Increasing availability and extent of biological ocean time series (from both in situ and satellite data) have helped reveal significant phenological variability of marine plankton. The extent to which the range of this variability is modified as a result of climate change is of obvious importance. Here we summarize recent research results on phenology of both phytoplankton and zooplankton. We suggest directions to better quantify and monitor future plankton phenology shifts, including (i) examining the main mode of expected future changes (ecological shifts in timing and spatial distribution to accommodate fixed environmental niches vs. evolutionary adaptation of timing controls to maintain fixed biogeography and seasonality), (ii) broader understanding of phenology at the species and community level (e.g. for zooplankton beyond Calanus and for phytoplankton beyond chlorophyll), (iii) improving and diversifying statistical metrics for indexing timing and trophic synchrony and (iv) improved consideration of spatio-temporal scales and the Lagrangian nature of plankton assemblages to separate time from space changes.
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Diatoms dominate spring bloom phytoplankton assemblages in temperate waters and coastal upwelling regions of the global ocean. Copepods usually dominate the zooplankton in these regions and are the prey of many larval fish species. Recent laboratory studies suggest that diatoms may have a deleterious effect on the success of copepod egg hatching. These findings challenge the classical view of marine food-web energy flow from diatoms to fish by means of copepods. Egg mortality is an important factor in copepod population dynamics, thus, if diatoms have a deleterious in situ effect, paradoxically, high diatom abundance could limit secondary production. Therefore, the current understanding of energy transfer from primary production to fisheries in some of the most productive and economically important marine ecosystems may be seriously flawed. Here we present in situ estimates of copepod egg hatching success from twelve globally distributed areas, where diatoms dominate the phytoplankton assemblage. We did not observe a negative relationship between copepod egg hatching success and either diatom biomass or dominance in the microplankton in any of these regions. The classical model for diatom-dominated system remains valid.
It is frequently put forward that variability in fisheries productivity is related to interannual variation in physical processes affecting phytoplankton productivity. Here, alternative views of the role of copepods as an intermediary link in North Atlantic marine food chains are discussed. Following Bainbridge & McKay (1968) and Cushing (1982), a strong link between phytoplankton and fisheries variability is proposed for some fish stocks, like cod and redfish, that spawn in spring in regions where Calanus finmarchicus dominates the plankton. Otherwise, in regions where small copepods and other microzooplankton dominate the prey field productivity for larval fish, a weak link is proposed. Experimental studies, including laboratory observations of copepod reproductive response to food concentration and incubation techniques for measuring in situ reproductive rates, are important for understanding how copepod dynamics may filter year-to-year differences in phytoplankton production cycles.
Johnson, C. L., Leising, A. W., Runge, J. A., Head, E. J. H., Pepin, P., Plourde, S., and Durbin, E. G. 2008. Characteristics of Calanus finmarchicus dormancy patterns in the Northwest Atlantic. – ICES Journal of Marine Science, 65: 339–350. Demographic time-series from four fixed stations in the Northwest Atlantic Ocean demonstrate variable timing of entry into and emergence from dormancy in subpopulations of the planktonic copepod Calanus finmarchicus. A proxy for timing of entry was established as the date each year when the proportion of the fifth copepodid stage (CV) in the subpopulation rose to half its overall climatological maximum CV proportion at that station. The proxy for timing of emergence at each station was set as the first date when adults were more than 10% of the total abundance of copepodid stages. An alternate emergence proxy date was determined by back-calculating the spawning dates of the first early copepodid stages appearing in spring, using a stage-structured, individual-based model. No single environmental cue (photoperiod, surface temperature, or average surface-layer chlorophyll a concentration) consistently explained entry or emergence dates across all stations. Among hypotheses put forward to explain dormancy in Calanus species, we cannot eliminate the lipid accumulation window hypothesis for onset of dormancy or a lipid-modulated endogenous timer controlling dormancy duration. The fundamental premise of these hypotheses is that individuals can only enter dormancy if their food and temperature history allows them to accumulate sufficient lipid to endure overwintering, moult, and undergo early stages of gonad maturation.
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