tardigrade

{{short description |Phylum of microscopic animals}}

{{redirect |Tardigrada |the suborder of mammals |sloth}}

{{redirect |Moss Piglets |the South Park episode |Moss Piglets (South Park){{!}}Moss Piglets (South Park)}}

{{good article}}

{{use British English|date=December 2024}}

{{use dmy dates|date=December 2024}}

{{Automatic taxobox

|fossil_range={{fossil range |Turonian |Recent |earliest=Cambrian}}

Middle Cambrian stem-group fossils

|image=SEM image of Milnesium tardigradum in active state - journal.pone.0045682.g001-2 (white background).png

|image_caption=Milnesium tardigradum, a eutardigrade

|image2=Echiniscus insularis (10.3897-evolsyst.5.59997) Figure 6 (white background).jpg

|image2_caption=Echiniscus insularis, a heterotardigrade

|display_parents=8

|taxon=Tardigrada

|authority=Spallanzani, 1776

|subdivision_ranks=Classes

|subdivision=*Eutardigrada

}}

Tardigrades ({{IPAc-en|ˈ|t|ɑr|d|ᵻ|g|r|eɪ|d|z|audio=en-us-Tardigrades.oga}}),{{cite Dictionary.com |tardigrade}} known colloquially as water bears or moss piglets,{{cite web |last=Miller |first=William |title=Tardigrades |url=https://www.americanscientist.org/article/tardigrades |publisher=American Scientist |access-date=2018-04-13 |date=2017-02-06}} are a phylum of eight-legged segmented micro-animals. They were first described by the German zoologist Johann August Ephraim Goeze in 1773, who called them {{lang |de |Kleiner Wasserbär |italics=no}} {{gloss|little water bear}}. In 1776, the Italian biologist Lazzaro Spallanzani named them Tardigrada, which means 'slow walkers'.

They live in diverse regions of Earth's biosphere{{snd}}mountaintops, the deep sea, tropical rainforests, and the Antarctic. Tardigrades are among the most resilient animals known, with individual species able to survive extreme conditions – such as exposure to extreme temperatures, extreme pressures (both high and low), air deprivation, radiation, dehydration, and starvation – that would quickly kill most other forms of life. Tardigrades have survived exposure to outer space.

There are about 1,500 known species in the phylum Tardigrada, a part of the superphylum Ecdysozoa. The earliest known fossil is from the Cambrian, some 500 million years ago. They lack several of the Hox genes found in arthropods, and the middle region of the body corresponding to an arthropod's thorax and abdomen. Instead, most of their body is homologous to an arthropod's head.

Tardigrades are usually about {{cvt|0.5|mm|sigfig=1}} long when fully grown. They are short and plump, with four pairs of legs, each ending in claws (usually four to eight) or sticky pads. Tardigrades are prevalent in mosses and lichens and can readily be collected and viewed under a low-power microscope, making them accessible to students and amateur scientists. Their clumsy crawling and their well-known ability to survive life-stopping events have brought them into science fiction and popular culture including items of clothing, statues, soft toys and crochet patterns.

Description

= Body structure =

File:Tardigrade anatomy.svg

Tardigrades have a short plump body with four pairs of hollow unjointed legs. Most range from {{cvt|0.1|to|0.5|mm|sigfig=1}} in length, although the largest species may reach {{cvt|1.3|mm}}. The body cavity is a haemocoel, an open circulatory system, filled with a colourless fluid. The body covering is a cuticle that is replaced when the animal moults; it contains hardened (sclerotised) proteins and chitin but is not calcified. Each leg ends in one or more claws according to the species; in some species, the claws are modified as sticky pads. In marine species, the legs are telescopic. There are no lungs, gills, or blood vessels, so tardigrades rely on diffusion through the cuticle and body cavity for gas exchange.{{cite book |last1=Brusca |first1=Richard C. |last2=Moore |first2=Wendy |last3=Shuster |first3=Stephen M. |date=2016 |title=Invertebrates |publisher=Sinauer Associates |edition=3rd |isbn=978-1605353753 |pages=711–717}} They are made up of only about 1000 cells.{{Cite journal |last=Gross |first=Vladimir |last2=Treffkorn |first2=Sandra |last3=Reichelt |first3=Julian |last4=Epple |first4=Lisa |last5=Lüter |first5=Carsten |last6=Mayer |first6=Georg |date=January 2019 |title=Miniaturization of tardigrades (water bears): Morphological and genomic perspectives |url=https://pubmed.ncbi.nlm.nih.gov/30447338/#:~:text=The%20five-segmented%20tardigrade%20body,to%20a%20single%20cell%20each. |journal=Arthropod Structure & Development |volume=48 |pages=12–19 |doi=10.1016/j.asd.2018.11.006 |issn=1873-5495 |pmid=30447338}}

= Nervous system and senses =

The tardigrade nervous system has a pair of ventral nerve cords with a pair of ganglia serving each pair of legs. The nerve cords end near the mouth at a pair of subpharyngeal (or suboesophageal) ganglia. These are connected by paired commissures (either side of the tube from the mouth to the pharynx) to the dorsally located cerebral ganglion or 'brain'. Also in the head are two eyespots in the brain, and several sensory cirri and pairs of hollow antenna-like clavae which may be chemoreceptors.

The tardigrade Dactylobiotus dispar can be trained by classical conditioning to curl up into the defensive 'tun' state in response to a blue light associated with a small electric shock, an aversive stimulus. This demonstrates that tardigrades are capable of learning.{{cite journal |last=Zhou |first=Sarah |last2=DeFranco |first2=Joseph P. |last3=Blaha |first3=Nicholas T. |last4=Dwivedy |first4=Pritty |last5=Culver |first5=Ashley |last6=Nallamala |first6=Hinduja |last7=Chelluri |first7=Srikanth |last8=Dumas |first8=Theodore C. |display-authors=3 |title=Aversive conditioning in the tardigrade, Dactylobiotus dispar |journal=Journal of Experimental Psychology: Animal Learning and Cognition |volume=45 |issue=4 |date=2019 |pmid=31368766 |pmc=6776688 |doi=10.1037/xan0000218 |doi-access=free |pages=405–412}}

= Locomotion =

Although the body is flexible and fluid-filled, locomotion does not operate mainly hydrostatically. Instead, as in arthropods, the muscles (sometimes just one or a few cells) work in antagonistic pairs that make each leg step backwards and forwards; there are also some flexors that work against hydrostatic pressure of the haemocoel. The claws help to stop the legs sliding during walking, and are used for gripping.

= Feeding and excretion =

Tardigrades feed by sucking animal or plant cell fluids, or on detritus. A pair of stylets pierce the prey; the pharynx muscles then pump the fluids from the prey into the gut. A pair of salivary glands secrete a digestive fluid into the mouth, and produce replacement stylets each time the animal moults. Non-marine species have excretory Malpighian tubules where the intestine joins the hindgut. Some species have excretory or other glands between or at the base of the legs.

