Ololaelaps
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Ordo: Mesostigmata
Familia: Laelapidae
Name
Ololaelaps Berlese, 1904: 260 – Wikispecies link – Pensoft Profile
- Pristolaelaps Womersley, 1956: 571. Synonymy by Ryke (1962)[1].
Type species
Laelaps (Hypoaspis) venetus Berlese, 1903
Diagnosis
(adult male and female, unless stated).Well-sclerotized hypoaspidine laelapid with a hologastric (genitiventrianal) shield in female, bearing 3–5 pairs of preanal setae (plus st5), as well as the following character states: dorsal shield covering entirely idiosoma dorsally, narrowly to broadly extending onto venter; bearing 39 or slightly fewer pairs of slender setae, including px2–3 and often one Jx. A pair of well-sclerotized presternal platelets. Female with seta st4 on sternal shield or on soft cuticle (or putatively on endopodal plate). Peritrematal shield free posteriorly or variously (narrowly) fused with hologastric and/or parapodal shields, via metapodal platelet; metapodal platelet free or variously fused to above-mentioned shields; parapodal plate well-developed, subtriangular. Soft opisthogastric cuticle with 5–10 pairs of setae. Male holoventral shield broad, fused to parapodal-exopodal plates, sometimes also to peritrematal shield. Gnathotectum convex, with few to numerous fine denticles; deutosternal groove with six rows of 1–10 denticles; female cheliceral movable digit with two teeth (rarely more), fixed digit with 3–5 (exceptionally 8); palp-apotele three-tined, third tine reduced. Leg chaetotaxy normal for Laelapidae; setae generally slender.
Description
Dorsal idiosoma.Dorsal shield relatively large (435–800 in female), broadly oval to narrowly suboval (length/width ratio 1.2–1.8), completely covering idiosoma dorsally, barely to moderately extending ventrally (this can be determined most accurately before slide-mounting); shield smooth (except for fine granulation or punctuation) to strongly reticulate; shield’s ventral extension (‘epipleura’ of Bregetova and Koroleva (1964)[2]) smooth to reticulate (sometimes in contrast to smooth dorsal region of shield); shield with a delineated marginal strip along its edge. Dorsal shield bearing 39 pairs of simple, slender, almost hair-like setae, short to moderately long, including px2–3, and often one unpaired median seta (Jx) inserted at a level between J2 and J3 (Table 2); sometimes fewer than 39 pairs of setae, with z1 (absent in O.sellnicki), z3 (see Evans and Till 1966[3]), or setae in r or S series apparently absent; shield never hypertrichous; setae slender and smooth, occasionally with a few light barbs on Z5 and J5 (Jordaan and Loots 1987[4]). Shield with 16 pairs of poroids and four or five pairs of gland openings (based on Bregetova and Koroleva (1964)[2] and specimens examined, representing a few species only): gd1, gd2 (sometimes absent), gd4 (usually conspicuous, on or near shield margin), gd6, gd9.
