A new family of Laniatores (Arachnida:Opiliones) from the Afrotropics

2011 ◽  
Vol 25 (2) ◽  
pp. 143 ◽  
Author(s):  
Prashant P. Sharma ◽  
Carlos E. Prieto ◽  
Gonzalo Giribet

Among Opiliones, Afrotropical lineages constitute some of the least studied groups in comparison with those endemic to other biogeographic provinces. Based upon morphological evidence, we erect Pyramidopidae, fam. nov. to distinguish a group of Laniatores from the family Phalangodidae. We review evidence from recent molecular phylogenetic studies that corroborate the independence of Pyramidopidae, fam. nov. from previously described families and support its sister relationship to another largely Afrotropical group, the family Assamiidae. The monotypic genus Maiorerus Rambla, 1993 is transferred to Pyramidopidae, fam. nov. The new family comprises 12 genera geographically restricted to Africa and the adjacent Canary Islands. Interfamilial relationships of the derived Laniatores are discussed in the context of gross and genitalic morphology.

2021 ◽  
Vol 151 ◽  
Author(s):  
Dieter Weber ◽  
Fabio Stoch ◽  
Lee R.F.D. Knight ◽  
Claire Chauveau ◽  
Jean-François Flot

Microniphargus leruthi Schellenberg, 1934 (Amphipoda: Niphargidae) was first described based on samples collected in Belgium and placed in a monotypic genus within the family Niphargidae. However, some details of its morphology as well as recent phylogenetic studies suggest that Microniphargus may be more closely related to Pseudoniphargus (Amphipoda: Pseudoniphargidae) than to Niphargus. Moreover, M. leruthi ranges over 1,469 km from Ireland to Germany, which is striking since only a few niphargids have confirmed ranges in excess of 200 km. To find out the phylogenetic position of M. leruthi and check whether it may be a complex of cryptic species, we collected material from Ireland, England and Belgium then sequenced fragments of the mitochondrial cytochrome c oxidase subunit 1 gene as well as of the nuclear 28S ribosomal gene. Phylogenetic analyses of both markers confirm that Microniphargus is closer to Pseudoniphargus than to Niphargus, leading us to reallocate Microniphargus to Pseudoniphargidae. We also identify three congruent mito-nuclear lineages present respectively in Ireland, in both Belgium and England, and in England only (with the latter found in sympatry at one location), suggesting that M. leruthi is a complex of at least three species with a putative centre of origin in England.


2021 ◽  
Vol 46 (4) ◽  
pp. 891-915
Author(s):  
Susan Fawcett ◽  
Alan R. Smith ◽  
Michael Sundue ◽  
J. Gordon Burleigh ◽  
Emily B. Sessa ◽  
...  

Abstract— The generic classification of the Thelypteridaceae has been the subject of much controversy. Proposed taxonomic systems have varied from recognizing the approximately 1200 species in the family within the single genus Thelypteris, to systems favoring upwards of 30 genera. Insights on intrafamilial relationships, especially for neotropical taxa, have been gained from recent phylogenetic studies; however, in the most recent classification, 10 of 30 recognized genera are either non-monophyletic or untested. We sequenced 407 nuclear loci for 621 samples, representing all recognized genera and approximately half the known species diversity. These were analyzed using both maximum likelihood analysis of a concatenated matrix and multi-species coalescent methods. Our phylogenomic results, informed by recently published morphological evidence, provide the foundation for a generic classification which recircumscribed 14 genera and recognized seven new genera. The 37 monophyletic genera sampled demonstrate greater geographic coherence than previous taxonomic concepts suggested. Additionally, our results demonstrate that certain morphological characters, such as frond division, are evolutionarily labile and are thus inadequate for defining genera.


2020 ◽  
Vol 189 (3) ◽  
pp. 762-827 ◽  
Author(s):  
Tatiana Korshunova ◽  
Karin Fletcher ◽  
Bernard Picton ◽  
Kennet Lundin ◽  
Sho Kashio ◽  
...  

