scholarly journals Negative correleations between larval and juvenile growth rates in winter flounder: implications of compensatory growth for variation in size-at-age

1993 ◽  
Vol 96 ◽  
pp. 209-215 ◽  
Author(s):  
DR Bertram ◽  
RO Chambers ◽  
WC Leggett
1971 ◽  
Vol 28 (8) ◽  
pp. 1153-1165 ◽  
Author(s):  
V. S. Kennedy ◽  
D. H. Steele

Monthly samples of winter flounder taken in Long Pond from November 1962 to October 1963 indicated that the flounder moved into deeper water (7–10 m) during the summer and returned to shallow water (1–2 m) from September to June. These movements corresponded to the end of the spawning season and the ripening of the gonads respectively. Spawning occurred from March until early June, most of it in May and early June. Most males were mature at age 6 and most females at age 7. Fifty percent of the males and females were mature at 21 and 25 cm respectively. The growth rates of the males and females were similar until the age of 8, after which the females apparently outgrew the males. Early growth and fecundity were similar to those reported for other areas. No feeding took place in December or January but the flounder fed in March and continued to feed throughout the summer; food intake decreased in the fall. They were omnivorous and the type of food eaten varied with the locality. Polychaetes, plant material, and molluscs were the most common food items throughout the year. Capelin eggs and fish remains were found only during a few months of the year but were eaten in great quantities.


PeerJ ◽  
2015 ◽  
Vol 3 ◽  
pp. e1392
Author(s):  
Juan C. Levesque

Ladyfish (Elopssp) are a common and economically valuable coastal nearshore species found along coastal beaches, bays, and estuaries of the southeastern United States, and subtropical and tropical regions worldwide. Previously, ladyfish were a substantial bycatch in Florida’s commercial fisheries, but changes in regulations significantly reduced commercial landings. Today, ladyfish are still taken in commercial fisheries in Florida, but many are also taken by recreational anglers. Life-history information and research interest in ladyfish is almost non-existent, especially information on age and growth. Thus, the overarching purpose of this study was to expand our understanding of ladyfish age and growth characteristics. The specific objectives were to describe, for the first time, age, growth, and recruitment patterns of juvenile ladyfish from the east coast of Florida (USA). In the Indian River Lagoon (IRL), annual monthly length-frequency distributions were confounded because a few small individuals recruited throughout the year; monthly length-frequency data generally demonstrated a cyclical pattern. The smallest were collected in September and the largest in May. Post-hoc analysis showed no significant difference in length between August and May, or among the other months. In Volusia County (VC), annual monthly length-frequency distribution demonstrated growth generally occurred from late-winter and spring to summer. The smallest ladyfish were collected in February and the largest in August. On average, the absolute growth rate in the IRL was 36.3 mm in 60 days or 0.605 mm day−1. Cohort-specific daily growth rates, elevations, and coincidentals were similar among sampling years. Cohort-specific growth rates ranged from 1.807 in 1993 to 1.811 mm day−1in 1994. Overall, growth was best (i.e., goodness of fit) described by exponential regression. On average, the absolute growth rate in VC was 28 mm in 150 days or 0.1866 mm day−1. Cohort-specific daily growth rates were significantly different among sampling years; however, the elevations and coincidentals were similar. Cohort-specific growth rates ranged from 1.741 in 1994 to 1.933 mm day−1in 1993. Mean ladyfish growth was best described by linear regression; however, natural growth was explained better by exponential regression. In the IRL, the corrected exponential growth equation yielded a size-at-age 1 of 156.0 mm SL, which corresponded to an estimated growth rate of 0.4356 mm day−1. In VC, the corrected exponential growth equation yielded a size-at-age 1 of 80 mm SL corresponding to an estimated growth rate of 0.2361 mm day−1.


2021 ◽  
Vol 74 ◽  
pp. 106526
Author(s):  
A.A. Miszura ◽  
M.V.C. Ferraz ◽  
R.C. Cardoso ◽  
D.M. Polizel ◽  
G.B. Oliveira ◽  
...  

1981 ◽  
Vol 59 (9) ◽  
pp. 1790-1795 ◽  
Author(s):  
Norman W. S. Quinn ◽  
Daniel M. Keppie

The influences of date of hatch, and age and prelaying body weight of brood female on the growth rate of juvenile spruce grouse (Canachites canadensis) were studied in central New Brunswick in 1977 and 1978. Because of differential timing of hatch of broods of adult and yearling females, it was not clear whether a difference in juvenile growth rates during 5–14 days of age in 1977 was related to date of hatch, age of brood female, or both. Differences in juvenile growth rates within and between years apparently were not influenced by body weight of brood females prior to egg laying. Results suggest that posthatch factors are more important in determining growth rate than a prehatch or "maternal" influence.


