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Tardigrades (/ˈtɑːrdɪˌɡreɪd/; also known colloquially as water bears, or moss piglets)[2][3][4][5] are water-dwelling, eight-legged, segmented micro-animals.[2][6] They were first discovered by the German zoologist Johann August Ephraim Goeze
Johann August Ephraim Goeze
in 1773. The name Tardigrada (meaning "slow stepper") was given three years later by the Italian biologist Lazzaro Spallanzani.[7] They have been found everywhere: from mountain tops to the deep sea and mud volcanoes;[8] from tropical rain forests to the Antarctic.[9] Tardigrades are one of the most resilient known animals,[10][11] with individual species able to survive extreme conditions that would be rapidly fatal to nearly all other known life forms, such as exposure to extreme temperatures, extreme pressures (both high and low), air deprivation, radiation, dehydration, and starvation. About 1,150 known species[12][13] form the phylum Tardigrada, a part of the superphylum Ecdysozoa. The group includes fossils dating from 530 million years ago, in the Cambrian
Cambrian
period.[14] Usually, tardigrades are about 0.5 mm (0.02 in) long when they are fully grown.[2] They are short and plump, with four pairs of legs, each with four to eight claws also known as "disks".[2] Tardigrades are prevalent in mosses and lichens and feed on plant cells, algae, and small invertebrates. When collected, they may be viewed under a very low-power microscope, making them accessible to students and amateur scientists.[15]

Contents

1 Description 2 Anatomy and morphology 3 Reproduction 4 Ecology and life history 5 Physiology 6 Taxonomy 7 Genomes
Genomes
and genome sequencing 8 Ecological importance 9 See also 10 References 11 External links

Description[edit]

Johann August Ephraim Goeze

Lazzaro Spallanzani

Johann August Ephraim Goeze
Johann August Ephraim Goeze
originally named the tardigrade kleiner Wasserbär (Bärtierchen today), meaning "little water bear" in German. The name Tardigradum means "slow walker" and was given by Lazzaro Spallanzani
Lazzaro Spallanzani
in 1776.[16] The name "water bear" comes from the way they walk, reminiscent of a bear's gait. The biggest adults may reach a body length of 1.5 mm (0.059 in), the smallest below 0.1 mm. Newly hatched tardigrades may be smaller than 0.05 mm.

SEM image of Hypsibius dujardini

The most convenient place to find tardigrades is on lichens and mosses. Other environments are dunes, beaches, soil, and marine or freshwater sediments, where they may occur quite frequently (up to 25,000 animals per liter). Tardigrades, in the case of Echiniscoides wyethi,[17] may be found on barnacles.[18] Often, tardigrades can be found by soaking a piece of moss in water.[19] Anatomy and morphology[edit] Tardigrades have barrel-shaped bodies with four pairs of stubby legs. Most range from 0.3 to 0.5 mm (0.012 to 0.020 in) in length, although the largest species may reach 1.2 mm (0.047 in). The body consists of a head, three body segments each with a pair of legs, and a caudal segment with a fourth pair of legs. The legs are without joints, while the feet have four to eight claws each. The cuticle contains chitin and protein and is moulted periodically. The first three pairs of legs are directed downward along the sides, and are the primary means of locomotion, while the fourth pair is directed backward on the last segment of the trunk and is used primarily for grasping the substrate.[20] All adult tardigrades of the same species have the same number of cells (see eutely). Some species have as many as 40,000 cells in each adult, while others have far fewer.[21][22] The body cavity consists of a haemocoel, but the only place where a true coelom can be found is around the gonad. No respiratory organs are found, with gas exchange able to occur across the entirety of the body. Some tardigrades have three tubular glands associated with the rectum; these may be excretory organs similar to the Malpighian tubules of arthropods, although the details remain unclear.[23] The tubular mouth is armed with stylets, which are used to pierce the plant cells, algae, or small invertebrates on which the tardigrades feed, releasing the body fluids or cell contents. The mouth opens into a triradiate, muscular, sucking pharynx. The stylets are lost when the animal molts, and a new pair is secreted from a pair of glands that lie on either side of the mouth. The pharynx connects to a short esophagus, and then to an intestine that occupies much of the length of the body, which is the main site of digestion. The intestine opens, via a short rectum, to an anus located at the terminal end of the body. Some species only defecate when they molt, leaving the feces behind with the shed cuticle.[23] The brain develops in a bilaterally symmetric pattern.[24] The brain includes multiple lobes, mostly consisting of three bilaterally paired clusters of neurons.[25] The brain is attached to a large ganglion below the esophagus, from which a double ventral nerve cord runs the length of the body. The cord possesses one ganglion per segment, each of which produces lateral nerve fibres that run into the limbs. Many species possess a pair of rhabdomeric pigment-cup eyes, and numerous sensory bristles are on the head and body.[26] Tardigrades all possess a buccopharyngeal apparatus (swallowing device made of muscles and spines that activates an inner jaw and begins digestion and movement along the throat and intestine[27]) which, along with the claws, is used to differentiate among species. Reproduction[edit]

