Diminishing infectious animal disease prevalence amounts to a
global public good. This has in part motivated the long tradition of
public involvement in infectious animal disease control. But
appropriately designed public intervention requires a clear
understanding of failure in private incentives.
Two important features of communicable disease are spatial spread
and the possibility of costly private actions to reduce spread. In
addition, since routine biosecurity actions by growers are typically
costly to verify by veterinary authorities, voluntary compliance is
often essential. To this end, growers must recognize the consequences of
their actions and must have adequate incentives to take socially
desirable actions. The intent of this article is to provide a better
understanding of private incentives to protect against the spread of
infectious animal disease. We do so by developing a model that
emphasizes spatial relations in infection, prevention technology, and
externalities across agent payoffs.
The economics literature on public goods aspects of animal diseases
is limited. Indeed, a surprisingly small body of work exists on the
economics of infectious human diseases (Gersovitz and Hammer 2004).
Animal diseases have been the subject of formal models (Chi et al.
2002), but the issue generally addressed is that of internal costs and
not how farms inter-relate. A strongly related theme is that of
controlling invasive species. Economic perspective on this issue is
expanding, but has been confined largely to quarantine (Mumford 2002)
and other public behaviors given an assumed exogenous stochastic dynamic
process for infection (Olson and Roy 2002).
The direction in Hennessy, Roosen, and Jensen (2005) is closest to
that in the present work. While theirs is not a spatial model, the
biosecuring decisions involve whether to trade in young stock and the
extent of production. Private benefits from trade are shown to lead to
socially excessive losses from an endemic communicable disease.
Furthermore, communicable disease is shown to alter the format and scale
of production.
This article emphasizes protecting a farm's borders in a
spatial model of private behavior to prevent the spread of infection.
For farms arranged on a circle, we show how biosecuring actions are
local substitutes and explain what this means for behavioral patterns
under simultaneous-moves Nash equilibrium. Two insights obtained are
that losses from disease-spread externalities are smaller when
production is concentrated, and subsidies to small producers may
exacerbate overall disease losses. We also consider a line topology for
farms in order to show how the model can be adapted, and how locational
asymmetries can affect incentives to protect farm boundaries. We find
that more centrally located farms, which are more vulnerable, will take
more care than other farms, all else equal. But they may not adopt
enough protective measures for the social good. More isolated farms take
less care, all else equal, but over protect.
Circle Topology
A region has N [greater than or equal to] 3 farms labeled n [member
of] {1, 2, ..., N} = [[OMEGA].sub.N], where each seeks to protect
potential production to the value of [V.sub.n] > 0. The N [greater
than or equal to] 3 assumption on the extent of the outbreak is
convenient, but could be relaxed at only the cost of substantially more
tedious algebra. An infected farm loses all of [V.sub.n]. The farms are
located on a circle (see figure 1). The circle topology was chosen
because farms are located symmetrically on it. It enables a
consideration of many of the article's main points but not the role
of location asymmetry. Location asymmetry issues are examined in a
separate section using a line spatial structure.
[FIGURE 1 OMITTED]
Infection is rare and can enter the region at some farm with
probability [theta], where each farm is equally likely to be the first
infected. By "rare" we mean it is almost certainly true that
at most one farm inside the region becomes infected from outside the
region at any time. The first farm to be infected within a region is
labeled as the "originating farm." It will also be assumed
that public authorities intervene to suppress a disease outbreak after
the disease spreads to no more than the most proximate two farms
(clockwise), if indeed it spreads at all. We allow infection to occur
only in one (arbitrarily, the clockwise) direction to simplify algebra.
Condition N [greater than or equal to] 3 was imposed to avoid
double-counting on the circle, where the disease spreads clockwise back
to the originating farm. The case where infection occurs in both
clockwise and anticlockwise directions is available upon request.
Farm-level care taking is modeled through actions taken at the farm
border. If infection has reached its direct anticlockwise neighbor, the
nth farm will become infected with probability [a.sub.n]. The grower can
change this probability at a cost. The nth farm is said to take
comparatively less care when the value of [a.sub.n] is comparatively
high. Before representing the cost of reducing probability [a.sub.n],
consider the expected revenue loss.
Farm 1 may be the first infected, where the probability of first
infection is [theta]. Or it may contract the disease from its neighbor.
Anticlockwise is farm N. If farm N is infected first, then farm 1
becomes infected through farm N with probability [theta][a.sub.1]. The
originating farm's probability does not enter the calculation
because we assume a farm has no incentive to try preventing the disease
from exiting the farm. Farm N - 2 may also be the source of infection to
farm 1, where the probability this occurs is [theta][a.sub.1][a.sub.N].
