The measurement of growth and reproductive rates

By J. Runge, J. Roff. 2000

183 citations recorded by the source corpus.

Subfields: Health, Toxicology and Mutagenesis, Oceanography

View Paper: https://www.semanticscholar.org/paper/c74a2d3d9824b9925296e3e1eb30fc4956268ada

How researchers see this paper

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

In Health, Toxicology and Mutagenesis

1. E. Durbin
2. R. Campbell
3. M. Wagner
4. M. Heath
5. M. Ohman
6. Adrian Bunker
7. A. Hirst
8. B. Niehoff

In Oceanography

1. K. Eiane
2. M. Ohman
3. E. Durbin
4. J. Runge
5. R. Campbell
6. Adrian Bunker
7. A. Hirst
8. T. Nielsen

Citations in the corpus

• CO2-induced acidification affects hatching success in Calanus finmarchicus (2007, methodology): “%) of the eggs produced each day was calculated as the number of nauplii present after 72 h / the number of eggs added at the start of the incubation × 100, because eggs without properly formed membranes may disintegrate quickly (Runge & Roff 2000).”
• On birth and death in the sea (2002, background): “Experimental work has shown that adult females (Runge & Roff, 2000) and C5’s (Runge et al., unpubl.) of C. finmarchicus ingest eggs and nauplii of conspecifics, and do so with clearance rates that are comparable to optimal clearance rates measured on other microzooplankton prey (cf. Ohman & Runge,…”
• The North Atlantic Ocean as habitat for Calanus finmarchicus: Environmental factors and life history traits (2014, background): “Thus, it has been assumed that average egg production rates of freshly caught females are the same during the 24 h following capture as they would have been in situ (Runge and Roff, 2000).”
• Growth and development rates of the copepod Calanus finmarchicus reared in the laboratory (2001, methodology): “In the high food treatments at 4 and 8°C, egg production rates were determined for females collected from the tanks at the end of the experiment following the methods described in Runge & Roff (2000).”
• Fecundity of marine planktonic copepods: global rates and patterns in relation to chlorophyll a, temperature and body weight (2004, background): “…permitted without written consent of the publisher Mar Ecol Prog Ser 279: 161–181, 2004 determines the potential rate of recruitment to a population, and has often been used to assess growth and secondary production in copepods (Runge & Roff 2000; although for problems see Hirst & McKinnon 2001).”
• A comparative study of Calanus finmarchicus mortality patterns at five localities in the North Atlantic (2004, background): “We have suggested elsewhere (Ohman and Hirche, 2001; Ohman et al., 2002) that the most parsimonious explanation for the density-dependent mortality in both regions is cannibalism by late copepodids and adult females of Calanus on their own young (cf. Runge and Roff, 2000; Runge et al., pers. obs.).”
• Interannual variation in phytoplankton blooms and zooplankton productivity and abundance in the Gulf of Maine during Winter (2003, methodology): “Egg production (EP) rates of Calanus finmarchicus followed the procedure described in Runge & Roff (2000).”
• Changes in the structure and function of the North Sea fish foodweb, 1973–2000, and the impacts of fishing and climate (2005, background): “Then, the use of temperature-dependent weightspecific growth rates estimated from empirical relationships (Huntley and Lopez, 1992) to determine production is also debatable (Runge and Roff, 2000).”