Springtails(classCollembola) form the largest of the three lineages of modernhexapodsthat are no longer consideredinsects.Although the three orders are sometimes grouped together in a class calledEntognathabecause they have internalmouthparts,they do not appear to be any more closely related to one another than they are to all insects, which have external mouthparts.

Springtails
Temporal range:Early Devonian – present
Orchesella cincta
Scientific classificationEdit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Clade: Pancrustacea
Subphylum: Hexapoda
Class: Collembola
Lubbock,1871
Orders
Synonyms[1]
  • Oligentoma
  • Oligoentoma

Springtails areomnivorous,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[2]and the control of soil microbial communities.[3]The wordCollembolais from the ancient Greekκόλλαkólla"glue" andἔμβολοςémbolos"peg"; this name was given due to the existence of thecollophore,which was previously thought to stick to surfaces to stabilize the creature.[4]

EarlyDNA sequencestudies[5][6][7]suggested that Collembola represent a separateevolutionary linefrom the otherHexapoda,but others disagree;[8]this seems to be caused by widely divergent patterns ofmolecular evolutionamong thearthropods.[9]The adjustments of traditionaltaxonomic rankfor springtails reflect the occasional incompatibility of traditional groupings with moderncladistics:when they were included with the insects, they were ranked as anorder;as part of the Entognatha, they are ranked as asubclass.If they are considered abasallineage of Hexapoda, they are elevated to fullclassstatus.

Morphology

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Isotoma anglicana(Entomobryomorpha) with visible furcula
Deutonura monticola(Poduromorpha)

Members of the Collembola are normally less than 6 mm (0.24 in) long, have six or fewerabdominalsegments,and possess a tubularappendage(thecollophoreor ventral tube) with reversible, sticky vesicles, projecting ventrally from the first abdominal segment.[10]It is believed to be associated with fluid uptake and balance, excretion, and orientation of the organism itself.[11]Most species have an abdominal, tail-like appendage known as afurcula(or furca). It is located on the fourth abdominal segment of springtails and is folded beneath the body, held under tension by a small structure called theretinaculum(or tenaculum). When released, it snaps against the substrate, flinging the springtail into the air and allowing for rapid evasion and travel. All of this takes place in as little as 18 milliseconds.[12][11]

Springtails also possess the ability to reduce their body size by as much as 30% through subsequentecdyses(moulting) 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.[13]

ThePoduromorphaandEntomobryomorphahave an elongated body, while theSymphypleonaandNeelipleonahave a globular body. Collembola lack atrachealrespiration system, which forces them to respire through aporouscuticle,except for the two familiesSminthuridaeand Actaletidae, which exhibit a single pair ofspiraclesbetween the head and thethorax,leading to a rudimentary, although fully functional, tracheal system.[14][10]The anatomical variance present between different species partially depends onsoil morphologyand composition. Surface-dwellers are generally larger, have darker pigments, have longer antennae and functioning furcula. Sub-surface-dwellers are usually unpigmented, have elongated bodies, and reduced furcula. They can be categorized into four main forms according to soil composition and depth: atmobiotic, epedaphic, hemiedaphic, and euedaphic. Atmobiotic species inhabit macrophytes and litter surfaces. They are generally 8-10 millimeters (about ⅓ ") in length, pigmented, have long limbs, and a full set ofocelli(photoreceptors). Epedaphic species inhabit upper litter layers and fallen logs. They are slightly smaller and have less pronounced pigments, as well as less developed limbs and ocelli than the atmobiotic species. Hemiedaphic species inhabit the lower litter layers of decomposing organic material. They are 1-2 millimeters (about 1/16 ") in length, have dispersed pigmentation, shortened limbs, and a reduced number of ocelli. Euedaphic species inhabit upper mineral layers known as the humus horizon. They are smaller than hemiedaphic species; have soft, elongated bodies; lack pigmentation and ocelli; and have reduced or absent furca.[15][16][17]

Poduromorphs are characterized by their elongated bodies and conspicuous segmentation – three thoracic segments, six abdominal segments, including a well-developedprothoraxwith tergal chaetae,[17]while the first thoracic segment in Entomobryomorpha is clearly reduced and bears no chaetae.

The digestive tract of springtails consists of three main components: the foregut, midgut, and hindgut. The midgut is surrounded by a network of muscles and lined with a monolayer of columnar or cuboidal cells. Its function is to mix and transport food from the lumen into the hindgut through contraction. Many species of syntrophic bacteria, archaea, and fungi are present in the lumen. These different digestive regions have varying pH to support specific enzymatic activities and microbial populations. The anterior portion of the midgut and hindgut is slightly acidic (with a pH of approximately 6.0) while the posterior midgut portion is slightly alkaline (with a pH of approximately 8.0). Between the midgut and hindgut is an alimentary canal called the pyloric region, which is a muscular sphincter.[11]Malpighian tubulesare absent.[18]

Systematics and evolution

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Allacma fusca(Symphypleona) on rotting wood

Traditionally, the springtails were divided into theordersArthropleona,Symphypleona,and occasionally alsoNeelipleona.The Arthropleona were divided into twosuperfamilies,theEntomobryoideaand thePoduroidea.However, recent phylogenetic studies show Arthropleona isparaphyletic.[19][20][21]Thus, the Arthropleona are abolished in modern classifications, and their superfamilies are raised in rank accordingly, being now ordersEntomobryomorphaand thePoduromorpha.Technically, the Arthropleona are thus a partialjunior synonymof the Collembola.[22]

