fisheries research services populations by a rod fishery ... · in wildlife telemetry: remote...

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Photo by James Butler Photo by James Butler Photo by Ian Neale Acknowledgements We are extremely grateful to all the River Spey proprietors, ghillies and anglers who participated in the project. We would also like to thank John Webb (Atlantic Salmon Trust) and Iain McLaren (Fisheries Research Services) for their assistance with tagging training. The project was generously supported by Diageo and the Edinburgh Smoked Salmon Company Ltd. References Davidson IC, Cove RJ, Milner NJ & Purvis WK (1996) Estimation of Atlantic salmon (Salmo salar L.) and sea trout (Salmo trutta L.) run size and angling exploitation on the Welsh Dee, using mark-recapture and trap indices. In Stock Assessment in Inland Fisheries (Cowx IG, ed.), pp.293-307. Fishing News Books, Oxford, England. Hilborn R, Quinn TP, Schindler DE & Rogers DE (2003) Biocomplexity and fisheries sustainability. PNAS, 100:6564-6568. Laughton R & Smith GW (1992) The relationship between the date of entry and the estimated spawning position of adult Atlantic salmon (Salmo salar L.) in two major East coast rivers. In Wildlife Telemetry: Remote Monitoring and Tracking of Animals (Priede IG & Swift SM, eds.), pp.423-433. Ellis Horwood Ltd, Chichester, England. Stewart DC, Smith GW & Youngson AF (2002) Tributary-specific variation in timing of return of adult Atlantic salmon (Salmo salar) to fresh water has a genetic component. Canadian Journal of Fisheries and Aquatic Sciences, 59:276-281. Youngson AF, MacLean JC & Fryer FJ (2002) Rod catch trends for early-running MSW salmon in Scottish rivers (1952-1997): divergence among stock components. ICES Journal of Marine Science, 59:836-849. Acknowledgements We are extremely grateful to all the River Spey proprietors, ghillies and anglers who participated in the project. We would also like to thank John Webb (Atlantic Salmon Trust) and Iain McLaren (Fisheries Research Services) for their assistance with tagging training. The project was generously supported by Diageo and the Edinburgh Smoked Salmon Company Ltd. References Davidson IC, Cove RJ, Milner NJ & Purvis WK (1996) Estimation of Atlantic salmon (Salmo salar L.) and sea trout (Salmo trutta L.) run size and angling exploitation on the Welsh Dee, using mark-recapture and trap indices. In Stock Assessment in Inland Fisheries (Cowx IG, ed.), pp.293-307. Fishing News Books, Oxford, England. Hilborn R, Quinn TP, Schindler DE & Rogers DE (2003) Biocomplexity and fisheries sustainability. PNAS, 100:6564-6568. Laughton R & Smith GW (1992) The relationship between the date of entry and the estimated spawning position of adult Atlantic salmon (Salmo salar L.) in two major East coast rivers. In Wildlife Telemetry: Remote Monitoring and Tracking of Animals (Priede IG & Swift SM, eds.), pp.423-433. Ellis Horwood Ltd, Chichester, England. Stewart DC, Smith GW & Youngson AF (2002) Tributary-specific variation in timing of return of adult Atlantic salmon (Salmo salar) to fresh water has a genetic component. Canadian Journal of Fisheries and Aquatic Sciences, 59:276-281. Youngson AF, MacLean JC & Fryer FJ (2002) Rod catch trends for early-running MSW salmon in Scottish rivers (1952-1997): divergence among stock components. ICES Journal of Marine Science, 59:836-849. Differential Exploitation of Atlantic Salmon Populations by a Rod Fishery on the River Spey, Scotland Joseph Thorley 1 , Robert Laughton 2 and Alan Youngson 1 1. Freshwater Laboratory, Faskally, Pitlochry, Perthshire, PH16 5LB, UK. 2. Spey Fishery Board Research Office, 1 Nether Borlum Cottage, Knockando, Morayshire, AB38 7SD, UK. Discussion The results have to be interpreted carefully because the recapture probabilities estimate re-exploitation level - which may not be the same as exploitation level. A discrepancy could arise in four ways. Firstly, (1) if individual salmon differ in their catchability then tagged salmon will tend to be the most catchable fish and re-exploitation will exceed exploitation. Alternatively, (2) if capture decreases the probability of capture at a later date, through for example a higher mortality rate, then exploitation will exceed re-exploitation. This will also be the case (3) if fish lose their tags or recaptures are unreported. Finally, (4) if the probability of capture declines from date of river entry then exploitation will once again