the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Diversity and assembly processes of microeukaryotic community in Fildes Peninsula Lakes (West Antarctica)
- 1Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai 200136, China
- 2State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
- 3Antarctic Great Wall Ecology National Observation and Research Station, Polar Research Institute of China, Ministry of Natural Resources, Shanghai 200136, China
- 4School of Oceanography, Shanghai Jiao Tong University, Shanghai 200030, China
- 5Key Laboratory of Marine Ecosystem Dynamics, Second Institute of Oceanography, Ministry of Natural Resources, Hangzhou 310012, China
- 1Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai 200136, China
- 2State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
- 3Antarctic Great Wall Ecology National Observation and Research Station, Polar Research Institute of China, Ministry of Natural Resources, Shanghai 200136, China
- 4School of Oceanography, Shanghai Jiao Tong University, Shanghai 200030, China
- 5Key Laboratory of Marine Ecosystem Dynamics, Second Institute of Oceanography, Ministry of Natural Resources, Hangzhou 310012, China
Abstract. The diversity, co-occurrence patterns, and assembly processes of microeukaryotes in Antarctic freshwater lakes are not well understood, despite its wide distribution and ecological importance. This study used Illumina high-throughput sequencing to explore five freshwater lakes' microeukaryotic communities on the Fildes Peninsula during three summer seasons. A total of 33 phyla were detected, with the phytoplankton occupying the highest percentage of sequences (accounting for up to 98 %). Meanwhile, the main dominant taxa were Chrysophyta, Chlorophyta, and Cryptophyta. Alpha diversity varied among lakes, with Changhu (CH), Kitec (KT) lake having higher values, and Yue Ya (YY) lake having the lowest value. There were significant differences in microeukaryotic communities between lakes, with spatial and temporal variation in the relative abundance of dominant taxa (P<0.05). Environmental variables only explained about 30 % of the variation in community structure. In the co-occurrence network, microeukaryotes tended to be more symbiotic than competitive with each other (positive correlation 82 % vs. negative correlation 18 %), with only 8 % of OTUs significantly associated with environmental factors. The neutral community model found that neutral processes explained more than 56 % of the community variation. The stochastic processes (e.g., homogenizing dispersal and undominated process) predominated in community assembly than the deterministic processes. These findings revealed the diversity of the microeukaryotic community and have important implications for understanding the community assembly in the freshwater lakes of the Fildes Peninsula (Antarctica).
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Chunmei Zhang et al.
Status: open (until 03 Jun 2022)
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RC1: 'Comment on bg-2022-75', Shoubing Wang, 17 May 2022
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Microeukaryotes are wide distribution and play importance role in aquatic ecosystem. Diversity and assembly processes of microeukaryotes should be paid more attention. Antarctic freshwater lakes are a kind of non-pollution freshwater ecosystem and Microeukaryotes are important contributor of primary producer. Diversity and assemblage of microeukaryotes would give us a clue to get insight into the whole ecosystem. Five freshwater lakes' microeukaryotic communities on the Fildes Peninsula were screened in this manuscript, ample data were provided, diversity, co-occurrence patterns and assembly processes have been analyzed. In my opinion, this work is very interesting and provided a better understanding of the dynamic patterns and ecological processes of microeukaryotic community structure inc oligotrophic lakes. I recommend it is worthy to be published after minor revision.
1. As parameter of diversity, Shannon index should be mentioned in the abstract.
2. WT and PO4-P should be mentioned in the abstract, but not the “Environmental factors”.
3. In the discussion, dominant taxa and keystone species were mentioned, is there any difference between the two? If there is no difference, please use the same one.
4. The conclusion is too long and should be shortened. -
RC2: 'Comment on bg-2022-75', Anonymous Referee #2, 23 May 2022
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The article “Diversity and assembly processes of microeukaryotic community in Fildes Peninsula Lakes (West Antarctica)” by authors Zhang et al. is an impressive effort to characterize and interpret protist communities in hard to reach and understudied ecosystems. The authors analyze protist communities from the same lakes every austral summer for three years. This provides a unique opportunity to understand how stable these communities are over time. The authors discuss the dominant taxa—Crysophyta, Cryptophyta, and Chlorophyta—and how their abundance relates to environmental factors and is influenced by biotic interactions, and whether the community assembly processes are mainly deterministic or stochastic. Overall, the authors conclude that environmental factors contribute little to community composition, interactions are mainly positive between taxa, and stochastic factors primarily shape community assembly. This is a unique study, due to its temporal component, and it documents important aspects of rapidly changing ecosystems in Antarctica. Below are comments that I believe will help improve the manuscript.
