Enarthronotides

Major mite taxa

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Taxonomy

Name

Enarthronota Grandjean, 1969

Classification

Superorder Acariformes » Order Sarcoptiformes » Suborder Oribatida » Infraorder Enarthronota

Children

superfamilies: Atopochthonioidea, Brachychthonioidea, Heterochthonioidea, Hypochthonioidea, Protoplophoroidea

Common names

enarthronote oribatid mites

Probability of encounter

low

Quarantine importance

No known quarantine importance. Most species are small to minute fungivores in mostly dry soils, including house dust and rarely stored products.

Diagnosis

White to yellow, tan, brown, or rarely more brightly coloured armoured oribatid mites with 1–3 hysterosomal scissures, or their remnants, or pytchoidy. Pedofossae sometimes present. Bodies rectangular, elongate, oval or globular; opisthosomal glandsopisthosomal glands:
see oil glands.  
absent. Setaeseta:
(pl. setae, from L. = bristle) cuticular process composed of a hollow shaft (sometimes filled with a refractive material) produced from a membranous socket (the alveolus); the hair-like, spine-like, branched or variously expanded structures on the surfaces of the legs and body.  Most setae function as mechanoreceptors, but others (e.g., solenidia) are chemoreceptors or have unknown or ambiguous functions.
ranging from setiform, to brush-like, to highly modified leaf-like shapes or ornate dendritic arrangements. Capitulumgnathosoma:
(= capitulum) the anteriormost part of a mite or ricinuleid, composed of the cheliceral and pedipalpal segments and separated from the body (idiosoma) by a ring of soft cuticle.
usually withdrawn into a camerostomecamerostome:
a recess under the rostral tectum that allows retraction of the chelicerae and palps of oribatid mites and that is sealed by the subcapitulum when retracted; a deep recess containing the gnathosoma in Uropodina.
; chelicerae sometimes visible from above; a pair of lateral eyes rarely present. Macropyline, 3 pairs of genital papillaegenital papillae:
 1-3 pairs of extrusible finger-like to button-like projections, usually retracted into in the genital vestibule of acariform mites; sometimes formed as sessile disks around the genital opening; thought to be osmoregulatory structures; modified or multiplied and dispersed over the body in many freshwater mites.  Genital papillae are absent in the larva, but may be added ontogenetically: protonymphs have one pair, deutonymphs two pairs, and tritonymphs (and adults) three pairs.  The tritonymphal pair of papillae is often lost.  The serially homologous Claparède's organ is usually present in the larvae (and prelarvae) of mites exhibiting genital papillae in nymphs and adults (Oudeman's Rule).
.

Similar taxa

Some Endeostigmata somewhat resemble enarthronotes, but are soft-bodied and lack scissures (although remnants of primary segmentation may be present).

Ecology and distribution

Fossil enarthronotes are known from the Devonian. Extant taxa are found in most soil types, but are especially abundant in the drier soils and in mosses. Many species are all female parthenogens. The feeding ecology of this group is poorly understood, but many have highly modified chelicerae, cheliceral setaeseta:
(pl. setae, from L. = bristle) cuticular process composed of a hollow shaft (sometimes filled with a refractive material) produced from a membranous socket (the alveolus); the hair-like, spine-like, branched or variously expanded structures on the surfaces of the legs and body.  Most setae function as mechanoreceptors, but others (e.g., solenidia) are chemoreceptors or have unknown or ambiguous functions.
, and adoral setaeseta:
(pl. setae, from L. = bristle) cuticular process composed of a hollow shaft (sometimes filled with a refractive material) produced from a membranous socket (the alveolus); the hair-like, spine-like, branched or variously expanded structures on the surfaces of the legs and body.  Most setae function as mechanoreceptors, but others (e.g., solenidia) are chemoreceptors or have unknown or ambiguous functions.
. Brachychthonioids are found everywhere, usually in high diversity, feed on algae and other microbes, and are among the smallest of all oribatid mites. Hypochthonioids are generally dorsoventrally flattened, but Mesoplophoridae are globular, lack any scissures, and exhibit ptychoidyptychoidy:
the ability of some oribatid mites to withdraw the legs between two body regions like a penknife being closed or a box being closed (hence box mites), and resulting in a seed-like appearance.  A derived form of dichoidy.
. Protoplophoroids range from poorly sclerotised endeostigmatanendeostigmatan:
a member of the Endeostigmata; characteristic of or belonging to the Endeostigmata.
-like mites (e.g., Paralycus), to rather brachythonioid-like mites (e.g., Haplochthonius), to strongly ornamented mites with elongate erectile setaeseta:
(pl. setae, from L. = bristle) cuticular process composed of a hollow shaft (sometimes filled with a refractive material) produced from a membranous socket (the alveolus); the hair-like, spine-like, branched or variously expanded structures on the surfaces of the legs and body.  Most setae function as mechanoreceptors, but others (e.g., solenidia) are chemoreceptors or have unknown or ambiguous functions.
(e.g., Cosmochthonius), to light-bulb shaped subsub:
 - as prefix used to indicate (1) under (see subcapitulum) or (2) not quite, e.g., subrectangular = not quite rectangular; subtriangular = not cleanly triangular.
-ptychoid mites (e.g., Sphaerochthonius), to fully ptychoid taxa (e.g., Protoplophora).

