Hydrophiloidea, Latreille, 1802
publication ID |
https://doi.org/10.37520/aemnp.2020.018 |
publication LSID |
lsid:zoobank.org:pub:9D78C2BB-8042-4883-9578-A370E8152D9A |
persistent identifier |
https://treatment.plazi.org/id/03A6EF51-FFD8-1F15-3B25-FDD9FA37FDF0 |
treatment provided by |
Tatiana |
scientific name |
Hydrophiloidea |
status |
|
of Japanese Hydrophiloidea
All families of Hydrophiloidea except Epimetopidae are recorded from Japan (HANඌൾN 1999, KıŦANƟ et al. 2019). Although the larvae of Japanese species of Georissidae , Hydrochidae and Spercheidae are not described, larvae of the Japanese hydrophiloid families may be identified using the following key (adapted from RıർIJMƟNĐ 1920, BøඏıNǤ & HൾNRıĸඌൾN 1938, ARർIJANǤൾĿඌĸY 1997):
1. Abdominal segment 9 complete ( Fig. 5E View Fig ; see also fig. 6A, C in Archangelsky 1997 for Georissidae , which has slightly reduced segment 9), thus segments 8 to 10 not forming spiracular atrium; antenna with two sensoria (SE1 and SE2) on outer face of the intersegmental membrane between antennomeres 2 and 3 ( Figs 4A View Fig , 7A View Fig ). ................................................. 2
– Abdominal segment 9 modified as part of the spiracular atrium, not or only partly visible from dorsal view, thus segments 8 to 10 forming spiracular atrium (spiracular atrium highly reduced in hydrophilid genus Berosus Leach, 1817 , e.g., fig. 5D in Minoshima & Hayashi 2015); antenna with one sensorium (SE1) on outer face of the intersegmental membrane between antennomeres 2 and 3 (often SE1 is reduced in size and very small; e.g., fig. 53A in Minoshima & Hayashi 2011). .......... 3
2. Legs well developed, five-segmented ( Figs 5C, D View Fig ); urogomphi well developed, long, three-segmented ( Fig. 5E View Fig ). ............................................. Helophoridae
– Legs reduced, minute, three-segmented (fig. 8A in Archangelsky 1997); urogomphi reduced. .................. ................................................................. Georissidae
3. Inner tooth of mandible situated close to mandibular apex, thus mandibular apex looks bifid; inner face of stipes strongly extending anteromesally, forming well developed, large inner lobe (lacinia); labium developed; mentum fused with prementum, forming plate-like structure ( Archangelsky 1997, 2001; Fikáček 2019a); legs five-segmented, very long. ........ ................................................................ Spercheidae
– Inner tooth of mandible situated on median part, thus mandibular apex simple; inner face of stipes not extending anteromesally or weakly extending anteromesally, forming small inner lobe (lacinia) (see Archangelsky 1997); labium well developed or reduced; if labium well developed, mentum not fused with prementum (rarely fused but not in Japanese species); legs variable, minute to long. .................... 4
4. Submentum fused with head capsule (Figs 2B, 6B); antennomere 1 variable in length but never very long and stout ( Archangelsky 1997, Minoshima & Hayashi 2011); second segment of the labial palpus without a large sensorium; legs usually well developed in aquatic species, moderately to highly reduced in some terrestrial groups ( Arriaga-Varela et al. 2017, Archangelsky 2018, Minoshima 2019) ....................... ............................................................. Hydrophilidae
– Submentum not fused with head capsule; antennomere 1 very long and stout; second segment of labial palpus with two large sensoria of almost same size as the second palpomere; legs well developed, fivesegmented ( Richmond 1920, Archangelsky 1997, Fikáček 2019b). .................................... Hydrochidae
ARCHANGELSKY M. 1997: Studies on the biology, ecology, and systematics of the immature stages of New World Hydrophiloidea (Coleoptera: Staphyliniformia). Bulletin of the Ohio Biological Survey, New Series 12: 1 - 207.
