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    The Dynamics of an Open Access FisheryAuthor(s): Trond Bjrndal and Jon M. ConradSource: The Canadian Journal of Economics / Revue canadienne d'Economique, Vol. 20, No. 1(Feb., 1987), pp. 74-85Published by: Blackwell Publishing on behalf of the Canadian Economics AssociationStable URL: http://www.jstor.org/stable/135232

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    The dynamics of an open access fisheryTROND BJORNDAL Norwegian School of EconomicsJON M. CONRAD Cornell University

    Abstract. A discrete time non-linear deterministic model for an open access fishery isdeveloped and the equilibrium is characterized. The open access exploitation of NorthSea herring during the period 1963-77 is analysed. Alternative production functions areconsidered and estimated for the Norwegian purse seine fishery. The bionomicequilibrium and approach dynamics are presented when prices and costs are changing.The results indicate that the resource stock was saved from possible extinction by theclosure of the fishery at the end of the 1977 season.Sur la dynamiqued'une zone de peches quand l'entr&est libre. Les auteurs d6veloppentun modele deterministe non-lineaire en temps discret d'une zone de peches oiul'entr6eest libre et definissent les caract6ristiques de l'equilibre. L'exploitation du hareng de laMer du Nord qui s'est faite sans entraves a l'entree pendant la periode 1963-1977 estanalys6e avec ce modele. Des fonctions de production de rechange sont examinees etcalibrees pour la peche a l'essaugue par la flotte norvegienne. L'equilibre bionomiqueet la dynamiquede l'approche 'acet 6quilibresont examinesdans un universoiu es prix etles couits sont changeants. Les r6sultats de l'analyse montrentque le stock de ressourceaechappe a la disparition possible grace a la fermeture de la zone de peches a la fin de lasaison de 1977.INTRODUCTIONOpen access exploitation of common property fish resources frequently causessevere stock depletion. Indeed, the question whether open access may causestock extinction has been analysed by several authors (Smith, 1968 and 1975;Berck, 1979; Hartwick, 1982). Moreover, as Smith (1968) has pointed out,although stock equilibrium under open access may be positive, the stock maybe driven to extinction along the path of adjustment. Stock equilibriummay also be stable and positive with fixed prices and technology and still drifttowards extinction over time, since these fixed variables drift in the long run.Canadian Journal of Economics Revue canadienne d'Economique, xx, No. IFebruary fevrier 1987. Printed in Canada Imprime au Canada0008-4085 / 87 / 74-85 1.50 ? Canadian Economics Association

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    Dynamics of an open access fishery 75With the exception of Wilen (1976) the work on the dynamics of open accessor free entry fisheries is mainly theoretical. The purpose of this paper is to

    provide an empirical application, based on the North Sea herring fishery, withspecial reference to the question of stock extinction under open access. Herringis a schooling species. The schooling behaviour has permitted the developmentof very effective harvesting techniques. With modem fish-finding equipment,harvesting can remain profitable even at low stock levels. Open accessexploitation of a number of schooling species has caused severe stock depletion(Murphy, 1977). The question of possible stock extinction thus takes on specialimportance for schooling species.In the second section we shall develop a deterministic model for an openaccess fishery based on Smith (1968) and give a characterizationof open accessequilibrium. In the following section open access exploitation of North Seaherring during the period 1963-77 will be analysed. Alternative productionfunctions are considered and estimated for the Norwegian purse seine fishery.The bionomic equilibrium and approach dynamics are presented when pricesand costs are changing. Finally, the work is summarized and some policyimplications are discussed.THE OPEN ACCESS MODELIn this section we construct a simple open access model to discuss steady state(equilibrium) conditions and system dynamics. The model will be specified indiscrete time as a system of difference equations. Timne s partitioned intoannual increments, a procedure consistent with the data used to estimateproduction and growth functions and the equation for capital (vessel)dynamics. It is also consistent with the observation that vessel owners arereluctant to incur the cost of regearing once a decision has been made to enterthe herring fishery which, in the North Sea, has a season running from Mayuntil September. While the steady state equilibria for differential equationsystems and their difference-equation analogues are usually equivalent, thestability and thus approach dynamics can be qualitatively different.The distinction becomes more than a mathematical curiosity in resourcesystems, where discrete-time and possibly lagged adjustment to biological andeconomic conditions can lead to overshoot and greater potential foroverharvest and possibly species extinction.The model presumes an industry production function

