Eucharitidae

Superregnum: Eukaryota
Cladus: Unikonta
Cladus: Opisthokonta
Cladus: Holozoa
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Cladus: Protostomia
Cladus: Ecdysozoa
Cladus: Panarthropoda
Phylum: Arthropoda
Subphylum: Crustacea
Superclassis: Allotriocarida
Classis: Hexapoda
Classis: Insecta
Cladus: Dicondylia
Subclassis: Pterygota
Cladus: Metapterygota
Infraclassis: Neoptera
Cladus: Eumetabola
Cladus: Endopterygota
Superordo: Hymenopterida
Ordo: Hymenoptera
Subordo: Apocrita
Superfamilia: Chalcidoidea

Familia: Eucharitidae
Subfamiliae: Akapalinae - Eucharitinae - Gollumiellinae - Oraseminae
Overview of genera (57)

Akapala – Ancylotropus – Anorasema – Apometagea – Athairocharis – Austeucharis – Babcockiella – Carletonia – Chalcura – Cherianella – Colocharis – Cyneucharis – Dicoelothorax – Dilocantha – Eucharis – Eucharissa – Galearia – Gollumiella – Hydrorhoa – Indosema – Isomerala – Kapala – Lasiokapala – Latina – Leurocharis – Lirata – Liratella – Lophyrocera – Mateucharis – Mictocharis – Mimistaka – Neolosbanus – Neostilbula – Obeza – Orasema – Orasemorpha – Parakapala – Parapsilogastrus – Pogonocharis – Pseudochalcura – Pseudometagea – Psilocharis – Psilogasteroides – Rhipipalloidea – Saccharissa – Schizaspidia – Stilbula – Stilbuloida – Striostilbula – Substilbula – Thoracantha – Thoracanthoides – Timioderus – Tricoryna – Zulucharis – †Palaeocharis
Source(s) of checklist:
Name

Eucharitidae Latreille, 1809

References

Latreille, P.A. 1809. Genera crustaceorum et insectorum secundum ordinem naturalem in familias disposita, iconibus exemplisque plurimis explicata. Tomus quartus et ultimus. Parisiis: A. Koenig, 399 pp. BHL Reference page.
Burks, R.A., Mottern, J.L. & Heraty, J.M. 2015: Revision of the Orasema festiva species group (Hymenoptera: Chalcidoidea: Eucharitidae). Zootaxa 3972(4): 521–534. DOI: 10.11646/zootaxa.3972.4.4. Preview (PDF) Full article (PDF) Reference page.
Heraty, J.M.; Darling, D.C. 2009: Fossil Eucharitidae and Perilampidae (Hymenoptera: Chalcidoidea) from Baltic Amber. Zootaxa, 2306: 1–16. Abstract & excerpt
Gadallah, N.S.; Edmardash, Y.A.; Heraty, J.M. 2013: A review of the family Eucharitidae (Hymenoptera: Chalcidoidea) of Egypt. Zootaxa 3717(3): 389–394. DOI: 10.11646/zootaxa.3717.3.9 Reference page.
da Silva, T.S.R., Silva-Freitas, J.M. & Schoeninger, K. 2019. A synopsis of the Brazilian Eucharitidae (Hymenoptera: Chalcidoidea) fauna: an annotated checklist of the family in the country, with a revised key for the New World genera. Zootaxa 4564(2): 347–366. DOI: 10.11646/zootaxa.4564.2.3 Paywall Reference page.
Torréns, J. 2013: A review of the biology of Eucharitidae (Hymenoptera: Chalcidoidea) from Argentina. Psyche, 2013: Article ID 926572. DOI: 10.1155/2013/926572
Torréns, J.; Heraty, J.M. 2013: A new genus of Eucharitidae (Hymenoptera: Chalcidoidea), with notes on life history and immature stages. Zootaxa 3630(2): 347–358. DOI: 10.11646/zootaxa.3630.2.9 Reference page.

