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Endeostigmata
Superorder Acariformes
Order Sarcoptiformes
Suborder Endeostigmata
Cohorts (Superfamilies): Alycina (Alycoidea), Nematalycina (Nematalycoidea), Terpnacarina (Oeserchestoidea, Terpnacaroidea), Alicorhagiina (Alicorhagioidea)
Common names: endeostigmatans
Probability of Encounter: medium
Quarantine importance:
None. Most endeostigmatans are rare and all
that have been studied are fungivores, algivores or predators of small
invertebrates.
Diagnosis. Soft-bodied,
sometimes hypertrichous, acariform mites, often with remnants of
primary segmentation. Body cuticle usually
plicate, sometimes with secondary ornamentation; colorless (white) to pale
lilac, bright pink or yellowish brown.
Prodorsum unsclerotized, usually with 5-6 pairs of setae (Vertex-scapular
system: vi, ve,
sci, sce, in, exp; also, Rostral-bothridial system,
respectively: ro, le, bo, exa, in, exp) and, except in the usually
worm-like Nematalycidae,
prodorsal setae sci (and sometimes sce) formed as trichobothria; dorso-sejugal furrow
distinct; naso and/or median eye often present; lens-like lateral ocellus and
post-ocular body often present.
Subcapitulum with lateral lips bearing 0-3 pairs of adoral setae, narrow
rutella with distal blade or teeth; 2-3 or more pairs of setae in the genal
area; and usually a pair of peg-like epicoxal setae (ep); palps usually
with 5 free segments (sometimes with femora
subdivided) and without a palptibial claw. Chelicerae often distinctly 3-segmented (trochanter well developed), chelate-dentate
to attenuate-edentate stylets and bearing 0-2 setae;
subcapitulum sometimes suctorial.
Genital shields unsclerotized, bearing numerous genital setae, and
covering 3 (rarely 2) pairs genital papillae in the adult. Legs well supplied with solenidia and other
setae, but without trichobothria; epicoxal seta epI sometimes present;
pretarsi usually with empodium and often with claws; legs IV often modified for
jumping.
Similar mites. Some endeostigmatans
resemble small, soft-bodied prostigmatans (especially members of the Eupodina),
but usually have rutella and 6 rather than
3-5 prodorsal setae. Species of Nanorchestidae (Speleorchestes,
Nanorchestes) are especially common
in very dry habitats (sand dunes, hot desert soils, cold deserts) and can be
distinguished by their 2 pairs of prodorsal trichobothria and heavily
sclerotized, finger-like labrum. Members of the Terpnacaridae
resemble soft-bodied oribatid mites.
Ecology & Distribution.
Endeostigmatans are mostly tiny, globular or bizarrely elongate
sarcoptiform mites that bear numerous primitive morphological characters.
They are often found in extreme soil habitats (e.g. cold and hot deserts, microbial
crusts, seashores, sandy soils, deep soil).
Fossil endeostigmatans have been described from some of the earliest
terrestrial faunas known, and their life styles tend to reflect their early
derivation. For example, most
endeostigmatans have the fundamental acariform ontogeny, i.e. an egg, an
inactive hexapod prelarva, an active hexapod larva, and active octopod
protonymph, deutonymph, tritonymph and adult.
In some taxa the prelarva is retained within the egg; but in others it
expands, pops the egg shell, and then remains quiescent. In some Nanorchestidae the prelarva is able
to move, but not feed. The stage
between molts is quiescent and unable to move. The number of eggs matured at one time by a female seems to vary
with size: small species tend to mature a single egg and large species
many. A short ovipositor is primitively
present, but has been lost in many groups.
Males usually have a well developed spermatophoric organ for producing
spermatophores, but all female parthenogenesis is common in the Terpnacarina
and males are unknown for many taxa. In
Alicorhagia, silken cocoons are spun for the deposition of eggs and
before molts. Cocoons of other
endeostigmatans can be found in soil extractions using flotation methods.
In the Terpnacarina and
Alicorhagiina
larvae and other active stages feed by ingesting pieces of solid food (i.e.
particulate feeding) which form discrete gut boluses, a behavior shared with some Opiliones,
opilioacarans and sarcoptiform mites.
Within the Terpnacarina, fungi and sclerotized bits of small
invertebrates can be identified in gut boluses. Outside of the Terpnacarina little is known about feeding
biology. Some Bimichaeliidae (e.g. Alycus
roseus Koch) appear to be exclusively predatory on nematodes, but others
(e.g. Bimichaelia) have highly modified, elongate, needle-like digits
that serve an unknown function. The
Nanorchestidae are fluid-feeders and have a sclerotized tubular labium with an
unknown function. Nanorchestes
amphibius Topsent & Trouessart is reported to feed on green algae.
References
Gilyarov, M.S. (ed.) 1978. Identification
key of soil inhabiting mites. Trombidiformes. Nauka: Moscow [In Russian].
Grandjean F. 1939. Quelques genres d’acariens appartenant au
groupe des Endeostigmata. Ann. Sci.
nat. Zool. 11(ser. 2):1-122.
Kethley JB. 1982. Endeostigmata. pp. 118-120, In: Parker SP (ed.) Synopsis and Classification of Living Organisms. McGraw-Hill, NY.
Kethley JB. 1990. Acarina: Prostigmata (Actinedida). pp. 667-756, In: DL Dindal (ed), Soil
Biology Guide. John Wiley &
Sons, Brisbane.
Krantz GW. 1976.
A Manual of Acarology.
OSU Bookstores: Corvallis.
Walter DE. 1988. Predation and mycophagy by endeostigmatid mites (Acariformes: Prostigmata). Experimental & Applied Acarology 4: 159-166.
Walter
DE. 2001. Endemism and cryptogenesis in 'segmented' mites: A review
of Australian Alicorhagiidae, Terpnacaridae, Oehserchestidae, and
Grandjeanicidae (Acari: Sarcoptiformes). Australian Journal of
Entomology 40: 207-218.