    t= H(Kt, St), (1)where Y is yield (harvest) in year t, Kt are the number of vessels in the fisheryduring year t, and St is the fishable stock at the beginning of year t.The number of vessels, Kt, may be a crude measure of actual fishing effort.In demersal fisheries the best measure might be the volume of water 'screened'by nets during the season (Clark, 1985). However, in a fishery on a schooling

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    76 Trond Bj0rndal and Jon M. Conradspecies like herring, search for schools of herringis of predominant importance.Accordingly, in such fisheries the number of participating vessels may be anappropriate measure of effort.For schooling stocks, like herring, there is some question as to 'elasticity' ofyield with respect to stock size, St. If as a population declines it continues toconcentrate in (fewer) schools of the same approximate size, and if theseschools can be located with relative ease by electronic search, then yield may beessentially determined by effort, independent of stock, until the populationdeclines to a small number of schools. If this were the case, the produc-tion function H(Q)might depend strictly on Kt, and catch per unit effort, oftenused to estimate stock, would not predict the collapse of the fishery (Clark andMangel, 1979; Ulltang, 1980).Assuming that vessel numbers are an appropriate measure of effort and thatyield is stock dependent, the standard open access model proceeds by definingindustry profit (net revenue) in year t as

    t = pH() - cKt, (2)where p and c are the per unit price for yield and cost per vessel, respectively.Two additional assumptions are implicit in equation (2). First, the fishery mustbe one of several sources of the species in question; otherwise price woulddepend on yield, that is, pt = p(t) where p() is an inverse demand function.Cost per vessel is also assumed given. Second, the unit prices and costs areassumed constant through time. Neither assumption is likely to hold in 'realworld' fisheries, but theirmaintenance permits the estimation of an open accessor bionomic equilibrium, which may give an indication of the extent ofoverfishing.Vessels are assumed to enter a profitable fishery and exit an unprofitablefishery according to

    Kt+- Kt = n7Tt (3)where n > 0 is an adjustment parameter (unit: vessels/ ). With n positive, itwill be the case that (a) Kt?I > Kt if 7Tt > 0; (b) Kt+I < Kt if 7Tt < 0;and(c) Kt,I = Kt f7Tt = 0. It is possiblethattheratesof entryand exit maydiffer, in which case n+ might apply if 7Tt> 0 and n might apply if 7Tt< 0where n+, n- > 0, n+ t n.Finally, the resource stock is assumed to adjust according to

    vSt+1 - St = F(St) - H(Kt, St), (4)where F(St) is a net natural growth function. It is often assumed that thereexist stock levels S and S where F(S) = F(S) = 0, F(S) < 0 for 0 < S < S,F(S) > 0 for S < S < S, and F(S) < 0 for S > S.Taken together equations (3) and (4) constitute a dynamical system (or aniterative map). More specifically, with given values for So and Ko the system

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    Dynamics of an open accessfishery 77

    K,+l= K, + n[pH(Kt,St) -- cKt] (5)St + = St + F(St) - H(Kt, St)

    can be iterated forward in time. The trajectory (St, Kt) may be plotted inphase-space. A stationary point (S, K) is one for which K,t l Kt = K andSt+ -= St = S for all future t. Such a point must satisfy K pH(K, S)/cand H(K, S) = F(S).For the Gordon-Schaefer model (Clark, 1976) where F(S,) = rS,(l - St/L)and H(Kt, St) = qKtSt,the differential equation system takes the form

    K = n(pqKS - cK) (6)S =rS(l - S/L) - qKS,where r is the intrinsic growth rate, L is the environmental carrying capac-ity, and q is the catchability coefficient. The system has an equilibrium at

