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| image = Orchesella cincta.jpg | image = Orchesella cincta.jpg
| image_caption = '']'' | image_caption = '']''
| display_parents = 2
| taxon = Collembola | taxon = Collembola
| authority = ], 1871 | authority = ], 1871
| subdivision_ranks = ] | subdivision_ranks = ]
| subdivision = | subdivision = * ]
* ]
* ] * ]
* ] * ]
* ] <small>(disputed)</small> * ] <small>(disputed)</small>
| synonyms = | synonyms = * Oligentoma
* Oligentoma
* Oligoentoma * Oligoentoma
| synonyms_ref = &nbsp;<ref>{{cite book |last=Gillott |first=Cedric|year=2005 |edition=3rd |title=Entomology |publisher=] |location=Berlin |isbn=978-0-306-44967-3 |chapter=Apterygote hexapods |pages=113–125 |doi=10.1007/1-4020-3183-1_5}}</ref> | synonyms_ref = <ref>{{cite book |last=Gillott |first=Cedric|year=2005 |edition=3rd |title=Entomology |publisher=] |location=Berlin |isbn=978-0-306-44967-3 |chapter=Apterygote hexapods |pages=113–125 |doi=10.1007/1-4020-3183-1_5}}</ref>
}} }}


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


Collembolans are ], 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<ref name="brady">{{cite book|last1=Brady |first1=Nyle C. |last2=Weil |first2=Ray R. |name-list-style=amp |title =Elements of the nature and properties of soils |edition=3rd |chapter=Organisms and ecology of the soil |publisher=] |location=Upper Saddle River |year =2009 |isbn=978-0-13-501433-2 |oclc=276340542 }}</ref> and the control of soil microbial communities.<ref>{{cite journal |last1=Thimm |first1=Torsten |last2=Hoffmann |first2=Andrea |last3=Borkott |first3=Heinz |last4=Munch |first4=Jean Charles |last5=Tebbe |first5=Christoph C. |name-list-style=amp |year=1998 |title=The gut of the soil microarthropod ''Folsomia candida'' (Collembola) is a frequently changeable but selective habitat and a vector for microorganisms |journal=] |volume=64 |issue=7 |pages=2660–2669 |doi=10.1128/AEM.64.7.2660-2669.1998 |pmid=9647845 |pmc=106441|bibcode=1998ApEnM..64.2660T }}</ref> The word ''Collembola'' is from the ancient Greek {{lang|grc|κόλλα}} {{transl|grc|kólla}} "glue" and {{lang|grc|ἔμβολος}} {{transl|grc|émbolos}} "peg"; this name was given due to the existence of the ], which was previously thought to stick to surfaces to stabilize the creature.<ref name="lubbock">{{cite book |last=Lubbock |first=John |year=1873 |title=Monograph of the Collembola and Thysanura |url=https://archive.org/stream/monographofcolle00lubb#page/36/mode/2up |page=36 |publisher=Ray Society |place=London |author-link=John Lubbock, 1st Baron Avebury}}</ref> Springtails are ], 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<ref name="brady">{{cite book|last1=Brady |first1=Nyle C. |last2=Weil |first2=Ray R. |name-list-style=amp |title =Elements of the nature and properties of soils |edition=3rd |chapter=Organisms and ecology of the soil |publisher=] |location=Upper Saddle River |year =2009 |isbn=978-0-13-501433-2 |oclc=276340542 }}</ref> and the control of soil microbial communities.<ref>{{cite journal |last1=Thimm |first1=Torsten |last2=Hoffmann |first2=Andrea |last3=Borkott |first3=Heinz |last4=Munch |first4=Jean Charles |last5=Tebbe |first5=Christoph C. |name-list-style=amp |year=1998 |title=The gut of the soil microarthropod ''Folsomia candida'' (Collembola) is a frequently changeable but selective habitat and a vector for microorganisms |journal=] |volume=64 |issue=7 |pages=2660–2669 |doi=10.1128/AEM.64.7.2660-2669.1998 |pmid=9647845 |pmc=106441|bibcode=1998ApEnM..64.2660T }}</ref> The word ''Collembola'' is from the ancient Greek {{lang|grc|κόλλα}} {{transl|grc|kólla}} "glue" and {{lang|grc|ἔμβολος}} {{transl|grc|émbolos}} "peg"; this name was given due to the existence of the ], which was previously thought to stick to surfaces to stabilize the creature.<ref name="lubbock">{{cite book |last=Lubbock |first=John |year=1873 |title=Monograph of the Collembola and Thysanura |url=https://archive.org/stream/monographofcolle00lubb#page/36/mode/2up |page=36 |publisher=Ray Society |place=London |author-link=John Lubbock, 1st Baron Avebury}}</ref>


Some ] studies<ref>{{cite journal|last1=Nardi|first1=Francesco|last2=Spinsanti|first2=Giacomo|last3=Boore|first3=Jeffrey L.|last4=Carapelli|first4=Antonio|last5=Dallai|first5=Romano|last6=Frati|first6=Francesco|name-list-style=amp|year=2003|title=Hexapod origins: monophyletic or paraphyletic?|url=ftp://ftp.soest.hawaii.edu/engels/Stanley/Textbook_update/Science_299/Nardi-03.pdf|journal=]|volume=299|issue=5614|pages=1887–1889|doi=10.1126/science.1078607|pmid=12649480|bibcode=2003Sci...299.1887N|s2cid=38792657}}</ref><ref>{{cite journal|last1=Delsuc|first1=Frédéric|last2=Phillips|first2=Matthew J.|last3=Penny|first3=David|name-list-style=amp|year=2003|title=Comment on ''Hexapod origins: monophyletic or paraphyletic?''|url=http://www.sciencemag.org/cgi/reprint/301/5639/1482d.pdf|journal=]|volume=301|issue=5639|pages=1482|doi=10.1126/science.1086558|pmid=12970547|s2cid=43942720}}</ref><ref>{{cite journal|last1=Nardi|first1=Francesco|last2=Spinsanti|first2=Giacomo|last3=Boore|first3=Jeffrey L.|last4=Carapelli|first4=Antonio|last5=Dallai|first5=Romano|last6=Frati|first6=Francesco|name-list-style=amp|year=2003|title=Response to comment on ''Hexapod origins: monophyletic or paraphyletic?''|url=https://www.researchgate.net/publication/235235283|format=]|journal=]|volume=301|issue=5639|pages=1482|doi=10.1126/science.1087632|s2cid=82407120}}</ref> suggest that Collembola represent a separate ] from the other ], but others disagree;<ref name="Gao">{{cite journal|last1=Gao|first1=Yan|last2=Bu|first2=Yun|last3=Luan|first3=Yun-Xia|name-list-style=amp|year=2008|title=Phylogenetic relationships of basal hexapods reconstructed from nearly complete 18S and 28S rRNA gene sequences|url=http://decapoda.nhm.org/pdfs/31595/31595.pdf|journal=]|volume=25|issue=11|pages=1139–1145|doi=10.2108/zsj.25.1139|pmid=19267625|s2cid=10783597}}</ref> this seems to be caused by widely divergent patterns of ] among the ]s.<ref>{{cite journal|last=Hassanin|first=Alexandre|year=2006|title=Phylogeny of Arthropoda inferred from mitochondrial sequences: strategies for limiting the misleading effects of multiple changes in pattern and rates of substitution|url=http://www.csulb.edu/~dlunderw/entomology/Arthropodphylogeny2006.pdf|journal=]|volume=38|issue=1|pages=100–116|doi=10.1016/j.ympev.2005.09.012|pmid=16290034}}</ref> The adjustments of traditional ] for springtails reflects the occasional incompatibility of traditional groupings with modern ]: when they were included with the insects, they were ranked as an ]; as part of the Entognatha, they are ranked as a ]. If they are considered a ] lineage of Hexapoda, they are elevated to full ] status. Early ] studies<ref>{{cite journal |last1=Nardi |first1=Francesco |last2=Spinsanti |first2=Giacomo |last3=Boore |first3=Jeffrey L. |last4=Carapelli |first4=Antonio |last5=Dallai |first5=Romano |last6=Frati |first6=Francesco |title=Hexapod Origins: Monophyletic or Paraphyletic? |journal=Science |date=21 March 2003 |volume=299 |issue=5614 |pages=1887–1889 |doi=10.1126/science.1078607 |pmid=12649480 |bibcode=2003Sci...299.1887N |s2cid=38792657 }}</ref><ref>{{cite journal |last1=Delsuc |first1=Frédéric |last2=Phillips |first2=Matthew J. |last3=Penny |first3=David |title=Comment on 'Hexapod Origins: Monophyletic or Paraphyletic?' |journal=Science |date=12 September 2003 |volume=301 |issue=5639 |pages=1482 |doi=10.1126/science.1086558 |pmid=12970547 |s2cid=43942720 |url=https://hal.archives-ouvertes.fr/halsde-00192990/file/Delsuc-Science03_HAL.pdf }}</ref><ref>{{cite journal |last1=Nardi |first1=Francesco |last2=Spinsanti |first2=Giacomo |last3=Boore |first3=Jeffrey L. |last4=Carapelli |first4=Antonio |last5=Dallai |first5=Romano |last6=Frati |first6=Francesco |title=Response to Comment on 'Hexapod Origins: Monophyletic or Paraphyletic?' |journal=Science |date=12 September 2003 |volume=301 |issue=5639 |pages=1482 |doi=10.1126/science.1087632 |s2cid=82407120 |doi-access=free }}</ref> suggested that Collembola represent a separate ] from the other ], but others disagree;<ref name="Gao">{{cite journal |last1=Gao |first1=Yan |last2=Bu |first2=Yun |last3=Luan |first3=Yun-Xia |title=Phylogenetic Relationships of Basal Hexapods Reconstructed from Nearly Complete 18S and 28S rRNA Gene Sequences |journal=Zoological Science |date=25 November 2008 |volume=25 |issue=11 |pages=1139–1145 |doi=10.2108/zsj.25.1139 |pmid=19267625 |s2cid=10783597 }}</ref> this seems to be caused by widely divergent patterns of ] among the ]s.<ref>{{cite journal |last1=Hassanin |first1=Alexandre |title=Phylogeny of Arthropoda inferred from mitochondrial sequences: Strategies for limiting the misleading effects of multiple changes in pattern and rates of substitution |journal=Molecular Phylogenetics and Evolution |date=January 2006 |volume=38 |issue=1 |pages=100–116 |doi=10.1016/j.ympev.2005.09.012 |pmid=16290034 }}</ref> The adjustments of traditional ] for springtails reflect the occasional incompatibility of traditional groupings with modern ]: when they were included with the insects, they were ranked as an ]; as part of the Entognatha, they are ranked as a ]. If they are considered a ] lineage of Hexapoda, they are elevated to full ] status.


== Morphology == == Morphology ==
]'' with visible furcula]] ]'' (]) with visible furcula]]
]'' (])]]


Members of the Collembola are normally less than {{convert|6|mm|abbr=on}} long, have six or fewer ] ], and possess a tubular ] (the ] or ventral tube) with reversible, sticky vesicles, projecting ventrally from the first abdominal segment.<ref name=":0">{{cite journal|last=Davies|first=W. Maldwyn|year=1927|title=On the tracheal system of Collembola, with special reference to that of ''Sminthurus viridis'', Lubb.|url=http://jcs.biologists.org/content/joces/s2-71/281/15.full.pdf|journal=]|volume=71|issue=281|pages=15–30}}</ref> It is believed to be associated with fluid uptake and balance, excretion, and orientation of the organism itself.<ref name=":1" /> Most species have an abdominal, tail-like appendage known as a ]. It is located on the fourth abdominal segment of collembolans and is folded beneath the body, held under tension by a small structure called the ] (or tenaculum). When released, it snaps against the substrate, flinging the springtail into the air and allowing for rapid evasion and migration. All of this takes place in as little as 18&nbsp;milliseconds.<ref name="Piper">{{cite book |last=Piper |first=Ross |year=2007 |title=Extraordinary animals: an encyclopedia of curious and unusual animals |url=https://archive.org/details/extraordinaryani0000pipe |url-access=registration |publisher=] |location=Santa Barbara, California |isbn=9780313339226 |author-link=Ross Piper|oclc=124074839 }}</ref><ref name=":1" /> Members of the Collembola are normally less than {{convert|6|mm|abbr=on}} long, have six or fewer ] ], and possess a tubular ] (the ] or ventral tube) with reversible, sticky vesicles, projecting ventrally from the first abdominal segment.<ref name=":0">{{cite journal |last1=Davies |first1=W. Maldwyn |title=On the Tracheal System of Collembola, with special reference to that of Sminthurus viridis, Lubb |journal=Journal of Cell Science |date=1 May 1927 |volume=S2-71 |issue=281 |pages=15–30 |doi=10.1242/jcs.s2-71.281.15 }}</ref> It is believed to be associated with fluid uptake and balance, excretion, and orientation of the organism itself.<ref name=":1" /> Most species have an abdominal, tail-like appendage known as a ] (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 the ] (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&nbsp;milliseconds.<ref name="Piper">{{cite book |last=Piper |first=Ross |year=2007 |title=Extraordinary animals: an encyclopedia of curious and unusual animals |url=https://archive.org/details/extraordinaryani0000pipe |url-access=registration |publisher=] |location=Santa Barbara, California |isbn=9780313339226 |author-link=Ross Piper|oclc=124074839 }}</ref><ref name=":1" />


Springtails also possess the ability to reduce their body size by as much as 30% through subsequent ] (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.<ref>{{cite journal |url=http://www.sciencemagazinedigital.org/sciencemagazine/30_august_2013?pg=17#pg17 |journal=] |volume = 341 |pages = 945 |date = 30 August 2013 |doi=10.1126/science.341.6149.945-a |issue=6149 |title=The incredible shrinking springtail}}</ref> Springtails also possess the ability to reduce their body size by as much as 30% through subsequent ] (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.<ref>{{cite journal |title=Random Sample |journal=Science |date=30 August 2013 |volume=341 |issue=6149 |pages=945 |doi=10.1126/science.341.6149.945-a }}</ref>