File:Tardigrade in real time.ogv|Video of tardigrade under the microscope

File:Тихоходки, темное поле 280х.webm|Living tardigrades moving around, filmed using dark-field microscopy

= Reproduction and life cycle =

File:TardigradeEggsInShedCuticle.jpg

Most tardigrades have both male and female animals which copulate by a variety of methods. The females lay eggs; those of Austeruseus faeroensis are spherical, 80 μm in diameter, with a knobbled surface. In other species the eggs can be ovoid, as in Hypsibius annulatus, or may be spherical with pyramidal or bottle-shaped surface ornamentation. Some species appear to have no males, suggesting that parthenogenesis is common.

Both sexes have a single gonad (an ovary or testis) located above the intestine. A pair of ducts run from the testis, opening through a single gonopore in front of the anus. Females have a single oviduct opening either just above the anus or directly into the rectum, which forms a cloaca.

The male may place his sperm into the cloaca, or may penetrate the female's cuticle and place the sperm straight into her body cavity, for it to fertilise the eggs directly in the ovary. A third mechanism in species such as H. annulatus is for the male to place the sperm under the female's cuticle; when she moults, she lays eggs into the cast cuticle, where they are fertilised. Courtship occurs in some aquatic tardigrades, with the male stroking his partner with his cirri to stimulate her to lay eggs; fertilisation is then external.

Up to 30 eggs are laid, depending on the species. Terrestrial tardigrade eggs have drought-resistant shells. Aquatic species either glue their eggs to a substrate or leave them in a cast cuticle. The eggs hatch within 14 days, the hatchlings using their stylets to open their egg shells.

Ecology and life history

Tardigrades as a group are cosmopolitan, living in many environments on land, in freshwater, and in the sea. Their eggs and resistant life-cycle stages (cysts and tuns) are small and durable enough to enable long-distance transport, whether on the feet of other animals or by the wind.

Individual species have more specialised distributions, many being both regional and limited to a single type of habitat, such as mountains. Some species have wide distributions: for instance, Echiniscus lineatus is pantropical. Halobiotus is restricted to cold Holarctic seas. Species such as Borealibius and Echiniscus lapponicus have a discontinuous distribution, being both polar and on tall mountains. This could be a result of long-distance transport by the wind, or the remains of an ancient geographic range when the climate was colder. A small percentage of species may be cosmopolitan.{{cite journal |last=Gąsiorek |first=Piotr |title=Catch me if you can, or how paradigms of tardigrade biogeography evolved from cosmopolitism to 'localism' |journal=Zoological Journal of the Linnean Society |volume=202 |issue=2 |date=1 October 2024 |doi=10.1093/zoolinnean/zlad191 |doi-access=free}}

The majority of species live in damp habitats such as on lichens, liverworts, and mosses, and directly in soil and leaf litter. In freshwater and the sea they live on and in the bottom, such as in between particles or around seaweeds. More specialised habitats include hot springs and as parasites or commensals of marine invertebrates. In soil there can be as many as 300,000 per square metre; on mosses they can reach a density of over 2 million per square metre.

Tardigrades are host to many microbial symbionts and parasites. In glacial environments, the bacterial genera Flavobacterium, Ferruginibacter, and Polaromonas are common in tardigrades' microbiomes.{{cite journal |last=Zawierucha |first=Krzysztof |last2=Trzebny |first2=Artur |last3=Buda |first3=Jakub |last4=Bagshaw |first4=Elizabeth |last5=Franzetti |first5=Andrea |last6=Dabert |first6=Miroslawa |last7=Ambrosini |first7=Roberto |title=Trophic and symbiotic links between obligate-glacier water bears (Tardigrada) and cryoconite microorganisms |journal=PLOS ONE |volume=17 |issue=1 |date=12 January 2022 |pmid=35020747 |pmc=8754347 |doi=10.1371/journal.pone.0262039 |doi-access=free |page=e0262039}} Many tardigrades are predatory; Milnesium lagniappe includes other tardigrades such as Macrobiotus acadianus among its prey.{{cite journal |last=Meyer |first=Harry A |last2=Larsen |first2=Hannah E |last3=Akobi |first3=Nézira O |last4=Broussard |first4=Garret |title=Predator and prey detection in two species of water bear (Tardigrada) |journal=Zoological Journal of the Linnean Society |volume=188 |issue=3 |date=16 March 2020 |doi=10.1093/zoolinnean/zlz141 |doi-access=free |pages=860–864 |url=https://academic.oup.com/zoolinnean/article-pdf/188/3/860/32916282/zlz141.pdf}} Tardigrades consume prey such as nematodes, and are themselves predated upon by soil arthropods including mites, spiders and cantharid beetle larvae.{{cite journal |last=Hyvonen |first=R. |last2=Persson |first2=T. |title=Effects of fungivorous and predatory arthropods on nematodes and tardigrades in microcosms with coniferous forest soil |journal=Biology and Fertility of Soils |volume=21 |issue=1-2 |date=1996 |doi=10.1007/BF00336003 |pages=121–127}}

With the exception of 62 exclusively freshwater species, all non-marine tardigrades are found in terrestrial environments. Because the majority of the marine species belongs to Heterotardigrada, the most ancestral class, the phylum evidently has a marine origin.{{Cite journal |last=van Straalen |first=Nico M. |date=August 2021 |title=Evolutionary terrestrialization scenarios for soil invertebrates |journal=Pedobiologia |volume=87-88 |pages=150753 |doi=10.1016/j.pedobi.2021.150753 |bibcode=2021Pedob..8750753V |doi-access=free }}

Environmental tolerance

{{main|Environmental tolerance in tardigrades}}

Tardigrades are not considered universally extremophilic because they are not adapted to exploit many of the extreme conditions that their environmental tolerance has been measured in, only to endure them. This means that their chances of dying increase the longer they are exposed to these extreme environments, whereas true extremophiles thrive there.{{cite journal |last1=Rothschild |first1=Lynn J. |author-link=Lynn J. Rothschild |last2=Mancinelli |first2=Rocco L. |title=Life in extreme environments |journal=Nature |volume=409 |issue=6823 |pages=1092–1101 |year=2001 |bibcode=2001Natur.409.1092R |s2cid=529873 |doi=10.1038/35059215 |pmid=11234023 |url=https://zenodo.org/record/1233097 }}

= Dehydrated 'tun' state =

File:Richtersius coronifer in active and tun states.png in active and 'tun' states.
A↔P = anterior-posterior; mg = midgut; go = gonad;
pb = pharyngeal bulb; mo = mouth; st = stylet
Scale bars = 100 μm]]

