Minimum Size Regulations and the Implications for Yield and Value in the Canadian Atlantic Halibut (Hippoglossus hippoglossus) Fishery

1989 ◽  
Vol 46 (11) ◽  
pp. 1899-1903 ◽  
Author(s):  
John D. Neilson ◽  
W. R. Bowering
Keyword(s):  
Mortality Rate ◽  
Size Composition ◽  
Minimum Size ◽  
Atlantic Halibut ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Hippoglossus Hippoglossus ◽  
Size Regulation ◽  
Size Limit ◽  
Yield Per Recruit

The effect of a minimum size regulation on yield and value per recruit in the Canadian Atlantic halibut fishery was examined. The model indicated that under most scenarios, the size limit would not result in increased yield per recruit. In general, yield per recruit was more sensitive to fishing mortality than age of first entry to the fishery. While reduced yields were usually associated with the minimum size limit, the value per recruit increased with increasing age at entry to the fishery until age 7. The changes in value per recruit reflected the size composition of landings following the imposition of the size limit and the different values associated with various size categories. Both yield and value per recruit were sensitive to the choice of the natural mortality rate.

Eggs-per-recruit model for management of the California market squid (Loligo opalescens) fishery

2005 ◽  
Vol 62 (7) ◽  
pp. 1640-1650 ◽  
Author(s):  
Michael R Maxwell ◽  
Larry D Jacobson ◽  
Ramon J Conser
Keyword(s):  
Mortality Rate ◽  
Egg Laying ◽  
Reference Points ◽  
Model Parameters ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Loligo Opalescens ◽  
Maturation Rate ◽  
Sampling Procedures ◽  
Yield Per Recruit

We develop a per-recruit model for the management of the California market squid (Loligo opalescens) fishery. Based on recent confirmation of determinate fecundity in this species, we describe how catch fecundity (i.e., eggs remaining in the reproductive tracts of harvested females) can be used to simultaneously infer fishing mortality rate along with management reference points such as yield-per-recruit, spawned eggs-per-recruit, and proportional egg escapement. Rates of mortality and egg laying have important effects on these reference points. Somewhat surprisingly, increasing the rate of natural mortality decreased spawned eggs-per-recruit while increasing proportional egg escapement. Increasing the rate of egg laying increased both spawned eggs-per-recruit and egg escapement. Other parameters, such as the maturation rate and gear vulnerability of immature females, affected the reference points. In actual practice, the influence of these parameters for immature squid may go undetected if immature squid are excluded from analysis of the catch. Application of this model to routine management is feasible but requires refinement of sampling procedures, biological assumptions, and model parameters. This model is useful because it is grounded on empirical data collected relatively inexpensively from catch samples (catch fecundity) while allowing for the simultaneous calculation of instantaneous fishing mortality rate and egg escapement.

Survival of Atlantic Halibut (Hippoglossus hippoglossus) Caught by Longline and Otter Trawl Gear

1989 ◽  
Vol 46 (5) ◽  
pp. 887-897 ◽  
Author(s):  
John D. Neilson ◽  
Kenneth G. Waiwood ◽  
Stephen J. Smith
Keyword(s):  
Handling Time ◽  
Bottom Trawl ◽  
Minimum Size ◽  
Otter Trawl ◽  
Fish Length ◽  
Atlantic Halibut ◽  
Small Fish ◽  
Total Catch ◽  
Hippoglossus Hippoglossus ◽  
Size Limit

To assess the effectiveness of a proposed minimum size limit (81 cm) for Atlantic halibut (Hippoglossus hippoglossus) in Canadian waters, the survival of small fish caught in longline and bottom trawl gear was examined using live holding facilities onboard a research vessel and subsequently, in a land-based laboratory. Commercial practices were simulated during fishing operations. Of halibut less than the proposed size limit, 35% of the otter trawl catch and 77% of the longline catch survived more than 48 h. Factors potentially influencing halibut survival (handling time, total catch, fish length, maximum depth fished, and trawl duration) were examined using proportional hazard models. On the basis of those analyses, it was concluded that in bottom trawl sets of duration used in the commercial fishery (≥ 2 h), higher survival times were associated with shorter handling time, larger fish size, and comparatively small total catch weight. Supplemental information on the condition of trawl-caught halibut was also obtained from observers stationed onboard commercial trawlers.

Yield-per-recruit and egg-per-recruit analyses of the Omani abalone, Haliotis mariae

1995 ◽  
Vol 46 (3) ◽  
pp. 663 ◽  
Author(s):  
SA Shepherd ◽  
JL Baker ◽  
DW Johnson
Keyword(s):  
Mortality Rate ◽  
Sexual Maturity ◽  
Egg Production ◽  
Arabian Sea ◽  
Total Mortality ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Northern Arabian Sea ◽  
Size At Sexual Maturity ◽  
Yield Per Recruit

