Dytiscidae
The Dytiscidae - based on the Greek dytikos, "able to dive" - are the predaceous diving beetles, a family of water beetles. They occur in virtually any freshwater habitat around the world, but a few species live among leaf litter. The adults of most are between long, though much variation is seen between species. The European Dytiscus latissimus and Brazilian Megadytes ducalis are the largest, reaching up to and respectively. In contrast, the smallest is likely the Australian Limbodessus atypicali of subterranean waters, which only is about long. Most are dark brown, blackish, or dark olive in color with golden highlights in some subfamilies. The larvae are commonly known as water tigers due to their voracious appetite. They have short, but sharp mandibles and immediately upon biting, they deliver digestive enzymes into prey to suck their liquefied remains. The family includes more than 4,000 described species in numerous genera.
Habitat
Diving beetles are the most diverse beetles in the aquatic environment and can be found in almost every kind of freshwater habitat, from small rock pools to big lakes. Some dytiscid species are also found in brackish water. Diving beetles live in water bodies in various landscapes, including agricultural and urban landscapes. Some species, such as Agabus uliginosus and Acilius canaliculatus, are found to be relatively tolerant to recent urbanization.Larvae and development
When still in larval form, the beetles vary in size from about 1 to 5 cm. The larval bodies are shaped like crescents, with the tail long and covered with thin hairs. Six legs protrude from along the thorax, which also sports the same thin hairs. The head is flat and square, with a pair of long, large pincers. When hunting, they cling to grasses or pieces of wood along the bottom, and hold perfectly still until prey passes by, then they lunge, trapping their prey between their front legs and biting down with their pincers. The larvae are also known to partially consume prey and discard the carcass if another potential prey swims nearby. Their usual prey includes tadpoles and glassworms, among other smaller water-dwelling creatures. As the larvae mature, they crawl from the water on the sturdy legs, and bury themselves in the mud for pupation. After about a week, or longer in some species, they emerge from the mud as adults. Adult diving beetles have been found to oviposit their eggs within frog spawn in highly ephemeral habitats, with their eggs hatching within 24 hours after the frogs and the larvae voraciously predating on the recently hatched tadpoles.Edibility
Adult Dytiscidae, particular of the genus Cybister, are edible. Remnants of C. explanatus were found in prehistoric human coprolites in a Nevada cave, likely sourced from the Humboldt Sink. In Mexico, C. explanatus is eaten roasted and salted to accompany tacos. In Japan, C. japonicus has been used as food in certain regions such as Nagano prefecture. In the Guangdong Province of China, the latter species, as well as C. bengalensis, C. guerini, C. limbatus, C. sugillatus, C. tripunctatus, and probably also the well-known Great diving beetle are bred for human consumption, though as they are cumbersome to raise due to their carnivorous habit and have a fairly bland taste and little meat, this is decreasing. Dytiscidae are reportedly also eaten in Taiwan, Thailand, and New Guinea.Large but slow on land, adults are also eaten with relish by many midsized birds, mammals, reptiles, and other larger predators. The larvae are usually safer, due to their camouflage and ability to escape by water jet; they can be quite hard to catch and may become apex predators in small ponds. Although not considered particularly fierce, adults have been observed working as a group and attacking much larger vertebrates such as tadpoles.
