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Temporal range: Early Devonian–Recent
Orchesella cincta.jpg
Orchesella cincta
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Hexapoda
Class: Entognatha (but see text)
Subclass: Collembola
Lubbock, 1870
Synonyms [1]
  • Oligentoma
  • Oligoentoma

Springtails (Collembola) form the largest of the three lineages of modern hexapods that are no longer considered insects (the other two are the Protura and Diplura). Although the three orders are sometimes grouped together in a class called Entognatha because they have internal mouthparts, they do not appear to be any more closely related to one another than they all are to insects, which have external mouthparts.[2]

Some DNA sequence studies[3][4][5] suggest that Collembola represent a separate evolutionary line from the other Hexapoda, but others disagree;[6] this seems to be caused by widely divergent patterns of molecular evolution among the arthropods.[7] The adjustments of traditional taxonomic rank for springtails reflects the occasional incompatibility of traditional groupings with modern cladistics: when they were included with the insects, they were ranked as an order; as part of the Entognatha, they are ranked as a subclass. If they are considered a basal lineage of Hexapoda, they are elevated to full class status.

Collembolans are omnivorous, free-living organisms that prefer moist conditions. They do not directly engage in the decomposition of organic matter, but contribute to it indirectly through the fragmentation of organic matter[8] and the control of soil microbial communities.[9] The word "collembola" is from the ancient Greek kolla meaning glue and embolon meaning wedge or plug.


Isotoma with visible furcula

Members of Collembola are normally less than 6 mm (0.24 in) long, have six or fewer abdominal segments and possess a tubular appendage (the collophore or ventral tube) with eversible sticky vesicles, projecting ventrally from the first abdominal segment. The Poduromorpha and Entomobryomorpha have an elongated body, while the Symphypleona and Neelipleona have a globular body. Collembola lack a tracheal respiration system, which forces them to respire through a porous cuticle, to the notable exception of Sminthuridae which exhibit a rudimentary, although fully functional, tracheal system.[10]

Most species have an abdominal, tail-like appendage, the furcula, that is folded beneath the body to be used for jumping when the animal is threatened. It is held under tension by a small structure called the retinaculum and when released, snaps against the substrate, flinging the springtail into the air. All of this takes place in as little as 18 milliseconds.[11]

Springtails also possess the ability to reduce their body size by as much as 30% through subsequent ecdyses (molting) if temperatures rise high enough. The shrinkage is genetically controlled. Since warmer conditions increase metabolic rates and energy requirements in organisms, the reduction in body size is advantageous to their survival.[12]

Systematics and evolution

Allacma fusca (Symphypleona) on rotting wood

Traditionally, the springtails were divided into the orders Arthropleona, Symphypleona and occasionally also Neelipleona. The Arthropleona were divided into two superfamilies, the Entomobryoidea and the Poduroidea. But actually, these two and the Symphypleona form three lineages, each of which is equally distant from the other two. Thus, the Arthropleona are abolished in modern classifications, and their superfamilies are raised in rank accordingly, being now the Entomobryomorpha and the Poduromorpha. Technically, the Arthropleona are thus a partial junior synonym of the Collembola.[13] The term "Neopleona" is essentially synonymous with Symphypleona + Neelipleona.[citation needed]

The Neelipleona were originally seen as a particular advanced lineage of Symphypleona, based on the shared global body shape. But the global body of Neelipleona is realised in a completely different way than in Symphypleona. Subsequently, the Neelipleona were considered as being derived from the Entomobryomorpha. But analysis of 18S and 28S rRNA sequence data suggests that they form the most ancient lineage of springtails, which would explain their peculiar apomorphies.[6]

Springtails are attested to since the Early Devonian.[14] The fossil from 400 million years ago, Rhyniella praecursor, is the oldest terrestrial arthropod, and was found in the famous Rhynie chert of Scotland. Given its morphology resembles extant species quite closely, the radiation of the Hexapoda can be situated in the Silurian, 420 million years ago or more.[15]

Fossil collembola are rare. Instead, most are found in amber.[16] Even these are rare and many amber deposits carry few or no collembola. The best deposits are from the early Eocene of Canada and Europe,[17] Miocene of Central America,[18] and the mid-Cretaceous of Burma and Canada.[19] They display some unusual characteristics: first, all but one of the fossils from the Cretaceous belong to extinct genera, whereas none of the specimens from the Eocene or the Miocene are of extinct genera; second, the species from Burma are more similar to the modern fauna of Canada than are the Canadian Cretaceous specimens.

