scholarly journals Shell growth of sea scallops (Placopecten magellanicus) in the southern and northern Great South Channel, USA

2006 ◽  
Vol 63 (5) ◽  
pp. 811-821 ◽  
Author(s):  
Bradley P. Harris ◽  
Kevin D.E. Stokesbury

Abstract Shell growth of sea scallops in two commercially productive regions of the Great South Channel (GSC) (41°4′N 69°16′W) was studied using tag–recapture experiments. Commercial fishers captured and returned 9.7% of the 11 704 sea scallops tagged in the southern GSC study area, and 7.9% of the 18 274 sea scallops tagged in the northern GSC study area. Scallop density and shell height distribution were sampled with underwater video in the two study areas. In the southern GSC tagged scallops grew faster, reached larger asymptotic size, and had higher growth performance (Φ′) than in the northern GSC study area. Mean sea scallop density in the southern GSC was 0.117 scallops m−2 (s.e. = 0.01), and 2.601 scallops m−2 (s.e. = 0.28) in the northern GSC. Environmental factors, fishing pressure, and sea scallop density all influence shell growth on a fine geographic scale (1–100 km2) and should be considered in area-specific management strategies, such as that currently used in the USA sea scallop fishery.

2016 ◽  
Vol 19 (1) ◽  
pp. 1 ◽  
Author(s):  
Adi Santoso

A study of the growth of the sea scallop, Placopecten magellanicus, under suspended culture conditions was carried out over a seven month period at a culture site in Graves Shoal, Mahone Bay,Nova Scotia – Canada. Scallop spat were cultivated in pearl nets at a density of 30-35 per net set at four locations corresponding to the surface (7 m) and bottom (14 m) at the outer edge and the center of the site. Shell height was measured at monthly intervals. Environmental conditions represented as temperature and food availability at the surface and bottom over the same period were also monitored. Shell Height growth rate was slightly greater at the surface than at the bottom. At the surface sites growth was greater at the outside (SUROUT) than at the center locations, but at the bottom growth was greater at the centre location (BOTIN). The only significant relationship between shell growth and temperature - food variables was chlorophyll a concentration.  Key words: temperature, food availability, shell height, sea scallop


2009 ◽  
Vol 66 (5) ◽  
pp. 751-758 ◽  
Author(s):  
Deborah R. Hart ◽  
Antonie S. Chute

We tracked the growth of large cohorts of sea scallops ( Placopecten magellanicus ) at four sites located in areas closed to scallop fishing and compared the observed growth with that inferred from rings on sea scallop shells collected at the same sites. Stochastic growth transition matrices were constructed for each site based on the shell growth increments, assuming annual ring formation. These matrices were used to predict the annual growth of the scallops, which were compared with direct observations of growth obtained by repeated sampling. Additionally, the observed growth of the scallops was used to estimate the parameters of a stochastic von Bertalanffy model for each site, which were used to estimate the mean annual growth increments as a function of starting shell height. These were compared with the mean growth increments on the shells. There was a close correspondence, in most cases, between the observed growth and the growth inferred from the shell rings, implying that the shell rings were formed annually. The lack of fishing mortality in the areas meant that there was no confounding of size-selective fishing with growth and allowed us to track cohorts longer than would otherwise have been possible.


1987 ◽  
Vol 44 (1) ◽  
pp. 91-98 ◽  
Author(s):  
J. F. Uthe ◽  
C. L. Chou

Over 90% of the total cadmium in the soft tissues of sea scallops (Placopecten magellanicus) was in the digestive gland with less than 1% in the adductor muscle. The amount of cadmium in the digestive gland was significantly related to shell height. Shell height was superior to age as an independent (predictor) variable due to difficulties in ageing scallops. Based on these relationships, scallops of approximately 100 mm shell height were selected to study interregional differences. Neither cadmium concentration nor burden could be used to identify contaminated areas. The ratio of digestive gland cadmium to that in the adductor muscle was lowest for scallops from Chaleur Bay, which had received substantial anthropogenic cadmium input, and for scallops that had been starved for approximately 14 mo. We suggest that the high tissue cadmium levels in scallops from Georges Bank and Browns Bank are not due to contamination from anthropogenic or natural sources but rather reflect feeding and the nutritional inadequacy of the diets. Conversely, the high levels of cadmium input to Chaleur Bay were not reflected in high tissue concentrations or burdens in scallops.


1978 ◽  
Vol 7 (2) ◽  
pp. 111-118
Author(s):  
David A. Storey ◽  
Cleve E. Willis

The Atlantic sea scallop (Placopecten magellanicus) is harvested in the waters off the coast of the northeastern United States and Canada by vessels from both countries. The Atlantic sea scallop fishery has been an important fishery in the Northeastern U.S. in recent decades. This is particularly true for New England where, during the quarter-century ending in 1976, over 10 percent of the value of all fish and shellfish landed was attributable to the harvest of sea scallops.


1997 ◽  
Vol 54 (4) ◽  
pp. 907-913 ◽  
Author(s):  
D J Douglas ◽  
E R Kenchington ◽  
C J Bird ◽  
R Pocklington ◽  
B Bradford ◽  
...  