The fecundity, size at sexual maturity, sex ratios and total mortality of Haliotis mariae on the Dhofar coast of the northern Arabian Sea were measured. These data, and estimates of the growth rate, were used for yield-per-recruit and egg-per-recruit analyses. Maximum yields occur at 3+ to 4+ years of age, depending on the natural mortality rate chosen. At the present age at first capture egg production levels are 2-29% of the unfished stock, depending on estimates of the fishing mortality rate and the natural mortality rate, and are considered to be far too low to maintain recruitment. At 40% egg production, of the maximum possible the age at first capture is 4 to 4.5 years, i.e. 105-115 mm shell length, depending on site.

scholarly journals Yield per recruit of the peacock bass Cichla monoculus (Spix and Agassiz, 1831) caught in Lago Grande at Manacapuru (Amazonas – Brazil)

2014 ◽  
Vol 74 (1) ◽  
pp. 226-230 ◽  
Author(s):  
CP Campos ◽  
CEC Freitas
Keyword(s):  
Growth Parameters ◽  
Fishing Effort ◽  
Maximum Sustainable Yield ◽  
Minimum Size ◽  
Small Scale ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Yield Per Recruit ◽  
Peacock Bass ◽  
Actual Size

We evaluated the stock of peacock bass Cichla monoculus caught by a small-scale fishing fleet in Lago Grande at Manacapuru. The database was constructed by monthly samplings of 200 fish between February 2007 and January 2008. We measured the total length (cm) and total weight (gr) of each fish. We employed previously estimated growth parameters to run a yield per recruit model and analyse scenarios changing the values of the age of the first catch (Tc), natural mortality (M), and fishing mortality (F). Our model indicated an occurrence of overfishing because the fishing effort applied to catch peacock in Lago Grande at Manacapuru is greater than that associated with the maximum sustainable yield. In addition, the actual size of the first catch is almost half of the estimated value. Although there are difficulties in enforcing a minimum size of the catch, our results show that an increase in the size of the first catch to at least 25 cm would be a good strategy for management of this fishery.

Movement, Growth and natural mortality rate of the Red Spot King Prawn, Penaeus longistylus Kubo, from the Great Barrier Reef Lagoon

1990 ◽  
Vol 41 (3) ◽  
pp. 399 ◽  
Author(s):  
MCL Dredge
Keyword(s):  
Growth Rate ◽  
Mortality Rate ◽  
Great Barrier Reef ◽  
Annual Variation ◽  
Growth Parameters ◽  
Natural Mortality ◽  
Barrier Reef ◽  
Fishing Mortality ◽  
Nursery Areas ◽  
Reef Lagoon

Movement, growth and natural mortality rate of the red spot king prawn, Penaeus longistylus, occurring in waters of the Great Barrier Reef off Townsville, Queensland, were investigated in a series of tagging experiments. Adult P. longistylus did not migrate after leaving nursery areas. Their growth rate was slower than that of the conspecific species P. plebejus, and significant inter-annual variation in growth parameters was observed. The natural mortality rate, assessed by sequential tagging experiments that eliminated the possibility of confounding with the rate of fishing mortality, was estimated to be 0.072 (week-1).

Influence of errors in natural mortality estimates in cohort analysis

1997 ◽  
Vol 54 (7) ◽  
pp. 1608-1612 ◽  
Author(s):  
G Mertz ◽  
R A Myers
Keyword(s):  
Mortality Rate ◽  
Similar Pattern ◽  
Cohort Analysis ◽  
Transient Behavior ◽  
Natural Mortality ◽  
Exact Formulation ◽  
Fishing Mortality ◽  
Bias Factor ◽  
Special Case ◽  
Mortality Estimates

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.

scholarly journals POPULATION DYNAMICS OF MALAYAN LEAF FISH (Pristolepisgrooti Blkr.) IN RANAU LAKE, SOUTH SUMATRA

2018 ◽  
Vol 24 (2) ◽  
pp. 125
Author(s):  
Sevi Sawetri ◽  
Subagdja Subagdja ◽  
Dina Muthmainnah
Keyword(s):  
Mortality Rate ◽  
Growth Parameters ◽  
Total Mortality ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Frequency Data ◽  
Length Frequency ◽  
Lake Ecosystems ◽  
Exploitation Rate ◽  
Length Frequency Data

The Malayan leaf fish or locally named as kepor (Pristolepis grooti) is one of important biotic components in Ranau Lake ecosystems. This study aimed to estimate population dynamic and exploitation rate of kepor in Ranau Lake, South Sumatera. The population parameters are estimated based on length frequency data which were collected in March to October 2013. Growth parameters and fishing mortality rates were calculated using FiSAT software package. The results showed that kepor’s growth was negative allometric, which tended to gain length faster than weight. Kepor population was dominated (42%) by individual length of 10.0 to 11.0 cm. Predicted length infinity (L) was 17.28 cm with high value of growth rates (K) of 1.4 year-1. The natural mortality rate (M) is 2.57 year-1, the fishing mortality rate (F) is 5.36 year-1 and total mortality rate (Z) is 7.93 year-1. The exploitation rate of Malayan leaf fish in Ranau Lake (E = 0.68 year-1) has passed the optimum score.  