Tardigrades are capable of suspending their metabolism, going into a state of cryptobiosis. Terrestrial and freshwater tardigrades are able to tolerate long periods when water is not available, such as when the moss or pond they are living in dries out, by drawing their legs in and forming a desiccated cyst, the cryptobiotic 'tun' state, where no metabolic activity takes place. In this state, they can go without food or water for several years. Further, in that state they become highly resistant to environmental stresses, including temperatures from as low as {{cvt|-272|C|F|0}} to as much as {{cvt|+149|C|F|0}} (at least for short periods of time{{cite book |last1=Horikawa |first1=Daiki D. |chapter=Survival of Tardigrades in Extreme Environments: A Model Animal for Astrobiology |doi=10.1007/978-94-007-1896-8_12 |editor1-first=Alexander V. |editor1-last=Altenbach |editor2-first=Joan M. |editor2-last=Bernhard |editor3-first=Joseph |editor3-last=Seckbach |title=Anoxia |volume=21 |pages=205–217 |series=Cellular Origin, Life in Extreme Habitats and Astrobiology |year=2012 |isbn=978-94-007-1895-1}}), lack of oxygen, vacuum, ionising radiation,{{cite journal |title=Radiation tolerance in the tardigrade Milnesium tardigradum |year=2006 |doi=10.1080/09553000600972956 |last1=Horikawa |first1=Daiki D. |last2=Sakashita |first2=Tetsuya |last3=Katagiri |first3=Chihiro |last4=Watanabe |first4=Masahiko |last5=Kikawada |first5=Takahiro |last6=Nakahara |first6=Yuichi |last7=Hamada |first7=Nobuyuki |last8=Wada |first8=Seiichi |last9=Funayama |first9=Tomoo |last10=Higashi |first10=Seigo |last11=Kobayashi |first11=Yasuhiko |last12=Okuda |first12=Takashi |last13=Kuwabara |first13=Mikinori |display-authors=5 |journal=International Journal of Radiation Biology |volume=82 |issue=12 |pages=843–848 |pmid=17178624 |s2cid=25354328}} and high pressure.{{cite journal |last1=Seki |first1=Kunihiro |last2=Toyoshima |first2=Masato |title=Preserving tardigrades under pressure |journal=Nature |volume=395 |issue=6705 |pages=853–854 |year=1998 |doi=10.1038/27576 |bibcode=1998Natur.395..853S |s2cid=4429569}}

= Surviving other stresses =

Marine tardigrades such as Halobiotus crispae alternate each year (cyclomorphosis) between an active summer morph and a hibernating winter morph (a pseudosimplex) that can resist freezing and low salinity, but which remains active throughout. Reproduction however takes place only in the summer morph.

Tardigrades can survive impacts up to about {{convert|900|m/s}}, and momentary shock pressures up to about {{convert|1.14| GPa}}.{{cite journal |doi=10.1126/science.abj5282 |title=Hardy water bears survive bullet impacts—up to a point |year=2021 |last=O'Callaghan |first=Jonathan |journal=Science |s2cid=236376996}}

= Exposure to space =

{{main|Tardigrades in space}}

File:Biopan Space Expo 001.jpg mission carrying the BIOPAN astrobiology payload (illustrated) exposed tardigrades to vacuum, solar ultraviolet, or both, showing their ability to survive in the space environment.]]

Tardigrades have survived exposure to space. In 2007, dehydrated tardigrades were taken on the FOTON-M3 mission and exposed to vacuum, or to both vacuum and solar ultraviolet, for 10 days. Back on Earth, more than 68% of the subjects protected from ultraviolet were reanimated by rehydration, and many produced viable embryos.{{cite journal |last1=Jönsson |first1=K. Ingemar |last2=Rabbow |first2=Elke |last3=Schill |first3=Ralph O. |last4=Harms-Ringdahl |first4=Mats |last5=Rettberg |first5=Petra |title=Tardigrades survive exposure to space in low Earth orbit |journal=Current Biology |volume=18 |issue=17 |pages=R729–R731 |year=2008 |s2cid=8566993 |doi=10.1016/j.cub.2008.06.048 |doi-access=free |pmid=18786368 |bibcode=2008CBio...18.R729J }}

In contrast, hydrated samples exposed to vacuum and solar ultraviolet survived poorly, with only three subjects of Milnesium tardigradum surviving. The space vacuum did not much affect egg-laying in either R. coronifer or M. tardigradum, whereas UV radiation reduced egg-laying in M. tardigradum.{{Cite journal |last1=Jönsson |first1=K. Ingemar |last2=Rabbow |first2=Elke |last3=Schill |first3=Ralph O. |last4=Harms-Ringdahl |first4=Mats |last5=Rettberg |first5=Petra |date= September 2008 |title=Tardigrades survive exposure to space in low Earth orbit |journal=Current Biology |volume=18 |issue=17 |pages=R729–R731 |doi=10.1016/j.cub.2008.06.048 |pmid=18786368 |s2cid=8566993 |doi-access=free |bibcode=2008CBio...18.R729J }} In 2011, tardigrades went on the International Space Station STS-134,{{cite web |author=NASA Staff |url=http://www.nasa.gov/mission_pages/station/research/experiments/BIOKIS.html |archive-url=https://web.archive.org/web/20110417085459/http://www.nasa.gov/mission_pages/station/research/experiments/BIOKIS.html |url-status=dead |archive-date=17 April 2011 |title=BIOKon In Space (BIOKIS) |date=17 May 2011 |publisher=NASA |access-date=2011-05-24}} showing that they could survive microgravity and cosmic radiation,{{cite book |hdl=2434/239127 |first1=L. |last1=Rebecchi |first2=T. |last2=Altiero |first3=A. M. |last3=Rizzo |first4=M. |last4=Cesari |first5=G. |last5=Montorfano |first6=T. |last6=Marchioro |first7=R. |last7=Bertolani |first8=R. |last8=Guidetti |chapter=Two tardigrade species on board of the STS-134 space flight |page=89 |title=12th International Symposium on Tardigrada |chapter-url=http://www.tardigrada.net/newsletter/images/symposia/12_Booklet.pdf |isbn=978-989-96860-7-6 |year= 2012 }}{{Cite web |url=https://news.harvard.edu/gazette/story/2019/07/harvard-study-suggests-asteroids-might-play-key-role-in-spreading-life/ |title=Harvard study suggests asteroids might play key role in spreading life |last=Reuell |first=Peter |date=2019-07-08 |website=Harvard Gazette |access-date=2019-11-30}} and should be suitable model organisms.{{cite journal |last=Guidetti |first=Roberto |last2=Rizzo |first2=Angela Maria |last3=Altiero |first3=Tiziana |last4=Rebecchi |first4=Lorena |title=What can we learn from the toughest animals of the Earth? Water bears (tardigrades) as multicellular model organisms in order to perform scientific preparations for lunar exploration |journal=Planetary and Space Science |volume=74 |issue=1 |date=2012 |doi=10.1016/j.pss.2012.05.021 |pages=97–102}}

In 2019, a capsule containing tardigrades in a cryptobiotic state was on board the Israeli lunar lander Beresheet which crashed on the Moon.{{cite journal |last=Ledford |first=Heidi |date=2008-09-08 |title=Spacesuits optional for 'water bears' |url=https://www.nature.com/articles/news.2008.1087 |journal=Nature |doi=10.1038/news.2008.1087}}