The ] and ] have an elongated body, while the ] and ] have a globular body. Collembola lack a ] respiration system, which forces them to respire through a ] ], with the notable exception of the ], which exhibit a rudimentary, although fully functional, tracheal system.<ref name=":0" /> The anatomical variance present between different species partially depends on soil morphology and composition. Surface-dwellers are generally larger, have darker pigments, have longer antennae and functioning ]. Sub-surface-dwellers are usually unpigmented, have elongated bodies, and reduced ]. 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 in length, pigmented, have long limbs, and a full set of ] (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 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.<ref name=":2" /><ref>{{Cite journal|last1=Potapov|first1=Anton A.|last2=Semenina|first2=Eugenia E.|last3=Korotkevich|first3=Anastasiya Yu.|last4=Kuznetsova|first4=Natalia A.|last5=Tiunov|first5=Alexei V.|date=2016-10-01|title=Connecting taxonomy and ecology: Trophic niches of collembolans as related to taxonomic identity and life forms|url=http://www.sciencedirect.com/science/article/pii/S0038071716301377|journal=Soil Biology and Biochemistry|language=en|volume=101|pages=20–31|doi=10.1016/j.soilbio.2016.07.002|issn=0038-0717}}</ref><ref name=":3">{{Cite journal|last1=Jordana|first1=Rafael|last2=Baquero Martín|first2=Enrique|last3=Ledesma|first3=Enrique|last4=Sendra|first4=Alberto|last5=Ortuño|first5=Vicente|date=2020-02-01|title=Poduromorpha (Collembola) from a sampling in the mesovoid shallow substratum of the Sierra de Guadarrama National Park (Madrid and Segovia, Spain): Taxonomy and Biogeography|url=https://www.researchgate.net/publication/339121044|journal=Zoologischer Anzeiger|doi=10.1016/j.jcz.2020.02.001|volume=285|pages=81–96|s2cid=214349457}}</ref> The ] and ] have an elongated body, while the ] and ] have a globular body. Collembola lack a ] respiration system, which forces them to respire through a ] ], except for the two families ] and Actaletidae, which exhibit a single pair of ]s between the head and the ], leading to a rudimentary, although fully functional, tracheal system.<ref>{{Cite book|url=https://books.google.com/books?id=x7vtCAAAQBAJ&dq=sminthuridae+actaletidae+spiracles&pg=PA264|title=Multicellular Animals: Volume II: The Phylogenetic System of the Metazoa|first=Peter|last=Ax|date=March 9, 2013|publisher=Springer Science & Business Media|isbn=978-3-662-10396-8 |via=Google Books}}</ref><ref name=":0" /> The anatomical variance present between different species partially depends on ] and 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 of ] (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.<ref name=":2" /><ref>{{cite journal |last1=Potapov |first1=Anton A. |last2=Semenina |first2=Eugenia E. |last3=Korotkevich |first3=Anastasiya Yu. |last4=Kuznetsova |first4=Natalia A. |last5=Tiunov |first5=Alexei V. |title=Connecting taxonomy and ecology: Trophic niches of springtails as related to taxonomic identity and life forms |journal=Soil Biology and Biochemistry |date=October 2016 |volume=101 |pages=20–31 |doi=10.1016/j.soilbio.2016.07.002 }}</ref><ref name=":3">{{cite journal |last1=Jordana |first1=Rafael |last2=Baquero |first2=Enrique |last3=Ledesma |first3=Enrique |last4=Sendra |first4=Alberto |last5=Ortuño |first5=Vicente M. |title=Poduromorpha (Collembola) from a sampling in the mesovoid shallow substratum of the Sierra de Guadarrama National Park (Madrid and Segovia, Spain): Taxonomy and Biogeography |journal=Zoologischer Anzeiger |date=March 2020 |volume=285 |pages=81–96 |doi=10.1016/j.jcz.2020.02.001 |s2cid=214349457 }}</ref>


Poduromorphs inhabit the epedaphic, hemiedaphic, and euedaphic layers and are characterized by their elongated bodies and conspicuous segmentation – three thoracic segments, six abdominal segments, and a ].<ref name=":3" /> Poduromorphs are characterized by their elongated bodies and conspicuous segmentation – three thoracic segments, six abdominal segments, including a well-developed ] with tergal chaetae,<ref name=":3" /> while the first thoracic segment in Entomobryomorpha is clearly reduced and bears no chaetae.


The digestive tract of collembolan species 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.<ref name=":1" /> 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.<ref name=":1" /> ] are absent.<ref>{{Cite web|url=https://journals.biologists.com/jeb/article/222/10/jeb200691/33925/Water-and-ion-transport-across-the-eversible|title=Water and ion transport across the eversible vesicles in the collophore of the springtail Orchesella cincta &#124; Journal of Experimental Biology &#124; The Company of Biologists}}</ref>


== Systematics and evolution == == Systematics and evolution ==
]) on rotting wood]] ]) on rotting wood]]
Traditionally, the springtails were divided into the ] ], ], and occasionally also ]. The Arthropleona were divided into two ], the ] and the ]. However, recent phylogenetic studies show Arthropleona is ].<ref name="XiongGao2008">{{cite journal|last1=Xiong|first1=Y|last2=Gao|first2=Y|last3=Yin|first3=W|last4=Luan|first4=Y|title=Molecular phylogeny of Collembola inferred from ribosomal RNA genes|journal=Molecular Phylogenetics and Evolution|volume=49|issue=3|year=2008|pages=728–735|issn=1055-7903|doi=10.1016/j.ympev.2008.09.007|pmid=18835455}}</ref><ref name="LeoCarapelli2019">{{cite journal|last1=Leo|first1=Chiara|last2=Carapelli|first2=Antonio|last3=Cicconardi|first3=Francesco|last4=Frati|first4=Francesco|last5=Nardi|first5=Francesco|title=Mitochondrial Genome Diversity in Collembola: Phylogeny, Dating and Gene Order|journal=Diversity|volume=11|issue=9|year=2019|pages=169|issn=1424-2818|doi=10.3390/d11090169|doi-access=free}}</ref><ref name="SunDing2020">{{cite journal|last1=Sun|first1=Xin|last2=Ding|first2=Yinhuan|last3=Orr|first3=Michael C.|last4=Zhang|first4=Feng|title=Streamlining universal single‐copy orthologue and ultraconserved element design: A case study in Collembola|journal=Molecular Ecology Resources|volume=20|issue=3|year=2020|pages=706–717|issn=1755-098X|doi=10.1111/1755-0998.13146|pmid=32065730|s2cid=211133755}}</ref> Thus, the Arthropleona are abolished in modern classifications, and their superfamilies are raised in rank accordingly, being now orders ] and the ]. Technically, the Arthropleona are thus a partial ] of the Collembola.<ref>{{cite web |url=http://www.collembola.org/ |title=Checklist of the Collembola |access-date= January 2, 2016}}</ref> Traditionally, the springtails were divided into the ] ], ], and occasionally also ]. The Arthropleona were divided into two ], the ] and the ]. However, recent phylogenetic studies show Arthropleona is ].<ref name="XiongGao2008">{{cite journal |last1=Xiong |first1=Y |last2=Gao |first2=Y |last3=Yin |first3=W |last4=Luan |first4=Y |title=Molecular phylogeny of Collembola inferred from ribosomal RNA genes |journal=Molecular Phylogenetics and Evolution |date=December 2008 |volume=49 |issue=3 |pages=728–735 |doi=10.1016/j.ympev.2008.09.007 |pmid=18835455 }}</ref><ref name="LeoCarapelli2019">{{cite journal |last1=Leo |first1=Chiara |last2=Carapelli |first2=Antonio |last3=Cicconardi |first3=Francesco |last4=Frati |first4=Francesco |last5=Nardi |first5=Francesco |title=Mitochondrial Genome Diversity in Collembola: Phylogeny, Dating and Gene Order |journal=Diversity |date=17 September 2019 |volume=11 |issue=9 |pages=169 |doi=10.3390/d11090169 |doi-access=free |hdl=11365/1079696 |hdl-access=free }}</ref><ref name="SunDing2020">{{cite journal |last1=Sun |first1=Xin |last2=Ding |first2=Yinhuan |last3=Orr |first3=Michael C. |last4=Zhang |first4=Feng |title=Streamlining universal single-copy orthologue and ultraconserved element design: A case study in Collembola |journal=Molecular Ecology Resources |date=May 2020 |volume=20 |issue=3 |pages=706–717 |doi=10.1111/1755-0998.13146 |pmid=32065730 |s2cid=211133755 }}</ref> Thus, the Arthropleona are abolished in modern classifications, and their superfamilies are raised in rank accordingly, being now orders ] and the ]. Technically, the Arthropleona are thus a partial ] of the Collembola.<ref>{{cite web |url=http://www.collembola.org/ |title=Checklist of the Collembola |access-date= January 2, 2016}}</ref>


The term "Neopleona" is essentially synonymous with Symphypleona + Neelipleona.<ref>{{cite journal |last1=Sánchez-García |first1=Alba |last2=Engel |first2=Michael S. |name-list-style=amp |year=2016 |title=Long-term stasis in a diverse fauna of Early Cretaceous springtails (Collembola: Symphypleona) |journal=] |pages=1–25 |url=https://www.researchgate.net/publication/303955438 |format=]}}</ref> 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 of ] and ] ] ] data, though, suggests that they form the most ancient lineage of springtails, which would explain their peculiar ].<ref name="Gao"/> This phylogenetic relationship was also confirmed using a phylogeny based on ]<ref name="LeoCarapelli2019"/> and ].<ref name="SunDing2020"/> The term "Neopleona" is essentially synonymous with Symphypleona + Neelipleona.<ref>{{cite journal |last1=Sánchez-García |first1=Alba |last2=Engel |first2=Michael S. |title=Long-term stasis in a diverse fauna of Early Cretaceous springtails (Collembola: Symphypleona) |journal=Journal of Systematic Palaeontology |date=3 July 2017 |volume=15 |issue=7 |pages=513–537 |doi=10.1080/14772019.2016.1194575 |bibcode=2017JSPal..15..513S |s2cid=88641582 }}</ref> 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 of ] and ] ] ] data, though, suggests that they form the most ancient lineage of springtails, which would explain their peculiar ].<ref name="Gao"/> This phylogenetic relationship was also confirmed using a phylogeny based on ]<ref name="LeoCarapelli2019"/> and ].<ref name="SunDing2020"/>


The latest whole-genome phylogeny supporting four orders of collembola:<ref name="SunDing2020"/> The latest whole-genome phylogeny supporting four orders of Collembola:<ref name="SunDing2020"/>
{{clade {{clade
|1={{clade |1={{clade
|1=] ] |1=] ]
|2={{clade |2={{clade
|1=] ] |1=] ]
|2={{clade |2={{clade
|1=] ] |1=] ]
|2=] ] |2=] ]
}} }}
}} }}
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}} }}


Springtails are attested to since the ].<ref>{{cite book |last1=Daly |first1=Howell V. |last2=Doyen |first2=John T. |last3=Purcell |first3=Alexander H. |name-list-style=amp |year=1998 |title=Introduction to insect biology and diversity |edition=2nd |publisher=] |location=New York |isbn= 978-0-19-510033-4 |oclc=925231875 }}</ref> The fossil from {{Ma|400}}, '']'', is the oldest terrestrial arthropod, and was found in the famous ] of ]. Given its morphology resembles extant species quite closely, the radiation of the ] can be situated in the ], {{Ma|420}} or more.<ref>{{cite web |work=] |url=http://tolweb.org/Hexapoda/2528 |title=Hexapoda. Insects, springtails, diplurans, and proturans |date=January 1, 2002 |access-date=March 26, 2017}}</ref> Additional research concerning the coprolites (fossilized feces) of ancient collembolans allowed researchers to track their lineages back some 412 million years.<ref name=":1" /> Springtails are attested to since the ].<ref>{{cite book |last1=Daly |first1=Howell V. |last2=Doyen |first2=John T. |last3=Purcell |first3=Alexander H. |name-list-style=amp |year=1998 |title=Introduction to insect biology and diversity |edition=2nd |publisher=] |location=New York |isbn= 978-0-19-510033-4 |oclc=925231875 }}</ref> The fossil from {{Ma|400}}, '']'', is the oldest terrestrial arthropod, and was found in the famous ] of ]. Given its morphology resembles extant species quite closely, the radiation of the ] can be situated in the ], {{Ma|420}} or more.<ref>{{cite web |work=] |url=http://tolweb.org/Hexapoda/2528 |title=Hexapoda. Insects, springtails, diplurans, and proturans |date=January 1, 2002 |access-date=March 26, 2017}}</ref> Additional research concerning the coprolites (fossilized feces) of ancient springtails allowed researchers to track their lineages back some 412 million years.<ref name=":1" />


