Density Dependent Growth and Size Specific Competitive Interactions in Young Fish

Oikos ◽  
1999 ◽  
Vol 86 (2) ◽  
pp. 217 ◽  
Author(s):  
Par Bystrom ◽  
Emili Garcia-Berthou
Oecologia ◽  
2010 ◽  
Vol 165 (4) ◽  
pp. 959-969 ◽  
Author(s):  
Sigurd Einum ◽  
Grethe Robertsen ◽  
Keith H. Nislow ◽  
Simon McKelvey ◽  
John D. Armstrong

Nature ◽  
1974 ◽  
Vol 250 (5469) ◽  
pp. 739-741 ◽  
Author(s):  
IIH-NAN CHOU ◽  
PAUL H. BLACK ◽  
RICHARD O. ROBLIN

2002 ◽  
Vol 59 (1) ◽  
pp. 57-65 ◽  
Author(s):  
Geir Ottersen ◽  
Kristin Helle ◽  
Bjarte Bogstad

For the large Arcto-Norwegian stock of cod (Gadus morhua L.) in the Barents Sea, year-to-year variability in growth is well documented. Here three hypotheses for the observed inverse relation between abundance and the mean length-at-age of juveniles (ages 1–4) are suggested and evaluated. Based on comprehensive data, we conclude that year-to-year differences in length-at-age are mainly determined by density-independent mechanisms during the pelagic first half year of the fishes' life. Enhanced inflow from the southwest leads to an abundant cohort at the 0-group stage being distributed farther east into colder water masses, causing lower postsettlement growth rates. We can not reject density-dependent growth effects related to variability in food rations, but our data do not suggest this to be the main mechanism. Another hypothesis suggests that lower growth rates during periods of high abundance are a result of density-dependent mechanisms causing the geographic range of juveniles to extend eastwards into colder water masses. This is rejected mainly because year-to-year differences in mean length are established by age 2, which is too early for movements over large distances.


1979 ◽  
Vol 34 (3-4) ◽  
pp. 279-283 ◽  
Author(s):  
Jürgen van der Bosch ◽  
Ilse Sommer ◽  
Heinz Maier ◽  
Willy Rahmig

Abstract Lowered extracellular [Ca2+] causes low growth rates and low stationary cell densities in 3T3 cell cultures as compared to physiological [Ca2+]. Under otherwise constant conditions the extra­ cellular [Ca2+] determines a stable stationary cell density, which can be readied by increase of net cell number or decrease of net cell number, depending on cell density at the time of [Ca2+] adjustment. SV40-3T3 cells do not show this [Ca2+] dependency. At 39 °C 3T3 and SV40-3T3 cell populations show an increased growth rate at low cell densities as compared to cell populations at 35 °C. Approaching the stationary density the growth rate of both cell sorts is reduced faster at 39 °C than at 35 °C, leading to lower stationary cell densities at 39 °C than at 35 °C. A temperature change from 39 °C to 35 °C or in the opposite direction can affect the stationary cell density of 3T3 cell populations only if applied before reduction of growth rate by density-dependent growth-inhibiting principles has taken place.


1987 ◽  
Vol 44 (1) ◽  
pp. 48-53 ◽  
Author(s):  
Randall M. Peterman ◽  
Michael J. Bradford

We tested whether English sole (Parophrys vetulus) in Oregon and Washington waters show density-dependent growth. We found that there is a significant negative effect of cohort abundance on annual growth rate of age 1 fish, but not on growth of ages 2–7. Unlike most similar studies of density dependence, this result was not confounded by time trends in abundance and growth. The multiple regression of age 1 growth on cohort abundance and temperature accounted for 91% of the interannual variation in growth, which was a significant increase in r2 over that of the previously published relation with temperature alone. However, stock assessments which take into account only the previously published temperature effect on growth for this stock will probably not seriously overestimate the impact of management regulations which increase cohort abundance.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Takashi Nakajima ◽  
Xiaolong Wang ◽  
Souvik Chatterjee ◽  
Tetsuo Sakka

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