    ScO< c/(pq) and K,, = r(l - S,/L)/q, which is the focus of a stable spiral(see figure la). The difference equation analogue might be writtenKt+l -[1 + n(pqSt - c)]Kt (7)St+l = [1 + r(1 - St/L) - qKt]St,

    and is capable of more complex behaviour, including limit cycles (seefigure 1b).1THE NORTH SEA HERRING FISHERY 1963-77

    The North Sea herring fishery takes place in the central and northern NorthSea, with the main season in the months May to September.In the present casestudy data for the Norwegian purse seine fleet will be used to estimateproduction functions and vessel dynamics. The fishery, utilizing this technolo-gy, started in 1963. In the middle of the 1970s, however, the stock was severelydepleted under an open access regime and the fishery was closed at the end of1977. Severe regulations have been in effect ever since to allow the stock torecover.Table 1 contains data on stock size, Norwegian purse seine harvest and thenumber of Norwegian purse seiners for the period 1963-77. Other countries(Denmark, the Netherlands, Germany, and the United Kingdom) were alsoharvesting the herring stock using a variety of gear, including single and pairI For system (6) with S. = c/(pq) > 0 and K,, = r(l - S,/L)/q > 0 the open accessequilibrium is stable (a node or spiral) and limit cycles are precluded by the Bendixon-duLac test (see Clark, 1976, 203-4). For the difference equations in system (7), simulation forp = 1,000, c = 3,000, q = 3.8 X 10 5, n = 0.0001, r = 0.5, and L = 250,000 fromSO = 250,000 and Ko = 1,000, results in a convergent spiral. Changing n to 0.000175 leadsto a limit cycle and with n = 0.000175 and r = 2.6, ceteris paribus, an invariant circle isobtained. The difference equation system, with its inherent lag, is capable of much morecomplex, possibly 'chaotic' behaviour.

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    78 Trond Bj0rndal and Jon M. Conrad

    K0 ~ ~ ~ =

    8~~~~~~~~=

    K=O ~ ~ ~ S=

    SS =c/(pq)FIGURE I a: Phase plane analysis of system (6). The point (S., K.) is the focus of a stablespiral.

    K

    Cy)

    L S.

    SOO=c/(pq)FIGURE Ib: Phase plane analysis of system (7). The point (S., K.) is the focus of a limit cycle.

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    Dynamrics of an open access fishery 79

    TABLE INorth Sea herring stock, Norwegian purse seine harvest, and the number of Norwegian purseseiners

    Stock size Norwegian harvest Number of participatingYear S, (tonnes) Y (tonnes) purse seiners K,1963 2,325,000 3,454 81964 2,529,0)00 147,933 1211965 2,348,000 586,318 2091966 1,871,000 448,511 2981967 1,434,000 334,449 3191968 1,056,000 286,198 3521969 696,000 134,886 2531970 717,000 220,854 2011971 501,000 210,733 2301972 509,000 136,969 2031973 521,000 135,338 1531974 345,000 66,236 1651975 259,000 34,221 1021976 276,000 33,057 921977 166,000 3,911 24SOURCE: Bjo0ridal 1984)trawl and drift nets. After 1963, however, the purse seine technology becamethe dominant gear, and lacking data on the number and harvest of other geartypes, we used the Norwegian purse seine data to estimate parameters forseveral alternative production forms. The stock estimates (S,) were obtained byvirtual population analysis (Ricker, 1975). Unrestricted OLS regressions wererun, and table 2 shows four estimating equations (a)(i)-(d)(i) and fourassociated production functions (a)(ii)-(d)(ii). The exponents on K, in (a)(ii)and (b)(ii) would indicate a yield/vessel elasticity greater than one. This ispresumably the result of economies of scale in searchingfor schools of herring,since information about locations of schools tends to be shared between boatsin this fishery. The yield-stock elasticity in (b)(ii) and (d)(ii) are bothsignificantly positive and less than one. Thus, as stock declines, catch per vesselwill decline and there will be a stock-dependent incentive to exit from theindustry, as indicated by the rather rapid departure of Norwegian purse seinersfrom the fishery after 1968. The remaining vessels, however, seemed more thanadequate to continue harvest in excess of natural growth and recruitment, andfrom inspection of table 1 it is still not clear whether exit would have beenrapid enough for the stock to increase.The expression for profits was specified as

    7Tt = ptH(Kt, St) - ctKt, (8)where c, = et`Zt+ ft; e, is the average number of days spent fishing herring, ?i, isthe operating cost per day in year t, andf, are the fixed and opportunity costsincurred during the herring season.

