Showing posts with label Subgenus. Show all posts
Showing posts with label Subgenus. Show all posts

Wednesday, August 14, 2024

[Botany • 2024] A Synopsis of Carex subgenus Psyllophorae, sect. Junciformes (Cyperaceae) in South America


 Carex subgenus Psyllophorae, sect. Junciformes

in Morales-Alonso, Muñoz-Schüler, Pereira-Silva, Donadío, Martín-Bravo et Jiménez-Mejías, 2024. 
 
Abstract
This is the second study of a series of thorough studies into the taxonomy and systematics of Carex in South America. Here, we present the systematic placement, taxonomic account, formal typifications, and summarized distributions for the 31 accepted South America species of Carex subg. Psyllophorae, all belonging to sect. Junciformes. We have conducted an exhaustive revision of literature, more than 400 specimens from 32 South and North American and European herbaria have been studied, and a Sanger phylogenetic study with four DNA regions and morphometric analyses for the C. phalaroides group have been performed. We present an enlarged phylogenetic study where sect. Junciformes sampling has increased by 11 species regarding previous studies, only lacking four species of the group (C. herba-alpacae, C. moorei, C. nelmesiana, and C. transandina). South American species of sect. Junciformes are grouped into four major lineages: C. camptoglochin Clade, Aciculares Clade (South America and Australia–New Zealand), C. phalaroides group, and Junciformes Clade. We have resolved the C. phalaroides complex into six independent species with a clear geographic structure. We successfully unravelled the systematic placement of three species included here for the first time (C. boelckeiana, C. reicheana, and C. manuelbarrosii). An identification key is provided for the studied species. We propose 30 new typifications, and four new species are described (C. herba-alpacae, C. manuelbarrosii, C. melliza, and C. via-montana).

neotropics, phylogeny, taxonomy

 Representative images of living specimens of sect. Junciformes.
A, C. andina (Chile, Ñuble). B, C. aphylla (Chile, Biobío). C, C. argentina (Chile, Metropolitana de Santiago). D, C. herba-alpacae (Peru, Lima),
E, C. camptoglochin (Chile, Los Lagos). F, C. boelckeiana (Chile, Araucaní). G, C. caduca (Chile, Los Lagos). H, C. reicheana (Chile, Araucanía).
I, C. setifolia (Chile, Maule). J, C. pungens (Chile, Valparaíso). K, C. sorianoi (Chile, O’ Higgins). L, C. vallis-pulchrae subsp. barrosiana (Argentina, Tierra del Fuego).
M, C. chlorolepis (Chile, Biobío). N, C. phalaroides (Brazil, Paraná). O, C. paraguayensis (Brazil, Rio Grande do Sul). P, C. via-montana (Ecuador, Pichincha).
Pictures: P. Muñoz-Schüler(A, B, E, I, J, M), M. Maldonado (D), P. Jiménez-Mejías (F, G, O), S. Martín-Bravo (C, H), M. Luceño (K, L, N), and A. Morales-Alonso (P).

Representative inflorescence variation displayed by sect. Junciformes species. 
From A to J, Aciculares Clade; from L to Y, Junciformes Clade; and from Z to AE, C. phalaroides group. ...
Scale bar = 4 cm.


Ana Morales-Alonso, Paulo Muñoz-Schüler, Luciana Pereira-Silva, Sabina Donadío, Santiago Martín-Bravo and Pedro Jiménez-Mejías. 2024. A Synopsis of Carex subgenus Psyllophorae, sect. Junciformes (Cyperaceae) in South America. Botanical Journal of the Linnean Society. boae038. DOI: doi.org/10.1093/botlinnean/boae038

Sunday, January 28, 2024

[Entomology • 2024] Lasioglossum iridescens, L. dilisena & L. silveirai • A Problematic Species Complex of Lasioglossum Subgeneric Diagnostics in North America (Hymenoptera: Halictidae)


Lasioglossum (Sphecodogastra) dilisena
 Hettiarachchi & Gibbs, 2024

 
Abstract
A problematic species complex within Lasioglossum subgenus Sphecodogastra with unusual metallic reflections on the mesosoma is described from North America. Three new species in this complex are described and illustrated: Lasioglossum (Sphecodogastrairidescens sp. nov., Lasioglossum (Sphecodogastra) dilisena sp. nov., and Lasioglossum (Sphecodogastrasilveirai sp. nov. Our study addresses the challenge of diagnosing Lasioglossum subgenera within North America. We present an updated key for the North American Lasioglossum subgenera.

Key words: Apoidea, classification, cryptic species, new species, taxonomy


Lasioglossum (Sphecodogastra) iridescens sp. nov. 

Etymology. The specific epithet refers to the iridescent colouration of the new species.


Lasioglossum (Sphecodogastra) dilisena sp. nov. , ♀, holotype.
A. Dorsal habitus. b. Face. C. Lateral habitus. D.Metasoma.
Scale bars = 1 mm.

Lasioglossum (Sphecodogastra) dilisena sp. nov. 

