The velvet spiders: an atlas of the Eresidae (Arachnida, Araneae) (original) (raw)
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A completely resolved phylogenetic tree of British spiders (Arachnida: Araneae)
Ecologica Montenegrina
The recent accumulation of increasingly densely sampled phylogenetic analyses of spiders has greatly advanced our understanding of evolutionary relationships within this group. Here, this diverse literature is reviewed and combined with earlier morphological analyses in an attempt to reconstruct the first fully resolved phylogeny for the spider fauna of the British Isles. The resulting tree highlights parts of the group where data are still too limited for a confident assessment of relationships, proposes a number of deviations from previously suggested phylogenetic hypotheses, and can serve as a framework for evolutionary and ecological interpretations of the biology of British spiders, as well as a starting point for future studies on a larger geographical scale.
Phylogeny of pholcid spiders (Araneae: Pholcidae): Combined analysis using morphology and molecules
Molecular Phylogenetics and Evolution, 2005
The spider family Pholcidae comprises a large number of mainly tropical, web-weaving spiders, and is among the most diverse and dominant spider groups in the world. The phylogeny of this family has so far been investigated exclusively using morphological data. Here, we present the Wrst molecular data for the family analyzed in a phylogenetic context. Four diVerent gene regions (12S rRNA, 16S rRNA, cytochrome c oxidase subunit I, 28S rRNA) and 45 morphological characters were scored for 31 pholcid and three outgroup taxa. The data were analyzed both for individual genes, combined molecular data, and molecular plus morphological data, using parsimony, maximum likelihood, and Bayesian methods. Some of the phylogenetic hypotheses obtained previously using morphology alone were also supported by our results, like the monophyly of pholcines and of the New World clade. On the other hand, some of the previous hypotheses could be discarded with some conWdence (monophyly of holocnemines, the position of Priscula), and still others need further investigation (the position of holocnemines, ninetines, and Metagonia). The data obtained provide an excellent basis for future investigations of phylogenetic patterns both within the family and among spider families.
Molecular Phylogenetics and Evolution, 2010
Penestomine spiders were first described from females only and placed in the family Eresidae. Discovery of the male decades later brought surprises, especially in the morphology of the male pedipalp, which features (among other things) a retrolateral tibial apophysis (RTA). The presence of an RTA is synapomorphic for a large clade of spiders exclusive of Eresidae. A molecular data matrix based on four loci was constructed to test two alternative hypotheses: (1) penestomines are eresids and the RTA is convergent, or (2) penestomines belong within the RTA clade. Taxon sampling concentrated on the Eresidae and the RTA clade, especially outside of the Dionycha and Lycosoidea. Evolution of the cribellum, conventionally characterized as a primitive araneomorph spinning organ lost multiple times, is explored. Parsimony optimization indicates repeated appearances of the cribellum. Exploration of asymmetric rates of loss and gain in both a likelihood framework and using a Sankoff matrix under parsimony reveals that cribellum homology is supported when losses are two times more likely than gains. We suggest that when complicated characters appear (under parsimony optimization) to evolve multiple times, investigators should consider alternative reconstructions featuring a relatively high rate of loss. Evolution of other morphological characters is also investigated. The results imply revised circumscription of some RTA-clade families, including Agelenidae, Amaurobiidae, Cybaeidae, Dictynidae and Hahniidae. Some nomenclatural changes are formally proposed here; others await further investigation. The family Penestomidae (NEW RANK) is established. Tamgrinia, not Neoramia, is the cribellate sister clade of the ecribellate Agelenidae. Tamgrinia and the subfamily Coelotinae are transferred from the family Amaurobiidae to the family Agelenidae. Zanomys and its relatives are not coelotines but belong to a clade tentatively identified as Macrobuninae.