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    80 Trond Bjorndal and Jon M. Conrad

    TABLE 2Estimates of production function parametersfor the Norwegian purse seine fleet; all regressionsOLSwith t-statistics in parenthesesa(a)(i) In , = 4.5408 + 1.4099 In K, (adjusted R2 = 0.85)(5.86) (9.11)

    (ii) }; =93.769 K,'4'(b)(i) In Y = -2.7876 + 1.3556 In K, + 0.5621 In S, (adjusted R2 0.96)(2.11) (16.39) (5.84)

    (ii) = 0.06157 Kt1356s 0.562(c)(i) In (S, - Yt)= -0.5683' + 1.0398' In S, - 0.0011 K, (adjusted R2 0.99)(1.29) (30.81) (3.74)

    (ii) t = S,t( - (--.OI IK,)b ~~~~~~~~~~~~~2(d)(i) In (t K,) -1.6718 + 0.6086 In S, (adjusted R = 0.54)(0.84) (4.16)

    (ii) ; X0.609( Autocorrelation was indicated only in equations (a) and (d). First-order correction did not

    significantly alter the magnitude of the estimated coefficients. Two-stage least squares didnot indicate the presence of simultaneous equations bias which can occur if estimates of St arebased on current period harvest. This is less of a problem when stock estimates are obtained byvirtual population analysis.Not significantly different from zero; parameterassumed to be zero in the associated productionfunction.Not significantly different from 1.00; parameter set equal to one in the associated productionfunction.

    Vessel dynamics were assumed to occur according toKt+I -KtK n7,/(pK,). (9)

    Equation (9) assumes that entry or exit will depend on the sign of normalizedprofit per boat. This form was employed to take advantage of previous analysisby Bj0rndal and Conrad (1985). Estimates of n ranged between 0.08 and0.10.A discrete-time analogue to the logistic growth function might be writtenasSt+, - St = rSt(l -StIL), (10)where estimates of r and L were 0.8 and 3.2 X 106 metric tonnes. Equation (10)is an approximation to a more complex delay-difference equation discussed inBj0rndal (1984).Of the four production models the Cobb-Douglas form t = aKbStresulted in the most plausible values for the bionomic equilibrium and openaccess dynamics. The open access system may be written as

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    Dynamics of an open accessfishery 81

    TABLE 3Costs (per season per vessel) and herring price (per tonne); figures in Norwegian kroneraYear Ct Pt1963 190,380 2321964 195,840 2031965 198,760 2051966 201,060 2141967 204,880 1411968 206,800 1281969 215,200 1851970 277,820 2621971 382,880 2441972 455,340 2141973 565,780 3841974 686,240 4981975 556,580 7351976 721,640 8531977 857,000 1,415a Price figures have been adjusted by a factor of 0.6, which represents the boat owner's share ofincome. Costs cover only costs incurred by the boatowner.

    SOURCES: p,: The Directorate of Fisheries, NorwayCt:The Budget Committee for the Fishing Industry, Norway

    Kt+ I = Kt + n (aKb- St9 -- Ct/Pt)St+] = St + rSt(l - St/L) - aKt(SgIf ct = c and p = p, then one obtains the following equations for thebionomic equilibriumSO = [c/(paKoo1 (I 12)Koo = [rS00(l - S./L)/(aSo.g)) Ib(1

