Deforestation and land‐use change in tropical regions result in habitat loss and extinction of species that are unable to adapt to the conditions in agricultural landscapes. If the associated loss of functional diversity is not compensated by species colonizing the converted habitats, extinctions might be followed by a reduction or loss of ecosystem functions including biological control. To date, little is known about how land‐use change in the tropics alters the functional diversity of invertebrate predators and which key environmental factors may mitigate the decline in functional diversity and predation in litter and soil communities. We applied litter sieving and heat extraction to study ground spider communities and assessed structural characteristics of vegetation and parameters of litter in rainforest and agricultural land‐use systems (jungle rubber, rubber, and oil palm monocultures) in a Southeast Asian hotspot of rainforest conversion: Sumatra, Indonesia. We found that (1) spider density, species richness, functional diversity, and community predation (energy flux to spiders) were reduced by 57–98% from rainforest to oil palm monoculture; (2) jungle rubber and rubber monoculture sustained relatively high diversity and predation in ground spiders, but small cryptic spider species strongly declined; (3) high species turnover compensated losses of some functional trait combinations, but did not compensate for the overall loss of functional diversity and predation per unit area; (4) spider diversity was related to habitat structure such as amount of litter, understory density, and understory height, while spider predation was better explained by plant diversity. Management practices that increase habitat‐structural complexity and plant diversity such as mulching, reduced weeding, and intercropping monocultures with other plants may contribute to maintaining functional diversity of and predation services provided by ground invertebrate communities in plantations.
Pirate spiders (Mimetidae) are well known for their specialised feeding ecology. They are vagrant araneophagic predators, enter the webs of their prey spiders and exhibit patterns of aggressive mimicry to overcome the web owner. The mimetid fauna of Australia and New Zealand currently consists of 26 species in the following three genera: Australomimetus Heimer, 1986 (18 species), Mimetus Hentz, 1832 (six species), and Ero C.L. Koch, 1836 (two species). The systematic position of the majority of Australasian mimetids was investigated through phylogenetic techniques utilising morphological character systems of 29 exemplar taxa and 87 characters, including the first examination of spinneret structure in species of Australomimetus. The results support an expanded concept for Australomimetus, which, apart from the introduced Ero aphana (Walckenaer, 1802), is found to contain the entire Australian and New Zealand mimetid fauna, also recorded from Asia. The following taxonomic changes are proposed: A. catulli (Heimer, 1989), comb. nov., A. hannemanni (Heimer, 1989), comb. nov., A. japonicus (Uyemura, 1938), comb. nov., A. mendicus (O. P. Cambridge, 1879), comb. nov. and A. sennio (Urquhart, 1891), comb. nov.; Ero luzoniensis Barrion & Litsinger, 1995 is synonymised with Ero aphana, and A. andreae Heimer, 1989 is synonymised with A. daviesianus Heimer, 1986; Mimetus tikaderi Gajbe, 1992 from India is excluded from Mimetidae, and referred to Liocranidae. The Western Australian mimetid fauna is described for the first time and comprises nine species of Australomimetus, including the following five new species: A. diabolicus, sp. nov., A. djuka, sp. nov., A. dunlopi, sp. nov., A. nasoi, sp. nov. and A. stephanieae, sp. nov. Several species-groups of Australomimetus are identified.
Abstract. Pseudoscorpions, given their resemblance to scorpions, have attracted human attention since the time of Aristotle, although they are much smaller and lack the sting and elongated tail. These arachnids have a long evolutionary history but their origins and phylogenetic affinities are still being debated. Here, we summarise their fossil record based on a comprehensive review of the literature and data contained in other sources. Pseudoscorpions are one of the oldest colonisers of the land, with fossils known since the Middle Devonian (ca. 390 Ma). The only arachnid orders with an older fossil record are scorpions, harvestmen and acariform mites, plus two extinct groups. Pseudoscorpions do not fossilise easily, and records from the Mesozoic and Cenozoic consist almost exclusively of amber inclusions. Most Mesozoic fossils come from Archingeay and Burmese ambers (Late Cretaceous) and those from the Cenozoic are primarily from Eocene Baltic amber, although additional fossils from, for example, Miocene Dominican and Mexican ambers, are known. Overall, 16 of the 26 families of living pseudoscorpions have been documented from fossils and 49 currently valid species are recognised in the literature. Pseudoscorpions represent a case of morphological stasis and even the Devonian fossils look rather modern. Indeed, most amber fossils are comparable to Recent groups despite a major gap in the fossil record of almost 250 Myr. Baltic amber inclusions indicate palaeofauna inhabiting much warmer climates than today and point to climatic shifts in central Europe since the Eocene. They also indicate that some groups (e.g. Feaellidae and Pseudogarypidae) had much wider Eocene distributions. Their present-day occurrence is relictual and highlights past extinction events. Faunas from younger tropical amber deposits (e.g. Dominican and Mexican amber) are comparable to Recent ones. Generally, there is a strong bias in the amber record towards groups that live under tree bark, whereas those from litter habitats are underrepresented. We also discuss challenges in interpreting fossils: their cryptic morphology warranting novel techniques of morphological reconstruction, the massive gap in the fossil record between the Palaeozoic and Mesozoic, and problems with the classification of (historically) old amber material. Finally, we discuss aspects of the palaeoecology and biology of the fossils compared with the Recent fauna, such as phoresy.
