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Final Note of Special Issue “Tardigrades Taxonomy, Biology and Ecology”

Final Note of Special Issue “Tardigrades Taxonomy, Biology and Ecology” diversity Editorial Final Note of Special Issue “Tardigrades Taxonomy, Biology and Ecology” Łukasz Kaczmarek Department of Animal Taxonomy and Ecology, Adam Mickiewicz University, Poznan, ´ Uniwersytetu Poznanskiego ´ 6, 61-614 Poznan, ´ Poland; kaczmar@amu.edu.pl Received: 19 April 2020; Accepted: 20 April 2020; Published: 25 April 2020 Abstract: Tardigrada (water bears) are microscopic invertebrates inhabiting aquatic (freshwater and marine) and terrestrial habitats. They are thriving in almost all Earth ecosystems from deepest oceans to highest mountains, from tropics to polar regions. Water bears are probably most famous for their cryptobiotic abilities, which allow them to survive a broad spectrum of extreme environmental conditions. The Special Issue on tardigrades was launched to popularize research on these fascinating microinvertebrates. The published papers were focused on (a) marine and terrestrial tardigrades diversity, (b) interpopulation variability of Antarctic eutardigrade Paramacrobiotus fairbanksi, (c) encystment in freshwater eutardigrade Thulinius ru oi and (d) use of a metabarcoding approach to community structures studies in microenvironments. Keywords: diversity; encystment; interpopulation variability; metabarcoding; new species; Tardigrada; taxonomy Tardigrada (known colloquially as water bears or moss piglets) are microscopic invertebrates inhabiting aquatic (freshwater and marine) and terrestrial habitats. They are very frequent in almost all of Earth’s ecosystems from deepest oceans to highest mountains, from tropics to polar regions. They can be found in lichens, mosses, soil and aquatic sediments [1–6]. Tardigrades are relatively poorly known, up to now ca. 1300 species of tardigrades have been described [7] and new species are still being described every year (http://www.tardigrada.net/newsletter/index.htm.). Water bears have a bilaterally symmetrical body and four pairs of legs mostly terminating in claws. A tardigrade’s body is divided into a head (cephalic) segment and four trunk segments each bearing a pair of legs. Body length ranges from 50 m in marine or juveniles of freshwater or terrestrial, to 1200 m in adults with an average of 250–500 m. The cuticle is soft in Eutardigrada or covered by cuticular plates in Heterotardigrada. They have a complete digestive system and body cavity, with numerous free-floating storage cells, which is responsible for respiration and circulation. The nervous system consists of a simple brain and a ventral nerve chain with four bilobed ganglia. Tardigrades are bisexual, parthenogenetic or hermaphroditic [1]. Tardigrades can be herbivorous and feed on algae, bacteria or plant cells; carnivorous, feeding mainly on microscopic invertebrates such as rotifers or nematodes, but also on other tardigrades; or omnivorous and feed both on plants and invertebrates, see [1–8]. Water bears are probably the most famous for their cryptobiotic abilities, which allow them to survive a broad spectrum of extreme environmental conditions, e.g., lack of water, very low and high temperatures, ionizing radiation, starvation, lack of oxygen, high levels of di erent types of chemicals or space vacuum, see [9–12]. What is even more exciting, tardigrades can possibly “cheat death” and do not age during anhydrobiosis [13]. Although the tardigrades are known in general, there are numerous knowledge gaps to be fulfilled. For this reason, as a guest editor, I thought about proposing the Special Issue: “Tardigrades Taxonomy, Biology and Ecology” in the Diversity journal. Overall, five papers were published, providing novel insights into this fascinating group of invertebrate animals. Diversity 2020, 12, 169; doi:10.3390/d12050169 