    While it is not possible to solve for explicit expressions for SOO nd Koo it ispossible to solve for SOOnd Koonumerically. By making an initial guess forKoo,the first equation in (12) provides a value for SO. Substituting this valueinto the second equation one obtains a value for K.0, consistent with growthand yield. Calling the initial guess ZO, one can evaluate 1Z0 - K.J. If this isnot within an arbitraryE,readjust the guess according to Z. = (ZOO KJ)/2.This process will converge to the bionomic equilibrium from above orbelow K,.During the period 1963-77 prices and costs were changing as indicated intable 3. If the 1975 values of c = 556,580 and p = 735 (both in Norwegiankroner) were somehow fixed into the future and all other parametersremainedunchanged, then the bionomic equilibrium is calculated at S,, = 430,191(tonnes), K.0 = 393 (boats), and Y. = 297,887 (tonnes). When c, and p, areallowed to vary as per table 3, the time paths for St and K, are given in table 4

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    82 Trond Bj0rndal and Jon M. Conrad

    TABLE 4Bionomic equilibrium and open access dynamicsSystemKt+ = Kt + n (aKb Stg - C'/pt)St+ I = St + rS,(1 - St/L) -aKt StParanmeteraluesa = 0.06157, h = 1.356, c = 556,580, g = 0.562L = 3,200,000, a7= 0.1, p = 735, r = 0.8Biononlic equilibriunmSO = 430,191, Koo= 393, YO = 297,887Open access dnanihicsWith c, and p, as given in table 3, S( = 2,325,000, Ko 120, thenYear St Kt1963 2,325,000 120 153,6981964 2,679,895 166 258,5311965 2,769,820 225 398,3761966 2,669,323 305 588,8741967 2,434,586 404 818,5641968 2,081,887 461 897,0771969 1,766,756 494 898,0251970 1,501,779 559 970,0031971 1,169,363 626 983,0511972 779,950 626 782,754a1973 469,075 538 479,2321974 310,096 480 325,0611975 209,071 410 210,2871976 155,113 385 163,5801977 109,609 343 115,016a After 1972 harvest exceeds St but n7ot S, plus growth. This is possible, since growth to theresource occurs before harvesting (see equation for S,+ 1,above).and plotted in phase-space in figure 2. The values for Ktmight be interpreted asan estimate of 'purse seine equivalents' fishing herring in the entire North Sea.Thus Kt is larger than the number of Norwegian purse seiners that participatedin the fishery during the period. The stock actually increases until 1965 andthen decreases monotolically. The estimates of the herring stock in table 1 area bit more ragged, lower than the simulated estimates until 1973 and higherthereafter. Of particular interest is the overshoot 'past' the 1975-basedbionomic equilibrium and the continued decline in stock. In contrast to theresults of Wilen, there is no increase in the stock and the 'first loop' of aconvergent spiral has not been completed.In 1977 Norway and the EEC agreed to close the fishery. There are no official

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    Dynamics of an open accessfishery 83

    K700

    ) 600-'2)'2) 500-0 -1975\E 400-- (SOKO

    300-0CI)o 200-< 1963O 100-

    ~~~~~~~~~~ S0 0.5 1 1.5 2 2.5 3

    HERRING TOCK(million onnes)FIGURE 2. Simulation of North Sea herring fishery.prices nor data to estimate costs after this year. One can only speculate whatthe future evolution of stock and vessel numbers would have been. It seemsentirely plausible that with declining harvest, relative price increases wouldhave exceeded relative cost increases with species extinction the result. If theprice in 1978 were increased to 2,000 NoK/metric tonne and costs held steady,the species 'simulates' to extinction in 1983. Under the moratorium whichlasted until 1981 the stock was allowed to recover, and fisheries scientistsestimated the 1983 stock level at 600,000 metric tonnes.CONCLUSIONS AND POLICY IMPLICATIONSIn the empirical analysis of open access systems it is important to note that