Abstract Dorids are one of the largest nudibranch groups, encompassing more than 2000 species. One of the crucial problems with tracing the evolution of dorids is the relationship between cryptobranch dorids (gill cavity present) and phanerobranch dorids (gill cavity absent). Integrative morphological and molecular studies of the enigmatic Japanese dorid species of the cryptobranch genus Cadlina, C. japonica and ‘C.’ sagamiensis, which were collected by the Emperor of Japan (Shōwa era), are presented here for the first time. It is shown that while C. japonica does belong to the Cadlina clade, another Japanese species ‘C.’ sagamiensis is not part of the cryptobranch dorids of the family Cadlinidae, but is related to both the phanerobranch dorid family, Hexabranchidae, and to the cryptobranch family Cadlinellidae stat. nov. A new genus, Showajidaia gen. nov., and new family, Showajidaiidae fam. nov., are proposed for ‘C.’ sagamiensis, and four new species of the genus Cadlina are described based on a dorid-wide molecular phylogenetic analysis, which is the first substantial update of the dorid family system since 2010. Integration of phylogenetic data with an ontogenetic model of dorid evolution suggests that cryptobranch organization can be most reliably assessed as the ancestral state for the majority of dorids.


2020 ◽  
Vol 86 (1) ◽  
pp. 1-26
Author(s):  
S T Williams ◽  
Y Kano ◽  
A Warén ◽  
D G Herbert

ABSTRACT The assignment of species to the vetigastropod genus Solariella Wood, 1842, and therefore the family Solariellidae Powell, 1951, is complicated by the fact that the type species (Solariella maculata Wood, 1842) is a fossil described from the Upper Pliocene. Assignment of species to genera has proved difficult in the past, and the type genus has sometimes acted as a ‘wastebasket’ for species that cannot easily be referred to another genus. In the light of a new systematic framework provided by two recent publications presenting the first molecular phylogenetic data for the group, we reassess the shell characters that are most useful for delimiting genera. Shell characters were previously thought to be of limited taxonomic value above the species level, but this is far from the case. Although overall shell shape is not a reliable character, our work shows that shell characters, along with radular and anatomical characters, are useful for assigning species to genera. Sculpture of the early teleoconch (the region immediately following the protoconch) and the columella are particularly useful characters that have not been used regularly in the past to distinguish genera. However, even with the combination of all morphological characters used in this study (shell, radular and eye), a few species are still difficult to assign to genera and in such cases molecular systematic data are essential. In the present study, we discuss 13 genera—12 of which were recovered as well-supported clades in recent molecular systematic studies—and provide morphological characters to distinguish them. We describe several new taxa: Chonospeira n. gen. (referred to as ‘clade B’ in previous molecular systematic studies), Phragmomphalina n. gen. (Bathymophila in part in molecular systematic studies) and Phragmomphalina vilvensi n. sp. (type species of Phragmomphalina n. gen.). We synonymize Hazuregyra Shikama, 1962 with Minolia A. Adams, 1860, Minolia subangulata Kuroda & Habe, 1952 with Minolia punctata A. Adams, 1860 and M. gemmulata Kuroda & Habe, 1971 with M. shimajiriensis (MacNeil, 1960). We also present the following new combinations: Bathymophila bairdii (Dall, 1889), B. dawsoni (Marshall, 1979), B. regalis (Marshall, 1999), B. wanganellica (Marshall, 1999), B. ziczac (Kuroda & Habe in Kuroda, Habe & Oyama, 1971), Chonospeira nuda (Dall, 1896), C. iridescens (Habe, 1961), C. ostreion (Vilvens, 2009), C. strobilos (Vilvens, 2009), Elaphriella corona (Lee & Wu, 2001), E. diplax (Marshall, 1999), E. meridiana (Marshall, 1999), E. olivaceostrigata (Schepman, 1908), E. opalina (Shikama & Hayashi, 1977), Ilanga norfolkensis (Marshall, 1999), I. ptykte (Vilvens, 2009), I. zaccaloides (Vilvens, 2009), Minolia shimajiriensis (MacNeil, 1960), M. watanabei (Shikama, 1962), Phragmomphalina alabida (Marshall, 1979), P. diadema (Marshall, 1999), P. tenuiseptum (Marshall, 1999), Spectamen euteium (Vilvens, 2009), S. basilicum (Marshall, 1999), S. exiguum (Marshall, 1999) and S. flavidum (Marshall, 1999).


