Small-scale spatial and temporal patterns in spawning of Atlantic cod (Gadus morhua) in coastal Newfoundland waters

2000 ◽  
Vol 57 (5) ◽  
pp. 1011-1024 ◽  
Author(s):  
Gareth L Lawson ◽  
George A Rose

Acoustic surveys were used to locate coastal Atlantic cod (Gadus morhua) spawning grounds and examine spatial and temporal patterns of spawning in Placentia Bay, Newfoundland, Canada. The same three grounds were used in 1997 and 1998 (Bar Haven in the inner bay and Cape St. Mary's and Oderin Bank in the outer bay). Grounds had densities >0.1 fish·m-2 over scales of 100 m and >13% of mature females in spawning condition. Ground use and spawning timing differed between years. Mean spawning female densities were highest at Cape St. Mary's in 1997 (1.6 × 10-2 fish·m-2) and Oderin Bank in 1998 (1.0 × 10-2 fish·m-2). At all grounds, spawning peaked earlier in 1997 (April) than in 1998 (June-July). In both years, cod spawned at sub- or near-zero temperatures. "Spawning columns" were observed at sites and times having high densities of spawning females. Sex ratios suggested that males arrived first and stayed later, while females followed when ready to spawn, accompanied by juveniles. Older females spawned earlier and later than younger females. Peaks in density of spawning females and the proportion of females spawning did not coincide. Hence, the location and timing of spawning cannot be quantified solely from the proportions of females in spawning condition.

2003 ◽  
Vol 60 (9) ◽  
pp. 1111-1121 ◽  
Author(s):  
Tara M McIntyre ◽  
Jeffrey A Hutchings

Life histories of Atlantic cod (Gadus morhua) from the Gulf of St. Lawrence south to Georges Bank differ significantly through time and space. Within the Southern Gulf, fecundity per unit body mass differed by more than 40% over short (2 years) and long (42–45 years) periods of time. Significant variation in size-specific fecundity is also evident among populations: Southern Gulf cod produce almost 30% more eggs per unit body mass than those on Georges Bank, whereas fecundity of Scotian Shelf cod is almost half that of cod in Sydney Bight. Compared with those on Georges Bank, Southern Gulf cod life histories are characterized by high fecundity, late maturity, high gonadosomatic index, and large eggs. Relative to the influence of body size, neither temporal nor spatial differences in fecundity can be attributed to physiological condition, as reflected by liver weight, hepatosomatic index, and Fulton's K. Delayed maturity and higher reproductive allotment among Southern Gulf cod can be explained as selection responses to slower growth, higher prereproductive mortality, and fewer lifetime reproductive events. Patterns of covariation in heritable, fitness-related traits suggest the existence of adaptive variation and evolutionarily significant units at spatial scales considerably smaller than the species range in the Northwest Atlantic.


1998 ◽  
Vol 49 (3) ◽  
pp. 241 ◽  
Author(s):  
A. J. Underwood ◽  
M. G. Chapman

Data were collected in New South Wales from replicate sites on five wave-exposed shores separated by hundreds of kilometres at three-monthly intervals for four years, to examine large and small spatial and temporal patterns in low-shore algal assemblages. These data were used to test hypotheses from the models that algal assemblages show large-scale, predictable changes in structure or, alternatively, that variation from time to time is small-scale and differs from shore to shore or site to site on a shore. There was considerable variation at all scales examined — among replicate quadrats within sites, between sites on a shore and among shores. Similarly, assemblages differed from one sampling period to the next and changes in the assemblages over time periods of three months were as great as from year to year. These changes were interactive, with no two sites or shores showing similar temporal patterns. Thus, understanding diversity along a coast-line requires detailed understanding of local processes. Without adequate spatial and temporal replication in sampling designs and without explanatory models, the large and complex variability in intertidal assemblages at different scales cannot be documented and understood.


2018 ◽  
Vol 75 (12) ◽  
pp. 2302-2312 ◽  
Author(s):  
Victoria Neville ◽  
George Rose ◽  
Sherrylynn Rowe ◽  
Robyn Jamieson ◽  
Glenn Piercey

Stable oxygen isotope assays of otoliths (δ18Ooto) from migrant Atlantic cod (Gadus morhua Linnaeus, 1758) that overwintered in Smith Sound, Newfoundland, during 1995–2006 differed from those of nonmigrating summer residents and cod from Placentia Bay and Halibut Channel but did not differ from those of cod from the adjacent offshore Bonavista Corridor in summer. All fish sampled were of the 1990 year class (founder of the Smith Sound aggregation) at ages 8–10 years. Hence, overwintering Smith Sound and summering Bonavista Corridor cod likely experienced similar temperatures and salinities in each year of life, representing different migration stages of an intermixed group. Moreover, predictions of δ18Ooto from near-bottom ocean temperatures and salinities differed between inshore and offshore sites and, in general, matched observed signatures of inshore and offshore cod. The Bonavista Corridor cod, however, were an exception, having δ18Ooto signatures suggestive of inshore exposure. Our findings provide direct evidence of metapopulation structure in the Northern cod and are consistent with offshore rebuilding having been spurred by dispersal of cod from inshore Smith Sound.


