Search

To explore the spider species diversity and its environmental associations on artificial grasslands in karst areas, we investigated the species diversity of spider in the New Zealand pasture of the Youshanhe in northwestern Guizhou Province, using sampling, trap, and line sampling methods, and further assessed species diversity–environment relationship. The results of the study showed: (1)1642 spiders, belonging to 15 families, 53 genera, and 69 species, were collected. The order of different functional groups was: Round-web spiders > Ambush spiders > wandering-spiders > Net-type spiders. The dominant four families were Araneidae (25.15% of all species), Theridiidae (20.52% of all species), Philodromidae (15.1% of all species), and Thomisidae (13.28% of all species). Furthermore, the two dominant species were Araneus diffinis (17.17% of all individuals) and Philodromus fallax (14.49% of all individuals). (2) The number of individual spiders, the number of species, and the Shannon-wiener index were the smallest in December, which was significantly lower than that in September, October, November and January. The spider richness index decreased first and then increased, and was the smallest in December, significantly lower than in September, October and January. (3) The linear fitting showed that altitude, air humidity, and number of vegetation species had significantly positive associations with spider abundance. (4) Canonical correspondence analysis revealed that 9 environmental factors accounted for 70.98% of the variation for spider species diversity. The vegetation Pielou index had a significantly negative associations with spider species diversity, and soil temperature and air temperature had a significant and positive effect on spider species diversity. Among them, soil temperature had the greatest impact on spider composition, with a contribution rate of 78.52%. The species diversity of spider communities on artificial grasslands in karst areas had a strong correlation with factors such as seasons, climate, and vegetation. Spiders must be closely integrated with local vegetation, climatic and soil factors to control grassland pests and diseases. [ABSTRACT FROM AUTHOR]

The new Australo-Pacific orb-weaving spider genus Socca is established to include 12 species from Australia: Socca pustulosa (Walckenaer, 1841) comb. nov. (type species; also present in New Zealand); S. arenasp. nov., S. australissp. nov.S. caigunasp. nov., S. elvispresleyisp. nov., S. eugenisp. nov., S. johnnywarrenisp. nov., S. kullmannisp. nov., S. levyashinisp. nov., S. pleiasp. nov., S. senicaudata (Simon, 1908) comb. nov. (= Araneus senicaudatus simplex Simon, 1908 syn. nov.) and S. sydneyica (Keyserling, 1887) comb. nov. (= Epeira inquieta Keyserling, 1887 syn. nov.). Soccagen. nov. includes medium-sised, nocturnal orb-weaving spiders. It differs from other backobourkiine genera by five tubercles posteriorly on the abdomen and a tri-partite terminal apophysis of the male pedipalp. The epigyne plate in females is about as wide as long and the scape elongate and reaches posteriorly beyond the epigyne plate. Specimens of five Soccagen. nov. species were sequenced for the mitochondrial gene cytochrome c oxidase subunit 1 (COI). The preliminary phylogeny supports our morphological species but does not confirm species-groups based on morphology and suggests that New Zealand S. pustulosacomb. nov. populations originate from south-eastern Australia. Zoobank LSID: [ABSTRACT FROM AUTHOR]

A new monotypic orb-weaving spider (Araneidae Clerck, 1757) genus, Courtaraneusgen. nov., is described to accommodate the New Zealand species C. orientalis (Urquhart, 1887) comb. nov. This new genus is proposed, as the male pedipalp of the species is unique amongst orb-weaving spiders by the presence of two complex tibial apophyses and a heavily sclerotised cymbial lobe at the base of a strong, elongated paracymbium. The pedipalp bulb is complex with heavily sclerotised sclerites. The median apophysis is situated transverse, the radix strong and wedge-shaped and the terminal apophysis heavily sclerotised and flat, U-shaped. The embolus is accompanied by three terminal apophyses on the elongated stipes. The female epigyne scape forms a tongue, surrounded by an elevated rim, the spermathecae are spherical. The unique autapomorphic characters of the new genus make the phylogenetical placement of the genus difficult. Courtaraneus orientaliscomb. nov. is one of the largest endemic orb-weaving spiders in New Zealand and has been found in multiple locations in the North Island in scrub and forest margins. The orb-web is vertical, large, and the catching threads are widely spaced; however, the hub is poorly structured and the orb often incomplete. [ABSTRACT FROM AUTHOR]

