Dynamics and Exploitation of Lake Whitefish in Southern Georgian Bay

1966 ◽  
Vol 23 (2) ◽  
pp. 221-274 ◽  
Author(s):  
Daniel Cucin ◽  
Henry A. Regier

Instability of the population of Coregonus clupeaformis (Mitchill) in southern Georgian Bay from 1948 to 1964 was evidently partly due to intensive fishing.The population was discrete at least from 1956 to 1964 as determined by extensive tagging. From 1948 to 1964, estimated effective fishing effort varied 10-fold and annual yields almost 20-fold, with two cycles of abundance and scarcity. Strength of 1951–59 year-classes, defined as population size at age III, varied 40-fold. In spite of the marked instability, the population was in recent years more stable than any other whitefish population in Georgian Bay or Lake Huron.Almost all the commercial catch was made with gill nets of [Formula: see text] mesh. In 1957, fishing depended largely on age VII–IX fish; by 1964, on those of age V and VI. Apparent growth rate increased during this period: in 1957 age XII fish weighed 3.4 lb; in 1964 age VI weighed 3.7 lb. From 1959 to 1964, reproduction depended largely on males age IV+ and older and longer than 17 inches, and on females age V+ and older and longer than 18 inches.Natural mortality coefficients (exponential model) averaged 0.41 for fish of the 1948–58 year-classes beyond age III. Gillnetting was largely restricted to 2 months in late spring and two in fall. In each fishing season these gill nets took about 40% of the survivors of a year-class after it became fully vulnerable, at ages V, VI, and VII during the early 1960s.Combining growth and natural mortality rates in a biomass curve indicated that individual year-classes would provide highest yields when fished intensively at age IV, or slightly earlier than they were fished in the early 1960s. Yet the only hypothesis that might explain the continued existence of a fishable population was that relatively large parts of the habitat were either legally closed or unsuitable for fishing. Evidently the fishing was intense and increasing the effort would mean risk of a population collapse.

1995 ◽  
Vol 52 (5) ◽  
pp. 1018-1029 ◽  
Author(s):  
Robert W. Hannah

Interannual variation in geographic stock area, catchability, and natural mortality of age 2 ocean shrimp (Pandalus jordani) was investigated for the years 1980–1990, using commercial catch and logbook data. Stock area changed gradually from 1980–1990, but showed wide variation, demonstrating that an assumption of constant catchability is not valid for ocean shrimp. Stock area was positively correlated with total catch, suggesting that stock area increases roughly in proportion to shrimp abundance. The time series of fishing effort and effort per unit stock area were quite different, showing that fishing effort probably gives incorrect information on time trends in ocean shrimp fishing mortality. Natural mortality rates varied widely over the study period also and were positively correlated with the abundance of age 2+ Pacific hake (Merluccius productus), a known shrimp predator. The best correlations were between natural mortality rates and the number of age 2–7 Pacific hake. Hake abundance indices that included only age 3+ fish were not significantly correlated with shrimp natural mortality rates, suggesting that if a trophic interaction exists between these two species, it may be influenced by hake recruitment events.


2001 ◽  
Vol 58 (12) ◽  
pp. 2490-2501 ◽  
Author(s):  
S D Frusher ◽  
J M Hoenig

Fishing and natural mortality rates and tag reporting rate for rock lobsters (Jasus edwardsii) in northwest Tasmania, Australia, were estimated using multiyear tagging models. These estimates are necessary for assessment of the resource. Several models were examined that had either two or three tagging events each year, and either combined sexes or kept sexes separate. The model that best described the dynamics of the fishery utilized three tagging events within a year. The year was divided into discrete periods and, within each year, fishing effort and duration of period were used to apportion fishing and natural mortalities, respectively, to the periods. The separation of fishing mortalities by sex was not found to improve the models. Although high (1.0–1.2·year–1), the instantaneous fishing mortality estimates were comparable to estimates obtained from other methods and the relative standard errors were low. Reporting rate estimates were also precise and indicated a lack of participation by the fishing industry. Estimates of natural mortality were low (0.00–0.02·year–1) but imprecise.


