An Island Geographical Approach to Island Tourism and Biodiversity
Transcript of An Island Geographical Approach to Island Tourism and Biodiversity
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An Island Biogeographical Approach to IslandTourism and Biodiversity: An Exploratory Study of
the Caribbean and Pacific Islands
C. Michael Hall1–3∗1Department of Management, University of Canterbury, Christchurch, New Zealand
2Department of Geography, University of Oulu, Oulu, Finland3Linnaeus University School of Business and Economics, Kalmar, Sweden
Islands are especially susceptible to the loss of indigenous species following anthropogenicchange. Although tourism has long been cited as a justification for conserving biodiversityvia the establishment of national parks and reserves, it also contributes to biodiversity lossas a result of direct habitat change and human activities, as well as more indirectly via theintroduction of exotic species and environmental change. An island biogeographical approach is used to provide an exploratory analysis of tourism and biodiversity relation-ships in the Caribbean and Pacific Islands. Data suggest that the islands are under heavyanthropogenic pressure, of which tourism is just one element, although for some countries
tourism represents a substantial real increase in the size of the human population. Few of the countries examined have anywhere near the recommended percentage of area pro-tected, with marine ecosystems being least conserved. The study concludes that there aresignificant data gaps for examining tourism and biodiversity relations at the national level, but suggests that island biogeographical approaches may yield significant insightsinto the pressures of tourism on biodiversity at smaller scales if adequate data can be gained.
Key words: island biogeography, biodiversity, tourism, conservation, Caribbean, PacificIslands
Introduction
Islands have long played a pivotal role in
the understanding of natural processes. For
example, the Galapagos Islands have long been
recognized as a significant source of inspiration
for Darwin’s theory of natural selection and
continue to be an important natural history
research site, and tourist attraction, to the
present day. One of the most significant
Asia Pacific Journal of Tourism Research, Vol. 15, No. 3, September 2010
∗Email: [email protected]
Asia Pacific Journal of Tourism Research, Vol. 15, No. 3, September 2010
ISSN 1094-1665 print/ISSN 1741-6507 online/10/030383–17# 2010 Asia Pacific Tourism Association
DOI: 10.1080/10941665.2010.503628
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contributions of islands to the understanding of
the richness of biodiversity for ecological com-
munities is the concept of island biogeography,
which examines the relationships between
species and a given area (MacArthur &
Wilson, 1963, 1967; Preston, 1962). The con-ventional expression of the species– area
relationship is S ¼ CAz, where S and A are
species count and area, respectively, and C and
z are fitted species-specific constants. However,
significantly for the wider applicability of the
species–area relationship, an “island” can be
regarded as any area of suitable habitat that is
surrounded by unsuitable habitat, for instance
a national park surrounded by agricultural
land. Therefore, the concept has importantimplications for conservation reserve design
and broader strategies to conserve biodiversity.
This article seeks to examine the implications
of island biogeographical theory with respect
to understanding some of the possible effects
of tourism on the biodiversity of small island
economies as well as the potential relationship
between island biogeographic theory and
steady-state approaches of ecological econ-
omics. The article is divided into three main
sections. First, a discussion of island biogeo-
graphic theory and its potential connections to
sustainable tourism and biodiversity conserva-
tion; second, an exploratory study of tourism
and biodiversity conservation on small island
economies; and finally, a series of observations
with respect to the need to integrate better bio-
geographical and ecological economic insights
into the development of sustainable tourism
research and biodiversity conservation strategies
for islands and equivalent areas.
The Theory of Island Biogeography
The number of species that are found on an
island depends on a number of factors,
including its area and topography, diversity of
habitats, shape, spatial and temporal isolation,
connection to previous landmasses, climate,
accessibility to its source of colonists (i.e. not
just distance to nearest source region but
location relative to ocean currents), and theequilibrium rate of colonization by new
species and the rate of extinction of existing
species (Cox, Healey, & Moore, 1973). The
equilibrium model of the biota of a single
island proposes that the equilibrial species
number is reached at the intersection between
the curve of the rate of new species immigration,
not already on the island, and the curve of
extinction of species on the island (Figure 1).