Fossil Collembola are rare. Instead, most are found in amber.<ref>{{cite journal |last=Mari Mutt |first=José A. |year=1983 |title=Collembola in amber from the Dominican Republic |journal=] |volume=85 |issue=3 |pages=575–587 |url=http://www.uprm.edu/biology/profs/marimutt/37.pdf }}</ref> 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,<ref>{{cite journal |last1=Nel |first1=André |last2=De Ploëg |first2=Gaėl |last3=Milliet |first3=Jacqueline |last4=Menier |first4=Jean-Jacques |last5=Waller |first5=Alain |name-list-style=amp |year=2004 |title=The French ambers: a general conspectus and the Lowermost Eocene amber deposit of Le Quesnoy in the Paris Basin |journal=] |volume=2 |issue=1 |pages=3–8 |url=http://revistes.ub.edu/index.php/GEOACTA/article/view/1827/4123 |format=]}}</ref> Miocene of Central America,<ref>{{cite journal |last1=Penney |first1=David |last2=McNeil |first2=Andrew |last3=Green |first3=David I. |last4=Bradley |first4=Robert S. |last5=Jepson |first5=James E. |last6=Withers |first6=Philip J. |last7=Preziosi |first7=Richard F. |name-list-style=amp |year=2012 |title=Ancient Ephemeroptera-Collembola symbiosis fossilized in amber predicts contemporary phoretic associations |journal=] |volume=7 |issue=10 |pages=e47651 |doi=10.1371/journal.pone.0047651 |pmid=23082186 |pmc=3474712 |bibcode=2012PLoSO...747651P |doi-access=free }}</ref> and the mid-Cretaceous of Burma and Canada.<ref>{{cite journal |last1=Christiansen |first1=Kenneth |last2=Nascimbene |first2=Paul |name-list-style=amp |year=2006 |title=Collembola (Arthropoda, Hexapoda) from the mid Cretaceous of Myanmar (Burma) |journal=] |volume=27 |issue=3 |pages=318–33 |doi=10.1016/j.cretres.2005.07.003 |url=https://www.researchgate.net/publication/235005863 |format=]}}</ref> 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. Fossil Collembola are rare. Instead, most are found in amber.<ref>{{cite journal |last=Mari Mutt |first=José A. |year=1983 |title=Collembola in amber from the Dominican Republic |journal=] |volume=85 |issue=3 |pages=575–587 |url=http://www.uprm.edu/biology/profs/marimutt/37.pdf }}</ref> 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,<ref>{{cite journal |last1=Nel |first1=André |last2=De Ploëg |first2=Gaėl |last3=Milliet |first3=Jacqueline |last4=Menier |first4=Jean-Jacques |last5=Waller |first5=Alain |name-list-style=amp |year=2004 |title=The French ambers: a general conspectus and the Lowermost Eocene amber deposit of Le Quesnoy in the Paris Basin |journal=] |volume=2 |issue=1 |pages=3–8 |url=http://revistes.ub.edu/index.php/GEOACTA/article/view/1827/4123 |format=]}}</ref> Miocene of Central America,<ref>{{cite journal |last1=Penney |first1=David |last2=McNeil |first2=Andrew |last3=Green |first3=David I. |last4=Bradley |first4=Robert S. |last5=Jepson |first5=James E. |last6=Withers |first6=Philip J. |last7=Preziosi |first7=Richard F. |name-list-style=amp |year=2012 |title=Ancient Ephemeroptera-Collembola symbiosis fossilized in amber predicts contemporary phoretic associations |journal=] |volume=7 |issue=10 |pages=e47651 |doi=10.1371/journal.pone.0047651 |pmid=23082186 |pmc=3474712 |bibcode=2012PLoSO...747651P |doi-access=free }}</ref> and the mid-Cretaceous of Burma and Canada.<ref>{{cite journal |last1=Christiansen |first1=Kenneth |last2=Nascimbene |first2=Paul |title=Collembola (Arthropoda, Hexapoda) from the mid Cretaceous of Myanmar (Burma) |journal=Cretaceous Research |date=June 2006 |volume=27 |issue=3 |pages=318–363 |doi=10.1016/j.cretres.2005.07.003 |bibcode=2006CrRes..27..318C }}</ref> 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.<ref>{{cite web |last1=Koehler |first1=Philip G. |last2=Aparicio |first2=M. L. |last3=Pfiester |first3=Margaret |name-list-style=amp |title=Springtails |publisher=University of Florida IFAS Extension |location=Gainesville, Florida |date=July 2011 |url=http://edis.ifas.ufl.edu/pdffiles/IG/IG12400.pdf |access-date=March 26, 2017}}</ref> There are about 3,600 different species.<ref>{{cite web |last1=Koehler |first1=Philip G. |last2=Aparicio |first2=M. L. |last3=Pfiester |first3=Margaret |name-list-style=amp |title=Springtails |publisher=University of Florida IFAS Extension |location=Gainesville, Florida |date=July 2011 |url=http://edis.ifas.ufl.edu/pdffiles/IG/IG12400.pdf |access-date=March 26, 2017}}</ref>
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=== Eating behavior === === Eating behavior ===
Specific feeding strategies and mechanisms are employed to match specific niches.<ref>{{Cite journal|last1=Sechi|first1=Valentina|last2=D'Annibale|first2=Alessandra|last3=Ambus|first3=Per|last4=Sárossy|first4=Zsuzsa|last5=Krogh|first5=Paul Henning|last6=Eriksen|first6=Jørgen|last7=Holmstrup|first7=Martin|date=2014-07-01|title=Collembola feeding habits and niche specialization in agricultural grasslands of different composition|url=http://www.sciencedirect.com/science/article/pii/S0038071714000728|journal=Soil Biology and Biochemistry|language=en|volume=74|pages=31–38|doi=10.1016/j.soilbio.2014.02.019|issn=0038-0717}}</ref> 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.<ref>{{Cite journal |last=Rusek |first=Josef |date=September 1998 |title=Biodiversity of Collembola and their functional role in the ecosystem |url=http://dx.doi.org/10.1023/a:1008887817883 |journal=Biodiversity and Conservation |volume=7 |issue=9 |pages=1207–1219 |doi=10.1023/a:1008887817883 |s2cid=22883809 |issn=0960-3115}}</ref> Carnivorous species maintain populations of small invertebrates such as nematodes, rotifers, and other collembolan species.<ref name=":1">{{Cite book|last=Hopkin|first=Stephen P.|title=Biology of the springtails (Insecta: Collembola)|publisher=Oxford University Press|year=1997|location=Oxford}}</ref><ref name=":2">{{Citation|last1=Coleman|first1=David C.|title=Chapter 5 - Soil Fauna: Occurrence, Biodiversity, and Roles in Ecosystem Function|date=2015-01-01|url=http://www.sciencedirect.com/science/article/pii/B9780124159556000050|work=Soil Microbiology, Ecology and Biochemistry (Fourth Edition)|pages=111–149|editor-last=Paul|editor-first=Eldor A.|publisher=Academic Press|language=en|isbn=978-0-12-415955-6|access-date=2020-03-16|last2=Wall|first2=Diana H.}}</ref> 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.<ref>{{Cite journal |last1=Chen |first1=Benrong |last2=Snider |first2=Richard J. |last3=Snider |first3=Renate M. |name-list-style=amp |year=1996 |title=Food consumption by Collembola from northern Michigan deciduous forest |journal=Pedobiologia |volume=40 |issue=2 |pages=149–161 |url=https://www.researchgate.net/publication/280136843 |format=]}}</ref> Specific feeding strategies and mechanisms are employed to match specific niches.<ref>{{cite journal |last1=Sechi |first1=Valentina |last2=D'Annibale |first2=Alessandra |last3=Ambus |first3=Per |last4=Sárossy |first4=Zsuzsa |last5=Krogh |first5=Paul Henning |last6=Eriksen |first6=Jørgen |last7=Holmstrup |first7=Martin |title=Collembola feeding habits and niche specialization in agricultural grasslands of different composition |journal=Soil Biology and Biochemistry |date=July 2014 |volume=74 |pages=31–38 |doi=10.1016/j.soilbio.2014.02.019 }}</ref> 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.<ref>{{cite journal |last1=Rusek |first1=Josef |title=Biodiversity of Collembola and their functional role in the ecosystem |journal=Biodiversity and Conservation |date=September 1998 |volume=7 |issue=9 |pages=1207–1219 |doi=10.1023/a:1008887817883 |bibcode=1998BiCon...7.1207R |s2cid=22883809 }}</ref> Carnivorous species maintain populations of small invertebrates such as nematodes, rotifers, and other collembolan species.<ref name=":1">{{Cite book|last=Hopkin|first=Stephen P.|title=Biology of the springtails (Insecta: Collembola)|publisher=Oxford University Press|year=1997|location=Oxford}}</ref><ref name=":2">{{cite book |doi=10.1016/B978-0-12-415955-6.00005-0 |chapter=Soil Fauna |title=Soil Microbiology, Ecology and Biochemistry |date=2015 |last1=Coleman |first1=David C. |last2=Wall |first2=Diana H. |pages=111–149 |isbn=978-0-12-415955-6 }}</ref> 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.<ref>{{Cite journal |last1=Chen |first1=Benrong |last2=Snider |first2=Richard J. |last3=Snider |first3=Renate M. |name-list-style=amp |year=1996 |title=Food consumption by Collembola from northern Michigan deciduous forest |journal=Pedobiologia |volume=40 |issue=2 |pages=149–161 |doi=10.1016/S0031-4056(24)00348-2 |url=https://www.researchgate.net/publication/280136843 |format=]|doi-access=free }}</ref>

=== Predators ===
Springtails are consumed by ]n mites in various families, including ], ], ], ] and ].<ref>{{cite book |doi=10.1016/b978-0-444-50019-9.50022-4 |chapter=Predatory mites (Gamasina, Mesostigmata) |title=Invertebrate Biodiversity as Bioindicators of Sustainable Landscapes |date=1999 |last1=Koehler |first1=H.H. |pages=395–410 |isbn=978-0-444-50019-9 }}</ref>

Cave-dwelling springtails are a food source for ]s and ] in the same environment, such as the endangered harvestman '']''.<ref>{{Cite web |last=City of Austin and Travis County |date=September 3, 2020 |title=Support for Maintaining Endangered Status For the Bone Cave Harvestman (Texella reyesi) |url=https://www.austintexas.gov/edims/document.cfm?id=347313 |access-date=October 6, 2022}}</ref>

To protect themselves, some species have evolved chemical defenses.<ref>{{Cite book|url=https://books.google.com/books?id=HoMqBgAAQBAJ&dq=springtails+chemical+defenses&pg=PA44|title=Insect Molecular Biology and Ecology|first=Klaus H.|last=Hoffmann|date=December 19, 2014|publisher=CRC Press|isbn=978-1-4822-3189-2 |via=Google Books}}</ref>


=== Distribution === === Distribution ===
Springtails are ] frequently found in ] and other decaying material,<ref name="Hopkin">{{cite web |last=Hopkin |first=Stephen P. |year=1997 |title=The biology of the Collembola (springtails): the most abundant insects in the world |publisher=] |url=http://www.nhm.ac.uk/resources-rx/files/35feat_springtails_most_abundent-3056.pdf |access-date=January 2, 2016}}</ref> where they are primarily ] and ]s, and one of the main biological agents responsible for the control and the dissemination of soil ]s.<ref>{{cite journal |last=Ponge |first=Jean-François |year=1991 |title=Food resources and diets of soil animals in a small area of Scots pine litter |journal=Geoderma |volume=49 |issue=1–2 |pages=33–62 |doi=10.1016/0016-7061(91)90090-G |bibcode=1991Geode..49...33P |url=https://www.researchgate.net/publication/47537958 |format=]|citeseerx=10.1.1.635.8529 }}</ref> 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.<ref name="Hopkin1997">{{cite book |author=Hopkin, Stephen P. |title=Biology of the Springtails: (Insecta: Collembola)|url=https://books.google.com/books?id=F_Eo6r5xAzEC |year=1997 |publisher=OUP Oxford|isbn=978-0-19-158925-6 |page=127}}</ref> Springtails are ] frequently found in ] and other decaying material,<ref name="Hopkin">{{cite web |last=Hopkin |first=Stephen P. |year=1997 |title=The biology of the Collembola (springtails): the most abundant insects in the world |publisher=] |url=http://www.nhm.ac.uk/resources-rx/files/35feat_springtails_most_abundent-3056.pdf |access-date=January 2, 2016}}</ref> where they are primarily ] and ]s, and one of the main biological agents responsible for the control and the dissemination of soil ]s.<ref>{{cite journal |last=Ponge |first=Jean-François |year=1991 |title=Food resources and diets of soil animals in a small area of Scots pine litter |journal=Geoderma |volume=49 |issue=1–2 |pages=33–62 |doi=10.1016/0016-7061(91)90090-G |bibcode=1991Geode..49...33P |citeseerx=10.1.1.635.8529 }}</ref> 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.<ref name="Hopkin1997">{{cite book |author=Hopkin, Stephen P. |title=Biology of the Springtails: (Insecta: Collembola) |year=1997 |publisher=OUP Oxford |isbn=978-0-19-158925-6 |page=127 }}</ref>


] ]
] (]: ])]] ] (]: ])]]


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,<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Arpin |first2=Pierre |last3=Sondag |first3=Francis |last4=Delecour |first4=Ferdinand |name-list-style=amp|year=1997 |title=Soil fauna and site assessment in beech stands of the Belgian Ardennes |journal=] |volume=27 |issue=12 |pages=2053–2064 |doi=10.1139/cjfr-27-12-2053 |url=https://www.researchgate.net/publication/45341271 |format=]}}</ref> essentially everywhere on Earth where soil and related habitats (] cushions, fallen ], ] tufts, ] and ] nests) occur.<ref name="Ponge 1993">{{cite journal |last=Ponge |first=Jean-François |year=1993 |title=Biocenoses of Collembola in atlantic temperate grass-woodland ecosystems |journal=Pedobiologia |volume=37 |issue=4 |pages=223–244 |url=https://www.researchgate.net/publication/46396173 |format=]}}</ref> Only ]s, ]s, and ]s 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 ] and crustaceans a ]. Most springtails are small and difficult to see by casual observation, but one springtail, the so-called ] ('']''), is readily observed on warm winter days when it is active and its dark color contrasts sharply with a background of snow.<ref>{{cite journal |last1=Lyford |first1=Walter H. |year=1975 |title=Overland migration of Collembola (Hypogastrura nivicola Fitch) colonies |journal=] |volume=94 |issue=1 |pages=205–209 |doi=10.2307/2424550 |url=http://harvardforest.fas.harvard.edu/sites/harvardforest.fas.harvard.edu/files/publications/pdfs/Lyford_AmMidlandNaturalist_1975.pdf |jstor=2424550 }}</ref> 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,<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Arpin |first2=Pierre |last3=Sondag |first3=Francis |last4=Delecour |first4=Ferdinand |title=Soil fauna and site assessment in beech stands of the Belgian Ardennes |journal=Canadian Journal of Forest Research |date=December 1997 |volume=27 |issue=12 |pages=2053–2064 |doi=10.1139/x97-169 |url=https://hal.science/hal-00505482/ }}</ref> essentially everywhere on Earth where soil and related habitats (] cushions, fallen ], ] tufts, ] and ] nests) occur.<ref name="Ponge 1993">{{cite journal |last1=Ponge |first1=Jean-François |title=Biocenoses of Collembola in atlantic temperate grass-woodland ecosystems |journal=Pedobiologia |date=1993 |volume=37 |issue=4 |pages=223–244 |doi=10.1016/S0031-4056(24)00100-8 |url=https://hal.science/hal-00506012/ }}</ref> Only ]s, ]s, and ]s 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 ] and crustaceans a ]. Most springtails are small and difficult to see by casual observation, but one springtail, the so-called ] ('']''), is readily observed on warm winter days when it is active and its dark color contrasts sharply with a background of snow.<ref>{{cite journal |last1=Lyford |first1=Walter H. |title=Overland Migration of Collembola (Hypogastrura nivicola Fitch) Colonies |journal=The American Midland Naturalist |date=1975 |volume=94 |issue=1 |pages=205–209 |doi=10.2307/2424550 |jstor=2424550 }}</ref>


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.<ref>{{cite journal |last1=Shaw |first1=Peter |last2=Ozanne |first2=Claire |last3=Speight |first3=Martin |last4=Palmer |first4=Imogen |name-list-style=amp |year=2007 |title=Edge effects and arboreal Collembola in coniferous plantations |journal=Pedobiologia |volume=51 |issue=4 |pages=287–293 |doi=10.1016/j.pedobi.2007.04.010 |url=https://www.academia.edu/1951148 |format=]}}</ref><ref>{{cite journal |last1=Zettel |first1=Jürg |last2=Zettel |first2=Ursula |last3=Egger |first3=Beatrice |name-list-style=amp |year=2000 |title=Jumping technique and climbing behaviour of the collembolan Ceratophysella sigillata (Collembola: Hypogastruridae) |journal=] |volume=97 |issue=1 |pages=41–45 |doi=10.14411/eje.2000.010 |url=http://www.eje.cz/pdfs/eje/2000/01/10.pdf |doi-access=free }}</ref> These tend to be the larger (>2&nbsp;mm) species, mainly in the genera '']'' and '']'', 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. '']'' spp., ''Entomobrya albocincta'', '']'', '']'') are almost exclusively arboreal.<ref name="Ponge 1993"/> In tropical regions a single square meter of canopy habitat can support many species of Collembola.<ref name="Piper"/> 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.<ref>{{cite journal |last1=Shaw |first1=Peter |last2=Ozanne |first2=Claire |last3=Speight |first3=Martin |last4=Palmer |first4=Imogen |title=Edge effects and arboreal Collembola in coniferous plantations |journal=Pedobiologia |date=October 2007 |volume=51 |issue=4 |pages=287–293 |doi=10.1016/j.pedobi.2007.04.010 }}</ref><ref>{{cite journal |last1=Zettel |first1=Joerg |last2=Zettel |first2=Ursula |last3=Egger |first3=Beatrice |title=Jumping technique and climbing behaviour of the collembolan Ceratophysella sigillata (Collembola: Hypogastruridae) |journal=European Journal of Entomology |date=15 April 2000 |volume=97 |issue=1 |pages=41–45 |doi=10.14411/eje.2000.010 |doi-access=free }}</ref> These tend to be the larger (>2&nbsp;mm) species, mainly in the genera '']'' and '']'', 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. '']'' spp., ''Entomobrya albocincta'', '']'', '']'') are almost exclusively arboreal.<ref name="Ponge 1993"/> In tropical regions a single square meter of canopy habitat can support many species of Collembola.<ref name="Piper"/>