Ventral idiosoma.Tritosternum normal, with two pilose laciniae. Presternal region with a pair of sclerotized platelets, wedge-shaped to subrectangular, lineate (typically with 2–4 transversal lineae); typically an additional, poorly sclerotized area, lineate and granulate, anteriorly or anteromesally adjoining each platelet. Female sternal shield as long as or longer than wide, sometimes wider than long; shield length/width ratio 0.6–1.8; Shield posterior margin straight, slightly to moderately concave, or sometimes convex; shield reticulate, smooth in its posterior fourth or fifth, bearing 3–4 pairs of simple setae and 2–3 pairs of poroids, therefore sometimes including seta st4 and poroid iv3; seta st4 on sternal shield (near or on its posterolateral edge), on soft cuticle, or apparently on endopodal plate (Table 2; see Discussion). Female hologastric shield broad, laterally extending to or beyond margin of parapodal (or adcoxal, Bregetova (1977a)[5]) plate, overlapping sternal and endopodal shields, bearing usually five pairs of preanal setae (JV1–3, ZV1–2) in addition to seta st5, occasionally only three or four pairs of preanals (JV3 and/or ZV2 off shield) or exceptionally six (ZV3 apparently on shield in O.rectagoni); shield setae usually moderately long, sometimes short; hologastric shield ornamented with reticulation, cells polygonal, scale-like or elongate transversally (note that shield reticulation is not drawn for some species in Ryke (1962)[1], but probably present; compare O.mooiensis in Ryke (1962)[1] vs Marais and Loots (1972)[6]); circumanal setae shorter than preanals, and postanal usually shorter than paranal setae; cribrum typically with 2–3 rows of spicules. Endopodal plate besides coxae III–IV well-developed (appears reduced in O.dililoensis, but the portion of endopodal plate that is overlapped by hologastric shield may have been overlooked); plate free, more or less contiguous with sternal shield (or apparently fused to it, e.g., O.expansus (Ma 2015[7])) or slightly overlapped by it. Peritrematal shield well-developed, fused to dorsal shield anteriorly, usually free posteriorly, reaching approximately posterior margin of coxa IV, occasionally only mid-coxa IV, or moderately surpassing coxa; sometimes narrowly connected to hologastric shield and/or parapodal element; peritrematal shield posteriorly bifid in some species (O.interruptus, O.leptochelae, and an undescribed species from North America). Peritreme narrow, usually reaching anteriorly level of coxa I, sometimes slightly less. Parapodal plate well-developed, subtriangular, with outer margin convex (especially when peritrematal shield free and not extending beyond coxa IV) or straight (typically when peritrematal shield extended posteriorly or fused to hologastric shield); parapodal exceptionally not produced in O.rectagoni (Table 2) and an undescribed species from Costa Rica; parapodal posteriorly free, more or less abutting hologastric shield, or narrowly fused to hologastric and/or peritrematal shields, via metapodal element as connecting ‘bridge’. Metapodal platelet entirely free, suboval to strip-like, or variously fused to hologastric shield, parapodal and/or peritrematal plates. Exopodal strip well-developed, fused to parapodal element posteriorly, and anteriorly to sternal shield between coxae I–II. Soft opisthogastric cuticle surrounding shield with 5–10 pairs of simple setae, often including 1–2 pairs of r-R setae isolated at level near parapodal plate; never hypertrichous. Male holoventral shield fused to parapodal-exopodal elements, sometimes also to peritrematal shield, bearing 3–5 preanals (JV1–3, ZV1–2; JV3 and ZV2 sometimes off shield, e.g., O.ussuriensis); metapodal element merged with holoventral shield.
Gnathosoma.Gnathotectum with subtriangular to rounded margin, usually finely denticulate, may appear smooth when denticles sparse or (possibly) absent. Deutosternal groove of moderate, regular width, or slightly tapering posteriorly, with six (occasionally seven, and rarely five) rows of denticles, each row bearing 1–10 denticles, most of the rows with 3–7 denticles; denticulate rows usually preceded by a smooth ridge anteriorly, and sometimes also posteriorly. Corniculi horn-like, of moderate length. Internal malae with two pairs of long projections, median pair fimbriate on its basal portion, lateral pair smooth or branched or fimbriate in its apical portion; lateral projection absent in males (and apparently in the female of O.sitalaensis). Palptarsal claw three-tined, third tine reduced. Chelicerae of moderate length, chelate-dentate; female movable digit with two moderately-sized teeth, rarely more (two additional small teeth between the two typical large teeth in O.interruptus; Table 2); fixed digit with 3–5 teeth, variously sized, rarely more (eight in O.leptochelae), including a subapical, laterally offset tooth (gabelzhan); male digits each with a single tooth; pilus dentilis setiform; arthrodial process a simple corona. Male spermatodactyl 0.7–2.0 × as long as movable digit, from its departure from edge of digit; more or less straight or variously bent; junction between spermatodactyl and movable digit straight to strongly angled (O.translineatus); duct inside spermatodactyl straight or sinuous. Chaetotaxy of subcapitulum and palps normal for Laelapidae (sensu Evans and Till 1965[8]).