2008 ◽  
Vol 48 (7) ◽  
pp. 966 ◽  
Author(s):  
S. Hatcher ◽  
J. Eppleston ◽  
R. P. Graham ◽  
J. McDonald ◽  
S. Schlunke ◽  
...  

Two monitoring projects were conducted to investigate weaner mortality in commercial Merino flocks in the Yass and the Central Tablelands Rural Lands Protection Boards located in the Southern Tablelands agricultural region of New South Wales. The projects were conducted in Yass in 2005 and in the Central Tablelands in 2006. A random sample of weaners from four flocks in the Yass board and 11 flocks in the Central Tablelands board were regularly weighed, growth rates were calculated after weaning and survival was determined by the continuing presence of an individual weaner at subsequent weighing activities. Weaning weight was the most important factor in determining postweaning liveweight, growth rates and survival with the significant impact of weaning weight on liveweight persisting for up to 6 months after weaning. Despite the lightest weaners being capable of considerable compensatory growth given sufficient postweaning nutrition, the lightest 25% of weaners were more than twice as likely to die as heavier weaners. A focus on ewe nutrition and parasite control during late pregnancy and lactation will allow Merino producers to achieve higher weaning weights that will set their weaners up for strong postweaning growth with a decreased likelihood of mortality.


2010 ◽  
Vol 67 (6) ◽  
pp. 1119-1127 ◽  
Author(s):  
Ángel F. González ◽  
Jaime Otero ◽  
Graham J. Pierce ◽  
Ángel Guerra

Abstract González, Á. F., Otero, J., Pierce, G. J., and Guerra, Á. 2010. Age, growth, and mortality of Loligo vulgaris wild paralarvae: implications for understanding of the life cycle and longevity. – ICES Journal of Marine Science, 67: 1119–1127. Age, growth, and mortality were estimated for the first time in wild paralarvae of the common squid, Loligo vulgaris, by examining growth increments in the statoliths of 273 animals collected off the Ría de Vigo (NW Spain, NE Atlantic). Hatching was all year round for the period 2003–2005, with a peak during late spring and a secondary peak during early autumn. Paralarvae varied from 1260 to 7580 µm, and their abundance decreased abruptly as they grew. Statolith increments were clearly visible without grinding in almost all material, allowing reliable estimation of age. Paralarvae are planktonic for at least 3 months. Growth in dorsal mantle length (DML) during that period fitted an exponential equation. The instantaneous relative growth rates were 2.11, 2.15, and 1.82% DML d−1 for 2003, 2004, and 2005, respectively, and there were no significant differences in size-at-age between the 3 years. Taking into account the growth rates estimated for the whole cycle of L. vulgaris, we suggest that the lifespan may previously have been underestimated by 3 months, because the proximity of the rings deposited during paralarval and early juvenile stages would prevent accuracy in enumerating the number of growth increments in later stages. The estimated instantaneous rate of total mortality during the first 90 d of a paralarva life was 9.6, 5.3, and 4.8% d−1 for 2003, 2004, and 2005, respectively. Eye diameter was a reliable and rapid way of estimating DML and age.


2012 ◽  
Vol 63 (12) ◽  
pp. 1231 ◽  
Author(s):  
Carina J. Sim-Smith ◽  
Andrew G. Jeffs ◽  
Craig A. Radford

For many fish species, growth and mortality of larvae are closely coupled, with faster-growing larvae generally experiencing higher survivorship in the plankton, which may lead to higher recruitment. Using back-calculated growth trajectories derived from otolith increments we used the modified Fry model to estimate the growth rate of larvae and early juveniles of the commercially important sparid, Chrysophrys auratus, at four sites around northern New Zealand. Back-calculated growth rates were used to test the hypothesis that fish with a short pelagic larval duration (≤20 days) grew faster than did fish with a long pelagic larval duration (>24 days) during both the larval and juvenile periods. At three of the four sites, fish with a short larval duration grew significantly faster during the larval period, and these larvae generally continued to have a larger size-at-age as juveniles up to 70-day-old. Growth rates for both the larval and early juvenile period were also found to vary significantly among the four sites and were found to be unrelated to differences in water temperature. Localised variation in early growth of C. auratus among sites may be important in helping explain differences in their contribution to the recruitment to C. auratus populations.


1996 ◽  
Vol 125 (1) ◽  
pp. 119-127 ◽  
Author(s):  
J. A. Pechenik ◽  
T. J. Hilbish ◽  
L. S. Eyster ◽  
D. Marshall

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