The term "Neopleona" is essentially synonymous with Symphypleona + Neelipleona.[23]The Neelipleona was originally seen as a particularly advanced lineage of Symphypleona, based on the shared global body shape, but the global body of the Neelipleona is realized in a completely different way than in Symphypleona. Subsequently, the Neelipleona were considered as being derived from the Entomobryomorpha. Analysis of18Sand28SrRNAsequencedata, though, suggests that they form the most ancient lineage of springtails, which would explain their peculiarapomorphies.[8]This phylogenetic relationship was also confirmed using a phylogeny based onmtDNA[20]andwhole-genome data.[21]

The latest whole-genome phylogeny supporting four orders of Collembola:[21]

Springtails are attested to since theEarly Devonian.[24]The fossil from400million years ago,Rhyniella praecursor,is the oldest terrestrial arthropod, and was found in the famousRhynie chertofScotland.Given its morphology resembles extant species quite closely, the radiation of theHexapodacan be situated in theSilurian,420million years agoor more.[25]Additional research concerning the coprolites (fossilized feces) of ancient springtails allowed researchers to track their lineages back some 412 million years.[11]

Fossil Collembola are rare. Instead, most are found in amber.[26]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,[27]Miocene of Central America,[28]and the mid-Cretaceous of Burma and Canada.[29]They display some unexplained 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.[30]

Ecology

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Eating behavior

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Specific feeding strategies and mechanisms are employed to match specific niches.[31]Herbivorous and detritivorous species fragment biological material present in soil and leaf litter, supporting decomposition and increasing the availability of nutrients for various species of microbes and fungi.[32]Carnivorous species maintain populations of small invertebrates such as nematodes, rotifers, and other collembolan species.[11][15]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.[33]

Predators

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Springtails are consumed bymesostigmatanmites in various families, includingAscidae,Laelapidae,Parasitidae,RhodacaridaeandVeigaiidae.[34]

Cave-dwelling springtails are a food source forspidersandharvestmenin the same environment, such as the endangered harvestmanTexella reyesi.[35]

To protect themselves, some species have evolved chemical defenses.[36]

Distribution

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Springtails arecryptozoafrequently found inleaf litterand other decaying material,[37]where they are primarilydetritivoresandmicrobivores,and one of the main biological agents responsible for the control and the dissemination of soilmicroorganisms.[38]In a mature deciduous woodland in temperate climate, leaf litter and vegetation typically support 30 to 40 species of springtails, and in the tropics the number may be over 100.[39]

"Snow flea"
A species ofSminthurinae(Symphypleona:Sminthuridae)

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,[40]essentially everywhere on Earth where soil and related habitats (mosscushions, fallenwood,grasstufts,antandtermitenests) occur.[41]Onlynematodes,crustaceans,andmitesare 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 aphylumand crustaceans asubphylum.Most springtails are small and difficult to see by casual observation, but one springtail, the so-calledsnow 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.[42]

In addition, a few species routinely climb trees and form a dominant component of canopy fauna, where they may be collected by beating or insecticide fogging.[43][44]These tend to be the larger (>2 mm) species, mainly in the generaEntomobryaandOrchesella,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.Anurophorusspp.,Entomobrya albocincta,Xenylla xavieri,Hypogastrura arborea) are almost exclusively arboreal.[41]In tropical regions a single square meter of canopy habitat can support many species of Collembola.[12]

The mainecological factordriving the local distribution of species is the vertical stratification of the environment: inwoodlanda continuous change in species assemblages can be observed from treecanopiesto groundvegetationthen toplant litterdown to deepersoil horizons.[41]This is a complex factor embracing bothnutritionalandphysiologicalrequirements, together with behavioural trends,[45]dispersal limitation[46]and probable speciesinteractions.Some species have been shown to exhibit negative[47]or positive[45]gravitropism,which adds abehaviouraldimension 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".[48]

Dicyrtominasp. on leaf

As a group, springtails are highly sensitive todesiccation,because of their tegumentaryrespiration,[49]although some species with thin, permeable cuticles have been shown to resist severe drought by regulating the osmotic pressure of their body fluid.[50]The gregarious behaviour of Collembola, mostly driven by the attractive power ofpheromonesexcreted by adults,[51]gives more chance to every juvenile or adult individual to find suitable, better protected places, where desiccation could be avoided andreproductionandsurvivalrates (therebyfitness) could be kept at an optimum.[52]Sensitivity to drought varies from species to species[53]and increases duringecdysis.[54]Given that springtailsmoultrepeatedly during their entire life (anancestralcharacter inHexapoda) they spend much time in concealed micro-sites where they can find protection againstdesiccationandpredationduring ecdysis, an advantage reinforced by synchronized moulting.[55]The high humidity environment of many caves also favours springtails and there are numerous cave adapted species,[56][57]including one,Plutomurus ortobalaganensisliving 1,980 metres (6,500 ft) down theKrubera Cave.[58]

Anurida maritimaon water

The horizontal distribution of springtail species is affected by environmental factors which act at the landscape scale, such as soilacidity,moistureandlight.[41]Requirements forpHcan be reconstructed experimentally.[59]Altitudinal changes in species distribution can be at least partly explained by increased acidity at higher elevation.[60]Moisture requirements, among other ecological and behavioural factors, explain why some species cannot live aboveground,[61]or retreat in the soil during dry seasons,[62]but also why someepigealspringtails are always found in the vicinity of ponds and lakes, such as the hygrophilousIsotomurus palustris.[63]Adaptivefeatures, such as the presence of a fan-like wettable mucro, allow some species to move at the surface of water in freshwater and marine environments.[64]Podura aquatica,a unique representative of the familyPoduridae(and one of the first springtails to have been described byCarl 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.[65]A few genera are capable of being submerged, and after molting young springtails lose their water repellent properties and are able to survive submerged under water.[66]