Etymology. The specific epithet ‘dilisena’ is derived from the Sinhala word ‘dilisena’ දිලිසෙන, which means ‘shining’, but is used here as a noun in apposition. This name was chosen because all three species described in this paper have an unusual metallic reflection on the mesosoma that is not seen in other known North American species in the subgenus Sphecodogastra. The first author is also a native speaker of Sinhala from Sri Lanka. Sinhala language is one of the official and national languages of Sri Lanka and the mother tongue of the majority people of Sri Lanka. Through this naming choice, we hope to honour all the linguistic and cultural diversity of the world.

 
Lasioglossum (Sphecodogastrasilveirai sp. nov., ♀, holotype.
A. Dorsal habitus. b. Face. C. Lateral habitus. D. Metasoma.
Scale bars = 1 mm.

Lasioglossum (Sphecodogastrasilveirai sp. nov.

Etymology. This species is named in honour of the late Fernando Silveira (Universidade Federal de Minas Gerais) for his contributions to bee taxonomy and his warm, jovial spirit, which made it a delight to attend international conferences on pollinators.

  
Thilina Hettiarachchi and Jason Gibbs. 2024. A Problematic Species Complex of Lasioglossum Subgeneric Diagnostics in North America (Hymenoptera: Halictidae). Zootaxa. 5404(1); 206-235. DOI: 10.11646/zootaxa.5404.1.13

Saturday, November 25, 2023

[Herpetology • 2023] Nanorana laojunshanensis • A New Species of Nanorana (Anura: Dicroglossidae) from Northwestern Yunnan, China, with Comments on the Taxonomy of Nanorana arunachalensis and Allopaa


 Nanorana laojunshanensis 
Tang, Liu & Yu, 2023

Laojunshan Slow Frog | 老君山倭蛙  ||  DOI: 10.3390/ani13213427 

 Abstract

The genus Nanorana contains three subgenera, namely Nanorana, Paa, and Chaparana, and currently, there are four species known to science in Nanorana (Nanorana). In this study, we describe a new species belonging to the subgenus Nanorana from northwestern Yunnan, China. Phylogenetically, the new species, Nanorana laojunshanensis sp. nov., is the sister to the clade of N. pleskei and N. ventripunctata. Morphologically, the new species can be distinguished from known congeners by the combination of following characters: present tympanum, equal fingers I and II, small body size, yellow ventral surface of limbs, distinct vomerine teeth, indistinct subarticular tubercles, head width greater than head length, slender supratympanic fold, absent dorsolateral fold, nuptial spines present on fingers I and II in adult males, absent vocal sac, and paired brown spines on the chest. Moreover, we suggest moving the genus Allopaa into Nanorana (Chaparana) and consider that N. arunachalensis is neither an Odorrana species nor a member of the subfamily Dicroglossinae (therefore Nanorana), but probably represents a distinct genus closely related to Ingerana or belongs to Ingerana, pending more data. Additionally, we consider that Nanorana minica deserves the rank of an independent subgenus, and we suggest assigning N. arnoldi, N. blanfordii, N. ercepeae, N. polunini, N. rarica, N. rostandi, N. vicina, N. xuelinensis, and N. zhaoermii into the subgenus Paa and placing N. kangxianensis, N. phrynoides, and N. sichuanensis in the subgenus Chaparana.

Keywords: Nanorana; Paa; Chaparana; Allopaa; northwestern Yunnan

 Holotype of Nanorana laojunshanensis sp. nov.
in life (A,B) and in preservative (C,D).

Nanorana (Nanorana) laojunshanensis sp. nov. 

Diagnosis: The new species was assigned to Nanorana (Nanorana) using the following morphological characters: oval tongue, shallowly notched posterior; blunt finger and toe tips; absent webbing between fingers, absent supernumerary tubercle; developed webbing between toes; paired patches of spine on chest [Fei, et al., 2009]. The new species can be distinguished from other members of Nanorana by having a combination of the following characters: (1) present tympanum; (2) small body size; (3) distinct vomerine teeth; (4) indistinct subarticular tubercles; (5) head width greater than head length; (6) slender supratympanic fold; (7) finger I equal to finger II; (8) absence of dark blotches on ventral surface and yolk-yellow ventral surface of limbs; (9) absent dorsolateral fold; (10) nuptial spines present only on fingers I and II in adult males; (11) absent vocal sac; and (12) paired brown spines on chest.
...

Etymology: The specific epithet is named after the type locality, Mt. Laojun, Lijiang, Yunnan, China. We suggested “laojunshan slow frog” for the common English name and “老君山倭蛙 (Lǎo Jūn Shān Wō Wā)” for the common Chinese name.

Minipaa subgen. nov.
Type species: Nanorana minica (Dubois, 1975)
Included species: Nanorana minica (Dubois, 1975).

Distribution: Nepal, India, Bhutan.

Etymology: From the Latin mini, “small”, and from the generic name Paa, Dubois, 1975 (from the Tamang name paa, “frog”), in which this species was originally placed. This name refers to the small body size of this taxon.