Shed cuticle of female tardigrade, containing eggs.

Although some species are parthenogenic, both males and females are usually present, each with a single gonad located above the intestine. Two ducts run from the testes in males, opening through a single pore in front of the anus. In contrast, females have a single duct opening either just above the anus or directly into the rectum, which thus forms a cloaca.[23] Tardigrades are oviparous, and fertilization is usually external. Mating occurs during the molt with the eggs being laid inside the shed cuticle of the female and then covered with sperm. A few species have internal fertilization, with mating occurring before the female fully sheds her cuticle. In most cases, the eggs are left inside the shed cuticle to develop, but some species attach them to nearby substrate.[23] The eggs hatch after no more than 14 days, with the young already possessing their full complement of adult cells. Growth to the adult size therefore occurs by enlargement of the individual cells (hypertrophy), rather than by cell division. Tardigrades may molt up to 12 times.[23] Ecology and life history[edit]

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Most tardigrades are phytophagous (plant eaters) or bacteriophagous (bacteria eaters), but some are carnivorous to the extent of eating other smaller species of tardigrades (e.g., Milnesium tardigradum).[28][29] Tardigrades share morphological characteristics with many species that differ largely by class. Biologists have a difficult time finding verification among tardigrade species because of this relationship. These animals are most closely related to the early evolution of arthropods.[30] Tardigrade
Tardigrade
fossils go as far back as the Cretaceous period in North America. This specific species is considered cosmopolitan and can be located in regions all over the world. The eggs and cysts of tardigrades are so resistant to other dangers that they are carried great distances, on the feet of other animals, to a different location.[31]  The lifespan of tardigrades range from 3–4 months for some species, up to 2 years for other species, not counting the time they spend in dormant states.[32] Physiology[edit]

Hypsibius dujardini
Hypsibius dujardini
imaged with a scanning electron microscope