ARCHANGELSKY M. 2001: A new neotropical species of Spercheus Kugelann, and its larval stages (Coleoptera, Hydrophiloidea: Spercheidae). Studies on Neotropical Fauna and Environment 36 (3): 199 - 204.
ARCHANGELSKY M. 2018: Larval chaetotaxy and morphometry of Oosternum costatum (Coleoptera: Hydrophilidae: Sphaeridiinae, Megasternini) and a discussion of larval characters with phylogenetic relevance. Acta Entomologica Musei Nationalis Pragae 58 (2): 499 - 511.
ARRIAGA-VARELA E., SEIDEL M., DELER-HERNANDEZ A., SEN- DEROV V. & FIKACEK M. 2017: A review of the Cercyon Leach (Coleoptera, Hydrophilidae, Sphaeridiinae) of the Greater Antilles. ZooKeys 681: 39 - 93.
FIKACEK M. 2019 a: 18. Hydrochidae Thomson, 1859. Pp. 258 - 264. In: LAWRENCE J. F. & SLIPINSKI A. (eds.): Australian Beetles Volume 2, Archostemata, Myxophaga, Adephaga, Polyphaga (part). CSIRO Publishing, Melbourne, vii + 784 pp.
FIKACEK M. 2019 b: 20. Hydrophilidae Latreille, 1802. Pp. 271 - 337. In: LAWRENCE J. F. & SLIPINSKI A. (eds.): Australian Beetles Volume 2, Archostemata, Myxophaga, Adephaga, Polyphaga (part). CSIRO Publishing, Melbourne, vii + 784 pp.
MINOSHIMA Y. & HAYASHI M. 2011: Larval morphology of the Japanese species of the tribes Acidocerini, Hydrobiusini and Hydrophilini (Coleoptera: Hydrophilidae). Acta Entomologica Musei Nationalis Pragae 51 (supplementum): 1 - 118.
MINOSHIMA Y. N. & HAYASHI M. 2015: Description of the larval stages of berosine genera Berosus and Regimbartia (Coleoptera, Hydrophilidae) based on Japanese B. japonicus and R. attenuata. Acta Entomologica Musei Nationalis Pragae 55 (1): 47 - 83.
MINOSHIMA Y. N. 2019: First known larva of omicrine genus Psalitrus d'Orchymont (Coleoptera, Hydrophilidae). Deutsche Entomologische Zeitschrift 66 (1): 107 - 118.
RICHMOND E. A. 1920: Studies on the biology of the aquatic Hydrophilidae. Bulletin of the American Museum of Natural History 42: 1 - 94, pls. 1 - 16.
Fig. 5. Larvae of Helophorus auriculatus Sharp, 1884. A – head, second instar larva, dorsal (left) and ventral (right) view; B – head, third instar larva, dorsal (left) and ventral (right) view; C – posterior leg, first instar, anterior view; D – posterior leg, third instar, anterior view; E – abdominal apex, third instar, dorsal view.
Fig. 4. First instar larva of Helophorus auriculatus Sharp, 1884. Head appendages. A, B – antenna, dorsal (A) and ventral (B) view; C–E – mandibles (C – right mandible, dorsal view, D – right mandible, ventral surface (drawn from dorsal), E – left mandible, dorsal view); F–H – maxilla (F – ventral view, gMX omitted; G, H – maxilla, slightly modified by pressure of cover glass for examination, dorsal (G) and ventral (H) face, both drawn from dorsal view). I–K – labium, dorsal (I), dorsolateral (J), ventral (K) view.
Fig. 7. Third instar larva of Helophorus auriculatus Sharp, 1884.A – antenna, dorsal (left) and ventral (right) surface, both drawn from dorsal view, gAN omitted; B – mandible, dorsal view; C – ventral surface of basal part of mandible; D – maxilla, dorsal (left) and ventral (right) surface, both drawn from dorsal view; E – labium, dorsal view (left) and labium and its adjacent structure, ventral view (right), gAN omitted.
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