www.mdpi.com/journal/diversity Diversity 2020, 12, 169 2 of 3 Janelt and Poprawa [14] analyzed the poorly studied phenomenon of encystment in the freshwater eutardigrade, Thulinius ru oi (Bertolani [15]). Authors described in detail a process of cyst formation, as well as the morphology of cysts and animals inside the cyst. In the main conclusions, they stated that the cyst capsule is composed of three cuticle layers. Cuticle layers are increasingly simplified (from outside to inside). Tardigrades inside the cyst are covered with a cuticle that develops like nonencysted specimens of this species and possesses claws and produces only one functional buccal-pharyngeal apparatus [14]. Gomes-Júnior et al. [16] studied deep sea (between 150 and 3000 m bsl) tardigrades of the genus Coronarctus Renaud-Mornant [17] from the south-western Atlantic Ocean and described three species new for science. The authors also discussed the most important morphological characters in the genus and presented identification key to all known Coronarctus species [16]. Berdi and Altındag ˘ [18] studied terrestrial tardigrades in the province of Karabük (Turkey) and reported two species, Echiniscus granulatus (Doyère [19]) and Diaforobiotus islandicus (Richters [20]), new for this province. Moreover, the authors provided a current checklist of tardigrade species reported from Turkey, indicating their localities and geographic distribution [18]. In the next paper of the SI, Kaczmarek et al. [21] focused on terrestrial Antarctic tardigrades. Authors reported eight tardigrade taxa from this region including parthenogenetic Paramacrobiotus fairbanksi Schill, Förster, Dandekar and Wolf [22], which are considered by authors as cosmopolitan species which confirm the “everything is everywhere” hypothesis. Moreover, Kaczmarek et al. [21] analyzed morphological and genetic di erences between the few populations of Pam. fairbanksi from distant localities and small statistically important genetic and morphological di erences were shown. Arakawa [23] studied community structures within xeric and mesic mosses. The author used metabarcoding to identify all prokaryotes and eukaryotes, including tardigrades. In xeric mosses xerophilic tardigrades and other anhydrobiotic invertebrates seem to have limited diversity and the prokaryotic population was dominated by cyanobacteria, which suggests that in such environments only organisms resistant to extreme desiccation are able to survive. In conclusion, such combined metabarcoding approaches can be highly useful to study community structures within microscopic ecosystems, i.e., microecology [23]. As a guest editor for this Special Issue, I would like to express my gratitude to all the authors for their contributors and the reviewers for their work in the manuscript evaluations. I am confident that this Special Issue not only shows the diversity of studies carried out in the field of tardigrades but also will inspire di erent research teams to conduct subsequent investigations and further explore this fascinating phylum of microinvertebrates. I also want to thank the sta members at the MDPI editorial (in particular Ms. Wei Zhang and Ms. Emma Li, managing editors) for their support during the editorial process. Conflicts of Interest: The author declare no conflict of interest. References 1. Nelson, D.R.; Guidetti, R.; Rebecchi, L. Phylum tardigrada. In Vol. 1: Thorp and Covich’s Freshwater Invertebrates, 4th ed.; Ecology and General Biology; Elsevier Press: Amsterdam, The Netherlands, 2015; pp. 347–380. 