 
 Shangjing Tang, Shuo Liu and Guohua Yu. 2023. A New Species of Nanorana (Anura: Dicroglossidae) from Northwestern Yunnan, China, with Comments on the Taxonomy of Nanorana arunachalensis and AllopaaAnimals. 13(21), 3427. DOI: 10.3390/ani13213427 
 
Simple Summary: Currently, the genus Nanorana contains thirty-two species, and four of them belong to the subgenus Nanorana, namely N. bangdaensis, N. parkeri, N. pleskei, and N. ventripunctata. In this study, on the basis of molecular and morphological evidence, we described a new species of Nanorana (Nanorana) from northwestern Yunnan, China, where only one member (N. ventripunctata) of Nanorana (Nanorana) has been reported. Additionally, the taxonomic status of Nanorana arunachalensis and Allopaa hazarensis were discussed, and subgeneric allocations of Nanorana species were suggested. The findings in this study bring the number of Nanorana species to 33 and improve our understanding on the taxonomy of genus Nanorana and the species diversity of Nanorana (Nanorana), an alpine group widely distributed in the southern and southeastern Qinghai–Tibetan Plateau.

Thursday, January 26, 2023

[Botany • 2023] Phylogeny based Generic Reclassification of Muscari sensu lato (Asparagaceae) using Plastid and Genomic DNA


Inflorescences of Muscari species incorporated in this study.
A–H, M. subg. Muscari: A, M. anatolicum; B, M. adilii; C, M. armeniacum; D, M. discolor; E, M. sivrihisardaghlarense; F, M. vuralii; G, M. neglectum; H, M. commutatum.
I, M. subg. Muscarimia: M. macrocarpum.
J–L, Muscari subg. Pulchella (subg. nov.): J, M. latifolium; K, M. pulchellum; L, M. bourgaei.
 — Names listed above follow the new classification here proposed. 

in Böhnert, Neumann, Quandt & Weigend, 2023.
Images: T. Böhnert. twitter.com/TimBoeh

Abstract
The grape hyacinth (Muscari) represents an important ornamental plant group in Asparagaceae subfamily Scilloideae, comprising some 80 species distributed mainly in the Mediterranean. However, genus delimitation has repeatedly shifted over the past two centuries and a general consensus has not been reached so far. The present study investigates the phylogeny of Muscari s.l. (i.e., including the disputed segregates Pseudomuscari and Leopoldia) with a broad sampling of about half the currently recognized species using both chloroplast markers (trnK(matK)-psbA, trnL-trnF, rpl16) and genome-wide single nucleotide polymorphism (SNP) data generated by double-digest restriction site-associated DNA sequencing (ddRAD). We perform concatenated maximum likelihood inference for both datasets as well as a coalescent-based approach and principal component analysis (PCA) on the ddRAD data. We find that the morphological characters traditionally used to distinguish different genera are not diagnostic for the clades here retrieved. Also, the segregates Pseudomuscari and Leopoldia are deeply nested in Muscari and we therefore propose a broadly defined Muscari with five subgenera. The subgenera roughly correspond to previously recognized entities, with the exception of the newly identified clade here proposed as M. subg. Pulchella subg. nov. We provide a provisional assignment of the 80 currently accepted taxa to these subgenera.

Keywords: ddRAD, geophyte, Leopoldia, Mediterranean, Pseudomuscari, Scilloideae

Inflorescences of 16 Muscari species incorporated in this study.
A–H, Msubg. Muscari: A, M. anatolicum; B, M. adilii; C, M. armeniacum; D, M. discolor; E, M. sivrihisardaghlarense; F, M. vuralii; G, M. neglectum; H, M. commutatum.
I, M. subg. MuscarimiaM. macrocarpum.
J–L, M. subg. Pulchella (subg. nov.): J, M. latifolium; K, M. pulchellum; L, M. bourgaei.
M–P, M. subg. Pseudomuscari: M, M. parviflorum; N, M. chalusicum; O, M. inconstrictum; P, Mcoeruleum.
 — Names listed above follow the new classification here proposed. 
Images: T. Böhnert.

CONCLUSION AND OUTLOOK: 
Muscari is a very natural group, best recognized as a single genus. The ddRAD data are able to reconstruct a highly resolved and highly supported phylogeny. Comprehensive sampling of the remaining ca. 45 species would be highly desirable to reach a comprehensive understanding of this important geophyte genus. Our data show evidence for lineage admixture and future analyses should be directed towards understanding the role of hybridization in the evolution of the genus by testing for introgression and possibly ongoing gene flow. It would also be expected that the evolution of Muscari is correlated to the geological and climatic history of the Mediterranean basin and this could be tested with a dated phylogeny of this genus. Beyond molecular data, additional and critical morphological analyses are required to hopefully provide a morphological characterization of the different subgenera.


Tim Böhnert, Michael Neumann, Dietmar Quandt and Maximilian Weigend. 2023. Phylogeny based Generic Reclassification of Muscari sensu lato (Asparagaceae) using Plastid and Genomic DNA. TAXON. DOI: 10.1002/tax.12864

Friday, September 30, 2022

[Entomology • 2022] Dasypolia sejilaensis & D. cerritula • Taxonomic Review of the Subgenus Tatsipolia of the Genus Dasypolia (Lepidoptera: Noctuidae) with Descriptions of Two New Species from southern Xizang, China


 Dasypolia (Tatsipoliasejilaensis
 Dasypolia (Tatsipoliacerritula

 Chen, Pan, Volynkin, Saldaitis & Benedek, 2022.

