Phylogenomic re-evaluation of Triaenonychoidea (Opiliones : Laniatores), and systematics of Triaenonychidae, including new families, genera and species

Author(s):  
Shahan Derkarabetian ◽  
Caitlin M. Baker ◽  
Marshal Hedin ◽  
Carlos E. Prieto ◽  
Gonzalo Giribet

The Opiliones superfamily Triaenonychoidea currently includes two families, the monogeneric New Zealand–endemic Synthetonychiidae Forster, 1954 and Triaenonychidae Sørensen, 1886, a diverse family distributed mostly throughout the temperate Gondwanan terranes, with ~110 genera and ~500 species and subspecies currently described. Traditionally, Triaenonychidae has been divided into subfamilies diagnosed by very few morphological characters largely derived from the troublesome ‘Roewerian system’ of morphology, and classifications based on this system led to many complications. Recent research within Triaenonychoidea using morphology and traditional multilocus data has shown multiple deeply divergent lineages, non-monophyly of Triaenonychidae, and non-monophyly of subfamilies, necessitating a revision based on phylogenomic data. We used sequence capture of ultraconserved elements across 164 samples to create a 50% taxon occupancy matrix with 704 loci. Using phylogenomic and morphological examinations, we explored family-level relationships within Triaenonychoidea, including describing two new families: (1) Lomanellidae Mendes & Derkarabetian, fam. nov., consisting of Lomanella Pocock, 1903, and a newly described genus Abaddon Derkarabetian & Baker, gen. nov. with one species, A. despoliator Derkarabetian, sp. nov.; and (2) the elevation to family of Buemarinoidae Karaman, 2019, consisting of Buemarinoa Roewer, 1956, Fumontana Shear, 1977, Flavonuncia Lawrence, 1959, and a newly described genus Turonychus Derkarabetian, Prieto & Giribet, gen. nov., with one species, T. fadriquei Derkarabetian, Prieto & Giribet, sp. nov. With our dataset we also explored phylogenomic relationships within Triaenonychidae with an extensive taxon set including samples representing ~80% of the genus-level diversity. Based on our results we (1) discuss systematics of this family including the historical use of subfamilies, (2) reassess morphology in the context of our phylogeny, (3) hypothesise placement for all unsampled genera, (4) highlight lineages most in need of taxonomic revision, and (5) provide an updated species-level checklist. Aside from describing new taxa, our study provides the phylogenomic context necessary for future evolutionary and systematic research across this diverse lineage. ZooBank Registration: urn:lsid:zoobank.org:pub:81683834-98AB-43AA-B25A-C28C6A404F41


2015 ◽  
Vol 89 (1) ◽  
pp. 72-81 ◽  
Author(s):  
William I. Ausich ◽  
Mark A. Wilson ◽  
Olev Vinn

AbstractStudy of new collections of the Wenlock and Pridoli, Silurian, crinoids from Saaremaa, western Estonia, result in taxonomic revision, expanded ranges, and new taxa. Eucalyptocrinites regularis and Periechocrinus laevis are recognized outside of Sweden for the first time. Desmidocrinus laevigatus Ausich et al., 2012 is reassigned to Methabocrinus. Because the type species of Methabocrinus was previously known only from glacial sediments, the age and provenance of this genus are constrained for the first time. A new crotalocrinitid, Velocrinus coniculus new genus and species, is described. Although the Pridoli faunas of western Estonia contain only twelve species-level taxa assigned to nine genera, this fauna is one of the four richest Pridoli faunas known.



