Tardigrade Ecology: Difference between revisions
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In some marine tardigrade species, zonation has been found. In one study, for example, the species composition shifted from littoral (near the shore) to submarine to deep sea caves(Grimaldi de Zio 1984; Grimaldi de Zio and Gallo D’Addabbo 2001). Intertidal tardigrades, like other meiofauna, migrate both horizontally and vertically with the tides(Giere 2009), which dynamically stratifiy beach environments with respect to water saturation and oxygen content. Additionally, competitive interactions between marine tardigrade species have been suggested based on non-overlapping distributions, impacting beach tardigrades(Martinex 1975) and vertical distribution patterns of barnacle-dependent species(Kristensen and Hallas 1980).<br> | In some marine tardigrade species, zonation has been found. In one study, for example, the species composition shifted from littoral (near the shore) to submarine to deep sea caves(Grimaldi de Zio 1984; Grimaldi de Zio and Gallo D’Addabbo 2001). Intertidal tardigrades, like other meiofauna, migrate both horizontally and vertically with the tides(Giere 2009), which dynamically stratifiy beach environments with respect to water saturation and oxygen content. Additionally, competitive interactions between marine tardigrade species have been suggested based on non-overlapping distributions, impacting beach tardigrades(Martinex 1975) and vertical distribution patterns of barnacle-dependent species(Kristensen and Hallas 1980).<br> | ||
Generally smaller, marine tardigrades have telescopic legs. They can have either up to 13 claws or 4 tows with complex claws. Alternatively, interstitial species have 4 to 6 toes with an adhesive round or rod-shaped disk on each that allows them to tightly adhere to shifting sand grains<ref name="source"></ref>. Tardigrades living in deep-sea muds have cylindrical, wormlike bodies with reduced legs. Epibenthic species and those on algae often have elongated appendages and claws with multiple hooks | Generally smaller, marine tardigrades have telescopic legs. They can have either up to 13 claws or 4 tows with complex claws. Alternatively, interstitial species have 4 to 6 toes with an adhesive round or rod-shaped disk on each that allows them to tightly adhere to shifting sand grains<ref name="source"></ref>. Tardigrades living in deep-sea muds have cylindrical, wormlike bodies with reduced legs. Epibenthic species and those on algae often have elongated appendages and claws with multiple hooks<ref name="source"></ref>. And the eutardigrade Halobioutus crispae possesses enlarged Malpighian tubules attributed to a secondary shift to seawater(Crisp and Kistensen 1983;Mobjerg and Dahl 1996). Many marine tardigrades are found the world over, suggesting substantial dispersal capabilities<ref name="source"></ref>, but the mechanisms for dispersal are poorly understood. Passive dispersal may be utilized. Semibenthic species, like Halechiniscidae semibenthics, have a diversity of structures that facilitate swimming and drifting. Some semibenthic and interstitial species have cuticular extensions that increase surface area and may increase passive dispersion(Grimaldi de Zio 1984; Jorgensen and Kristensen 2001; Giere 2001; Kristensen and Sorensen 2004). Tantarctus bubulubus has 18-20 balloon or float-like appendages attached to the fourth pair of legs (Jorgensen and Kristensen 2001). However marine species often lack cryptobiotic states, which would seemingly limit passive dispersion. Additionally, tardigrades possess weak swimming ability, calling into question their aptitude for active dispersion in a marine environment<ref name="source"></ref>. Eggs of one species were found in the exuvium (shed skin) of its host barnacle, suggesting that this is its means of dispersal(Kristensen and Hallas, 1980). They may also spread by the ballast water from or barnacles and algal lawns beneath marine vessels (Giere 2009) as well as various forms of free-floating vegetation and plastic-anchored barnacles(Giere 2009; Arroyo 2006).<br> | ||