exceed re-exploitation. To the best of our knowledge, the only study to consider inter-individual variation in catchability found that salmon which entered the Welsh Dee in the same month did not experience any difference in exploitation level associated with sea-age (Davidson et al., 1996). Since the other three mechanisms, which are all probably operative, cause exploitation to exceed re-exploitation, the recapture probabilities presented in this study are likely to be conservative estimates of the levels of exploitation. In Scotland, early-running (or so-called ‘spring’) salmon belong to genetically distinct populations which typically spawn in the upper parts of catchments (Laughton & Smith, 1992; Stewart et al., 2002). Spring salmon are large, multi-sea winter fish that are sought after by anglers. As this study demonstrates, they are also highly exploitable – a property that further increases their value to the rod fishery. However, due at least partly to changes in the marine environment, early-running salmon are declining in abundance (Youngson et al., 2002). Unless fisheries managers protect these populations, the genetic diversity underlying run- timing may be compromised. This could leave the ‘stock complex’ unable to rapidly respond to future environmental change and therefore vulnerable to collapse (Hilborn et al., 2003). Fisheries managers must consider differential exploitation of the various run-timing groups when implementing conservation measures. Introduction Due to heritable population differences in run-timing, Atlantic salmon (Salmo salar) enter Scottish rivers throughout the year. Maintenance of this diversity is vital for the continued commercial and recreational value of the associated rod fisheries, which extend on most rivers from February to September. However, as the data we present demonstrate, management of the rod fishery on the River Spey, Scotland, is complicated by differential exploitation of the Atlantic salmon from the various run-timing groups. Method & Results During the 2000 to 2002 fishing seasons on the River Spey, Scotland, 862 rod-caught Atlantic salmon were Floy- tagged by trained ghillies (guides) and released. Of these three were later found in a diseased state and were excluded from the study. The numbers tagged and released in each month are shown in Figure 1. Thirty-nine salmon were re-caught by anglers before October. The proportion of fish tagged in each month that were subsequently re- caught is shown in Figure 2. Fish of different sea-age classes are not distinguished. The probability of recapture by Julian Day was estimated by a logistic model with recapture coded as a binary variable. Since an additive logistic model did not significantly improve the fit and since year was not a significant explanatory variable, the following logistic regression model was fitted: The adequacy of the model was established by simulating data. The logistic regression complete with confidence intervals is shown in Figure 3. The probability of recapture from date of tagging, by days, was estimated for fish tagged in March, April or May by a Cox proportional hazards model. Too few fish from the remaining months were re-caught for inclusion in the model. Since the fish became re-exploitable in September, captures after the 31st of August were excluded. Salmon tagged in March had a significantly different baseline hazard to those tagged in April and May (p<0.005). The two separate models are plotted in Figure 4. Julian Day of tagging was a significant negative coefficient of proportionality for the salmon in the April-May model (p<0.05) but not the March model (p>0.5). Figure 3. The probability of recapture before October by Julian Day tagged as estimated by logistic regression. The dashed lines are pointwise 95% confidence intervals. Julian Day Probability of Recapture 50 100 150 200 250 0.0 0.05 0.10 0.15 0.20 0.25 0.30 Figure 4. The proportion of tagged salmon remaining uncaught by days from tagging. Days Proportion Remaining Uncaught 0 50 100 150 0.8 0.9 1.0 March April-May Figure 1. The number of salmon tagged in each month. Feb Mar Apr May Jun Jul Aug Sep 0 50 100 150 200 Number Tagged Figure 2. The proportion of salmon tagged in each month and subsequently re-caught before October. Feb Mar Apr May Jun Jul Aug Sep 0.0 0.05 0.10 0.15 0.20 0.25 0.30 Proportion Re-caught 1+ exp(1.33 – 0.0335JulianDay) = exp(1.33 – 0.0335JulianDay) (Recapture) Ρ Fisheries Research Services

