3 research outputs found

    Phylogeny, taxonomy and species delimitation of water mites and velvet mites

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    This study is part of the Swedish Taxonomy Initiative (STI) - one of the most ambitious all taxa biodiversity inventories in the world. One of the pillars in STI is to support taxonomic research on the most neglected taxonomic groups with the aim to lift the level of knowledge of biodiversity in the country. There is still a lot to be discovered, especially in the microscopic world, and this includes mites. Many aspects of mite biology and diversity are poorly known, such as species richness, abundance, distribution, lifestyle and behavior of species. Mites inhabits all sorts of aquatic, terrestrial, arboreal and parasitic habitats, nevertheless even in well-studied systems mites are often overlooked. Despite being among the smallest of arthropods, they are of medical and economical importance and may be very abundant in the ecosystems they inhabit. This thesis focuses on Parasitengona (Acariformes: Prostigmata), one of the most diverse taxa among the arachnids. It includes the aquatic Hydrachnidia (water mites) and the terrestrial Trombidia (e.g. velvet mites, chiggers). A unifying characteristic of Parasitengona is their complex life cycle of active and inactive stages, parasitic larvae and predatory deutonymphs and adults. They typically parasitize and prey on arthropods, except the chiggers which have vertebrates as hosts. The aim of this thesis is to shed light on the phylogeny and taxonomy of Parasitengona with emphasis on the Swedish fauna. To achieve this, mites were collected from different localities throughout the country between the years 2007-2016. Water mites were sampled with a hand net. Larvae of terrestrial Parasitengona were collected with sweeping nets and sorted out from malaise trap samples from the Swedish Malaise Trap Project. To collect the adults Berlese-Tullgren extractor and pitfall traps were used as well as hand collecting and sifting with litter reducer. The material collected abroad was kindly provided through collaboration.  Methods used in the papers included morphometrics, multivariate analyses, experimental rearing, DNA extraction and sequencing, Bayesian phylogenetic analyses and molecular species delimitation. In paper I and II, we combine molecular species delimitation models and morphological data to resolve taxonomical issues. This integrative taxonomic approach of combining data resulted in Piona dispersa Sokolow, 1926 as a valid species and redescriptions, new synonyms and neotypes provided for Erythraeus phalangoides (De Geer, 1778),  E. cinereus (Dugès, 1834) and E. regalis (C.L. Koch, 1837). Based on the new inventories we produce an updated and annotated checklist of 105 terrestrial Parasitengona species for Fennoscandia in paper III, and use metadata to increase the knowledge on distribution, habitat preferences, life stages and abundance. Out of these, 20 species are new findings for the region and five are potential new species for science. In paper IV, we provide a molecular phylogeny of Parasitengona based on the genes 18S, 28S and COI for 80 taxa with a sampling focus on the terrestrial lineages. Based on the results we offer a revised higher-level classification of the group. In particular the analyses supported Tanaupodoidea Thor, 1935 as a separate superfamily, but Trombiculoidea Ewing, 1929 was not monophyletic and was synonymized, along with Chyzerioidea Womersley, 1954, with Trombidioidea Leach, 1815.At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript. Paper 4: Manuscript. </p

    Checklist of terrestrial Parasitengona mites in Fennoscandia with new species- and distribution records (Acariformes: Prostigmata)

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    The knowledge of terrestrial Parasitengona in Fennoscandia lies far behind that of their aquatic counterparts, the water mites (Hydrachnidia). Based on new inventories, we provide primary data and an annotated checklist of terrestrial Parasitengona in Fennoscandia including 107 species. Out of these, nineteen species are new findings for the region and five are species potentially new for science. Twenty-three species are new for Norway, fourteen for Finland and eleven for Sweden. The known recorded fauna today of terrestrial Parasitengona is 80 species for Norway, 54 for Sweden and 48 for Finland. Primary data include georeferenced locality data as well as collecting techniques and microhabitat to increase the knowledge on species' habitat requirements

    Towards resolving the double classification in Erythraeus (Actinotrichida: Erythraeidae): matching larvae with adults using 28S sequence data and experimental rearing

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    The taxonomy of free-living adults and heteromorphic parasitic larvae of Parasitengona mites has in the past been treated independently resulting in a double classification. Correct linkage of names still remains unknown for many species. A holistic understanding of species is imperative for understanding their role in ecosystems. This is particularly true for groups like parasitengone mites with a radically altered lifestyle during development—parasitic to predatory. Here, we infer linkages of three nominal species of Erythraeus, using matching with 28S DNA sequence data from field-collected specimens and through laboratory rearing. The general mixed Yule coalescent method (GMYC) was used to explicitly test if field-collected specimens representing heteromorphic life instars were conspecific. The field-collected larvae were allocated to adults of Erythraeus cinereus and Erythraeus regalis, respectively. Laboratory rearing of the same two species confirmed the matching done by DNA. Rearing was also successful for Erythraeus phalangoides after eggs were treated to an imitated winter diapause. This integrative taxonomic approach of molecular, morphological, and rearing data resulted in the following synonyms: E. phalangoides (De Geer, 1778) [= Erythraeus adrastus(Southcott, 1961), syn. nov.], E. cinereus (Dugès, 1834) [= Erythraeus jowitae Haitlinger, 1987, syn. nov.], and E. regalis (C.L. Koch, 1837) [= Erythraeus kuyperi (Oudemans, 1910), syn. nov., = Erythraeus gertrudae Haitlinger, 1987, syn. nov.]. The molecular evidence confirmed the separate identity of three further members of the genus. We provide redescriptions of E. phalangoides, E. cinereus, and E. regalis after modern standards, and neotypes are designated
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