In a variegated landscape, made of a patchwork of closed (woodland) and open (meadows,cereal crops) environments, mostsoil-dwelling species are not specialized and can be found everywhere, but mostepigealandlitter-dwelling species are attracted to a particular environment, either forested or not.[41][67]As a consequence ofdispersallimitation,landusechange, when too rapid, may cause the local disappearance of slow-moving,specialist species,[68]a phenomenon the measure of which has been called colonisation credit.[69][70]

Relationship with humans

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Tomocerussp. from Germany

Springtails are well known aspestsof some agricultural crops.Sminthurus viridis,the lucerne flea, has been shown to cause severe damage to agricultural crops,[71]and is considered as a pest in Australia.[72][73]Onychiuridae are also known to feed on tubers and to damage them to some extent.[74]However, by their capacity to carry spores ofmycorrhizal fungiandmycorrhiza helper bacteriaon their tegument, soil springtails play a positive role in the establishment of plant-fungalsymbiosesand thus are beneficial to agriculture.[75]They also contribute to controlling plantfungal diseasesthrough their active consumption ofmyceliaandsporesofdamping-offandpathogenicfungi.[76][77]It has been suggested that they could be reared to be used for the control ofpathogenic fungiin greenhouses and other indoor cultures.[78][79]

Various sources and publications have suggested that some springtails mayparasitizehumans, 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 springtails can cause irritation when rubbed onto the skin.[80]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 asdelusional 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 ofpareidolia;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.[80][81][82][83][84]However, Steve Hopkin reports one instance of an entomologistaspiratinganIsotomaspecies 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.[39]

In 1952,Chinaaccused theUnited Statesmilitary of spreading bacteria-laden insects and other objects during theKorean Warby dropping them fromP-51fighters above rebel villages overNorth Korea.In all, the U.S. was accused of dropping ants, beetles, crickets, fleas, flies, grasshoppers, lice, springtails, and stoneflies as part of abiological warfareeffort. The alleged associated diseases includedanthrax,cholera,dysentery,fowl septicemia,paratyphoid,plague,scrub typhus,small pox,andtyphoid.China created an international scientific commission for investigating possible bacterial warfare, eventually ruling that the United States probably did engage in limited biological warfare in Korea. TheUS governmentdenied all the allegations, and instead proposed that the United Nations send a formal inquiry committee to China and Korea, but China and Korea refused to cooperate. U.S. and Canadian entomologists further claimed that the accusations were ridiculous and argued that anomalous appearances of insects could be explained through natural phenomena.[85]Springtail species cited inallegations of biological warfare in the Korean WarwereIsotoma (Desoria) negishina(a local species) and the "white rat springtail"Folsomia candida.[86]

Captive springtails are often kept in aterrariumas part of aclean-up crew.[87]

Ecotoxicology laboratory animals

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Springtails are currently used in laboratory tests for the early detection ofsoil pollution.Acuteandchronic toxicitytests have been performed by researchers, mostly using theparthenogeneticisotomidFolsomia candida.[88]These tests have been standardized.[89]Details on aringtest,on the biology andecotoxicologyofFolsomia candidaand comparison with the sexual nearby speciesFolsomia fimetaria(sometimes preferred toFolsomia candida) are given in a document written by Paul Henning Krogh.[90]Care should be taken that different strains of the same species may be conducive to different results. Avoidance tests have been also performed.[91]They have been standardized, too.[92]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.[93]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 toearthworms,and like many insects and molluscs, Collembola are very sensitive toherbicidesand thus are threatened in no-tillage agriculture, which makes a more intense use of herbicides than conventional agriculture.[94] The springtailFolsomia candidais also becoming agenomicmodel organism for soil toxicology.[95][96]Withmicroarraytechnology the expression of thousands of genes can be measured in parallel. The gene expression profiles ofFolsomia candidaexposed 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.[97]

Climate warming impact

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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.[98]There are negative,[99][100]positive[101][102]and neutral responses reported.[100][103]Neutral responses to experimental warming have also been reported in studies of non-polar regions.[104]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.[105]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.[103]

Reproduction

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Sexual reproductionoccurs through the clustered or scattered deposition of spermatophores bymaleadults. Stimulation ofspermatophoredeposition by femalepheromoneshas been demonstrated inSinella curviseta.[106]Mating behaviorcan be observed inSymphypleona.[107]Among Symphypleona, males of someSminthuridaeuse a clasping organ located on theirantenna.[37]Many springtails, mostly those living in deeper soil horizons, are parthenogenetic, which favorsreproductionto the detriment ofgenetic diversityand thereby topopulationtolerance ofenvironmental hazards.[108]Parthenogenesis(also calledthelytoky) is under the control of symbioticbacteriaof the genusWolbachia,which live, reproduce and are carried in female reproductive organs and eggs of Collembola.[109]FeminizingWolbachiaspecies are widespread inarthropods[110]andnematodes,[111]where they co-evolved with most of theirlineages.

