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Ants
Formicinae
EOL Text
The Formicinae share the following characters with the Aneuretinae and Dolichoderinae (Bolton 2003):
- Dorsal cuticular flap of the metapleural gland anteriorly reduced and posteromedially extended
- Petiole with complete tergosternal fusion
- Postpygidial glands absent
... and have the following synapomorphies (Bolton 2003):
- Acidopore at apex of hypopygium
- Glands producing formic acid
- Sting nonfunctional (vestigial to absent)
- Lancets disarticulated from sting
- Pygidial gland absent
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Rights holder/Author | Tree of Life web project |
Source | http://tolweb.org/Formicinae/22203 |
Depth range based on 4 specimens in 1 taxon.
Environmental ranges
Depth range (m): 0 - 0
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Rights holder/Author | Ocean Biogeographic Information System |
Source | http://www.iobis.org/mapper/?taxon_id=817985 |
Barcode of Life Data Systems (BOLD) Stats
Specimen Records: | 19,434 | Public Records: | 3,866 |
Specimens with Sequences: | 16,258 | Public Species: | 465 |
Specimens with Barcodes: | 15,423 | Public BINs: | 479 |
Species: | 1,220 | ||
Species With Barcodes: | 947 | ||
Collection Sites: world map showing specimen collection locations for Formicinae
The Formicinae are a subfamily within the Formicidae containing ants of moderate evolutionary development.
Formicines retain some primitive features, such as the presence of cocoons around pupae, the presence of ocelli in workers, and little tendency toward reduction of palp or antennal segmentation in most species, except subterranean groups. Extreme modification of mandibles is rare, except in the genera Myrmoteras and Polyergus. However, some members show considerable evolutionary advancement in behaviors such as slave-making and symbiosis with root-feeding homopterans. Finally, all formicines have very reduced stings and enlarged venom reservoirs, with the venom gland, specialized (uniquely among ants) for the production of formic acid.[citation needed]
All members of the Formicinae "have a one-segmented petiole in the form of a vertical scale".[1]
Identification[edit]
Formicine ants have a single node-like or scale-like petiole (postpetiole entirely lacking) and the apex of the abdomen has a circular or U-shaped opening (the acidopore), usually fringed with hairs. A functional sting is absent, and defense is provided by the ejection of formic acid through the acidopore. If the acidopore is concealed by the pygidium and difficult to discern, then the antennal sockets are located well behind the posterior margin of the clypeus (cf. Dolichoderinae). In most formicines, the eyes are well developed (ocelli may also be present), the antennal insertions are not concealed by the frontal carinae, and the promesonotal suture is present and flexible.[2]
Tribes and genera[edit]
The tribal structure of Formicinae is not completely understood. This list follows the scheme at AntCat,[3] but other schemes and names are used.
- Camponotini Forel, 1878
- Calomyrmex Emery, 1895
- Camponotus Mayr, 1861 – carpenter ants (global)
- †Chimaeromyrma Dlussky, 1988
- Echinopla Smith, 1857
- Forelophilus Kutter, 1931
- Opisthopsis Dalla Torre, 1893
- Overbeckia Viehmeyer, 1916
- Phasmomyrmex Stitz, 1910
- Polyrhachis Smith, 1857 (Asian, African tropics)
- †Pseudocamponotus Carpenter, 1930
- Formicini Latreille, 1809
- Alloformica Dlussky, 1969
- Bajcaridris Agosti, 1994
- Cataglyphis Foerster, 1850
- †Cataglyphoides Dlussky, 2008
- †Conoformica Dlussky, 2008
- Formica Linnaeus, 1758
- Iberoformica Tinaut, 1990
- Polyergus Latreille, 1804 – Amazon ants
- Proformica Ruzsky, 1902
- †Protoformica Dlussky, 1967
- Rossomyrmex Arnol'di, 1928
- Gesomyrmecini Ashmead, 1905
- Gesomyrmex Mayr, 1868
- †Prodimorphomyrmex Wheeler, 1915
- Santschiella Forel, 1916
- †Sicilomyrmex Wheeler, 1915
- Gigantiopini Ashmead, 1905
- Gigantiops Roger, 1863 (Neotropical)