2010 ◽  
Vol 24 (2) ◽  
pp. 131 ◽  
Author(s):  
Lorraine D. Cook ◽  
Steven A. Trewick ◽  
Mary Morgan-Richards ◽  
Peter M. Johns

The New Zealand Rhaphidophoridae Walker, 1869 comprise 18 endemic genera (including 8 that are monotypic). Although there are many new species to be described, rationalisation at the genus level is also required due to inconsistencies in their current systematics. Even the largest and best known taxa, including those that occupy cave systems and are the most frequently encountered by people, require taxonomic revision. These cave weta include species assigned to three poorly differentiated genera, Pachyrhamma Brunner v. Wattenwyl, 1888, Gymnoplectron Hutton, 1897 and Turbottoplectron Salmon, 1948, that are best known from North Island New Zealand. We used mitochondrial DNA sequence data to examine their relationships using representatives of each genus. The results indicate that a single genus Pachyrhamma would be appropriate for all, as Gymnoplectron and Turbottoplectron nest phylogenetically within it. There are insufficient morphological, spatial or ecological reasons to justify retention of all three. However, we also note that species level diversity does not correlate with genetic or spatial diversity; some species are genetically well partitioned and widespread while others have narrow ranges in single cave systems and are closely related to one another.



2002 ◽  
Vol 16 (6) ◽  
pp. 957 ◽  
Author(s):  
J. T. Jennings ◽  
A. D. Austin

This study examines the phylogeny, taxonomy, distribution and biology of the gasteruptiid subfamily Hyptiogastrinae and, at the same time, presents an overview of the family. Following a cladistic analysis of 35 discrete morphological characters, two monophyletic genera are recognised, Hyptiogaster Kieffer and Pseudofoenus s. l. Kieffer. As a consequence, the genera Aulacofoenus Kieffer, Crassifoenus Crosskey, and Eufoenus Szépligeti are synonymised with Pseudofoenus. A total of 88 species are recognised for the subfamily, 10 species of Hyptiogaster, which are restricted to mainland Australia, and 78 species of Pseudofoenus, 40 of which are described as new. Pseudofoenus has a restricted Gondwanan distribution and is found in Australia including Tasmania (65 spp.), New Guinea and New Britain (5 spp.), the south-west Pacific (New Caledonia, New Hebrides and Fiji – 2 spp.), New Zealand (4 spp.) and South America (2 spp.). No new species have been recorded from either New Zealand or South America. For Pseudofoenus, information on the distribution of each species, their biology (if known) and an identification key are presented.Following a taxonomic revision, the following new species are described: P. baileyi, sp. nov., P. baitetaensis, sp. nov., P. beverlyae, sp. nov., P. caperatus, sp. nov., P. cardaleae, sp. nov., P. carrabinensis, sp. nov., P. claireae, sp. nov., P. collessi, sp. nov., P. coorowensis, sp. nov., P. crosskeyi, sp. nov., P. douglasorum, sp. nov., P. eliseae, sp. nov., P. ericae, sp. nov., P. eustonensis, sp. nov., P. feckneri, sp. nov., P. gressitti, sp. nov., P. gullanae, sp. nov., P. hackeri, sp. nov., P. imbricatus, sp. nov., P. iqbali, sp. nov., P. kadowi, sp. nov., P. karimuiensis, sp. nov., P. kelleri, sp. nov., P. leinsterensis, sp. nov., P. macdonaldi, sp. nov., P. malkini, sp. nov., P. marshalli, sp. nov., P. masneri, sp. nov., P. mitchellae, sp. nov., P. morganensis, sp. nov., P. nalbarraensis, sp. nov., P. pumilis, sp. nov., P. schmidti, sp. nov., P. stevensi, sp. nov., P. tasmaniensis, sp. nov., P. taylori, sp. nov., P. umboiensis, sp. nov., P. walkeri, sp. nov. and P. zborowskii, sp. nov. The synonymy of Aulacofoenus, Crassifoenus and Eufoenus with Pseudofoenus result in the following new combinations: from Aulacofoenus: P. bungeyi (Jennings & Austin), comb. nov., P. deletangi (Schletterer), comb. nov., P. fallax (Schletterer), comb. nov., P. fletcheri (Jennings & Austin), comb. nov., P. goonooensis (Jennings & Austin), comb. nov., P. infumatus (Schletterer), comb. nov., P. kurmondi (Jennings & Austin), comb. nov., P. loxleyi (Jennings & Austin), comb. nov., P. marionae (Jennings & Austin), comb. nov., P. perenjorii (Jennings & Austin), comb. nov., P. swani (Jennings & Austin), comb. nov., P. thoracicus (Guérin Menéville), comb. nov., P. whiani (Jennings & Austin), comb. nov. and P. wubinensis (Jennings & Austin), comb. nov.; from Crassifoenus: P. houstoni (Jennings & Austin), comb. nov., P. grossitarsis (Kieffer), comb. nov and P. macronyx (Schletterer), comb. nov.; and from Eufoenus: P. antennalis (Schletterer), comb. nov., P. australis (Westwood), comb. nov., P. crassitarsis (Kieffer), comb. nov., P. darwini (Westwood), comb. nov., P. extraneus (Turner), comb. nov., P. ferrugineus (Crosskey), comb. nov., P. floricolus (Turner), comb. nov., P. inaequalis (Turner), comb. nov., P. melanopleurus (Crosskey), comb. nov., P. minimus (Turner), comb. nov., P. nitidiusculus (Turner), comb. nov., P. patellatus (Westwood), comb. nov., P. pilosus (Kieffer), comb. nov., P. reticulatus (Crosskey), comb. nov., P. rieki (Crosskey), comb. nov., P. ritae (Cheesman), comb. nov. and P. spinitarsis (Westwood), comb. nov. Pseudofoenus microcephalus (Crosskey), comb. nov. is transferred from Hyptiogaster and Eufoenus flavinervis (Kieffer) remains incertae sedis.