The main ] driving the local distribution of species is the vertical stratification of the environment: in ] a continuous change in species assemblages can be observed from tree ] to ground ] then to ] down to deeper ]s.<ref name="Ponge 1993"/> This is a complex factor embracing both ] and ] requirements, together with behavioural trends,<ref name="Didden 1987">{{cite journal |last=Didden |first=Wim A. M. |year=1987 |title=Reactions of ''Onychiurus fimatus'' (Collembola) to loose and compact soil: methods and first results |journal=Pedobiologia |volume=30 |issue=2 |pages=93–100 |url=https://www.researchgate.net/publication/40215122 |format=]}}</ref> dispersal limitation<ref>{{cite journal |last1=Rodgers |first1=Denis J. |last2=Kitching |first2=Rodger L. |name-list-style=amp |year=1998 |title=Vertical stratification of rainforest collembolan (Collembola: Insecta) assemblages: description of ecological patterns and hypotheses concerning their generation |journal=] |volume=21 |issue=4 |pages=392–400 |doi=10.1111/j.1600-0587.1998.tb00404.x |citeseerx=10.1.1.476.6663 |s2cid=85133291 }}</ref> and probable species ]. Some species have been shown to exhibit negative<ref>{{cite journal |last1=Bowden |first1=John |last2=Haines |first2=Ian H. |last3=Mercer |first3=D. |name-list-style=amp |year=1976 |title=Climbing Collembola |journal=Pedobiologia |volume=16 |issue=4 |pages=298–312}}</ref> or positive<ref name="Didden 1987"/> ], which adds a ] 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".<ref>{{cite journal |last1=Krab |first1=Eveline J. |last2=Oorsprong |first2=Hilde |last3=Berg |first3=Matty P. |last4=Cornelissen |first4=Johannes H. C. |name-list-style=amp |year=2010 |title=Turning northern peatlands upside down: disentangling microclimate and substrate quality effects on vertical distribution of Collembola |journal=] |volume=24 |issue=6 |pages=1362–1369 |doi=10.1111/j.1365-2435.2010.01754.x |url=https://www.researchgate.net/publication/227703962 |format=]}}</ref> The main ] driving the local distribution of species is the vertical stratification of the environment: in ] a continuous change in species assemblages can be observed from tree ] to ground ] then to ] down to deeper ]s.<ref name="Ponge 1993"/> This is a complex factor embracing both ] and ] requirements, together with behavioural trends,<ref name="Didden 1987">{{cite journal |last=Didden |first=Wim A. M. |year=1987 |title=Reactions of ''Onychiurus fimatus'' (Collembola) to loose and compact soil: methods and first results |journal=Pedobiologia |volume=30 |issue=2 |pages=93–100 |doi=10.1016/S0031-4056(23)00360-8 |s2cid=258140448 |doi-access=free }}</ref> dispersal limitation<ref>{{cite journal |last1=Rodgers |first1=Denis J. |last2=Kitching |first2=Rodger L. |name-list-style=amp |year=1998 |title=Vertical stratification of rainforest collembolan (Collembola: Insecta) assemblages: description of ecological patterns and hypotheses concerning their generation |journal=] |volume=21 |issue=4 |pages=392–400 |doi=10.1111/j.1600-0587.1998.tb00404.x |bibcode=1998Ecogr..21..392R |citeseerx=10.1.1.476.6663 |s2cid=85133291 }}</ref> and probable species ]. Some species have been shown to exhibit negative<ref>{{cite journal |last1=Bowden |first1=John |last2=Haines |first2=Ian H. |last3=Mercer |first3=D. |name-list-style=amp |year=1976 |title=Climbing Collembola |journal=Pedobiologia |volume=16 |issue=4 |pages=298–312|doi=10.1016/S0031-4056(23)02178-9 |s2cid=258572651 }}</ref> or positive<ref name="Didden 1987"/> ], which adds a ] 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".<ref>{{cite journal |last1=Krab |first1=Eveline J. |last2=Oorsprong |first2=Hilde |last3=Berg |first3=Matty P. |last4=Cornelissen |first4=Johannes H. C. |name-list-style=amp |year=2010 |title=Turning northern peatlands upside down: disentangling microclimate and substrate quality effects on vertical distribution of Collembola |journal=] |volume=24 |issue=6 |pages=1362–1369 |doi=10.1111/j.1365-2435.2010.01754.x |doi-access=free |bibcode=2010FuEco..24.1362K }}</ref>


]'' sp. on leaf]] ]'' sp. on leaf]]


As a group, springtails are highly sensitive to ], because of their tegumentary ],<ref>{{cite journal |last1=Nickerl |first1=Julia |last2=Helbig |first2=Ralf |last3=Schulz |first3=Hans-Jürgen |last4=Werner |first4=Carsten |last5=Neinhuis |first5=Christoph |name-list-style=amp |year=2013 |title=Diversity and potential correlations to the function of Collembola cuticle structures |journal=] |volume=132 |issue=2 |pages=183–195 |doi=10.1007/s00435-012-0181-0 |s2cid=14442664 |url=https://www.researchgate.net/publication/257425170 |format=]}}</ref> although some species with thin, permeable cuticles have been shown to resist severe drought by regulating the osmotic pressure of their body fluid.<ref>{{cite journal |last1=Holmstrup |first1=Martin |last2=Bayley |first2=Mark |name-list-style=amp |year=2013 |title=''Protaphorura tricampata'', a euedaphic and highly permeable springtail that can sustain activity by osmoregulation during extreme drought |journal=Journal of Insect Physiology |volume=59 |issue=11 |pages=1104–1110 |doi=10.1016/j.jinsphys.2013.08.015|pmid=24035747 }}</ref> The gregarious behaviour of Collembola, mostly driven by the attractive power of ] excreted by adults,<ref>{{cite journal |last=Verhoef |first=Herman A. |year=1984 |title=Releaser and primer pheromones in Collembola |journal=Journal of Insect Physiology |volume=30 |issue=8 |pages=665–670 |doi=10.1016/0022-1910(84)90052-0 |url=https://eurekamag.com/pdf.php?pdf=006306633 |format=]}}</ref> gives more chance to every juvenile or adult individual to find suitable, better protected places, where desiccation could be avoided and ] and ] rates (thereby ]) could be kept at an optimum.<ref>{{cite journal |last1=Benoit |first1=Joshua B. |last2=Elnitsky |first2=Michael A. |last3=Schulte |first3=Glen G. |last4=Lee |first4=Richard E. Jr|last5=Denlinger |first5=David L. |name-list-style=amp |year=2009 |title=Antarctic Collembolans use chemical signals to promote aggregation and egg laying |journal=Journal of Insect Behavior |volume=22 |issue=2 |pages=121–133 |doi=10.1007/s10905-008-9159-7 |s2cid=914560 |url=http://www.units.miamioh.edu/cryolab/publications/documents/BenoitElnitskyetal_2009.pdf }}</ref> Sensitivity to drought varies from species to species<ref>{{cite journal |last1=Prinzing |first1=Andreas |last2=D'Haese |first2=Cyrille A. |last3=Pavoine |first3=Sandrine |last4=Ponge |first4=Jean-François |name-list-style=amp |year=2014 |title=Species living in harsh environments have low clade rank and are localized on former Laurasian continents: a case study of ''Willemia'' (Collembola) |journal=] |volume=41 |issue=2 |pages=353–365 |doi=10.1111/jbi.12188 |s2cid=86619537 |url=https://www.researchgate.net/publication/259967386 |format=]}}</ref> and increases during ].<ref>{{cite journal |last=Verhoef |first=Herman A. |year=1981 |title=Water balance in Collembola and its relation to habitat selection: water content, haemolymph osmotic pressure and transpiration during an instar |journal=Journal of Insect Physiology |volume=27 |issue=11 |pages=755–760 |doi=10.1016/0022-1910(81)90065-2}}</ref> Given that springtails ] repeatedly during their entire life (an ] character in ]) they spend much time in concealed micro-sites where they can find protection against ] and ] during ], an advantage reinforced by synchronized moulting.<ref>{{cite journal |last=Leinaas |first=Hans Petter |year=1983 |title=Synchronized moulting controlled by communication in group-living Collembola |journal=] |volume=219 |issue=4581 |pages=193–195 |doi=10.1126/science.219.4581.193 |pmid=17841689|bibcode=1983Sci...219..193P |s2cid=41604935 }}</ref> The high humidity environment of many caves also favours springtails and there are numerous cave adapted species,<ref>{{cite journal |last=Wilson |first=Jane M. |year=1982 |title=A review of world Troglopedetini (Insecta, Collembola, Paronellidae), including an identification table and descriptions of new species |journal=Cave Science: Transactions of the British Cave Research Association |volume=9 |issue=3 |pages=210–226 |url=http://www.wcmt.org.uk/sites/default/files/report-documents/Jane%20Wilson%20Howarth.pdf }}</ref><ref>{{cite journal |last1=Palacios-Vargas |first1=José G. |last2=Wilson |first2=Jane |name-list-style=amp |year=1990 |title=''Troglobius coprophagus'', a new genus and species of cave collembolan from Madagascar with notes on its ecology |journal=] |volume=19 |issue=1–4 |pages=67–73 |doi=10.5038/1827-806x.19.1.6 |url=http://www.wilson-howarth.com/Scientific-publications/Troglobius-coprophagus.pdf }}</ref> including one, '']'' living {{convert|1980|m|ft}} down the ].<ref>{{cite journal |last1=Jordana |first1=Rafael |last2=Baquero |first2=Enrique |last3=Reboleira |first3=Sofía |last4=Sendra |first4=Alberto |name-list-style=amp |year=2012 |title=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 |journal=Terrestrial Arthropod Reviews |volume=5 |issue=1 |pages=35–85 |doi=10.1163/187498312X622430 |url=https://www.researchgate.net/publication/234091960 |format=]|hdl=10171/27607 |hdl-access=free }}</ref> As a group, springtails are highly sensitive to ], because of their tegumentary ],<ref>{{cite journal |last1=Nickerl |first1=Julia |last2=Helbig |first2=Ralf |last3=Schulz |first3=Hans-Jürgen |last4=Werner |first4=Carsten |last5=Neinhuis |first5=Christoph |title=Diversity and potential correlations to the function of Collembola cuticle structures |journal=Zoomorphology |date=June 2013 |volume=132 |issue=2 |pages=183–195 |doi=10.1007/s00435-012-0181-0 |s2cid=14442664 }}</ref> although some species with thin, permeable cuticles have been shown to resist severe drought by regulating the osmotic pressure of their body fluid.<ref>{{cite journal |last1=Holmstrup |first1=Martin |last2=Bayley |first2=Mark |name-list-style=amp |year=2013 |title=''Protaphorura tricampata'', a euedaphic and highly permeable springtail that can sustain activity by osmoregulation during extreme drought |journal=Journal of Insect Physiology |volume=59 |issue=11 |pages=1104–1110 |doi=10.1016/j.jinsphys.2013.08.015|pmid=24035747 }}</ref> The gregarious behaviour of Collembola, mostly driven by the attractive power of ] excreted by adults,<ref>{{cite journal |last=Verhoef |first=Herman A. |year=1984 |title=Releaser and primer pheromones in Collembola |journal=Journal of Insect Physiology |volume=30 |issue=8 |pages=665–670 |doi=10.1016/0022-1910(84)90052-0 }}</ref> gives more chance to every juvenile or adult individual to find suitable, better protected places, where desiccation could be avoided and ] and ] rates (thereby ]) could be kept at an optimum.<ref>{{cite journal |last1=Benoit |first1=Joshua B. |last2=Elnitsky |first2=Michael A. |last3=Schulte |first3=Glen G. |last4=Lee |first4=Richard E. Jr|last5=Denlinger |first5=David L. |name-list-style=amp |year=2009 |title=Antarctic Collembolans use chemical signals to promote aggregation and egg laying |journal=Journal of Insect Behavior |volume=22 |issue=2 |pages=121–133 |doi=10.1007/s10905-008-9159-7 |bibcode=2009JIBeh..22..121B |s2cid=914560 }}</ref> Sensitivity to drought varies from species to species<ref>{{cite journal |last1=Prinzing |first1=Andreas |last2=D'Haese |first2=Cyrille A. |last3=Pavoine |first3=Sandrine |last4=Ponge |first4=Jean-François |name-list-style=amp |year=2014 |title=Species living in harsh environments have low clade rank and are localized on former Laurasian continents: a case study of ''Willemia'' (Collembola) |journal=] |volume=41 |issue=2 |pages=353–365 |doi=10.1111/jbi.12188 |bibcode=2014JBiog..41..353P |s2cid=86619537 |url=https://hal.archives-ouvertes.fr/hal-00940083/file/JBI-12-0428-R1_incl_appendices_revision2.pdf }}</ref> and increases during ].<ref>{{cite journal |last=Verhoef |first=Herman A. |year=1981 |title=Water balance in Collembola and its relation to habitat selection: water content, haemolymph osmotic pressure and transpiration during an instar |journal=Journal of Insect Physiology |volume=27 |issue=11 |pages=755–760 |doi=10.1016/0022-1910(81)90065-2}}</ref> Given that springtails ] repeatedly during their entire life (an ] character in ]) they spend much time in concealed micro-sites where they can find protection against ] and ] during ecdysis, an advantage reinforced by synchronized moulting.<ref>{{cite journal |last=Leinaas |first=Hans Petter |year=1983 |title=Synchronized moulting controlled by communication in group-living Collembola |journal=] |volume=219 |issue=4581 |pages=193–195 |doi=10.1126/science.219.4581.193 |pmid=17841689|bibcode=1983Sci...219..193P |s2cid=41604935 }}</ref> The high humidity environment of many caves also favours springtails and there are numerous cave adapted species,<ref>{{cite journal |last=Wilson |first=Jane M. |year=1982 |title=A review of world Troglopedetini (Insecta, Collembola, Paronellidae), including an identification table and descriptions of new species |journal=Cave Science: Transactions of the British Cave Research Association |volume=9 |issue=3 |pages=210–226 |url=http://www.wcmt.org.uk/sites/default/files/report-documents/Jane%20Wilson%20Howarth.pdf |access-date=2016-01-03 |archive-date=2016-08-04 |archive-url=https://web.archive.org/web/20160804122528/http://www.wcmt.org.uk/sites/default/files/report-documents/Jane%20Wilson%20Howarth.pdf |url-status=dead }}</ref><ref>{{cite journal |last1=Palacios-Vargas |first1=José G. |last2=Wilson |first2=Jane |name-list-style=amp |year=1990 |title=''Troglobius coprophagus'', a new genus and species of cave collembolan from Madagascar with notes on its ecology |journal=] |volume=19 |issue=1–4 |pages=67–73 |doi=10.5038/1827-806x.19.1.6 }}</ref> including one, '']'' living {{convert|1980|m|ft}} down the ].<ref>{{cite journal |last1=Jordana |first1=Rafael |last2=Baquero |first2=Enrique |last3=Reboleira |first3=Sofía |last4=Sendra |first4=Alberto |name-list-style=amp |year=2012 |title=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 |journal=Terrestrial Arthropod Reviews |volume=5 |issue=1 |pages=35–85 |doi=10.1163/187498312X622430 |hdl=10171/27607 |hdl-access=free }}</ref>


]'' on water]] ]'' on water]]