= Damage protection proteins =

Tardigrades' ability to remain desiccated for long periods of time was thought to depend on high levels of the sugar trehalose,{{cite journal |last1=Hibshman |first1=Jonathan D. |last2=Clegg |first2=James S. |last3=Goldstein |first3=Bob |title=Mechanisms of Desiccation Tolerance: Themes and Variations in Brine Shrimp, Roundworms, and Tardigrades |journal=Frontiers in Physiology |volume=11 |date=2020-10-23 |page=592016 |pmid=33192606 |pmc=7649794 |doi=10.3389/fphys.2020.592016 |doi-access=free }} common in organisms that survive desiccation.{{cite journal |last1=Kamilari |first1=Maria |last2=Jørgensen |first2=Aslak |last3=Schiøtt |first3=Morten |last4=Møbjerg |first4=Nadja |title=Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages |journal=BMC Genomics |volume=20 |issue=1 |date=2019-07-24 |page=607 |pmid=31340759 |pmc=6652013 |doi=10.1186/s12864-019-5912-x |doi-access=free }} However, tardigrades do not synthesize enough trehalose for this function. Instead, tardigrades produce intrinsically disordered proteins in response to desiccation. Three of these are specific to tardigrades and have been called tardigrade specific proteins. These may protect membranes from damage by associating with the polar heads of lipid molecules.{{cite journal |last1=Boothby |first1=Thomas C. |last2=Tapia |first2=Hugo |last3=Brozena |first3=Alexandra H. |last4=Piszkiewicz |first4=Samantha |last5=Smith |first5=Austin E. |last6=Giovannini |first6=Ilaria |last7=Rebecchi |first7=Lorena |last8=Pielak |first8=Gary J. |author-link8=Gary J. Pielak |last9=Koshland |first9=Doug |author-link9=Douglas Koshland |last10=Goldstein |first10=Bob |display-authors=5 |title=Tardigrades Use Intrinsically Disordered Proteins to Survive Desiccation |journal=Molecular Cell |volume=65 |issue=6 |pages=975–984.e5 |year=2017 |doi=10.1016/j.molcel.2017.02.018 |pmid=28306513 |pmc=5987194}} The proteins may also form a glass-like matrix that protects cytoplasm from damage during desiccation.{{cite journal |last1=Boothby |first1=Thomas C. |last2=Piszkiewicz |first2=Samantha |last3=Holehouse |first3=Alex |last4=Pappu |first4=Rohit V. |last5=Pielak |first5=Gary J. |author-link5=Gary J. Pielak |date=December 2018 |title=Tardigrades use intrinsically disordered proteins to survive desiccation |url=https://linkinghub.elsevier.com/retrieve/pii/S0011224018304024 |journal=Cryobiology |volume=85 |pages=137–138 |doi=10.1016/j.cryobiol.2018.10.077 |hdl=11380/1129511 |s2cid=92411591 |hdl-access=free}}

Anhydrobiosis in response to desiccation has a complex molecular basis; in Hypsibius exemplaris, 1,422 genes are upregulated during the process. Of those, 406 are specific to tardigrades, 55 being intrinsically disordered and the others globular with unknown functions.{{cite journal |last=Arakawa |first=Kazuharu |title=Examples of Extreme Survival: Tardigrade Genomics and Molecular Anhydrobiology |journal=Annual Review of Animal Biosciences |volume=10 |issue=1 |date=15 February 2022 |doi=10.1146/annurev-animal-021419-083711 |doi-access=free |pages=17–37 |url=https://www.annualreviews.org/doi/pdf/10.1146/annurev-animal-021419-083711}}

Tardigrades possess a cold shock protein; Maria Kamilari and colleagues propose (2019) that this may serve "as a RNA-chaperone involved in regulation of translation [of RNA code to proteins] following freezing."

Tardigrade DNA is protected from radiation by the Dsup ("damage suppressor") protein.{{cite journal |doi=10.1038/ncomms12808 |pmid=27649274 |pmc=5034306 |title=Extremotolerant tardigrade genome and improved radiotolerance of human cultured cells by tardigrade-unique protein |journal=Nature Communications |volume=7 |pages=12808 |year=2016 |last1=Hashimoto |first1=Takuma |last2=Horikawa |first2=Daiki D |last3=Saito |first3=Yuki |last4=Kuwahara |first4=Hirokazu |last5=Kozuka-Hata |first5=Hiroko |last6=Shin-i |first6=Tadasu |last7=Minakuchi |first7=Yohei |last8=Ohishi |first8=Kazuko |last9=Motoyama |first9=Ayuko |last10=Aizu |first10=Tomoyuki |last11=Enomoto |first11=Atsushi |last12=Kondo |first12=Koyuki |last13=Tanaka |first13=Sae |last14=Hara |first14=Yuichiro |last15=Koshikawa |first15=Shigeyuki |last16=Sagara |first16=Hiroshi |last17=Miura |first17=Toru |last18=Yokobori |first18=Shin-Ichi |last19=Miyagawa |first19=Kiyoshi |last20=Suzuki |first20=Yutaka |last21=Kubo |first21=Takeo |last22=Oyama |first22=Masaaki |last23=Kohara |first23=Yuji |last24=Fujiyama |first24=Asao |last25=Arakawa |first25=Kazuharu |last26=Katayama |first26=Toshiaki |last27=Toyoda |first27=Atsushi |last28=Kunieda |first28=Takekazu |display-authors=5 |bibcode=2016NatCo...712808H }} The Dsup proteins of Ramazzottius varieornatus and H. exemplaris promote survival by binding to nucleosomes and protecting chromosomal DNA from hydroxyl radicals.{{cite journal |last1=Chavez |first1=Carolina |last2=Cruz-Becerra |first2=Grisel |last3=Fei |first3=Jia |last4=Kassavetis |first4=George A. |last5=Kadonaga |first5=James T. |date=2019-10-01 |title=The tardigrade damage suppressor protein binds to nucleosomes and protects DNA from hydroxyl radicals |journal=eLife |volume=8 |doi=10.7554/eLife.47682 |issn=2050-084X |pmc=6773438 |pmid=31571581 |doi-access=free}} The Dsup protein of R. varieornatus confers resistance to ultraviolet-C by upregulating DNA repair genes.{{Cite journal |last1=Ricci |first1=Claudia |last2=Riolo |first2=Giulia |last3=Marzocchi |first3=Carlotta |last4=Brunetti |first4=Jlenia |last5=Pini |first5=Alessandro |last6=Cantara |first6=Silvia |date=2021-09-27 |title=The Tardigrade Damage Suppressor Protein Modulates Transcription Factor and DNA Repair Genes in Human Cells Treated with Hydroxyl Radicals and UV-C |journal=Biology |volume=10 |issue=10 |page=970 |doi=10.3390/biology10100970 |pmc=8533384 |pmid=34681069 |doi-access=free}}

Some of these proteins are of interest to biomedical research. Potential is seen in Dsup's ability to protect against damage; in CAHS and LEA's ability to protect from desiccation; and some CAHS proteins could serve to prevent programmed cell death (apoptosis).{{cite journal |last=Kasianchuk |first=Nadiia |last2=Rzymski |first2=Piotr |last3=Kaczmarek |first3=Łukasz |title=The biomedical potential of tardigrade proteins: A review |journal=Biomedicine & Pharmacotherapy |volume=158 |year=2023 |doi=10.1016/j.biopha.2022.114063 |doi-access=free |page=114063}}