2019 ◽  
Vol 33 (6) ◽  
pp. 892
Author(s):  
Adriano B. Kury ◽  
Abel Pérez-González ◽  
Daniel N. Proud

The laniatorean family Phalangodidae has been largely reduced to a core of Holarctic species; however, many taxa were never formally transferred to other families. We examined a group of harvestmen related to Beloniscus Thorell, 1891, from South-east Asia and determined the nature of the relationships of the ‘Beloniscus-like harvestmen’, herein described as the new family Beloniscidae, fam. nov., in the broad context of Laniatores. Based on a molecular phylogenetic analysis of a broad representative laniatorean Sanger-sequences dataset we found support for our taxonomic hypotheses that (1) inclusion of Beloniscidae, fam. nov. in Phalangodidae would render the family non-monophyletic, and (2) Beloniscidae, fam. nov. represents a lineage that is morphologically and genetically distinct from all other known laniatorean families. The new family Beloniscidae is endemic to South-east Asia and comprises 37 species in two new subfamilies: Beloniscinae, subfam. nov. and Buparinae, subfam. nov. Beloniscinae includes the genera Beloniscellus Roewer, 1931, Beloniscops Roewer, 1949, Belonisculus Roewer, 1923, Beloniscus (type genus) and Kendengus Roewer, 1949. Buparinae includes the genera Buparellus Roewer, 1949, Bupares Thorell, 1889 (type genus) and Buparomma Roewer, 1949. Members of Beloniscidae are relatively homogeneous in their external morphology, but are recognised by well marked genitalic features. Male genitalia are described for exemplar species, and the morphology is compared with that of Epedanidae. Names are given to two new genitalic structures: sella curulis and pseudocalyx. http://zoobank.org/urn:lsid:zoobank.org:act:540BCE49-6F2E-4372-BFD4-D3C6068F045D http://zoobank.org/urn:lsid:zoobank.org:act:FE8B011B-AA6D-4E6C-A321-123542A0563F http://zoobank.org/urn:lsid:zoobank.org:act:E4A559CD-170A-40F2-924A-541C22974344


2017 ◽  
Vol 31 (5) ◽  
pp. 566 ◽  
Author(s):  
Michael G. Rix ◽  
Robert J. Raven ◽  
Barbara Y. Main ◽  
Sophie E. Harrison ◽  
Andrew D. Austin ◽  
...  