Legs.Chaetotaxy normal for Laelapidae (sensu Evans and Till 1965[8]); most setae slender; ventral and/or subapical setae of tarsi II–IV usually moderately thickened, sometimes lateral setae too (e.g., al2, pl2–3 of tarsus IV); setae on other leg segments occasionally thickened (e.g., pd2, ad3 on femur I, pd on femur III in O.placentula; also dorsally on femur IV in O.mooiensis (Jordaan and Loots 1987[4])). Males of some species with a spine-like seta on femur II (O.translineatus); pv thickened on genu or tibia III (in undescribed species); a ventral spine on tarsus II, apparently representing pv2 (position shifted proximad) (e.g., O.venetus, O.placentula, O.ussuriensis); or with cuticular tubercles on various leg segments (femur and genu of O.placentula, O.ussuriensis). Ambulacra I–IV with well-developed paired claws and pulvillus.
Spermatheca.
Spermathecal ducts well-sclerotized and discernable in some species.
Species | Shared features (mostly fusion of shields1) | Dorsal shield ornamentation1 | Epipleura2 ornament. | Dorsal seta Jx | Insertion of st43 | Other features1 | Notes and references (redescriptions) |
---|---|---|---|---|---|---|---|
venetus | (1) all shields (HOLOG + METAP + PERIT + PARAP) narrowly fused together; (2) spermatod. with sinuous duct; (3) spermathecae well-sclerotized, distinctive | smooth with sculptured areas anteriorly (Evans and Till’s text) | smooth | 1 | stern. | JV3, ZV2 setae sometimes off HOLOG | Ryke 1962[1], Bregetova and Koroleva 1964[2], Evans and Till 1966[3], Bregetova 1977a[5] |
placidus* | smooth except light reticul. near ant. margin | smooth | 0–1 | stern. | as above | Hennessey and Farrier 1988[9], F.B. pers. obs. | |
sellnicki | as venetus; reticul. visible only when freshly moulted (Bregetova and Koroleva 1964[2]) | smooth?4 | 1 | stern. | JV3, ZV2 off HOLOG; z1, z3 absent | Evans and Till 1966[3], Solomon 1968[10], Bregetova 1977a[5], Kavianpour et al. 2017[11]; also Sellnick (1940)[12], as O.haemisphaericus | |
hemisphaera | HOLOG + METAP + PERIT fused [PARAP apparently free] | ? | lineate-reticulate? | ? | soft cut.? | broad idiosoma | not illustr. in Berlese (1916b)[13]; partly illustr. in Ryke (1962)[1], possibly based on Berlese’s types or drawings (see Ryke’s introduction) |
interruptus | (1) HOLOG + METAP + PERIT narrowly fused [PARAP clearly free]; (2) PERIT notched post. | ? | ? | 1 | soft cut. | MD with 2 small teeth in-between the 2 standard teeth; broad idiosoma | |
leptochelae | ? | ? | ? | ? | FD with a total of 8 teeth | ||
burdwanensis | HOLOG + METAP + PARA narrowly fused [PERIT free] | ? | lineate-reticulate | 1 | soft cut.? | ||
translineatus | smooth? | lineate-reticulate | 1 | soft cut.? | sternal shield with transverse ridge; spermatod. at 90° angle from MD; spermath. distinctive | similar to O.burdwanensis | |
wangi | smooth except lineate anteriorly | lineate-reticulate | 0 | soft cut.? | only 2–4 deutosternal denticles / row | similar to O.burdwanensis; Keum et al. 2017[14] | |
formidabilis*,** | only METAP + PARAP fused | light reticul.; lighter and sparser anteriorly | reticulate | 0–1 | soft cuticle | HOLOG with inverse V-shaped ridges; spermatod. elongate; spermath. not discerned | O.formidabilis sensu Ryke (1962)[1] differs: METAP partly fused to HOLOG, not to PARAP |
caucasicus | only HOLOG + METAP (partly to completely) fused | similar to placentula or ussuriensis? | lineate-reticulate | 0–1 | stern. or soft cut. | broad idiosoma; spermatheca not discerned | similar to O.ussuriensis; Bregetova 1977a[5] |