There are about 3,600 different species.[20]


Food source

Springtails commonly consume fungal hyphae and spores, but also have been found to consume plant material and pollen, animal remains, colloidal materials, minerals and bacteria.[21]


Springtails are cryptozoa frequently found in leaf litter and other decaying material,[22] where they are primarily detritivores and microbivores, and one of the main biological agents responsible for the control and the dissemination of soil microorganisms.[23]

"Snow flea"

In sheer numbers, they are reputed to be one of the most abundant of all macroscopic animals, with estimates of 100,000 individuals per square meter of ground,[24] essentially everywhere on Earth where soil and related habitats (moss cushions, fallen wood, grass tufts, ant and termite nests) occur.[25] Only nematodes, crustaceans, and mites are likely to have global populations of similar magnitude, and each of those groups except mites is more inclusive: though taxonomic rank cannot be used for absolute comparisons, it is notable that nematodes are a phylum and crustaceans a subphylum. Most springtails are small and difficult to see by casual observation, but one springtail, the so-called snow flea (Hypogastrura nivicola), is readily observed on warm winter days when it is active and its dark color contrasts sharply with a background of snow.[26]

In addition, a few species routinely climb trees and form a dominant component of canopy faunas, where they may be collected by beating or insecticide fogging.[27][28] These tend to be the larger (>2 mm) species, mainly in the genera Entomobrya and Orchesella, though the densities on a per square meter basis are typically 1–2 orders of magnitude lower than soil populations of the same species. In temperate regions, a few species (e.g. Anurophorus spp., Entomobrya albocincta, Xenylla xavieri, Hypogastrura arborea) are almost exclusively arboreal.[25] In tropical regions a single square meter of canopy habitat can support many species of Collembola.[11]

The main ecological factor driving the local distribution of species is the vertical stratification of the environment: in woodland a continuous change in species assemblages can be observed from tree canopies to ground vegetation then to plant litter down to deeper soil horizons.[25] This is a complex factor embracing both nutritional and physiological requirements, together with behavioural trends,[29] dispersal limitation[30] and probable species interactions. Some species have been shown to exhibit negative[31] or positive[29] gravitropism, which adds a behavioural dimension to this still poorly understood vertical segregation. Experiments with peat samples turned upside down showed two types of responses to disturbance of this vertical gradient, called "stayers" and "movers".[32]

As a group, springtails are highly sensitive to desiccation, because of their tegumentary respiration.[33] although some species with thin, permeable cuticles have been shown to resist severe drought by regulating the osmotic pressure of their body fluid.[34] The gregarious behaviour of Collembola, mostly driven by the attractive power of pheromones excreted by adults,[35] gives more chance to every juvenile or adult individual to find suitable, better protected places, where desiccation could be avoided and reproduction and survival rates (thereby fitness) could be kept at an optimum.[36] Sensitivity to drought varies from species to species[37] and increases during ecdysis.[38] Given that springtails are moulting repeatedly during their entire life (an ancestral character in Hexapoda) they spend much time in concealed micro-sites where they can find protection against desiccation and predation during ecdysis, an advantage reinforced by synchronized moulting.[39] The high humidity environment of many caves also favours springtails and there are numerous cave adapted species,[40][41] including one, Plutomurus ortobalaganensis living 1,980 metres (6,500 ft) down the Krubera Cave.[42]

The horizontal distribution of springtail species is affected by environmental factors which act at the landscape scale, such as soil acidity, moisture and light.[25] Requirements for pH can be reconstructed experimentally.[43] Altitudinal changes in species distribution can be at least partly explained by increased acidity at higher elevation.[44] Moisture requirements, among other ecological and behavioural factors, explain why some species cannot live aboveground,[45] or retreat in the soil during dry seasons,[46] but also why some epigeal springtails are always found in the vicinity of ponds and lakes, such as the hygrophilous Isotomurus palustris.[47] Adaptive features, such as the presence of a fan-like wettable mucro, allow some species to move at the surface of water (Sminthurides aquaticus, Sminthurides malmgreni). Podura aquatica, a unique representative of the family Poduridae (and one of the first springtails to have been described by Linnaeus), spends its entire life at the surface of water, its wettable eggs dropping in water until the non-wettable first instar hatches then surfaces.[48]

In a variegated landscape, made of a patchwork of closed (woodland) and open (meadows, cereal crops) environments, most soil-dwelling species are not specialized and can be found everywhere, but most epigeal and litter-dwelling species are attracted to a particular environment, either forested or not.[25][49] As a consequence of dispersal limitation, landuse change, when too rapid, may cause the local disappearance of slow-moving, specialist species,[50] a phenomenon the measure of which was recently called colonisation credit.[51][52]