The horizontal distribution of springtail species is affected by environmental factors which act at the landscape scale, such as soil ], ] and ].<ref name="Ponge 1993"/> Requirements for ] can be reconstructed experimentally.<ref>{{cite journal |last1=Salmon |first1=Sandrine |last2=Ponge |first2=Jean-François |last3=Van Straalen |first3=Nico |name-list-style=amp |year=2002 |title=Ionic identity of pore water influences pH preference in Collembola |journal=Soil Biology and Biochemistry |volume=34 |issue=11 |pages=1663–1667 |doi=10.1016/S0038-0717(02)00150-5 |url=https://www.researchgate.net/publication/45162312 |format=]}}</ref> Altitudinal changes in species distribution can be at least partly explained by increased acidity at higher elevation.<ref>{{cite journal |last1=Loranger |first1=Gladys |last2=Bandyopadhyaya |first2=Ipsa |last3=Razaka |first3=Barbara |last4=Ponge |first4=Jean-François |name-list-style=amp |year=2001 |title=Does soil acidity explain altitudinal sequences in collembolan communities? |journal=Soil Biology and Biochemistry |volume=33 |issue=3 |pages=381–393 |doi=10.1016/S0038-0717(00)00153-X |s2cid=84523833 |url=https://www.researchgate.net/publication/45172737 |format=]}}</ref> Moisture requirements, among other ecological and behavioural factors, explain why some species cannot live aboveground,<ref>{{cite journal |last1=Faber |first1=Jack H. |last2=Joosse |first2=Els N.G. |name-list-style=amp |year=1993 |title=Vertical distribution of Collembola in a Pinus nigra organic soil |journal=Pedobiologia |volume=37 |issue=6 |pages=336–350}}</ref> or retreat in the soil during dry seasons,<ref>{{cite journal |last=Detsis |first=Vassilis |year=2000 |title=Vertical distribution of Collembola in deciduous forests under Mediterranean climatic conditions |journal=Belgian Journal of Zoology |volume=130 |issue=Supplement 1 |pages=57–61 |url=https://www.researchgate.net/publication/242773445 |format=]}}</ref> but also why some ] springtails are always found in the vicinity of ponds and lakes, such as the hygrophilous '']''.<ref>{{cite web |url=http://urweb.roehampton.ac.uk/collembola/taxonomy/(316IRpal)%20Isotomurus%20palustris.html |title=Isotomurus palustris (Muller, 1776) |access-date=April 2, 2017}}</ref> ] features, such as the presence of a fan-like wettable mucro, allow some species to move at the surface of water ('']'', '']''). '']'', a unique representative of the family ] (and one of the first springtails to have been described by ]), spends its entire life at the surface of water, its wettable eggs dropping in water until the non-wettable first instar hatches then surfaces.<ref>{{cite journal |last=Pichard |first=Sylvain |year=1973 |title=Contribution à l'étude de la biologie de ''Podura aquatica'' (Linné) Collembole |language=fr |journal=Bulletin Biologique de la France et de la Belgique |volume=107 |issue=4 |pages=291–299}}</ref> The horizontal distribution of springtail species is affected by environmental factors which act at the landscape scale, such as soil ], ] and ].<ref name="Ponge 1993"/> Requirements for ] can be reconstructed experimentally.<ref>{{cite journal |last1=Salmon |first1=Sandrine |last2=Ponge |first2=Jean-François |last3=Van Straalen |first3=Nico |name-list-style=amp |year=2002 |title=Ionic identity of pore water influences pH preference in Collembola |journal=Soil Biology and Biochemistry |volume=34 |issue=11 |pages=1663–1667 |doi=10.1016/S0038-0717(02)00150-5 |url=https://hal.archives-ouvertes.fr/hal-00499496/file/Publi_pH_revised.pdf }}</ref> Altitudinal changes in species distribution can be at least partly explained by increased acidity at higher elevation.<ref>{{cite journal |last1=Loranger |first1=Gladys |last2=Bandyopadhyaya |first2=Ipsa |last3=Razaka |first3=Barbara |last4=Ponge |first4=Jean-François |name-list-style=amp |year=2001 |title=Does soil acidity explain altitudinal sequences in collembolan communities? |journal=Soil Biology and Biochemistry |volume=33 |issue=3 |pages=381–393 |doi=10.1016/S0038-0717(00)00153-X |s2cid=84523833 |url=https://hal.archives-ouvertes.fr/hal-00501866/file/Article.pdf }}</ref> Moisture requirements, among other ecological and behavioural factors, explain why some species cannot live aboveground,<ref>{{cite journal |last1=Faber |first1=Jack H. |last2=Joosse |first2=Els N.G. |name-list-style=amp |year=1993 |title=Vertical distribution of Collembola in a Pinus nigra organic soil |journal=Pedobiologia |volume=37 |issue=6 |pages=336–350|doi=10.1016/S0031-4056(24)00108-2 |doi-access=free }}</ref> or retreat in the soil during dry seasons,<ref>{{cite journal |last=Detsis |first=Vassilis |year=2000 |title=Vertical distribution of Collembola in deciduous forests under Mediterranean climatic conditions |journal=Belgian Journal of Zoology |volume=130 |issue=Supplement 1 |pages=57–61 |url=https://www.researchgate.net/publication/242773445 |format=]}}</ref> but also why some ] springtails are always found in the vicinity of ponds and lakes, such as the hygrophilous '']''.<ref>{{cite web |url=http://urweb.roehampton.ac.uk/collembola/taxonomy/(316IRpal)%20Isotomurus%20palustris.html |title=Isotomurus palustris (Muller, 1776) |access-date=April 2, 2017}}</ref> ] features, 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.<ref>{{Cite book|url=https://books.google.com/books?id=dC2gEAAAQBAJ&dq=snow+hydrophilic+P.+aquatica&pg=PA227|title=Identification and Ecology of Freshwater Arthropods in the Mediterranean Basin|first1=Alain|last1=Maasri|first2=James H.|last2=Thorp|date=October 31, 2023|publisher=Elsevier|isbn=978-0-12-821856-3 |via=Google Books}}</ref> '']'', a unique representative of the family ] (and one of the first springtails to have been described by ]), spends its entire life at the surface of water, its wettable eggs dropping in water until the non-wettable first instar hatches then surfaces.<ref>{{cite journal |last=Pichard |first=Sylvain |year=1973 |title=Contribution à l'étude de la biologie de ''Podura aquatica'' (Linné) Collembole |language=fr |journal=Bulletin Biologique de la France et de la Belgique |volume=107 |issue=4 |pages=291–299}}</ref> 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.<ref>{{Cite book|url=https://books.google.com/books?id=98mcDwAAQBAJ&dq=P.+aquatica+springtail+eggs+water&pg=PA198|title=Aquatic Insects: Behavior and Ecology|first1=Kleber|last1=Del-Claro|first2=Rhainer|last2=Guillermo|date=June 10, 2019|publisher=Springer|isbn=978-3-030-16327-3 |via=Google Books}}</ref>


In a variegated landscape, made of a patchwork of closed (]) and open (]s, ]s) environments, most ]-dwelling species are not specialized and can be found everywhere, but most ] and ]-dwelling species are attracted to a particular environment, either forested or not.<ref name="Ponge 1993"/><ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Gillet |first2=Servane |last3=Dubs |first3=Florence |last4=Fédoroff |first4=Éric|last5=Haese |first5=Lucienne |last6=Sousa |first6=José Paulo |last7=Lavelle |first7=Patrick |name-list-style=amp |year=2003 |title=Collembolan communities as bioindicators of land use intensification |journal=Soil Biology and Biochemistry |volume=35 |issue=6 |pages=813–826 |doi=10.1016/S0038-0717(03)00108-1 |url=https://www.researchgate.net/publication/44986540 |format=]|hdl=10316/3875 |s2cid=86289373 |hdl-access=free }}</ref> As a consequence of ] limitation, ] change, when too rapid, may cause the local disappearance of slow-moving, ],<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Dubs |first2=Florence |last3=Gillet |first3=Servane |last4=Sousa |first4=José Paulo |last5=Lavelle |first5=Patrick |name-list-style=amp |year=2006 |title=Decreased biodiversity in soil springtail communities: the importance of dispersal and landuse history in heterogeneous landscapes |journal=Soil Biology and Biochemistry |volume=38 |issue=5 |pages=1158–1161 |doi=10.1016/j.soilbio.2005.09.004 |url=https://www.researchgate.net/publication/44859395 |format=]}}</ref> a phenomenon the measure of which has been called colonisation credit.<ref>{{cite journal |last1=Cristofoli |first1=Sara |last2=Mahy |first2=Grégory |name-list-style=amp |year=2010 |title=Colonisation credit in recent wet heathland butterfly communities |journal=Insect Conservation and Diversity |volume=3 |issue=2 |pages=83–91 |doi=10.1111/j.1752-4598.2009.00075.x|s2cid=86558143 }}</ref><ref>{{cite journal |last1=Heiniger |first1=Charlène |last2=Barot |first2=Sébastien |last3=Ponge |first3=Jean-François |last4=Salmon |first4=Sandrine |last5=Botton-Divet |first5=Léo |last6=Carmignac |first6=David |last7=Dubs |first7=Florence |name-list-style=amp |year=2014 |title=Effect of habitat spatiotemporal structure on collembolan diversity |journal=Pedobiologia |volume=57 |issue=2 |pages=103–117 |doi=10.1016/j.pedobi.2014.01.006 |url=https://www.researchgate.net/publication/260156195 |format=]}}</ref> In a variegated landscape, made of a patchwork of closed (]) and open (]s, ]s) environments, most ]-dwelling species are not specialized and can be found everywhere, but most ] and ]-dwelling species are attracted to a particular environment, either forested or not.<ref name="Ponge 1993"/><ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Gillet |first2=Servane |last3=Dubs |first3=Florence |last4=Fédoroff |first4=Éric|last5=Haese |first5=Lucienne |last6=Sousa |first6=José Paulo |last7=Lavelle |first7=Patrick |name-list-style=amp |year=2003 |title=Collembolan communities as bioindicators of land use intensification |journal=Soil Biology and Biochemistry |volume=35 |issue=6 |pages=813–826 |doi=10.1016/S0038-0717(03)00108-1 |hdl=10316/3875 |s2cid=86289373 |hdl-access=free }}</ref> As a consequence of ] limitation, ] change, when too rapid, may cause the local disappearance of slow-moving, ],<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Dubs |first2=Florence |last3=Gillet |first3=Servane |last4=Sousa |first4=José Paulo |last5=Lavelle |first5=Patrick |name-list-style=amp |year=2006 |title=Decreased biodiversity in soil springtail communities: the importance of dispersal and landuse history in heterogeneous landscapes |journal=Soil Biology and Biochemistry |volume=38 |issue=5 |pages=1158–1161 |doi=10.1016/j.soilbio.2005.09.004 |url=https://hal.archives-ouvertes.fr/hal-00495402/file/Dispersion.pdf }}</ref> a phenomenon the measure of which has been called colonisation credit.<ref>{{cite journal |last1=Cristofoli |first1=Sara |last2=Mahy |first2=Grégory |name-list-style=amp |year=2010 |title=Colonisation credit in recent wet heathland butterfly communities |journal=Insect Conservation and Diversity |volume=3 |issue=2 |pages=83–91 |doi=10.1111/j.1752-4598.2009.00075.x|s2cid=86558143 }}</ref><ref>{{cite journal |last1=Heiniger |first1=Charlène |last2=Barot |first2=Sébastien |last3=Ponge |first3=Jean-François |last4=Salmon |first4=Sandrine |last5=Botton-Divet |first5=Léo |last6=Carmignac |first6=David |last7=Dubs |first7=Florence |name-list-style=amp |year=2014 |title=Effect of habitat spatiotemporal structure on collembolan diversity |journal=Pedobiologia |volume=57 |issue=2 |pages=103–117 |doi=10.1016/j.pedobi.2014.01.006 |url=https://hal.archives-ouvertes.fr/hal-00964875v2/file/PEDOBI-D-13-00047R2.pdf }}</ref>


=== Relationship with humans === === Relationship with humans ===
]'' sp. from Germany]] ]'' sp. from Germany]]


