Termes flavipes Kollar
Reticulitermes flavipes, the eastern subterranean termite, is the most common termite found in North America. These termites are the most economically important wood destroying insects in the United States and are classified as pests. They feed on cellulose material such as the structural wood in buildings, wooden fixtures, paper, books, and cotton. A mature colony can range from 20,000 workers to as high as 5 million workers and the primary queen of the colony lays 5,000 to 10,000 eggs per year to add to this total.
The eastern subterranean termite (R. flavipes) is the most widely distributed Reticulitermes species. It occurs throughout the eastern United States, including Texas, and can be found as far north as southern Ontario. In 2006, R. flavipes was also recorded in Oregon, on the West coast of the United States.
Reticulitermes santonensis in France is now understood to be a synonym of R. flavipes. The species is now believed to originate in the southeastern United States and to be exotic or invasive in southern Canada, Europe (France, Germany), South America (Uruguay, Chile), and the Bahamas. An infestation of unknown origin was also discovered in an Italian house in 2008.
Eastern subterranean termites, like other social insects, share resources and divide labor based on a caste system. They live in loosely associated societies called colonies which are composed of both males and females. The termites in the colony are generally organized into the worker caste, the soldier caste, and the reproductive caste.
Workers are about 3 mm long and are blind, wingless, soft-bodied, creamy white to grayish-white with a round head. They make up the majority of the termites that actually eat the wood. They are sterile and forage for food and water, construct and repair shelter tubes, feed and groom other termites, care for eggs and young, and participate in colony defense.
Soldier termites are also wingless and resemble workers except that they have a large, rectangular, yellowish-brown head with long black mandibles. The soldiers’ primary function is colony defense  and the mandibles are mainly used for crushing enemy ants which may invade the colony. Additionally, R. flavipes has a fontanelle (frontal gland pore) on the forehead from which it secretes a blend of terpenoid compounds. These secretions are synthesised de novo and are also used to defend the colony from predators such as ants. The soldier caste only makes up 1 to 2% of the entire colony. The soldiers are not capable of feeding themselves and rely on the worker termites to provide them with regurgitated food.
Immature termites on the sexual, or reproductive, line are called nymphs and can be distinguished from workers by the presence of wing buds. Under natural conditions, the work that they do in the nest is negligible compared to that done by workers. They can feed themselves, but there is debate over how long (over how many instars) they retain this ability.
Alates (from the Latin ālātus, "having wings") are winged, sexually mature adults that are capable of dispersal and outbreeding. In R. flavipes, they are 8.5-10mm in length to the tips of their wings and have compound eyes, ocelli, and a dark brown to black fully sclerotized cuticle. As the species name suggests (flāvī, "yellow" + pēs, "foot"), the tarsi are yellowish. To distinguish R. flavipes from similar species (at least in the United States), the position of the ocelli can be used: looking at the head from the side, the distance between the ocellus and the nearest compound eye is at least as large as the diameter of the ocellus.
Alates always develop from nymphs, with the last nymphal stage characterised by particularly long wing buds. After leaving their nests and swarming, male and female alates pair, shed their wings, begin excavating a new nest, and mate. From this point onward, they are called kings and queens, dealates, or primary reproductives.
Secondary reproductives, or neotenics, develop from either the reproductive line (brachypterous neotenics) or, in rare cases, the worker line (ergatoids). Ergatoids are the only members of the reproductive caste that have neither wing buds nor wings. Like workers, soldiers, and nymphs, they are eyeless. Ergatoids are seldom found in nature.
Brachypterous neotenics, which are common in the French population of R. flavipes (formerly R. santonensis), and possibly other populations as well, develop from nymphs via a nymph-like pre-brachypterous neotenic stage. They can be distinguished from nymphs by their shorter wing buds (brachy-, "short" + -pterous, "having wings"), darker pigmentation, slight sclerotization, and longer abdomens. Like alates, brachypterous neotenics also have compound eyes and ocelli. Female neotenics lay eggs at a lower rate than queens, but when present in large numbers, they may play a significant role in the growth of the colony.
