Opiliones (Arachnida) of the superfamily Gonyleptoidea
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA556673 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR17068830_1.fastq.gz | Fastqsanger.gz | |||
| SRR17068830_2.fastq.gz | Fastqsanger.gz | |||
| SRR17068831_1.fastq.gz | Fastqsanger.gz | |||
| SRR17068831_2.fastq.gz | Fastqsanger.gz | |||
| SRR17068832_1.fastq.gz | Fastqsanger.gz |
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Project description:Raw read data from multiple Opiliones libraries enriched for ultraconserved elements shared among Opiliones Raw sequence reads
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Project description:High Phylogenetic Utility of an Ultraconserved Element Probe Set Designed for Arachnida
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Project description:As part of an ongoing revision of the family Gonyleptidae, we have identified many species that are synonyms of previously described species or misplaced in this family. This article summarizes these findings, adding previously unavailable information or correcting imprecise observations to justify the presented taxonomic changes. THE FOLLOWING NEW FAMILIAL OR SUBFAMILIAL ASSIGNMENTS ARE PROPOSED: Nemastygnus Roewer, 1929 and Taulisa Roewer, 1956 are transferred to Agoristenidae, Agoristeninae; Napostygnus Roewer, 1929 to Cranaidae; Ceropachylinus peruvianus Roewer, 1956 and Pirunipygus Roewer, 1936 are transferred to Gonyleptidae, Ampycinae; Gyndesops Roewer, 1943, Haversia Roewer, 1913 and Oxapampeus Roewer, 1963 are transferred to Gonyleptidae, Pachylinae. The following generic synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes Mello-Leitão, 1922 = Centroleptes Roewer, 1943; Acrographinotus Roewer, 1929 = Unduavius Roewer, 1929; Gonyleptes Kirby, 1819 = Collonychium Bertkau, 1880; Mischonyx Bertkau, 1880 = Eugonyleptes Roewer, 1913 and Gonazula Roewer, 1930; Parampheres Roewer, 1913 = Metapachyloides Roewer, 1917; Pseudopucrolia Roewer, 1912 = Meteusarcus Roewer, 1913; Haversia Roewer, 1913 = Hoggellula Roewer, 1930. The following specific synonymies are proposed for the family Gonyleptidae: Acanthogonyleptes singularis (Mello-Leitão, 1935) = Centroleptes flavus Roewer, 1943, syn. n.; Geraeocormobius sylvarum Holmberg, 1887 = Discocyrtus serrifemur Roewer, 1943, syn. n.; Gonyleptellus bimaculatus (Sørensen, 1884) = Gonyleptes cancellatus Roewer,1917, syn. n.; Gonyleptes atrus Mello-Leitão, 1923 = Weyhia brieni Giltay, 1928, syn. n.; Gonyleptes fragilis Mello-Leitão, 1923 = Gonyleptes banana Kury, 2003, syn. n.; Gonyleptes horridus Kirby, 1819 = Collonychium bicuspidatum Bertkau, 1880, syn. n., Gonyleptes borgmeyeri Mello-Leitão, 1932, syn. n., Gonyleptes curvicornis Mello-Leitão, 1932, syn. n., Metagonyleptes hamatus Roewer, 1913, syn. n. and Paragonyleptes simoni Roewer, 1930, syn. n.; Gonyleptes pustulatus Sørensen, 1884 = Gonyleptes guttatus Roewer, 1917, syn. n.; Haversia defensa (Butler, 1876) = Sadocus vallentini Hogg, 1913, syn. n.; Liogonyleptoides minensis (Piza, 1946) = Currala bahiensis Soares, 1972, syn. n.; Megapachylus grandis Roewer, 1913 = Metapachyloides almeidai Soares & Soares, 1946, syn. n.; Mischonyx cuspidatus (Roewer, 1913) = Gonazula gibbosa Roewer, 1930 syn. n.; Mischonyx scaber (Kirby, 1819) = Xundarava holacantha Mello-Leitão, 1927, syn. n.; Parampheres tibialis Roewer, 1917 = Metapachyloides rugosus Roewer, 1917, syn. n.; Parapachyloides uncinatus (Sørensen, 1879) = Goyazella armata Mello-Leitão, 1931, syn. n.; Pseudopucrolia mutica (Perty, 1833) = Meteusarcus armatus Roewer, 1913, syn. n.THE FOLLOWING NEW COMBINATIONS ARE PROPOSED: Acrographinotus ornatus (Roewer, 1929), comb. n. (ex Unduavius); Gonyleptellus bimaculatus (Sørensen, 1884),comb. n. (ex Gonyleptes);Gonyleptes perlatus (Mello-Leitão, 1935), comb. n. (exMoojenia);Mischonyx scaber (Kirby, 1819), comb. n. (ex Gonyleptes); and Neopachyloides peruvianus (Roewer, 1956), comb. n. (ex Ceropachylus). The following species of Gonyleptidae, Gonyleptinae are revalidated: Gonyleptes atrus Mello-Leitão, 1923 and Gonyleptes curvicornis (Roewer, 1913).