1987 ◽  
Vol 44 (S2) ◽  
pp. s275-s288 ◽  
Author(s):  
Lawrence D. Jacobson ◽  
Wayne R. MacCallum ◽  
George R. Spangler

Schnute's (1985. Can. J. Fish. Aquat. Sci. 42: 414–429) difference model was used to study the biomass dynamics of lake herring (Coregonus artedii) in Thunder Bay and Black Bay, Lake Superior, during 1948–79. Recruitment to both fisheries appeared to be independent of escapement during previous years. Abundance of lake herring in Black Bay varied without trend during the study period despite a strong peak in effective fishing effort during 1968–70 and a general trend of increasing effort throughout the study period. Abundance of Thunder Bay lake herring declined during 1948–50 and 1959–67 and increased when fishing effort declined. The estimated catchability coefficient for small-mesh gill nets (54–83 mm stretched measure) set in Black Bay for lake herring during November was 0.467/102 km net. The estimated catchability coefficient for small mesh gill nets set in Thunder Bay for lake herring during December was 0.132/102 km net. Estimates of natural mortality rates and recruitment levels for both fisheries were confounded and unreliable. This analysis demonstrates the utility of Schnute's model for management of Great Lakes herring stocks and some difficulties with its application.


1987 ◽  
Vol 44 (S2) ◽  
pp. s129-s135
Author(s):  
John J. Collins

During 1979–81, Lake Huron fishermen changed from using 36-mesh monofilament nets to deeper (50-mesh) nets in the commercial fishery for lake whitefish (Coregonus clupeaformis). Simultaneous catch comparisons between the two gears showed that overall, deep nets were 1.7 times more efficient (but varied seasonally) for whitefish. The increase in efficiency exceeded that expected from the increase in area of the deeper nets. Simulation modeling demonstrates that the expression of enhanced catchability of deep nets is inversely proportional to the intensity of the fishery and thus total mortality rates (Z). Further, the temporal distribution of yield to the fishery would be advanced within the fishing period. This most recent change in catchability has introduced further bias in commercial catch and effort statistics.


1973 ◽  
Vol 30 (11) ◽  
pp. 1667-1682 ◽  
Author(s):  
E. B. Davidoff ◽  
R. W. Rybicki ◽  
K. H. Doan

Whitefish catches have fluctuated since 1952, and except in 1964 each successive peak has decreased in magnitude. Recently the overall trend has been a diminishing fishery with increasing effort.There has been a drastic change in age composition with time. Age-groups 5, 6, and 7 accounted for 81% of the catch from 1944 to 1948, age-groups 4, 5, and 6 for 89% from 1949 to 1955, age-groups 4 and 5 for 86% from 1959 to 1968, and age-groups 3 and 4 for 88% in 1969. The fishery is now dependent upon two age-groups instead of three. Natural failure of one or more important year-classes would result in a serious decline in catch, and partial or complete collapse of this fishery.Annual survival rate decreased from 34%, 1944–48 to 12%, 1959–69. Instantaneous natural mortality rate was estimated to be 0.72, and may be overestimated. The 1938–39, 1945–47, 1949, and 1957 year-classes were strong, while the 1940–44, and 1956, 1958, and 1961 year-classes were weak. The 1959 and 1960 year-classes appeared to be somewhat above average. Examination of data on total dissolved solids and temperature indicated that ecological changes were not responsible for the decline of whitefish in Lake Winnipeg.We judge that the optimum rate of fishing has been exceeded, and that the fishery itself is largely responsible for the depleted condition of the whitefish stocks in Lake Winnipeg. Fishing effort must be reduced to the point where the fishery is again dependent upon three year-classes. This should result in higher catches, and provide less fluctuation in annual catches.