dililoensis | dense scale-like reticul. post., smooth or scattered reticul. ant. | reticulate | 0 | soft cut. | broad idiosoma | ||
holaspis | only HOLOG + METAP (partly to completely) fused | colspan="1" rowspan="1" | reticulate? (Oudemans’ text says “all shields with large scales”) | ? | ? | soft cut.? | elongate idiosoma | Oudemans (1903[15]: 11) provided a more complete description than Oudemans (1902b)[16]; partly illustr. by Ryke (1962)[1] |
mooiensis | reticulate; reticul. sparser anteriorly | ? | 0–1 | soft cut. or endop.? | elongate idiosoma; METAP rarely free (based on syn. O gamagarensis) | colspan="1" rowspan="1" | Marais and Loots 1972[6], Jordan and Loots 1987, Nemati et al. 2018[17] (notes on characters) | |
placentula* | colspan="1" rowspan="1" | essentially smooth (finely granulate) or faintly reticulate | lineate-reticulate | 0 | stern. | broad idiosoma; sternal shield wider than long, with concave margin; PERIT reaching past coxa IV; spermatheca not discerned | Sellnick 1940[12]: 69, Ryke 1962[1], Bregetova and Koroleva 1964[2], Evans and Till 1966[3], Bai and Ma 2014[18] | |
platensis | ? | ? | ? | soft cut.? | peritreme short, reaching between coxae I–II; ZV1 absent? | colspan="1" rowspan="1" | Ryke 1962[1] (partial illustration) | |
rectagoni | ? | ? | 0 | soft cut.? | j1 seta elongate; broad idiosoma and HOLOG; PARAP truncate; ZV3 apparently on HOLOG | Karg 1994[19] (male chelicera and spermatodactyl) | |
sinensis | ? | ? | ? | soft cut.? | Ryke 1962[1] (partial illustration) | ||
ussuriensis | polygonal reticul. scarcely evident (text) | lineate-reticulate | 0? | stern. | spermatheca not discerned; only 2–3 deutosternal denticles / row | Bregetova 1977a[5] | |
bregetovae | all shields (HOLOG, METAP, PERIT, PARAP) free | with (scale-like?) reticulation post. | ? | 0? | ? | elongate idiosoma | similar to O.tasmanicus and O.sitalensis? |
expansus | ? | ? | 0? | soft cut. | |||
nasri | finely granulate? | lineate-reticulate? | 0 | soft cut.? | broad dorsal and sternal shields | similar to O.obovatus | |
obovatus | smooth? | ? | ? | soft cut. | broad idiosoma; ZV1 absent? | colspan="1" rowspan="1" | | |
paratasmanicus | reticulate | ? | 0 | soft cut. | elongate idiosoma; HOLOG rounded laterally | similar to O.tasmanicus; Ma 2015[7] | |
sitalaensis | ? | reticulate | 1 | soft cut.? | elongate idiosoma | ||
tasmanicus | lightly reticulate (Womersley’s text) | ? | 0 | soft cut. | Tenorio (1982)[20] indicates broader idiosomal shields than those in Womersley (1956)[21] | Tenorio 1982[20] (photograph) |
Taxon Treatment
- Beaulieu, F; Quintero-Gutiérrez, E; Sandmann, D; Klarner, B; Widyastuti, R; Cómbita-Heredia, O; Scheu, S; 2019: Review of the mite genus Ololaelaps (Acari, Laelapidae) and redescription of O.formidabilis Berlese ZooKeys, 853: 1-36. doi
Images
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Other References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 Ryke P (1962) The genus Ololaelaps Berlese (Acarina: Laelaptidae).Revista de Biologia3: 124–130.
- ↑ 2.0 2.1 2.2 2.3 2.4 Bregetova N, Koroleva E (1964) Mites of the genus Ololaelaps Berlese, 1904 (Acarina: Laelaptide).Parazitologicheskii Sbornik22: 61–87.
- ↑ 3.0 3.1 3.2 3.3 Evans G, Till W (1966) Studies on the British Dermanyssidae (Acari: Mesostigmata) Part II. Classification.Bulletin of the British Museum (Natural History), Zoology14: 109–370.
- ↑ 4.0 4.1 Jordaan L, Loots G (1987) A new species of the genus Ololaelaps Berlese, 1904 (Acari: Laelapidae) from the Afrotropical region.Phytophylactica19: 49–51.