R. flavipes are opportunistic, and a newly hatched termite can develop into any of a number of castes. At first, it becomes a worker termite and is most likely to remain one for its entire lifespan. Molting can change the worker into a pre-soldier and subsequently, a soldier. The soldier caste is a terminal stage which can no longer molt.
R. flavipes also molts into nymphs, which are the precursors of winged adult termites called alates which are sexually mature. Nymphal termites are non terminal and can revert to the worker stage. These reverted nymphs are called pseudergates. Nymphs and workers can also develop into secondary and tertiary neotenic reproductives respectively.
Because termites are social insects, they share many of their tasks. This can be seen throughout the caste system, where different castes take on different responsibilities for the betterment of the whole colony. R. flavipes cooperate in the rearing of young and also share their resources with the nest.
Swarming is the sudden, dramatic appearance of R. flavipes alates in the daytime from February to April. After this behavior male and female alates lose their wings, pair up, and form new colonies.
R. flavipes is mobile throughout its life and no permanent central nest area exists. Therefore, all termite castes can be found in any of the different sites occupied by a colony. Their activity is determined by food, moisture and temperature, and movement is usually driven by one of these necessities. Termites feed on anything made of or containing cellulose, but can tunnel into non-cellulose containing material to gain access to their destination. This behavior can be destructive to human activities.
The first person to observe and formally describe symbiotic flagellates in R. flavipes was the American paleontologist Joseph Leidy. In 1877, he reported his findings to the Academy of Natural Sciences of Philadelphia, describing three new species which he mistakenly took to be parasitic ciliates: Trichonympha agilis, Pyrsonympha vertens, and Dinenympha gracilis.
Prof. LEIDY remarked that in seeking small animals beneath stones and fragments of wood in our forests, observing the very common White Ant, Termes flavipes, he noticed that the intestine of the insect, seen in the translucent abdomen, was distended with brown matter. Feeling curious to learn the exact nature of this matter, he was surprised to find that it consisted largely of infusorial and other parasites, mingled with minute particles of decayed wood. In many instances the parasites are so numerous as to make up the greater portion of the bulk of the intestinal pulp. Every individual he had examined, of workers, soldiers, and winged forms, was infested with the parasites, which may be estimated by millions.— Proceedings of the Academy of Natural Sciences of Philadelphia (1877)
Species present in Reticulitermes flavipes
- Dinenympha fimbriata Kirby, 1924
- Dinenympha gracilis Leidy, 1877
- Holomastigotes elongatum Grassi, 1892
- Microjoenia fallax (Duboscq & Grassé, 1928)
- Monocercomonas sp. Grassi, 1879
- Pyrsonympha major Powell, 1928
- Pyrsonympha vertens Leidy, 1877
- Spironympha kofoidi Koidzumi, 1917
- Spirotrichonympha flagellata (Grassi, 1892)
- Trichomitus trypanoides (Duboscq & Grassé, 1924)
- Trichonympha agilis Leidy, 1877
A 2003 study that focused on oxymonad flagellates found evidence of at least one additional undescribed Dinenympha species. They also found what they believe is an undescribed "second" Pyrsonympha species in addition to P. vertens. The authors question whether P. major, which was first described in Reticulitermes hesperus, is truly found in R. flavipes and consider it a case of mistaken identity.
Role in digestion
Flagellates are a feature of all termite families except Termitidae, the so-called "higher termites". They are found exclusively in the hindgut, especially the paunch, an enlarged section of the hindgut with an anaerobic interior that serves as a fermenter. In R. flavipes, wood eaten by the termite is first broken up with the mandibles, treated with host endoglucanases from the salivary glands, ground up into small particles in the gizzard, and then treated with additional host cellulases in the midgut, freeing glucose for immediate absorption. It then passes into the paunch, where flagellates take up the partly-digested wood particles through endocytosis. The flagellates break lignocellulose (xylan or cellulose) down into simple sugars, which they ferment for their own energy needs, producing CO2, H2, and short-chain fatty acids such as acetate as waste products. The short-chain fatty acids (which are also produced by homoacetogenic gut bacteria from CO2 and H2) can be directly absorbed by the termite host. The vast majority of digestion takes place in the paunch: almost all xylanase activity, just over one quarter of the endoglucanase activity, and almost two thirds of the exoglucanase activity in the R. flavipes digestive system is localised in the hindgut and attributed to gut flagellates.