2017 ◽  
Vol 4 (9) ◽  
pp. 170221 ◽  
Author(s):  
A. L. Vereshchaka

The phylogenetic analysis of Sergestoidea based on 253 morphological characters and encompassing all 99 valid species confirmed all previously recognized genus-level clades. Analysis retrieved five major robust clades that correspond to families Luciferidae, Sergestidae, Acetidae fam.n., Sicyonellidae fam.n. and Petalidiumidae fam.n. Synonymy, emended diagnoses and composition of revealed family-level clades are provided. Three types of morphological characters were important in the phylogeny of the Sergestoidea: general external characters, copulatory organs, and photophores. Novel metrics to quantify the contribution of these character types were tested. General external characters were significant in supporting the major clades (80% of the families and nearly half of the genera). Copulatory organ characters and photophores greatly supported the medium-level clades: Lucifer, Belzebub , Petalidium, Neosergestes, Challengerosergia (copulatory organ characters) and Lucensosergia , Challengerosergia, Gardinerosergia , Phorcosergia (photophores). An evolutionary model of the Sergestoidea showing their pathways into their principal biotopes is proposed: the major clades evolved in a vertical direction (from epi- to bathypelagic); further divergence at the genus level occurred within vertical zones in a horizontal direction, with the invasion of the benthopelagic and neritic (shelf and estuarine) habitats and speciation within these domains.



2017 ◽  
Vol 52 (1) ◽  
pp. 7-14
Author(s):  
SD Oyeyemi ◽  
J Kayode

Palynological analysis of honey samples from different localities in Kwara State, Nigeria was carried out to isolate and identified pollen types in the honey samples. Out of forty two pollen types belonging to twenty two botanical families recovered, twenty five were identified to species level, eight to genus level and eight to family level. A total of 849,978 pollen grains were counted with 46,355 in Shao, 101,356 in Ganmo, 22,000 in Idofian, 28,337 in Omupo, 200,090 in Iludun Oro, 298,079 in Ijagbo, 22,100 in Offa I and 131,142 in Afon. The major pollen occurrences in the honey samples include those of Sarcocephaluslatifolius, Parkiabiglobosa, Phyllantusdiscoideus, Tridaxprocubens, Combretaceae/Melastomataceae, Spondiasmombins and Hymenocardiaacida. Other important honey plants identified are Elaeisguineensis, Lanneasp, Parinarisp, Celtissp and Entadaabssynica. All these are characteristic plant taxa of the Forest-Savanna ecotype of the studied area. The presence of relatively high quantity of pollen shows their richness in pollen composition and also a clear evidence that the honey are from botanical sourceand also multifloral.Bangladesh J. Sci. Ind. Res. 52(1), 7-14, 2017



Zootaxa ◽  
2019 ◽  
Vol 4660 (1) ◽  
pp. 1-94
Author(s):  
JAIRO A. MORENO-GONZÁLEZ ◽  
RANULFO GONZÁLEZ O. ◽  
EDUARDO FLÓREZ D.