Very little is known about trophic interactions in marine species. Tardigrades comprise a minuscule portion of marine meiofauna, and so their specific roles in marine ecosystems have not been studied. However, polychaetes , bivalves, various crustaceans, fish, and birds rely heavily on meiofauna, sometimes depending solely on them at least during some phase of their life cycle(Coull 1990, 1999). Intertidal interstitial tardigrades live alongside meiofauna including nematodes, harpacticoid copepods, and turbellarians in lower relative concentration, as is often but not always the case | Very little is known about trophic interactions in marine species. Tardigrades comprise a minuscule portion of marine meiofauna, and so their specific roles in marine ecosystems have not been studied. However, polychaetes , bivalves, various crustaceans, fish, and birds rely heavily on meiofauna, sometimes depending solely on them at least during some phase of their life cycle(Coull 1990, 1999). Intertidal interstitial tardigrades live alongside meiofauna including nematodes, harpacticoid copepods, and turbellarians in lower relative concentration, as is often but not always the case<ref name="source"></ref>. 402 individuals of the commensal Echinoscoides sigismundi species have been found on a single barnacle(Kristensen and Hallas 1980). Most marine tardigrades probably feed on algal cells, including macroalgae and diatoms, using their paired piercing stylets and a muscular, sucking pharynx<ref name="source"></ref>. Others may be detritivores, bacterivores or ectoparasites (on the surface of the host)(Kristensen and Sorensen 2004). Some species are associated with organic slime growing on algae(Giere 2009).<br> | ||
Several commensal relationships have been observed among tardigrades, but they are likely facultative (circumstantial rather than necessary), as the same species are also found living freely in interstitial or algal habitats | Several commensal relationships have been observed among tardigrades, but they are likely facultative (circumstantial rather than necessary), as the same species are also found living freely in interstitial or algal habitats<ref name="source"></ref>. Some marine tardigrades live between the plates of barnacles, likely feeding on associated algae. Crevices of barnacle plates provide physical protection and shelter from temperature fluctuations especially when exposed by low tides(Faurby 2012). Ectoparasites include facultative parasitism on the pleopods (limbs) of the isopod Ligmoria lignorum<ref name="source"></ref> and obligate parasites with specific adaptations, like Echiniscoides hoepneri, which feeds on embryos in barnacles’ brood chamber and Tetrakentron synaptae, which only lives on the tentacles of the sea cucumber Leptosunapa galliennei<ref name="source"></ref>. Most species of Floractus and Eingstrandarctus genus have epicuticular vesicles associated with the buccal apparatus that house symbiotic bacteria, which, in their clean coral sand microhabitats, may provide their primary food source(Kristensen 1984). One final interspecific interaction has been seen in the epibenthic Tanarctus bubulubus, the balloon-appendaged tardigrade from earlier, whose entire dorsal side is covered in mucous, apparently providing adhesion for shed calcerous platelets which form the spherical shells of coccolithophores, perhaps providing chemical or mechanical camouflage(Jørgensen and Kristensen 2001). | ||
==Instructions== | ==Instructions== | ||
Revision as of 00:53, 7 December 2022
Overview
Taxonomy and Phylogeny
Morphology
Ecology
Marine Tardigrades
Composing almost all species in the Heterotardigrada class, including the order Arthrotardigrada and the family Echiniscoididae[1], marine tardigrades are found in all seas, from intertidal (exposed at low tide) and subtidal (covered at low tide) shores, to manganese nodules, abyssal mud, and deep-sea ooze on ocean floors 5730 m below sea level(Hansen 2003; J. Hansen pers. comm). Marine tardigrades are either interstitial, living between grains of sand in the soil or aquatic sediment, alongside others in the psammon community, or anchor to different substrates, detritus, or other organisms[1]. They are interstitial among coarser sands, often found in intertidal but also subtidal zones, and tend to be epibenthic (on sediment surface) in finer sands and mud due to lower oxygenation[1]. Marine tardigrades in microhabitats that are both intertidal and interstitial are usually found within the first few centimeters of the substrate, but they also live in communities up to 180 cm deep(Renaud-Mornaunt 1988). Additionally, some semibenthic species in the family Halechiniscidae sometimes drift or weakly swim above their substrate in order to settle on a new location(Kristensen and Renaud-Mornant 1983).
In some marine tardigrade species, zonation has been found. In one study, for example, the species composition shifted from littoral (near the shore) to submarine to deep sea caves(Grimaldi de Zio 1984; Grimaldi de Zio and Gallo D’Addabbo 2001). Intertidal tardigrades, like other meiofauna, migrate both horizontally and vertically with the tides(Giere 2009), which dynamically stratifiy beach environments with respect to water saturation and oxygen content. Additionally, competitive interactions between marine tardigrade species have been suggested based on non-overlapping distributions, impacting beach tardigrades(Martinex 1975) and vertical distribution patterns of barnacle-dependent species(Kristensen and Hallas 1980).