The model therefore suggests that althoughfluctuations will occur over time, there is a
finite limit on the species biodiversity of a
given area. This is significant in conservation
terms as, because every species runs the risk of
extinction, “the more that have arrived the
more species there are at risk. In addition, as
more species arrive, the average population
size of each will diminish as competition
increases” (Cox et al., 1973, p. 98).
As noted in the Introduction, McArthur and
Wilson (1963, 1967) concluded that for a
particular taxon and within any given region
of relatively uniform climate, the island
species –area relationship can be approxi-
mated by the power function model:
S = CAz
where S and A are species count of a given
taxon and area, respectively, and C and z are
fitted species-specific constants that will varyfrom system to system. MacArthur and
Wilson favoured logarithmic transformations
of both axes thereby enabling the constants C
and z to be determined by least squares
(linear) regression (Whittaker & Ferna ´ndez-
Palacios, 2007). MacArthur and Wilson
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(1967) found that in most cases z falls between
0.20 and 0.35 for islands. The model is highly
significant in that, even though it has heuristic
value without it, the contribution of the
theory to biogeography and conservation
biology provides a high degree of rigour with
respect to dynamic modelling of ecological
and biological population processes. As Brown
and Gibson (1983, p. 449) stated, “like any
good theory, the model goes beyond what isalready known to make additional predictions
that can only be tested with new observations
and experiments”, a situation that has led to a
significant reformulation of some of the
notions of equilibrium and species and island
difference (e.g. Brown & Lomolino, 2000;
Lomolino, 2000), as well as the importance of
anthropogenic and other disturbance. Indeed,
as Wilson (2001, p. viii) himself noted, “after
more than three decades, [the theory of island
biogeography] has been largely replaced by a
generation of far more detailed and sophisti-
cated studies. Yet I believe that its basic struc-
ture remains sounds, and the content still
serves as a good introduction to the subject”.
Lomolino (2000) has argued for a tripartitemodel of island biography that illustrates the
three fundamental biogeographic processes
of immigration, extinction and evolution as a
function of island characteristics of area and
isolation (Figure 2). Under such a model immi-
gration rates should increase with proximity
Figure 1 Equilibrium Model of the Biota of a Single Island.
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to a source region and the ability of species to
travel or be transported across immigration
barriers and filters. Extinction rates should
decrease as island area increases, or increase
with growing resource requirements of the
focal species. Finally, speciation should be
most important where extinction and immi-gration are lowest, and therefore it increases
in relation to increase in island area and iso-
lation and decreases with respect to resource
requirements and the capacity of species to
move or disperse within their environments
(Lomolino, 2000). However, just as signifi-
cantly, the interrelationships between island
characteristics and biogeographical processes
provide for the relative resilience of islands
to disturbance, whether from natural events
such as storms and tide surges, or from anthro-
pogenic pressures such as tourism. In addition,
recognition of the relationships between acces-sibility, area size and resilience also has direct
parallels with the identification of wilderness
areas in which remoteness and naturalness
are key factors (Hall & Page, 2006).
In conservation terms the theory is important
because it highlights the need for retaining large
Figure 2 Interrelationships between Biogeographical Processes and Island Characteristics.
386 C. Michael Hall
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areas of relatively undisturbed environments in
order to save species from extinction. National
parks, conservation reserves and other relatively
undisturbed environments under public or
private ownership act as islands for a large
number of species. The breaking up of suchnatural areas as a result of land clearing, agri-
culture or other natural and human processes
therefore can lead to the creation of smaller
islands, with significant effects for species as
these new “islands” develop their new ecosys-
tem equilibrium. Such fragmentation effects
are most pronounced on larger species that
require large ranges; however, they can affect
many plant and animal species as habitat is
reduced and/or competition among individualsand between species is increased. As a result,
island biogeography theory has led conserva-
tionists to advocate for the retention of
natural areas that are as large as possible,
ideally with a high ratio of area to boundary
(Soule ´ & Simberloff, 1986). In addition,
where fragmentation has occurred or is una-
voidable efforts have been made to retain or
regenerate natural area corridors (also referred
to as habitat corridors) between reserves in
order to assist the movement of species
between reserves and therefore increase the
number of species that can be supported and
the opportunities for species survival (Dobson,
Rodriguez, Roberts, & Wilcove, 1997; Prender-
gast, Quinn, Lawton, Eversham, & Gibbons,
1993).