2. McInnes, S.J. Zoogeographic distribution of terrestrial/freshwater tardigrades from current literature. J. Nat. Hist. 1994, 28, 257–352. [CrossRef] 3. Kaczmarek, Ł.; Michalczyk, Ł.; McInnes, S.J. Annotated zoogeography of non-marine Tardigrada. Part I: Central America. Zootaxa 2014, 3763, 1–62. [CrossRef] [PubMed] 4. Kaczmarek, Ł.; Michalczyk, Ł.; McInnes, S.J. Annotated zoogeography of non-marine Tardigrada. Part II: South America. Zootaxa 2015, 3923, 1–107. [CrossRef] [PubMed] 5. Kaczmarek, Ł.; Michalczyk, Ł.; McInnes, S.J. Annotated zoogeography of non-marine Tardigrada. Part III: North America and Greenland. Zootaxa 2016, 4203, 1–249. [CrossRef] [PubMed] Diversity 2020, 12, 169 3 of 3 6. McInnes, S.J.; Michalczyk, Ł.; Kaczmarek, Ł. Annotated zoogeography of non-marine Tardigrada. Part IV: Africa. Zootaxa 2017, 4284, 1–74. [CrossRef] 7. Degma, P.; Bertolani, R.; Guidetti, R. Actual Checklist of Tardigrada Species (2009–2019, 35th Edition: 31-07-2019). 2019. Available online: https://iris.unimore.it/retrieve/handle/11380/1178608/226739/Actual% 20checklist%20of%20Tardigrada%2035th%20Edition.pdf (accessed on 19 April 2020). [CrossRef] 8. Roszkowska, M.; Bartels, P.J.; Gołdyn, B.; Ciobanu, D.; Fontoura, P.; Michalczyk, Ł.; Nelson, D.R.; Ostrowska, M.; Moreno-Talamantes, A.; Kaczmarek, Ł. Is the gut content of Milnesium (Eutardigrada) related to buccal tube size? Zool. J. Linnean Soc. 2016, 178, 794–803. [CrossRef] 9. Rebecchi, L.; Altiero, T.; Guidetti, R. Anhydrobiosis: The extreme limit of desiccation tolerance. Invert. Surviv. J. 2007, 4, 65–81. 10. Wełnicz, W.; Grohme, M.A.; Kaczmarek, Ł.; Schill, R.O.; Frohme, M. Anhydrobiosis in tardigrades—The last decade. J. Insect Physiol. 2011, 57, 577–583. [CrossRef] [PubMed] 11. Guidetti, R.; Rizzo, A.M.; Altiero, T.; Rebecchi, L. 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. Planet. Space Sci. 2012, 74, 97–102. [CrossRef] 12. Erdmann, W.; Kaczmarek, Ł. Tardigrade in space research-past and future. Orig. Life Evol. Biosph. 2017, 47, 545–553. [CrossRef] 13. Kaczmarek, Ł.; Roszkowska, M.; Fontaneto, D.; Jezierska, M.; Pietrzak, B.; Wieczorek, R.; Poprawa, I.; Kosicki, J.Z.; Karachitos, A.; Kmita, H. Staying young and fit? Ontogenetic and phylogenetic consequences of animal anhydrobiosis. J. Zool. 2019, 309, 1–11. [CrossRef] 14. Janelt, K.; Poprawa, I. Analysis of encystment, excystment, and cyst structure in freshwater eutardigrade Thulinius ru oi (Tardigrada, Isohypsibioidea: Doryphoribiidae). Diversity 2020, 12, 62. [CrossRef] 15. Bertolani, R. Tardigradi Guide Per Il Riconoscimento Delle Specie Animali Delle Acque Interne Italiane; CNR Press: Verona, Italy, 1982; pp. 1–104. 16. Gomes-Júnior, E.; Santos, É.; da Rocha, C.M.C.; Santos, P.J.P.; Fontoura, P. The deep-sea genus Coronarctus (Tardigrada, Arthrotardigrada) in Brazil, south-western Atlantic Ocean, with the description of three new species. Diversity 2020, 12, 63. [CrossRef] 17. Renaud-Mornant, J. Une nouvelle famille de Tardigrades marins abyssaux: Les Coronarctidae fam. nov. (Heterotardigrada). CR Acad. Sci. 1974, 278, 3087–3090. 18. Berdi, D.; Altındag, ˘ A. Contribution to the Knowledge on Distribution of Tardigrada in Turkey. Diversity 2020, 12, 95. [CrossRef] 19. Doyère, P.L.N. Memoire sur les Tardigrades. Ann. Sci. Nat. Zool. Paris Series 2 1840, 14, 269–362. 20. Richters, F. Isländische Tardigraden. Zool. Anz 1904, 28, 373–377. 21. Kaczmarek, Ł.; Mioduchowska, M.; Kacar ˇ evic, ´ U.; Kubska, K.; Parnikoza, I.; Gołdyn, B.; Roszkowska, M. New records of Antarctic Tardigrada with comments on interpopulation variability of the Paramacrobiotus fairbanksi Schill, Förster, Dandekar and Wolf, 2010. Diversity 2020, 12, 108. [CrossRef] 22. Schill, R.O.; Forster, F.; Dandekar, T.; Wolf, N. Using compensatory base change analysis of internal transcribed spacer 2 secondary structures to identify three new species in Paramacrobiotus (Tardigrada). Org. Divers. Evol. 2010, 10, 287–296. [CrossRef] 23. Arakawa, K. Simultaneous metabarcoding of eukaryotes and prokaryotes to elucidate the community structures within tardigrade microhabitats. Diversity 2020, 12, 110. [CrossRef] © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Diversity Multidisciplinary Digital Publishing Institute