The Australasian spiny trapdoor spiders of the family Idiopidae (subfamily Arbanitinae) are revised at the generic level, using a multi-locus molecular phylogenetic foundation and comprehensive sampling of all known lineages. We propose a new family- and genus-group classification for the monophyletic Australasian fauna, and recognise 10 genera in four tribes. The Arbanitini Simon includes Arbanitis L. Koch, 1874 (61 species), Blakistonia Hogg, 1902 (one species) and Cantuaria Hogg, 1902 (43 species). The Aganippini Simon includes Bungulla Rix, Main, Raven & Harvey, gen. nov. (two species), Eucanippe Rix, Main, Raven & Harvey, gen. nov. (one species), Eucyrtops Pocock, 1897 (two species), Gaius Rainbow, 1914 (one species) and Idiosoma Ausserer, 1871 (14 species). The Cataxiini Rainbow and Euoplini Rainbow include just Cataxia Rainbow, 1914 (11 species) and Euoplos Rainbow, 1914 (12 species), respectively. Two distinctive new genera of Aganippini are described from Western Australia, and several previously valid genera are recognised as junior synonyms of existing genus-group names, including Misgolas Karsch, 1878 (= Arbanitis; new synonymy), Aganippe O. P.-Cambridge, 1877 (= Idiosoma; new synonymy) and Anidiops Pocock, 1897 (= Idiosoma; new synonymy). Gaius stat. rev. is further removed from synonymy of Anidiops. Other previously hypothesised generic synonyms are supported by both morphology and molecular phylogenetic data from 12 genes, including the synonymy of Neohomogona Main, 1985 and Homogona Rainbow, 1914 with Cataxia, and the synonymy of Albaniana Rainbow & Pulleine, 1918, Armadalia Rainbow & Pulleine, 1918, Bancroftiana Rainbow & Pulleine, 1918 and Tambouriniana Rainbow & Pulleine, 1918 with Euoplos. At the species level, the identifications of Eucy. latior (O. P.-Cambridge, 1877) and I. manstridgei (Pocock, 1897) are clarified, and three new species are described: Bungulla bertmaini Rix, Main, Raven & Harvey, sp. nov., Eucanippe bifida Rix, Main, Raven & Harvey, sp. nov. and Idiosoma galeosomoides Rix, Main, Raven & Harvey, sp. nov., the latter remarkable for its phragmotic abdominal morphology. The Tasmanian species Mygale annulipes C. L. Koch, 1842 is here transferred to the genus Stanwellia Rainbow & Pulleine, 1918 (family Nemesiidae), comb. nov., Arbanitis mestoni Hickman, 1928 is transferred to Cantuaria, comb. nov. and Idiosoma hirsutum Main, 1952 is synonymised with I. sigillatum (O. P.-Cambridge, 1870), new synonymy. In addition to the morphological synopses and an illustrated key to genera, molecular diagnoses are presented for all nominal taxa, along with live habitus and burrow images to assist in field identification. The Australasian idiopid fauna is highly diverse, with numerous new species known from all genera. As a result, this study provides a taxonomic and nomenclatural foundation for future species-level analyses, and a single reference point for the monographic documentation of a remarkable fauna. http://zoobank.org/?lsid=urn:lsid:zoobank.org:pub:BACE065D-1EF9-40C6-9134-AADC9235FAD8


Phytotaxa ◽  
2014 ◽  
Vol 181 (3) ◽  
pp. 151 ◽  
Author(s):  
Yuya Inoue ◽  
Hiromi Tsubota

Based on our molecular phylogenetic analysis of haplolepideous mosses with concatenated sequences of chloroplast rps4 and rbcL genes, a new family Timmiellaceae is erected to accommodate the genera Timmiella and Luisierella, both of which have been formerly included in the family Pottiaceae.  The family Timmiellaceae is resolved as a second-branching clade together with Distichium (Distichiaceae) within the Dicranidae (haplolepideous moss) lineages and phylogenetically distinct from the Pottiaceae.  Reassessment of morphological characters suggests that a combination of the characters: 1) adaxially bulging and abaxially flat leaf surfaces, 2) sinistrorse or straight peristomes, when present, and 3) sinistrorsely arranged operculum cells is unique to Timmiellaceae and discriminates it from other haplolepideous moss families.


Phytotaxa ◽  
2013 ◽  
Vol 100 (1) ◽  
pp. 6 ◽  
Author(s):  
S. ROBBERT GRADSTEIN

Lejeuneaceae are the largest family of the liverworts with at least one thousand species in 68 currently accepted genera. The number of genera is much lower than accepted previously and was reduced based on recent molecular work. This paper present a first classification of Lejeuneaceae based on integrated molecular-phylogenetic and morphological evidence. The family is subdivided into two broad subfamilies, Ptychanthoideae (19 genera) and Lejeuneoideae (49 genera). Ptychanthoideae are not further subdivided whereas Lejeuneoideae are classified into three tribes: Brachiolejeuneeae (8 genera), Symbiezidieae (new; 1 genus) and Lejeuneeae (40 genera). Lejeuneeae, the largest tribe in the family, are classified into eight subtribes: Ceratolejeuneinae (2 genera), Cheilolejeuneinae (4 genera), Cololejeuneinae (12 genera), Cyclolejeuneinae (3 genera), Drepanolejeuneinae (2 genera), Echinolejeuneinae (3 genera), Lejeuneinae (5 genera) and Lepidolejeuneinae (2 genera). Seven genera of Lejeuneeae have not yet been studied by molecular methods and are not classified.