Cultural significance
The diving beetle plays a role in a Cherokee creation story. According to the narrative, upon finding nowhere to rest in the "liquid chaos" the beetle brought up soft mud from the bottom. This mud then spread out to form all of the land on Earth.Ethnobiology
Adult Dytiscidae, as well as Gyrinidae, are collected by young girls in East Africa. It is believed that inducing the beetles to bite the nipples will stimulate breast growth.Parasites
of the genus Dytiscacarus were found to be are highly specialised parasites of beetles in the family Dytiscidae, undergoing their entire life cycle while inhabiting the space beneath the elytra of their hosts.Systematics
The following taxonomic sequence gives the subfamilies, their associated genera.Subfamily Agabinae Thomson, 1867
- Agabinus Crotch, 1873
- Agabus Leach, 1817
- Agametrus Sharp, 1882
- Andonectes Guéorguiev, 1971
- Hydronebrius Jakovlev, 1897
- Hydrotrupes Sharp, 1882
- Ilybiosoma Crotch, 1873
- Ilybius Erichson, 1832
- Leuronectes Sharp, 1882
- Platambus Thomson, 1859
- † Platynectes Régimbart, 1879
- Anisomeria Brinck, 1943
- Senilites Brinck, 1948
- Carabdytes Balke, Hendrich & Wewalka, 1992
- Bunites Spangler, 1972
- Colymbetes Clairville, 1806
- Hoperius Fall, 1927
- Meladema Laporte, 1835
- Melanodytes Seidlitz, 1887
- Neoscutopterus J.Balfour-Browne, 1943
- Rhantus Dejean, 1833
- Rugosus García, 2001
- Agaporomorphus Zimmermann, 1921
- Aglymbus Sharp, 1880
- Copelatus Erichson, 1832
- Exocelina Broun, 1886
- Lacconectus Motschulsky, 1855
- Liopterus Dejean, 1833
- Madaglymbus Shaverdo & Balke, 2008
- Rugosus García, 2001
- Coptotomus Say, 1830
- Austrodytes Watts, 1978
- Cybister Curtis, 1827
- Megadytes Sharp, 1882
- Onychohydrus Schaum & White, 1847
- Regimbartina Chatanay, 1911
- Spencerhydrus Sharp, 1882
- Sternhydrus Brinck, 1945
- Acilius Leach, 1817
- Aethionectes Sharp, 1882
- Austrodytes Watts, 1978
- Cybister Curtis, 1827
- Dytiscus Linnaeus, 1758
- Eretes Laporte, 1833
- Graphoderus Dejean, 1833
- Hydaticus Leach, 1817
- Hyderodes Hope, 1838
- Megadytes Sharp, 1882
- Miodytiscus Wickham, 1911
- Notaticus Zimmermann, 1928
- Onychohydrus Schaum & White, 1847
- Regimbartina Chatanay, 1911
- Rhantaticus Sharp, 1880
- Sandracottus Sharp, 1882
- Spencerhydrus Sharp, 1882
- Sternhydrus Brinck, 1945
- Thermonectus Dejean, 1833
- Tikoloshanes Omer-Cooper, 1956
- Hydrodytes K.B.Miller, 2001
- Microhydrodytes K.B.Miller, 2002
- Africodytes Biström, 1988
- Agnoshydrus Biström, Nilsson & Wewalka, 1997
- Allodessus Guignot, 1953
- Allopachria Zimmermann, 1924
- Amarodytes Régimbart, 1900
- Amurodytes Fery & Petrov, 2013
- Andex Sharp, 1882
- Anginopachria Wewalka, Balke & Hendrich, 2001
- Anodocheilus Babington, 1841
- Antiporus Sharp, 1882
- Barretthydrus Lea, 1927
- Bidessodes Régimbart, 1895
- Bidessonotus Régimbart, 1895
- Bidessus Sharp, 1882
- Boreonectes Angus, 2010
- Borneodessus Balke, Hendrich, Mazzoldi & Biström, 2002
- Brachyvatus Zimmermann, 1919
- Brancuporus Hendrich, Toussaint & Balke, 2014
- Canthyporus Zimmermann, 1919
- Carabhydrus Watts, 1978
- Celina Aubé, 1837
- Chostonectes Sharp, 1880
- Clypeodytes Régimbart, 1894
- Coelhydrus Sharp, 1882
- Comaldessus Spangler & Barr, 1995
- Crinodessus K.B. Miller, 1997
- Darwinhydrus Sharp, 1882
- Deronectes Sharp, 1882
- Derovatellus Sharp, 1882
- Desmopachria Babington, 1841
- Dimitshydrus Uéno, 1996
- Ereboporus K.B. Miller, Gibson & Alarie, 2009
- Etruscodytes Mazza, Cianferoni & Rocchi, 2013