The Eucharitidae are a family of parasitic wasps.[1] Eucharitid wasps are members of the superfamily Chalcidoidea and consist of three subfamilies: Oraseminae, Eucharitinae, and Gollumiellinae. Most of the 55 genera and 417 species of Eucharitidae are members of the subfamilies Oraseminae and Eucharitinae,[2] and are found in tropical regions of the world.[2]

Eucharitids are specialized parasitoids of ants, meaning each species is usually only parasitic of one genus of ant.[2] Furthermore, they are one of the few parasitoids that have been able to use ants as hosts, despite ants’ effective defense systems against most parasitoids.[3][4][5] Eucharitid parasitism occurs year-round, with a majority of it occurring during hot and humid months. However, the amount of parasitism that occurs depends primarily on the size of the ant colony and the number of host pupae in them, and not on the season.[3]
Life cycle

Female eucharitids oviposit rows of eggs into plant tissue, such as leaves and stems, away from ant colonies.[6] The eggs are a translucent white and are about 0.19 mm long and 0.08 mm wide. They are elliptical and flat on one side. As the eggs mature, they turn a brown color and ten days after oviposition, they hatch.[1] The larvae are solely responsible for their entry into the ant colony and the parasitism of their host.[2] They are 0.13 mm long and are able to travel several inches on the leaf but do not leave the egg cluster. After six to seven days, they attach themselves to foraging ants heading back to their brood; however, sometimes they will attach themselves to other insects, using them as intermediate hosts. Once in the brood, the larvae will attach to their host larva.[1] Some Eucharitidae are external parasites while others are internal parasites;[3] however, all eucharitid species finish their development as ectoparasites.[1]

Limited feeding on the host occurs until the host pupates, after which, most of it is consumed by the wasp.[2] Usually, only one parasite per host is found, but in some cases, superparasitism occurs, and two to four wasps will attach to, and emerge from one host.[3] Once the wasps emerge, the ant colony grooms and feeds them as if they were part of the ants’ brood. In some instances, worker ants have been observed assisting the wasps to emerge from their host. The wasps gain acceptance in these ways, and the ants show no signs of aggression because the wasps acquire their host's odor upon entry into the colony. By mimicking the odor of their host, eucharitid wasps are able to keep themselves safe until the scent wears off, at which point they leave the ant colony and begin mating.[6]

Adult wasps emerge from the ant nest in the morning; the males emerge before the females. In most cases, the males swarm one to two feet above the nest, and as soon as the females emerge, mating occurs. However, the males of certain species, such as Kapala terminalis, calmly wait on foliage surrounding the nest until the females emerge. Many times, the males will begin mating with the females before they have a chance to take flight, and in some instances, mating will occur while the wasps are still inside the ants' nest.[7] After mating, the females lay all their eggs in one day. The egg capacity of each female is 1000 to 10000.[6]
Anatomy

Most eucharitids are between 2.0 and 5.4 mm long and vary from metallic colors to black. They have 13 or fewer segments on their antennae, but some have up to 26.[8]

The main anatomical characteristics of eucharitid wasps are:

The prepectus lies in the same plane as, and fused, to pronotum.
The pronotum is small and hidden by the head dorsally.
The gaster is usually relatively small with a very long petiole.
The forewing marginal vein is moderately long and stigmal, and the postmarginal veins are extremely short.
Moderately large, about 2.0 to 5.4 mm in length.[9]

Subfamilies

The number of subfamilies of Eucharitidae has changed over the years, but the three most widely accepted are Oraseminae, Eucharitinae, and Gollumiellinae.
Oraseminae
Orasema simplex from Argentina

Oraseminae are parasitic on the ant genus Pheidole (Myrmicinae), as well as the fire ant in southern South America and the little red fire ant in the Caribbean.[2] They are distributed worldwide in tropical regions, such as Costa Rica, Ecuador,[4] Brazil, and Argentina.[3][6] They are also native to Texas, Florida, Massachusetts, Delaware,[10] and Colorado.[6]

The Oraseminae female punctures the plant tissue on which she will oviposit, and places an egg inside of each incision.[2] The eggs are deposited on the edges of the underside of leaves, and are sometimes found in the buds and stems of the plant.[6] They have been known to oviposite on blueberry leaves,[6] tea leaves (Das), oak leaves, olive leaves, mango leaves, flower heads, and banana fingers. Species of Eucharitidae are consistent in their choice of leaf for oviposition.[4]