Final Note of Special Issue “Tardigrades Taxonomy, Biology and Ecology”

Diversity , Volume 12 (5) – Apr 25, 2020

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Abstract

diversity Editorial Final Note of Special Issue “Tardigrades Taxonomy, Biology and Ecology” Łukasz Kaczmarek Department of Animal Taxonomy and Ecology, Adam Mickiewicz University, Poznan, ´ Uniwersytetu Poznanskiego ´ 6, 61-614 Poznan, ´ Poland; kaczmar@amu.edu.pl Received: 19 April 2020; Accepted: 20 April 2020; Published: 25 April 2020 Abstract: Tardigrada (water bears) are microscopic invertebrates inhabiting aquatic (freshwater and marine) and terrestrial habitats. They are thriving in almost all Earth ecosystems from deepest oceans to highest mountains, from tropics to polar regions. Water bears are probably most famous for their cryptobiotic abilities, which allow them to survive a broad spectrum of extreme environmental conditions. The Special Issue on tardigrades was launched to popularize research on these fascinating microinvertebrates. The published papers were focused on (a) marine and terrestrial tardigrades diversity, (b) interpopulation variability of Antarctic eutardigrade Paramacrobiotus fairbanksi, (c) encystment in freshwater eutardigrade Thulinius ru oi and (d) use of a metabarcoding approach to community structures studies in microenvironments. Keywords: diversity; encystment; interpopulation variability; metabarcoding; new species; Tardigrada; taxonomy Tardigrada (known colloquially as water bears or moss piglets) are microscopic invertebrates inhabiting aquatic (freshwater and marine) and terrestrial habitats. They are very frequent in almost all of Earth’s ecosystems from deepest oceans to highest mountains, from tropics to polar regions. They can be found in lichens, mosses, soil and aquatic sediments [1–6]. Tardigrades are relatively poorly known, up to now ca. 1300 species of tardigrades have been described [7] and new species are still being described every year (http://www.tardigrada.net/newsletter/index.htm.). Water bears have a bilaterally symmetrical body and four pairs of legs mostly terminating in claws. A tardigrade’s body is divided into a head (cephalic) segment and four trunk segments each bearing a pair of legs. Body length ranges from 50 m in marine or juveniles of freshwater or terrestrial, to 1200 m in adults with an average of 250–500 m. The cuticle is soft in Eutardigrada or covered by cuticular plates in Heterotardigrada. They have a complete digestive system and body cavity, with numerous free-floating storage cells, which is responsible for respiration and circulation. The nervous system consists of a simple brain and a ventral nerve chain with four bilobed ganglia. Tardigrades are bisexual, parthenogenetic or hermaphroditic [1]. Tardigrades can be herbivorous and feed on algae, bacteria or plant cells; carnivorous, feeding mainly on microscopic invertebrates such as rotifers or nematodes, but also on other tardigrades; or omnivorous and feed both on plants and invertebrates, see [1–8]. Water bears are probably the most famous for their cryptobiotic abilities, which allow them to survive a broad spectrum of extreme environmental conditions, e.g., lack of water, very low and high temperatures, ionizing radiation, starvation, lack of oxygen, high levels of di erent types of chemicals or space vacuum, see [9–12]. What is even more exciting, tardigrades can possibly “cheat death” and do not age during anhydrobiosis [13]. Although the tardigrades are known in general, there are numerous knowledge gaps to be fulfilled. For this reason, as a guest editor, I thought about proposing the Special Issue: “Tardigrades Taxonomy, Biology and Ecology” in the Diversity journal. Overall, five papers were published, providing novel insights into this fascinating group of invertebrate animals. Diversity 2020, 12, 169; doi:10.3390/d12050169 www.mdpi.com/journal/diversity