Relationship with humans

Tomocerus sp. from Germany

Springtails are well known as pests of some agricultural crops. Sminthurus viridis, the lucerne flea, has been shown to cause severe damage to agricultural crops,[53] and is considered as a pest in Australia.[54][55] Onychiuridae are also known to feed on tubers and to damage them to some extent.[56] However, by their capacity to carry spores of mycorrhizal fungi and mycorrhiza-helper bacteria on their tegument, soil springtails play a positive role in the establishment of plant-fungal symbioses and thus are beneficial to agriculture.[57] They also contribute to controlling plant fungal diseases through their active consumption of mycelia and spores of damping-off and pathogenic fungi.[58][59] It has been suggested that they could be reared to be used for the control of pathogenic fungi in greenhouses and other indoor cultures.[60][61]

Various sources and publications have suggested that some springtails may parasitize humans, but this is entirely inconsistent with their biology, and no such phenomenon has ever been scientifically confirmed, though it has been documented that the scales or hairs from collembolans can cause irritation when rubbed onto the skin.[62] They may sometimes be abundant indoors in damp places such as bathrooms and basements, and incidentally found on one's person. More often, claims of persistent human skin infection by springtails may indicate a neurological problem, such as Morgellons Syndrome, or delusory parasitosis, a psychological rather than entomological problem. Researchers themselves may be subject to psychological phenomena. For example, a publication in 2004 claiming that springtails had been found in skin samples was later determined to be a case of pareidolia; that is, no springtail specimens were actually recovered, but the researchers had digitally enhanced photos of sample debris to create images resembling small arthropod heads, which then were claimed to be springtail remnants.[62][63][64] However, Steve Hopkin reports one instance of an entomologist aspirating an Isotoma species and in the process accidentally inhaling some of their eggs, which hatched in his nasal cavity and made him quite ill until they were flushed out.[22]

Ecotoxicology laboratory animals

Springtails are currently used in laboratory tests for the early detection of soil pollution. Acute and chronic toxicity tests have been performed by researchers, mostly using the parthenogenetic isotomid Folsomia candida.[65] These tests have been standardized.[66] Details on a ringtest, on the biology and ecotoxicology of Folsomia candida and comparison with the sexual nearby species Folsomia fimetaria (sometimes preferred to Folsomia candida) are given in a document written by Paul Henning Krogh.[67] Care should be taken that different strains of the same species mays be conducive to different results. Avoidance tests have been also performed.[68] They have been standardized, too.[69] Avoidance tests are complementary to toxicity tests, but they also offer several advantages: they are more rapid (thus cheaper), more sensitive and they are environmentally more reliable, because in the real world Collembola move actively far from pollution spots.[70] It may be hypothesized that the soil could become locally depauperated in animals (and thus improper to normal use) while below thresholds of toxicity. Contrary to earthworms, and like many insects and molluscs, Collembola are very sensitive to herbicides and thus are threatened in no-tillage agriculture, which makes a more intense use of herbicides than conventional agriculture.[71] The springtail Folsomia candida is also becoming a genomic model organism for soil toxicology.[72][73] With microarray technology the expression of thousands of genes can be measured in parallel. The gene expression profiles of Folsomia candida exposed to environmental toxicants allow fast and sensitive detection of pollution, and additionally clarifies molecular mechanisms causing toxicology.

Collembola have been found to be useful as bio-indicators of soil quality. Laboratory studies have been conducted that validated that the jumping ability of springtails can be used to evaluate the soil quality of Cu- and Ni-polluted sites.[74]

Climate warming impact

In polar regions that are expected to experience among the most rapid impact from climate warming, springtails have shown contrasting responses to warming in experimental warming studies.[75] There are negative,[76][77] positive[78][79] and neutral responses reported.[77][80] Neutral responses to experimental warming have also been reported in studies of non-polar regions.[81] The importance of soil moisture has been demonstrated in experiments using infrared heating in an alpine meadow, which had a negative effect on mesofauna biomass and diversity in drier parts and a positive effect in moist sub-areas.[82] Furthermore, a study with 20 years of experimental warming in three contrasting plant communities found that small scale heterogeneity may buffer springtails to potential climate warming.[80]


Sexual reproduction occurs through the clustered or scattered deposition of spermatophores by male adults. Stimulation of spermatophore deposition by female pheromones has been demonstrated in Sinella curviseta.[83] Mating behaviour can be observed in Symphypleona.[84] Among Symphypleona, males of some Sminthuridae use a clasping organ located on their antenna.[22] Many collembolan species, mostly those living in deeper soil horizons, are parthenogenetic, which favours reproduction to the detriment of genetic diversity and thereby to population tolerance of environmental hazards.[85] Parthenogenesis (also called thelytoky) is under the control of symbiotic bacteria of the genus Wolbachia, which live, reproduce and are carried in female reproductive organs and eggs of Collembola.[86] Feminizing Wolbachia species are widespread in arthropods[87] and nematodes,[88] where they co-evolved with most of their lineages.