Although this is an obligate symbiosis, newly hatched larvae do not have gut flagellates. These are acquired when the larvae are fed with flagellate-containing anal fluids from other members of the colony (proctodeal trophallaxis). Proctodeal trophallaxis is also used to replenish flagellates and other gut symbionts after each moult.
Most bacterial species in the termite gut are difficult or impossible to culture, so methods like 16S ribosomal RNA sequencing are used to identify which groups are present. One such analysis of R. flavipes worker guts uncovered representatives of the Endomicrobia (Elusimicrobiota), Actinomycetota, Pseudomonadota, Bacillota, Bacteroidota, and Spirochaetota. The dominant bacterial taxon in the core gut microbiome is the genus Treponema (Spirochaetota), which accounted for approximately 32% of sequences in another 16S rRNA study. The same study identified Endomicrobia (phylum:Elusimicrobiota), which are predominant endosymbionts several protozoa in the termtie gut. Artificial defaunation of Reticulitermes species by force-feeding on starch or starvation leads to a loss of flagellates and, by association, these endosymbiotic Endomicrobia, and an increase in abundance of free-living relatives. A rare free-living member of this class, Endomicrobium proavitum, the first Endomicrobia species to be cultured and named, was isolated from sterile-filtered gut homogenates from defaunated (starch-fed) R. flavipes workers. It is believed to play a role in nitrogen fixation.
While some gut bacteria live free in the gut lumen or attached to the gut wall, many others live in close association with flagellates. These include uncultured members of Endomicrobia (Elusimicrobiota) and other taxa that live as cytoplasmic symbionts, as well as epibiotic symbionts that attach to the outer surface of cells. In R. flavipes, cytoplasmic symbionts have been identified in flagellates such as Trichonympha agilis (Hypermastigida) and Pyrsonympha vertens (Oxymonadida). The latter is also characterised by spirochaete epibiotic symbionts. In other termite species, members of the spirochaete genus Treponema have been identified as endo- and ectosymbionts of flagellates: similar associations may explain Treponema's dominance in the R. flavipes gut.
Archaea isolated from the R. flavipes hindgut include the H2- and CO2-utilizing methanogens Methanobrevibacter cuticularis and curvatus. These two species are believed to be the dominant methanogens in R. flavipes and are found in the peripheral, microxic region of the hindgut, on or in close proximity to the gut wall, where they are sometimes attached to filamentous prokaryotes.
Although there is a core microbiome shared among castes and colonies, the alate caste gut is characterised by a significantly lower abundances of bacteria in the genus Treponema (Spirochaetota) and the class Endomicrobia (Elusimicrobia) compared to workers and soldiers. Flagellates in the class Parabasalia and the order Oxymonadida are also significantly less abundant in the alate gut, with the latter significantly reduced in dealates as well.
Along with Reticulitermes virginica, R. flavipes is responsible for 80% of the $2.2 billion spent annually in the United States on termite control. Termites feed on wood cellulose, meaning that their presence in human made structures often goes unnoticed for lengthy periods of time. A termite infested timber will appear structurally sound from the outside, while inside it will have a honeycombed appearance. To detect the presence of R. flavipes the observer can test the integrity of the wood by tapping it with a screwdriver. If present, R. flavipes is found at, near or below ground level. Trim work, sub flooring, flooring, and the structural timbers are the areas of a building most susceptible to termite damage. The Eastern subterranean termite is considered a serious economic timber pest and it is estimated that in high activity areas more than 1 in 5 homes have been or will be attacked.
Termite control methods include: physical barriers, chemical treatments, and physical treatments (such as heat, freezing, electrocution and microwave irradiation).
Structural damage to buildings is not R. flavipes’ only impact on humans. Termites also play a critical role in the decomposition of organic matter in natural communities. Without termites, the accumulation of dead organic matter on the forest floor would become detrimental to integrity of that forest. The benefits provided by R. flavipes in terms of their contribution to environmental regulation may far outweigh the disadvantages they pose.