- Lasiini Ashmead, 1905
- Acropyga Roger, 1862
- Anoplolepis Santschi, 1914
- Cladomyrma Wheeler, 1920
- †Glaphyromyrmex Wheeler, 1915
- Lasiophanes Emery, 1895
- Lasius Fabricius, 1804
- Myrmecocystus Wesmael, 1838
- Prolasius Forel, 1892
- Stigmacros Forel, 1905
- Teratomyrmex McAreavey, 1957
- Melophorini Forel, 1912
- Melophorus Lubbock, 1883 (Australian)
- Myrmecorhynchini Wheeler, 1917
- Myrmecorhynchus André, 1896
- Notoncus Emery, 1895
- Pseudonotoncus Clark, 1934
- Myrmoteratini Emery, 1895
- Myrmoteras Forel, 1893
- Notostigmatini Bolton, 2003
- Notostigma Emery, 1920
- Oecophyllini Emery, 1895
- Oecophylla Smith, 1860 – weaver ants
- Plagiolepidini Forel, 1886
- Agraulomyrmex Prins, 1983
- Aphomomyrmex Emery, 1899
- Brachymyrmex Mayr, 1868
- Bregmatomyrma Wheeler, 1929
- Euprenolepis Emery, 1906
- Lepisiota Santschi, 1926
- Myrmelachista Roger, 1863
- Nylanderia Emery, 1906
- Paraparatrechina Donisthorpe, 1947
- Paratrechina Motschoulsky, 1863 – crazy ants
- Petalomyrmex Snelling, 1979
- Plagiolepis Mayr, 1861
- Prenolepis Mayr, 1861
- Pseudolasius Emery, 1887
- Tapinolepis Emery, 1925
- Zatania LaPolla, Kallal & Brady, 2012
- incertae sedis
- †Leucotaphus Donisthorpe, 1920
- †Liaoformica Hong, 2002
- †Longiformica Hong, 2002
- †Magnogasterites Hong, 2002
- †Orbicapitia Hong, 2002
- †Ovalicapito Hong, 2002
- †Ovaligastrula Hong, 2002
- †Protrechina Wilson, 1985
- †Sinoformica Hong, 2002
- †Sinotenuicapito Hong, 2002
- †Wilsonia Hong, 2002
References[edit]
- ^ Klotz, John H. (2008). "Formicinae". Urban ants of North America and Europe: identification, biology, and management. Cornell University Press. ISBN 978-0-8014-7473-6.
- ^ "Subfamily: Formicinae". antweb.org. AntWeb. Retrieved 21 September 2013.
- ^ Bolton, B. (2013), "An online catalog of the ants of the world.", AntCat, retrieved 22 September 2013
License | http://creativecommons.org/licenses/by-sa/3.0/ |
Rights holder/Author | Wikipedia |
Source | http://en.wikipedia.org/w/index.php?title=Formicinae&oldid=612424009 |
Honeypot ants, also called honey ants or repletes, are ants which are gorged with food by workers, to the point that their abdomens swell enormously, a condition called plerergate. Other ants then extract nourishment from them. They function as living larders. Honeypot ants belong to any of five genera, including Myrmecocystus.[1] They were first documented in 1881 by Henry C. McCook.
Many insects, notably honey bees and some wasps, collect and store liquid for use at a later date. However, these insects store their food within their nest or in combs. Honey ants are unique in using their own bodies as living storage, but they have more function than just storing food. Some store liquids, body fat, and water from insect prey brought to them by worker ants. They can later serve as a food source for their fellow ants when food is otherwise scarce. When the liquid stored inside a honeypot ant is needed, the worker ants stroke the antennae of the honeypot ant, causing the honeypot ant to regurgitate the stored liquid. In certain places such as the Australian Outback, honeypot ants are eaten by aboriginal people as sweets and are considered a delicacy.
Some worker ants turn into honeypots right from their emergence from pupa stage. The young ants stay in the nest, and the worker ants who collect food feed them. As the workers feed them with more food than they need, the surplus nutrients get stored in their abdomens. As their abdomens expand, the ants lose their mobility.
These ants can live anywhere in the nest, but in the wild, they are found deep underground, literally imprisoned by their huge abdomens, swollen to the size of grapes. They are so valued in times of little food and water that occasionally raiders from other colonies, knowing of these living storehouses, will attempt to steal these ants because of their high nutritional value and water content. These ants are also known to change colors. Some common colors are green, red, orange, yellow, and blue.