Taxonomic history

In 1773, Johann August Ephraim Goeze named the tardigrade {{lang|de|Kleiner Wasserbär}}, meaning 'little water-bear' in German (today, Germans often call them {{lang|de|Bärtierchen}} 'little bear-animal').{{Cite journal |last=Greven |first=Hartmut |journal=Acta Biologica Benrodis |volume=17 |year=2015 |pages=1–27 |url=https://www.researchgate.net/publication/283615362 |access-date=27 September 2024 |title=About the little water bear: A commented translation of GOEZE'S note "Ueber den kleinen Wasserbär" from 1773}}{{cite journal |last1=Cross |first1=Ryan |title=Secrets of the tardigrade |journal=C&EN Global Enterprise |date=2016-11-07 |volume=94 |issue=44 |pages=20–21 |doi=10.1021/cen-09444-scitech1 |url=https://pubs.acs.org/doi/abs/10.1021/cen-09444-scitech1 |access-date=31 May 2021}} The name water bear comes from the way they walk, reminiscent of a bear's gait. The name Tardigradum means 'slow walker' and was given by Lazzaro Spallanzani in 1776.{{cite book |last=Spallanzani |first=Lazzaro |author-link=Lazzaro Spallanzani |date=1776 |title=Opuscoli di fisica animale, e vegetabile |language=it |trans-title=Booklets on the structure of animals and plants |location=Modena |publisher=Presso La Societa' Tipografica |url=https://books.google.com/books?id=oYxfAAAAcAAJ}}{{cite web |first=Sarah |last=Bordenstein |title=Tardigrades (Water Bears) |work=Microbial Life Educational Resources |publisher=National Science Digital Library |url=http://serc.carleton.edu/microbelife/topics/tardigrade/index.html |access-date=2014-01-24}} In 1834, C.A.S. Schulze gave the first formal description of a tardigrade, Macrobiotus hufelandi, in a work subtitled "a new animal from the crustacean class, capable of reviving after prolonged asphyxia and dryness".{{cite journal |last=Bertolani |first=Roberto |last2=Rebecchi |first2=Lorena |last3=Giovannini |first3=Ilaria |last4=Cesari |first4=Michele |title=DNA barcoding and integrative taxonomy of Macrobiotus hufelandi C.A.S. Schultze 1834, the first tardigrade species to be described, and some related species |journal=Zootaxa |volume=2997 |issue=1 |date=2011-08-17 |doi=10.11646/zootaxa.2997.1.2 |pages=19–36}}{{cite book |last=Schultze |first=Karl August Sigismund |title=Macrobiotus hufelandii, animal e crustaceorum classe novum, reviviscendi post diuturnam asphyxiam et ariditatem potens |language=la |trans-title=Macrobiotus hufelandii, a new animal from the crustacean class, capable of reviving after prolonged asphyxia and dryness |publisher=Curths |year=1834 |url=https://www.google.co.uk/books/edition/_/afRAAAAAcAAJ}} This was soon followed by descriptions of species including Echiniscus testudo, Milnesium tardigradum, Hypsibius dujardini, and Ramazzottius oberhaeuseri by L.M.F. Doyère in 1840. All four of these are now the nominal species for higher tardigrade taxa.{{cite journal |last1=Gąsiorek |first1=Piotr |last2=Stec |first2=Daniel |last3=Morek |first3=Witold |last4=Michalczyk |first4=Łukasz |title=An integrative redescription of Hypsibius dujardini (Doyère, 1840), the nominal taxon for Hypsibioidea (Tardigrada: Eutardigrada) |journal=Zootaxa |volume=4415 |issue=1 |year=2018 |pages=45–75 |doi=10.11646/zootaxa.4415.1.2 |pmid=30313631 |doi-access=free}} The zoologist Hartmut Greven wrote that "The unanimous opinion of all later researchers is that Doyère's 1842 dissertation {{lang|fr|Memoire sur les Tardigrades}} is an indisputable milestone in tardigradology".{{cite book |last=Greven |first=Hartmut |year=2018 |chapter=From Johann August Ephraim Goeze to Ernst Marcus: A Ramble Through the History of Early Tardigrade Research (1773 Until 1929) |editor-last=Schill |editor-first=R. |title=Water Bears: The Biology of Tardigrades |series=Zoological Monographs |volume=2 |publisher=Springer |chapter-url=https://doi.org/10.1007/978-3-319-95702-9_1}}

Ferdinand Richters worked on the taxonomy of tardigrades from 1900 to 1913, with studies of Nordic, Arctic, marine, and South American species; he described many species at this time,{{cite web |last=Mach |first=Martin |title=Prof. Ferdinand Richters |url=http://www.baertierchen.de/wb_aug05.html |website=Water Bear web base |access-date=15 December 2024}} (with full Richters bibliography; first published in Bärtierchen-Journal, issue 62){{cite journal |last1=Michalczyk |first1=Łukasz |last2=Kaczmarek |first2=Łukasz |title=The Tardigrada Register: a comprehensive online data repository for tardigrade taxonomy |journal=Journal of Limnology |volume=72 |issue=1s |date=24 July 2013 |doi=10.4081/jlimnol.2013.s1.e22 |doi-access=free |url=https://www.jlimnol.it/index.php/jlimnol/article/download/jlimnol.2013.s1.e22/pdf |access-date=15 December 2024}} and in 1926 proposed the class Eutardigrada.{{cite web |title=Eutardigrada Richters, 1926 |url=https://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=155362#null |website=Integrated Taxonomic Information System |access-date=16 December 2024}}{{cite book |last1=Richters |first1=Ferdinand |author1-link=Ferdinand Richters |last2=Krumbach, T.H. |chapter=Tardigrada |editor1=Kŭkenthal, W. |editor2=Krumbach, T.H. |title=Handbook of Zoology |volume=3 |pages=1–68 |location=Berlin and Leipzig |year=1926}} In 1927, Ernst Marcus created the class Heterotardigrada.{{cite journal |last=Marcus |first=Ernst |year=1927 |title=Zur Anatomie und Ökologie mariner Tardigraden |language=de |trans-title=On Anatomy and Ecology of Underwater Tardigrades |journal=Zoologische Jahrbücher, Abteilung für Systematik |volume=53 |pages=487–558}}{{cite web |title=Heterotardigrada Marcus, 1927 |url=https://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=155167#null |website=Integrated Taxonomic Information System |access-date=16 December 2024}} and in 1929 a monograph on tardigrades{{cite book |last=Marcus |first=Ernst |year=1929 |chapter=Tardigrada |editor=Dahl, F. |title=Bronns Klassen und Ordnungen des Tierreichs |volume=5 |location=Leipzig |publisher=Akademische Verlagsgesellschaft |ref=none}} which Greven describes as "comprehensive" and "unsurpassed today". In 1937 Gilbert Rahm, studying the fauna of Japan's hot springs, distinguished the class Mesotardigrada, with a single species Thermozodium esakii;{{cite journal |last=Rahm |first=Gilbert |year=1937 |title=A new ordo of tardigrades from the hot springs of Japan (Furu-yu section, Unzen) |journal=日本動物学彙報 (Bulletin of the Zoological Society of Japan) |volume=16 |issue=4 |pages=345–352}} its validity is now doubted.