General comments:
My main concern is the pre-filtering step in the methods and how that might influence the subsequent results and interpretation. The methods state that the water was pre -filtered through 20 micron mesh-size to remove “mesoplankton and large particles” and then biomass was collected onto a 0.2 micron pore-size filter. This step actually removes all of the microplankton and leaves behind the nano and pico plankton. This has obvious implications for the title and the language throughout the manuscript, but also has more important implications for the interpretation of the results. The authors note that there is less diversity in these samples than in similar studies, which I suspect could be due to more aggressive filtering? The authors also note in the introduction that diatoms have been studied in Antarctic lakes previously but they do not report finding significant proportions of diatoms in their samples, which could also be an artifact of the size fractionation in this study. Finally, the authors report mainly positive relationships in their co-occurrence network analysis. Again, I think this may be due to the size selection, as microeukaryotes are more likely to graze nano and pico eukaryotes. However, the observation that there seems to be more niche-overlap than competition between nano and pico eukaryotes remains very interesting. Lastly, I feel that it is incorrect to refer to the positive interactions as symbiotic without further evidence documenting symbiotic relationships between the node OTUs being discussed.
Technical comments:
In the methods and throughout, I suggest choosing one spelling for each lake and sticking with it for consistency.
Line 123- I suggest abbreviating temperature just as Temp, similar to using Sal for salinity. WT adds an unnecessary additional acronym. And please complete the statement YSI Model 30 … what type of instrument, a CTD?
Line 143- “PCR products were pooled and purified using the DNA gel extraction kit.” I think this statement is a mistake as pooling should not occur at this step …
Line 148- please provide more information regarding the sequencing. The first line of the section states the instrument model, but which version chemistry was used? How many base pairs were sequenced (300?)? And paired or single end?
Line 149- the bioinformatics methods are a bit dated. For instance, why did you use qiime instead of qiime 2? Why OTUs instead of ASVs? Likewise, the SILVA database used is not the most recent and you might also consider using the PR2 database, which is curated specifically for protists. To be clear, I do not necessarily recommend redoing the analysis with more up to date methodology, but I do recommend justifying your decisions with an explanatory sentence.
Line 161- here and elsewhere the OTUs index is referred to and I am not sure what this means. Perhaps you are referring to richness?
167- define MNTD at first use
179- Bray-Curtis distance or dissimilarity, Not similarity
181- I think you may want to scale these variables, especially for variance partitioning (z-scores)
219- a range of 0.9 to 7.14ºC does not feel similar
222- molarity is mols per liter, so the units "uM L-1" is incorrect. Only uM should be reported.
226- the a of chlorophyll a should be italicized
227- salinity needs units (PSU?)
223- the Good’s coverage is calculated based on singletons, so please clarify that it was calculated before quality filtering. Also, providing rarefaction curves in the supplemental material will increase confidence in adequate sequencing depth and coverage.
246- SAR should be defined at its first appearance, I’m assuming stramenopiles-rhizaria-alveolates supergroup?
251- 70.09% Arthropoda is …. a lot. Potentially fecal material since the samples were filtered through such fine mesh? I would consider excluding this sample unless the remaining sequencing reads still reach OTU saturation after the Arthropoda reads are removed. In general, you might consider removing metazoan reads early in the analysis.
267- still unclear what the OTU index is
285- define UPGMA at first use
287- rather than saying “clustered into one clade,” I think it is more correct to simply say “clustered together”
345- while it is true that the taxa found in the samples are small cells and their small size makes them better adapted to low nutrient conditions, I think that it is hard to say whether they were more or less abundant than larger cells since all the larger cells were removed by pre-filtering with 20 um mesh. As such, this section probably should not take up so much space or prominence in the discussion.
363- I am not sure what is meant by “forming temporary groups”— maybe change the word choice?
378- please clarify whether the other studies you are referring to used similar size fractionation
426- “indicating that species coexistence was achieved mainly by symbiotic relationships between species” — I think this is an overstatement and not supported by the data.
465- unclear which “channel” is being referred to, more context is needed
478- what is “ecological scheduling”?
484- the statement regarding extreme conditions exerting less selection pressure seems incorrect?
511- again please be careful about assuming that positive co-occurrence patterns equate to symbioses, it seems niche-overlapping is more likely
520- please provide the PRJ number to make it easier to access all the sequences.
Figure 1- Please also include a large map that places the region in regional context (probably include Antarctic peninsula and tip of South America)
Figure 3-The significance indications of letters are not defined in the figure caption. What do “a” , “b”, and “ab” mean?
Other comments:
English editing is needed throughout the manuscript. Below are a few edits that stood out to me.
125- nutrient to nutrients
189- opening sentence needs to be rewritten
190- “OTUs represented Occurred” ??
217- Result to Results
310- “still keeps a high proportion” needs to be reworded
353x reference mistake “F R Pick”- remove 1st initials
406- “the nonconsecutive of environmental factors among different expedition seasons was deficient in our study” as is, I cannot make out the meaning of this sentence.
Chunmei Zhang et al.
Chunmei Zhang et al.
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