Abstract
The subgenus Tatsipolia Benedek, Behounek, Floriani & Saldaitis, 2011 of the genus Dasypolia Guenée, 1852 is reviewed. Two new species, D. (T.) sejilaensis sp. nov. and D. (T.) cerritula sp. nov. are described from the Linzhi (Nyingchi) Prefecture in southern Xizang, China. The adults and the male and female genitalia of all species in the subgenus are illustrated. Additionally, Dasypolia (Auropolia) carlotta Floriani, Benedek, Behounek & Saldaitis, 2011 is reported from Xizang for the first time.

Keywords: Antitypina, new record, Noctuinae, Owlet moth, systematics, taxonomy, Xylenini


Noctuidae Latreille, 1809
Noctuinae Latreille, 1809

Xylenini Guenée, 1837
Antitypina Forbes & Franclemont, 1954

Genus Dasypolia Guenée, 1852
 
Subgenus Tatsipolia Benedek, Behounek, Floriani & Saldaitis, 2011
Dasypolia (Tatsipolia) Benedek et al. 2011: 108. 
Type species: Dasypolia (Tatsipolia) ruficilia Benedek, Behounek, Floriani & Saldaitis, 2011, by original designation.

Diagnosis: Members of the subgenus are small moths (forewing length is 11-13 mm) externally similar to taxa of the subgenus Cteipolia. However, despite the external similarity, the subgenus is characterised by the following diagnostic features in the male genitalia: (1) The uncus is short but wide, triangular, dorso-ventrally flattened; (2) The harpe is reduced, tubercle- or spine-like; (3) The digitus is robust, thorn-like; (4) The juxta bears a medial process posteriorly; and (5) The phallus is relatively short but broad, with vesica bearing one or two clusters of spine-like cornuti. In the female genitalia, the broad ostium bursae and the sideways curved ductus and corpus bursae are characteristic for the subgenus.

Distribution: Species of the subgenus are known only from south-western China (Sichuan and southern Xizang).

Species content of Dasypolia (Tatsipolia)
D. (T.) sejilaensis sp. nov.
D. (T.) cerritula sp. nov.
D. (T.) vignai L. Ronkay & Zilli, 1993.
D. (T.) ruficilia Benedek, Behounek, Floriani & Saldaitis, 2011.

Dasypolia (Tatsipolia and Auropolia) spp., adults.
 Depositories of the specimens: 1–4 and 8 in TAAHU 5 in AFM 6 in HNHM (photo by B. Tóth) 7 in ZSM.


 Dasypolia (Tatsipolia) sejilaensis sp. nov.

Distribution: The new species is known only from Sejila Mountain in southern Xizang Province of China.

Etymology: The specific epithet refers to the type locality [Sejila Mountain].


 Dasypolia (Tatsipoliacerritula sp. nov.

Distribution: The new species is known only from Sejila Mountain in southern Xizang Province of China.

Etymology: In Latin, ‘cerritulus’ means ‘weird.’ The specific epithet refers to the unusual cucullus densely covered with robust, spine-like setae.


Enyong Chen, Zhaohui Pan, Anton V. Volynkin, Aidas Saldaitis and Balázs Benedek. 2022. Taxonomic Review of the Subgenus Tatsipolia Benedek, Behounek, Floriani & Saldaitis of the Genus Dasypolia Guenée with Descriptions of Two New Species from southern Xizang, China (Insecta, Lepidoptera, Noctuidae). ZooKeys. 1115: 187-198. DOI: 10.3897/zookeys.1115.84527

Saturday, October 2, 2021

[Botany • 2021] Indigofera wenholdiae (Fabaceae, Indigofereae) • A New Species from the Western Cape Province, South Africa


 Indigofera wenholdiae du Preez & Schrire, 

in du Preez, Dreyer, ... et Schrire, 2021. 

Abstract
In this study, Indigofera wenholdiae, a new species of Fabaceae from the Agulhas Plain Region of the Western Cape Province, South Africa, is described. A composite photographic plate is included along with a distribution map, description of habitat and ecology and proposed IUCN conservation status. Indigofera wenholdiae is unique in the I. brachystachya group by having digitately compound (vs. pinnately compound) leaves, white and unscented flowers (vs. pink and sweetly scented flowers) and grows on sandstone hillsides (vs. coastal limestone plains and outcrops).

Keywords: Indigofera, Leguminosae, Greater Cape Floristic Region, fynbos, taxonomy


Figure 1. Indigofera wenholdiae du Preez & Schrire
 A single inflorescence B flower lateral view C leaf abaxial view D multiple inflorescences on branches E whole plant.
Photographs by Brian du Preez. Voucher B. du Preez 836 (BOL).

Indigofera wenholdiae du Preez & Schrire, sp. nov.
 