Scientists have reported tardigrades in hot springs, on top of the Himalayas[33] (6,000 m; 20,000 ft, above sea level) to the deep sea (−4,000 m; −13,000 ft) and from the polar regions to the equator, under layers of solid ice, and in ocean sediments. Many species can be found in milder environments such as lakes, ponds, and meadows, while others can be found in stone walls and roofs. Tardigrades are most common in moist environments, but can stay active wherever they can retain at least some moisture. Tardigrades are considered to be able to survive even complete global mass extinction events due to astrophysical events, such as supernovae, gamma-ray bursts, or large meteorite impacts.[10][11] Some of them can withstand extremely cold temperatures down to 1 K (−458 °F; −272 °C) (close to absolute zero), while others can withstand extremely hot temperatures up to 420 K (300 °F; 150 °C)[34] for several minutes, pressures about six times greater than those found in the deepest ocean trenches, ionizing radiation at doses hundreds of times higher than the lethal dose for a human, and the vacuum of outer space.[35] They can go without food or water for more than 30 years, drying out to the point where they are 3% or less water, only to rehydrate, forage, and reproduce.[3][36][37][38][39] Tardigrades that live in harsh conditions undergo an annual process of cyclomorphosis, allowing for survival in sub-zero temperatures.[40] They are not considered extremophilic because they are not adapted to exploit these conditions, only to endure them. This means that their chances of dying increase the longer they are exposed to the extreme environments,[7] whereas true extremophiles thrive in a physically or geochemically extreme environment that would harm most other organisms.[3][41][42] Tardigrades are one of the few groups of species that are capable of suspending their metabolism (see cryptobiosis). Many species of tardigrade can survive in a dehydrated state up to five years, or in exceptional cases longer.[43][44] Depending on the environment, they may enter this state via anhydrobiosis, cryobiosis, osmobiosis, or anoxybiosis. While in this state, their metabolism lowers to less than 0.01% of normal and their water content can drop to 1% of normal.[35] Their ability to remain desiccated for such long periods was thought to be largely dependent on the high levels of the nonreducing sugar trehalose, which protects their membranes, although recent research suggests that tardigrades have a unique type of disordered protein that serves a similar purpose: It replaces water in the cells and adopts a glassy, vitrified state when the animals dry out.[45] Their DNA is further protected from radiation by a protein called "dsup" (short for damage suppressor).[46][47] In this cryptobiotic state, the tardigrade is known as a tun.[48] Tardigrades are able to survive in extreme environments that would kill almost any other animal. Extremes at which tardigrades can survive include those of:

Temperature
Temperature
– tardigrades can survive:

A few minutes at 151 °C (304 °F)[49] 30 years at −20 °C (−4 °F)[50] A few days at −200 °C (−328 °F; 73 K)[49] A few minutes at −272 °C (−458 °F; 1 K)[51]

Pressure
Pressure
– they can withstand the extremely low pressure of a vacuum and also very high pressures, more than 1,200 times atmospheric pressure. Tardigrades can survive the vacuum of open space and solar radiation combined for at least 10 days.[52] Some species can also withstand pressure of 6,000 atmospheres, which is nearly six times the pressure of water in the deepest ocean trench, the Mariana trench.[21] Dehydration
Dehydration
– the longest that living tardigrades have been shown to survive in a dry state is nearly 10 years,[37][38] although there is one report of leg movement, not generally considered "survival",[53] in a 120-year-old specimen from dried moss.[54] When exposed to extremely low temperatures, their body composition goes from 85% water to only 3%. As water expands upon freezing, dehydration ensures the tardigrades do not get ripped apart by the freezing ice.[55] Radiation
Radiation
– tardigrades can withstand 1,000 times more radiation than other animals,[56] median lethal doses of 5,000 Gy (of gamma rays) and 6,200 Gy (of heavy ions) in hydrated animals (5 to 10 Gy could be fatal to a human).[57] The only explanation found in earlier experiments for this ability was that their lowered water state provides fewer reactants for ionizing radiation.[57] However, subsequent research found that tardigrades, when hydrated, still remain highly resistant to shortwave UV radiation
UV radiation
in comparison to other animals, and that one factor for this is their ability to efficiently repair damage to their DNA resulting from that exposure.[58]

Irradiation of tardigrade eggs collected directly from a natural substrate (moss) showed a clear dose-related response, with a steep decline in hatchability at doses up to 4 kGy, above which no eggs hatched.[59] The eggs were more tolerant to radiation late in development. No eggs irradiated at the early developmental stage hatched, and only one egg at middle stage hatched, while eggs irradiated in the late stage hatched at a rate indistinguishable from controls.[59]