In 1962, Giuseppe Ramazzotti proposed the phylum Tardigrada.{{cite journal |last=Ramazzotti |first=Giuseppe |year=1962 |title=Il Phylum Tardigrada |language=it |trans-title=The Phylum Tardigrada |journal=Memorie dell'Istituto Italiano di Idrobiologia |volume=16 |pages=1–595}}

In 2019, Noemi Guil and colleagues proposed to promote the order Apochela to the new class Apotardigrada.{{cite journal |last1=Guil |first1=Noemi |last2=Jørgensen |first2=Aslak |last3=Kristensen |first3=Reinhardt |title=An upgraded comprehensive multilocus phylogeny of the Tardigrada tree of life |journal=Zoologica Scripta |volume=48 |issue=1 |date=2019 |issn=0300-3256 |doi=10.1111/zsc.12321 |doi-access=free |pages=120–137 }} There are some 1,488 described species of tardigrades, organised into 160 genera and 36 families.{{cite web |last1=Degma |first1=Peter |last2=Guidetti |first2=Roberto |title=Actual checklist of Tardigrada species (2009–2024, 43th Edition: 01-07-2024) |year=2024 |publisher=Università di Modena e Reggio Emilia |url=https://iris.unimore.it/bitstream/11380/1178608.20/10/Actual%20checklist%20of%20Tardigrada%2043rd%20edition%2005-07-24.pdf |access-date=29 December 2024 |doi=10.25431/11380_1178608}}

File:First Recorded Image of Tardigrade.jpg|The first drawing of a tardigrade, by Johann August Ephraim Goeze, 1773

File:Echiniscus testudo Doyere 1840 Pl 12 Fig 1.png |Drawing of Echiniscus testudo on a grain of sand by L.M.F. Doyère, 1840

File:Echiniscus sp.jpg |Drawing of Echiniscus sp. by C.A.S. Schultze, 1861

File:Macrobiotus ornatus var. spinifer by Ferdinand Richters 1900.jpg|Drawing of Calohypsibius (Macrobiotus) ornatus var. spinifer by Ferdinand Richters, 1900

Evolution

= Evolutionary history =

{{further|Panarthropoda}}

Tardigrade fossils are rare. The only known specimens are those from mid-Cambrian deposits in Siberia (in the Orsten fauna) and a few specimens in amber from the Cretaceous of North America and the Neogene of Dominica. The Siberian fossils differ from living tardigrades in several ways. They have three pairs of legs rather than four, they have a simplified head morphology, and they have no posterior head appendages, but they share with modern tardigrades their columnar cuticle construction. Scientists think they represent a stem group of living tardigrades.{{cite journal |doi=10.1078/0044-5231-00034 |title=Tardigrades as 'Stem-Group Arthropods': The Evidence from the Cambrian Fauna |journal=Zoologischer Anzeiger |volume=240 |issue=3–4 |pages=265–79 |year=2001 |last1=Budd |first1=Graham E |bibcode=2001ZooAn.240..265B |url=https://www.researchgate.net/publication/223465290}}

File:Entothryeos.png|The luolishaniids from the Cambrian and Ordovician are possibly the closest fossil relatives of tardigrades. Entothryeos reconstruction shown.

File:Aysheaia pedunculata2021.jpg|Tardigrades may be descended from a lobopodian like Aysheaia.

File:OrstenTardigrade.jpg |Reconstruction of the unnamed Orsten fauna tardigrade, from the Cambrian Kuonamka Formation, {{circa}} 500 mya

File:Fossil_Tardigrade_Dominican_Amber.png|Reconstruction of Paradoryphoribius, from the Miocene (23 to 5.3 mya)

Multiple lines of evidence show that tardigrades are secondarily miniaturised from a larger ancestor,{{cite journal |doi=10.1016/j.asd.2018.11.006 |pmid=30447338 |title=Miniaturization of tardigrades (water bears): Morphological and genomic perspectives |journal=Arthropod Structure & Development |volume=48 |pages=12–19 |year=2018 |last1=Gross |first1=Vladimir |last2=Treffkorn |first2=Sandra |last3=Reichelt |first3=Julian |last4=Epple |first4=Lisa |last5=Lüter |first5=Carsten |last6=Mayer |first6=Georg |s2cid=53669741}} probably a lobopodian, perhaps resembling the mid-Cambrian Aysheaia, which many analyses place close to the divergence of the tardigrade lineage.{{cite book |date=2001 |publisher=Chapman & Hall |isbn=978-0-412-75420-3 |title=Arthropod Relationships |first1=Richard A. |last1=Fortey |author-link=Richard Fortey |first2=Richard H. |last2=Thomas |page=383}}{{Cite journal |doi=10.1038/nature13576 |pmid=25132546 |title=Hallucigenia's onychophoran-like claws and the case for Tactopoda |journal=Nature |volume=514 |issue=7522 |pages=363–366 |year=2014 |last1=Smith |first1=Martin R. |last2=Ortega-Hernández |first2=Javier |bibcode=2014Natur.514..363S |s2cid=205239797 |url=http://dro.dur.ac.uk/19108/1/19108.pdf}} An alternative hypothesis derives tactopoda from a clade encompassing dinocaridids and Opabinia.{{cite journal |last1=Budd |first1=Graham E. |year=1996 |title=The morphology of Opabinia regalis and the reconstruction of the arthropod stem-group |journal=Lethaia |volume=29 |issue=1 |pages=1–14 |doi=10.1111/j.1502-3931.1996.tb01831.x |bibcode=1996Letha..29....1B }} The enigmatic panarthropodan Sialomorpha found in 30-million year old Dominican amber, while not a tardigrade, shows some apparent affinities.{{cite journal |last1=Poinar |first1=George |last2=Nelson |first2=Diane R. |date=September 28, 2019 |title=A new microinvertebrate with features of mites and tardigrades in Dominican amber |url=https://onlinelibrary.wiley.com/doi/abs/10.1111/ivb.12265 |journal=Invertebrate Biology |volume=138 |issue=4 |doi=10.1111/ivb.12265 |s2cid=204157733}} A 2023 morphological analysis concluded that luolishaniids, a group of Cambrian lobopodians, might be the tardigrades' closest known relatives.{{cite journal |last1=Kihm |first1=Ji-Hoon |last2=Smith |first2=Frank W. |last3=Kim |first3=Sanghee |last4=Rho |first4=Hyun Soo |last5=Zhang |first5=Xingliang |last6=Liu |first6=Jianni |last7=Park |first7=Tae-Yoon S. |title=Cambrian lobopodians shed light on the origin of the tardigrade body plan |year=2023 |journal=Proceedings of the National Academy of Sciences |volume=120 |issue=28 |page=e2211251120 |pmid=37399417 |pmc=10334802 |bibcode=2023PNAS..12011251K |doi=10.1073/pnas.2211251120 |doi-access=free }}