Studies of species– area relationships
suggest that 30–50% of a given community
or ecosystem type needs to be conserved to
maintain 80– 90% of the species (Groves,2003; Soule ´ & Sanjayan, 1998). However, in
their analysis of the conservation deficits for
the continental USA, Dietz and Czech (2005)
noted that even 30–50% may not be enough
to sustain species over the long term, with
research indicating that there is no single
threshold value that can be broadly applied
to conserve all species (Fahrig, 2001).
Although highly significant in conservation
ecology, the theory of island biogeography
has had relatively little influence on tourism
research except where there is a focus on thedesign of national parks and conservation
reserve areas that may attract visitors (e.g.
Newsome, Moore, & Dowling, 2002; Whit-
taker & Ferna ´ndez-Palacios, 2007) and, to a
very limited extent, with respect to the examin-
ation of the impact of tourism on island
environments (e.g. Go ¨ ssling, 2003). Although
perhaps not recognized by many students of
tourism, the theory of island biogeography
has also been extremely influential withrespect to the notion of the physical carrying
capacity of outdoor recreation land in terms
of the maximum number of people that can
use an area without an unacceptable change
in the environment or an unacceptable change
in perceived quality (Wall, 1999). Both carry-
ing capacity and the theory of island biogeo-
graphy suggest that capacity is the maximum
sustainable output of a system, i.e. that there
is an upper limit to the number of individuals
a population can reach in a closed environment.
Such ideas have also proved influential with
respect to broader concerns about the limits
to growth and sustainable development,
topics that also have significance in tourism
studies (e.g. Hall & Lew, 2009).
Tourism is an important element in the
maintenance of biodiversity for many islands,
both as a justification for conservation efforts
by virtue of being an attraction for visitors
interested in the natural environment (e.g.Christian, Potts, Burnett, & Lacher, 1996;
Go ¨ ssling, 1999), sometimes referred to as
ecotourism, and as a form of anthropogenic
disturbance (e.g. Go ¨ ssling & Hall, 2006;
Hall & Lew, 2009). For example, in the case
of islands tourism can: act as a means of
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transporting new species and diseases; directly
change and fragment habitat as a result of
developments such as golf courses, beaches,
marinas, roads and walkways and hotels;
and indirectly change habitats as a result of
requiring food for visitors, disturbinganimals, placing further demands on water
supply, as well as disturbing animals or tram-
pling plants. However, for many small island
economies tourism is often one of the few
means of development available, thereby
leading to increased attention as to how
tourism can become sustainable.
Sustainable tourism development is tourism
development without growth in throughput of
matter and energy beyond regenerative andabsorptive capacities (Hall, 2008). From such
a perspective the sustainability of tourism is
to be found in recognition of the high ecologi-
cal footprints of much tourism consumption
(Go ¨ ssling, Hansson, Ho ¨ rstmeier, & Saggel,
2002) and the need to adopt an approach
towards tourism development grounded in
ecological economics. Hall (2009) argues
that sustainable tourism needs to be under-
stood from a steady-state economic perspec-
tive that explicitly recognizes the extent to
which economic development is dependent
on the stock of natural capital. According to
Hall (2009), steady-state tourism is a tourism
system that encourages qualitative develop-
ment but not aggregate quantitative growth
to the detriment of natural capital. A steady-
state economy, including at the destination
level, can therefore be defined in terms of “a
constant flow of throughput at a sustainable
(low) level, with population and capital stockfree to adjust to whatever size can be main-
tained by the constant throughput beginning
with depletion and ending with pollution”
(Daly, 2008, p. 3). Such an approach therefore
recognizes that the human economy competes
with wildlife for use of scarce natural capital.
Figure 3 illustrates that natural capital (e.g.
soil, timber and water) is reallocated from
wildlife to humans in the process of economic
growth, thereby leading to species extinction
and threats. As the economy grows, the
natural capital comprising wildlife habitat(represented above the sigmoid curve) is con-
verted into goods and services in the human
economy (represented below the sigmoid
curve). K equals economic carrying capacity
(Czech, 2004).