Environmental toxins – tardigrades are reported to undergo chemobiosis, a cryptobiotic response to high levels of environmental toxins. However, as of 2001, these laboratory results have yet to be verified.[53][54] Outer space
Outer space
– tardigrades are the first known animal to survive in space. In September 2007, dehydrated tardigrades were taken into low Earth orbit on the FOTON-M3 mission carrying the BIOPAN
BIOPAN
astrobiology payload. For 10 days, groups of tardigrades were exposed to the hard vacuum of outer space, or vacuum and solar UV radiation.[3][60][61] After being rehydrated back on Earth, over 68% of the subjects protected from high-energy UV radiation revived within 30 minutes following rehydration, but subsequent mortality was high; many of these produced viable embryos.[52][62] In contrast, hydrated samples exposed to the combined effect of vacuum and full solar UV radiation had significantly reduced survival, with only three subjects of Milnesium tardigradum
Milnesium tardigradum
surviving.[52] In May 2011, Italian scientists sent tardigrades on board the International Space Station along with extremophiles on STS-134, the final flight of Space Shuttle
Space Shuttle
Endeavour.[63][64][65] Their conclusion was that microgravity and cosmic radiation "did not significantly affect survival of tardigrades in flight, confirming that tardigrades represent a useful animal for space research."[66] In November 2011, they were among the organisms to be sent by the U.S.-based Planetary Society on the Russian Fobos-Grunt
Fobos-Grunt
mission's Living Interplanetary Flight Experiment to Phobos; however, the launch failed. Tardigrades are one of the few groups to have survived Earth's five mass extinctions.[67]

Taxonomy[edit] See also: List of bilaterial animal orders

Illustration of Echiniscus
Echiniscus
sp. from 1861[citation needed]

Scientists have conducted morphological and molecular studies to understand how tardigrades relate to other lineages of ecdysozoan animals. Two plausible placements have been proposed: tardigrades are either most closely related to Arthropoda
Arthropoda
± Onychophora, or tardigrades are most closely related to nematodes. Evidence for the former is a common result of morphological studies; evidence of the latter is found in some molecular analyses. The latter hypothesis has been rejected by recent microRNA and expressed sequence tag analyses.[68] Apparently, the grouping of tardigrades with nematodes found in a number of molecular studies is a long branch attraction artifact. Within the arthropod group (called panarthropoda and comprising onychophora, tardigrades and euarthropoda), three patterns of relationship are possible: tardigrades sister to onychophora plus arthropods (the lobopodia hypothesis); onychophora sister to tardigrades plus arthropods (the tactopoda hypothesis); and onychophora sister to tardigrades.[69] Recent analyses indicate that the panarthropoda group is monophyletic, and that tardigrades are a sister group of Lobopodia, the lineage consisting of arthropods and Onychophora.[68][70]

Panarthropoda

Water bears (Tardigrada)

Lobopodia

Velvet worms (Onychophora)

Arthropods (Arthropoda)

The minute sizes of tardigrades and their membranous integuments make their fossilization both difficult to detect and highly unusual. The only known fossil specimens are those from mid- Cambrian
Cambrian
deposits in Siberia
Siberia
and a few rare specimens from Cretaceous
Cretaceous
amber.[71]

Echiniscus
Echiniscus
testudo[citation needed]