See also

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References

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  1. ^Gillott, Cedric (2005). "Apterygote hexapods".Entomology(3rd ed.). Berlin:Springer.pp. 113–125.doi:10.1007/1-4020-3183-1_5.ISBN978-0-306-44967-3.
  2. ^Brady, Nyle C. & Weil, Ray R. (2009). "Organisms and ecology of the soil".Elements of the nature and properties of soils(3rd ed.). Upper Saddle River:Prentice Hall.ISBN978-0-13-501433-2.OCLC276340542.
  3. ^Thimm, Torsten; Hoffmann, Andrea; Borkott, Heinz; Munch, Jean Charles & Tebbe, Christoph C. (1998)."The gut of the soil microarthropodFolsomia candida(Collembola) is a frequently changeable but selective habitat and a vector for microorganisms ".Applied and Environmental Microbiology.64(7): 2660–2669.Bibcode:1998ApEnM..64.2660T.doi:10.1128/AEM.64.7.2660-2669.1998.PMC106441.PMID9647845.
  4. ^Lubbock, John(1873).Monograph of the Collembola and Thysanura.London: Ray Society. p. 36.
  5. ^Nardi, Francesco; Spinsanti, Giacomo; Boore, Jeffrey L.; Carapelli, Antonio; Dallai, Romano; Frati, Francesco (21 March 2003). "Hexapod Origins: Monophyletic or Paraphyletic?".Science.299(5614): 1887–1889.Bibcode:2003Sci...299.1887N.doi:10.1126/science.1078607.PMID12649480.S2CID38792657.
  6. ^Delsuc, Frédéric; Phillips, Matthew J.; Penny, David (12 September 2003)."Comment on 'Hexapod Origins: Monophyletic or Paraphyletic?'"(PDF).Science.301(5639): 1482.doi:10.1126/science.1086558.PMID12970547.S2CID43942720.
  7. ^Nardi, Francesco; Spinsanti, Giacomo; Boore, Jeffrey L.; Carapelli, Antonio; Dallai, Romano; Frati, Francesco (12 September 2003)."Response to Comment on 'Hexapod Origins: Monophyletic or Paraphyletic?'".Science.301(5639): 1482.doi:10.1126/science.1087632.S2CID82407120.
  8. ^abGao, Yan; Bu, Yun; Luan, Yun-Xia (25 November 2008). "Phylogenetic Relationships of Basal Hexapods Reconstructed from Nearly Complete 18S and 28S rRNA Gene Sequences".Zoological Science.25(11): 1139–1145.doi:10.2108/zsj.25.1139.PMID19267625.S2CID10783597.
  9. ^Hassanin, Alexandre (January 2006). "Phylogeny of Arthropoda inferred from mitochondrial sequences: Strategies for limiting the misleading effects of multiple changes in pattern and rates of substitution".Molecular Phylogenetics and Evolution.38(1): 100–116.doi:10.1016/j.ympev.2005.09.012.PMID16290034.
  10. ^abDavies, W. Maldwyn (1 May 1927). "On the Tracheal System of Collembola, with special reference to that of Sminthurus viridis, Lubb".Journal of Cell Science.S2-71 (281): 15–30.doi:10.1242/jcs.s2-71.281.15.
  11. ^abcdeHopkin, Stephen P. (1997).Biology of the springtails (Insecta: Collembola).Oxford: Oxford University Press.
  12. ^abPiper, Ross(2007).Extraordinary animals: an encyclopedia of curious and unusual animals.Santa Barbara, California:Greenwood Press.ISBN9780313339226.OCLC124074839.
  13. ^"Random Sample".Science.341(6149): 945. 30 August 2013.doi:10.1126/science.341.6149.945-a.
  14. ^Ax, Peter (March 9, 2013).Multicellular Animals: Volume II: The Phylogenetic System of the Metazoa.Springer Science & Business Media.ISBN978-3-662-10396-8– via Google Books.
  15. ^abColeman, David C.; Wall, Diana H. (2015). "Soil Fauna".Soil Microbiology, Ecology and Biochemistry.pp. 111–149.doi:10.1016/B978-0-12-415955-6.00005-0.ISBN978-0-12-415955-6.
  16. ^Potapov, Anton A.; Semenina, Eugenia E.; Korotkevich, Anastasiya Yu.; Kuznetsova, Natalia A.; Tiunov, Alexei V. (October 2016). "Connecting taxonomy and ecology: Trophic niches of springtails as related to taxonomic identity and life forms".Soil Biology and Biochemistry.101:20–31.doi:10.1016/j.soilbio.2016.07.002.
  17. ^abJordana, Rafael; Baquero, Enrique; Ledesma, Enrique; Sendra, Alberto; Ortuño, Vicente M. (March 2020). "Poduromorpha (Collembola) from a sampling in the mesovoid shallow substratum of the Sierra de Guadarrama National Park (Madrid and Segovia, Spain): Taxonomy and Biogeography".Zoologischer Anzeiger.285:81–96.doi:10.1016/j.jcz.2020.02.001.S2CID214349457.
  18. ^"Water and ion transport across the eversible vesicles in the collophore of the springtail Orchesella cincta | Journal of Experimental Biology | The Company of Biologists".
  19. ^Xiong, Y; Gao, Y; Yin, W; Luan, Y (December 2008). "Molecular phylogeny of Collembola inferred from ribosomal RNA genes".Molecular Phylogenetics and Evolution.49(3): 728–735.doi:10.1016/j.ympev.2008.09.007.PMID18835455.
  20. ^abLeo, Chiara; Carapelli, Antonio; Cicconardi, Francesco; Frati, Francesco; Nardi, Francesco (17 September 2019)."Mitochondrial Genome Diversity in Collembola: Phylogeny, Dating and Gene Order".Diversity.11(9): 169.doi:10.3390/d11090169.hdl:11365/1079696.