References

  • Balogh and Balogh 1987bBalogh and Balogh 1987b:
    Balogh J, Balogh P. 1987b. A new outline of the family Lohmanniidae Berlese, 1916 (Acari, Oribatei). Acta Zoologica Academiae Scientiarum Hungaricae 33: 327–398.
  • Balogh and Mahunka 1983Balogh and Mahunka 1983:
    Balogh J, Mahunka S. 1983. Primitive Oribatids of the Palaearctic Region. The Soil Mites of the World, Vol. 1. Elsevier, Amsterdam. 327 pp.
  • Colloff and Halliday 1998Colloff and Halliday 1998:
    Colloff M, Halliday B. 1998. Oribatid mites: A catalogue of Australian genera and species. Monograph on Invertebrate Taxonomy, Vol. 6. CSIRO Publishing, Melbourne.
  • Gilyarov and Krivolutsky 1975Gilyarov and Krivolutsky 1975:
    Gilyarov MS and Krivolutsky DA, eds. 1975. Handbook for the identification of soil-inhabiting mites, Sarcoptiformes. Zoological Institute of the Academy of Sciences, Petrograd.
  • Hunt et al. 1998Hunt et al. 1998:
    Hunt GS, Norton RA, Kelly JPH, Colloff MJ, Lindsay SM, Dallwitz MJ, and Walter DE. 1998. Oribatid Mites: An Interactive Glossary of Oribatid Mites, An Interactive Key to the Oribatid Mites of Australia [Intkey software and user guide on CD-ROM]. CSIRO Publishing, Collingwood.
  • Lee 1982Lee 1982:
    Lee DC. 1982. Sarcoptiformes (Acari) of South Australian soils. 3. Arthronotina (Cryptostigmata). Records of the South Australian Museum 18: 327-359.
  • Norton 1975Norton 1975:
    Norton RA. 1975. Elliptochthoniidae, a new mite family (Acarina: Oribatei) from mineral soil in California. Journal of the New York Entomological Society 83: 209-216.
  • Norton 1982Norton 1982:
    Norton RA. 1982. Arborichthonius n. gen., an unusual enarthronote soil mite (Acarina: Oribatei) from Ontario. Proceedings of the Entomological Society of Washington 84: 85-96.
  • Norton 1984Norton 1984:
    Norton, RA. 1984. Monophyletic groups in the Enarthronota (Sarcoptiformes). pp. 233-240. In: Griffiths DA and Bowman CE, eds. Acarology VI, Vol. 1. Ellis Horwood, Chichester.
  • Norton 2001Norton 2001:
    Norton RA. 2001. Systematic relationships of Nothrolohmanniidae, and the evolutionary plasticity of body form in Enarthronota (Acari: Oribatida). pp. 58-75. In: Halliday RB, Walter DE, Proctor HC, Norton RA, and Colloff MJ, eds. Acarology: Proceedings of the 10th International Congress, Canberra. CSIRO Publishing, Melbourne.
  • Schatz 2003Schatz 2003:
    Schatz H. 2003. New Sphaerochthonius species from the Neotropical region (Acari: Oribatida). Revue Suisse de Zoologie 110: 111-124.
Ornate dendritic arrangements;  Cosmochthonius  dorso-lateral (DEW)
Ornate dendritic arrangements; Cosmochthonius dorso-lateral (DEW)
 Sphaerochthonius  venter (DEW)
Sphaerochthonius venter (DEW)
 Sphaerochthonius  mouthparts (DEW)
Sphaerochthonius mouthparts (DEW)
 Sphaerochthonius  scissures (DEW)
Sphaerochthonius scissures (DEW)
Hypochthonioid,  Eniochthonius  (DEW)
Hypochthonioid, Eniochthonius (DEW)
 Eniochthonius  venter (DEW)
Eniochthonius venter (DEW)
Brachychthonioid dorsum (DEW)
Brachychthonioid dorsum (DEW)
1–3 hysterosomal scissures; Brachychthonioid dorsum (DEW)
1–3 hysterosomal scissures; Brachychthonioid dorsum (DEW)
Brachychthonioid venter (DEW)
Brachychthonioid venter (DEW)
Bachychthonioid lateral (DEW)
Bachychthonioid lateral (DEW)
 Eohypochthonius  venter (divided genital shields internal) (DEW)
Eohypochthonius venter (divided genital shields internal) (DEW)
 Eohypochtonius  venter (CH)
Eohypochtonius venter (CH)
Mesoplophoridae lateral (DEW)
Mesoplophoridae lateral (DEW)
Mesoplophorid ventral (DEW)
Mesoplophorid ventral (DEW)
 Cosmochthonius  lateral (DEW)
Cosmochthonius lateral (DEW)
Lohmanniid (DEW)
Lohmanniid (DEW)
Venter of lohmanniid (DEW)
Venter of lohmanniid (DEW)
 Meristacarus  (Lohmanniidae) (DEW)
Meristacarus (Lohmanniidae) (DEW)
Remnants;  Verpacarus  (Lohmanniidae) (DEW)
Remnants; Verpacarus (Lohmanniidae) (DEW)
Pytchoidy (DEW)
Pytchoidy (DEW)
Macropyline, 3 pairs of genital papillae
Macropyline, 3 pairs of genital papillae