Honeypot ants such as Camponotus inflatus are edible and form an occasional part of the diet of various Australian Aboriginal peoples. Papunya, in Australia's Northern Territory is named after a honey ant creation story, or Dreaming, which belongs to the people there, such as the Warlpiri. The name of Western Desert Art Movement, Papunya Tula, means "honey ant dreaming".
Myrmecocystus nests are found in a variety of arid or semi-arid environments. Some species live in extremely hot deserts, others reside in transitional habitats, and still other species can be found in woodlands where it is somewhat cool but still very dry for a large part of the year.
References[edit]
Further reading[edit]
- Crane, Eva. The World History of Beekeeping and Honey Hunting. 1999.
License | http://creativecommons.org/licenses/by-sa/3.0/ |
Rights holder/Author | Wikipedia |
Source | http://en.wikipedia.org/w/index.php?title=Honeypot_ant&oldid=573882172 |
SUBFAMILY FORMICINAE HNS LEPELETIER
Workers and queens with ventral apex of gaster (hypopygium) produced into a conical structure terminating in a circular acidopore fringed with hairs. Petiole a large scale or distinct node. Gaster with 5 distinct tergites visible in dorsal view. Males have semi-erect hairs on dorsum of alitrunk.
Keys to genera of Formicinae HNS
Workers and queens
1 Antennal insertions set at a distance behind posterior clypeal margin; metapleural gland orifice absent (Figs. 114,116)........... Camponotus HNS Mayr (p. 86)
Antennal insertions more or less contiguous with posterior clypeal margin. Metapleural gland orifice present................................................................... 2
2(1) Antennae 11 segmented (Fig. 158)............................... Plagiolepis HNS Mayr (p. 110)
Antennae 12 segmented ................................................................................ 3
3 (2) Eyes at or in front of midlength of sides of head; petiole inclined forward, overhung by first gaster tergite (Fig. 156) ........ Paratrechina Motschulsky HNS (p. 108)
Eyes behind midlength of sides of head; petiole nodal or as a vertical scale not overhung by gaster........................................................................................ 4
4 (3) Mandibles falcate, pointed (Fig. 267)......................... Polyergus HNS Latreille (p. 155)
Mandibles with broad masticatory border, coarsely dentate............................. 5
5 (4) Propodeal spiracle ellipsoid or slitlike set at a distance from posterior propodeal declivity. Funiculus segments 2-5 as long or longer than segments 6-10 (Figs. 159, 176).............................................................. Formica HNS Linne (p. 111)
Propodeal spiracle circular or broadly oval set close to posterior margin of propodeum. Funiculus segments 2-5 shorter than segments 6-10 (Figs. 124, 135) Lasius HNS Fabricius (p. 92)
Males
1 Antennal insertions set at a distance behind posterior clypeal margin (Fig. 119) Camponotus HNS Mayr (p. 86)
Antennal insertions set close to or at posterior clypeal margin.......................... 3
2 (1) Eyes set in front of or at midlength of sides ofhead. Gonopalpi absent Paratrechina Motschulsky HNS (p. 108) Eyes set behind of sides of head. Gonopalpi present........................................ 3
3 (2) Antennae 12 segmented ............................................. Plagiolepis HNS Mayr (p. 110)
Antennae 13 segmented ................................................................................ 4
4 (3) Mandibles very reduced, falcate. Antennal scapes shorter than first four follow- ing segments. Maxillary palps 4 segmented very reduced Polyergus HNS Latreille (p. 155)
Mandibles broadening to apex. Antennal scapes longer than first five following segments. Maxillary palps 5-6 segmented ....................................................... 5
5 (4) Propodeal spiracle narrowly elliptical, set well forward from the posterior propodeal margin (Fig. 192)........................................... Formica HNS Linne (p. 111)
Propodeal spiracle broadly oval or circular, set close to or at the posterior propodeal margin (Fig. 129).......................................... Lasius HNS Fabricius (p. 92)
- Collingwood, C. A. (1979): The Formicidae (Hymenoptera) of Fennoscandia and Denmark. Fauna Entomologica Scandinavica 8, 1-174: 85-86, URL:http://antbase.org/ants/publications/6175/6175.pdf
License | Public Domain |
Rights holder/Author | No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation. |
Source | http://treatment.plazi.org/id/25304252AA708EE64713655D485C0505 |