scholarly journals Estimating natural and fishing mortality and tag reporting rate of southern rock lobster (Jasus edwardsii) from a multiyear tagging model

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.

2003 ◽  
Vol 60 (5) ◽  
pp. 1075-1085 ◽  
Author(s):  
Robert J. Latour ◽  
John M. Hoenig ◽  
Daniel A. Hepworth ◽  
Stewart D. Frusher

Abstract Multi-year tag-recovery models can be used to derive estimates of age- and year-specific annual survival rates and year-specific instantaneous fishing and natural mortality rates. The latter, which are often of interest to fisheries managers, usually can only be estimated when the tag-reporting rate (λ) and the short-term tag-induced mortality and tag-shedding rate (φ) are known a priori. We present a new multi-year tagging model that permits estimation of instantaneous mortality rates independently of φλ, provided tagged animals from two adjacent size groups are released simultaneously. If the two size groups comprise animals just above and below the minimum harvestable size limit, then it is possible to estimate year-specific instantaneous fishing and natural mortality rates after 2 yr of tagging and tag-recovery. In addition to the standard assumptions of multi-year tag-recovery models, it is necessary to assume that recruited animals have equal selectivity, pre-recruited animals become fully recruited in 1 or 2 yr, and the size groups experience the same natural mortality rate. Applicability of the model to the Tasmania southern rock lobster (Jasus edwardsii) fishery is evaluated using a simulation model and parameters based on data from the lobster fishery; assumptions are likely to be met and precision should be adequate if at least 1000 animals are tagged per year in each size group.


1998 ◽  
Vol 55 (6) ◽  
pp. 1466-1476 ◽  
Author(s):  
John M Hoenig ◽  
Nicholas J Barrowman ◽  
William S Hearn ◽  
Kenneth H Pollock

The Brownie models for multiyear tagging studies can be used to estimate age- and year-specific annual survival rates and tag recovery rates. The latter are composites of the exploitation rates and rates of tag reporting, tag shedding, and tag-induced mortality. It is possible to estimate the exploitation rates if the other components of the tag recovery rates can be quantified. Instantaneous rates of fishing and natural mortality can be estimated if information is available on the seasonal distribution of fishing effort. The estimated rates are only moderately dependent on the timing of the fishing; consequently, the relative effort data can be crude. Information on the timing of the catch over the course of the year can be used as a substitute for the effort data. Fishing mortality can also be assumed to be proportional to fishing effort over years; consequently, if fishing effort is known then the tag reporting rate, natural mortality rate, and a single catchability coefficient can be estimated (instead of natural mortality and a series of fishing mortalities). Although it is possible in theory to estimate both the tag reporting rate and the natural mortality rate with all of these models, in practice it appears necessary to obtain some additional data relating to tag reporting rate to obtain acceptable results. The additional data can come from a variable reward tagging study, a creel or port sampling survey, or from tagged animals that are secretly added to the fishers' catches.


1998 ◽  
Vol 55 (1) ◽  
pp. 199-205 ◽  
Author(s):  
William S Hearn ◽  
Kenneth H Pollock ◽  
Elizabeth N Brooks

Brownie et al. (1985, U.S. Fish Wildl. Serv. Resour. Publ. 156, p. 159) presented models for tag returns from multiple taggings of animals when tagging is done twice per year. Here, we present a reformulation of their model suitable for pre- and post-season fishery tag return studies. Under this model, it is possible to estimate fishing mortality, natural mortality, and reporting rate from the tag return data alone. (Under once-a-year tagging models, the reporting rate usually has to be estimated externally.) We consider two special cases: (i) a pulse fishery and (ii) a continuous fishery over part of the year. An artificial example and simulation results are presented to illustrate the methodology and the properties of the various estimators. Unlike for catch-based methods, the correlation between estimates of fishing mortality and natural mortality is moderate. While pre- and post-season tagging studies are likely to be difficult to run in practice, other methods of estimating reporting rate are also difficult to implement, and therefore, this approach may prove quite useful, especially in fisheries that have heavy exploitation rates.


1998 ◽  
Vol 55 (9) ◽  
pp. 2001-2010 ◽  
Author(s):  
Elizabeth N Brooks ◽  
Kenneth H Pollock ◽  
John M Hoenig ◽  
William S Hearn

We present generalizations of fishery models that allow for the separate estimation of fishing mortality when more than one user group is present (e.g., a commercial and a recreational fishery). This model also allows for the fisheries to be in operation for any length of time whereas previously fisheries were generally considered to be pulse or continuous. Three cases are considered: (i) fisheries operate consecutively, (ii) fisheries overlap for a part of their seasons, and (iii) fisheries are in operation for the whole year. The results of a simulation study are included, which provide estimates of fishing and natural mortality along with their proportional standard errors (CVs). All scenarios had good precision, with most CVs < 25% and usually very little difference between the three cases. Coefficients of interaction, the potential gain by one fishery if another is closed down, are also given along with a method for calculating them. Factors affecting these coefficients of interaction were the order in which fisheries operated, amount of overlap in fishing seasons, and intensity of fishing effort by each fishery. We believe that these models could provide useful information for the management of fisheries with multiple user groups where allocation conflicts may arise.