Diagnosis: Similar to I. brachystachya, but differs in its digitately compound, 5–7 foliolate leaves (versus pinnately compound, 7–9 foliolate leaves), leaflets 4–6 mm long (versus leaflets 9–15 mm long), racemes up to 7 mm long, flowers ± 4–5 per raceme (versus racemes > 10 mm long, flowers > 8 per raceme), flowers creamy white, unscented (versus flowers pale pink, scented), branching divaricate (versus branching random), populations restricted to sandstone fynbos (versus populations restricted to limestone fynbos).

Etymology: The specific epithet “wenholdiae” is assigned in honour of Mrs Hannerie Wenhold who has funded large-scale conservation efforts in this area, including the funding of the botanist post at Grootbos Nature Reserve of Miss Rebecca Dames who brought this species to our attention in April 2020.


 Brian du Preez, Leanne L. Dreyer, Charles H. Stirton, A. Muthama Muasya and Brian D. Schrire. 2021. Indigofera wenholdiae (Indigofereae, Fabaceae), A New Species from the Western Cape Province, South Africa. PhytoKeys. 182: 107-112.  DOI: 10.3897/phytokeys.182.72170


Tuesday, March 9, 2021

[Entomology • 2021] Ankylopteryx (A.) diffluens & A. (A.) rubrocincta • Two New Species of the Green Lacewing Subgenus Ankylopteryx Brauer, 1864 (s. str.) (Neuroptera, Chrysopidae) from China


Ankylopteryx (Ankylopteryx) diffluens 
Ma & Liu, 2021


Abstract
Two new species of the green lacewing subgenus Ankylopteryx Brauer are described from southern Yunnan, China, namely Ankylopteryx (A.) diffluens sp. nov. and Ankylopteryx (A.) rubrocincta sp. nov.. An updated key to the species of this subgenus is provided.

Keywords: Neuroptera, new species, green lacewing, key

 
Yunlong Ma and Xingyue Liu. 2021. Two New Species of the Green Lacewing Subgenus Ankylopteryx Brauer, 1864 (s. str.) (Neuroptera, Chrysopidae) from China. Zootaxa. 4941(3); 425–433. DOI: 10.11646/zootaxa.4941.3.7

Monday, February 15, 2021

[Botany • 2021] A Monograph of the Genus Polhillia (Fabaceae: Genisteae)

 

Polhillia fortunata B.du Preez, sp. nov.
  Polhillia groenewaldii B.du Preez, sp. nov.  
 
Subgen. Roseopolhillia B.du Preez, subgen. nov.
Polhillia involucrata (Thunb.) B.-E.van Wyk & A.L.Schutte

in du Preez, Dreyer, Stirton et Muasya, 2021. 
 Scale bars: 4 mm. Photographs by B. du Preez


Highlights: 
• Four new species are described.
Polhillia canescens synonymized under P. connata.
• Molecular phylogenetic reconstruction confirms monophyly of the genus.
• New monotypic subgenus described.
• Updated Red Data List status for all 11 Polhillia species.

Abstract
Polhillia is a small, but poorly known genus of legumes endemic to the Greater Cape Floristic Region (GCFR) of South Africa. The genus was described three decades ago to accommodate species erroneously placed in Argyrolobium and other Cape legume genera. Polhillia is the third most threatened plant genus in South Africa, hence priority for taxonomic study and current knowledge on distribution patterns are essential for conservation interventions. Eight species were known at the start of this study, all of which are threatened with extinction. Species boundaries were, however, unclear and many Renosterveld fragments, in particular in the Overberg, required further exploration in pursuit of the various Polhillia species. The phylogenetic relationships among species and monophyly of the genus, especially regarding the position of the morphological aberrant P. involucrata, had not been tested. This study was built upon a foundation of widespread field sampling and analysis of herbarium specimens. Having considered morphological, anatomical, palynological and molecular data, we present an updated taxonomy of the genus Polhillia. Morphological characters between species were often obscure and unique characters were uncommon, as such species are recognized based on unique combinations of characters. Pollen and leaf anatomical studies did not provide substantial taxonomically informative characters, although some interspecific differences were noted. Molecular phylogenetic reconstructions confirm Polhillia to be monophyletic and sister to Argyrolobium, and that Argyrolobium may not be monophyletic. The morphologically distinct species, P. involucrata, is strongly supported as sister to the rest of the genus. Internal phylogenetic resolution in Polhillia is weak in many clades, due to the low variability among DNA markers studied, and several polytomies are still present. Based on the morphological and molecular evidence, we place P. involucrata in the new monotypic subgenus Roseopolhillia. Four new species are described (P. fortunata B.du Preez, P. groenewaldii B.du Preez, P. stirtoniana B.du Preez, P. xairuensis B.du Preez), and a previously recognized species (P. canescens C.H.Stirt.) is placed in synonymy under P. connata (Harv.) C.H.Stirt. Red data list assessments are provided for all species to highlight their conservation importance. Maps and compound colour plates are provided for each species.
 
Keywords: Polhillia, Cape flora, Conservation, Legumes, New species, Phylogeny, Taxonomy



Polhillia C.H.Stirt. subgen. Polhillia 
Type species: Polhillia obsoleta (Harv.) B.-E.van Wyk 
(=Polhillia waltersii (C.H.Stirt.) C.H.Stirt.)