See also


  1. Cedric Gillott (2005). "Apterygote hexapods". Entomology (3rd ed.). Berlin: Springer. pp. 113–125. doi:10.1007/1-4020-3183-1_5. ISBN 978-0-306-44967-3.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  2. Reviews, Cram101 Textbook (2015-11-04). Vertebrate Life. Cram101 Textbook Reviews. ISBN 9781467269377.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  3. Frédéric Delsuc, Matthew J. Phillips & David Penny (2003). "Comment on Hexapod origins: monophyletic or paraphyletic?" (PDF). Science. 301 (5639): 1482. doi:10.1126/science.1086558. PMID 12970547.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  4. Francesco Nardi, Giacomo Spinsanti, Jeffrey L. Boore, Antonio Carapelli, Romano Dallai & Francesco Frati (2003). "Hexapod origins: monophyletic or paraphyletic?" (PDF). Science. 299 (5614): 1887–1889. doi:10.1126/science.1078607. PMID 12649480.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  5. Francesco Nardi, Giacomo Spinsanti, Jeffrey L. Boore, Antonio Carapelli, Romano Dallai & Francesco Frati (2003). "Response to comment on Hexapod origins: monophyletic or paraphyletic?" (PDF). Science. 301 (5639): 1482. doi:10.1126/science.1087632.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  6. 6.0 6.1 Yan Gao, Yun Bu & Yun-Xia Luan (2008). "Phylogenetic relationships of basal hexapods reconstructed from nearly complete 18S and 28S rRNA gene sequences" (PDF). Zoological Science. 25 (11): 1139–1145. doi:10.2108/zsj.25.1139. PMID 19267625.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  7. Alexandre Hassanin (2006). "Phylogeny of Arthropoda inferred from mitochondrial sequences: strategies for limiting the misleading effects of multiple changes in pattern and rates of substitution" (PDF). Molecular Phylogenetics and Evolution. 38 (1): 100–116. doi:10.1016/j.ympev.2005.09.012. PMID 16290034.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  8. Nyle C. Brady & Ray R. Weil (2009). "Organisms and ecology of the soil". Elements of the nature and properties of soils (3rd ed.). Upper Saddle River: Prentice Hall. ISBN 978-0-13-501433-2.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  9. Torsten Thimm, Andrea Hoffmann, Heinz Borkott, Jean Charles Munch & Christoph C. Tebbe (1998). "The gut of the soil microarthropod Folsomia candida (Collembola) is a frequently changeable but selective habitat and a vector for microorganisms" (PDF). Applied and Environmental Microbiology. 64 (7): 2660–2669. PMC 106441. PMID 9647845.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  10. W. Maldwyn Davies (1927). "On the tracheal system of Collembola, with special reference to that of Sminthurus viridis, Lubb" (PDF). Quarterly Journal of Microscopical Science. 71 (281): 15–30.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  11. 11.0 11.1 Ross Piper (2007). Extraordinary animals: an encyclopedia of curious and unusual animals. Santa Barbara: Greenwood Press.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  12. "The incredible shrinking springtail". Science. 341 (6149): 945. 30 August 2013. doi:10.1126/science.341.6149.945-a.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  13. "Checklist of the Collembola". Retrieved January 2, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  14. Howell V. Daly, John T. Doyen & Alexander H. Purcell (1998). Introduction to insect biology and diversity (2nd ed.). New York: Oxford University Press. ISBN 0-19-510033-6.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  15. "Hexapoda. Insects, springtails, diplurans, and proturans". Tree of Life Web Project. January 1, 2002. Retrieved January 2, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  16. José A. Mari Mutt (1983). "Collembola in amber from the Dominican Republic" (PDF). Proceedings of the Entomological Society of Washington. 85 (3): 575–587.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  17. André Nel, Gaėl De Ploëg, Jacqueline Milliet, Jean-Jacques Menier & Alain Waller (2004). "The French ambers: a general conspectus and the Lowermost Eocene amber deposit of Le Quesnoy in the Paris Basin" (PDF). Geologica Acta. 2 (1): 3–8.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  18. David Penney, Andrew McNeil, Andrew, David I. Green, Robert S. Bradley, Robert S., James E. Jepson, Philip J. Withers & Richard F. Preziosi (2012). "Ancient Ephemeroptera-Collembola symbiosis fossilized in amber predicts contemporary phoretic associations" (PDF). PlosOne. 7 (10): e47651. doi:10.1371/journal.pone.0047651.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  19. Kenneth Christiansen & Paul Nascimbene (2006). "Collembola (Arthropoda, Hexapoda) from the mid Cretaceous of Myanmar (Burma)" (PDF). Cretaceous Research. 27 (3): 318–33. doi:10.1016/j.cretres.2005.07.003.