Diversity 2020, 12, 169 2 of 3 Janelt and Poprawa [14] analyzed the poorly studied phenomenon of encystment in the freshwater eutardigrade, Thulinius ru oi (Bertolani [15]). Authors described in detail a process of cyst formation, as well as the morphology of cysts and animals inside the cyst. In the main conclusions, they stated that the cyst capsule is composed of three cuticle layers. Cuticle layers are increasingly simplified (from outside to inside). Tardigrades inside the cyst are covered with a cuticle that develops like nonencysted specimens of this species and possesses claws and produces only one functional buccal-pharyngeal apparatus [14]. Gomes-Júnior et al. [16] studied deep sea (between 150 and 3000 m bsl) tardigrades of the genus Coronarctus Renaud-Mornant [17] from the south-western Atlantic Ocean and described three species new for science. The authors also discussed the most important morphological characters in the genus and presented identification key to all known Coronarctus species [16]. Berdi and Altındag ˘ [18] studied terrestrial tardigrades in the province of Karabük (Turkey) and reported two species, Echiniscus granulatus (Doyère [19]) and Diaforobiotus islandicus (Richters [20]), new for this province. Moreover, the authors provided a current checklist of tardigrade species reported from Turkey, indicating their localities and geographic distribution [18]. In the next paper of the SI, Kaczmarek et al. [21] focused on terrestrial Antarctic tardigrades. Authors reported eight tardigrade taxa from this region including parthenogenetic Paramacrobiotus fairbanksi Schill, Förster, Dandekar and Wolf [22], which are considered by authors as cosmopolitan species which confirm the “everything is everywhere” hypothesis. Moreover, Kaczmarek et al. [21] analyzed morphological and genetic di erences between the few populations of Pam. fairbanksi from distant localities and small statistically important genetic and morphological di erences were shown. Arakawa [23] studied community structures within xeric and mesic mosses. The author used metabarcoding to identify all prokaryotes and eukaryotes, including tardigrades. In xeric mosses xerophilic tardigrades and other anhydrobiotic invertebrates seem to have limited diversity and the prokaryotic population was dominated by cyanobacteria, which suggests that in such environments only organisms resistant to extreme desiccation are able to survive. In conclusion, such combined metabarcoding approaches can be highly useful to study community structures within microscopic ecosystems, i.e., microecology [23]. As a guest editor for this Special Issue, I would like to express my gratitude to all the authors for their contributors and the reviewers for their work in the manuscript evaluations. I am confident that this Special Issue not only shows the diversity of studies carried out in the field of tardigrades but also will inspire di erent research teams to conduct subsequent investigations and further explore this fascinating phylum of microinvertebrates. I also want to thank the sta members at the MDPI editorial (in particular Ms. Wei Zhang and Ms. Emma Li, managing editors) for their support during the editorial process. Conflicts of Interest: The author declare no conflict of interest. References 1. Nelson, D.R.; Guidetti, R.; Rebecchi, L. Phylum tardigrada. In Vol. 1: Thorp and Covich’s Freshwater Invertebrates, 4th ed.; Ecology and General Biology; Elsevier Press: Amsterdam, The Netherlands, 2015; pp. 347–380. 