The south-western division of Australia is the only biodiversity hotspot in Australia and is well-known for extreme levels of local endemism. Climate change has been identified as a key threat for flora and fauna, but very few data are presently available to evaluate its impact on invertebrate fauna. Here, we derive a molecular phylogeography for pseudoscorpions of the genus Pseudotyrannochthonius that in the south-west are restricted to regions with the highest rainfall. A dated molecular phylogeny derived from six gene fragments is used for biogeographic reconstruction analyses, spatial mapping, environmental niche-modelling, and to infer putative species. Phylogenetic analyses uncover nine clades with mostly allopatric distributions and often small linear ranges between 0.5 and 130 km. Molecular dating suggests that the origins of contemporary diversity fall into a period of warm/humid Palaeogene climates, but splits in the phylogeny coincide with major environmental shifts, such as significant global cooling during the Middle Miocene. By testing several models of historical biogeography available for the south-west, we determine that Pseudotyrannochthonius is an ancient relict lineage that principally follows a model of allopatric speciation in mesic zone refugia, although there are derivations from this model in that some species are older and distribution patterns more complex than expected. Ecological niche models indicate that drier and warmer future climates will lead to range contraction towards refugia of highest rainfall, probably mimicking past variations that have generated high diversity in these areas. Their conservation management will be crucial for preserving the unique biodiversity heritage of the south-west.
Recently, the Society of Vertebrate Paleontology (SVP) has sent around a letter, dated 21st April, 2020 to more than 300 palaeontological journals, signed by the President, Vice President and a former President of the society (Rayfield et al. 2020). The signatories of this letter request significant changes to the common practices in palaeontology. With our present, multi-authored comment, we aim to argue why these suggestions will not lead to improvement of both practice and ethics of palaeontological research but, conversely, hamper its further development. Although we disagree with most contents of the SVP letter, we appreciate this initiative to discuss scientific practices and the underlying ethics. Here, we consider different aspects of the suggestions by Rayfield et al. (2020) in which we see weaknesses and dangers. It is our intent to compile views from many different fields of palaeontology, as our discipline is (and should remain) pluralistic. This contribution deals with the aspects concerning Myanmar amber. Reference is made to Haug et al. (2020a) for another comment on aspects concerning amateur palaeontologists/citizen scientists/private collectors.
Rainforest canopies, home to one of the most complex and diverse terrestrial arthropod communities, are threatened by conversion of rainforest into agricultural production systems. However, little is known about how predatory arthropod communities respond to such conversion. To address this, we compared canopy spider (Araneae) communities from lowland rainforest with those from three agricultural systems in Jambi Province, Sumatra, Indonesia, i.e., jungle rubber (rubber agroforest) and monoculture plantations of rubber and oil palm. Using canopy fogging, we collected 10,676 spider specimens belonging to 36 families and 445 morphospecies. The four most abundant families (Salticidae N = 2,043, Oonopidae N = 1,878, Theridiidae N = 1,533 and Clubionidae N = 1,188) together comprised 62.2% of total individuals, while the four most speciose families, Salticidae (S = 87), Theridiidae (S = 83), Araneidae (S = 48) and Thomisidae (S = 39), contained 57.8% of all morphospecies identified. In lowland rainforest, average abundance, biomass and species richness of canopy spiders was at least twice as high as in rubber or oil palm plantations, with jungle rubber showing similar abundances as rainforest, and intermediate biomass and richness. Community composition of spiders was similar in rainforest and jungle rubber, but differed from rubber and oil palm, which also differed from each other. Canonical Correspondence Analysis showed that canopy openness, aboveground tree biomass and tree density together explained 18.2% of the variation in spider communities at family level. On a morphospecies level, vascular plant species richness and tree density significantly affected the community composition but explained only 6.8% of the variance. While abundance, biomass and diversity of spiders declined strongly with the conversion of rainforest into monoculture plantations of rubber and oil palm, we also found that a large proportion of the rainforest spider community can thrive in extensive agroforestry systems such as jungle rubber. Despite being very different from rainforest, the canopy spider communities in rubber and oil palm plantations may still play a vital role in the biological control of canopy herbivore species, thus contributing important ecosystem services. The components of tree and palm canopy structure identified as major determinants of canopy spider communities may aid in decision-making processes toward establishing cash-crop plantation management systems which foster herbivore control by spiders.
: Fossil pirate spiders (Araneae: Mimetidae) are revised. The extinct genera Succinero Wunderlich, 2004a and Palaeoero Wunderlich, 2004a are interpreted as synonyms of the extant genus Ero C. L. Koch, 1836. We recognize here the following fossil species as valid: E. carboneana Petrunkevitch, 1942, E. longitarsus (Wunderlich, 2004a) comb. nov. and E. permunda Petrunkevitch, 1942, all from Baltic amber (Paleogene: Eocene), and E. rovnoensis (Wunderlich, 2004b) comb. nov. from Rovno (Ukranian) amber (Paleogene: Eocene). Mimetus bituberculatus Wunderlich, 1988 from Dominican Republic amber (Neogene: Miocene) can be assigned to a specifically American clade of Mimetus Hentz, 1932. Mimetus brevipes Wunderlich, 2004a from Baltic amber is synonymized with M. longipes Wunderlich, 2004a syn. nov. Of the other species (all Baltic amber), Ero aberrans Petrunkevitch, 1958 lacks taxonomically useful characters. Ero setulosa C. L. Koch and Berendt, 1854 is based on two non‐conspecific, and non‐mimetid, spiders. Mimetarchaea gintaras Eskov, 1992 is a subadult male mimetid. The putative oarcine ‘missing link’Praeoarces exitus Wunderlich, 2004a is a subadult female mimetine. All four are treated here as nomina dubia. Other fossil mimetid species in the literature are nomina nuda.
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