Generally smaller, marine tardigrades have telescopic legs. They can have either up to 13 claws or 4 tows with complex claws. Alternatively, interstitial species have 4 to 6 toes with an adhesive round or rod-shaped disk on each that allows them to tightly adhere to shifting sand grains[1]. Tardigrades living in deep-sea muds have cylindrical, wormlike bodies with reduced legs. Epibenthic species and those on algae often have elongated appendages and claws with multiple hooks[1]. And the eutardigrade Halobioutus crispae possesses enlarged Malpighian tubules attributed to a secondary shift to seawater(Crisp and Kistensen 1983;Mobjerg and Dahl 1996). Many marine tardigrades are found the world over, suggesting substantial dispersal capabilities[1], but the mechanisms for dispersal are poorly understood. Passive dispersal may be utilized. Semibenthic species, like Halechiniscidae semibenthics, have a diversity of structures that facilitate swimming and drifting. Some semibenthic and interstitial species have cuticular extensions that increase surface area and may increase passive dispersion(Grimaldi de Zio 1984; Jorgensen and Kristensen 2001; Giere 2001; Kristensen and Sorensen 2004). Tantarctus bubulubus has 18-20 balloon or float-like appendages attached to the fourth pair of legs (Jorgensen and Kristensen 2001). However marine species often lack cryptobiotic states, which would seemingly limit passive dispersion. Additionally, tardigrades possess weak swimming ability, calling into question their aptitude for active dispersion in a marine environment[1]. Eggs of one species were found in the exuvium (shed skin) of its host barnacle, suggesting that this is its means of dispersal(Kristensen and Hallas, 1980). They may also spread by the ballast water from or barnacles and algal lawns beneath marine vessels (Giere 2009) as well as various forms of free-floating vegetation and plastic-anchored barnacles(Giere 2009; Arroyo 2006).
Very little is known about trophic interactions in marine species. Tardigrades comprise a minuscule portion of marine meiofauna, and so their specific roles in marine ecosystems have not been studied. However, polychaetes , bivalves, various crustaceans, fish, and birds rely heavily on meiofauna, sometimes depending solely on them at least during some phase of their life cycle(Coull 1990, 1999). Intertidal interstitial tardigrades live alongside meiofauna including nematodes, harpacticoid copepods, and turbellarians in lower relative concentration, as is often but not always the case[1]. 402 individuals of the commensal Echinoscoides sigismundi species have been found on a single barnacle(Kristensen and Hallas 1980). Most marine tardigrades probably feed on algal cells, including macroalgae and diatoms, using their paired piercing stylets and a muscular, sucking pharynx[1]. Others may be detritivores, bacterivores or ectoparasites (on the surface of the host)(Kristensen and Sorensen 2004). Some species are associated with organic slime growing on algae(Giere 2009).
Several commensal relationships have been observed among tardigrades, but they are likely facultative (circumstantial rather than necessary), as the same species are also found living freely in interstitial or algal habitats[1]. Some marine tardigrades live between the plates of barnacles, likely feeding on associated algae. Crevices of barnacle plates provide physical protection and shelter from temperature fluctuations especially when exposed by low tides(Faurby 2012). Ectoparasites include facultative parasitism on the pleopods (limbs) of the isopod Ligmoria lignorum[1] and obligate parasites with specific adaptations, like Echiniscoides hoepneri, which feeds on embryos in barnacles’ brood chamber and Tetrakentron synaptae, which only lives on the tentacles of the sea cucumber Leptosunapa galliennei[1]. Most species of Floractus and Eingstrandarctus genus have epicuticular vesicles associated with the buccal apparatus that house symbiotic bacteria, which, in their clean coral sand microhabitats, may provide their primary food source(Kristensen 1984). One final interspecific interaction has been seen in the epibenthic Tanarctus bubulubus, the balloon-appendaged tardigrade from earlier, whose entire dorsal side is covered in mucous, apparently providing adhesion for shed calcerous platelets which form the spherical shells of coccolithophores, perhaps providing chemical or mechanical camouflage(Jørgensen and Kristensen 2001).
Instructions
Select a topic about genetics or evolution in a specific organism or ecosystem.
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Legend/credit: Electron micrograph of the Ebola Zaire virus. This was the first photo ever taken of the virus, on 10/13/1976. By Dr. F.A. Murphy, now at U.C. Davis, then at the CDC.
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Section 1 Genetics
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[3]
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For multiple use of the same inline citation or footnote, you can use the named references feature, choosing a name to identify the inline citation, and typing [5]
Second citation of Ref 1: [2]
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Include some current research, with a second image.
Conclusion
Overall text length (all text sections) should be at least 1,000 words (before counting references), with at least 2 images.
Include at least 5 references under References section.
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 R. O. (Ed.). (2018). Water Bears: The Biology of Tardigrades. Zoological Monographs, 2.
- ↑ 2.0 2.1 Hodgkin, J. and Partridge, F.A. "Caenorhabditis elegans meets microsporidia: the nematode killers from Paris." 2008. PLoS Biology 6:2634-2637.
- ↑ Bartlett et al.: Oncolytic viruses as therapeutic cancer vaccines. Molecular Cancer 2013 12:103.
- ↑ Lee G, Low RI, Amsterdam EA, Demaria AN, Huber PW, Mason DT. Hemodynamic effects of morphine and nalbuphine in acute myocardial infarction. Clinical Pharmacology & Therapeutics. 1981 May;29(5):576-81.
- ↑ 5.0 5.1 text of the citation
Edited by Zachary Spivack, student of Joan Slonczewski for BIOL 116 Information in Living Systems, 2022, Kenyon College.