The Siberian tardigrade 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.[1] Scientists think they represent a stem group of living tardigrades.[71] Rare specimens in Cretaceous
Cretaceous
amber have been found in two North American locations. Milnesium swolenskyi, from New Jersey, is the older of the two; its claws and mouthparts are indistinguishable from the living M. tardigradum. The other specimens from amber are from western Canada, some 15–20 million years earlier than M. swolenskyi. One of the two specimens from Canada
Canada
has been given its own genus and family, Beorn leggi, but it bears a strong resemblance to many living specimens in the family Hypsibiidae.[71][72] Aysheaia
Aysheaia
from the middle Cambrian
Cambrian
Burgess shale
Burgess shale
has been proposed as a sister taxon to an arthropod-tardigrade clade.[73] Tardigrades have been proposed to be among the closest living relatives of the Burgess shale oddity Opabinia.[74] Genomes
Genomes
and genome sequencing[edit] Tardigrade
Tardigrade
genomes vary in size, from about 75 to 800 megabase pairs of DNA.[75] Hypsibius dujardini
Hypsibius dujardini
has a compact genome of 100 megabase pairs [76] and a generation time of about two weeks; it can be cultured indefinitely and cryopreserved.[77] The genome of Ramazzottius varieornatus, one of the most stress-tolerant species of Tardigrades, was sequenced by a team of researchers from the University of Tokyo in 2015. Analysis revealed less than 1.2% of its genes were the result of horizontal gene transfer. They also found evidence of a loss of gene pathways that are known to promote damage due to stress. This study also found a high expression of novel Tardigrade-unique proteins, including Damage suppressor (Dsup), which was shown to protect against DNA damage from X-ray radiation. The same team applied the Dsup protein to human cultured cells and found that it suppressed X-ray damage to the human cells by ~40%.[47] Ecological importance[edit] Many organisms that live in aquatic environments feed on species such as nematodes, tardigrades, bacteria, algae, mites, and collembolans.[78] Tardigrades work as pioneer species by inhabiting new developing environments in which to live. This movement attracts other invertebrates to populate that space, while also attracting predators.[30] See also[edit]

List of microorganisms tested in outer space Living Interplanetary Flight Experiment – study of selected microorganisms in outer space Mopsechiniscus franciscae – tardigrade found in Victoria Land Antarctica

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tolerance in the tardigrade Milnesium tardigradum" (PDF). [permanent dead link] ^ a b Horikawa, Daiki D; Sakashita, Tetsuya; Katagiri, Chihiro; Watanabe, Masahiko; Kikawada, Takahiro; Nakahara, Yuichi; Hamada, Nobuyuki; Wada, Seiichi; Funayama, Tomoo; Higashi, Seigo; Kobayashi, Yasuhiko; Okuda, Takashi; Kuwabara, Mikinori (2009). "Radiation tolerance in the tardigrade Milnesium tardigradum". International Journal of Radiation
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External links[edit]

Wikispecies
Wikispecies
has information related to Tardigrada

Wikimedia Commons has media related to Tardigrada.

Tardigrade
Tardigrade
water bear NY Times, 2015 Tardigrada Newsletter Tardigrades – Pictures and Movies The Edinburgh Tardigrade
Tardigrade
project Instructions for finding tardigrades The incredible water bear! Tardigrade
Tardigrade
Reference Center Tardigrades in space Tardigrade
Tardigrade
data and analysis A short film about tardigrade research from NPR's Science Friday Tardigrada at the Tree of Life Web Project Swiss Center of Tardigrade
Tardigrade
Research – Ecology, Physiology and Evolutionary Biology of Tardigrades NASA
NASA
Astronomy Picture of the Day: Tardigrade
Tardigrade
in Moss
Moss
(6 March 2013) Video (07:54) – First Animal
Animal
to Survive in Space Video (00:38) – Tardigrade
Tardigrade
Movement in Water Tardigrades are so tough, they can survive outer space (March 2015). BBC The International Society of Tardigrade
Tardigrade
Hunters Tardigrades discussed on RNZ Critter of the Week, 14 July 2017

v t e

Extant Animal
Animal
phyla

Domain Archaea Bacteria Eukaryota (Supergroup Plant Hacrobia Heterokont Alveolata Rhizaria Excavata Amoebozoa Opisthokonta

Animal Fungi)

A n i m a l i a

Porifera (sponges)

Diploblasts (Eumetazoa)

Ctenophora
Ctenophora
(comb jellies)

ParaHoxozoa

Placozoa
Placozoa
(Trichoplax)

Planulozoa

Cnidaria
Cnidaria
(jellyfish and relatives)

Bilateria (Triploblasts)

(see below↓)

Bilateria

Xenacoelomorpha

Xenoturbellida (Xenoturbella) Acoelomorpha

acoels nemertodermatids

N e p h r o z o a

Deuterostomia

Chordata

lancelets tunicates craniates / vertebrates

Ambulacraria

Echinodermata (starfish and relatives) Hemichordata

acorn worms pterobranchs

P r o t o s t o m i a

Ecdysozoa

Scalidophora

Kinorhyncha
Kinorhyncha
(mud dragons) Priapulida
Priapulida
(penis worms)