Since infection is rare, the overall probability that farm 1 is infected
is approximately [theta] + [theta][a.sub.1] + [theta][a.sub.1][a.sub.N].
In order to develop a general expression for each farm's
infection risk, define [n + i] = n + i - zN where z is an integer chosen
such that [n + i] [member of] [[OMEGA].sub.N]. That is, clock algebra
(also called modular algebra) is used. For the nth farm, the infection
probability is approximately
[[omega].sub.n] = [theta] + [theta][a.sub.n] +
[theta][a.sub.n][a.sub.[n-1]]. (1)
The overall expected loss in revenue to the region is [MATHEMATICAL
EXPRESSION NOT REPRODUCIBLE IN ASCII].
Finally, a prevention technology exists. Farms differ in their
capacity to protect themselves, and the protection cost at entry
probability level [a.sub.n] is [C.sup.n]([a.sub.n]), a decreasing
function. Private profit to a farm is [L.sub.n] = [V.sub.n] - [V.sub.n]
[[omega].sub.n] - [C.sup.n]([a.sub.n]), while the overall expected
profit to the region is [MATHEMATICAL EXPRESSION NOT REPRODUCIBLE IN
ASCII]. The region is assumed to produce a small share of overall market
output, so that consumer surplus may be ignored. Thus, L represents
social surplus. Since actions by farm [n - 1] enter [L.sub.n] through
[[omega].sub.n], externalities exist and one should not expect market
competition to support the maximization of L.
In order to better understand protection incentives, the nth
farm's cost of protection is posited as
-[[alpha].sub.n]Ln([a.sub.n]) where [[alpha].sub.n] > 0. This ensures
that the cost of not protecting at all is -[[alpha].sub.n]Ln(1) = 0,
while the cost of complete protection--where [a.sub.n] = 0--is infinite.
This, we believe, reflects reality to the extent that not protecting at
all requires no expenditure, complete protection is prohibitively
expensive, and the protection cost increases with the extent of
protective action.
Private Incentives and Responses
The nth farm's profit is
[L.sub.n] = [V.sub.n] - [V.sub.n][[omega].sub.n] + [[alpha].sub.n]
Ln([a.sub.n]), n [member of] [[OMEGA].sub.N]. (2)
Substituting (1) into (2) and differentiating, we obtain [[partial
derivative].sup.2][L.sub.n]/[partial derivative][a.sub.k] [partial
derivative][a.sub.s] [less than or equal to] 0 [for all] k, s [member
of] [[OMEGA].sub.N], k [not equal to] s. Thus, an increase in care by
the nth farm reduces the marginal net benefit of own care by farms other
than the nth. This leads to the following:
PROPOSITION 1. If the probability of infection is as given in
equation (1), then farm biosecurity actions to prevent the spread of
infection are strategic substitutes.
This observation shows that the game being played is not of the
type involving global strategic complementarities (Vives 2005). (1)
Given substituting strategic interactions, the possibility exists for a
public intervention to do harm by indirectly discouraging important
actions while directly encouraging less important actions.
With Nash conjectures on payoffs (2), protective actions are chosen
as solutions to
[partial derivative][L.sub.n]/[partial derivative][a.sub.n] = -
[theta] [V.sub.n] (1 + [a.sub.[n-1]]) + [[alpha].sub.n]/[a.sub.n] = 0.
(3)
Solutions are denoted by [a.sup.*.sub.n]. The system is illustrated
for N = 3, so that profits are
Farm 1: [V.sub.1] - (1 + [a.sub.1] +
[a.sub.1][a.sub.3])[theta][V.sub.1] + [[alpha].sub.1] Ln([a.sub.1])
Farm 2: [V.sub.2] - (1 + [a.sub.2] + [a.sub.1][a.sub.2])[theta]
[V.sub.2] + [[alpha].sub.2]Ln([a.sub.2])
Farm 3: [V.sub.3] - (1 + [a.sub.3] + [a.sub.2][a.sub.3])[theta]
[V.sub.3] + [[alpha].sub.3]Ln([a.sub.3]). (4)
From (3), ith farm Nash private conjectures are given by
[a.sup.*.sub.i] + [a.sup*.sub.i][a.sup.*.sub.[i-1]] = [[lambda].sub.i]
where [[lambda].sub.i] = [[alpha].sub.i]/[[theta][V.sub.i]]. The unique
pure strategy interior solution is (2)
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