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Photo by James Butler Photo by James Butler

Photo by Ian Neale

AcknowledgementsWe are extremely grateful to all the River Spey proprietors, ghillies and anglers who participated in the project.We would also like to thank John Webb (Atlantic Salmon Trust) and Iain McLaren (Fisheries Research Services) fortheir assistance with tagging training. The project was generously supported by Diageo and the Edinburgh SmokedSalmon Company Ltd.

ReferencesDavidson IC, Cove RJ, Milner NJ & Purvis WK (1996) Estimation of Atlantic salmon (Salmo salar L.) and sea trout (Salmo trutta L.) run size and anglingexploitation on the Welsh Dee, using mark-recapture and trap indices. In Stock Assessment in Inland Fisheries (Cowx IG, ed.), pp.293-307. Fishing NewsBooks, Oxford, England.

Hilborn R, Quinn TP, Schindler DE & Rogers DE (2003) Biocomplexity and fisheries sustainability. PNAS, 100:6564-6568.

Laughton R & Smith GW (1992) The relationship between the date of entry and the estimated spawning position of adult Atlantic salmon (Salmo salarL.) in two major East coast rivers. In Wildlife Telemetry: Remote Monitoring and Tracking of Animals (Priede IG & Swift SM, eds.), pp.423-433. EllisHorwood Ltd, Chichester, England.

Stewart DC, Smith GW & Youngson AF (2002) Tributary-specific variation in timing of return of adult Atlantic salmon (Salmo salar) to fresh water hasa genetic component. Canadian Journal of Fisheries and Aquatic Sciences, 59:276-281.

Youngson AF, MacLean JC & Fryer FJ (2002) Rod catch trends for early-running MSW salmon in Scottish rivers (1952-1997): divergence among stockcomponents. ICES Journal of Marine Science, 59:836-849.

AcknowledgementsWe are extremely grateful to all the River Spey proprietors, ghillies and anglers who participated in the project.We would also like to thank John Webb (Atlantic Salmon Trust) and Iain McLaren (Fisheries Research Services) fortheir assistance with tagging training. The project was generously supported by Diageo and the Edinburgh SmokedSalmon Company Ltd.

ReferencesDavidson IC, Cove RJ, Milner NJ & Purvis WK (1996) Estimation of Atlantic salmon (Salmo salar L.) and sea trout (Salmo trutta L.) run size and anglingexploitation on the Welsh Dee, using mark-recapture and trap indices. In Stock Assessment in Inland Fisheries (Cowx IG, ed.), pp.293-307. Fishing NewsBooks, Oxford, England.

Hilborn R, Quinn TP, Schindler DE & Rogers DE (2003) Biocomplexity and fisheries sustainability. PNAS, 100:6564-6568.

Laughton R & Smith GW (1992) The relationship between the date of entry and the estimated spawning position of adult Atlantic salmon (Salmo salarL.) in two major East coast rivers. In Wildlife Telemetry: Remote Monitoring and Tracking of Animals (Priede IG & Swift SM, eds.), pp.423-433. EllisHorwood Ltd, Chichester, England.

Stewart DC, Smith GW & Youngson AF (2002) Tributary-specific variation in timing of return of adult Atlantic salmon (Salmo salar) to fresh water hasa genetic component. Canadian Journal of Fisheries and Aquatic Sciences, 59:276-281.

Youngson AF, MacLean JC & Fryer FJ (2002) Rod catch trends for early-running MSW salmon in Scottish rivers (1952-1997): divergence among stockcomponents. ICES Journal of Marine Science, 59:836-849.

Differential Exploitation of Atlantic SalmonPopulations by a Rod Fishery on the River Spey, Scotland

Joseph Thorley1, Robert Laughton2 and Alan Youngson1

1. Freshwater Laboratory, Faskally, Pitlochry, Perthshire, PH16 5LB, UK.2. Spey Fishery Board Research Office, 1 Nether Borlum Cottage, Knockando, Morayshire, AB38 7SD, UK.

DiscussionThe results have to be interpreted carefully because the recapture probabilities estimate re-exploitation level -which may not be the same as exploitation level. A discrepancy could arise in four ways. Firstly, (1) if individualsalmon differ in their catchability then tagged salmon will tend to be the most catchable fish and re-exploitationwill exceed exploitation. Alternatively, (2) if capture decreases the probability of capture at a later date, throughfor example a higher mortality rate, then exploitation will exceed re-exploitation. This will also be the case (3) iffish lose their tags or recaptures are unreported. Finally, (4) if the probability of capture declines from date of riverentry then exploitation will once again exceed re-exploitation.