  21. ^abcSun, Xin; Ding, Yinhuan; Orr, Michael C.; Zhang, Feng (May 2020). "Streamlining universal single-copy orthologue and ultraconserved element design: A case study in Collembola".Molecular Ecology Resources.20(3): 706–717.doi:10.1111/1755-0998.13146.PMID32065730.S2CID211133755.
  22. ^"Checklist of the Collembola".RetrievedJanuary 2,2016.
  23. ^Sánchez-García, Alba; Engel, Michael S. (3 July 2017). "Long-term stasis in a diverse fauna of Early Cretaceous springtails (Collembola: Symphypleona)".Journal of Systematic Palaeontology.15(7): 513–537.Bibcode:2017JSPal..15..513S.doi:10.1080/14772019.2016.1194575.S2CID88641582.
  24. ^Daly, Howell V.; Doyen, John T. & Purcell, Alexander H. (1998).Introduction to insect biology and diversity(2nd ed.). New York:Oxford University Press.ISBN978-0-19-510033-4.OCLC925231875.
  25. ^"Hexapoda. Insects, springtails, diplurans, and proturans".Tree of Life Web Project.January 1, 2002.RetrievedMarch 26,2017.
  26. ^Mari Mutt, José A. (1983)."Collembola in amber from the Dominican Republic"(PDF).Proceedings of the Entomological Society of Washington.85(3): 575–587.
  27. ^Nel, André; De Ploëg, Gaėl; Milliet, Jacqueline; Menier, Jean-Jacques & Waller, Alain (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.
  28. ^Penney, David; McNeil, Andrew; Green, David I.; Bradley, Robert S.; Jepson, James E.; Withers, Philip J. & Preziosi, Richard F. (2012)."Ancient Ephemeroptera-Collembola symbiosis fossilized in amber predicts contemporary phoretic associations".PLOS ONE.7(10): e47651.Bibcode:2012PLoSO...747651P.doi:10.1371/journal.pone.0047651.PMC3474712.PMID23082186.
  29. ^Christiansen, Kenneth; Nascimbene, Paul (June 2006). "Collembola (Arthropoda, Hexapoda) from the mid Cretaceous of Myanmar (Burma)".Cretaceous Research.27(3): 318–363.Bibcode:2006CrRes..27..318C.doi:10.1016/j.cretres.2005.07.003.
  30. ^Koehler, Philip G.; Aparicio, M. L. & Pfiester, Margaret (July 2011)."Springtails"(PDF).Gainesville, Florida: University of Florida IFAS Extension.RetrievedMarch 26,2017.
  31. ^Sechi, Valentina; D'Annibale, Alessandra; Ambus, Per; Sárossy, Zsuzsa; Krogh, Paul Henning; Eriksen, Jørgen; Holmstrup, Martin (July 2014). "Collembola feeding habits and niche specialization in agricultural grasslands of different composition".Soil Biology and Biochemistry.74:31–38.doi:10.1016/j.soilbio.2014.02.019.
  32. ^Rusek, Josef (September 1998). "Biodiversity of Collembola and their functional role in the ecosystem".Biodiversity and Conservation.7(9): 1207–1219.Bibcode:1998BiCon...7.1207R.doi:10.1023/a:1008887817883.S2CID22883809.
  33. ^Chen, Benrong; Snider, Richard J. & Snider, Renate M. (1996)."Food consumption by Collembola from northern Michigan deciduous forest"(PDF).Pedobiologia.40(2): 149–161.doi:10.1016/S0031-4056(24)00348-2.
  34. ^Koehler, H.H. (1999). "Predatory mites (Gamasina, Mesostigmata)".Invertebrate Biodiversity as Bioindicators of Sustainable Landscapes.pp. 395–410.doi:10.1016/b978-0-444-50019-9.50022-4.ISBN978-0-444-50019-9.
  35. ^City of Austin and Travis County (September 3, 2020)."Support for Maintaining Endangered Status For the Bone Cave Harvestman (Texella reyesi)".RetrievedOctober 6,2022.
  36. ^Hoffmann, Klaus H. (December 19, 2014).Insect Molecular Biology and Ecology.CRC Press.ISBN978-1-4822-3189-2– via Google Books.
  37. ^abHopkin, Stephen P. (1997)."The biology of the Collembola (springtails): the most abundant insects in the world"(PDF).Natural History Museum.RetrievedJanuary 2,2016.
  38. ^Ponge, Jean-François (1991). "Food resources and diets of soil animals in a small area of Scots pine litter".Geoderma.49(1–2): 33–62.Bibcode:1991Geode..49...33P.CiteSeerX10.1.1.635.8529.doi:10.1016/0016-7061(91)90090-G.
  39. ^abHopkin, Stephen P. (1997).Biology of the Springtails: (Insecta: Collembola).OUP Oxford. p. 127.ISBN978-0-19-158925-6.
  40. ^Ponge, Jean-François; Arpin, Pierre; Sondag, Francis; Delecour, Ferdinand (December 1997)."Soil fauna and site assessment in beech stands of the Belgian Ardennes".Canadian Journal of Forest Research.27(12): 2053–2064.doi:10.1139/x97-169.
  41. ^abcdePonge, Jean-François (1993)."Biocenoses of Collembola in atlantic temperate grass-woodland ecosystems".Pedobiologia.37(4): 223–244.doi:10.1016/S0031-4056(24)00100-8.
  42. ^Lyford, Walter H. (1975). "Overland Migration of Collembola (Hypogastrura nivicola Fitch) Colonies".The American Midland Naturalist.94(1): 205–209.doi:10.2307/2424550.JSTOR2424550.
  43. ^Shaw, Peter; Ozanne, Claire; Speight, Martin; Palmer, Imogen (October 2007). "Edge effects and arboreal Collembola in coniferous plantations".Pedobiologia.51(4): 287–293.doi:10.1016/j.pedobi.2007.04.010.
  44. ^Zettel, Joerg; Zettel, Ursula; Egger, Beatrice (15 April 2000)."Jumping technique and climbing behaviour of the collembolan Ceratophysella sigillata (Collembola: Hypogastruridae)".European Journal of Entomology.97(1): 41–45.doi:10.14411/eje.2000.010.