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  20. Koehler, Philip G.; Aparicio, ML; Pfiester, Margaret (July 2011). "Springtails" (PDF). University of Florida IFAS Extension. Retrieved January 2, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  21. Benrong Chen, Richard J. Snider & Renate M. Snider (1996). "Food consumption by Collembola from northern Michigan deciduous forest". Pedobiologia. 40 (2): 149–161.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  22. 22.0 22.1 22.2 Stephen P. Hopkin (1997). "The biology of the Collembola (springtails): the most abundant insects in the world" (PDF). Natural History Museum. Retrieved January 2, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  23. Jean-François Ponge (1991). "Food resources and diets of soil animals in a small area of Scots pine litter" (PDF). Geoderma. 49 (1–2): 33–62. doi:10.1016/0016-7061(91)90090-G.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  24. Jean-François Ponge, Pierre Arpin, Francis Sondag & Ferdinand Delecour (1997). "Soil fauna and site assessment in beech stands of the Belgian Ardennes" (PDF). Canadian Journal of Forest Research. 27 (12): 2053–2064. doi:10.1139/cjfr-27-12-2053.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  25. 25.0 25.1 25.2 25.3 25.4 Jean-François Ponge (1993). "Biocenoses of Collembola in atlantic temperate grass-woodland ecosystems" (PDF). Pedobiologia. 37 (4): 223–244.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  26. Island Creek Elementary School. "Snow Flea. Hypogastrura nivicola". Study of Northern Virginia Ecology. Fairfax County Public Schools. Retrieved January 2, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  27. Peter Shaw, Claire Ozanne, Martin Speight & Imogen Palmer (2007). "Edge effects and arboreal Collembola in coniferous plantations". Pedobiologia. 51 (4): 287–293. doi:10.1016/j.pedobi.2007.04.010.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  28. Jürg Zettel, Ursula Zettel & Beatrice Egger (2000). "Jumping technique and climbing behaviour of the collembolan Ceratophysella sigillata (Collembola: Hypogastruridae)" (PDF). European Journal of Entomology. 97 (1): 41–45. doi:10.14411/eje.2000.010.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  29. 29.0 29.1 Wim A. M. Didden (1987). "Reactions of Onychiurus fimatus (Collembola) to loose and compact soil: methods and first results". Pedobiologia. 30 (2): 93–100.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  30. Denis J. Rodgers & Rodger L. Kitching (1998). "Vertical stratification of rainforest collembolan (Collembola: Insecta) assemblages: description of ecological patterns and hypotheses concerning their generation" (PDF). Ecography. 21 (4): 392–400. doi:10.1111/j.1600-0587.1998.tb00404.x.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  31. John Bowden, Ian H. Haines & D. Mercer (1976). "Climbing Collembola". Pedobiologia. 16 (4): 298–312.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  32. Eveline J. Krab, Hilde Oorsprong, Matty P. Berg & Johannes H.C. Cornelissen (2010). "Turning northern peatlands upside down: disentangling microclimate and substrate quality effects on vertical distribution of Collembola" (PDF). Functional Ecology. 24 (6): 1362–1369. doi:10.1111/j.1365-2435.2010.01754.x.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  33. Julia Nickerl, Ralf Helbig, Hans-Jürgen Schulz, Carsten Werner, & Christoph Neinhuis (2013). "Diversity and potential correlations to the function of Collembola cuticle structures". Zoomorphology. 132 (2): 183–195. doi:10.1007/s00435-012-0181-0.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  34. Martin Holmstrup & Mark Bayley (2013). "Protaphorura tricampata, a euedaphic and highly permeable springtail that can sustain activity by osmoregulation during extreme drought". Journal of Insect Physiology. 59 (11): 1104–1110. doi:10.1016/j.jinsphys.2013.08.015.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  35. Herman A. Verhoef (1984). "Releaser and primer pheromones in Collembola". Journal of Insect Physiology. 30 (8): 665–670. doi:10.1016/0022-1910(84)90052-0.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  36. Joshua B. Benoit, Michael A. Elnitsky, Glen G. Schulte, Richard E. Lee Jr & David L. Denlinger (2009). "Antarctic Collembolans use chemical signals to promote aggregation and egg laying" (PDF). Journal of Insect Behavior. 22 (2): 121–133. doi:10.1007/s10905-008-9159-7.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  37. Andreas Prinzing, Cyrille A. D'Haese, Sandrine Pavoine & Jean-François Ponge (2014). "Species living in harsh environments have low clade rank and are localized on former Laurasian continents: a case study of Willemia (Collembola)" (PDF). Journal of Biogeography. 41 (2): 353–365. doi:10.1111/jbi.12188.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  38. Herman A. Verhoef (1981). "Water balance in Collembola and its relation to habitat selection: water content, haemolymph osmotic pressure and transpiration during an instar". Journal of Insect Physiology. 