Shrubs erect or spreading, sprouting from rootstock after fire; stipules 2, deltoid, sericeous, veins not visible, connate around base, sheathing stem, often persistent; leaves subsessile or petiolate in P. brevicalyx, pubescent, conduplicate (or flattened in P. ignota); flowers single, paired or in clusters (4–5 in P. brevicalyx, P. ignota and P. fortunata), subsessile or pseudo-pedunculate up to 15 mm long; flowers yellow, 8–13 mm long; calyx yellow-green, often flushed red, villous or sericeous; standard broadly ovate, apex emarginate, pubescent abaxially; wing petals variable in shape and sculpturing, mostly glabrous or pilose along midrib; keel petals variable in shape and level of pubescence, usually restricted to the fore edge; pistil green, sericeous or villous, ovules 7–12, style sub-erect to erect; fruit indehiscent, oblong, laterally compressed between seeds, plicate in P. ignota, P. obsoleta, P. groenewaldii, and P. fortunata, sericeous to glabrescent; seeds ovate-reniform, smooth, uniformly coloured, olive green to dark brown (except for P. connata and P. pallens that have occasional mottling).

 Species included: 
1. Polhillia brevicalyx (C.H.Stirt.) B.-E.van Wyk & A.L.Schutte
2. Polhillia connata (Harv.) C.H.Stirt.
3. Polhillia curtisiae C.H.Stirt. & Muasya
4. Polhillia fortunata B.du Preez
5. Polhillia groenewaldii B.du Preez
6. Polhillia ignota Boatwr.
7. Polhillia obsoleta (Harv.) B.-E.van Wyk
8. Polhillia pallens C.H.Stirt.
9. Polhillia stirtoniana B.du Preez
10. Polhillia xairuensis B.du Preez

 Etymology: The generic and subgeneric epithet Polhillia honours the renowned botanist and legume systematist Dr. Roger M. Polhill from the Royal Botanical Gardens, Kew (Stirton. 1986a).


Fig. 20. Composite plate of Polhillia involucrata.
 1 – Inflorescence with pink flowers; 2 – Inflorescence with white flowers; 3 – Side view of inflorescence showing pink-flushed sepals; 4 – Calyx; 5 – Flower side view; 6 – Flower bottom view; 7 – Wing petals; 8 – Keel petal; 9 – Androecium; 10 – Gynoecium; 11 – Fruit; 12 – Dehiscent fruit on bush; 13 – Close-up of leaves and stipules; 14 – Habit.
Scale bars: 4 mm. Photographs by B. du Preez

Fig. 20. Composite plate of Polhillia involucrata.
1 – Inflorescence with pink flowers; 2 – Inflorescence with white flowers;
3 – Side view of inflorescence showing pink-flushed sepals;12 – Dehiscent frfrfruit on bush;
 13 – Close-up of leaves and stipules; 14 – Habit.
Scale bars: 4 mm. Photographs by B. du Preez

Polhillia C.H.Stirt. Subgen. Roseopolhillia B.du Preez, subgen. nov.
 
Type species: Polhillia involucrata (Thunb.) B.-E.van Wyk & A.L.Schutte,
 Kew Bulletin 44: 3 (1989).

Shrubs erect, sprouting from rootstock after fire; stipules 2, deltoid-oblong, glabrous abaxially, villous adaxially with three prominent veins, connate around base, sheathing stem, often persistent; leaves digitately trifoliolate, shortly petiolate, glabrous or rarely sparsely hairy, conduplicate; inflorescence terminal, flowers in clusters of 2–5, subsessile, surrounded by enlarged stipules; flowers rose pink or rarely white, 10–12 mm long; calyx with trifid ventral lip, sparsely pilose, green, often flushed maroon; standard broadly elliptic to ovate, apex emarginate, pubescent only along abaxial midrib; wing petals broadly oblong with lamellate sculpturing along most part of dorsal half; keel petals lunate, pilose along ventral fore edge; stamens 10, monadelphous with single dorsal slit, filaments fused for most of their length, anthers alternating between long and short; pistil sericeous, variable in length, ovules 7, style sub-erect, stigma regular, capitate; fruit dehiscent, pale cream-brown, oblong, laterally compressed between seeds, sericeous; seeds ovate-squared, smooth, dark-brown to mottled pale-orange.

 Species included: Polhillia involucrata (Thunb.) B.-E.van Wyk & A.L.Schutte.

  Etymology: The subgeneric epithet Roseopolhillia was chosen to highlight the distinct and diagnostic rose pink coloured flowers unique to Polhillia species.


   

 Polhillia fortunata B.du Preez, sp. nov.  1 – Flower front view; 3 – Flower bottom view; 9 – Close-up of leaves and stipules; 11 – Habit.  
 Polhillia groenewaldii B.du Preez, sp. nov. 1 – Flower front view; 2 – Flower side view; 9 – Fruit; 10 – Habit.  