  45. ^abDidden, Wim A. M. (1987)."Reactions ofOnychiurus fimatus(Collembola) to loose and compact soil: methods and first results ".Pedobiologia.30(2): 93–100.doi:10.1016/S0031-4056(23)00360-8.S2CID258140448.
  46. ^Rodgers, Denis J. & Kitching, Rodger L. (1998). "Vertical stratification of rainforest collembolan (Collembola: Insecta) assemblages: description of ecological patterns and hypotheses concerning their generation".Ecography.21(4): 392–400.Bibcode:1998Ecogr..21..392R.CiteSeerX10.1.1.476.6663.doi:10.1111/j.1600-0587.1998.tb00404.x.S2CID85133291.
  47. ^Bowden, John; Haines, Ian H. & Mercer, D. (1976). "Climbing Collembola".Pedobiologia.16(4): 298–312.doi:10.1016/S0031-4056(23)02178-9.S2CID258572651.
  48. ^Krab, Eveline J.; Oorsprong, Hilde; Berg, Matty P. & Cornelissen, Johannes H. C. (2010)."Turning northern peatlands upside down: disentangling microclimate and substrate quality effects on vertical distribution of Collembola".Functional Ecology.24(6): 1362–1369.Bibcode:2010FuEco..24.1362K.doi:10.1111/j.1365-2435.2010.01754.x.
  49. ^Nickerl, Julia; Helbig, Ralf; Schulz, Hans-Jürgen; Werner, Carsten; Neinhuis, Christoph (June 2013). "Diversity and potential correlations to the function of Collembola cuticle structures".Zoomorphology.132(2): 183–195.doi:10.1007/s00435-012-0181-0.S2CID14442664.
  50. ^Holmstrup, Martin & Bayley, Mark (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.PMID24035747.
  51. ^Verhoef, Herman A. (1984). "Releaser and primer pheromones in Collembola".Journal of Insect Physiology.30(8): 665–670.doi:10.1016/0022-1910(84)90052-0.
  52. ^Benoit, Joshua B.; Elnitsky, Michael A.; Schulte, Glen G.; Lee, Richard E. Jr & Denlinger, David L. (2009). "Antarctic Collembolans use chemical signals to promote aggregation and egg laying".Journal of Insect Behavior.22(2): 121–133.Bibcode:2009JIBeh..22..121B.doi:10.1007/s10905-008-9159-7.S2CID914560.
  53. ^Prinzing, Andreas; D'Haese, Cyrille A.; Pavoine, Sandrine & Ponge, Jean-François (2014)."Species living in harsh environments have low clade rank and are localized on former Laurasian continents: a case study ofWillemia(Collembola) "(PDF).Journal of Biogeography.41(2): 353–365.Bibcode:2014JBiog..41..353P.doi:10.1111/jbi.12188.S2CID86619537.
  54. ^Verhoef, Herman A. (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.
  55. ^Leinaas, Hans Petter (1983). "Synchronized moulting controlled by communication in group-living Collembola".Science.219(4581): 193–195.Bibcode:1983Sci...219..193P.doi:10.1126/science.219.4581.193.PMID17841689.S2CID41604935.
  56. ^Wilson, Jane M. (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. Archived fromthe original(PDF)on 2016-08-04.Retrieved2016-01-03.
  57. ^Palacios-Vargas, José G. & Wilson, Jane (1990). "Troglobius coprophagus,a new genus and species of cave collembolan from Madagascar with notes on its ecology ".International Journal of Speleology.19(1–4): 67–73.doi:10.5038/1827-806x.19.1.6.
  58. ^Jordana, Rafael; Baquero, Enrique; Reboleira, Sofía & Sendra, Alberto (2012). "Reviews of the generaSchaefferiaAbsolon, 1900,DeuteraphoruraAbsolon, 1901,PlutomurusYosii, 1956 and theAnuridaLaboulbène, 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.hdl:10171/27607.
  59. ^Salmon, Sandrine; Ponge, Jean-François & Van Straalen, Nico (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.
  60. ^Loranger, Gladys; Bandyopadhyaya, Ipsa; Razaka, Barbara & Ponge, Jean-François (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.S2CID84523833.
  61. ^Faber, Jack H. & Joosse, Els N.G. (1993)."Vertical distribution of Collembola in a Pinus nigra organic soil".Pedobiologia.37(6): 336–350.doi:10.1016/S0031-4056(24)00108-2.
  62. ^Detsis, Vassilis (2000)."Vertical distribution of Collembola in deciduous forests under Mediterranean climatic conditions"(PDF).Belgian Journal of Zoology.130(Supplement 1): 57–61.
  63. ^"Isotomurus palustris (Muller, 1776)".RetrievedApril 2,2017.
  64. ^Maasri, Alain; Thorp, James H. (October 31, 2023).Identification and Ecology of Freshwater Arthropods in the Mediterranean Basin.Elsevier.ISBN978-0-12-821856-3– via Google Books.
  65. ^Pichard, Sylvain (1973). "Contribution à l'étude de la biologie dePodura aquatica(Linné) Collembole ".Bulletin Biologique de la France et de la Belgique(in French).107(4): 291–299.
  66. ^Del-Claro, Kleber; Guillermo, Rhainer (June 10, 2019).Aquatic Insects: Behavior and Ecology.Springer.ISBN978-3-030-16327-3– via Google Books.
  67. ^Ponge, Jean-François; Gillet, Servane; Dubs, Florence; Fédoroff, Éric; Haese, Lucienne; Sousa, José Paulo & Lavelle, Patrick (2003). "Collembolan communities as bioindicators of land use intensification".Soil Biology and Biochemistry.35(6): 813–826.doi:10.1016/S0038-0717(03)00108-1.hdl:10316/3875.S2CID86289373.