We present a taxonomic revision of the Colombian Tityus (Archaeotityus) species based on morphological and morphometric evidence. We examined more than 385 specimens and evaluated new and previously used qualitative and quantitative morphological characters. We redescribe the Colombian species and present morphological characters for both sexes and an emended diagnosis for the subgenus Tityus (Archaeotityus). We describe a new species Tityus guane sp. nov. from Santander department, Colombia, Tityus betschi Lourenço 1992 is synonymized with Tityus parvulus Kraepelin, 1914, and Tityus wayuu Rojas-Runjaic & Armas, 2007 is synonymized with Tityus tayrona Lourenço, 1991. We measured 186 specimens and performed a multivariate principal component analysis (PCA) for 34 selected morphometric ratios for each sex. We found that a few morphological ratios support species level distinctions within the Colombian species. We provide updated distributional maps with new records and an identification key for both sexes. Furthermore, we provide an updated checklist for the subgenus and a discussion about the character systems used within Tityus (Archaeotityus). The new morphological characters proposed and the traditional morphometry examined with a PCA are useful for studying Tityus (Archaeotityus) taxonomy.



2020 ◽  
Vol 51 (4) ◽  
pp. 696-752
Author(s):  
Marcelli K. Vieira ◽  
Fernando Z. Vaz-de-Mello ◽  
Fernando A. B. Silva

The subgenus Canthon (Pseudepilissus) Martínez, 1954 is revised. Four valid species are redescribed: Canthon (Pseudepilissus) muticus Harold, 1867; C. (P.) lunatus Schmidt, 1922; C. (P.) planus Lucas, 1857 and C. (P.) reichei Felsche, 1910. Three species assigned to other groups are transferred in the subgenus: C. (P.) quadratus Blanchard, 1843 [previously Canthon “incertae sedis”]; C. (P.) edentulus Harold, 1868 [previously Canthon “incertae sedis”] and C. (P.) seminulus Harold, 1867 comb. nov. [previously Vulcanocanthon]. The genus Vulcanocanthon Pereira & Martínez, 1960 syn. nov. is synonymized with Canthon (Pseudepilissus). Three subspecies are raised to species level: C. (P.) tibialis Schmidt, 1922 stat. nov. [previously C. (P.) lunatus tibialis]; C. (P.) granuliceps Felsche, 1910 stat. nov. [previously C. edentulus granuliceps] and C. (P.) hendrichsi Halffter & Martínez, 1968 stat. nov. [previously C. (P.) muticus hendrichsi]. C. (P.) honsi Balthasar, 1939 syn. nov. is synonymized with C. (P.) reichei Felsche, 1910. Four new species are described: Canthon (P.) arriagadai sp. nov., Canthon (P.) bonaerensis sp. nov., Canthon (P.) vidaurrei sp. nov. and Canthon (P.) ziggy sp. nov., bringing the number of species in the subgenus to 14. Lectotypes are designated for six species C. (P.) muticus Harold, 1867; C. (P.) reichei Felsche, 1910; C. (P.) planus Lucas, 1857; C. (P.) seminulus Harold, 1867; C. (P.) granuliceps Felsche, 1910 and C. (P.) quadratus Blanchard, 1843. A detailed literature review, synonymies, description, illustration of key morphological characters, data on the studied material and geographic distribution are provided for each species.