ZooKeys ◽  
2019 ◽  
Vol 821 ◽  
pp. 85-152 ◽  
Author(s):  
Shinichi Nakahara ◽  
Gerardo Lamas ◽  
Stephanie Tyler ◽  
Mario Alejandro Marín ◽  
Blanca Huertas ◽  
...  

We here propose a new, monotypic genus, Amiga Nakahara, Willmott & Espeland, gen. n., to harbor a common Neotropical butterfly, described as Papilioarnaca Fabricius, 1776, and hitherto placed in the genus Chloreuptychia Forster, 1964. Recent and ongoing molecular phylogenetic research has shown Chloreuptychia to be polyphyletic, with C.arnaca proving to be unrelated to remaining species and not readily placed in any other described genus. Amigaarnacagen. n. et comb. n. as treated here is a widely distributed and very common species ranging from southern Mexico to southern Brazil. A neotype is designated for the names Papilioarnaca and its junior synonym, Papilioebusa Cramer, 1780, resulting in the treatment of the latter name as a junior objective synonym of the former. A lectotype is designated for Euptychiasericeella Bates, 1865, which is treated as a subspecies, Amigaarnacasericeella (Bates, 1865), comb. n. et stat. n., based on molecular and morphological evidence. We also describe two new taxa, Amigaarnacaadela Nakahara & Espeland, ssp. n. and Amigaarnacaindianacristoi Nakahara & Marín, ssp. n., new subspecies from the western Andes and eastern Central America, and northern Venezuela, respectively.


Phytotaxa ◽  
2020 ◽  
Vol 451 (1) ◽  
pp. 97-102
Author(s):  
DIPANKAR BORAH ◽  
RAJEEV KUMAR SINGH ◽  
PURANJOY MIPUN ◽  
DEIJI NARAH

The monotypic genus Pseudobartsia Hong (1979: 406) is represented by Pseudobartsia glandulosa (Bentham) Yu & Li in Yu et al. (2015: 197) occurring in China and India (Yu et al. 2015, POWO 2020). In China, the species was collected in 1940 from Longtanying, Songming, Yunnan and since then this species was never collected or reported from these localities, hence it is believed to have gone extinct from here (Dong et al. 2013, Yu et al. 2015). In India, this species is known only by the type collection form Shivli, Uttarakhand in the year 1840 by Edgeworth (Khanna et al. 1999). Bentham (1846) described Euphrasia glandulosa based on specimens collected by Edgeworth in 1840 from Shivli, Uttarakhand, India. Later, Hooker (1884) made a combination for Euphrasia glandulosa Bentham (1846: 555) under the genus Phtheirospermum Bunge ex Fischer & Meyer (1835: 35). The genus Pseudobartsia was established by Hong (1979) with one species, Pseudobartsia yunnanensis Hong (1979: 406). Based on the study of the type specimens of Euphrasia glandulosa and Pseudobartsia yunnanensis, Tao (1993, 1996) found that Pseudobartsia yunnanensis cannot be distinguished from Phtheirospermum glandulosum (≡ Euphrasia glandulosa), therefore he treated Pseudobartsia as a synonym of Phtheirospermum and synonymized Pseudobartsia yunnanensis under Phtheirospermum glandulosum. However, recent phylogenetic studies (Dong et al. 2013; McNeal et al. 2013), pollen morphological evidence (Lu et al. 2007) and seed characters (Dong et al. 2013), support Pseudobartsia as distinct and independent genus. Because the name Euphrasia glandulosa as priority over Pseudobartsia yunnanensis, Yu & Li in Yu et al. (2015) made a new combination Pseudobartsia glandulosa to replace the latter in the genus Pseudobartsia.


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