1992 ◽  
Vol 43 (1) ◽  
pp. 195 ◽  
Author(s):  
TI Walker

A dynamic pool simulation model is derived and applied to the gummy shark stock of the southern shark fishery. Inputs to the model are fishing effort reported by fishers for hooks and for gill-nets with mesh sizes of 6 inches (152 mm), 7 inches (178 mm) and 8 inches (203 mm) along with estimates for growth, natural mortality, catchability, hook and gill-net mesh selectivity, size at maturity and fecundity of females, sex ratio at birth, and length-weight relationships. Growth is described by the von Bertalanffy equation; hook selectivity is constant with length for sharks recruited to the fishery; gill-net selectivity is based on the probability density distribution of the gamma function where selectivity varies with the mesh size of the gill-nets and the length of the sharks; number of births is related to the proportion of females mature at each length, and the relationship between number of births and maternal weight is linear; parturition is annual and time is standardized so that parturition occurs at the beginning of each year; sex ratio at birth is based on observations of a 1: 1 sex ratio of embryos; and allometric weight-length is based on the power curve. Natural mortality of recruits, catchability, reproduction and growth parameters are held constant, but density-dependent natural mortality of prerecruits is varied in proportion to stock abundance. The model is used to simulate effects of historical longline fishing effort and gill-net fishing effort for each mesh size on stock biomass, numbers of sharks in the stock, and numbers of births. The performance of the model is evaluated by comparing simulated annual catches and the simulated mean weight of sharks captured with annual catches reported by the fishers and the mean weight of sharks sampled in commercial landings. Uncertainties surrounding estimates of some of the parameters are discussed. Notwithstanding its shortcomings, the model indicates that the stock of gummy shark has been severely reduced and is in danger of further depletion unless immediate action is taken to reduce the commercial catch.


2017 ◽  
Vol 74 (7) ◽  
pp. 1061-1076 ◽  
Author(s):  
Julianne E. Harris ◽  
Joseph E. Hightower

We developed an integrated tagging model to estimate mortality rates and run sizes of Albemarle Sound – Roanoke River striped bass (Morone saxatilis), including (i) a multistate component for telemetered fish with a high reward external tag; (ii) tag return components for fish with a low reward external or PIT tag; and (iii) catch-at-age data. Total annual instantaneous mortality was 1.08 for resident (458–899 mm total length, TL) and 0.45 for anadromous (≥900 mm TL) individuals. Annual instantaneous natural mortality was higher for resident (0.70) than for anadromous (0.21) fish due to high summer mortality in Albemarle Sound. Natural mortality for residents was substantially higher than currently assumed for stock assessment. Monthly fishing mortality from multiple sectors (including catch-and-release) corresponded to seasonal periods of legal harvest. Run size estimates were 499 000–715 000. Results and simulation suggest increasing sample size for the multistate component increases accuracy and precision of annual estimates and low reward tags are valuable for estimating monthly fishing mortality rates among sectors. Our results suggest that integrated tagging models can produce seasonal and annual mortality estimates needed for stock assessment and management.


2019 ◽  
Vol 27 (2) ◽  
pp. 86-101
Author(s):  
Paweł Buras ◽  
Wiesław Wiśniewolski

Abstract Fisheries simulation models are tools used for forecasting the effects of exploitation and determining the directions of managing fisheries resources. The Numerical Model of Fish Exploitation (NMFE) and its capabilities were tested on a population of common bream, Abramis brama (L.) in a dam reservoir that is exploited by commercial and recreational fisheries. Based on the designated population parameters of N0, Fij, Mi, and ei and the size and structure of the common bream population in the reservoir, the model was used to examine hypothetical simulation variants of changes in fishing intensity E1 with nets and rods, changes in fishing intensity based on actual fishing effort with nets, changes in natural mortality, changes in the size of fish caught, and the impact of this on the size of the resources. Initial catches with nets and rods were calculated. Increasing fishing effort did not translate proportionally to increased catches, and the function was curvilinear. The results of simulations that reduced the intensity of fishing with nets and decreased catch sizes concurred with data from actual catches. Simulations of changes in natural mortality had various effects on the size of catches. Reducing parameter M did not impact the level of catches, while increasing parameter M reduced the size of catches significantly.


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