Growth and development rates of the copepod Calanus finmarchicus reared in the laboratory

By R. Campbell, M. Wagner, G. Teegarden, C. -. Boudreau, E. Durbin. 2001

351 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/fabc904de3830adeef2423bad4bb7052fbbff6fe

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Global and Planetary Change

1. K. Eiane
2. M. Ohman
3. J. Runge
4. E. Durbin
5. Aditee Mitra
6. Malin Daase
7. B. Niehoff
8. C. Johnson

In Oceanography

1. K. Eiane
2. M. Ohman
3. Aditee Mitra
4. E. Durbin
5. Malin Daase
6. J. Runge
7. A. Calbet
8. R. Campbell

Citations in the corpus

• Life history and biogeography of Calanus copepods in the Arctic Ocean: An individual-based modeling study (2012, methodology): “The development duration (D) becomes D ¼ aðT þ aÞb=½1 expðF=KÞ ; ð3Þ where F is food concentration (unit: lg chl l 1), and K was a constant associated with the intensity of food limitation (0.8 lg chl l 1 in this model, derived from Campbell et al., 2001).”
• Inhibition of population growth in the copepods Acartia clausi and Calanus helgolandicus during diatom blooms (2003, background): “…production has rarely been measured in the ocean, and there is still much concern as to what methods to adopt for its measurement (Hirst & McKinnon 2001), especially for lipid-storing copepods such as Calanus species, in which growth is not equivalent for all stages (Campbell et al. 2001).”
• A comparative study of Calanus finmarchicus mortality patterns at five localities in the North Atlantic (2004, methodology): “Comparison of development times predicted from Belehrádek functions (Campbell et al., 2001a) with measurements made for C. finmarchicus during the FLEX experiments (Williams and Lindley, 1980b) reveals that Calanus was developing through each copepodid stage at rates corresponding to…”
• Stage-specific mortality of Calanus finmarchicus, Pseudocalanus elongatus and Oithona similis on Fladen Ground, North Sea, during a spring bloom (2004, methodology): “…effect of food-restricted developmental rates or other physiological effects that prolong development during specific time periods, we analyzed the sensitivity of the estimated mortality rates to increases in stage duration of 50 to 100% as reported for C. finmarchicus by Campbell et al. (2001).”
• Stage‐specific mortality of Calanus spp. under different predation regimes (2002, methodology): “To estimate developmental duration for Calanus spp., we applied the a parameters derived for C. finmarchicus (Campbell et al. 2001) and forced the equation with the observed vertical temperature fields.”
• Ocean-scale modelling of the distribution, abundance, and seasonal dynamics of the copepod Calanus finmarchicus (2006, background): “The development time depends strongly on water temperature and to a lesser degree phytoplankton abundance (Campbell et al. 2001).”
• Characteristics of Calanus finmarchicus dormancy patterns in the Northwest Atlantic (2008, methodology): “…separately determined for each stage, P the concentration of prey (mg Chl a l21) at the vertical location of each copepod, and Vi and mi are coefficients that affect the development rate as a function of food concentration, derived empirically from laboratory studies (Campbell et al., 2001).”
• Climate change in the southeastern Bering Sea: impacts on pollock stocks and implications for the oscillating control hypothesis (2011, background): “Calanoids which store lipids have longer stage duration in the copepodid stages (Campbell et al., 2001).”
• On birth and death in the sea (2002, methodology): “This appears to be a reasonable assumption until the late copepodid stages, as most stage pairs last a relatively short time (3–10 days until C4/C5, at which point it extends to about 18 days at 8 ◦ C [ Campbell et al., 2001a ]).”
• Differential gene expression in diapausing and active Calanus finmarchicus (Copepoda) (2008, background): “…in different envi- 202 1 2 3 4 5 Principal component ELOV FABP RDH Ferritin EcR 20.8 82.7 9.3 92.0 5.6 97.6 2.4% 100.0% Variance explained: 62.0 Cumulative variance explained: 62.0 a Tarrant et al.: Differential gene expression in Calanus finmarchicus ronmental conditions (Campbell et al. 2001).”
• How do organisms change size with changing temperature? The importance of reproductive method and ontogenetic timing (2011, background): “2006), and Calanus finmarchicus (Campbell et al. 2001), and included”
• Dynamics of coexisting Calanus finmarchicus, Calanus glacialis and Calanus hyperboreus populations in a high-Arctic fjord (2005, methodology): “Adult males were determined to species by the procedure specified by Campbell et al. (2001).”
• Climate-induced variability in Calanus marshallae populations (2003, methodology): “Effects of food limitation on C. finmarchicus on Georges Bank were most severe during late naupliar (N4–N5) and early copepodite (C2–C4) stages (Campbell et al., 2001a).”
• Mesozooplankton distribution in northern Svalbard waters in relation to hydrography (2007, background): “As temperature scales with most growth processes (Vidal 1980; Campbell et al. 2001), and as temperature scaling coeYcients were positive in most (5 of 6) cases we suggest this reXect positive temperature eVects on production, growth or development in surface waters where biological production…”
• Interannual variation in phytoplankton blooms and zooplankton productivity and abundance in the Gulf of Maine during Winter (2003, positive): “Based on studies in other regions and in the laboratory (Campbell et al. 2001a,b) we would expect growth and reproduction of C. finmarchicus to be limited by the low food concentrations normally present at this time prior to the spring bloom.”