27 (11): 755–760. doi:10.1016/0022-1910(81)90065-2.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  39. Hans Petter Leinaas (1983). "Synchronized moulting controlled by communication in group-living Collembola". Science. 219 (4581): 193–195. doi:10.1126/science.219.4581.193.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  40. Jane M. Wilson (1982). "A review of world Troglopedetini (Insecta, Collembola, Paronellidae), including an identification table and descriptions of new species" (PDF). Cave Science: Transactions of the British Cave Research Association. 9 (3): 210–226.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  41. José G. Palacios-Vargas & Jane Wilson (1990). "Troglobius coprophagus, a new genus and species of cave collembolan from Madagascar with notes on its ecology" (PDF). International Journal of Speleology. 19 (1–4): 67–73. doi:10.5038/1827-806x.19.1.6.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  42. Rafael Jordana, Enrique Baquero, Sofía Reboleira & Alberto Sendra (2012). "Reviews of the genera Schaefferia Absolon, 1900, Deuteraphorura Absolon, 1901, Plutomurus Yosii, 1956 and the Anurida Laboulbène, 1865 species group without eyes, with the description of four new species of cave springtails (Collembola) from Krubera-Voronya cave, Arabika Massif, Abkhazia". Terrestrial Arthropod Reviews. 5 (1): 35–85. doi:10.1163/187498312X622430.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  43. Sandrine Salmon, Jean-François Ponge & Nico Van Straalen (2002). "Ionic identity of pore water influences pH preference in Collembola" (PDF). Soil Biology and Biochemistry. 34 (11): 1663–1667. doi:10.1016/S0038-0717(02)00150-5.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  44. Gladys Loranger, Ipsa Bandyopadhyaya, Barbara Razaka & Jean-François Ponge (2001). "Does soil acidity explain altitudinal sequences in collembolan communities?" (PDF). Soil Biology and Biochemistry. 33 (3): 381–393. doi:10.1016/S0038-0717(00)00153-X.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  45. Jack H. Faber & Els N.G. Joosse (1993). "Vertical distribution of Collembola in a Pinus nigra organic soil". Pedobiologia. 37 (6): 336–350.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  46. Vassilis Detsis (2000). "Vertical distribution of Collembola in deciduous forests under Mediterranean climatic conditions" (PDF). Belgian Journal of Zoology. 130 (Supplement 1): 57–61.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  47. "Isotomurus palustris (Muller, 1776)". Retrieved January 3, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  48. Sylvain Pichard (1973). "Contribution à l'étude de la biologie de Podura aquatica (Linné) Collembole". Bulletin Biologique de la France et de la Belgique (in French). 107 (4): 291–299.CS1 maint: unrecognized language (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  49. Jean-François Ponge, Servane Gillet, Florence Dubs, Eric Fédoroff, Lucienne Haese, José Paulo Sousa & Patrick Lavelle (2003). "Collembolan communities as bioindicators of land use intensification" (PDF). Soil Biology and Biochemistry. 35 (6): 813–826. doi:10.1016/S0038-0717(03)00108-1.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  50. Jean-François Ponge, Florence Dubs, Servane Gillet, Jose Paulo Sousa & Patrick Lavelle (2006). "Decreased biodiversity in soil springtail communities: the importance of dispersal and landuse history in heterogeneous landscapes" (PDF). Soil Biology and Biochemistry. 38 (5): 1158–1161. doi:10.1016/j.soilbio.2005.09.004.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  51. Sara Cristofoli & Grégory Mahy (2010). "Colonisation credit in recent wet heathland butterfly communities". Insect Conservation and Diversity. 3 (2): 83–91. doi:10.1111/j.1752-4598.2009.00075.x.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  52. Charlène Heiniger, Sébastien Barot, Jean-François Ponge, Sandrine Salmon, Léo Botton-Divet, David Carmignac & Florence Dubs (2014). "Effect of habitat spatiotemporal structure on collembolan diversity" (PDF). Pedobiologia. 57 (2): 103–117. doi:10.1016/j.pedobi.2014.01.006.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  53. Michael W. Shaw & G. M. Haughs (1983). "Damage to potato foliage by Sminthurus viridis (L.)". Plant Pathology. 32 (4): 465–466. doi:10.1111/j.1365-3059.1983.tb02864.x.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  54. Alan L. Bishop, Anne M. Harris, Harry J. McKenzie (2001). "Distribution and ecology of the lucerne flea, Sminthurus viridis (L.) (Collembola: Sminthuridae), in irrigated lucerne in the Hunter dairying region of New South Wales". Australian Journal of Entomology. 40 (1): 49–55. doi:10.1046/j.1440-6055.2001.00202.x.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  55. "Lucerne Flea Sminthurus viridis". Western Australia Department of Agriculture and Food. 2008. Retrieved January 3, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  56. A. N. Baker & R. A. Dunning (1975). "Association of populations of onychiurid Collembola with damage to sugar-beet seedlings". Plant Pathology. 