| S-EPMC3368255 | biostudies-literature
Project description:This dataset provides information on specimens of harvestmen (Arthropoda, Arachnida, Opiliones) collected in French Guiana. Field collections have been initiated in 2012 within the framework of the CEnter for the Study of Biodiversity in Amazonia (CEBA: www.labex-ceba.fr/en/). This dataset is a work in progress. Occurrences are recorded in an online database stored at the EDB laboratory after each collecting trip and the dataset is updated on a monthly basis. Voucher specimens and associated DNA are also stored at the EDB laboratory until deposition in natural history Museums. The latest version of the dataset is publicly and freely accessible through our Integrated Publication Toolkit at http://130.120.204.55:8080/ipt/resource.do?r=harvestmen_of_french_guiana or through the Global Biodiversity Information Facility data portal at http://www.gbif.org/dataset/3c9e2297-bf20-4827-928e-7c7eefd9432c.
| S-EPMC4290495 | biostudies-other
Project description:Praelibitia Roewer, 1956 and its type species, Praelibitia titicaca Roewer, 1956, are respectively synonymized with Platygyndes Roewer, 1943 and its type species Platygyndes titicaca Roewer, 1943, and furthermore the genus is transferred from the Gonyleptidae to the Cosmetidae. On the basis of domed and unarmed ocularium, increased number of granules on scutal areas, unarmed dorsal scutum and general body shape, Platygyndes seems to be closely related to Moselabius Roewer, 1956 and Caracarana Roewer, 1956. External morphological characters that are useful to revealing relationships among cosmetid genera are discussed.
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Project description:Comprising more than 6500 species, Opiliones is the third most diverse order of Arachnida, after the megadiverse Acari and Araneae. The database referred here is part 1 of 12 of a project containing an intended worldwide checklist of species and subspecies of Opiliones as Darwin Core archives, and it includes the superfamilies Travunioidea and Triaenonychoidea. These two superfamilies are often treated together under the denomination of Insidiatores. In this Part 1, a total of 571 species and subspecies are listed. Briggsidae and Cladonychiidae are both downgraded to subfamilies of Travuniidae. Peltonychia Roewer, 1935 is an available name and senior synonym of Hadziana Roewer, 1935 and is herein revalidated. Seven genera of Triaenonychidae described by Lawrence between 1931 and 1933 originally failed to comply ICZN rules for availability (Art. 13.3). All of them only became available when Staręga (1992) designated a type species for each. Therefore, the correct authorships of Austromontia Lawrence, 1931, Biacumontia Lawrence, 1931, Graemontia Lawrence, 1931, Larifugella Lawrence, 1933, Mensamontia Lawrence, 1931, Monomontia Lawrence, 1931 and Rostromontia Lawrence, 1931 are all Staręga, 1992. Fumontana Shear, 1977, originally referred only to subfamily Triaenonychinae (as opposed to Soerensenellinae then and not corresponding to present Triaenonychinae), not to any tribe (which in turn correspond to modern subfamilies) is herein included in the subfamily Triaenonychinae. Picunchenops Maury, 1988 originally not included in any tribe of Triaenonychidae, is herein included in the subfamily Triaenonychinae. Trojanella Karaman, 2005, originally ranked as Travunioidea incertae sedis, is herein included in the TravuniidaeTravuniinae. Nunciaovata Roewer, 1915 (synonymized with Triaenonyxcockayni Hogg, 1920 by Forster (1954), but with inverted precedence) is here combined as Nunciacoriaceaovata Roewer, 1915 as correct senior synonym instead of Nunciacoriaceacockayni (Hogg, 1920), which is current in the literature. Neonunciaenderbei (Hogg, 1909) is reaffirmed as the correct spelling for the species, while the deliberate change to Neonunciaenderbyi by Forster (1954) is an incorrect subsequent spelling.
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Project description:Nuptial gifts are material donations given from male to female before or during copulation and are subject to sexual selection in a wide variety of taxa. The harvestman genus Leiobunum has emerged as a model system for understanding the evolution of reproductive morphology and behavior, as transitions between solicitous and antagonistic modes of courtship have occurred multiple times within the lineage and are correlated with convergence in genital morphology. We analyzed the free amino acid content of nuptial gift secretions from five species of Leiobunum using gas chromatography-mass spectrometry. Multivariate analysis of the free amino acid profiles revealed that, rather than clustering based on phylogenetic relationships, nuptial gift chemical composition was better predicted by genital morphology and behavior, suggesting that convergent evolution has acted on the chemical composition of the nuptial gift. In addition, we found that, species with solicitous courtship produce gifts consisting of a 19% larger proportion of essential amino acids as compared to those with more antagonistic courtship interactions. This work represents the first comparative study of nuptial gift chemistry within a phylogenetic framework in any animal group and as such contributes to our understanding of the evolution of reproductive diversity and the participant role of nuptial gift chemistry in mating system transitions.
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