The steady-state approach to tourism desti-
nations as well as the theory of island biogeo-
graphy suggests that there are limits to the
exploitation of natural capital. However,
time remains an important element in under-standing how anthropogenic change may
affect species immigration and extinction. As
Burt (2003) noted with respect to issues of
scale in the physical environment, in general
terms, short-term studies tend to focus on
process dynamics whereas longer-term
studies are more likely to involve statistical
analysis of form and structure. The temporal
and spatial scale at which studies are con-
ducted also has implications for understanding
causality (Schumm & Lichty, 1965). At the
shortest timescale, processes operate within
an essentially fixed environment. Over the
Figure 3 Competition for Natural Capital
between People and Wildlife.
388 C. Michael Hall
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longer term, properties that were fixed at the
shorter timescale now become variable. As
Burt (2003, p. 212) commented, “Process
now controls form and a ‘steady-state equili-
brium’ may be identified. Large events may
perturb the system but there is then recoveryto a characteristic form”.
It is widely recognized that human activity is
having a significant impact on the world’s
biodiversity, with a third of amphibians, a
quarter of mammals and one-in-eight birds
being threatened with extinction (BBC,
2009). Human activity can serve to fragment
existing natural habitat and change environ-
mental conditions so as to suit species that
are identified as economically desirable.Figure 4 combines the insights of island
biographic theory and steady-state economic
thinking to illustrate the way in which anthro-
pogenic change in island environments serves
to reduce the extent of natural capital avail-
able to indigenous species. The figure also
highlights that there is a need to differentiate
between the manner in which this process
occurs in human timescales as against under-
standing its operation in evolutionary time.
Arguably this process is occurring at the
moment, as island environments come increas-
ingly under pressure from human activities
(Quammen, 1997). The insights of island
biogeographical research may therefore have
significant implications for understanding the
impacts of tourism on island environments.
Tourism and Threats to Biodiversity in
Island Economies
The theory of island biogeography highlights
how human impact, including tourism, may
threaten the biodiversity of island environ-
ments in a relatively short period of time.
This section therefore examines some of the
small island economies that are most depen-
dent on tourism in order to ascertain potential
threats and issues with respect to biodiversity
conservation. Two main data sets are utilized.
For economic, population and tourism infor-
mation UNCTAD (2008) statistical data areused while biodiversity information is primar-
ily gained from the IUCN Red List of Threa-
tened SpeciesTM (see http://www.iucnredlist.
org/ ). Unfortunately, there are several gaps in
both sets of information as a result of lack of
national data gathering. Nevertheless, the
information that is available does provide for
an exploratory analysis of some of the poten-
tial relationships between biodiversity and
the significance of tourism for island states.For the purpose of this study, data from the
Caribbean and Pacific Island regions are
examined as not only is tourism of recognized
importance in these areas but the islands in the
two regions also share common climatic fea-
tures. The small number of countries exam-
ined highlights that any relationships found
should be noted with caution, but as noted in
the Introduction, the value of such exploratory
analysis is to highlight potential future paths
for research.
Table 1 provides information on the biodi-
versity status of a number of island territories
in the Caribbean and Pacific. Some territories
are not included in IUCN data as they are
regarded as overseas departments or territories
of continental countries such as France or the
USA. The table provides information on the
percentage of marine and terrestrial territory
that is protected and various categories of
threatened species. Unfortunately, changeover time of threatened species is only avail-
able for a limited number of categories of
animals (birds, mammals and amphibia), but
it is noticeable that most countries have had
an increase in the number of species in those
categories with threatened species status
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Figure 4 Anthropogenic Change and Reduction of Natural Capital in Island Environments.