2. McInnes, S.J. Zoogeographic distribution of terrestrial/freshwater tardigrades from current literature. J. Nat. Hist. 1994, 28, 257–352. [CrossRef] 3. Kaczmarek, Ł.; Michalczyk, Ł.; McInnes, S.J. Annotated zoogeography of non-marine Tardigrada. Part I: Central America. Zootaxa 2014, 3763, 1–62. [CrossRef] [PubMed] 4. Kaczmarek, Ł.; Michalczyk, Ł.; McInnes, S.J. Annotated zoogeography of non-marine Tardigrada. Part II: South America. Zootaxa 2015, 3923, 1–107. [CrossRef] [PubMed] 5. Kaczmarek, Ł.; Michalczyk, Ł.; McInnes, S.J. Annotated zoogeography of non-marine Tardigrada. Part III: North America and Greenland. Zootaxa 2016, 4203, 1–249. [CrossRef] [PubMed] Diversity 2020, 12, 169 3 of 3 6. McInnes, S.J.; Michalczyk, Ł.; Kaczmarek, Ł. Annotated zoogeography of non-marine Tardigrada. Part IV: Africa. Zootaxa 2017, 4284, 1–74. [CrossRef] 7. Degma, P.; Bertolani, R.; Guidetti, R. Actual Checklist of Tardigrada Species (2009–2019, 35th Edition: 31-07-2019). 2019. Available online: https://iris.unimore.it/retrieve/handle/11380/1178608/226739/Actual% 20checklist%20of%20Tardigrada%2035th%20Edition.pdf (accessed on 19 April 2020). [CrossRef] 8. Roszkowska, M.; Bartels, P.J.; Gołdyn, B.; Ciobanu, D.; Fontoura, P.; Michalczyk, Ł.; Nelson, D.R.; Ostrowska, M.; Moreno-Talamantes, A.; Kaczmarek, Ł. Is the gut content of Milnesium (Eutardigrada) related to buccal tube size? Zool. J. Linnean Soc. 2016, 178, 794–803. [CrossRef] 9. Rebecchi, L.; Altiero, T.; Guidetti, R. Anhydrobiosis: The extreme limit of desiccation tolerance. Invert. Surviv. J. 2007, 4, 65–81. 10. Wełnicz, W.; Grohme, M.A.; Kaczmarek, Ł.; Schill, R.O.; Frohme, M. Anhydrobiosis in tardigrades—The last decade. J. Insect Physiol. 2011, 57, 577–583. [CrossRef] [PubMed] 11. Guidetti, R.; Rizzo, A.M.; Altiero, T.; Rebecchi, L. 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. Planet. Space Sci. 2012, 74, 97–102. [CrossRef] 12. Erdmann, W.; Kaczmarek, Ł. Tardigrade in space research-past and future. Orig. Life Evol. Biosph. 2017, 47, 545–553. [CrossRef] 13. Kaczmarek, Ł.; Roszkowska, M.; Fontaneto, D.; Jezierska, M.; Pietrzak, B.; Wieczorek, R.; Poprawa, I.; Kosicki, J.Z.; Karachitos, A.; Kmita, H. Staying young and fit? Ontogenetic and phylogenetic consequences of animal anhydrobiosis. J. Zool. 2019, 309, 1–11. [CrossRef] 14. Janelt, K.; Poprawa, I. Analysis of encystment, excystment, and cyst structure in freshwater eutardigrade Thulinius ru oi (Tardigrada, Isohypsibioidea: Doryphoribiidae). Diversity 2020, 12, 62. [CrossRef] 15. Bertolani, R. Tardigradi Guide Per Il Riconoscimento Delle Specie Animali Delle Acque Interne Italiane; CNR Press: Verona, Italy, 1982; pp. 1–104. 16. Gomes-Júnior, E.; Santos, É.; da Rocha, C.M.C.; Santos, P.J.P.; Fontoura, P. The deep-sea genus Coronarctus (Tardigrada, Arthrotardigrada) in Brazil, south-western Atlantic Ocean, with the description of three new species. Diversity 2020, 12, 63. [CrossRef] 17. Renaud-Mornant, J. Une nouvelle famille de Tardigrades marins abyssaux: Les Coronarctidae fam. nov. (Heterotardigrada). CR Acad. Sci. 1974, 278, 3087–3090. 18. Berdi, D.; Altındag, ˘ A. Contribution to the Knowledge on Distribution of Tardigrada in Turkey. Diversity 2020, 12, 95. [CrossRef] 19. Doyère, P.L.N. Memoire sur les Tardigrades. Ann. Sci. Nat. Zool. Paris Series 2 1840, 14, 269–362. 20. Richters, F. Isländische Tardigraden. Zool. Anz 1904, 28, 373–377. 21. Kaczmarek, Ł.; Mioduchowska, M.; Kacar ˇ evic, ´ U.; Kubska, K.; Parnikoza, I.; Gołdyn, B.; Roszkowska, M. New records of Antarctic Tardigrada with comments on interpopulation variability of the Paramacrobiotus fairbanksi Schill, Förster, Dandekar and Wolf, 2010. Diversity 2020, 12, 108. [CrossRef] 22. Schill, R.O.; Forster, F.; Dandekar, T.; Wolf, N. Using compensatory base change analysis of internal transcribed spacer 2 secondary structures to identify three new species in Paramacrobiotus (Tardigrada). Org. Divers. Evol. 2010, 10, 287–296. [CrossRef] 23. Arakawa, K. Simultaneous metabarcoding of eukaryotes and prokaryotes to elucidate the community structures within tardigrade microhabitats. Diversity 2020, 12, 110. [CrossRef] © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Journal

DiversityMultidisciplinary Digital Publishing Institute

Published: Apr 25, 2020

References