1643 as another. However, the latter is commonly misdated to 1543. Both examples, along with others that could be included in a broader list of early modern Psalter versions, are, in fact, Christian revisions of the Greek text and cannot be considered Jewish translations or adaptations. This study examines these texts in detail, beginning with the Vatican Vernacular Psalter, Codex Vaticanus gr. 343 (§ 1). It then explores a seventeenth-century version partly attributed to Maximos Peloponnesios and Athanasios Patellaros (§ 2), and finally, discusses various seventeenth to eighteenth-century versions, including the supposed Jewish print from 1643, which is actually a version by Agapios Landos of Crete, as well as the versions by Georgios Palamedes and Ioannes Litinos (§ 3). Contrary to the assertions of Fernández Marcos and other scholars, none of these Psalter translations originated from Jewish sources; they are all Christian adaptations from the early modern period. From a linguistic perspective, the Vatican Vernacular Psalter and the versions attributed to Maximos Peloponnesios and Athanasios Patellaros provide captivating examples of early modern Greek vernacular, while from a poetic point of view, the version by Georgios Palamedes is particularly interesting.
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