Polhillia stirtoniana B.du Preez, sp. nov. 1 – Flower front view; 2 – Flower side view; 8 – Fruit; 9 – Close-up of recurved leaves and stipules; 10 – Habit. 
Polhillia xairuensis B.du Preez, sp. nov. 1 – Flower front view; 2 – Flower side view; 9 – Leaves and stipules; 10 – Close-up of leaf; 11 – Habit. 
 Scale bars: 4 mm. Photographs by B. du Preez


Polhillia fortunata B.du Preez, sp. nov.  1 – Flower front view; 3 – Flower bottom view; 9 – Close-up of leaves and stipules; 11 – Habit. Scale bars: 4 mm. 
 Polhillia groenewaldii B.du Preez, sp. nov. 1 – Flower front view; 2 – Flower side view; 9 – Fruit; 10 – Habit. Scale bars: 4 mm. 
 Scale bars: 4 mm. Photographs by B. du Preez

Polhillia fortunata B.du Preez

 Etymology: The specific epithet is a direct translation from Latin meaning “lucky”. This epithet was selected as the discovery of this species was fortuitous. The area in which this species occurs was burnt in a massive fire for the first time in nearly 100 years in February 2018, allowing profusion of resprouting shrubs to be visible from the road in what was previously near-senescent Renosterveld vegetation.


Polhillia groenewaldii B.du Preez

Etymology: The specific epithet “groenewaldii” honours Mr Jannie Groenewald who first discovered this species and brought it to our attention. This honours the incredible work he has done in increasing our knowledge of new species and also new populations of threatened species in the Overberg region. This is also in recognition of the tremendous help he provided during fieldwork conducted for this study.


Polhillia stirtoniana B.du Preez, sp. nov. 1 – Flower front view; 2 – Flower side view; 8 – Fruit; 9 – Close-up of recurved leaves and stipules; 10 – Habit. 
Polhillia xairuensis B.du Preez, sp. nov. 1 – Flower front view; 2 – Flower side view; 9 – Leaves and stipules; 10 – Close-up of leaf; 11 – Habit.
 Scale bars: 4 mm. Photographs by B. du Preez
    
Polhillia stirtoniana B.du Preez

Etymology: The specific epithet honours Prof. Charles Howard Stirton for his extensive work on Cape legumes and his late wife, Dr Jana Stirton (Born Žantovská) who shared his love and passion for the diversity and conservation of the Overberg Renosterveld. They assisted in the formation of the Overberg Renosterveld Conservation Trust and establishment of the Haarwegskloof Private Nature Reserve and research centre. Prof. Stirton has significantly mentored the first author in his development as botanist.


Polhillia xairuensis B.du Preez

Etymology: The specific epithet is derived from the Hessequa Khoi name for the Suurbraak area, namely “!Xairu” which means ‘Beauty’ or ‘A place called Paradise’, referring to the beautiful nature of the area (Fourie, 2013). Pronunciation of the epithet can be with or without a click. Although much of the area has now been transformed for agriculture, the Langeberg Mountains above the town of Suurbraak remain scenic and lowland vegetation fragments hold beautiful floral gems such as this Polhillia species.


  B. du Preez, L. L. Dreyer, C. H. Stirton and A. M. Muasya. 2021. A Monograph of the Genus Polhillia (Genisteae: Fabaceae).  South African Journal of Botany. 138; 156-183. DOI: 10.1016/j.sajb.2020.12.022 
 

Sunday, January 31, 2021

[Entomology • 2021] Bolbelasmus (Bolbelasmus) zagrosensis • A New Species (Coleoptera: Scarabaeoidea: Bolboceratidae) from Iran, Along with An Updated Key to the western Palaearctic Species of the Subgenus

  

Bolbelasmus (Bolbelasmuszagrosensis 
Sommer, Hillert, Hrůzová & Král, 2021


Abstract
Bolbelasmus (Bolbelasmuszagrosensis Sommer, Hillert, Hrůzová & Král, new species, from Iran is described, illustrated and compared with its congeners known from the western Palaearctic region. An updated key to the western Palaearctic species of the nominotypical subgenus is provided. New country record of B. (B.) nireus (Reitter, 1895) from Greece (island of Rhodes) is reported. Distribution of B. (B.) makrisi Miessen, 2011, B. (B.) nireus and the new species is summarized and mapped.

Keywords: Coleoptera, Scarabaeoidea, Bolboceratidae, Bolboceratinae, Bolbelasmus, taxonomy, new species, distribution, Iran, Rhodes, Palaearctic region



Bolbelasmus (Bolbelasmuszagrosensis Sommer, Hillert, Hrůzová & Král


David Sommer, Oliver Hillert, Lucie Hrůzová and David Král. 2021. Bolbelasmus (Bolbelasmuszagrosensis (Coleoptera: Scarabaeoidea: Bolboceratidae), A New Species from Iran, Along with An Updated Key to the western Palaearctic Species of the Subgenus. Zootaxa. 4920(3); 380–394. DOI:  10.11646/zootaxa.4920.3.4

Thursday, January 28, 2021

[Herpetology • 2021] Brookesia nana • Extreme Miniaturization of A New Amniote Vertebrate and insights into the Evolution of Genital Size in Chameleons


Brookesia nana 
Glaw, Köhler, Hawlitschek, Ratsoavina, Rakotoarison, Scherz & Vences, 2021 