Springtails are well known as ] of some agricultural crops. '']'', the lucerne flea, has been shown to cause severe damage to agricultural crops,<ref>{{cite journal |last1=Shaw |first1=Michael W. |last2=Haughs |first2=G. M. |name-list-style=amp |year=1983 |title=Damage to potato foliage by ''Sminthurus viridis'' (L.) |journal=] |volume=32 |issue=4 |pages=465–466 |doi=10.1111/j.1365-3059.1983.tb02864.x |url=https://eurekamag.com/pdf.php?pdf=001179151 |format=]}}</ref> and is considered as a pest in Australia.<ref>{{cite journal |last1=Bishop |first1=Alan L. |last2=Harris |first2=Anne M. |last3=McKenzie |first3=Harry J. |name-list-style=amp |year=2001 |title=Distribution and ecology of the lucerne flea, ''Sminthurus viridis'' (L.) (Collembola: Sminthuridae), in irrigated lucerne in the Hunter dairying region of New South Wales |journal=] |volume=40 |issue=1 |pages=49–55 |doi=10.1046/j.1440-6055.2001.00202.x |url=https://eurekamag.com/pdf.php?pdf=003408913 |format=]}}</ref><ref>{{cite web |publisher=] |year=2017 |url=http://agriculture.vic.gov.au/agriculture/pests-diseases-and-weeds/pest-insects-and-mites/lucerne-flea |title=Lucerne Flea |access-date=June 2, 2018}}</ref> Onychiuridae are also known to feed on tubers and to damage them to some extent.<ref>{{cite journal |last1=Baker |first1=A. N. |last2=Dunning |first2=Andrew R. |name-list-style=amp |year=1975 |title=Association of populations of onychiurid Collembola with damage to sugar-beet seedlings |journal=] |volume=24 |issue=3 |pages=150–154 |doi=10.1111/j.1365-3059.1975.tb01882.x |url=https://eurekamag.com/pdf.php?pdf=000025743 |format=]}}</ref> However, by their capacity to carry spores of ] and ] on their tegument, soil springtails play a positive role in the establishment of plant-fungal ] and thus are beneficial to agriculture.<ref>{{cite journal |last1=Klironomos |first1=John N. |last2=Moutoglis |first2=Peter |name-list-style=amp |year=1999 |title=Colonization of nonmycorrhizal plants by mycorrhizal neighbours as influenced by the collembolan, ''Folsomia candida'' |journal=Biology and Fertility of Soils |volume=29 |issue=3 |pages=277–281 |doi=10.1007/s003740050553 |s2cid=11014525 |url=https://eurekamag.com/pdf.php?pdf=003071115 |format=]}}</ref> They also contribute to controlling plant ] through their active consumption of ] and ] of ] and ] fungi.<ref>{{cite journal |last1=Sabatini |first1=Maria Agnese |last2=Innocenti |first2=Gloria |name-list-style=amp |year=2001 |title=Effects of Collembola on plant-pathogenic fungus interactions in simple experimental systems |journal=Biology and Fertility of Soils |volume=33 |issue=1 |pages=62–66 |doi=10.1007/s003740000290 |s2cid=9273050 |url=https://eurekamag.com/pdf.php?pdf=003424094 |format=]}}</ref><ref>{{cite journal |last1=Shiraishi |first1=Hiroyoshi |last2=Enami |first2=Yoshinari |last3=Okano |first3=Seigo |name-list-style=amp |year=2003 |title=''Folsomia hidakana'' (Collembola) prevents damping-off disease in cabbage and Chinese cabbage by ''Rhizoctonia solani'' |journal=Pedobiologia |volume=47 |issue=1 |pages=33–38 |doi=10.1078/0031-4056-00167 |url=https://eurekamag.com/pdf.php?pdf=003774597 |format=]}}</ref> It has been suggested that they could be reared to be used for the control of ] in greenhouses and other indoor cultures.<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Charpentié |first2=Marie-José |name-list-style=amp |year=1981 |title=Étude des relations microflore-microfaune: expériences sur ''Pseudosinella alba'' (Packard), Collembole mycophage |language=fr |journal=Revue d'Écologie et de Biologie du Sol |volume=18 |pages=291–303 |url=https://eurekamag.com/pdf.php?pdf=017192513 |format=]}}</ref><ref>{{cite journal |last1=Lartey |first1=Robert T. |last2=Curl |first2=Elroy A. |last3=Peterson |first3=Curt M. |last4=Harper |first4=James D. |name-list-style=amp |year=1989 |title=Mycophagous grazing and food preference of ''Proisotoma minuta'' (Collembola: Isotomidae) and ''Onychiurus encarpatus'' (Collembola: Onychiuridae) |journal=Environmental Entomology |volume=18 |issue=2 |pages=334–337|doi=10.1093/ee/18.2.334}}</ref> Springtails are well known as ] of some agricultural crops. '']'', the lucerne flea, has been shown to cause severe damage to agricultural crops,<ref>{{cite journal |last1=Shaw |first1=Michael W. |last2=Haughs |first2=G. M. |name-list-style=amp |year=1983 |title=Damage to potato foliage by ''Sminthurus viridis'' (L.) |journal=] |volume=32 |issue=4 |pages=465–466 |doi=10.1111/j.1365-3059.1983.tb02864.x }}</ref> and is considered as a pest in Australia.<ref>{{cite journal |last1=Bishop |first1=Alan L. |last2=Harris |first2=Anne M. |last3=McKenzie |first3=Harry J. |name-list-style=amp |year=2001 |title=Distribution and ecology of the lucerne flea, ''Sminthurus viridis'' (L.) (Collembola: Sminthuridae), in irrigated lucerne in the Hunter dairying region of New South Wales |journal=] |volume=40 |issue=1 |pages=49–55 |doi=10.1046/j.1440-6055.2001.00202.x }}</ref><ref>{{cite web |publisher=] |year=2017 |url=http://agriculture.vic.gov.au/agriculture/pests-diseases-and-weeds/pest-insects-and-mites/lucerne-flea |title=Lucerne Flea |access-date=June 2, 2018}}</ref> Onychiuridae are also known to feed on tubers and to damage them to some extent.<ref>{{cite journal |last1=Baker |first1=A. N. |last2=Dunning |first2=Andrew R. |name-list-style=amp |year=1975 |title=Association of populations of onychiurid Collembola with damage to sugar-beet seedlings |journal=] |volume=24 |issue=3 |pages=150–154 |doi=10.1111/j.1365-3059.1975.tb01882.x }}</ref> However, by their capacity to carry spores of ] and ] on their tegument, soil springtails play a positive role in the establishment of plant-fungal ] and thus are beneficial to agriculture.<ref>{{cite journal |last1=Klironomos |first1=John N. |last2=Moutoglis |first2=Peter |name-list-style=amp |year=1999 |title=Colonization of nonmycorrhizal plants by mycorrhizal neighbours as influenced by the collembolan, ''Folsomia candida'' |journal=Biology and Fertility of Soils |volume=29 |issue=3 |pages=277–281 |doi=10.1007/s003740050553 |bibcode=1999BioFS..29..277K |s2cid=11014525 }}</ref> They also contribute to controlling plant ] through their active consumption of ] and ] of ] and ] fungi.<ref>{{cite journal |last1=Sabatini |first1=Maria Agnese |last2=Innocenti |first2=Gloria |name-list-style=amp |year=2001 |title=Effects of Collembola on plant-pathogenic fungus interactions in simple experimental systems |journal=Biology and Fertility of Soils |volume=33 |issue=1 |pages=62–66 |doi=10.1007/s003740000290 |bibcode=2001BioFS..33...62S |s2cid=9273050 }}</ref><ref>{{cite journal |last1=Shiraishi |first1=Hiroyoshi |last2=Enami |first2=Yoshinari |last3=Okano |first3=Seigo |name-list-style=amp |year=2003 |title=''Folsomia hidakana'' (Collembola) prevents damping-off disease in cabbage and Chinese cabbage by ''Rhizoctonia solani'' |journal=Pedobiologia |volume=47 |issue=1 |pages=33–38 |doi=10.1078/0031-4056-00167 }}</ref> It has been suggested that they could be reared to be used for the control of ] in greenhouses and other indoor cultures.<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Charpentié |first2=Marie-José |title=Étude des relations microflore-microfaune: expériences sur Pseudosinella alba (Packard), Collembole mycophage |journal=Revue d'Écologie et de Biologie du Sol |date=1981 |volume=18 |issue=3 |pages=291–303 |url=https://hal.science/hal-00507105/ }}</ref><ref>{{cite journal |last1=Lartey |first1=Robert T. |last2=Curl |first2=Elroy A. |last3=Peterson |first3=Curt M. |last4=Harper |first4=James D. |name-list-style=amp |year=1989 |title=Mycophagous grazing and food preference of ''Proisotoma minuta'' (Collembola: Isotomidae) and ''Onychiurus encarpatus'' (Collembola: Onychiuridae) |journal=Environmental Entomology |volume=18 |issue=2 |pages=334–337|doi=10.1093/ee/18.2.334}}</ref>


Various sources and publications have suggested that some springtails may ] 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.<ref name="J&C2007">{{cite web |last1=Janssens |first1=Frans |last2=Christiansen |first2=Kenneth A. |name-list-style=amp |work=Checklist of the Collembola |url=http://www.collembola.org/publicat/sidney.htm |title=Synanthropic Collembola, springtails in association with Man |date=November 22, 2007 |access-date=April 9, 2017}}</ref> 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 ], 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 ]; 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.<ref name="J&C2007"/><ref>{{cite journal |last=Berenbaum |first=May |year=2005 |title=Face time |journal=] |volume=51 |issue=2 |pages=68–69 |doi=10.1093/ae/51.2.68 |url=http://www.entsoc.org/PDF/Pubs/Periodicals/AE/AE-2005/Summer/buzzwords.pdf }}</ref><ref>{{cite journal |last1=Christiansen |first1=Kenneth |last2=Bernard |first2=Ernest C. |name-list-style=amp |year=2008 |title=Critique of the article "Collembola (Springtails) (Arthropoda: Hexapoda: Entognatha) found in scrapings from individuals diagnosed with delusory parasitosis" |journal=] |volume=119 |issue=5 |pages=537–540 |doi=10.3157/0013-872x-119.5.537|s2cid=83870937 }}</ref><ref>{{cite journal |last1=Lim |first1=Christopher Seng-Hong |last2=Lim |first2=Scott L. |last3=Chew |first3=Fook Tim |last4=Deharveng |first4=Louis |name-list-style=amp |year=2009 |title=Collembola are unlikely to cause human dermatitis |journal=] |volume=9 |issue=3 |pages=1–5 |doi=10.1673/031.009.0301 |pmc=3011850 |pmid=19611235}}</ref><ref>{{cite journal |last=Shelomi |first=Matan |title=Evidence of photo manipulation in a delusional parasitosis paper |journal=] |year=2013 |volume=99 |issue=3 |pages=583–585 |doi=10.1645/12-12.1 |pmid=23198757 |s2cid=6473251 |url=https://www.researchgate.net/publication/233825102 |access-date=29 January 2019 |format=]}}</ref> However, Steve Hopkin reports one instance of an entomologist ] an '']'' 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.<ref name="Hopkin1997"/> Various sources and publications have suggested that some springtails may ] 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 springtails can cause irritation when rubbed onto the skin.<ref name="J&C2007">{{cite web |last1=Janssens |first1=Frans |last2=Christiansen |first2=Kenneth A. |name-list-style=amp |work=Checklist of the Collembola |url=http://www.collembola.org/publicat/sidney.htm |title=Synanthropic Collembola, springtails in association with Man |date=November 22, 2007 |access-date=April 9, 2017}}</ref> 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 ], 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 ]; 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.<ref name="J&C2007"/><ref>{{cite journal |last=Berenbaum |first=May |year=2005 |title=Face time |journal=] |volume=51 |issue=2 |pages=68–69 |doi=10.1093/ae/51.2.68 }}</ref><ref>{{cite journal |last1=Christiansen |first1=Kenneth |last2=Bernard |first2=Ernest C. |name-list-style=amp |year=2008 |title=Critique of the article "Collembola (Springtails) (Arthropoda: Hexapoda: Entognatha) found in scrapings from individuals diagnosed with delusory parasitosis" |journal=] |volume=119 |issue=5 |pages=537–540 |doi=10.3157/0013-872x-119.5.537|s2cid=83870937 }}</ref><ref>{{cite journal |last1=Lim |first1=Christopher Seng-Hong |last2=Lim |first2=Scott L. |last3=Chew |first3=Fook Tim |last4=Deharveng |first4=Louis |name-list-style=amp |year=2009 |title=Collembola are unlikely to cause human dermatitis |journal=] |volume=9 |issue=3 |pages=1–5 |doi=10.1673/031.009.0301 |pmc=3011850 |pmid=19611235}}</ref><ref>{{cite journal |last=Shelomi |first=Matan |author1-link=Matan Shelomi |title=Evidence of photo manipulation in a delusional parasitosis paper |journal=] |year=2013 |volume=99 |issue=3 |pages=583–585 |doi=10.1645/12-12.1 |pmid=23198757 |s2cid=6473251 }}</ref> However, Steve Hopkin reports one instance of an entomologist ] an '']'' 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.<ref name="Hopkin1997"/>


In 1952, ] accused the ] military of spreading bacteria-laden insects and other objects during the ] by dropping them from ] fighters above rebel villages over ]. In all, the U.S. was accused of dropping ants, beetles, crickets, fleas, flies, grasshoppers, lice, springtails, and stoneflies as part of a ] effort. The alleged associated diseases included ], ], ], ], ], ], ], ], and ]. 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. The ] denied 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.<ref></ref> Springtail species cited in ] were ''Isotoma (Desoria) negishina'' (a local species) and the "white rat springtail" '']''.<ref>{{cite book |last=Lockwood |first=Jeffrey A. |title=Six-legged soldiers: using insects as weapons of war |edition=1st |publisher=] |location=Oxford, UK |year=2009 |isbn=978-0-19-533305-3}}</ref> In 1952, ] accused the ] military of spreading bacteria-laden insects and other objects during the ] by dropping them from ] fighters above rebel villages over ]. In all, the U.S. was accused of dropping ants, beetles, crickets, fleas, flies, grasshoppers, lice, springtails, and stoneflies as part of a ] effort. The alleged associated diseases included ], ], ], ], ], ], ], ], and ]. 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. The ] denied 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.<ref>{{Cite web |title=Insects as Biological Weapons - Insects, Disease, and History {{!}} Montana State University |url=https://www.montana.edu/historybug/insects-as-bioweapons.html |access-date=2022-10-06 |website=www.montana.edu}}</ref> Springtail species cited in ] were ''Isotoma (Desoria) negishina'' (a local species) and the "white rat springtail" '']''.<ref>{{cite book |last=Lockwood |first=Jeffrey A. |title=Six-legged soldiers: using insects as weapons of war |edition=1st |publisher=] |location=Oxford, UK |year=2009 |isbn=978-0-19-533305-3}}</ref>


Captive springtails are often kept in a ] as part of a ].<ref>{{cite web |url=https://www.reptilecentre.com/blog/2015/12/top-5-bioactive-clean-up-crew/ |title=The Top 5 Bioactive Clean Up Crew |work=Northampton Reptile Centre |date=16 December 2015 |access-date=6 July 2021 |url-status=live}}</ref> Captive springtails are often kept in a ] as part of a ].<ref>{{cite web |url=https://www.reptilecentre.com/blog/2015/12/top-5-bioactive-clean-up-crew/ |title=The Top 5 Bioactive Clean Up Crew |work=Northampton Reptile Centre |date=16 December 2015 |access-date=6 July 2021 }}</ref>