- "Eastern Subterranean Termites Fact Sheet" (PDF). pestcontrol.basf.us. Archived from the original (PDF) on March 5, 2012. Retrieved February 20, 2009.
- Austin, James W.; Szalanski, Allen L.; Scheffrahn, R. H.; Messenger, M. T.; Dronnet, Stéphanie; Bagnères, Anne-Geneviève (1 May 2005). "Genetic Evidence for the Synonymy of Two Reticulitermes Species: Reticulitermes flavipes and Reticulitermes santonensis". Annals of the Entomological Society of America. 98 (3): 395–401. doi:10.1603/0013-8746(2005)098[0395:GEFTSO]2.0.CO;2.
- "ITIS Standard Report Page: Reticulitermes flavipes". ITIS. Retrieved 7 May 2017.
- Clarke, Matthew W.; Thompson, Graham J.; Sinclair, Brent J. (1 August 2013). "Cold Tolerance of the Eastern Subterranean Termite, Reticulitermes flavipes (Isoptera: Rhinotermitidae), in Ontario". Environmental Entomology. 42 (4): 805–810. doi:10.1603/EN12348. PMID 23905745. S2CID 37734178.
- McKern, Jackie A.; Szalanski, Allen L.; Austin, James W. (December 2006). "First Record of Reticulitermes Flavipes and Reticulitermes Hageni in Oregon (Isoptera: Rhinotermitidae)". Florida Entomologist. 89 (4): 541–542. doi:10.1653/0015-4040(2006)89[541:FRORFA]2.0.CO;2.
- Evans, Theodore A.; Forschler, Brian T.; Grace, J. Kenneth (7 January 2013). "Biology of Invasive Termites: A Worldwide Review". Annual Review of Entomology. 58 (1): 455–474. doi:10.1146/annurev-ento-120811-153554. PMID 23020620.
- Vieau, F. (March 2001). "Comparison of the spatial distribution and reproductive cycle of Reticulitermes santonensis Feytaud and Reticulitermes lucifugus grassei Clément (Isoptera, Rhinotermitidae) suggests that they represent introduced and native species, respectively". Insectes Sociaux. 48 (1): 57–62. doi:10.1007/PL00001746. S2CID 22218798.
- Sellenschlo, U. (August 1988). "Termiten in Hamburg". Anzeiger für Schädlingskunde Pflanzenschutz Umweltschutz. 61 (6): 105–108. doi:10.1007/BF01906764. S2CID 11468548.
- Scheffrahn, Rudolf H.; Chase, James A.; Mangold, John R.; Krĕcĕk, Jan; Su, Nan-Yao; Krecek, Jan (September 1999). "First Record of Reticulitermes (Isoptera: Rhinotermitidae) from the West Indies: R. flavipes on Grand Bahama Island". The Florida Entomologist. 82 (3): 480. doi:10.2307/3496875. JSTOR 3496875.
- Ghesini, Silvia; Messenger, Matthew T.; Pilon, Nicola; Marini, Mario (June 2010). "First Report of Reticulitermes flavipes (Isoptera: Rhinotermitidae) in Italy". Florida Entomologist. 93 (2): 327–328. doi:10.1653/024.093.0233.
- dBugger.org. "Subterranean Termite Identification & Castes". Retrieved 2013-07-26.
- Susan C. Jones. "Termite Control". Ohio State University. Retrieved February 20, 2009.
- Lori J. Nelson; Laurence G. Cool; Brian T. Forschler; Michael I. Haverty (2001). "Correspondence of Soldier Defense Secretion Mixtures with Cuticular Hydrocarbon Phenotypes for Chemotaxonomy of the Termite Genus Reticulitermes in North America". Journal of Chemical Ecology. 27 (7): 1449–1479. doi:10.1023/A:1010325511844. PMID 11504039. S2CID 9781034.
- Haverty, M. I.; Howard, R. W. (March 1981). "Production of soldiers and maintenance of soldier proportions by laboratory experimental groups of Reticulitermes flavipes (Kollar) and Reticulitermes virginicus (Banks) (Isoptera:Rhinotermitidae)". Insectes Sociaux. 28 (1): 32–39. doi:10.1007/BF02223620. ISSN 0020-1812. S2CID 20011514.
