TL;DR: The conclusion from this topology is that myobiid mites have developed some gnathosomal structures convergently with Cheyletoidea, including the stylet-like chelicerae and stylophore fused with the subcapitulum.
Abstract: The position of the family Myobiidae in the infraorder Eleutherengona (Prostigmata) was analyzed with a cladistic parsimony approach for the first time. Species of the genera Anystis von Heyden (Anystidae), Pomerantzia Baker (Pomerantziidae), and Walytydeus Kuznetzov (Paratydeidae) were selected as outgroups. Among Eleutherengona, species of the following genera were selected as ingroup taxa: Hirstiella Berlese (Pterygosomatidae), Eucheyletia Baker, Cheyletiella Canestrini (Cheyletidae), Syringophilus Heller (Syringophilidae), Tarsocheylus Berlese (Tarsocheylidae), Heterocheylus Lombardini (Heterocheylidae), Pygmephorus Kramer (Pygmephoridae), Raphignathus Duges (Raphignathidae), Neognathus Willmann (Caligonellidae), Storchia Oudemans (Stigmaeidae), and Tuckerella Womersley (Tuckerellidae). Three most parsimonious trees with similar topology were obtained. In all these trees, the family Myobiidae is situated outside of the clade joining the higher Raphignathae (Raphignathoidea and Cheyletoidea) and represents a branch within the earlier derivative Raphignathae. This result is based primarily on characters from leg setation and postembryonic development. The conclusion from this topology is that myobiid mites have developed some gnathosomal structures convergently with Cheyletoidea, including the stylet-like chelicerae and stylophore fused with the subcapitulum. The evolution of animal eleutherengone parasitism is discussed. Parasitism arisen independently in numerous phyletic lineages or superfamilies of Eleutherengona. The representatives of some phylogenetically distant eleutherengone lineages developed similar adaptations to predation and parasitism. However, in spite of some similarities in these adaptations, the evolutionary trends and pathways for switching to a parasitic mode of life are quite different in particular eleutherengone lineages.
TL;DR: The accepted taxonomic classification of Acariformes is updated to reflect the results, which show that a clade comprising early derivative Endeostigmata (Alycidae, Nanorchestidae, Nematalyc Families, and maybe Alicorhagiidae) should be treated as a taxon with the same rank as Sarcoptiformes and Trombidiformes.
Abstract: Acariformes is the most species-rich and morphologically diverse radiation of chelicerate arthropods, known from the oldest terrestrial ecosystems. It is also a key lineage in understanding the evolution of this group, with the most vexing question whether mites, or Acari (Parasitiformes and Acariformes) is monophyletic. Previous molecular studies recovered Acari either as monophyletic or non-monophyletic, albeit with a limited taxon sampling. Similarly, relationships between basal acariform groups (include little-known, deep-soil 'endeostigmatan' mites) and major lineages of Acariformes (Sarcoptiformes, Prostigmata) are virtually unknown. We infer phylogeny of chelicerate arthropods, using a large and representative dataset, comprising all main in- and outgroups (228 taxa). Basal diversity of Acariformes is particularly well sampled. With this dataset, we conduct a series of phylogenetically explicit tests of chelicerate and acariform relationships and present a phylogenetic framework for internal relationships of acariform mites. Our molecular data strongly support a diphyletic Acari, with Acariformes as the sister group to Solifugae (PP =1.0; BP = 100), the so called Poecilophysidea. Among Acariformes, some representatives of the basal group Endeostigmata (mainly deep-soil mites) were recovered as sister-groups to the remaining Acariformes (i. e., Trombidiformes + and most of Sarcoptiformes). Desmonomatan oribatid mites (soil and litter mites) were recovered as the monophyletic sister group of Astigmata (e. g., stored product mites, house dust mites, mange mites, feather and fur mites). Trombidiformes (Sphaerolichida + Prostigmata) is strongly supported (PP =1.0; BP = 98–100). Labidostommatina was inferred as the basal lineage of Prostigmata. Eleutherengona (e. g., spider mites) and Parasitengona (e. g., chiggers, fresh water mites) were recovered as monophyletic. By contrast, Eupodina (e. g., snout mites and relatives) was not. Marine mites (Halacaridae) were traditionally regarded as the sister-group to Bdelloidea (Eupodina), but our analyses show their close relationships to Parasitengona. Non-trivial relationships recovered by our analyses with high support (i.e., basal arrangement of endeostigmatid lineages, the position of marine mites, polyphyly of Eupodina) had been proposed by previous underappreciated morphological studies. Thus, we update currently the accepted taxonomic classification to reflect these results: the superfamily Halacaroidea Murray, 1877 is moved from the infraorder Eupodina Krantz, 1978 to Anystina van der Hammen, 1972; and the subfamily Erythracarinae Oudemans, 1936 (formerly in Anystidae Oudemans, 1902) is elevated to family rank, Erythracaridae stat. ressur., leaving Anystidae only with the nominal subfamily. Our study also shows that a clade comprising early derivative Endeostigmata (Alycidae, Nanorchestidae, Nematalycidae, and maybe Alicorhagiidae) should be treated as a taxon with the same rank as Sarcoptiformes and Trombidiformes, and the scope of the superfamily Bdelloidea should be changed. Before turning those findings into nomenclatural changes, however, we consider that our study calls for (i) finding shared apomorphies of the early derivative Endeostigmata clade and the clade including the remaining Acariformes; (ii) a well-supported hypothesis for Alicorhagiidae placement; (iii) sampling the families Proterorhagiidae, Proteonematalycidae and Grandjeanicidae not yet included in molecular analyses; (iv) undertake a denser sampling of clades traditionally placed in Eupodina, Anystina (Trombidiformes) and Palaeosomata (Sarcoptiformes), since consensus networks and Internode certainty (IC) and IC All (ICA) indices indicate high levels of conflict in these tree regions. Our study shows that regions of ambiguous alignment may provide useful phylogenetic signal when secondary structure information is used to guide the alignment procedure and provides an R implementation to the Bayesian Relative Rates test.