Integrating catch-at-age and multiyear tagging data: a combined Brownie and Petersen estimation approach in a fishery context

2006 ◽  
Vol 63 (3) ◽  
pp. 534-548 ◽  
Author(s):  
Tom Polacheck ◽  
J Paige Eveson ◽  
Geoff M Laslett ◽  
Kenneth H Pollock ◽  
William S Hearn
Keyword(s):  
Mortality Rate ◽  
Population Size ◽  
Stock Assessment ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Catch Data ◽  
Coefficients Of Variation ◽  
Southern Bluefin Tuna ◽  
Catch Rates ◽  
Comprehensive Framework

A comprehensive framework for modelling data from multiyear tagging experiments in a fishery context is presented that incorporates catch data into the traditional Brownie tag–recapture model. Incorporation of catch data not only allows for improved estimation of natural and fishing mortality rates, but also for direct estimation of population size at the time of tagging. These are the primary quantities required to be estimated in stock assessments — having an approach for directly estimating them that does not require catch rates provides a potentially powerful alternative for augmenting traditional stock assessment methods. Simulations are used to demonstrate the value of directly incorporating catch data in the model. Results from the range of scenarios considered suggest that in addition to providing a precise estimate of population size (coefficients of variation ranging from ~15% to 30%), including catch data can decrease biases in the mortality rate estimates (natural mortality especially) and improve precision of fishing mortality rate estimates (by as much as 60% at age 1). The model is applied to southern bluefin tuna (Thunnus maccoyii) tag–recapture and catch data collected in the 1990s to provide estimates of natural mortality, fishing mortality, and abundance for five cohorts of fish.

The Effect of Reduction of Fishing Effort on Yield

1962 ◽  
Vol 19 (4) ◽  
pp. 521-529 ◽  
Author(s):  
Syoiti Tanaka
Keyword(s):  
Mortality Rate ◽  
Sudden Change ◽  
Japan Sea ◽  
Fish Population ◽  
Fishing Effort ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Yield Curves ◽  
Before And After ◽  
Steady Level

When a fish population has been depleted by heavy exploitation, with the yield from the population maintaining an unfavourable level, it is usual to expect that the situation will be improved by reduction of fishing effort. Following a sudden reduction of fishing mortality, p, from p1 to p2 at time τ = 0, the yield at once decreases and then increases gradually until it reaches another steady level higher than the former level.The present paper deals, using Baranov's model, with the transition stage of the population following a sudden change in p, as well as with the steady state before and after the change. Relations between equilibrium yield and fishing mortality rate (effort-yield curves) are calculated for various values of the parameters, λ0 (= l0/u, where l0 is the length of a recruit and u is the yearly increase in length), q (natural mortality rate), and b (remaining life span of a fish at the time of recruitment) (Fig. 2). It is noteworthy that for species that grow slowly after recruitment, i.e. when λ0 is large, reduction of fishing would have scarcely any effect on the yield (Fig. 4).Yield curves for the period of transition from the present to various lower levels of fishing are calculated for the case in which λ0 = 4, q = 0.15, b = 10 and p1 = 1.35. These represent parameters for the present state of the stock of sohachi flounders Cleisthenes herzensteini (Schmidt), in the southwestern area of the Japan Sea (Fig. 5).Possible density effects on growth rate and natural mortality rate, which are briefly discussed, appear to diminish considerably the effectiveness of any reduction in fishing effort (Fig. 6).

scholarly journals The effect of including length structure in yield-per-recruit estimates for northeast Arctic cod

2007 ◽  
Vol 64 (2) ◽  
pp. 357-368 ◽  
Author(s):  
Cecilie Kvamme ◽  
Bjarte Bogstad
Keyword(s):  
Alternative Model ◽  
Gadus Morhua ◽  
The Other ◽  
Natural Mortality ◽  
Fishing Mortality ◽  
Structured Model ◽  
Arctic Cod ◽  
Traditional Age ◽  
Size At Age ◽  
Yield Per Recruit

Abstract Kvamme, C., and Bogstad, B. 2007. The effect of including length structure in yield-per-recruit estimates for northeast Arctic cod. – ICES Journal of Marine Science, 64: 357–368. For northeast Arctic cod (Gadus morhua), traditional age-based estimates of yield per recruit (YPR) are compared with alternative, though comparable, YPR estimates calculated using an age–length-structured model. In the age–length-structured model, growth, fishing mortality, and natural mortality depend only on length, not on age. This model considers possible changes in size-at-age caused by, for example, a length-selective fishery, and therefore, by comparing the different YPR estimates, the importance of considering the stock's length structure can be evaluated. Length- and weight-at-age of stock and catches were influenced by exploitation pattern and pressure. Such changes are not considered in traditional estimates of YPR, for which weight-at-age is fixed and strictly speaking only representative for the current fishery. Consequently, traditional YPR estimates were somewhat higher than the age–length-based estimates for exploiting smaller fish than at present, and the other way round for exploiting larger fish. Both models indicated a gain in YPR for reducing just exploitation pressure (traditional YPR, 13%; alternative model, 20%) or both reducing exploitation pressure and postponing exploitation (traditional YPR, 23–31%; alternative model, 33–48%), compared with the current fishery.

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