- Tian, Li; Zhou, Xuguo (2014). "The Soldiers in Societies: Defense, Regulation, and Evolution". International Journal of Biological Sciences. 10 (3): 296–308. doi:10.7150/ijbs.6847. ISSN 1449-2288. PMC 3957085. PMID 24644427.
- Lainé, L.V.; Wright, D.J. (2003). "The life cycle of Reticulitermes spp. (Isoptera: Rhinotermitidae): what do we know?". Bulletin of Entomological Research. 93 (4): 267–278. doi:10.1079/BER2003238. PMID 12908912.
- Scheffrahn, Rudolf H.; Su, Nan-Yao (December 1994). "Keys to Soldier and Winged Adult Termites (Isoptera) of Florida". The Florida Entomologist. 77 (4): 460. doi:10.2307/3495700. JSTOR 3495700.
- Jaques, Roger G. Bland, H.E. (2010). How to know the Insects (3rd ed.). Long Grove, IL.: Waveland Press. p. 116. ISBN 978-1577666844.
- Messenger, Matthew T. (2004). "The Termite Species of Louisiana: An Identification Guide". New Orleans Mosquito & Termite Control Board Bulletin. No. 04-04, 3rd Edition.
- Leidy, Joseph (1877). "On Intestinal Parasites of Termes flavipes". Proceedings of the Academy of Natural Sciences of Philadelphia. 29: 146–149. JSTOR 4060180.
- Lewis, J. L.; Forschler, B. T. (1 November 2006). "A Nondichotomous Key to Protist Species Identification of Reticulitermes (Isoptera: Rhinotermitidae)". Annals of the Entomological Society of America. 99 (6): 1028–1033. doi:10.1603/0013-8746(2006)99[1028:anktps]2.0.co;2.
- Lewis, J. L.; Forschler, B. T. (1 November 2004). "Protist Communities from Four Castes and Three Species of Reticulitermes (Isoptera: Rhinotermitidae)". Annals of the Entomological Society of America. 97 (6): 1242–1251. doi:10.1603/0013-8746(2004)097[1242:pcffca]2.0.co;2.
- Stingl, Ulrich; Brune, Andreas (April 2003). "Phylogenetic Diversity and Whole-Cell Hybridization of Oxymonad Flagellates from the Hindgut of the Wood-Feeding Lower Termite Reticulitermes flavipes". Protist. 154 (1): 147–155. doi:10.1078/143446103764928530. PMID 12812374.
- Zhou, Xuguo; Smith, Joseph A.; Oi, Faith M.; Koehler, Philip G.; Bennett, Gary W.; Scharf, Michael E. (June 2007). "Correlation of cellulase gene expression and cellulolytic activity throughout the gut of the termite Reticulitermes flavipes". Gene. 395 (1–2): 29–39. doi:10.1016/j.gene.2007.01.004. PMID 17408885.
- Bignell, David Edward; Roisin, Yves; Lo, Nathan (2011). Biology of Termites: A Modern Synthesis. Dordrecht: Springer. ISBN 978-90-481-3977-4.
- Brune, Andreas (3 February 2014). "Symbiotic digestion of lignocellulose in termite guts". Nature Reviews Microbiology. 12 (3): 168–180. doi:10.1038/nrmicro3182. PMID 24487819. S2CID 5220210.
- Fisher, Marc; Miller, Dini; Brewster, Carlyle; Husseneder, Claudia; Dickerman, Allan (25 July 2007). "Diversity of Gut Bacteria of Reticulitermes flavipes as Examined by 16S rRNA Gene Sequencing and Amplified rDNA Restriction Analysis". Current Microbiology. 55 (3): 254–259. doi:10.1007/s00284-007-0136-8. PMID 17657534. S2CID 2199228.
- Benjamino, Jacquelynn; Graf, Joerg (17 February 2016). "Characterization of the Core and Caste-Specific Microbiota in the Termite, Reticulitermes flavipes". Frontiers in Microbiology. 7: 171. doi:10.3389/fmicb.2016.00171. PMC 4756164. PMID 26925043.