Zootaxa ◽  
2017 ◽  
Vol 4338 (3) ◽  
pp. 401 ◽  
Author(s):  
ANDRÉS F. GARCÍA ◽  
ADRIANO B. KURY

The Andean genus Rhaucus Simon 1879 is revised. Five valid species are recognized, including Rhaucus florezi sp. nov. The following nomenclatural acts are proposed. At genus level: Megarhaucus Mello-Leitão, 1941, Neorhaucus Pickard-Cambridge, 1905 and Pararhaucus Pickard-Cambridge, 1905 are considered junior subjective synonyms of Rhaucus. At species level: Neorhaucus aurolineatus Pickard-Cambridge, 1905 is considered a junior subjective synonym of Rhaucus vulneratus Simon, 1879; Rhaucus (Rhaucus) tristis Sørensen, 1932, Rhaucus (Rhaucus) muticus Sørensen, 1932 and Pararhaucus obscurus Pickard-Cambridge, 1905 are considered junior subjective synonyms of Rhaucus quinquelineatus Simon, 1879 (the latter combination is restored from current combination Flirtea quinquelineata); Flirtea paucimaculata Roewer, 1963, Rhaucus (Rhaucus) geographicus Sørensen, 1932, Metarhaucus reticulatus Roewer, 1912 and Metarhaucus fuscus Pickard-Cambridge, 1905 are considered junior subjective synonyms of Erginus serripes Simon, 1879 (that is here combined as Rhaucus serripes comb. rest.). Megarhaucus robustus Mello-Leitão, 1941 is newly combined as Rhaucus robustus (Mello-Leitão, 1941) comb. nov. Distribution maps of the species are provided. The new term multicapitate apophysis (mca) is introduced here for a special type of apophysis on coxa IV of males. 



Phytotaxa ◽  
2017 ◽  
Vol 330 (1) ◽  
pp. 1 ◽  
Author(s):  
PETER B. HEENAN

A taxonomic revision of the cosmopolitan genus Cardamine is presented for New Zealand. Previous systematic research and the taxonomic history of Cardamine in New Zealand is reviewed, and a phylogenetic analysis of DNA sequences shows most of the species of Cardamine in New Zealand and Australia are closely related. Forty one taxa indigenous to New Zealand are recognised, with thirty-one species newly named and described, ten previously named taxa are accepted, including C. depressa with two subspecies and a new name is provided for one species. An additional four species are accepted as naturalised in New Zealand. Descriptions are presented for all taxa, along with information on distribution, habitats and conservation status. All taxa are illustrated, distribution maps provided, and a dichotomous key presented to assist with identification.



Zootaxa ◽  
2011 ◽  
Vol 2782 (1) ◽  
pp. 1 ◽  
Author(s):  
DAVID G. CHAPPLE ◽  
TRENT P. BELL ◽  
STEPHANIE N. J. CHAPPLE ◽  
KIMBERLY A. MILLER ◽  
CHARLES H. DAUGHERTY ◽  
...  

The New Zealand skink fauna is highly diverse and contains numerous cryptic, undescribed or hitherto undiscovered species. We completed a taxonomic revision of the cryptic skink (Oligosoma inconspicuum) species complex using molecular (550 bp of the ND2 mitochondrial gene) and morphological analyses. Four new species are described, with each diagnosable by a range of morphological characters and genetic differentiation from several closely related species: O. inconspicuum (sensu stricto), O. notosaurus, O. maccanni, O. stenotis and O. grande. Oligosoma tekakahu sp. nov. is restricted to Chalky Island in Fiordland, and is most closely related to O. inconspicuum and O. notosaurus. The other three new species are restricted to particular mountainous regions in central and western Otago (O. burganae sp. nov., Lammermoor and Rock and Pillar Ranges; O. toka sp. nov., Nevis Valley; O. repens sp. nov., Eyre Mountains) and are most closely related to O. stenotis and O. grande. We also re-described O. inconspicuum. Two proposed new taxa, the ‘Big Bay’ skink and ‘Mahogany’ skink, were found to represent Westland/Fiordland populations of O. inconspicuum rather than distinct taxa. We discuss the evolutionary and phylogeographic implications of cryptic and ‘anti-cryptic’ species within the O. inconspicuum species complex, and suggest that morphologically aberrant populations are the result of local adaptation to novel selective regimes.



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