  68. ^Ponge, Jean-François; Dubs, Florence; Gillet, Servane; Sousa, José Paulo & Lavelle, Patrick (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.
  69. ^Cristofoli, Sara & Mahy, Grégory (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.S2CID86558143.
  70. ^Heiniger, Charlène; Barot, Sébastien; Ponge, Jean-François; Salmon, Sandrine; Botton-Divet, Léo; Carmignac, David & Dubs, Florence (2014)."Effect of habitat spatiotemporal structure on collembolan diversity"(PDF).Pedobiologia.57(2): 103–117.doi:10.1016/j.pedobi.2014.01.006.
  71. ^Shaw, Michael W. & Haughs, G. M. (1983). "Damage to potato foliage bySminthurus viridis(L.) ".Plant Pathology.32(4): 465–466.doi:10.1111/j.1365-3059.1983.tb02864.x.
  72. ^Bishop, Alan L.; Harris, Anne M. & McKenzie, Harry J. (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.
  73. ^"Lucerne Flea".State of Victoria.2017.RetrievedJune 2,2018.
  74. ^Baker, A. N. & Dunning, Andrew R. (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.
  75. ^Klironomos, John N. & Moutoglis, Peter (1999). "Colonization of nonmycorrhizal plants by mycorrhizal neighbours as influenced by the collembolan,Folsomia candida".Biology and Fertility of Soils.29(3): 277–281.Bibcode:1999BioFS..29..277K.doi:10.1007/s003740050553.S2CID11014525.
  76. ^Sabatini, Maria Agnese & Innocenti, Gloria (2001). "Effects of Collembola on plant-pathogenic fungus interactions in simple experimental systems".Biology and Fertility of Soils.33(1): 62–66.Bibcode:2001BioFS..33...62S.doi:10.1007/s003740000290.S2CID9273050.
  77. ^Shiraishi, Hiroyoshi; Enami, Yoshinari & Okano, Seigo (2003). "Folsomia hidakana(Collembola) prevents damping-off disease in cabbage and Chinese cabbage byRhizoctonia solani".Pedobiologia.47(1): 33–38.doi:10.1078/0031-4056-00167.
  78. ^Ponge, Jean-François; Charpentié, Marie-José (1981)."Étude des relations microflore-microfaune: expériences sur Pseudosinella alba (Packard), Collembole mycophage".Revue d'Écologie et de Biologie du Sol.18(3): 291–303.
  79. ^Lartey, Robert T.; Curl, Elroy A.; Peterson, Curt M. & Harper, James D. (1989). "Mycophagous grazing and food preference ofProisotoma minuta(Collembola: Isotomidae) andOnychiurus encarpatus(Collembola: Onychiuridae) ".Environmental Entomology.18(2): 334–337.doi:10.1093/ee/18.2.334.
  80. ^abJanssens, Frans & Christiansen, Kenneth A. (November 22, 2007)."Synanthropic Collembola, springtails in association with Man".Checklist of the Collembola.RetrievedApril 9,2017.
  81. ^Berenbaum, May (2005). "Face time".American Entomologist.51(2): 68–69.doi:10.1093/ae/51.2.68.
  82. ^Christiansen, Kenneth & Bernard, Ernest C. (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.S2CID83870937.
  83. ^Lim, Christopher Seng-Hong; Lim, Scott L.; Chew, Fook Tim & Deharveng, Louis (2009)."Collembola are unlikely to cause human dermatitis".Journal of Insect Science.9(3): 1–5.doi:10.1673/031.009.0301.PMC3011850.PMID19611235.
  84. ^Shelomi, Matan(2013). "Evidence of photo manipulation in a delusional parasitosis paper".Journal of Parasitology.99(3): 583–585.doi:10.1645/12-12.1.PMID23198757.S2CID6473251.
  85. ^"Insects as Biological Weapons - Insects, Disease, and History | Montana State University".montana.edu.Retrieved2022-10-06.
  86. ^Lockwood, Jeffrey A. (2009).Six-legged soldiers: using insects as weapons of war(1st ed.). Oxford, UK:Oxford University Press.ISBN978-0-19-533305-3.
  87. ^"The Top 5 Bioactive Clean Up Crew".Northampton Reptile Centre.16 December 2015.Retrieved6 July2021.
  88. ^Fountain, Michelle T. & Hopkin, Steve P. (2001). "Continuous monitoring ofFolsomia candida(Insecta: Collembola) in a metal exposure test ".Ecotoxicology and Environmental Safety.48(3): 275–286.doi:10.1006/eesa.2000.2007.PMID11222037.
  89. ^ISO 11267 (2014)."Soil quality. Inhibition of reproduction of Collembola (Folsomia candida) by soil contaminants ".Geneva:International Organization for Standardization.{{cite web}}:CS1 maint: numeric names: authors list (link)
  90. ^Krogh, Paul Henning (August 1, 2008)."Toxicity testing with the collembolansFolsomia fimetariaandFolsomia candidaand the results of a ringtest "(PDF).RetrievedApril 17,2017.
  91. ^Lors, Christine; Martínez Aldaya, Maite; Salmon, Sandrine & Ponge, Jean-François (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.
  92. ^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.{{cite web}}:CS1 maint: numeric names: authors list (link)
  93. ^Chauvat, Matthieu & Ponge, Jean-François (2002)."Colonization of heavy metal-polluted soils by collembola: preliminary experiments in compartmented boxes"(PDF).Applied Soil Ecology.21(2): 91–106.Bibcode:2002AppSE..21...91C.doi:10.1016/S0929-1393(02)00087-2.