390 C. Michael Hall
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Table 1 Biodiversity Status
Economy
Land
Area
% Area Protected Threatened Species (TS)
Marine Terrestrial Mammals Birds Amphibia Reptiles Fish Molluscs
Other
Inverts
Su
tota
(km2) 2008 2008 2004 2008 2004 2008 2004 2008 2008 2008 2008 2008 20
Caribbean
Bermuda 53.1 5.12% 14.43% 2 4 3 1 0 0 2 12 0 28
Anguilla 102 0.01% 11.04% 0 1 0 0 0 0 3 14 0 10
Montserrat 102 0.02% 10.39% 1 3 2 2 1 1 2 14 0 11
Aruba 193 0.00% 0.06% 1 3 1 1 0 0 2 15 0 1
Saint Kitts and Nevis 261 0.41% 5.06% 1 2 1 1 1 1 5 14 0 10
Cayman Islands 262 1.32% 58.00% 0 1 1 1 0 0 4 14 1 10
Grenada 344 0.01% 1.96% 1 3 1 1 1 1 4 15 0 10
Saint Vincent and the
Grenadines
389 0.31% 16.34% 2 2 2 2 1 1 3 18 0 10
Barbados 431 0.07% 0.11% 0 3 2 1 0 0 4 15 0 10
Antigua and Barbuda 442.6 0.77% 10.25% 1 2 1 1 0 0 6 14 0 11
Turks and Caicos
Islands
430 2.85% 28.48% 0 2 4 2 0 0 4 14 0 10
Saint Lucia 616 0.11% 18.53% 2 2 5 5 4 0 5 15 0 11
Dominica 754 0.09% 26.69% 1 3 3 3 2 2 3 15 0 11
Trinidad and Tobago 5,128 0.27% 35.00% 1 2 2 2 9 9 5 19 0 10
Jamaica 10,991 3.56% 20.90% 5 5 12 10 17 17 9 15 0 14
Bahamas 13,940 0.44% 11.37% 4 7 7 5 0 0 6 20 0 11
Pacific Islands
Cook Islands 236.7 0.04% 2.61% 1 1 15 15 0 0 1 7 0 25
Palau 458 8.74% 1.30% 3 4 1 2 0 0 2 12 5 97 1
Micronesia (Federated
States of)
702 0.03% 10.08% 6 6 8 9 0 0 3 13 4 104 1
Tonga 748 2.20% 25.53% 2 2 4 4 0 0 2 9 2 33
Kiribati 811 0.00% 55.01% 0 1 5 5 0 0 1 7 1 72
Samoa 2,944 1.34% 3.62% 3 2 7 7 0 0 1 8 1 52
French Polynesia 4,167 0.08% 1.07% 3 1 31 32 0 0 1 13 29 26 1
Vanuatu 12,200 0.05% 4.46% 5 8 8 8 0 0 2 11 1 78 1
Fiji 18,270 0.11% 2.16% 5 6 13 10 1 1 6 11 3 87 1
New Caledonia 19,060 0.22% 7.39% 6 9 15 14 1 0 2 17 11 84 1
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Table 1 Continued
Economy
Land
Area
% Area Protected Threatened Species (TS)
Marine Terrestrial Mammals Birds Amphibia Reptiles Fish Molluscs
Other
Inverts
Su
tota
(km2) 2008 2008 2004 2008 2004 2008 2004 2008 2008 2008 2008 2008 20
Solomon Islands 28,450 0.05% 0.76% 20 17 22 20 2 2 4 12 2 138 1
Papua New Guinea 462,840 0.45% 9.70% 58 41 32 36 10 11 9 38 2 167 3
Sources: Land area from CIA World Factbook. Percentage area protected derived from nationally designated protected areason Protected Areas (WDPA), a joint project of UNEP and IUCN, hosted and managed by UNEP-World Conservation Monito31, 2008. Threatened species figures for 2004 derived from Baillie et al. (2004), appendix 3j. The numbers of threatened spendemic per country for mammals, birds, amphibians, turtles, chondrichthyan fishes (elasmobranches), conifers and cycadspresent exclude uncertain occurrences and vagrants. These will therefore differ from figures obtained through a country seaThreatened SpeciesTM, which includes all countries listed within the species’ range. Threatened species figures for 2008 deriveSpeciesTM (2009), table 5. Number of threatened species in each major group of organisms in each country (critically endancategories only) (totals by taxonomic group); table 6a Red List Category summary country totals (animals); table 6b Red L(plants).