- Fontidessus K.B. Miller & Spangler, 2008
- Geodessus Brancucci, 1979
- Gibbidessus Watts, 1978
- Glareadessus Wewalka & Biström, 1998
- Graptodytes Seidlitz, 1887
- Haideoporus Young & Longley, 1976
- Hemibidessus Zimmermann, 1921
- Heroceras Guignot, 1949
- Herophydrus Sharp, 1880
- Heterhydrus Fairmaire, 1869
- Heterosternuta Strand, 1935
- Hovahydrus Biström, 1982
- Huxelhydrus Sharp, 1882
- Hydrocolus Roughley & Larson in Larson, Alarie & Roughley, 2000
- Hydrodessus J. Balfour-Browne, 1953
- Hydroglyphus Motschulsky, 1853
- Hydropeplus Sharp, 1882
- Hydroporus Clairville, 1806
- Hydrovatus Motschulsky, 1853
- Hygrotus Stephens, 1828
- Hyphoporus Sharp, 1880
- Hyphovatus Wewalka & Biström, 1994
- Hyphydrus Illiger, 1802
- Hypodessus Guignot, 1939
- Iberoporus Castro & Delgado, 2001
- Incomptodessus K.B. Miller & García, 2011
- Kakadudessus Hendrich & Balke, 2009
- Laccornellus Roughley & Wolfe, 1987
- Laccornis Gozis, 1914
- Leiodytes Guignot, 1936
- Limbodessus Guignot, 1939
- Liodessus Guignot, 1939
- Lioporeus Guignot, 1950
- Megaporus Brinck, 1943
- Metaporus Guignot, 1945
- Methles Sharp, 1882
- Microdessus Young, 1967
- Microdytes J. Balfour-Browne, 1946
- Morimotoa Uéno, 1957
- Nebrioporus Régimbart, 1906
- Necterosoma W.J. Macleay, 1871
- Neobidessodes Hendrich & Balke, 2009
- Neobidessus Young, 1967
- Neoclypeodytes Young, 1967
- Neoporus Guignot, 1931
- Oreodytes Seidlitz, 1887
- Pachydrus Sharp, 1882
- Pachynectes Régimbart, 1903
- Papuadessus Balke, 2001
- Paroster Sharp, 1882
- Peschetius Guignot, 1942
- Petrodessus K.B. Miller, 2012
- Phreatodessus Ordish, 1976
- Platydytes Biström, 1988
- Porhydrus Guignot, 1945
- Primospes Sharp, 1882
- Pseuduvarus Biström, 1988
- Psychopomporus Jean, Telles & K.B. Miller, 2012
- Pteroporus Guignot, 1933
- Queda Sharp, 1882
- Rhithrodytes Bameul, 1989
- Sanfilippodytes Franciscolo, 1979
- Scarodytes Gozis, 1914
- Schistomerus Palmer, 1957
- Sekaliporus Watts, 1997
- Sharphydrus Omer-Cooper, 1958
- Siamoporus Spangler, 1996
- Siettitia Abeille de Perrin, 1904
- Sinodytes Spangler, 1996
- Spanglerodessus K.B. Miller & García, 2011
- Sternopriscus Sharp, 1880
- Stictonectes Brinck, 1943
- Stictotarsus Zimmermann, 1919
- Stygoporus Larson & LaBonte, 1994
- Suphrodytes Gozis, 1914
- Tepuidessus Spangler, 1981
- Terradessus Watts, 1982
- Tiporus Watts, 1985
- Trichonectes Guignot, 1941
- Trogloguignotus Sanfilippo, 1958
- Tyndallhydrus Sharp, 1882
- Typhlodessus Brancucci, 1985
- Uvarus Guignot, 1939
- Vatellus Aubé, 1837
- Yola Gozis, 1886
- Yolina Guignot, 1936
- † Calicovatellus K.B. Miller & Lubkin, 2001
- † Kuschelydrus Ordish, 1976
- † Procoelambus Théobald, 1937
- Africophilus Guignot, 1948
- Agabetes Crotch, 1873
- Australphilus Watts, 1978
- Japanolaccophilus Satô, 1972
- Laccodytes Régimbart, 1895
- Laccophilus Leach, 1815
- Laccoporus J. Balfour-Browne, 1939
- Laccosternus Brancucci, 1983
- Napodytes Steiner, 1981
- Neptosternus Sharp, 1882
- Philaccolilus Guignot, 1937
- Philaccolus Guignot, 1937
- Philodytes J. Balfour-Browne, 1939
- Lancetes Sharp, 1882
- Allomatus Mouchamps, 1964
- Batrachomatus Clark, 1863
- Matus Aubé, 1836
- † Liadroporus Prokin & Ren, 2010
- † Liadytiscus Prokin & Ren, 2010
- † Mesoderus Prokin & Ren, 2010
- † Liadyxianus Prokin, Petrov, B. Wang & Ponomarenko, 2013
- † Mesodytes Prokin, Petrov, Wang & Ponomarenko, 2013
- † Cretodytes Ponomarenko, 1977
- † Palaeodytes Ponomarenko, 1987
- † Sinoporus Prokin & Ren, 2010