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. 2022 Dec 31;12(1):22631.
doi: 10.1038/s41598-022-26004-5.

Protistan epibionts affect prey selectivity patterns and vulnerability to predation in a cyclopoid copepod

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Protistan epibionts affect prey selectivity patterns and vulnerability to predation in a cyclopoid copepod

Ram Kumar et al. Sci Rep. .

Abstract

Colonisation of crustacean zooplankton with ciliate epibionts is widespread in freshwater and marine environments. However, the ecology of such association are little studied as yet. The occurrence of ciliate epibionts on copepods and the preference towards this association with different life stages of Mesocyclops were studied from winter to spring. Relative susceptibility of zooplankton species was evaluated by analysing the epibiont colonies and zooids and relate this to the surface area of the host. The maximum epibiont infestation per unit body surface area was recorded on copepodites followed by copepod nauplii rather than other zooplankton species, whereas the rotifer Asplanchna was never affected. Influence of climatic factors such as temperature on the colonisation of epibionts on basibionts was found significant. In winter (November to February) samples, copepods were infested by autotrophic epibionts whereas in late spring and early summer (March-April) heterotrophic protists (peritrichian ciliates) were the sole epibionts on copepods. We conducted experiments in the laboratory on prey selection pattern of predators by direct visual and video-graphic observations of various events (encounter, attack, capture, ingestion, prey escape) during predation by infested and uninfested copepodites and adults of Mesocyclops. Postencounter the attack probability was significantly lower in infested than in uninfested copepods. The present paper reports on substrate preference by epibionts and their impacts in food rich and food scarce environments. Furthermore, major environmental interactions were studied with the reproductive phenology of copepods with respect to epibionts and the cause and effect of long term association of epibionts with copepods need to be addressed.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Zooplankton species loaded with epibionts (a) Copepod nauplii (b) Copepod adults (c) Keratella cochlearis (d) Polyarthra vulgaris (e) Filinia longiseta (f) Brachionus rubens (g) Hexarthra mira.
Figure 2
Figure 2
Total abundance and individual numbers colonized (individuals 5 L−1) by epibionts at each sampling date during November 2013 to April 2014, from the flood plain wetland of the river Ganges.
Figure 3
Figure 3
Monthly average of abundance (Individuals 5L−1 and No. of epibionts Individual−1 of ovigerous and non-ovigerous rotifers (A) Polyarthra, (B) Hexarthra (C) Filinia and (D) Keratella during November 2013 to April 2014, from the flood plain wetland of the river Ganges.
Figure 4
Figure 4
Monthly average of abundance (Individuals 5L−1) and infestation load (No. of epibiont individual−1) of ovigerous and non-ovigerous copepods, Mesocyclops (A) nauplii, (B) copepodid and (C) adults during November 2013 to April 2014, from the flood plain wetland of the river Ganges.
Figure 5
Figure 5
Prey ingestion rate (A), prey selectivity index value (ɑ) and prey selectivity as a function of body size (B) of Mesocyclops given a choice of ciliate, rotifer and cladoceran prey in the laboratory (see Table 1 for prey size).
Figure 6
Figure 6
Prey ingestion rate and prey selectivity index value (ɑ) for fish Punitus sarana and Gambusia affinis given a choice of colonised (burden level for adults: 21.6 ± 3.06; for nauplii 6.3 ± 2.01 epibionts Individual−1) and uncolonised adults and nauplii of Mesocyclops sp.

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