- ↑ 5.0 5.1 5.2 5.3 5.4 Bregetova N (1977a) Family Laelaptidae Berlese, 1892. In: Ghilyarov M Bregetova N (Eds) A Key to the Soil-Inhabiting Mites of the Mesostigmata (In Russian).Nauka, Leningrad, 483–553.
- ↑ 6.0 6.1 Marais J, Loots G (1972) A new mite of the genus Ololaelaps Berlese from the Congo.Revue de zoologie et de botanique africaines85: 30–36.
- ↑ 7.0 7.1 Ma M (2015) Discovery of the genus Pristolaelaps in China, with descriptions of a new species and a new record (Acari: Mesostigmata: Laelapidae).Acta Arachnologica Sinica24: 95–97.
- ↑ 8.0 8.1 Evans G, Till W (1965) Studies on the British Dermanyssidae (Acari: Mesostigmata). Part 1. External morphology.Bulletin of the British Museum (Natural History), Zoology13: 247–294. https://doi.org/10.5962/bhl.part.16752
- ↑ Hennessey M, Farrier M (1988) Systematic revision of thirty species of free-living, soil-inhabiting gamasine mites (Acari: Mesostigmata) of North America.North Carolina Agricultural Research Technical Bulletin285: 1–123.
- ↑ Solomon L (1968) Contribution à la connaissance de l’acaroparasitofaune des petits mammifères de Dobroudja.Travaux du Muséum d’Histoire Naturelle “Grigore Antipa”8: 671–692.
- ↑ Kavianpour M, Karimpour Y, Nemati A, Mirfakhraei S (2017) A faunistic study on laelapid mites in Urmia, Iran.Iranian Journal of Animal Biosystematics13: 159–170.
- ↑ 12.0 12.1 Sellnick M (1940) Die Milbenfauna Islands.Göteborgs Kungl. Vetenskaps- och Viterhets-Samhälles Handlingar, Series B, Band 6, 14: 1–129.
- ↑ Berlese A (1916b) Centuria terza di Acari nuovi.Redia12: 289–338.
- ↑ Keum E, Jung C, Joharchi O (2017) New species and new records of the family Laelapidae (Acari: Mesostigmata) from Republic of Korea.Zootaxa4353: 485–505. https://doi.org/10.11646/zootaxa.4353.3.5
- ↑ Oudemans A (1903) Notes sur les acariens. Xe Série (1). Parasitidae (Vel Gamasidae) Thrombididae et Oribatidae d’Italie.Mémoires de la Société zoologique de France16: 5–32. [pls I–III]
- ↑ Oudemans A (1902b) Verslag van de zeven-en-vijftigste Zomervergadering der Nederlandsche Entomologische Vereeniging. Tijdschrift voor Entomologie XLV, Verslag: 48–64.
- ↑ Nemati A, Riahi E, Khalili-Moghadam A, Gwiazdowicz D (2018) A catalogue of the Iranian Mesostigmata (Acari): Additions and updates of the previous catalogue.Persian Journal of Acarology7: 115–191. doi: 10.22073/pja.v7i2.36985
- ↑ Bai X, Ma L (2014) A new record of the genus Ololaelaps and a new record of the genus Ameroseius from China (Acari: Mesostigmata: Laelapidae, Ameroseiidae).Acta Arachnologica Sinica23: 29–31.
- ↑ Karg W (1994) Raubmilben der Cohors Gamasina Leach (Acarina, Parasitiformes) vom Galapagos-Archipel.Mitteilungen aus dem Zoologischen Museum in Berlin70: 179–216. https://doi.org/10.1002/mmnz.19940700202
- ↑ 20.0 20.1 Tenorio J (1982) Hypoaspidinae (Acari: Gamasida: Laelapidae) of the Hawaiian Islands.Pacific Insects24: 259–274.
- ↑ Womersley H (1956) On some new Acarina-Mesostigmata from Australia, New Zealand and New Guinea.The Journal of the Linnean Society of London, Zoology42: 505–599. https://doi.org/10.1111/j.1096-3642.1956.tb02218.x