1997 ◽  
Vol 54 (7) ◽  
pp. 1608-1612 ◽  
Author(s):  
G Mertz ◽  
R A Myers

The accuracy of the estimation of cohort strength from catch data may be greatly degraded if a poor estimate of the natural mortality rate is entered into the calculation. A straightforward, exact formulation for the error in cohort reconstruction due to a misspecified natural mortality rate is presented. The special case of constant fishing mortality is particularly transparent, allowing the error to be segmented into easily interpreted terms. A change in the fishing mortality may result in a distinct hump in the transient behavior of the bias factor, rather than a simple monotonic adjustment. This implies a similar pattern in estimated cohort strength.


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.


2020 ◽  
Vol 48 (4) ◽  
pp. 613-625
Author(s):  
Felipe Lopez ◽  
Jorge Jimenez ◽  
Cristian Canales

Since 1979, southern hake (Merluccius australis) has been exploited in Chile from the Bio Bio to the Magallanes regions, between the parallels 41°28.6'S and 57°S. There is evidence of a constant fishing effort and a sustained reduction of the fish population, consistent with a progressive decrease in total annual catches. Management strategies based on the maximum sustainable yield (MSY) and quota assignment/ distribution criteria have not been able to sustain acceptable biomass levels. A non-linear optimization model with two objective functions was proposed to determine an optimal total catch quota for more sustainable exploitation of this fishery. The first function maximizes the total catch over time in response to an optimal assignment of fishing mortality rates per fleet; the second function maximizes the total economic benefit associated with the total catch. The dynamics of the fish population were represented with the equations of a predictive age-structured model. Decision variables were fishing mortality rates and annual catch quotas per fleet, subject to constraints that guarantee a minimum level of biomass escape over a long-term period. The input parameters were obtained from the last stock evaluation report carried out by the Instituto de Fomento Pesquero (IFOP) of Chile. The historical background data of the fishery and the regulatory framework were relevant aspects of the methodology. Five scenarios were evaluated with the two objective functions, including a base scenario, which considered the referential mortality rate as input data as the average mortality rate per fleet from 2007 to 2012. Total economic benefits fluctuate between 102 and USD 442 million for total catches in the range of 108 to 421 thousand tons, which were obtained from maximizing the economic and biological objective functions. Economic benefit/catch ratios were reduced for scenarios with higher constraints on catch limits, and they were more efficient from a biological point of view. Situations with lighter constraints showed in general higher economic benefits and better performance ratios than those with stronger restrictions. The use of optimization models may provide a useful tool to evaluate the effect of regulations for adequate conservation and economical utilization of a limited resource.


2006 ◽  
Vol 63 (6) ◽  
pp. 961-968 ◽  
Author(s):  
Joe Horwood ◽  
Carl O'Brien ◽  
Chris Darby

AbstractRecovery of depleted marine, demersal, commercial fish stocks has proved elusive worldwide. As yet, just a few shared or highly migratory stocks have been restored. Here we review the current status of the depleted North Sea cod (Gadus morhua), the scientific advice to managers, and the recovery measures in place. Monitoring the progress of North Sea cod recovery is now hampered by considerable uncertainties in stock assessments associated with low stock size, variable survey indices, and inaccurate catch data. In addition, questions arise as to whether recovery targets are achievable in a changing natural environment. We show that current targets are achievable with fishing mortality rates that are compatible with international agreements even if recruitment levels remain at the current low levels. Furthermore, recent collations of data on international fishing effort have allowed estimation of the cuts in fishing mortality achieved by restrictions on North Sea effort. By the beginning of 2005, these restrictions are estimated to have reduced fishing mortality rates by about 37%. This is insufficient to ensure recovery of North Sea cod within the next decade.


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.


2012 ◽  
Vol 69 (4) ◽  
pp. 770-783 ◽  
Author(s):  
Hilaire Drouineau ◽  
Louise Savard ◽  
Mathieu Desgagnés ◽  
Daniel Duplisea

Despite the economic importance of Pandalus shrimp fisheries, few analytical tools have been developed to assess their stocks, and traditional stock assessment models are not appropriate because of biological specificities of Pandalus species. In this context, we propose SPAM (Sex-Structured Pandalus Assessment Model), a model dedicated to protandric hermaphrodite pandalids stock assessment. Pandalids are difficult to assess because the cues affecting sex change, size at recruitment, and mortality variability are not well understood or characterized. The novel structure of the model makes it possible to adequately describe variability in natural mortality by stage and in time, as well as variability in size at sex change and recruitment. The model provides traditional stock assessment outputs, such as fishing mortality estimates and numbers of individuals, and provides in addition yearly natural mortality estimates. The model is applied to the exploited shrimp stock of Pandalus borealis in Sept-Îles (Québec, Canada) as an illustrative example of the utility of the approach.


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