TL;DR: This research was carried out in twenty counties of the following regions in the state of Rio Grande do Sul to find out the diversity of mite predators in these places to separate the families, genus and species of the mites.
Abstract: This research was carried out in twenty counties of the following regions in the state of Rio Grande do Sul: Plain, Central Depression, Plateau and Coast Plain to find out the diversity of mite predators in these places Forty-six vegetable species were sampled, thirty species of miles of the families Anystidae, Ascidae, Cheyletidae, Cunaxidae, Phyloseiidae and Stigmaeidae were mel The Phytoseiidae were the mite that presented the greatest diversity, being present in the majority of the sample plants Most of the Phytoseiidae that were met belong to five species of the Euseius Wainstein, 1962 genus, the second genus of this family was Iphiseiodes DeLeon, 1966, with just one species The Stigmaeidae come up as second family in number but fewer than Phytoseiidae In this family, the most common mite belong to the Agistemus Sumers, 1960 genus The biggest of the mites species (13 species), was met in Morus spp (Moraceae) and Tabebuia spp (Bignoniaceae); Phaseolus vulgaris (Papilionaceae); only one species of the mite was met in Campomanesia spp (Myrtaceae), Phaseolus vulgaris (Papilionaceae) and Rosa spp (Rosaceae) In Alamanda spp(Apocinaceae), Ficus spp (Moraceae), Jacaranda mimosifolia (Bignoniaceae) and Solanum spp (Solanaceae) were met mites predators A dichotomic key is presented to separate the families, genus and species of the mites
TL;DR: Investigation of the relationship of the abundance of the predatory mite and its leafhopper prey is influenced by two different cover crops and a manually weeded inter-row treatment as a contrast to naturally growing vegetation in a tea plantation in China suggests that the abundant mite Anystis baccarum in aTea plantation is affected by intercropping and it can affect its leaf Hopper prey, albeit with varying levels of suppression.
TL;DR: Analysis of fruit, leaf and orchard ground cover plant samples collected in fall (October) 2005 showed greater abundance of phytoseiid mites on ground cover plants than on citrus fruit and leaves, suggesting that ground cover Plants may serve as overwintering reservoirs for predacious mites.
Abstract: Nine Satsuma citrus orchards (seven conventionally sprayed and two unsprayed) in southern Alabama were sampled (mainly leaf samples) for predacious mites at eight different sampling dates from March 2005 to February 2006. At least 29 species of predacious mites from nine families (Anystidae, Ascidae, Bdellidae, Cheyletidae, Cunaxidae, Erythraeidae, Eupalopsellidae, Phytoseiidae, and Stigmaeidae) were identified. In addition, six primarily fungivorous species from three families (Parasitidae, Tydeidae, and Tarsonemidae) were recorded. Predacious mites in the families Phytoseiidae (18 species) and Stigmaeidae (one species) were the most abundant. The dominant species were Typhlodromalus peregrinus (Muma) and Proprioseiopsis mexicanus (Garman) (Phytoseiidae), and Agistemus floridanus Gonzalez (Stigmaeidae). Phytoseiid mites were most abundant in the spring with populations declining at the start of the summer and remaining at very low levels through the fall and winter. Analysis of fruit, leaf and orchard ground cover plant samples collected in fall (October) 2005 showed greater abundance of phytoseiid mites on ground cover plants than on citrus fruit and leaves, suggesting that ground cover plants may serve as overwintering reservoirs for predacious mites. In general, predacious mites were relatively more abundant in the conventionally sprayed orchards compared with the unsprayed orchards, as were the two key phytophagous species, Panonychus citri (McGregor) and Phyllocoptruta oleivora (Ashmead). The results are discussed in relation to the potential of the dominant predacious mite species as candidates for biological control of key phytophagous mites on Alabama Satsuma citrus.