Because Oraseminae eggs are laid on plants that are not always visited by foraging ants, the larvae will most often attach to intermediate hosts,[11] or “insect prey” that will eventually be devoured by ants.[3] Sometimes, however, foraging ants are present and there is no need for an intermediate host.[6] Upon arriving at the ants’ brood, the larva burrows into the host's thorax and feeds there. The wasp feeds until the host larva pupates; after the host pupates, the wasp will resume feeding until it emerges from its host.[2] The average time of development from planidia to adult is 29.5 days; the average pupal stage is 8.2 days.[6]

Because Oraseminae larvae, pupae, and adults are easily distinguished from their host,[12] the wasps disguise themselves by passively obtaining the odor of the fire ants. After a few days in the nest, the odor wears off and the ants begin to notice the wasps are not a part of their brood. At this point, the wasps leave the nest to mate and lay eggs.[4] Though Oraseminae have a high fertility rate, only a small percentage of eggs survive to adulthood.[6]
Eucharitinae

Eucharitinae are parasites of poneromorph ants, Ectatommatinae, Ponerinae, and Formicinae, although one genus from Australia is parasitic on the bulldog ant.[2]

Female Eucharitinae bear up to 4500 eggs and begin oviposition soon after emerging from the nest.[3] They deposit their eggs in groups of eight to 15[9] on plant buds, on the undersides of leaves or on fruit skin.[2] Eucharitinae attach themselves to foraging ants and do not use an intermediate host. Some species of Eucharitinae, such as Kapala terminalis and other Kapala sp., have been known for their jumping capabilities. They stand erect on the plant on which they hatched, and without any distinguishable preparation, jump about 10 mm from the leaf onto a foraging ant.[7] The larvae are external parasites of their hosts,[3] and are not noticed due to their acquisition of the host’s odor.[12] After the wasps are fully developed, they emerge in large numbers. The males swarm around the nest in wait of the females. Mating takes place immediately, and oviposition occurs soon after.[9] A fossil genus, Palaeocharis is known from Eocene Baltic amber. [13]
Gollumiellinae

Gollumiellinae are unique in that they hook their eggs onto the plants and connect a ropey secretion to them, which stand erect. This acts as an attraction mechanism for Paratrechina ants. Gollumiellinae larvae burrow into the hosts' thoraces and feed there.[2] The rest of its life cycle is similar to the aforementioned life cycle of eucharitids. Two Indo‐Pacific genera are included here:[14]

Anorasema Boucek, 1988
Gollumiella Hedqvist, 1978

Unplaced Genera

In addition to the above, the Global Biodiversity Information Facility lists the following genera:[15]

Akapala Girault, 1934
Apometagea Heraty, 2002
Astilbula Girault, 1913
Carletonia Heraty, 2002
Chalcurella Girault, 1913
Chalcurelloides Girault, 1913
Chalcuroidella Girault, 1913
Chalcuroides Girault, 1913
Colocharis Heraty, 2002
Dicoelothorax Ashmead, 1899
Dilocantha Shipp, 1894
Epimetagea Girault, 1913
Galearia (insect) Brullé, 1846
Isomerala Shipp, 1894
Kapaloides Mani, 1942
Kapatella Girault, 1932
Laetocantha Shipp, 1894
Lasiokapala Ashmead, 1899
Laurella Heraty, 2002
Leurocharis Heraty, 2002
Lirata Cameron, 1884
Liratella Girault, 1913
Lophyrocera Cameron, 1884
Metagea Kirby, 1886
Mimistaka Heraty, 2005
Neokapala Girault, 1913
Neolirata Torrens & Heraty, 2013
Palaeocharis Heraty & Darling, 2009
Parachalcura Girault, 1940
Parakapala Gemignani, 1937
Pogonocharis Heraty, 2002
Propsilogaster Girault, 1940
Pseudokapala Gemignani, 1947
Psygmatocera Enderlein, 1912
Rhipipallus Kirby, 1886
Schizaspidia Westwood, 1835
Stibulaspis Cameron, 1907
Tetramelia Kirby, 1886
Thoracanth Berthold, 1827
Thoracanthella Girault, 1940