=== Ecotoxicology laboratory animals === === Ecotoxicology laboratory animals ===
Springtails are currently used in laboratory tests for the early detection of ]. ] and ] tests have been performed by researchers, mostly using the ] ] ''Folsomia candida''.<ref>{{cite journal |last1=Fountain |first1=Michelle T. |last2=Hopkin |first2=Steve P. |name-list-style=amp |year=2001 |title=Continuous monitoring of ''Folsomia candida'' (Insecta: Collembola) in a metal exposure test |journal=Ecotoxicology and Environmental Safety |volume=48 |issue=3 |pages=275–286 |doi=10.1006/eesa.2000.2007 |pmid=11222037 |url=https://eurekamag.com/pdf.php?pdf=003392782 |format=]}}</ref> These tests have been standardized.<ref>{{cite web |author=ISO 11267 |year=2014 |title=Soil quality. Inhibition of reproduction of Collembola (''Folsomia candida'') by soil contaminants |publisher=] |location=Geneva |url=http://www.iso.org/iso/home/store/catalogue_ics/catalogue_detail_ics.htm?csnumber=57582}}</ref> Details on a ], on the biology and ] 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.<ref>{{cite web |last=Krogh |first=Paul Henning |url=http://www.oecd.org/chemicalsafety/testing/41389036.pdf |title=Toxicity testing with the collembolans ''Folsomia fimetaria'' and ''Folsomia candida'' and the results of a ringtest |date=August 1, 2008 |access-date=April 17, 2017 }}</ref> Care should be taken that different strains of the same species may be conducive to different results. Avoidance tests have been also performed.<ref>{{cite journal |last1=Lors |first1=Christine |last2=Martínez Aldaya |first2=Maite |last3=Salmon |first3=Sandrine |last4=Ponge |first4=Jean-François |name-list-style=amp |year=2006 |title=Use of an avoidance test for the assessment of microbial degradation of PAHs |journal=Soil Biology and Biochemistry |volume=38 |issue=8 |pages=2199–2204 |doi=10.1016/j.soilbio.2006.01.026 |url=https://eurekamag.com/pdf.php?pdf=012727453 |format=]}}</ref> They have been standardized, too.<ref>{{cite web |author=ISO 17512-2 |year=2011 |title=Soil quality. Avoidance test for determining the quality of soils and effects of chemicals on behaviour. Part 2: Test with collembolans (''Folsomia candida'') |publisher=] |location=Geneva |url=http://www.iso.org/iso/iso_catalogue/catalogue_tc/catalogue_detail.htm?csnumber=50779}}</ref> 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.<ref>{{cite journal |last1=Chauvat |first1=Matthieu |last2=Ponge |first2=Jean-François |name-list-style=amp |year=2002 |title=Colonization of heavy metal-polluted soils by collembola: preliminary experiments in compartmented boxes |journal=Applied Soil Ecology |volume=21 |issue=2 |pages=91–106 |doi=10.1016/S0929-1393(02)00087-2 |url=https://eurekamag.com/pdf.php?pdf=003683138 |format=]}}</ref> 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 ]s, and like many insects and molluscs, Collembola are very sensitive to ]s and thus are threatened in no-tillage agriculture, which makes a more intense use of herbicides than conventional agriculture.<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Bandyopadhyaya |first2=Ipsa |last3=Marchetti |first3=Valérie |name-list-style=amp |year=2002 |title=Interaction between humus form and herbicide toxicity to Collembola (Hexapoda) |journal=Applied Soil Ecology |volume=20 |issue=3 |pages=239–253 |doi=10.1016/S0929-1393(02)00026-4 |url=https://eurekamag.com/pdf.php?pdf=003820483 |format=]}}</ref> Springtails are currently used in laboratory tests for the early detection of ]. ] and ] tests have been performed by researchers, mostly using the ] ] ''Folsomia candida''.<ref>{{cite journal |last1=Fountain |first1=Michelle T. |last2=Hopkin |first2=Steve P. |name-list-style=amp |year=2001 |title=Continuous monitoring of ''Folsomia candida'' (Insecta: Collembola) in a metal exposure test |journal=Ecotoxicology and Environmental Safety |volume=48 |issue=3 |pages=275–286 |doi=10.1006/eesa.2000.2007 |pmid=11222037 }}</ref> These tests have been standardized.<ref>{{cite web |author=ISO 11267 |year=2014 |title=Soil quality. Inhibition of reproduction of Collembola (''Folsomia candida'') by soil contaminants |publisher=] |location=Geneva |url=http://www.iso.org/iso/home/store/catalogue_ics/catalogue_detail_ics.htm?csnumber=57582}}</ref> Details on a ], on the biology and ] 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.<ref>{{cite web |last=Krogh |first=Paul Henning |url=http://www.oecd.org/chemicalsafety/testing/41389036.pdf |title=Toxicity testing with the collembolans ''Folsomia fimetaria'' and ''Folsomia candida'' and the results of a ringtest |date=August 1, 2008 |access-date=April 17, 2017 }}</ref> Care should be taken that different strains of the same species may be conducive to different results. Avoidance tests have been also performed.<ref>{{cite journal |last1=Lors |first1=Christine |last2=Martínez Aldaya |first2=Maite |last3=Salmon |first3=Sandrine |last4=Ponge |first4=Jean-François |name-list-style=amp |year=2006 |title=Use of an avoidance test for the assessment of microbial degradation of PAHs |journal=Soil Biology and Biochemistry |volume=38 |issue=8 |pages=2199–2204 |doi=10.1016/j.soilbio.2006.01.026 |url=https://hal.archives-ouvertes.fr/hal-00495395/file/Microflora.pdf }}</ref> They have been standardized, too.<ref>{{cite web |author=ISO 17512-2 |year=2011 |title=Soil quality. Avoidance test for determining the quality of soils and effects of chemicals on behaviour. Part 2: Test with collembolans (''Folsomia candida'') |publisher=] |location=Geneva |url=http://www.iso.org/iso/iso_catalogue/catalogue_tc/catalogue_detail.htm?csnumber=50779}}</ref> 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.<ref>{{cite journal |last1=Chauvat |first1=Matthieu |last2=Ponge |first2=Jean-François |name-list-style=amp |year=2002 |title=Colonization of heavy metal-polluted soils by collembola: preliminary experiments in compartmented boxes |journal=Applied Soil Ecology |volume=21 |issue=2 |pages=91–106 |doi=10.1016/S0929-1393(02)00087-2 |bibcode=2002AppSE..21...91C |url=https://hal.archives-ouvertes.fr/hal-00498579/file/ARTICLE.pdf }}</ref> 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 ]s, and like many insects and molluscs, Collembola are very sensitive to ]s and thus are threatened in no-tillage agriculture, which makes a more intense use of herbicides than conventional agriculture.<ref>{{cite journal |last1=Ponge |first1=Jean-François |last2=Bandyopadhyaya |first2=Ipsa |last3=Marchetti |first3=Valérie |name-list-style=amp |year=2002 |title=Interaction between humus form and herbicide toxicity to Collembola (Hexapoda) |journal=Applied Soil Ecology |volume=20 |issue=3 |pages=239–253 |doi=10.1016/S0929-1393(02)00026-4 |bibcode=2002AppSE..20..239P |url=https://hal.archives-ouvertes.fr/hal-00499536/file/Herbicide.pdf }}</ref>
The springtail '']'' is also becoming a ] model organism for soil toxicology.<ref>{{cite journal |last1=Nota |first1=Benjamin |last2=Timmermans |first2=Martijn J.T.N. |last3=Franken |first3=Oscar |last4=Montagne-Wajer |first4=Kora |last5=Mariën |first5=Janine |last6=De Boer |first6=Muriel E. |last7=De Boer |first7=Tjalf E. |last8=Ylstra |first8=Bauke |last9=Van Straalen |first9=Nico M. |last10=Roelofs |first10=Dick |name-list-style=amp |year=2008 |title=Gene expression analysis of Collembola in cadmium containing soil |journal=] |volume=42 |issue=21 |pages=8152–8157 |pmid=19031917 |doi=10.1021/es801472r |bibcode=2008EnST...42.8152N |url=https://www.researchgate.net/publication/23495797 |format=]}}</ref><ref>{{cite journal |last1=Nota |first1=Benjamin |last2=Bosse |first2=Mirte |last3=Ylstra |first3=Bauke |last4=Van Straalen |first4=Nico M. |last5=Roelofs |first5=Dick |name-list-style=amp |year=2009 |title=Transcriptomics reveals extensive inducible biotransformation in the soil-dwelling invertebrate ''Folsomia candida'' exposed to phenanthrene |journal=] |volume=10 |pages=236 |pmid=19457238 |doi=10.1186/1471-2164-10-236 |pmc=2688526 |url=}}</ref> With ] 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. The springtail '']'' is also becoming a ] model organism for soil toxicology.<ref>{{cite journal |last1=Nota |first1=Benjamin |last2=Timmermans |first2=Martijn J.T.N. |last3=Franken |first3=Oscar |last4=Montagne-Wajer |first4=Kora |last5=Mariën |first5=Janine |last6=De Boer |first6=Muriel E. |last7=De Boer |first7=Tjalf E. |last8=Ylstra |first8=Bauke |last9=Van Straalen |first9=Nico M. |last10=Roelofs |first10=Dick |name-list-style=amp |year=2008 |title=Gene expression analysis of Collembola in cadmium containing soil |journal=] |volume=42 |issue=21 |pages=8152–8157 |pmid=19031917 |doi=10.1021/es801472r |bibcode=2008EnST...42.8152N }}</ref><ref>{{cite journal |last1=Nota |first1=Benjamin |last2=Bosse |first2=Mirte |last3=Ylstra |first3=Bauke |last4=Van Straalen |first4=Nico M. |last5=Roelofs |first5=Dick |name-list-style=amp |year=2009 |title=Transcriptomics reveals extensive inducible biotransformation in the soil-dwelling invertebrate ''Folsomia candida'' exposed to phenanthrene |journal=] |volume=10 |pages=236 |pmid=19457238 |doi=10.1186/1471-2164-10-236 |pmc=2688526 |url= |doi-access=free }}</ref> With ] 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.<ref>{{Cite journal |last1=Kim |first1=Shin Woong |last2=An |first2=Youn-Joo |name-list-style=amp |year=2014 |title=Jumping behavior of the springtail ''Folsomia candida'' as a novel soil quality indicator in metal-contaminated soils |journal=Ecological Indicators |volume=38|pages=67–71 |doi=10.1016/j.ecolind.2013.10.033 }}</ref> 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.<ref>{{Cite journal |last1=Kim |first1=Shin Woong |last2=An |first2=Youn-Joo |name-list-style=amp |year=2014 |title=Jumping behavior of the springtail ''Folsomia candida'' as a novel soil quality indicator in metal-contaminated soils |journal=Ecological Indicators |volume=38|pages=67–71 |doi=10.1016/j.ecolind.2013.10.033 }}</ref>


==Climate warming impact== ==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.<ref>{{cite journal |last1=Nielsen |first1=Uffe N. |last2=Wall |first2=Diana H. |name-list-style=amp |year=2013 |title=The future of soil invertebrate communities in polar regions: different climate change responses in the Arctic and Antarctic? |journal=] |volume=16 |issue=3 |pages=409–419 |pmid= 23278945 |doi=10.1111/ele.12058 |doi-access=free }}</ref> There are negative,<ref>{{cite journal |last1=Coulson |first1=Stephen James |last2=Hodkinson |first2=Ian D. |last3=Woolley |first3=Christopher |last4=Webb |first4=Nigel R. |last5=Block |first5=William |last6=Worland |first6=M. Rodger |last7=Bale |first7=Jeff S. |last8=Strathdee |first8=Andrew T. |name-list-style=amp |year=1996 |title=Effects of experimental temperature elevation on high-arctic soil microarthropod populations |journal=] |volume=16 |issue=2 |pages=147–153 |doi=10.1007/BF02390435 |s2cid=13826340 |url=https://eurekamag.com/pdf.php?pdf=008566942 |format=]}}</ref><ref name="Sjursen, H. 2005">{{cite journal |last1=Sjursen |first1=Heidi |last2=Michelsen |first2=Anders |last3=Jonasson |first3=Sven |name-list-style=amp |year=2005 |title=Effects of long-term soil warming and fertilisation on microarthropod abundances in three sub-arctic ecosystems |journal=Applied Soil Ecology |volume=30 |issue=3 |pages=148–161 |doi=10.1016/j.apsoil.2005.02.013 |url=https://eurekamag.com/pdf.php?pdf=004424159 |format=]}}</ref> positive<ref>{{cite journal |last1=Dollery |first1=Rebecca |last2=Hodkinson |first2=Ian D. |last3=Jónsdóttir |first3=Ingibjörg S. |name-list-style=amp |year=2006 |title=Impact of warming and timing of snow melt on soil microarthropod assemblages associated with Dryas-dominated plant communities on Svalbard |journal=] |volume=29 |issue=1 |pages=111–119 |doi=10.1111/j.2006.0906-7590.04366.x |url=https://www.researchgate.net/publication/229527988 |format=]}}</ref><ref>{{cite journal |last1=Hågvar |first1=Sigmund |last2=Klanderud |first2=Kari |name-list-style=amp |year=2009 |title=Effect of simulated environmental change on alpine soil arthropods |journal=Global Change Biology |volume=15 |issue=12 |pages=2972–2980 |doi=10.1111/j.1365-2486.2009.01926.x |bibcode=2009GCBio..15.2972H |url=http://www.uib.no/filearchive/hagvar-klanderud-gcb2009.pdf |citeseerx=10.1.1.658.1606 |s2cid=36287733 }}</ref> and neutral responses reported.<ref name="Sjursen, H. 2005"/><ref name="Alatalo, JM 2015">{{cite journal |last1=Alatalo |first1=Juha M. |last2=Jägerbrand |first2=Annika K. |last3=Čuchta |first3=Peter |name-list-style=amp |year=2015 |title=Collembola in three alpine subarctic sites resistant to twenty years of experimental warming |journal=] |volume=5 |issue=18161 |pages=18161 |doi=10.1038/srep18161 |pmc=4680968 |pmid=26670681|bibcode=2015NatSR...518161A }}</ref> Neutral responses to experimental warming have also been reported in studies of non-polar regions.<ref>{{cite journal|last1=Kardol|first1=Paul|last2=Reynolds|first2=W. Nicholas|last3=Norby|first3=Richard J.|last4=Classen|first4=Aimée T.|author-link4=Aimée Classen|year=2011|title=Climate change effects on soil microarthropod abundance and community structure|url=https://www.researchgate.net/publication/225292391|format=]|journal=Applied Soil Ecology|volume=47|issue=1|pages=37–44|doi=10.1016/j.apsoil.2010.11.001|via=|name-list-style=amp}}</ref> 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.<ref>{{cite journal |last1=Harte |first1=John |last2=Rawa |first2=Agnieszka |last3=Price |first3=Vanessa |name-list-style=amp |year=1996 |title=Effects of manipulated soil microclimate on mesofaunal biomass and diversity |journal=Soil Biology and Biochemistry |volume=28 |issue=3 |pages=313–322 |doi=10.1016/0038-0717(95)00139-5 |url=https://eurekamag.com/pdf.php?pdf=002823138 |format=]}}</ref> 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.<ref name="Alatalo, JM 2015"/> 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.<ref>{{cite journal |last1=Nielsen |first1=Uffe N. |last2=Wall |first2=Diana H. |name-list-style=amp |year=2013 |title=The future of soil invertebrate communities in polar regions: different climate change responses in the Arctic and Antarctic? |journal=] |volume=16 |issue=3 |pages=409–419 |pmid= 23278945 |doi=10.1111/ele.12058 |doi-access= |bibcode=2013EcolL..16..409N }}</ref> There are negative,<ref>{{cite journal |last1=Coulson |first1=Stephen James |last2=Hodkinson |first2=Ian D. |last3=Woolley |first3=Christopher |last4=Webb |first4=Nigel R. |last5=Block |first5=William |last6=Worland |first6=M. Rodger |last7=Bale |first7=Jeff S. |last8=Strathdee |first8=Andrew T. |name-list-style=amp |year=1996 |title=Effects of experimental temperature elevation on high-arctic soil microarthropod populations |journal=] |volume=16 |issue=2 |pages=147–153 |doi=10.1007/BF02390435 |bibcode=1996PoBio..16..147C |s2cid=13826340 }}</ref><ref name="Sjursen, H. 2005">{{cite journal |last1=Sjursen |first1=Heidi |last2=Michelsen |first2=Anders |last3=Jonasson |first3=Sven |name-list-style=amp |year=2005 |title=Effects of long-term soil warming and fertilisation on microarthropod abundances in three sub-arctic ecosystems |journal=Applied Soil Ecology |volume=30 |issue=3 |pages=148–161 |doi=10.1016/j.apsoil.2005.02.013 |bibcode=2005AppSE..30..148S }}</ref> positive<ref>{{cite journal |last1=Dollery |first1=Rebecca |last2=Hodkinson |first2=Ian D. |last3=Jónsdóttir |first3=Ingibjörg S. |name-list-style=amp |year=2006 |title=Impact of warming and timing of snow melt on soil microarthropod assemblages associated with Dryas-dominated plant communities on Svalbard |journal=] |volume=29 |issue=1 |pages=111–119 |doi=10.1111/j.2006.0906-7590.04366.x |bibcode=2006Ecogr..29..111D }}</ref><ref>{{cite journal |last1=Hågvar |first1=Sigmund |last2=Klanderud |first2=Kari |name-list-style=amp |year=2009 |title=Effect of simulated environmental change on alpine soil arthropods |journal=Global Change Biology |volume=15 |issue=12 |pages=2972–2980 |doi=10.1111/j.1365-2486.2009.01926.x |bibcode=2009GCBio..15.2972H |citeseerx=10.1.1.658.1606 |s2cid=36287733 }}</ref> and neutral responses reported.<ref name="Sjursen, H. 2005"/><ref name="Alatalo, JM 2015">{{cite journal |last1=Alatalo |first1=Juha M. |last2=Jägerbrand |first2=Annika K. |last3=Čuchta |first3=Peter |name-list-style=amp |year=2015 |title=Collembola in three alpine subarctic sites resistant to twenty years of experimental warming |journal=] |volume=5 |issue=18161 |pages=18161 |doi=10.1038/srep18161 |pmc=4680968 |pmid=26670681|bibcode=2015NatSR...518161A }}</ref> Neutral responses to experimental warming have also been reported in studies of non-polar regions.<ref>{{cite journal |last1=Kardol |first1=Paul |last2=Reynolds |first2=W. Nicholas |last3=Norby |first3=Richard J. |last4=Classen |first4=Aimée T. |title=Climate change effects on soil microarthropod abundance and community structure |journal=Applied Soil Ecology |date=January 2011 |volume=47 |issue=1 |pages=37–44 |doi=10.1016/j.apsoil.2010.11.001 |bibcode=2011AppSE..47...37K }}</ref> 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.<ref>{{cite journal |last1=Harte |first1=John |last2=Rawa |first2=Agnieszka |last3=Price |first3=Vanessa |name-list-style=amp |year=1996 |title=Effects of manipulated soil microclimate on mesofaunal biomass and diversity |journal=Soil Biology and Biochemistry |volume=28 |issue=3 |pages=313–322 |doi=10.1016/0038-0717(95)00139-5 }}</ref> 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.<ref name="Alatalo, JM 2015"/>