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    84 Trond Bj0rndal and Jon M. Conradnon-linear difference equations, with or without longer lags, are capable ofmore complex dynamic behaviour than their continuous-time (differentialequation) analogues. The lag in adjustment by both the exploited species andthe harvesters themselves is often a more accurate depiction of dynamics,and the differential equation systems are best viewed as theoretical approxima-tions.If adjustment in an open access system is discrete, there is a greaterlikelihood of overshoot, severe depletion, and possibly extinction. Whendiscrete adjustment takes place in a system where the species exhibitsschooling, declining stocks may fail to reduce profits rapidly enough to turn thecritical 'first corner' in an approach to bionomic equilibrium. The fact thatthe economic and natural environments are subject to fluctuations placesgreater importance on modelling the dynamics of non-autonomous systems asopposed to the calculation of equilibria based on long-run or average values.The analysis of the North Sea herring fishery would seem to support manyof the above points. During the 1963-77 period the resource (1) was subject toopen access exploitation by Norway and members of the EEC; (2) exhibited aweak yield-stock elasticity (because of schooling) which failed to encouragea rapid enough exit of vessels from the fishery; and (3) was saved from moresevere overfishing and possibly extinction by the closure of the fishery at theend of the 1977 season.Recent analysis by Bj0rndal (1985) indicates that the optimal stock level islikely to be in the range 1.0-1.4 million tonnes, supporting a harvest of550,000-600,000 tonnes. With the recovery of the resource, the stock might beinitially managed through a system of internationally assigned but intranation-ally transferable quotas. In the longer run a system allowing fisheries managersfrom one country to purchase or lease the quota rights of another shouldpermit the total allowable catch (TAC) to be harvested at least cost. The theoryand institutions for the management of transboundary resources are still at anearly stage of development, but likely to be of critical importance if the value offisheries resources are to be maximized among coastal countries.REFERENCES

    Berck, P. (1979) 'Open access and extinction.' Econometrica47, 877-82Bj0rndal, T. (1984) 'The optimal management of an ocean fishery.' Unpublished PH Ddissertation, Department of Economics, University of British Columbia(1985), 'The optimal rmanagementof North Sea herring.'Working PaperNo. 2/1985, Centre for Applied Research, Norwegian School of Economics andBusiness Administration, BergenBjorndal, T. and J.M. Conrad (1985) 'Capital dynamics in the North Sea herringfishery.' Working Paper No. 01/85, Institute of Fisheries Economics, NorwegianSchool of Economics and Business Administration, BergenClark, C.W. (1976) MathematicalBioeconomics: The OptimalManagement ofRenewableResources(New York: Wiley)

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    Dynamics of an open access fishery 85

    - (1982) 'Concentration profiles and the production and management of marinefisheries.' In W. Eichhorn, et al. eds, Economic Theory of'Natural Resources(Wurzburg: Physica Verlag)- (1985) BioeconomicModelling and Fisheries Management (New York: Wiley)Clark, C.W. and M. Mangel (1979) 'Aggregation and fishery dynamics: a theoreticalstudy of schooling and the purse seine tuna fisheries.' Fishery Bulletin 77, 317-37Hartwick, J.M. (1982) 'Free access and the dynamics of the fishery.' In L.J. Mirmanand D.F. Spulber, eds, Essays in the Economics of'RenewableResources(Amsterdam, New York, Oxford: North-Holland)Murphy, G.I. (1977) 'Clupeids' In J.A. Gulland, ed., Fish PopulationDynamics (NewYork: Wiley)Ricker, W.E. (1975) Computationand Interpretationof Biological Statistics of'FishPopulations(Ottawa: Environment Canada)Smith, V.L. (1968) 'Economics of production from natural resources.'AmericanEconomicReview 58, 409--31

    -(1975) 'The primitive hunter culture, Pleistocene extinction, and the rise of agricul-ture.' Journal of'Political Economy 83, 727-55Ulltang, 0. (1980) 'Factors affecting the reactions of pelagic fish stocks to exploita-tion and requiringa new approach to assessment and management.' Rapp. P.-VReun. Cons. Int. Explor. Mer. 177, 489-504Wilen, J.E. (1976) 'Common property resources and the dynamics of over-exploita-tion: the case of the North Pacific ful seal.' Paper No. 3 in the ProgrammeinResource Economics, Department of Economics, University of British Columbia