Growth of marine planktonic copepods: Global rates and patterns in relation to chlorophyll a, temperature, and body weight

By A. Hirst, Adrian Bunker. 2003

365 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/79c36dfdd2e25e0b1d9cf330326c1d41990a0150

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Citations in the corpus

Biogeochemical fluxes through mesozooplankton (2006, positive): “Since mesozooplankton growth rate decreases with body mass ( Hirst and Bunker , 2003) this could also lead to a negative correlation between chlorophyll a and the mesozooplankton to chlorophyll a ratio in the ocean, while this process is not included in the model.”
Impact of climate change on marine pelagic phenology and trophic mismatch (2004, background): “The relationship between SST and the seasonal development of some plankton taxa, particularly the meroplankton and holozooplankton, can be explained by the species-specific effects of temperature on many aspects of plankton physiology, such as adult mortality, reproduction, respiration, embryonic an”
Differences in plankton community structure along the Godthåbsfjord, from the Greenland Ice Sheet to offshore waters (2010, methodology): “The production rates of this species were probably not representative of the copepod species dominating the fjord stations, as the growth and fecundity rates of different species can vary significantly (Hirst & Bunker 2003).”
The effects of temperature and salinity on egg production and hatching success of Baltic Acartia tonsa (Copepoda: Calanoida): a laboratory investigation (2006, background): “These differences between species and populations may contribute to the consistently low Q10 values for EP (i.e., 1.33–1.93) derived from data sets containing mixtures of copepod species (Ikeda 1985; Hirst and Bunker 2003 ) that have different (and perhaps contrasting) temperature optima.”
Zooplankton communities of the Arctic’s Canada Basin: the contribution by smaller taxa (2005, background): “This also agrees with the maximum reproductive rate of 7.1% at 15 C (Hirst and Bunker 2003), which corrected by his Q10 of 1.49 for sac spawning adults, would predict a rate of 0.039 day)1 at 0 C, although caution is warranted in extrapolating his relationships below 5 C.”
An overview of Southern Ocean zooplankton data: abundance, biomass, feeding and functional relationships (2012, background): “Numerous compilations of literature data now quantify rate processes of zooplankton in relation to body mass (e.g. Peters and Downing, 1984; Hansen et al., 1997; Huntley and Lopez, 1992; Kiørboe and Sabatini, 1995; Hirst et al., 1998; Ikeda et al., 2001; Hirst and Kiørboe, 2002; Hirst and Bunker, 20”
Body size in freshwater planktonic crustaceans: an overview of extrinsic determinants and modifying influences of biotic interactions (2011, background): “Some fundamental contrasts between these groups are evident from the comprehensive survey by Hirst & Bunker (2003).”
Extension of methods for jellyfish and ctenophore trophic ecology to large-scale research (2008, background): “…abundant data for copepods have enabled development of algorithms for predicting their feeding, growth, fecundity, and mortality rates in relation to Chl a, temperature, and size (e.g., Hansen et al., 1997; Hirst & Bunker, 2003; Bunker & Hirst, 2004; Hirst & Kiørboe, 2002; Hirst et al., 2003).”
Fecundity of marine planktonic copepods: global rates and patterns in relation to chlorophyll a, temperature and body weight (2004, methodology): “Increased variability in fecundity and weight-specific growth of broadcasters at low chl a concentrations may also be due to a steep slope in the relationship over a small range, but also to possible prey-switching and the use of non-chl a bearing particles (Hirst & Bunker 2003).”
Growth and development of nauplii and copepodites of the estuarine copepod Acartia tonsa from southern Europe (Ria de Aveiro, Portugal) under saturating food conditions (2006, methodology): “1998), which have recently proved not to be equivalent to the somatic growth of the juveniles (e.g. Koski et al. 1998; Hirst and Bunker 2003).”