31 citations as recorded by crossref.

1. Scale-dependence in geographic variation in a freshwater gastropod across the Palearctic M. Vinarski & S. Kramarenko https://doi.org/10.1080/13235818.2018.1497570
2. Environmental stability and long-term variability of harpacticoid copepod assemblages A. Azovsky et al. https://doi.org/10.1007/s00227-022-04059-2
3. Community-level spatiotemporal synchrony: new metric and application to White Sea meiobenthic harpacticoids A. Azovsky et al. https://doi.org/10.3354/meps14159
4. Power-law scaling in dimension-to-biomass relationship of fish schools H. Niwa https://doi.org/10.1016/j.jtbi.2005.01.022
5. Species composition and structure of testate amoebae community in a sphagnum bog at the initial stage of its formation Y. Mazei & O. Bubnova https://doi.org/10.1134/S1062359007060131
6. Integrity of benthic assemblages along the arctic estuarine-coastal system A. Udalov et al. https://doi.org/10.1016/j.ecolind.2020.107115
7. Body size determines the strength of the latitudinal diversity gradient H. Hillebrand & A. Azovsky https://doi.org/10.1034/j.1600-0587.2001.240302.x
8. Diversity of unicellular aquatic organisms scaled to body size H. Hillebrand https://doi.org/10.1080/03680770.2001.11902602
9. Monitoring Bioindication of Plankton through the Analysis of the Fourier Spectra of the Underwater Digital Holographic Sensor Data V. Dyomin et al. https://doi.org/10.3390/s24072370
10. Structure of a community of testate amoebae in a sphagnum dominated bog in upper sura flow (Middle Volga Territory) Y. Mazei et al. https://doi.org/10.1134/S1062359007040115
11. Accuracy of fractal dimension estimates for small samples of ecological distributions A. Kallimanis et al. https://doi.org/10.1023/A:1020285932506
12. Scale invariance of biosystems: From embryo to community B. Yakimov et al. https://doi.org/10.1134/S1062360414030084
13. Hierarchical drivers of cryptic biodiversity on coral reefs K. Wolfe et al. https://doi.org/10.1002/ecm.1586
14. Multi-scale beta-diversity patterns in testate amoeba communities: species turnover and nestedness along a latitudinal gradient J. Su et al. https://doi.org/10.1007/s00442-024-05602-2
15. Factors affecting regional diversity and distribution of freshwater microcrustaceans (Cladocera, Copepoda) at high latitudes A. Novichkova & A. Azovsky https://doi.org/10.1007/s00300-016-1943-9
16. Marine protected areas: Theoretical background for design and operation V. Mokievsky https://doi.org/10.1134/S1063074009060091
17. Spatial homogeneity of benthic macrofaunal biodiversity across small spatial scales R. Barnes https://doi.org/10.1016/j.marenvres.2016.10.006
18. Inter- and intra-estuarine fish assemblage variability patterns along the Portuguese coast S. França et al. https://doi.org/10.1016/j.ecss.2010.10.035
19. Small-scale diversity of Harpacticoida (Crustacea, Copepoda) from an intertidal sandflat in the Jade Bay (German Bight, North Sea) A. Rose & S. Seifried https://doi.org/10.1007/BF03043724
20. Do microbes have macroecology? Large‐scale patterns in the diversity and distribution of marine benthic ciliates A. Azovsky & Y. Mazei https://doi.org/10.1111/j.1466-8238.2012.00776.x
21. Exploring benthic habitat assessments on coral reefs: a comparison of direct field measurements versus remote sensing L. Lutzenkirchen et al. https://doi.org/10.1007/s00338-024-02468-x
22. Local and regional ecological drivers of fish assemblages in Brazilian estuaries C. Vilar et al. https://doi.org/10.3354/meps10343
23. Relevant scales of variability of the benthic allochthonous microalga Chrysophaeum taylorii S. Caronni et al. https://doi.org/10.1007/s00227-014-2461-3
24. Uses and abuses of fractal methodology in ecology J. Halley et al. https://doi.org/10.1111/j.1461-0248.2004.00568.x
25. Macroecological Patterns of Estuarine Nematodes G. Fonseca & S. Netto https://doi.org/10.1007/s12237-014-9844-z
26. Spectroscopic aspects of underwater digital holography of plankton V. Dyomin et al. https://doi.org/10.1038/s41598-025-85790-w
27. Fractal dimension of birds population sizes time series A. Garmendia & A. Salvador https://doi.org/10.1016/j.mbs.2005.03.014
28. Size‐dependent species‐area relationships in benthos: is the world more diverse for microbes? A. Azovsky https://doi.org/10.1034/j.1600-0587.2002.250303.x
29. Spatio-temporal variability of micro- and meiobenthic communities in a White Sea intertidal sandflat A. Azovsky et al. https://doi.org/10.1016/j.ecss.2004.03.005
30. Structural complexity of species assemblages and spatial scale of community organization: A case study of marine benthos A. Azovsky https://doi.org/10.1016/j.ecocom.2008.12.001
31. What is the optimum sample size for the study of peatland testate amoeba assemblages? Y. Mazei et al. https://doi.org/10.1016/j.ejop.2017.09.004