Abstract
Evolutionary reduction of adult body size (miniaturization) has profound consequences for organismal biology and is an important subject of evolutionary research. Based on two individuals we describe a new, extremely miniaturized chameleon, which may be the world’s smallest reptile species. The male holotype of Brookesia nana sp. nov. has a snout–vent length of 13.5 mm (total length 21.6 mm) and has large, apparently fully developed hemipenes, making it apparently the smallest mature male amniote ever recorded. The female paratype measures 19.2 mm snout–vent length (total length 28.9 mm) and a micro-CT scan revealed developing eggs in the body cavity, likewise indicating sexual maturity. The new chameleon is only known from a degraded montane rainforest in northern Madagascar and might be threatened by extinction. Molecular phylogenetic analyses place it as sister to B. karchei, the largest species in the clade of miniaturized Brookesia species, for which we resurrect Evoluticauda Angel, 1942 as subgenus name. The genetic divergence of B. nana sp. nov. is rather strong (9.9‒14.9% to all other Evoluticauda species in the 16S rRNA gene). A comparative study of genital length in Malagasy chameleons revealed a tendency for the smallest chameleons to have the relatively largest hemipenes, which might be a consequence of a reversed sexual size dimorphism with males substantially smaller than females in the smallest species. The miniaturized males may need larger hemipenes to enable a better mechanical fit with female genitals during copulation. Comprehensive studies of female genitalia are needed to test this hypothesis and to better understand the evolution of genitalia in reptiles.


Brookesia nana sp. nov. in life. 
(A–C) male holotype (ZSM 1660/2012).
(D, E) female paratype (UADBA-R/FGZC 3752).

Molecular phylogeny of specimens in the subgenus Evoluticauda (known as Brookesia minima species group), based on the nuclear CMOS gene (alignment length 847 bp, but only about 400 bp available for all samples) and inferred under the Maximum Likelihood optimality criterion (K2P + G substitution model). Values at nodes are support values from a bootstrap analysis in percent (500 replicates) and are only shown if > 50%. The tree was rooted with B. brygooi (removed for better graphical representation).

Systematics
Order Squamata Oppel, 181115.
Family Chamaeleonidae Rafinesque, 181516.
Subfamily Brookesiinae Angel, 194217.

Genus Brookesia Gray, 186517.

Subgenus Evoluticauda Angel, 1942 (resurrected herein, justification below).

Brookesia nana sp. nov
 
 Diagnosis: A diminutive chameleon species assigned to the genus Brookesia on the basis of its small body size, short tail, presence of rows of dorsolateral tubercles along vertebral column, presence of pelvic spine, and molecular phylogenetic relationships. Brookesia nana sp. nov. is distinguished by the following unique suite of morphological characters: (1) male SVL 13.5 mm, female SVL 19.2 mm; (2) male TL mm 21.6 mm, female TL 28.9 mm; (3) TaL/SVL ratio of 0.51 in male; (4) absence of lateral or dorsal spines on the tail; (5) absence of dorsal pelvic shield in sacral area; (6) presence of distinct pelvic spine; (7) pale brown dorsal colouration with slightly darker markings in life; (8) absence of apical spines on the hemipenis.

Etymology: The specific epithet is the Latin noun nana (meaning female dwarf) in the nominative singular.


Map of northern Madagascar, showing the distribution of species of the subgenus Evoluticauda (known as Brookesia minima group) in this region (only showing records verified by molecular data). Note that B. dentata, B. exarmata, and B. ramanantsoai occur further south and are not included in the map. Orange (dry forest) and green (rainforest) show remaining primary vegetation in 2003–2006.



....
Due to the old divergence and the morphological distinctness of the two clades we here suggest to consider them as different subgenera:

Subgenus Brookesia Gray, 1865 (large-bodied clade)
Type species: Chamaeleo superciliaris Kuhl, 1820.

Contents: Brookesia antakarana, B. bekolosy (attribution tentative), B. betschi, B. bonsi, B. brunoi, B. brygooi, B. decaryi, B. ebenaui, B. griveaudi, B. lambertoni, B. lineata, B. perarmata, B. stumpffi, B. superciliaris, B. therezieni, B. thieli, B. vadoni, B. valerieae.

Distribution: Madagascar.


Subgenus Evoluticauda Angel, 1942 (miniaturized clade, known as B. minima group)
Type species: Brookesia tuberculata Mocquard, 1894.

Contents: Brookesia confidens, B. dentata, B. desperata, B. exarmata, B. karchei, B. micra, B. minima, B. nana, B. peyrierasi, B. ramanantsoai, B. tedi, B. tristis, B. tuberculata.

Distribution: Northern half of Madagascar.
 

Frank Glaw, Jörn Köhler, Oliver Hawlitschek, Fanomezana M. Ratsoavina, Andolalao Rakotoarison, Mark D. Scherz and Miguel Vences. 2021. Extreme Miniaturization of A New Amniote Vertebrate and insights into the Evolution of Genital Size in Chameleons. Scientific Reports. 11, 2522. DOI: 10.1038/s41598-020-80955-1