Biological control

Eucharitids are candidates for biological control because each subfamily targets a specific ant genus.[4] On the other hand, some eucharitids, including the genus Kapala, are classified as pests for several different reasons.[3] First, a few days after oviposition occurs, the leaves dry up where each egg was located. Second, tea leaves with such marks reportedly do not have as strong of a flavor as tea leaves without these marks.[11] Third, not all eucharitids have a significant effect on the size of their hosts' colony.[7]

Orasema species are sometimes used as means of biological control for many ants, including the fire ant and little fire ant, because pesticides can cause damage to the environment, and they do not always work on fire ants. In addition, at least two eucharitid species groups are specialized parasites of these ants. Heraty stated, “Leaving aside the philosophical problems associated with introducing any organism for biological control, I believe that species of Orasema do have potential as biological control agents and deserve more study.”[4]
References

Ayre, G.L. Pseudometagea schwarzii (Ashm.) (Eucharitidae: Hymenoptera), a parasite of Lasius neoniger Emery (Formicidae: Hymenoptera). Canadian Journal of Zoology 40 (1962) : 157-164.
Heraty, John. Eucharitidae. Hymenopteran Systematics, University of California, Riverside (2002): Web. 16 Sep. 2011.
Lachaud, Jean-Paul and Perez-Lachaud, Gavriela. Impact of natural parasitism by two eucharitid wasps on a potential biocontrol agent ant in southeastern Mexico. Biological Control 48 (2009): 92-99.
Heraty, J.M. Biology and importance of two eucharitid parasites of Wasmannia and Solenopsis. (1994): Pages 104-120 in Williams, D. (ed), Exotic Ants: Biology, Impact and Control of Introduced Species. Boulder, CO: Westview Press. 332 pp.
Brues, C. T. (1 March 1919). "A New Chalcid-Fly Parasitic on the Australian Bull-Dog Ant". Annals of the Entomological Society of America. 12 (1): 13–21. doi:10.1093/aesa/12.1.13.
Varone, L. and Briano, J. Bionomics of Orasema simplex (Hymenoptera: Eucharitidae), a parasitoid of Solenopsis fire ants (Hymenoptera: Formicidae) in Argentina. Biological Control 48 (2009): 204-209.
Clausen, C.P. The habits of the Eucharidae. Psyche 48 (1941): 57-69.
Heraty, J.M. Family Eucharitidae. (1995) Pages 309-314. in Gauld, I.D.; Hanson, P., Hymenoptera of Costa Rica. Oxford: Oxford University Press. ??
Pitkin, B. R. Dr. “Eucharitidae”. Natural History Museum (2004) Universal Chalcidoidea Database Notes on families. Web. 30 Sep. 2011.
Ashmead, W.H. Studies on North American Chalcididae, with descriptions of new species from Florida. Transactions of the American Entomological Society 12 (1885[30]): 10-14.
Das, G.M. Preliminary studies on the biology of Orasema assectator Kerrich (Hymenoptera: Eucharitidae) parasitic on Pheidole and causing damage to leaves of tea in Assam. Bulletin of Entomological Research 54 (1963): 393-398.
Vander Meer, R.K., Jouvenaz, D.P. and Wojcik, D.P. Chemical mimicry in a parasitoid (Hymenoptera: Eucharitidae) of fire ants (Hymenoptera: Formicidae). Journal of Chemical Ecology 15 (1989): 2247-2261.
HERATY, JOHN M.; DARLING, D. CHRISTOPHER (2009-12-08). "Fossil Eucharitidae and Perilampidae (Hymenoptera: Chalcidoidea) from Baltic Amber". Zootaxa. 2306 (1): 1–16. doi:10.11646/zootaxa.2306.1.1. ISSN 1175-5334.
Heraty J, Hawks D, Kostecki JS, Carmichael A (2004) Phylogeny and behaviour of the Gollumiellinae, a new subfamily of the ant‐parasitic Eucharitidae (Hymenoptera: Chalcidoidea). Systematic Entomology 29[4] 544-559.

Global Biodiversity Information Facility: Eucharitidae (retrieved 24 December 2020)

Additional references

UC Riverside Eucharitid Page
Primary descriptions pdfs