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from 2004 to 2008. In the Caribbean the pro-
portion of threatened animal species as a pro-
portion of all animal species in the country
ranges from a low of 6.6% in Trinidad and
Tobago to a high of 18.1% in Bermuda. The
proportion of threatened animal species ismuch higher overall in the Pacific Islands,
which range from a low of 14.8% for Tonga
to 22.4% for French Polynesia. Of the 16
Caribbean countries studied, only two (the
Cayman Islands and Trinidad and Tobago)
have over 30% of their land area set aside as
protected areas, although the Turks and
Caicos Islands, Dominica and Jamaica have
over 20% of their land area protected. In the
Pacific only Kiribati has set aside more than30% of its land area as protected area, while
Tonga has a protected area of just over 25%.
The proportion of protected marine area in
both regions is much lower than terrestrial
area. In the Caribbean, Jamaica has the
highest proportion of marine area set aside at
3.56% and in the Pacific, Palau has 8.74%
of its marine territory as protected area.
Table 2 sets out information with respect to
tourism and the small island economies of the
Caribbean and the Pacific and includes data
with respect to UNCTAD economic grouping,
population and tourist data in terms of
number of visitors and visitor expenditure.
Data on average length of stay are included
so as to provide a measure of the actual
annual population equivalent in real terms
(permanent population plus visitors) (see
Mu ¨ ller & Hall (2003) for further information
on this approach to population determination
in tourist regions; where no official figures areavailable for length of stay a surrogate period
of average length of stay for the region has
been used).
The data indicate that there is a reasonably
strong relationship between the terrestrial
area of the territory and the number of
threatened species (a correlation of 0.62 for
the Caribbean and 0.76 for the Pacific). A
relatively weak relationship between GDP and
number of threatened species was observed
for the Caribbean (0.44), although a stronger
relationship exists in the Pacific (0.77). Norelationship was seen to exist in terms of per
capita GDP. The extent of the relationship
between GDP and threatened species has been
briefly noted because of the extent to which
this relationship has been observed in other
studies (e.g. Czech et al., 2005; Dietz &
Adger, 2003), including with respect to the
extent that economic growth is meant to lead
to increased biodiversity (the so-called environ-
mental Kuznets curve) (Mills & Waite, 2009). Aslightly negative relationship was found in both
regions with respect to the relationship between
tourism’s contribution to the economy and the
number of endangered species.
For small islands the size of the human
population may have a significant impact on
biodiversity (McMaster, 2005). In both the
Caribbean and the Pacific there is a strong
relationship between population and the
number of endangered species for each terri-
tory, 0.91 and 0.76, respectively. Including
international visitors in the island population
(see Table 2) provides only a very marginal
increase in the strength of the relationship.
Table 2 clearly indicates the potential extra
impacts that visitors may have on island
environments by virtue of their consumption
and increased density, thereby leading to dis-
turbance and anthropogenic change. In the
case of Anguilla, the annual visitor numbers
are equivalent to a 30.5% increase in perma-nent population, whereas the Cayman
Islands is equivalent to a staggering 89%.
However, the figures indicated in Tables 1
and 2 are effectively only a single-shot analysis
of island biodiversity and tourism economies.
Instead, more dynamic approaches that plot
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Table 2 Tourism and Developing Small Island Economies
Economy
UNCTAD
Category
Population
Estimate
2006 (’000)
Visitor
Estimate
2006
(’000)
Visitors as %
of Population
(Annual
Basis)
Visitors as
Ratio to
Population
(Annual
Basis)
Average
Length of
Stay
(Days)
Equivalent
Additional
Population
per Annum
As %
To
Perm
Popu
Caribbean
Anguilla A 12 167 1,392% 1:13.92 8.0 3,660 30.Aruba A 104 1,285 1,236% 1:12.36 7.9 10,152 9.
Turks and
Caicos
Islands
A 25 248 992% 1:9.92 7.0 4,756 19.
Saint Lucia A, F 163 670 411% 1:4.11 – –
Antigua and
Barbuda
A, F 84 745 887% 1:8.87 9.5 19,390 23.
Bahamas A, F 327 4,731 1,474% 1:14.74 6.4 82,954 25.
Barbados A, F 293 1,102 376% 1:3.76 9.8 29,588 10.
Saint Kitts and
Nevis
A, F 50 339 678% 1:6.78 – –
Saint Vincent
and theGrenadines
B, F 120 306 255% 1:2.55 12.5 10,479 8.7
Grenada A, F 106 342 323% 1:3.23 7.6 7,121 6.7
Dominica B, F 68 465 684% 1:6.84 9.2 11,721 17.