N+L+P

Nematoida

Nematoda (roundworms) Nematomorpha
Nematomorpha
(horsehair worms)

L+P

Loricifera

Panarthropoda

Arthropoda
Arthropoda
(arthropods) Tardigrada (waterbears) Onychophora
Onychophora
(velvet worms)

S p i r a l i a

Gnathifera¹

Chaetognatha
Chaetognatha
(arrow worms) Gnathostomulida (jaw worms) Micrognathozoa (Limnognathia) Syndermata

Rotifera Acanthocephala

Platytrochozoa

R+M

Mesozoa

Orthonectida Dicyemida
Dicyemida
or Rhombozoa

Rouphozoa¹

Platyhelminthes (flatworms) Gastrotricha (hairybacks)

Lophotrochozoa

Cycliophora (Symbion) Mollusca
Mollusca
(molluscs)

A+N

Annelida (ringed worms) Nemertea
Nemertea
(ribbon worms)

Lophophorata

Bryozoa

Entoprocta
Entoprocta
or Kamptozoa Ectoprocta (moss animals)

Brachiozoa

Brachiopoda (lamp shells) Phoronida (horseshoe worms)

Major groups within phyla

Sponges

Calcareous Hexactinellid Demosponge Homoscleromorpha

Cnidarians

Anthozoa
Anthozoa
inc. corals Medusozoa
Medusozoa
inc. jellyfish Myxozoa

Vertebrates

Jawless fish Cartilaginous fish Bony fish Amphibians Reptiles/Birds Mammals

Echinoderms

Sea lilies Asterozoa
Asterozoa
inc. starfish Echinozoa

Nematodes

Chromadorea Enoplea Secernentea

Arthropods

Chelicerates/Arachnids Myriapods Crustaceans Hexapods/Insects

Platyhelminths

Turbellaria Trematoda Monogenea Cestoda

Bryozoans

Phylactolaemata Stenolaemata Gymnolaemata

Annelids

Polychaetes Clitellata Echiura

Molluscs

Gastropods Cephalopods Bivalves Chitons Tusk shells

Phyla with ≥5000 extant species bolded See also Diploblasts Monoblastozoa (nomen dubium)

¹Platyzoa

v t e

Extremophiles

Types

Acidophile Alkaliphile Capnophile Cryozoa Endolith Halophile Hypolith Lipophile Lithoautotroph Lithophile Methanogen Metallotolerant Oligotroph Osmophile Piezophile Polyextremophile Psammophile Psychrophile Radioresistant Thermophile / Hyperthermophile Thermoacidophile Xerophile

Notable extremophiles

Bacteria

Chloroflexus aurantiacus Deinococcus radiodurans Deinococcus–Thermus Snottite Thermus aquaticus Thermus thermophilus Spirochaeta americana GFAJ-1

Archaea

Pyrococcus furiosus Strain 121 Pyrolobus fumarii

Eukaryota

Cyanidioschyzon merolae Galdieria sulphuraria Paralvinella sulfincola Halicephalobus mephisto Pompeii worm Tardigrada

Related articles

Abiogenic petroleum origin Acidithiobacillales Acidobacteria Acidophiles in acid mine drainage Archaeoglobaceae Berkeley Pit Blood Falls Crenarchaeota Grylloblattidae Halobacteria Halobacterium Helaeomyia petrolei Hydrothermal vent Methanopyrus Movile Cave Radiotrophic fungus Rio Tinto Taq polymerase Thermostability Thermotogae

Taxon identifiers

Wd: Q5194 ADW: Tardigrada EoL: 3204 Fauna Europaea: 12674 Fossilworks: 272408 iNaturalist: 124337 ITIS: 155166 NCBI: 42241 WoRMS: 1276

Authority control

GND: 41439