To the best of our knowledge, the only study to consider inter-individual variation in catchability found that salmonwhich entered the Welsh Dee in the same month did not experience any difference in exploitation level associatedwith sea-age (Davidson et al., 1996). Since the other three mechanisms, which are all probably operative, causeexploitation to exceed re-exploitation, the recapture probabilities presented in this study are likely to be conservativeestimates of the levels of exploitation.

In Scotland, early-running (or so-called ‘spring’) salmon belong to genetically distinct populations which typicallyspawn in the upper parts of catchments (Laughton & Smith, 1992; Stewart et al., 2002). Spring salmon are large,multi-sea winter fish that are sought after by anglers. As this study demonstrates, they are also highly exploitable– a property that further increases their value to the rod fishery.

However, due at least partly to changes in the marine environment, early-running salmon are declining in abundance(Youngson et al., 2002). Unless fisheries managers protect these populations, the genetic diversity underlying run-timing may be compromised. This could leave the ‘stock complex’ unable to rapidly respond to future environmentalchange and therefore vulnerable to collapse (Hilborn et al., 2003). Fisheries managers must consider differentialexploitation of the various run-timing groups when implementing conservation measures.

IntroductionDue to heritable population differences in run-timing, Atlantic salmon (Salmo salar) enter Scottish rivers throughoutthe year. Maintenance of this diversity is vital for the continued commercial and recreational value of the associatedrod fisheries, which extend on most rivers from February to September. However, as the data we present demonstrate,management of the rod fishery on the River Spey, Scotland, is complicated by differential exploitation of the Atlanticsalmon from the various run-timing groups.

Method & ResultsDuring the 2000 to 2002 fishing seasons on the River Spey, Scotland, 862 rod-caught Atlantic salmon were Floy-tagged by trained ghillies (guides) and released. Of these three were later found in a diseased state and wereexcluded from the study. The numbers tagged and released in each month are shown in Figure 1. Thirty-nine salmonwere re-caught by anglers before October. The proportion of fish tagged in each month that were subsequently re-caught is shown in Figure 2. Fish of different sea-age classes are not distinguished.

The probability of recapture by Julian Day was estimated by a logistic model with recapture coded as a binaryvariable. Since an additive logistic model did not significantly improve the fit and since year was not a significantexplanatory variable, the following logistic regression model was fitted:

The adequacy of the model was established by simulating data. The logistic regression complete with confidenceintervals is shown in Figure 3.

The probability of recapture from date of tagging, by days, was estimated for fish tagged in March, April or May bya Cox proportional hazards model. Too few fish from the remaining months were re-caught for inclusion in themodel. Since the fish became re-exploitable in September, captures after the 31st of August were excluded. Salmontagged in March had a significantly different baseline hazard to those tagged in April and May (p<0.005). The twoseparate models are plotted in Figure 4. Julian Day of tagging was a significant negative coefficient of proportionalityfor the salmon in the April-May model (p<0.05) but not the March model (p>0.5).

Figure 3.The probability of recapture before October by Julian Daytagged as estimated by logistic regression. The dashedlines are pointwise 95% confidence intervals.

Julian Day

Prob

abili

ty o

f Rec

aptu

re

50 100 150 200 250

0.0

0.05

0.10

0.15

0.20

0.25

0.30

Figure 4.The proportion of tagged salmon remaining uncaught bydays from tagging.

Days

Prop

orti

on R

emai

ning

Unc

augh

t

0 50 100 150

0.8

0.9

1.0

March

April-May

Figure 1.The number of salmon tagged in each month.

Feb Mar Apr May Jun Jul Aug Sep

050

100

150

200

Num

ber T

agge

d

Figure 2.The proportion of salmon tagged in each month andsubsequently re-caught before October.

Feb Mar Apr May Jun Jul Aug Sep

0.0

0.05

0.10

0.15

0.20

0.25

0.30

Prop

orti

on R

e-ca

ught

1+ exp(1.33 – 0.0335JulianDay)=

exp(1.33 – 0.0335JulianDay)(Recapture)Ρ

Fisheries Research Services