Cayman
Islands
A 46 2,197 4,776% 1:47.76 6.8 40,930 89.
Jamaica B, F 2,699 3,016 112% 1:1.12 9.8 80,977
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Montserrat A 6 9.5 158% 1:1.58 – –
Bermuda A 65 635 977% 1:9.77 6.5 11,308 17.
Trinidad and
Tobago
A, F, H 1,328 543 41% 1:0.41 14.8 22,018 1.7
Pacific Islands
Palau A, F 20 86 430% 1:4.3 – –
Cook Islands B 14 92 657% 1:6.57 10.4 2,621 18.
Vanuatu B, F, G 221 154 70% 1:0.7 9.8 4,135 1.9
Fiji B, F 833 545 65% 1:0.65 8.9 13,289 1.6
Samoa B, F, G 185 116 63% 1:0.63 – –
French
Polynesia
A 259 222 86% 1:0.86 13.2 8,028 3.
Micronesia
(Federated
States of)
B, F 111 19.1 17% 1:0.17 – –
Tonga B, F 100 54 54% 1:0.54 – –
New Caledonia A 238 219 92% 1:0.92 19.1 11,460 4.
Kiribati C, F, G 94 4.4 5% 1:0.05 – – Solomon
Islands
C, F, G 484 11.5 2% 1:0.02 – –
Papua New
Guinea
C, F 6,202 78 0% 0 9.1 1,944 0
aVisitor expenditure excluding transport.bMost recently available figure/estimate.UNCTAD Economic Groupings: A: 2000 per capita current GDP above US$4,500: High-income (42); B: 2000 per capita cUS$4,500: Middle-income (50); C: 2000 per capita current GDP below US$1,000: Low-income (65); D: Heavily indebted Landlocked developing countries – LLDCs (31); F: Small island developing states – SIDS (29); G: Least-developed countriexporters (22); I: Major exporters of manufactured goods (12); J: Emerging economies (10); K: Newly industrialized econoSource: Derived from UNCTAD (2008).
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the relationship of tourism growth over time in
relation to biodiversity concerns are needed to
assess more accurately the role that tourism
might play with respect to placing extra
pressures on indigenous island species.
Conclusions: Integrating Ecological andEconomic Dimensions of Island Tourism
Many of the Caribbean and Pacific Islands are
highly dependent on tourism for economic
growth (Duval, 2004; Harrison, 2004).
However, although sustainable island
tourism development has been a significant
issue in tourism studies, there has been rela-tively little attempt to try and integrate
tourism within ecological frameworks that
have been developed for island studies. This
paper has therefore sought to suggest ways
in which theories of island biogeography
and ecological economics could underpin
the development of steady-state tourism
approaches (Hall, 2009) to island tourism. In
the case of the small Caribbean and Pacific
Islands, the article has highlighted the extent
to which tourism, while important economi-
cally, also makes a very substantial addition
to the “real” population of the island,
human density, and consequent resource
consumption and anthropogenic change. It
has also tentatively suggested, similar to the
results of other developing country research,
that economic growth as measured by GDP
may not provide positive results for the
retention of biodiversity and a reduction in
the number of endangered species (Dietz &Adger, 2003; Czech et al., 2005). Such an
observation may have profound implications
for strategies that argue that biodiversity
maintenance in developing countries may be
enhanced by encouraging tourism as a means
of economic development, so-called pro-poor
tourism (Hall 2007), particularly as inter-
national medium and long-haul travel to
island economies also contributes substantial
greenhouse gas emissions (Go ¨ ssling, Hall, &
Scott, 2009).
With respect to island biodiversity, the dataemphasize that in the case of the islands
studied there is a significant number of endan-
gered species. In the case of animal species in
the Caribbean, the proportion of animal
species identified by the IUCN as threatened
ranges from a low of 7.6% of all animal
species in Aruba to a high of 18.1% in
Bermuda. In the Pacific the average number
of animal species threatened is much higher,
ranging from a low of 14.8% in Tonga to22.5% in French Polynesia. The differences
can be explained, at least in part, by theories
of island biogeography, whereby more iso-
lated islands, as in the case of the Pacific, are
more vulnerable to anthropogenic impacts,
and therefore have higher potential for
species extinction. Yet, although the mainten-
ance of biodiversity is recognized as a critical
element in sustainable development, the pro-
portion of area protected, especially marine
areas, remains significantly lower than rec-
ommendations as to what would be required
to conserve 80–90% of species (Groves,
2003; Soule ´ & Sanjayan, 1998).