== Reproduction == == Reproduction ==
] occurs through the clustered or scattered deposition of spermatophores by ] adults. Stimulation of ] deposition by female ] has been demonstrated in '']''.<ref>{{cite journal |last=Waldorf |first=Elizabeth S. |year=1974 |title=Sex pheromone in the springtail ''Sinella curviseta'' |journal=Environmental Entomology |volume=3 |issue=6 |pages=916–918 |doi=10.1093/ee/3.6.916 }}</ref> ] can be observed in ].<ref>{{cite journal |last1=Kozlowski |first1=Marek Wojciech |last2=Aoxiang |first2=Shi |name-list-style=amp |year=2006 |title=Ritual behaviors associated with spermatophore transfer in ''Deuterosminthurus bicinctus'' (Collembola : Bourletiellidae) |journal=Journal of Ethology |volume=24 |issue=2 |pages=103–110 |doi=10.1007/s10164-005-0162-6 |s2cid=12056710 }}</ref> Among Symphypleona, males of some ] use a clasping organ located on their ].<ref name="Hopkin"/> Many collembolan species, mostly those living in deeper soil horizons, are parthenogenetic, which favors ] to the detriment of ] and thereby to ] tolerance of ].<ref>{{cite journal |last1=Simon |first1=Jean-Christophe |last2=Delmote |first2=François |last3=Rispe |first3=Claude |last4=Crease |first4=Teresa |name-list-style=amp |year=2003 |title=Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals |journal=] |volume=79 |issue=1 |pages=151–153 |doi=10.1046/j.1095-8312.2003.00175.x |url=https://eurekamag.com/pdf.php?pdf=011148810 |format=]|doi-access=free }}</ref> ] (also called ]) is under the control of symbiotic ] of the genus '']'', which live, reproduce and are carried in female reproductive organs and eggs of Collembola.<ref>{{cite journal |last1=Czarnetzki |first1=Alice B. |last2=Tebbe |first2=Christoph C. |name-list-style=amp |year=2004 |title=Detection and phylogenetic analysis of ''Wolbachia'' in Collembola |journal=Environmental Microbiology |volume=6 |issue=1 |pages=35–44 |doi=10.1046/j.1462-2920.2003.00537.x |pmid=14686939 |url=https://eurekamag.com/pdf.php?pdf=004098500 |format=]}}</ref> Feminizing '']'' species are widespread in ]s<ref>{{cite journal |last1=Werren |first1=John H. |last2=Zhang |first2=Wan |last3=Guo |first3=Li Rong |name-list-style=amp |year=1995 |title=Evolution and phylogeny of ''Wolbachia'': reproductive parasites of arthropods |journal=] |volume=261 |issue=1360 |pages=55–63 |pmid=7644549 |jstor=50047 |doi=10.1098/rspb.1995.0117 |bibcode=1995RSPSB.261...55W |s2cid=8585323 |url=https://eurekamag.com/pdf.php?pdf=008645644 |format=]}}</ref> and ]s,<ref>{{cite journal |last1=Fenn |first1=Katelyn |last2=Blaxter |first2=Mark |name-list-style=amp |year=2004 |title=Are filarial nematode ''Wolbachia'' obligate mutualist symbionts? |journal=] |volume=19 |issue=4 |pages=163–166 |doi=10.1016/j.tree.2004.01.002 |pmid=16701248 |url=https://eurekamag.com/pdf.php?pdf=004046986 |format=]}}</ref> where they co-evolved with most of their ]. ] occurs through the clustered or scattered deposition of spermatophores by ] adults. Stimulation of ] deposition by female ] has been demonstrated in '']''.<ref>{{cite journal |last=Waldorf |first=Elizabeth S. |year=1974 |title=Sex pheromone in the springtail ''Sinella curviseta'' |journal=Environmental Entomology |volume=3 |issue=6 |pages=916–918 |doi=10.1093/ee/3.6.916 }}</ref> ] can be observed in ].<ref>{{cite journal |last1=Kozlowski |first1=Marek Wojciech |last2=Aoxiang |first2=Shi |name-list-style=amp |year=2006 |title=Ritual behaviors associated with spermatophore transfer in ''Deuterosminthurus bicinctus'' (Collembola : Bourletiellidae) |journal=Journal of Ethology |volume=24 |issue=2 |pages=103–110 |doi=10.1007/s10164-005-0162-6 |s2cid=12056710 }}</ref> Among Symphypleona, males of some ] use a clasping organ located on their ].<ref name="Hopkin"/> Many springtails, mostly those living in deeper soil horizons, are parthenogenetic, which favors ] to the detriment of ] and thereby to ] tolerance of ].<ref>{{cite journal |last1=Simon |first1=Jean-Christophe |last2=Delmote |first2=François |last3=Rispe |first3=Claude |last4=Crease |first4=Teresa |name-list-style=amp |year=2003 |title=Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals |journal=] |volume=79 |issue=1 |pages=151–153 |doi=10.1046/j.1095-8312.2003.00175.x |doi-access=free }}</ref> ] (also called ]) is under the control of symbiotic ] of the genus '']'', which live, reproduce and are carried in female reproductive organs and eggs of Collembola.<ref>{{cite journal |last1=Czarnetzki |first1=Alice B. |last2=Tebbe |first2=Christoph C. |name-list-style=amp |year=2004 |title=Detection and phylogenetic analysis of ''Wolbachia'' in Collembola |journal=Environmental Microbiology |volume=6 |issue=1 |pages=35–44 |doi=10.1046/j.1462-2920.2003.00537.x |pmid=14686939 |bibcode=2004EnvMi...6...35C }}</ref> Feminizing '']'' species are widespread in ]s<ref>{{cite journal |last1=Werren |first1=John H. |last2=Zhang |first2=Wan |last3=Guo |first3=Li Rong |name-list-style=amp |year=1995 |title=Evolution and phylogeny of ''Wolbachia'': reproductive parasites of arthropods |journal=] |volume=261 |issue=1360 |pages=55–63 |pmid=7644549 |jstor=50047 |doi=10.1098/rspb.1995.0117 |bibcode=1995RSPSB.261...55W |s2cid=8585323 }}</ref> and ]s,<ref>{{cite journal |last1=Fenn |first1=Katelyn |last2=Blaxter |first2=Mark |name-list-style=amp |year=2004 |title=Are filarial nematode ''Wolbachia'' obligate mutualist symbionts? |journal=] |volume=19 |issue=4 |pages=163–166 |doi=10.1016/j.tree.2004.01.002 |pmid=16701248 }}</ref> where they co-evolved with most of their ].


== See also == == See also ==
{{Portal|Arthropods}} {{Portal|Arthropods}}
* ]
* '']'', a predator of Collembola


== References == == References ==
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* {{cite EB1911|wstitle=Springtail |volume=25 |short=x}} * {{cite EB1911|wstitle=Springtail |volume=25 |short=x}}
* *
* * {{Webarchive|url=https://web.archive.org/web/20190422055046/http://urweb.roehampton.ac.uk/collembola/taxonomy/ |date=2019-04-22 }}
* *
* *

Latest revision as of 22:22, 30 December 2024

Subclass of arthropods

Springtails
Temporal range: Early Devonian – present PreꞒ O S D C P T J K Pg N
Orchesella cincta
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Clade: Pancrustacea
Subphylum: Hexapoda
Class: Collembola
Lubbock, 1871
Orders
Synonyms
  • Oligentoma
  • Oligoentoma

Springtails (class Collembola) form the largest of the three lineages of modern hexapods that are no longer considered insects. 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 are to all insects, which have external mouthparts.

Springtails 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 and the control of soil microbial communities. The word Collembola is from the ancient Greek κόλλα kólla "glue" and ἔμβολος émbolos "peg"; this name was given due to the existence of the collophore, which was previously thought to stick to surfaces to stabilize the creature.

Early DNA sequence studies suggested that Collembola represent a separate evolutionary line from the other Hexapoda, but others disagree; this seems to be caused by widely divergent patterns of molecular evolution among the arthropods. The adjustments of traditional taxonomic rank for springtails reflect 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.

Morphology

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 fewer abdominal segments, and possess a tubular appendage (the collophore or ventral tube) with reversible, sticky vesicles, projecting ventrally from the first abdominal segment. It is believed to be associated with fluid uptake and balance, excretion, and orientation of the organism itself. Most species have an abdominal, tail-like appendage known as a furcula (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 the retinaculum (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.

Springtails also possess the ability to reduce their body size by as much as 30% through subsequent ecdyses (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.

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, except for the two families Sminthuridae and Actaletidae, which exhibit a single pair of spiracles between the head and the thorax, leading to a rudimentary, although fully functional, tracheal system. The anatomical variance present between different species partially depends on soil morphology and 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 of ocelli (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.

Poduromorphs are characterized by their elongated bodies and conspicuous segmentation – three thoracic segments, six abdominal segments, including a well-developed prothorax with tergal chaetae, 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. Malpighian tubules are absent.

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. However, recent phylogenetic studies show Arthropleona is paraphyletic. Thus, the Arthropleona are abolished in modern classifications, and their superfamilies are raised in rank accordingly, being now orders Entomobryomorpha and the Poduromorpha. Technically, the Arthropleona are thus a partial junior synonym of the Collembola.

The term "Neopleona" is essentially synonymous with Symphypleona + Neelipleona. 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 of 18S and 28S rRNA sequence data, though, suggests that they form the most ancient lineage of springtails, which would explain their peculiar apomorphies. This phylogenetic relationship was also confirmed using a phylogeny based on mtDNA and whole-genome data.

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

Neelipleona

Poduromorpha

Symphypleona

Entomobryomorpha

Springtails are attested to since the Early Devonian. 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. Additional research concerning the coprolites (fossilized feces) of ancient springtails allowed researchers to track their lineages back some 412 million years.

Fossil Collembola are rare. Instead, most are found in amber. 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, Miocene of Central America, and the mid-Cretaceous of Burma and Canada. 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.

Ecology

Eating behavior

Specific feeding strategies and mechanisms are employed to match specific niches. 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. Carnivorous species maintain populations of small invertebrates such as nematodes, rotifers, and other collembolan species. 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.

Predators

Springtails are consumed by mesostigmatan mites in various families, including Ascidae, Laelapidae, Parasitidae, Rhodacaridae and Veigaiidae.

Cave-dwelling springtails are a food source for spiders and harvestmen in the same environment, such as the endangered harvestman Texella reyesi.

To protect themselves, some species have evolved chemical defenses.

Distribution

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

"Snow flea"
A species of Sminthurinae (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, essentially everywhere on Earth where soil and related habitats (moss cushions, fallen wood, grass tufts, ant and termite nests) occur. 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.

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. 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. In tropical regions a single square meter of canopy habitat can support many species of Collembola.

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. This is a complex factor embracing both nutritional and physiological requirements, together with behavioural trends, dispersal limitation and probable species interactions. Some species have been shown to exhibit negative or positive 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".

Dicyrtomina sp. on leaf

As a group, springtails are highly sensitive to desiccation, because of their tegumentary respiration, although some species with thin, permeable cuticles have been shown to resist severe drought by regulating the osmotic pressure of their body fluid. The gregarious behaviour of Collembola, mostly driven by the attractive power of pheromones excreted by adults, 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. Sensitivity to drought varies from species to species and increases during ecdysis. Given that springtails moult 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. The high humidity environment of many caves also favours springtails and there are numerous cave adapted species, including one, Plutomurus ortobalaganensis living 1,980 metres (6,500 ft) down the Krubera Cave.

Anurida maritima on water

The horizontal distribution of springtail species is affected by environmental factors which act at the landscape scale, such as soil acidity, moisture and light. Requirements for pH can be reconstructed experimentally. Altitudinal changes in species distribution can be at least partly explained by increased acidity at higher elevation. Moisture requirements, among other ecological and behavioural factors, explain why some species cannot live aboveground, or retreat in the soil during dry seasons, but also why some epigeal springtails are always found in the vicinity of ponds and lakes, such as the hygrophilous Isotomurus palustris. Adaptive features, 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. Podura aquatica, a unique representative of the family Poduridae (and one of the first springtails to have been described by Carl 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. 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.

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. As a consequence of dispersal limitation, landuse change, when too rapid, may cause the local disappearance of slow-moving, specialist species, a phenomenon the measure of which has been called colonisation credit.

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, and is considered as a pest in Australia. Onychiuridae are also known to feed on tubers and to damage them to some extent. 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. They also contribute to controlling plant fungal diseases through their active consumption of mycelia and spores of damping-off and pathogenic fungi. It has been suggested that they could be reared to be used for the control of pathogenic fungi in greenhouses and other indoor cultures.

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 springtails can cause irritation when rubbed onto the skin. 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 delusional 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. 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.

In 1952, China accused the United States military of spreading bacteria-laden insects and other objects during the Korean War by dropping them from P-51 fighters above rebel villages over North Korea. In all, the U.S. was accused of dropping ants, beetles, crickets, fleas, flies, grasshoppers, lice, springtails, and stoneflies as part of a biological warfare effort. The alleged associated diseases included anthrax, cholera, dysentery, fowl septicemia, paratyphoid, plague, scrub typhus, small pox, and typhoid. 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. The US government denied 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. Springtail species cited in allegations of biological warfare in the Korean War were Isotoma (Desoria) negishina (a local species) and the "white rat springtail" Folsomia candida.

Captive springtails are often kept in a terrarium as part of a clean-up crew.

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. These tests have been standardized. 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. Care should be taken that different strains of the same species may be conducive to different results. Avoidance tests have been also performed. They have been standardized, too. 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. 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. The springtail Folsomia candida is also becoming a genomic model organism for soil toxicology. 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.

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. There are negative, positive and neutral responses reported. Neutral responses to experimental warming have also been reported in studies of non-polar regions. 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. 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.

Reproduction

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. Mating behavior can be observed in Symphypleona. Among Symphypleona, males of some Sminthuridae use a clasping organ located on their antenna. Many springtails, mostly those living in deeper soil horizons, are parthenogenetic, which favors reproduction to the detriment of genetic diversity and thereby to population tolerance of environmental hazards. 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. Feminizing Wolbachia species are widespread in arthropods and nematodes, where they co-evolved with most of their lineages.

See also

References

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External links

Extant Arthropoda classes by subphylum
Chelicerata
Euchelicerata
Mandibulata
Myriapoda
Pancrustacea
Crustacea
Hexapoda
italic are paraphyletic groups
Taxon identifiers
Collembola
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