Mortality of marine planktonic copepods: global rates and patterns
By A. Hirst, T. Kiørboe. 2002
340 citations recorded by the source corpus.
Subfields: Global and Planetary Change, Oceanography
View Paper: https://www.semanticscholar.org/paper/297867956c4fbac68fc29fd6c6e8cb1e303b4fc4
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In Global and Planetary Change
In Oceanography
Citations in the corpus
- Temperature, Growth Rate, and Body Size in Ectotherms: Fitting Pieces of a Life-History Puzzle1 (2004, neutral): “4) and copepods (Hirst and Kiørboe, 2002).”
- Production, mortality, and infectivity of planktonic larval sea lice, Lepeophtheirus salmonis (Krøyer, 1837): current knowledge and implications for epidemiological modelling (2018, background): “Global approximations of the partitioning of wider zooplankton mortality suggest that predation accounts for 67–75% of total mortality in the plankton (Hirst and Kiørboe, 2002).”
- Bridging the gap between marine biogeochemical and fisheries sciences; configuring the zooplankton link (2014, background): “Predation, which includes cannibalism of copepod eggs and nauplii by older copepodites (Ohman and Hirche, 2001; Hirst and Kiørboe, 2002; Ohman et al., 2008; Neuheimer et al., 2009), typically dominates mortality losses (e.g., Hirst et al., 2010; ICES WKMOR Report, 2010), with estimated rates not…”
- Stage-specific mortality of Calanus finmarchicus, Pseudocalanus elongatus and Oithona similis on Fladen Ground, North Sea, during a spring bloom (2004, background): “6), and not negatively, as predicted from allometric arguments (Hirst & Kiørboe 2002).”
- 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”
- Clearance rates of jellyfish and their potential predation impact on zooplankton and fish larvae in a neritic ecosystem (Limfjorden, Denmark) (2005, background): “This constitutes a relatively large fraction of total copepod mortality rate, which typically is approximately 0.1 d–1 at those temperatures (Hirst & Kiørboe 2002).”
- Ocean-scale modelling of the distribution, abundance, and seasonal dynamics of the copepod Calanus finmarchicus (2006, background): “More recently, Hirst & Kiørboe (2002) used the balanced mortality hypothesis to estimate average mortality rates for a wide range of marine copepod species and found a significant positive association between temperature and mortality.”
- Motility patterns and mate encounter rates in planktonic copepods (2005, background): “Given adult longevities on the order of 10 d in 1 mm-sized copepods (Hirst and Kiørboe 2002), this implies a potential for many mating events in the lifetime of an adult female.”
- Climate control on the long‐term anomalous changes of zooplankton communities in the Northwestern Mediterranean (2007, background): “Temperature further increases food limitation that impairs growth and enhances mortality of adult stages of copepods (Hirst & Kiorboe, 2002).”
- Non-consumptive mortality in copepods: occurrence of Calanus spp. carcasses in the Arctic Ocean during winter (2014, background): “Hirst and Kiorboe (Hirst and Kiorboe, 2002) estimated that a quarter to a third of the total mortality of marine planktonic copepods may be due to non-predatory mortality.”
- Occurrence of copepod carcasses in the lower Chesapeake Bay and their decomposition by ambient microbes (2006, background): “The so estimated mortality rate is 0.12 d 1, within the reported mortality rate for broadcast-spawning copepods (Hirst and Kiørboe, 2002).”
- Fecundity of marine planktonic copepods: global rates and patterns in relation to chlorophyll a, temperature and body weight (2004, background): “6 of Hirst & Kiørboe 2002) and total egg to adult development times and sex ratios (Hirst & Kiørboe 2002).”