Although the sample of island economies is
small the paper has also sought to relate biodi-
versity conservation to the economic and
tourism characteristics of islands in a more
dynamic fashion. As island biogeographic
theory would suggest there is a reasonably
strong relationship between island size andnumber of threatened species. However,
human impact on the natural capital of
islands is also seen in the strong relationship
between population size and the number of
endangered species for countries. By them-
selves, neither the number of tourists nor the
396 C. Michael Hall
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relative size of tourism’s contribution to the
economy appears related to the number of
endangered species. Nevertheless, the combi-
nation of tourist numbers and permanent
population is strongly positively related to
the number of endangered species.This article has suggested some interesting
potential directions for future research on the
sustainability of the relationship between
tourism, economic development and biodiver-
sity conservation in small island environments.
It has argued for a more theoretically informed
account of sustainable island tourism that
seeks to integrate ecological approaches, and
island biogeography in particular, with
studies of tourism development. However,the size of the sample used to try and study
this phenomenon is extremely small and
suggests a range of methodological issues
that need to be addressed. First, with respect
to data availability this study has only utilized
data available at the national level; even here
some significant gaps in terms of both infor-
mation on tourism and biodiversity were
found that prevented some islands being
studied. For example, the IUCN Red Book
has valuable information on endangered
species and biodiversity; however, there are
some significant limitations in its use and
methods used (see Mace et al., 2008).
Second, there are significant issues of scale.
The use of national data for the territories
studied has treated all countries as individual
islands. Yet some territories, such as the
Bahamas, are island archipelagos, thereby
potentially significantly changing the nature
of island biogeographic relationships, particu-larly in terms of area-to-boundary ratios of
landmasses, which can affect species’ range
and distribution and their relative suscepti-
bility to disturbance. Just as importantly,
there is a need to incorporate understanding
of the proportion of territory that is actually
affected by habitat change as there are, in
effect, “islands” of relatively natural environ-
ment with the terrestrial and marine areas of
each country. Such relationships cannot be
understood by looking at protected areas
alone, as there may be areas of relativelyundisturbed environment outside protected
areas, while some protected areas may have
been subject to significant disturbance. In
addition, with respect to scale there is also a
clear need to undertake analysis of change
over time so that contributing factors that
lead to biodiversity loss are recorded. This
will include not only economic, demographic,
tourism and biodiversity data, but also infor-
mation on natural disturbances such as high-magnitude weather events such as storms,
floods and drought. Nevertheless, the gather-
ing of such information will provide a basis
by which to identify areas that may be most
resilient to anthropogenic environmental
change, including climate change, and may
also provide the identification of sites that
can be used as analogue for other island
environments at threat as well as benchmark
locations with which to measure the impacts
of change.
Finally, as noted above, it is suggested that
the island biogeographical approach can be
applied to a range of different “island” environ-
ments, not necessarily surrounded by water!
The fragmentation of private and public
natural areas creates islands of relatively
natural environment surrounded by environ-
mental change. Many national parks and con-
servation reserves have these characteristics,
as do wilderness areas that may act as refugiafrom global environmental and climate
change (Crist, Wilmer, & Aplet, 2005; Hall
& Page, 2006). Therefore, in seeking to under-
stand better the role that tourism plays in con-
tributing to biodiversity in such environments,
there is considerable potential not only to
An Island Biogeographical Approach to Island Tourism 397
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examine the population effects of visitation and
tourist consumption but also to identify sites of
highest resilience with respect to the conserva-
tion of insular biodiversity.
Acknowledgements
The author would like to acknowledge the
comments of David Duval on an earlier
version of the paper as well as conversations
with Stefan Go ¨ ssling, Dan Scott, Murray
Simpson and Sandra Wilson.
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