24 (3): 150–154. doi:10.1111/j.1365-3059.1975.tb01882.x.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  57. John N. Klironomos & Peter Moutoglis (1999). "Colonization of nonmycorrhizal plants by mycorrhizal neighbours as influenced by the collembolan, Folsomia candida". Biology and Fertility of Soils. 29 (3): 277–281. doi:10.1007/s003740050553.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  58. Maria Agnese Sabatini & Gloria Innocenti (2001). "Effects of Collembola on plant-pathogenic fungus interactions in simple experimental systems". Biology and Fertility of Soils. 33 (1): 62–66. doi:10.1007/s003740000290.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  59. Hiroyoshi Shiraishi, Yoshinari Enami & Seigo Okano (2003). "Folsomia hidakana (Collembola) prevents damping-off disease in cabbage and Chinese cabbage by Rhizoctonia solani". Pedobiologia. 47 (1): 33–38. doi:10.1078/0031-4056-00167.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  60. Jean-François Ponge & Marie-José Charpentié (1981). "Étude des relations microflore-microfaune: expériences sur Pseudosinella alba (Packard), Collembole mycophage" (PDF). Revue d'Écologie et de Biologie du Sol (in french). 18: 291–303.CS1 maint: unrecognized language (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  61. Robert T. Lartey, Elroy A. Curl, Curt M. Peterson & James D. Harper (1989). "Mycophagous grazing and food preference of Proisotoma minuta (Collembola: Isotomidae) and Onychiurus encarpatus (Collembola: Onychiuridae)". Environmental Entomology. 18 (2): 334–337. doi:10.1093/ee/18.2.334.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  62. 62.0 62.1 Frans Janssens & Kenneth A. Christiansen (November 22, 2007). "Synanthropic Collembola, springtails in association with Man". Checklist of the Collembola. Retrieved January 10, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  63. May Berenbaum (2005). "Face Time" (PDF). American Entomologist. 51 (2): 68–69. doi:10.1093/ae/51.2.68.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  64. Kenneth Christiansen & Ernest C. Bernard (2008). "Critique of the article "Collembola (Springtails) (Arthropoda: Hexapoda: Entognatha) found in scrapings from individuals diagnosed with delusory parasitosis"". Entomological News. 119 (5): 537–540. doi:10.3157/0013-872x-119.5.537.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  65. Michelle T. Fountain & Steve P. Hopkin (2001). "Continuous monitoring of Folsomia candida (Insecta: Collembola) in a metal exposure test" (PDF). Ecotoxicology and Environmental Safety. 48 (3): 275–286. doi:10.1006/eesa.2000.2007. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  66. ISO 11267 (2014). "Soil quality. Inhibition of reproduction of Collembola (Folsomia candida) by soil contaminants". Geneva: International Organization for Standardization.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  67. Paul Henning Krogh (August 1, 2008). "Toxicity testing with the collembolans Folsomia fimetaria and Folsomia candida and the results of a ringtest" (PDF). Retrieved January 10, 2016.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  68. Christine Lors, Maite Martínez Aldaya, Sandrine Salmon & Jean-François Ponge (2006). "Use of an avoidance test for the assessment of microbial degradation of PAHs" (PDF). Soil Biology and Biochemistry. 38 (8): 2199–2204. doi:10.1016/j.soilbio.2006.01.026.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  69. ISO 17512-2 (2011). "Soil quality. Avoidance test for determining the quality of soils and effects of chemicals on behaviour. Part 2: Test with collembolans (Folsomia candida)". Geneva: International Organization for Standardization.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  70. Matthieu Chauvat & Jean-François Ponge (2002). "Colonization of heavy metal-polluted soils by collembola: preliminary experiments in compartmented boxes" (PDF). Applied Soil Ecology. 21 (2): 91–106. doi:10.1016/S0929-1393(02)00087-2.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  71. Jean-François Ponge, Ipsa Bandyopadhyaya & Valérie Marchetti (2002). "Interaction between humus form and herbicide toxicity to Collembola (Hexapoda)" (PDF). Applied Soil Ecology. 20 (3): 239–253. doi:10.1016/S0929-1393(02)00026-4.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  72. Benjamin Nota, Martijn J.T.N. Timmermans, Oscar Franken, Kora Montagne-Wajer, Janine Mariën, Muriel E. De Boer, Tjalf E. De Boer, Bauke Ylstra, Nico M. Van Straalen & Dick Roelofs (2008). "Gene expression analysis of Collembola in cadmium containing soil" (PDF). Environmental Science and Technology. 42 (21): 8152–8157. doi:10.1021/es801472r. PMID 19031917.