  94. ^Ponge, Jean-François; Bandyopadhyaya, Ipsa & Marchetti, Valérie (2002)."Interaction between humus form and herbicide toxicity to Collembola (Hexapoda)"(PDF).Applied Soil Ecology.20(3): 239–253.Bibcode:2002AppSE..20..239P.doi:10.1016/S0929-1393(02)00026-4.
  95. ^Nota, Benjamin; Timmermans, Martijn J.T.N.; Franken, Oscar; Montagne-Wajer, Kora; Mariën, Janine; De Boer, Muriel E.; De Boer, Tjalf E.; Ylstra, Bauke; Van Straalen, Nico M. & Roelofs, Dick (2008). "Gene expression analysis of Collembola in cadmium containing soil".Environmental Science and Technology.42(21): 8152–8157.Bibcode:2008EnST...42.8152N.doi:10.1021/es801472r.PMID19031917.
  96. ^Nota, Benjamin; Bosse, Mirte; Ylstra, Bauke; Van Straalen, Nico M. & Roelofs, Dick (2009)."Transcriptomics reveals extensive inducible biotransformation in the soil-dwelling invertebrateFolsomia candidaexposed to phenanthrene ".BMC Genomics.10:236.doi:10.1186/1471-2164-10-236.PMC2688526.PMID19457238.
  97. ^Kim, Shin Woong & An, Youn-Joo (2014). "Jumping behavior of the springtailFolsomia candidaas a novel soil quality indicator in metal-contaminated soils ".Ecological Indicators.38:67–71.doi:10.1016/j.ecolind.2013.10.033.
  98. ^Nielsen, Uffe N. & Wall, Diana H. (2013). "The future of soil invertebrate communities in polar regions: different climate change responses in the Arctic and Antarctic?".Ecology Letters.16(3): 409–419.Bibcode:2013EcolL..16..409N.doi:10.1111/ele.12058.PMID23278945.
  99. ^Coulson, Stephen James; Hodkinson, Ian D.; Woolley, Christopher; Webb, Nigel R.; Block, William; Worland, M. Rodger; Bale, Jeff S. & Strathdee, Andrew T. (1996). "Effects of experimental temperature elevation on high-arctic soil microarthropod populations".Polar Biology.16(2): 147–153.Bibcode:1996PoBio..16..147C.doi:10.1007/BF02390435.S2CID13826340.
  100. ^abSjursen, Heidi; Michelsen, Anders & Jonasson, Sven (2005). "Effects of long-term soil warming and fertilisation on microarthropod abundances in three sub-arctic ecosystems".Applied Soil Ecology.30(3): 148–161.Bibcode:2005AppSE..30..148S.doi:10.1016/j.apsoil.2005.02.013.
  101. ^Dollery, Rebecca; Hodkinson, Ian D. & Jónsdóttir, Ingibjörg S. (2006). "Impact of warming and timing of snow melt on soil microarthropod assemblages associated with Dryas-dominated plant communities on Svalbard".Ecography.29(1): 111–119.Bibcode:2006Ecogr..29..111D.doi:10.1111/j.2006.0906-7590.04366.x.
  102. ^Hågvar, Sigmund & Klanderud, Kari (2009). "Effect of simulated environmental change on alpine soil arthropods".Global Change Biology.15(12): 2972–2980.Bibcode:2009GCBio..15.2972H.CiteSeerX10.1.1.658.1606.doi:10.1111/j.1365-2486.2009.01926.x.S2CID36287733.
  103. ^abAlatalo, Juha M.; Jägerbrand, Annika K. & Čuchta, Peter (2015)."Collembola in three alpine subarctic sites resistant to twenty years of experimental warming".Scientific Reports.5(18161): 18161.Bibcode:2015NatSR...518161A.doi:10.1038/srep18161.PMC4680968.PMID26670681.
  104. ^Kardol, Paul; Reynolds, W. Nicholas; Norby, Richard J.; Classen, Aimée T. (January 2011). "Climate change effects on soil microarthropod abundance and community structure".Applied Soil Ecology.47(1): 37–44.Bibcode:2011AppSE..47...37K.doi:10.1016/j.apsoil.2010.11.001.
  105. ^Harte, John; Rawa, Agnieszka & Price, Vanessa (1996). "Effects of manipulated soil microclimate on mesofaunal biomass and diversity".Soil Biology and Biochemistry.28(3): 313–322.doi:10.1016/0038-0717(95)00139-5.
  106. ^Waldorf, Elizabeth S. (1974). "Sex pheromone in the springtailSinella curviseta".Environmental Entomology.3(6): 916–918.doi:10.1093/ee/3.6.916.
  107. ^Kozlowski, Marek Wojciech & Aoxiang, Shi (2006). "Ritual behaviors associated with spermatophore transfer inDeuterosminthurus bicinctus(Collembola: Bourletiellidae) ".Journal of Ethology.24(2): 103–110.doi:10.1007/s10164-005-0162-6.S2CID12056710.
  108. ^Simon, Jean-Christophe; Delmote, François; Rispe, Claude & Crease, Teresa (2003)."Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals".Biological Journal of the Linnean Society.79(1): 151–153.doi:10.1046/j.1095-8312.2003.00175.x.
  109. ^Czarnetzki, Alice B. & Tebbe, Christoph C. (2004). "Detection and phylogenetic analysis ofWolbachiain Collembola ".Environmental Microbiology.6(1): 35–44.Bibcode:2004EnvMi...6...35C.doi:10.1046/j.1462-2920.2003.00537.x.PMID14686939.
  110. ^Werren, John H.; Zhang, Wan & Guo, Li Rong (1995). "Evolution and phylogeny ofWolbachia:reproductive parasites of arthropods ".Proceedings of the Royal Society B.261(1360): 55–63.Bibcode:1995RSPSB.261...55W.doi:10.1098/rspb.1995.0117.JSTOR50047.PMID7644549.S2CID8585323.
  111. ^Fenn, Katelyn & Blaxter, Mark (2004). "Are filarial nematodeWolbachiaobligate mutualist symbionts? ".Trends in Ecology and Evolution.19(4): 163–166.doi:10.1016/j.tree.2004.01.002.PMID16701248.
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