Taxonomy notes on twenty-eight spider species (Arachnida: Araneae) from Asia
Zenodo (CERN European Organization for Nuclear Research), 2022
Twenty-eight spiders from Asia 199 2 Materials and methods All specimens were preserved in 80% ethanol. The spermathecae were cleared in trypsin enzyme solution to dissolve non-chitinous tissues. Specimens were examined under a LEICA M205C stereomicroscope. Photomicrographs were taken with an Olympus C7070 zoom digital camera (7.1 megapixels). Laboratory habitus photographs were taken with a Sony A7RIV digital camera equipped with a Sony FE 90mm Goss lens. Photos were stacked with Helicon Focus® (Version 7.6.1) or Zerene Stacker® (Version 1.04) and processed in Adobe Photoshop CC2019®. All measurements are in millimetres (mm) and were obtained with an Olympus SZX16 stereomicroscope with a Zongyuan CCD industrial camera. All measurements of body lengths do not include the chelicerae. Eye sizes are measured as the maximum diameter from either the dorsal or frontal view. Leg measurements are given as follows: total length (femur, patella+tibia, metatarsus, tarsus), in Telemidae: total length (femur, patella, tibia, metatarsus, tarsus). In Anyphaenidae, the terminology used in the text and figures follows Lin et al., (2021), in Ctenidae, the terminology used in the text and figures follows Jäger (2012), in Leptonetidae, the terminology used in the text and figures follows Wang and Li (2011), in Liocranidae, the terminology used in the text and figures follows Marusik, Zheng and Li (2008), in Ochyroceratidae, the terminology used in the text and figures follows Tong et al. (2019), in Selenopidae, the terminology used in the text and figures follows Dankittipakul and Corronca (2009), in Tetrablemmidae, the terminology used in the text and figures follows Yan and Lin (2018), in Theridiidae, the terminology used in the text and figures follows Agnarsson (2004), in Theridiosomatidae, the terminology used in the text and figures follows Coddington (1986) and in Titanoecidae, the terminology used in the text and figures follows Almeida-Silva, Griswold and Brescovit (2010). Types from the current study are deposited in the Institute of Zoology, Chinese Academy of Sciences in Beijing (IZCAS). Abbreviations used in text and figures are as following. Ocular area: ALE-anterior lateral eyes; AME-anterior median eyes; PLE-posterior lateral eyes; PME-posterior median eyes. Male palp: C-conductor; Ca-cymbial apophysis; CEBP-ectobasal cymbial process; Cy-cymbium; dRTA-dorsal retrolateral tibial apophysis; DTA-dorsal tibial apophysis; E-embolus; Et-embolic tip; MA-median apophysis; MLT-median lobe of tibial apophysis; P-paracymbium; Pa-patellar apophysis; Pb-bulb; PCB-prolateral cymbial bulge; PLT-prolateral lobe of tibial apophysis; RBA-basal apophysis; 200 Lin et al.
Molecular Phylogenetics and Evolution, 2010
Penestomine spiders were first described from females only and placed in the family Eresidae. Discovery of the male decades later brought surprises, especially in the morphology of the male pedipalp, which features (among other things) a retrolateral tibial apophysis (RTA). The presence of an RTA is synapomorphic for a large clade of spiders exclusive of Eresidae. A molecular data matrix based on four loci was constructed to test two alternative hypotheses: (1) penestomines are eresids and the RTA is convergent, or (2) penestomines belong within the RTA clade. Taxon sampling concentrated on the Eresidae and the RTA clade, especially outside of the Dionycha and Lycosoidea. Evolution of the cribellum, conventionally characterized as a primitive araneomorph spinning organ lost multiple times, is explored. Parsimony optimization indicates repeated appearances of the cribellum. Exploration of asymmetric rates of loss and gain in both a likelihood framework and using a Sankoff matrix under parsimony reveals that cribellum homology is supported when losses are two times more likely than gains. We suggest that when complicated characters appear (under parsimony optimization) to evolve multiple times, investigators should consider alternative reconstructions featuring a relatively high rate of loss. Evolution of other morphological characters is also investigated. The results imply revised circumscription of some RTA-clade families, including Agelenidae, Amaurobiidae, Cybaeidae, Dictynidae and Hahniidae. Some nomenclatural changes are formally proposed here; others await further investigation. The family Penestomidae (NEW RANK) is established. Tamgrinia, not Neoramia, is the cribellate sister clade of the ecribellate Agelenidae. Tamgrinia and the subfamily Coelotinae are transferred from the family Amaurobiidae to the family Agelenidae. Zanomys and its relatives are not coelotines but belong to a clade tentatively identified as Macrobuninae.
Progress in erigonine spider phylogeny—the Savignia-group is not monophyletic (Araneae: Linyphiidae)
Organisms Diversity & Evolution, 2010
We present the most inclusive study on the higher-level phylogeny of erigonine spiders, including about 30% of all erigonine genera. By expanding the previously most comprehensive analysis (Miller and Hormiga Cladistics 20:385-442, 2004) we tested the robustness of its results to the addition of closely related taxa, and also the monophyly of the Savignia-group defined by Millidge (Bulletin of the British Arachnological Society 4:1-60, 1977). The character matrix was expanded by adding 18 newly scored species in 15 genera, and also includes all species scored by other authors. This adds up to 98 species in 91 erigonine genera plus 13 outgroup taxa. The parsimony analysis led to eight fully resolved most parsimonious trees (L=1084). The topology concerning the taxa basal to the 'distal erigonines' remained unchanged, and the latter clade still shares 67% of all nodes with the original analysis. The Savignia-group is not monophyletic at genus level with respect to Saloca diceros and Alioranus pastoralis, and the same applies at species level in Diplocephalus and Erigonella. From the Savignia-group, Glyphesis servulus, Diplocephalus cristatus, Savignia frontata, and two representatives each of Erigonella, Dicymbium and Araeoncus combine to form a monophyletic clade.