Sea scallops (Placopecten magellanicus) were fed Pseudo-nitzschia multiseries (formerly P. pungens f. multiseries, Nitzschia pungens f. multiseries) cells of high domoic acid (DA) content (4.0-6.7 pg DA cdot cell-1) for 22 days, followed by 14 days of feeding with nontoxic microalgae. DA was incorporated within 24 h by the scallops, with increased uptake after 6 days, and was concentrated in tissues in the following order: digestive gland >> remaining soft tissue >> adductor muscle. A maximum DA concentration of 3108 mu g cdot g-1 was recorded in the digestive gland, approximately 150 times the regulatory limit (20 mu g DA cdot g-1) and among the highest levels observed in bivalve molluscs; however, only trace amounts, 0.7-1.5 mu g cdot g-1, were found concomitantly in the adductor muscle. At the end of the exposure period, 50.9% of the DA that had been supplied to the scallops had been incorporated into the tissues. Concentrations in the digestive gland 14 days after termination of the toxic diet remained high, 752 mu g DA cdot g-1. Throughout the experiment, there was no sign of illness or mortality attributable to high DA loading, although the destructive sampling of animals did not allow us to assess the effects of the toxin in the longer term.


2004 ◽  
Vol 61 (8) ◽  
pp. 1338-1354 ◽  
Author(s):  
Stephen J Smith ◽  
Paul Rago

In this paper, we concentrate on spatial aspects of growth and reproduction for sea scallops (Placopecten magellanicus) to advance the general theory for development of reference points for sessile animals and to illustrate the general points with several specific examples. Nonlinear mixed effects models can be used to define the spatial distribution of growth rates and their implications for the definition of growth overfishing. We develop a basin model to illustrate that the typical "boom and bust" effects, often attributed to environmental factors, are explained equally well by spatial variations in habitat quality, spatial concentration of fisheries, and dispersal of larvae among areas. Results suggest that incentives to concentrate fishing effort in lower productivity areas may be an effective tool for reducing recruitment variation and improving yields. Reductions in fishing mortality might be possible with closed areas as they can be used to reduce the concentration of effort on high scallop densities. Further, rotational area management strategies can offer the promise of balancing demands for increased yield, prevention of recruitment overfishing, maintaining spawning reserves, and reducing habitat damage and bycatch.


1993 ◽  
Vol 71 (5) ◽  
pp. 953-959 ◽  
Author(s):  
Jonathan Grant ◽  
Craig W. Emerson ◽  
Sandra E. Shumway

Passive transport and orientation of sea scallops (Placopecten magellanicus; 27–120 mm shell height) were studied in a laboratory flume to assess flow-mediated control of movement and position on the seabed. Additional experiments were conducted to characterize patterns of sediment transport around the scallop shell in relation to recesses occupied by scallops. The critical shear velocity of scallop transport was not correlated with shell height or other size measures, and most scallops were transported with the ventral shell margin facing downstream. Frontal exposure of scallops to the flow as indicated by fineness (shell height/shell depth) was greater in larger scallops, but when pallial gape was included in fineness (shell height/shell depth + gape)), frontal exposure was not correlated with scallop size. This suggests that variation in the drag component of transport was responsible for the lack of correlation between shell morphometry and critical shear velocity. Sediment transport created a horseshoe-shaped trough around the shell and several smaller erosion–deposition features downstream. The dimensions of sediment transport features were dependent on shell allometry, and it is likely that sediment transport contributes to the formation of scallop recesses typically observed in scallop beds. These results indicate that passive transport of sea scallops has a behavioural component related to gape that is independent of shell size. In contrast, scallop orientation and recessing may be explained by physical processes rather than simply by behaviour. Studies of bivalve hydrodynamics require consideration of living animals in addition to shell specimens and must include conditions of benthic boundary layer flow and sediment transport.


1994 ◽  
Vol 51 (2) ◽  
pp. 348-356 ◽  
Author(s):  
E. L. Kenchington ◽  
W. E. Full

Sea scallops (Placopecten magellanicus) were sampled from each of four scallop beds: the northeast peak of Georges Bank, Western Bank, St. Pierre Bank, and the Bay of Fundy near Digby, N.S. The outlines of scallop top shells were captured by video imagery using a semiautomated approach. Fourier shape descriptors were calculated and analyzed. Age and year-class effects were shown to be important factors influencing scallop shell shape. Allometric effects on Fourier harmonics also have a significant influence on shell shape in this species. Comparisons of Fourier harmonics between scallop beds separated by age and sampling year, and corrected for allometry, revealed significant differences in the majority of harmonic numbers. Post hoc analyses identified St. Pierre Bank and the Bay of Fundy as being significantly different from the other beds in a suite of separate analyses.


2019 ◽  
Vol 76 (6) ◽  
pp. 847-855 ◽  
Author(s):  
Timothy J. Miller ◽  
Deborah R. Hart ◽  
Karen Hopkins ◽  
Norman H. Vine ◽  
Richard Taylor ◽  
...  

The efficiency of survey gear is an important measure that can be used to estimate the absolute scale of populations in assessment models. We develop a general hierarchical model for estimating the efficiency of a New Bedford-style sea scallop (Placopecten magellanicus) survey dredge from paired dredge and Habcam camera system tows. Habcam data for each tow consist of multiple images that give information on within-tow variability of scallop density. The model accounts for these multiple observations as well as the possibility of differences between the true densities in dredge and Habcam pairs due to the pairs not covering exactly the same ground. We fit several models with alternative assumptions to observations on Atlantic sea scallops and compare the relative performance using Akaike’s information criterion. The best performing model estimated higher dredge efficiency on fine substrates than on coarse ones (approximately 0.40 and 0.27, respectively). Our results inform the scale of annual abundance estimates from dredge surveys and reduce uncertainty in the sea scallop stock assessments.


Sign in / Sign up

Export Citation Format

Share Document