The oldest remains of modern tardigrades are those of Milnesium swolenskyi, belonging to the living genus Milnesium known from a Late Cretaceous (Turonian) aged specimen of New Jersey amber, around 90 mya. Another fossil species, Beorn leggi, is known from a Late Campanian (~72 mya) specimen of Canadian amber, belonging to the family Hypsibiidae.{{cite journal |doi=10.1155/1964/48418 |first=Kenneth W. |last=Cooper |title=The first fossil tardigrade: Beorn leggi, from Cretaceous Amber |journal=Psyche: A Journal of Entomology |date=1964 |volume=71 |issue=2 |pages=41–48 |doi-access=free }} The related hypsibioidean Aerobius dactylus was found in the same amber piece.{{Cite journal |last1=Mapalo |first1=Marc A. |last2=Wolfe |first2=Joanna M. |last3=Ortega-Hernández |first3=Javier |date=2024-08-06 |title=Cretaceous amber inclusions illuminate the evolutionary origin of tardigrades |journal=Communications Biology |volume=7 |issue=1 |page=953 |doi=10.1038/s42003-024-06643-2 |pmid=39107512 |issn=2399-3642 |pmc=11303527 }}{{Citation |last1=Guidetti |first1=Roberto |title=Paleontology and Molecular Dating |date=2018 |url=http://link.springer.com/10.1007/978-3-319-95702-9_5 |work=Water Bears: The Biology of Tardigrades |volume=2 |pages=131–143 |editor-last=Schill |editor-first=Ralph O. |place=Cham |publisher=Springer International Publishing |doi=10.1007/978-3-319-95702-9_5 |isbn=978-3-319-95701-2 |access-date=2020-11-24 |last2=Bertolani |first2=Roberto |series=Zoological Monographs }} The youngest known fossil tadigrade genus, Paradoryphoribius, was discovered in amber dated to about 16 mya.{{cite journal |last1=Mapalo |first1=M. A. |last2=Robin |first2=N. |last3=Boudinot |first3=B. E. |last4=Ortega-Hernández |first4=J. |last5=Barden |first5=P. |year=2021 |title=A tardigrade in Dominican amber |journal=Proceedings of the Royal Society B: Biological Sciences |volume=288 |issue=1960 |at=Article 20211760 |doi=10.1098/rspb.2021.1760 |pmid=34610770 |pmc=8493197 |doi-access=free }}

Morphological and molecular phylogenetics studies have attempted to define how tardigrades relate to other ecdysozoan groups; alternative placements have been proposed within the Panarthropoda.{{Cite journal |last1=Yoshida |first1=Yuki |last2=Koutsovoulos |first2=Georgios |last3=Laetsch |first3=Dominik R. |last4=Stevens |first4=Lewis |last5=Kumar |first5=Sujai |last6=Horikawa |first6=Daiki D. |last7=Ishino |first7=Kyoko |last8=Komine |first8=Shiori |last9=Kunieda |first9=Takekazu |last10=Tomita |first10=Masaru |last11=Blaxter |first11=Mark |last12=Arakawa |first12=Kazuharu |display-authors=5 |date=2017-07-27 |editor-last=Tyler-Smith |editor-first=Chris |title=Comparative genomics of the tardigrades Hypsibius dujardini and Ramazzottius varieornatus |journal=PLOS Biology |volume=15 |issue=7 |page=e2002266 |doi=10.1371/journal.pbio.2002266 |pmc=5531438 |pmid=28749982 |doi-access=free}} The Tactopoda hypothesis holds that Tardigrada are sister to Arthropoda; the Antennopoda hypothesis is that Tardigrada are sister to (Onychophora + Arthropoda); and the Lobopodia (sensu Smith & Goldstein 2017) hypothesis is that Tardigrada are sister to Onychophora. The relationships have been debated on the basis of conflicting evidence.{{cite journal |last1=Smith |first1=Frank W. |last2=Goldstein |first2=Bob |date=2017-05-01 |title=Segmentation in Tardigrada and diversification of segmental patterns in Panarthropoda |url=https://www.sciencedirect.com/science/article/pii/S1467803916301487 |journal=Arthropod Structure & Development |series=Evolution of Segmentation |volume=46 |issue=3 |pages=328–340 |doi=10.1016/j.asd.2016.10.005 |pmid=27725256 |bibcode=2017ArtSD..46..328S}}

= Genomics =

Tardigrade genomes vary widely in size.{{cite web |url=http://www.genomesize.com/search.php?search=type&value=Tardigrades&display=100 |last=Gregory |first=T.R. |title=Tardigrades |website=Animal Genome Size Database |access-date=28 December 2024}} Hypsibius exemplaris (part of the Hypsibius dujardini group) has a compact genome of 100 megabase pairs and a generation time of about two weeks; it can be cultured indefinitely and cryopreserved.{{cite journal |doi=10.1016/j.ydbio.2007.09.055 |pmid=17996863 |title=The tardigrade Hypsibius dujardini, a new model for studying the evolution of development |journal=Developmental Biology |volume=312 |issue=2 |pages=545–559 |year=2007 |last1=Gabriel |first1=Willow N. |last2=McNuff |first2=Robert |last3=Patel |first3=Sapna K. |last4=Gregory |first4=T. Ryan |last5=Jeck |first5=William R. |last6=Jones |first6=Corbin D. |last7=Goldstein |first7=Bob }} The genome of Ramazzottius varieornatus, one of the most stress-tolerant species of tardigrades, is about half as big, at 55 Mb. About 1.6% of its genes are the result of horizontal gene transfer from other species, not implying any dramatic effect.

Genomic studies across different tardigrade groups help reconstruct the evolution of their genome, such as the relationship of tardigrade body segments to those of other Panarthropoda. A 2023 review concludes that despite the diversity of body plan among the Panarthropoda, the tardigrade body plan maps best with "a simple one-to-one alignment of anterior segments". Such studies may eventually reveal how they miniaturised themselves from larger ecdysozoans.{{cite journal |last=Smith |first=Frank W. |last2=Game |first2=Mandy |last3=Mapalo |first3=Marc A. |last4=Chavarria |first4=Raul A. |last5=Harrison |first5=Taylor R. |last6=Janssen |first6=Ralf |title=Developmental and genomic insight into the origin of the tardigrade body plan |journal=Evolution & Development |volume=26 |issue=4 |date=2023 |doi=10.1111/ede.12457 |doi-access=free |url=https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/ede.12457}}

Tardigrades lack several of the Hox genes found in arthropods, and a large intermediate region of the body axis. In insects, this corresponds to the entire thorax and abdomen. Practically the whole body, except for the last pair of legs, is made up of just the segments that are homologous to the head region in arthropods. This implies that tardigrades evolved from an ancestral ecdysozoan with a longer body and more segments.{{cite journal |title=The Compact Body Plan of Tardigrades Evolved by the Loss of a Large Body Region |first1=Frank W. |last1=Smith |first2=Thomas C. |last2=Boothby |first3=Ilaria |last3=Giovannini |first4=Lorena |last4=Rebecchi |first5=Elizabeth L. |last5=Jockusch |first6=Bob |last6=Goldstein |date=1 January 2016 |journal=Current Biology |volume=26 |issue=2 |pages=224–229 |doi=10.1016/j.cub.2015.11.059 |pmid=26776737 |doi-access=free |bibcode=2016CBio...26..224S |hdl=11380/1083953 |hdl-access=free}}

File:Tardigrade body plan compared to other phyla.svg compared to arthropods, onychophora, and annelids. Tardigrades have lost the whole middle section of the ecdysozoan body plan, and its Hox genes.]]