Author(s):  
Fei Liu ◽  
Pengcheng Lin ◽  
Huanzhang Liu ◽  
Jun Wang

The spatial-temporal patterns of fish assemblages in lotic systems can provide useful information in developing effective conservation measures. This study aimed to explore the spatiotemporal changes in fish assemblage and their association with environmental factors in mountain streams of Ren River, southwest China. Filed investigations were conducted at 18 sites during rainy and dry season in 2017. A total of 21 species, belonged to 3 orders, 8 families and 19 genera, were collected. Analysis of similarities (ANOSIM) showed fish assemblages structure varied significantly at the spatial scale, but not at the temporal scale. In low order sites, fish assemblages were mainly dominated by cold water and rheophilic species (e.g. Rhynchocypris oxycephalus, Scaphesthes macrolepis, Metahomaloptera omeiensis and Gnathopogon herzensteini), while those in high order sites were predominated by warm water and eurytopicity or stagnophilic species (e.g. Squalidus argentatus, Hemiculter leucisculus and Zacco platypus). Canonical correspondence analysis (CCA) showed fish assemblages were structured by a combination of large-scale landscape factors (e.g. altitude and C-link) and small-scale habitat features (e.g. channel width, water temperature and depth). Among these factors, landscape factors had the greatest influence on fish assemblage, while local habitat measures played less important roles or just acted in certain season.


2015 ◽  
Vol 72 (2) ◽  
pp. 252-261 ◽  
Author(s):  
Keno Ferter ◽  
Klaas Hartmann ◽  
Alf Ring Kleiven ◽  
Even Moland ◽  
Esben Moland Olsen

Studying the sublethal effects of catch-and-release (C&R) is challenging, as there are several potential sources of bias. For example, if behavioural alterations immediately after the release event are to be studied, separation of tagging effects from actual C&R effects is required, which is a challenge in the wild, particularly in marine environments. To investigate the effects of C&R on Atlantic cod (Gadus morhua) in their natural environment, 80 cod were caught in fyke nets, fitted with acoustic transmitters, and released. After recovery from tagging and handling for at least 14 days, nine individuals were recaptured and released at least once during experimental angling, following best release practice. All cod survived the C&R event and did not show any large-scale behavioural changes (i.e., changes in diel vertical migrations). However, analysis of small-scale vertical movements showed that three individuals underwent short-term alterations (e.g., reduced or increased swimming activity). This study showed that pretagging fish with acoustic transmitters before experimental angling is an option when investigating fish behaviour immediately after the release event in marine environments. Moreover, release guidelines for cod should be developed, as cod can recover quickly if caught in shallow waters (<20 m) and properly handled and released.


1998 ◽  
Vol 55 (6) ◽  
pp. 1430-1442 ◽  
Author(s):  
David A Methven ◽  
David C Schneider

Habitat and size of juvenile Atlantic cod (Gadus morhua) change substantially during the first 3 years after settlement, and hence, cohort size cannot be followed using a single gear. We investigated whether catch could be calibrated across gear types by deploying pairs of gears repeatedly in the same habitat. As expected, size selectivity differed substantially among gears. Trawls and seines generally collected individuals <200 mm. Gillnets and jiggers collected individuals >150 mm. Size modes, corresponding to age-classes, were common to catches of most gears. Highest catches were taken by trawls and seines. Gillnet catches were orders of magnitude lower. Standardized catches could not be calibrated across pairs of gears deployed in the same habitat at approximately the same time. However, it was possible to identify spatial depth gradients and diel changes in catch that were independent of gear. Consistent spatial and temporal patterns across gears were interpreted as characteristic of fish populations, not just of gears. Density in coastal habitats was higher at night and was higher at 4-7 m than at greater depths. These results, in conjunction with other studies, establish that coastal depths of 4-7 m represent the centre, and not the edge, of the distribution of age 0 cod in Newfoundland during autumn. Hence nursery areas during the early 1990s, a time of historically low spawning stock biomass, must be identified as the coastal zone, not offshore.


2015 ◽  
Vol 73 (2) ◽  
pp. 304-315 ◽  
Author(s):  
José M. González-Irusta ◽  
Peter J. Wright

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