The orb-weaving spider genus Novakiella Court & Forster, 1993 (family Araneidae Clerck, 1757) is reviewed to include two species, N. trituberculosa (Roewer, 1942) (type species, Australia and New Zealand) and N. boletus sp. nov. (Australia). Novakiella belongs to the informal, largely Australian 'backobourkiine' clade and shares with the other genera of the clade a single macroseta on the male pedipalp patella and a median apophysis of the male pedipalp that forms an arch over the radix. The proposed genus synapomorphies are the presence of a large basal conductor lobe expanding apically over the radix and the shape of the median apophysis, which extends into a basally directed, pointy projection. Males have an apico-prolateral spur on the tibia of the second leg that carries a distinct spine. Females have an epigyne with triangular base plate bearing transverse ridges and an elongate triangular scape, which is almost always broken off. The humeral humps of the abdomen are distinct. Novakiella trituberculosa build characteristic domeshaped webs; however, the foraging behaviour and web-shape of N. boletus sp. nov., currently only known from museum specimens, are not known. [ABSTRACT FROM AUTHOR]

We present a new phylogeny of the spider family Araneidae based on five genes (28S, 18S, COI, H3 and 16S) for 158 taxa, identified and mainly sequenced by us. This includes 25 outgroups and 133 araneid ingroups representing the subfamilies Zygiellinae Simon, 1929, Nephilinae Simon, 1894, and the typical araneids, here informally named the "ARA Clade". The araneid genera analysed here include roughly 90% of all currently named araneid species. The ARA Clade is the primary focus of this analysis. In taxonomic terms, outgroups comprise 22 genera and 11 families, and the ingroup comprises three Zygiellinae and four Nephilinae genera, and 85 ARA Clade genera (ten new). Within the ARA Clade, we recognize ten informal groups that contain at least three genera each and are supported under Bayesian posterior probabilities (≥ 0.95): "Caerostrines" (Caerostris, Gnolus and Testudinaria), "Micrathenines" (Acacesia, Micrathena, Ocrepeira, Scoloderus and Verrucosa), "Eriophorines" (Acanthepeira, Alpaida, Eriophora, Parawixia and Wagneriana), "Backobourkiines" (Acroaspis, Backobourkia, Carepalxis, Novakiella, Parawixia, Plebs, Singa and three new genera), "Argiopines" (Arachnura, Acusilas, Argiope, Cyrtophora, Gea, Lariniaria and Mecynogea), "Cyrtarachnines" (Aranoethra, Cyrtarachne, Paraplectana, Pasilobus and Poecilopachys), "Mastophorines" (Celaenia, Exechocentrus and Mastophora,), "Nuctenines" (Larinia, Larinioides and Nuctenea), "Zealaraneines" (Colaranea, Cryptaranea, Paralarinia, Zealaranea and two new genera) and "Gasteracanthines" (Augusta, Acrosomoides, Austracantha, Gasteracantha, Isoxya, Macracantha, Madacantha, Parmatergus and Thelacantha). Few of these groups are currently corroborated by morphology, behaviour, natural history or biogeography. We also include the large genus Araneus, along with Aculepeira, Agalenatea, Anepsion, Araniella, Cercidia, Chorizopes, Cyclosa, Dolophones, Eriovixia, Eustala, Gibbaranea, Hingstepeira, Hypognatha, Kaira, Larinia, Mangora, Metazygia, Metepeira, Neoscona, Paraplectanoides, Perilla, Poltys, Pycnacantha, Spilasma and Telaprocera, but the placement of these genera was generally ambiguous, except for Paraplectanoides, which is strongly supported as sister to traditional Nephilinae. Araneus, Argiope, Eriophora and Larinia are polyphyletic, Araneus implying nine new taxa of genus rank, and Eriophora and Larinia two each. In Araneus and Eriophora, polyphyly was usually due to north temperate generic concepts being used as dumping grounds for species from southern hemisphere regions, e.g. South‐East Asia, Australia or New Zealand. Although Araneidae is one of the better studied spider families, too little natural history and/or morphological data are available across these terminals to draw any strong evolutionary conclusions. However, the classical orb web is reconstructed as plesiomorphic for Araneidae, with a single loss in "cyrtarachnines"–"mastophorines". Web decorations (collectively known as stabilimenta) evolved perhaps five times. Sexual dimorphism generally results from female body size increase with few exceptions; dimorphic taxa are not monophyletic and revert to monomorphism in a few cases. [ABSTRACT FROM AUTHOR]