= Phylogeny =

In 2012, the phylogeny of the phylum was studied using molecular markers (ribosomal RNA), finding that the Heterotardigrada and Arthrotardigrada seemed to be paraphyletic.{{cite journal |last1=Guil |first1=Noemí |last2=Giribet |first2=Gonzalo |title=A comprehensive molecular phylogeny of tardigrades—adding genes and taxa to a poorly resolved phylum-level phylogeny |journal=Cladistics |volume=28 |issue=1 |date=2012 |doi=10.1111/j.1096-0031.2011.00364.x |doi-access=free |pages=21–49 |pmid=34856729 }}

{{barlabel |size=7 |at1=0.3 |label1="Heterotardigrada"

|cladogram={{clade

|label1=Tardigrada

|1={{clade

|1="Arthrotardigrada" 70px |barbegin1=red

|2={{clade

|1=Echiniscoidea 69px |barend1=red

|label2=Eutardigrada

|2={{clade

|label1=Apochela

|1=Milnesiidae 70px

|label2=Parachela

|2={{clade

|1=Isohypsibiodea 70px

|2={{clade

|1=Macrobiotoidea 70px

|2=Hypsibioidea 70px

}}

}}

}}

}}

}}

}}

}}

In 2018, a report integrating multiple morphological and molecular studies concluded that while the Arthrotardigrada appear to be paraphyletic, the Heterotardigrada is an accepted clade. All the lower-level taxa have been much reorganised, but the major groupings remain in place.{{cite book |last1=Jørgensen |first1=Aslak |last2=Kristensen |first2=Reinhardt M. |last3=Møbjerg |first3=Nadja |title=Water Bears: The Biology of Tardigrades |chapter=Phylogeny and Integrative Taxonomy of Tardigrada |publisher=Springer International Publishing |volume=2 |date=2018 |isbn=978-3-319-95701-2 |doi=10.1007/978-3-319-95702-9_3 |pages=95–114}}

{{clade

|label1=Tardigrada

|1={{clade

|label1=Heterotardigrada

|1={{clade

|1="Arthrotardigrada" 70px

|2=Echiniscoidea 69px

}}

|label2=Eutardigrada

|2={{clade

|1={{clade

|label1=Apochela

|1=Milnesiidae 70px

|label2=Parachela

|2={{clade

|1=Isohypsibiodea 70px

|2={{clade

|1=Macrobiotoidea 70px

|2=Hypsibioidea 70px

}}

}}

}}

}}

}}

}}

In culture and society

= Early 20th century beginnings =

Possibly the first time that tardigrades appear in non-scientific literature is in the short-story "Bathybia" by the geologist and explorer Douglas Mawson. Published in the 1908 book Aurora Australis and printed in the Antarctic, it deals with an expedition to the South Pole where the team encounters giant mushrooms and arthropods. The team watches a giant tardigrade fighting a similarly enormous rotifer; another giant water bear bites a man's toe, rendering him comatose for half an hour with its anaesthetic bite. Finally, a four-foot-long tardigrade, waking from hibernation, scares the narrator from his sleep, and he realizes it was all a dream.{{cite book |last=Blum |first=Hester |title=The News at the Ends of the Earth: The Print Culture of Polar Exploration |date=2019 |publisher=Duke University Press |isbn=9781478004486 |page=170 |url=https://ia803005.us.archive.org/13/items/newsatendsofeart00blum/newsatendsofeart00blum.pdf}}{{cite book |last=Mawson |first=Douglas |author-link=Douglas Mawson |chapter=Bathybia |editor-last=Shackleton |editor-first=Ernest |editor-link=Ernest Shackleton |title=Aurora Australis |publisher=British Antarctic Expedition |date=July 1908 |pages=179–213 |url=https://en.wikisource.org/wiki/Aurora_Australis/Bathybia}}

= Popularity =

Tardigrades are common in mosses and lichens on walls and roofs, and can readily be collected and viewed under a low-power microscope. If they are dry, they can be reanimated on a microscope slide by adding a little water, making them accessible to beginning students and amateur scientists.{{cite web |url=http://tardigrade.us/how-to-articles/how-to-find-tardigrades/ |title=How to Find Tardigrades |last=Shaw |first=Michael W. |publisher=Tardigrade USA |archive-url=https://web.archive.org/web/20140210001506/http://tardigrade.us/how-to-articles/how-to-find-tardigrades/ |archive-date=10 February 2014 |url-status=dead |access-date=2013-01-14}} Current Biology attributed their popularity to "their clumsy crawling [which] is about as adorable as can be."{{cite journal |last1=Goldstein |first1=Bob |last2=Blaxter |first2=Mark |title=Tardigrades |journal=Current Biology |volume=12 |issue=14 |page=R475 |year=2002 |bibcode=2002CBio...12.R475G |doi=10.1016/S0960-9822(02)00959-4 |doi-access=free |pmid=12176341}} The zoologists James F. Fleming and Kazuhuru Arakawa called them "a charismatic phylum".{{cite journal |last1=Fleming |first1=James F. |last2=Arakawa |first2=Kazuharu |title=Systematics of tardigrada: A reanalysis of tardigrade taxonomy with specific reference to Guil et al. (2019) |journal=Zoologica Scripta |volume=50 |issue=3 |date=2021 |doi=10.1111/zsc.12476 |doi-access=free |pages=376–382 }} They have been famous for their ability to survive life-stopping events such as being dried out since Spallanzani first resuscitated them from some dry sediment in a gutter in the 18th century.{{cite news |last=Marshall |first=Michael |title=Tardigrades: nature's great survivors |url=https://www.theguardian.com/science/2021/mar/20/tardigrades-natures-great-survivors |work=The Observer |date=20 March 2021}} In 2015, the astrophysicist and science communicator Neil deGrasse Tyson described Earth as "the planet of the tardigrades", and they were nominated for the American Name Society's Name of the Year Award.{{cite journal |last=Evans |first=Cleveland |title=2015 Name of the Year Award |journal=Names |volume=64 |issue=2 |date=2 April 2016 |doi=10.1080/00277738.2016.1169034 |pages=120–122}} Live Science notes that they are popular enough to appear on merchandise like clothes, earrings, and keychains, with crochet patterns for people to make their own tardigrade.{{cite web |last=Saplakoglu |first=Yasemin |url=https://www.livescience.com/63945-tardigrade-gifts.html|title=The Best Gifts for Tardigrade Lovers |website=Live Science |date=29 October 2018}} The Dutch artist {{ill|Arno Coenen|nl}} created statues for St Eusebius' Church, Arnhem of microscopic organisms including a tardigrade and a coronavirus.{{cite web |title=Eusebius Church Arnhem, Netherlands |url=https://www.atlasobscura.com/places/eusebius-church |website=Atlas Obscura |access-date=14 December 2024 |date=3 January 2023}}

Milnesium tardigradum was voted the winner of The Guardian{{'s}} "2025 invertebrate of the year" competition, from a shortlist of ten. The article describing the conclusion of the contest stated that the species had "endured all five previous planetary extinction events".{{cite news |last1=Barkham |first1=Patrick |title=It’s heroic, hardy and less than a millimetre long: meet the 2025 invertebrate of the year |url=https://www.theguardian.com/commentisfree/2025/apr/07/guardian-invertebrate-of-the-year-2025-natural-history |access-date=7 April 2025 |work=The Guardian |date=7 April 2025}}

File:'Ark van Noach 3.0' door Arno Coenen, Eusebiuskerk, Arnhem 01 (cropped).jpg|Tardigrade sculpture Noah's Ark 3.0 by Arno Coenen, St Eusebius' Church, Arnhem, the Netherlands

File:Tardigrade reading a book.jpg|Tardigrade soft toy

See also

References

{{reflist|30em}}