- Mikaelyan, Aram; Thompson, Claire L.; Meuser, Katja; Zheng, Hao; Rani, Pinki; Plarre, Rudy; Brune, Andreas (2017). "High-resolution phylogenetic analysis of Endomicrobia reveals multiple acquisitions of endosymbiotic lineages by termite gut flagellates". Environmental Microbiology Reports. 9 (5): 477–483. doi:10.1111/1758-2229.12565. ISSN 1758-2229. PMID 28677262. S2CID 22715293.
- Zheng, Hao; Dietrich, Carsten; Radek, Renate; Brune, Andreas (1 January 2016). "Endomicrobium proavitum, the first isolate of Endomicrobia class. nov. (phylum Elusimicrobia) – an ultramicrobacterium with an unusual cell cycle that fixes nitrogen with a Group IV nitrogenase". Environmental Microbiology. 18 (1): 191–204. doi:10.1111/1462-2920.12960. ISSN 1462-2920. PMID 26119974.
- Stingl, U.; Radek, R.; Yang, H.; Brune, A. (3 March 2005). ""Endomicrobia": Cytoplasmic Symbionts of Termite Gut Protozoa Form a Separate Phylum of Prokaryotes". Applied and Environmental Microbiology. 71 (3): 1473–1479. doi:10.1128/AEM.71.3.1473-1479.2005. PMC 1065190. PMID 15746350.
- Smith, H. E.; Arnott, H. J. (April 1974). "Epi- and Endobiotic Bacteria Associated with Pyrsonympha vertens, a Symbiotic Protozoon of the Termite Reticulitermes flavipes". Transactions of the American Microscopical Society. 93 (2): 180–94. doi:10.2307/3225286. JSTOR 3225286. PMID 4598584.
- Ohkuma, Moriya; Noda, Satoko; Hattori, Satoshi; Iida, Toshiya; Yuki, Masahiro; Starns, David; Inoue, Jun-ichi; Darby, Alistair C.; Hongoh, Yuichi (18 August 2015). "Acetogenesis from H2 plus CO2 and nitrogen fixation by an endosymbiotic spirochete of a termite-gut cellulolytic protist". Proceedings of the National Academy of Sciences. 112 (33): 10224–10230. doi:10.1073/pnas.1423979112. PMC 4547241. PMID 25979941.
- Wenzel, Marika; Radek, Renate; Brugerolle, Guy; König, Helmut (January 2003). "Identification of the ectosymbiotic bacteria of Mixotricha paradoxa involved in movement symbiosis". European Journal of Protistology. 39 (1): 11–23. doi:10.1078/0932-4739-00893.
- Leadbetter, JR; Breznak, JA (October 1996). "Physiological ecology of Methanobrevibacter cuticularis sp. nov. and Methanobrevibacter curvatus sp. nov., isolated from the hindgut of the termite Reticulitermes flavipes". Applied and Environmental Microbiology. 62 (10): 3620–31. doi:10.1128/aem.62.10.3620-3631.1996. PMC 168169. PMID 8837417.
- Nan-Yao Su; Rudolf H. Scheffrahn & Brian Cabrera (April 2009). "Native Subterraneans". Featured Creatures. University of Florida. Retrieved February 2, 2010.
- "Eastern Subterranean Termites". Fumapest Group. Retrieved February 20, 2009.
- "Termites". University of Toronto. Archived from the original on October 21, 2008. Retrieved February 2, 2010.
- Maynard, Daniel; Crowther, Thomas; King, Joshua; Warren, Robert; Bradford, Mark (June 2015). "Temperate Forest Termites: ecology, biogeography, and ecosystem impacts". Ecological Entomology. 40 (3): 199–210. doi:10.1111/een.12185.
- Biology of Subterranean Termites in the Eastern United States - Ohioline Bulletin 1209, Ohio State University
- Subterranean Termite Fact Sheet from the National Pest Management Association with information on habits, habitat and prevention
- Eastern Subterranean Termite Fact Sheet - Penn State Entomology Department