Hydrophiloidea, Latreille, 1802

Minoshima, Yûsuke N. & Watanabe, Reiya, 2020, Morphology of immature stages of Helophorus (Gephelophorus) auriculatus (Coleoptera, Helophoridae), Acta Entomologica Musei Nationalis Pragae 60 (1), pp. 319-332 : 331

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.

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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.

Gallery Image

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.

Gallery Image

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.