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  73. Benjamin Nota, Mirte Bosse, Bauke Ylstra, Nico M. Van Straalen & Dick Roelofs (2009). "Transcriptomics reveals extensive inducible biotransformation in the soil-dwelling invertebrate Folsomia candida exposed to phenanthrene" (PDF). BMC Genomics. 10: 236. doi:10.1186/1471-2164-10-236. PMC 2688526. PMID 19457238.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  74. Shin Woong Kim & Youn-Joo An (2014). "Jumping behavior of the springtail Folsomia candida as a novel soil quality indicator in metal-contaminated soils". Ecological Indicators. 38: 67–71. doi:10.1016/j.ecolind.2013.10.033.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  75. Uffe N. Nielsen, Diana H. Wall (2013). "The future of soil invertebrate communities in polar regions: different climate change responses in the Arctic and Antarctic?" (PDF). Ecology Letters. 16 (3): 409–419. doi:10.1111/ele.12058. PMID 23278945. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  76. Stephen James Coulson, Ian D. Hodkinson, Christopher Woolley, Nigel R. Webb, William Block, M. Rodger Worland, Jeff S. Bale & Andrew T. Strathdee (1996). "Effects of experimental temperature elevation on high-arctic soil microarthropod populations". Polar Biology. 16 (2): 147–153. doi:10.1007/BF02390435.CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  77. 77.0 77.1 Heidi Sjursen, Anders Michelsen & Sven Jonasson (2005). "Effects of long-term soil warming and fertilisation on microarthropod abundances in three sub-arctic ecosystems". Applied Soil Ecology. 30 (3): 148–161. doi:10.1016/j.apsoil.2005.02.013.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  78. Rebecca Dollery, Ian D. Hodkinson & Ingibjörg S. Jónsdóttir (2006). "Impact of warming and timing of snow melt on soil microarthropod assemblages associated with Dryas-dominated plant communities on Svalbard" (PDF). Ecography. 29 (1): 111–119. doi:10.1111/j.2006.0906-7590.04366.x. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  79. Sigmund Hågvar & Kari Klanderud (2009). "Effect of simulated environmental change on alpine soil arthropods" (PDF). Global Change Biology. 15 (12): 2972–2980. doi:10.1111/j.1365-2486.2009.01926.x. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  80. 80.0 80.1 Juha M. Alatalo, Annika K. Jägerbrand & Peter Čuchta (2015). "Collembola in three alpine subarctic sites resistant to twenty years of experimental warming" (PDF). Scientific Reports. 5 (18161). doi:10.1038/srep18161. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  81. Paul Kardol, W. Nicholas Reynolds, Richard J. Norby & Aimee T. Classen (2011). "Climate change effects on soil microarthropod abundance and community structure" (PDF). Applied Soil Ecology. 47 (1): 37–44. doi:10.1016/j.apsoil.2010.11.001. Italic or bold markup not allowed in: |journal= (help)CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  82. John Harte, Agnieszka Rawa & Vanessa Price (1996). "Effects of manipulated soil microclimate on mesofaunal biomass and diversity" (PDF). Soil Biology and Biochemistry. 28 (3): 313–322. doi:10.1016/0038-0717(95)00139-5. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  83. Elizabeth S. Waldorf (1974). "Sex pheromone in the springtail Sinella curviseta". Environmental Entomology. 3 (6): 916–918. doi:10.1093/ee/3.6.916. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  84. Marek Wojciech Kozlowski & Shi Aoxiang (2006). "Ritual behaviors associated with spermatophore transfer in Deuterosminthurus bicinctus (Collembola : Bourletiellidae)". Journal of Ethology. 24 (2): 103–110. doi:10.1007/s10164-005-0162-6. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  85. Jean-Christophe Simon, François Delmote, Claude Rispe & Teresa Crease (2003). "Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals" (PDF). Biological Journal of the Linnean Society. 79 (1): 151–153. doi:10.1046/j.1095-8312.2003.00175.x. Italic or bold markup not allowed in: |journal= (help)CS1 maint: multiple names: authors list (link)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  86. Alice B. Czarnetzki & Christoph C. Tebbe (2004). "Detection and phylogenetic analysis of Wolbachia in Collembola". Environmental Microbiology. 6 (1): 35–44. doi:10.1046/j.1462-2920.2003.00537.x. PMID 14686939. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  87. John H. Werren, Wan Zhang & Li Rong Guo (1995). "Evolution and phylogeny of Wolbachia: reproductive parasites of arthropods" (PDF). Proceedings of the Royal Society B. 261 (1360): 55–63. doi:10.1098/rspb.1995.0117. JSTOR 50047. PMID 7644549. Italic or bold markup not allowed in: |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  88. Katelyn Fenn & Mark Blaxter (2004). "Are filarial nematode Wolbachia obligate mutualist symbionts?". Trends in Ecology and Evolution. 19 (4): 163–166. doi:10.1016/j.tree.2004.01.002. PMID 16701248.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>

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