35 citations as recorded by crossref.

1. Meiofauna winners and losers of coastal hypoxia: case study harpacticoid copepods M. Grego et al. https://doi.org/10.5194/bg-11-281-2014
2. Distribution of Meiofauna in Bathyal Sediments Influenced by the Oxygen Minimum Zone Off Costa Rica C. Neira et al. https://doi.org/10.3389/fmars.2018.00448
3. Polar micro- and meiobenthos is resistant to prolonged light limitation: Mesocosm shading experiment in the White Sea intertidal A. Azovsky et al. https://doi.org/10.1016/j.jembe.2025.152149
4. Ecological properties of life forms of marine harpacticoid copepods A. Azovsky et al. https://doi.org/10.1007/s10750-025-06074-y
5. Recovery of deep-sea meiofauna community in Kaikōura Canyon following an earthquake-triggered turbidity flow K. Bigham et al. https://doi.org/10.7717/peerj.17367
6. Patterns in nematode community during and after experimentally induced anoxia in the northern Adriatic Sea M. Taheri et al. https://doi.org/10.1016/j.marenvres.2015.08.004
7. Performance and stratified microbial community of vermi-filter affected by Acorus calamus and Epipremnum aureum during recycling of concentrated excess sludge K. Huang et al. https://doi.org/10.1016/j.chemosphere.2021.130609
8. Benthic invertebrate biodiversity enhancement with reef cubes®, evidenced by environmental DNA analysis of sediment samples S. Hickling et al. https://doi.org/10.1016/j.ecoleng.2023.107064
9. Assessing environmental effects of the bay scallop Argopecten irradians culture in China: Using abiotic and biotic indicators Q. Huang et al. https://doi.org/10.1016/j.aquaculture.2018.09.050
10. Environmental DNA metabarcoding for benthic monitoring: A review of sediment sampling and DNA extraction methods J. Pawlowski et al. https://doi.org/10.1016/j.scitotenv.2021.151783
11. Organic enrichment negatively impacts meiobenthic copepods on Argentinean coasts M. Sciberras et al. https://doi.org/10.1016/j.jembe.2025.152118
12. Impact of seasonal hypoxia on benthic copepod communities in Omura Bay, a highly enclosed coastal sea in southwestern Japan K. Kawano et al. https://doi.org/10.3800/pbr.16.93
13. Trophic guild structure, feeding overlap and diet-associated anthropogenic particles in the fishes of Manori Creek, Mumbai, India R. Bandyopadhyay et al. https://doi.org/10.1016/j.rsma.2025.104272
14. Occurrence of <i>Geehydrosoma</i> cf. <i>intermedia</i> (Chislenko, 1978), a harpacticoid copepod species in the family Cletodidae assessed by DNA barcoding in Omura Bay, a seasonally hypoxic enclosed bay, in Japan M. Wada et al. https://doi.org/10.3800/pbr.20.s86
15. Ecological Responses of Meiofauna to a Saltier World—A Case Study in the Van Uc River Continuum (Vietnam) in the Dry Season H. Nguyen et al. https://doi.org/10.3390/w15071278
16. Is the meiofauna a good indicator for climate change and anthropogenic impacts? D. Zeppilli et al. https://doi.org/10.1007/s12526-015-0359-z
17. Subsea permafrost thaw fuels meiobenthic hotspots in the East Siberian Sea D. Portnova et al. https://doi.org/10.1007/s00027-026-01282-7
18. Resilient amphipods: Gammarid predatory behaviour is unaffected by microplastic exposure and deoxygenation R. Griffith et al. https://doi.org/10.1016/j.scitotenv.2023.163582
19. Characteristics of meiofauna in extreme marine ecosystems: a review D. Zeppilli et al. https://doi.org/10.1007/s12526-017-0815-z
20. Impact of farming non-indigenous scallop Argopecten irradians on benthic ecosystem functioning: a case-study in Laizhou Bay, China Q. Huang et al. https://doi.org/10.3354/aei00264
21. Is meiofauna a good bioindicator of artificial reef impact? F. Semprucci et al. https://doi.org/10.1007/s12526-016-0484-3
22. Temporal changes of the meiofaunal assemblage as a tool for the assessment of the ecological quality status F. Semprucci et al. https://doi.org/10.1017/S0025315414001271
23. Metabolic rate and tolerance to hypoxia in the harpacticoid copepod Amphiascoides atopus A. García-Bernal et al. https://doi.org/10.1016/j.jembe.2025.152151
24. Multiple human pressures in coastal habitats: variation of meiofaunal assemblages associated with sewage discharge in a post-industrial area I. Bertocci et al. https://doi.org/10.1016/j.scitotenv.2018.11.121
25. Does vertical distribution of meiobenthic community structure differ among various mangrove habitats of Sundarban Estuarine System? M. Ghosh & S. Mandal https://doi.org/10.1016/j.rsma.2019.100778
26. Integrity of benthic assemblages along the arctic estuarine-coastal system A. Udalov et al. https://doi.org/10.1016/j.ecolind.2020.107115
27. Meiofaunal distribution patterns and trophic structure in response to abiotic conditions in Coringa mangroves on the east coast of India R. Pandiya rajan et al. https://doi.org/10.1007/s13131-026-2640-3
28. Artificially induced migration of redox layers in a coastal sediment from the Northern Adriatic E. Metzger et al. https://doi.org/10.5194/bg-11-2211-2014
29. Spatial marine meiofauna variations in areas undergoing different disturbance levels on the Amazon coast M. Santos et al. https://doi.org/10.1007/s11756-023-01536-x
30. Chronic contamination in the southern Gulf of Mexico coastal zone, as evidenced by meiofauna biological traits N. Santibañez-Aguascalientes et al. https://doi.org/10.1016/j.rsma.2024.103757
31. Foraminiferal species responses to in situ, experimentally induced anoxia in the Adriatic Sea D. Langlet et al. https://doi.org/10.5194/bg-11-1775-2014
32. Effect of hypoxia and anoxia on invertebrate behaviour: ecological perspectives from species to community level B. Riedel et al. https://doi.org/10.5194/bg-11-1491-2014
33. Taxonomic and functional biodiversity variations of meiobenthic and nematode assemblages across an extreme environment: a study case in a Blue Hole cave R. Sandulli et al. https://doi.org/10.1080/11250003.2014.952356
34. Spatiotemporal changes in meiofaunal composition on soft substrates in the semi-enclosed inner section of the northern Yatsushiro Sea M. Shimanaga et al. https://doi.org/10.1007/s10872-015-0274-8
35. Structure and function of nematode communities across the Indian western continental margin and its oxygen minimum zone R. Singh & B. Ingole https://doi.org/10.5194/bg-13-191-2016