Ecological
May 2011
Volume 81 No. 2
M O N O G R A P H S
A PUBLICATION OF THE ECOLOGICAL SOCIETY OF AMERICA
Reviews
The value of estuarine and coastal ecosystem services
Concepts & Synthesis
The underpinnings of the relationship of species richness with space and time
Articles
Stability, resilience, and phase shifts in rocky subtidal communities
along the west coast of Vancouver Island, Canada
REVIEWS
Ecological Monographs, 81(2), 2011, pp. 169–193
Ó 2011 by the Ecological Society of America
The value of estuarine and coastal ecosystem services
EDWARD B. BARBIER,1,5 SALLY D. HACKER,2 CHRIS KENNEDY,1 EVAMARIA W. KOCH,3 ADRIAN C. STIER,4
4
AND BRIAN R. SILLIMAN
1
3
Department of Economics and Finance, University of Wyoming, Laramie, Wyoming 82071 USA
2
Department of Zoology, Oregon State University, Corvallis, Oregon 97331 USA
Horn Point Laboratory, University of Maryland Center for Environmental Science, Cambridge, Maryland 21613 USA
4
Department of Biology, University of Florida, Gainesville, Florida 32611 USA
Abstract. The global decline in estuarine and coastal ecosystems (ECEs) is affecting a
number of critical benefits, or ecosystem services. We review the main ecological services
across a variety of ECEs, including marshes, mangroves, nearshore coral reefs, seagrass beds,
and sand beaches and dunes. Where possible, we indicate estimates of the key economic values
arising from these services, and discuss how the natural variability of ECEs impacts their
benefits, the synergistic relationships of ECEs across seascapes, and management implications.
Although reliable valuation estimates are beginning to emerge for the key services of some
ECEs, such as coral reefs, salt marshes, and mangroves, many of the important benefits of
seagrass beds and sand dunes and beaches have not been assessed properly. Even for coral
reefs, marshes, and mangroves, important ecological services have yet to be valued reliably,
such as cross-ecosystem nutrient transfer (coral reefs), erosion control (marshes), and
pollution control (mangroves). An important issue for valuing certain ECE services, such as
coastal protection and habitat–fishery linkages, is that the ecological functions underlying
these services vary spatially and temporally. Allowing for the connectivity between ECE
habitats also may have important implications for assessing the ecological functions
underlying key ecosystems services, such coastal protection, control of erosion, and
habitat–fishery linkages. Finally, we conclude by suggesting an action plan for protecting
and/or enhancing the immediate and longer-term values of ECE services. Because the
connectivity of ECEs across land–sea gradients also influences the provision of certain
ecosystem services, management of the entire seascape will be necessary to preserve such
synergistic effects. Other key elements of an action plan include further ecological and
economic collaborative research on valuing ECE services, improving institutional and legal
frameworks for management, controlling and regulating destructive economic activities, and
developing ecological restoration options.
Key words: coral reef; economic value; ecosystem service; estuarine and coastal ecosystem; mangrove;
salt marsh; sand beach and dune; seagrass; seascape.
INTRODUCTION
Estuarine and coastal ecosystems (ECEs) are some of
the most heavily used and threatened natural systems
globally (Lotze et al. 2006, Worm et al. 2006, Halpern et
al. 2008). Their deterioration due to human activities is
intense and increasing; 50% of salt marshes, 35% of
mangroves, 30% of coral reefs, and 29% of seagrasses
are either lost or degraded worldwide (Valiela et al.
2001, MEA 2005, Orth et al. 2006, UNEP 2006, FAO
Manuscript received 5 August 2010; revised 12 October 2010;
accepted 12 October 2010. Corresponding Editor: A. M.
Ellison.
5
E-mail: ebarbier@uwyo.edu
2007, Waycott et al. 2009). This global decrease in ECEs
is known to affect at least three critical ecosystem
services (Worm et al. 2006): the number of viable (noncollapsed) fisheries (33% decline); the provision of
nursery habitats such as oyster reefs, seagrass beds,
and wetlands (69% decline); and filtering and detoxification services provided by suspension feeders, submerged vegetation, and wetlands (63% decline). The loss
of biodiversity, ecosystem functions, and coastal vegetation in ECEs may have contributed to biological
invasions, declining water quality, and decreased coastal
protection from flooding and storm events (Braatz et al.
2007, Cochard et al. 2008, Koch et al. 2009).
169
170
EDWARD B. BARBIER ET AL.
Such widespread and rapid transformation of ECEs
and their services suggest that it is important to
understand what is at stake in terms of critical benefits
and values. The purpose of this paper is to provide an
overview of the main ecological services across a variety
of ECEs, including marshes, mangroves, nearshore coral
reefs, seagrass beds, and sand beaches and dunes. Where
available, we cite estimates of the key economic values
arising from the services provided by these ECEs. In
addition, we discuss how the natural variability in these
systems in space and time results in nonlinear functions
and services that greatly influence their economic value
(Barbier et al. 2008, Koch et al. 2009) and some of the
synergistic properties of ECEs. Because they exist at the
interface between the coast, land, and watersheds, ECEs
can produce cumulative benefits that are much more
significant and unique than the services provided by any
single ecosystem. Finally, we finish by highlighting the
main management implications of this review of ECE
services and their benefits, and provide an ‘‘action plan’’
to protect and/or enhance their immediate and longer
term value to humankind.
REVIEWS
METHODS: ASSESSING ECE SERVICES
AND
VALUES
In identifying the ecosystem services provided by
natural environments, a common practice is to adopt the
broad definition of the Millennium Ecosystem Assessment (MEA 2005) that ‘‘ecosystem services are the
benefits people obtain from ecosystems.’’ Thus, the term
‘‘ecosystem services’’ is usually interpreted to imply the
contribution of nature to a variety of ‘‘goods and
services,’’ which in economics would normally be
classified under three different categories (Barbier
2007): (1) ‘‘goods’’ (e.g., products obtained from
ecosystems, such as resource harvests, water, and genetic
material), (2) ‘‘services’’ (e.g., recreational and tourism
benefits or certain ecological regulatory and habitat
functions, such as water purification, climate regulation,
erosion control, and habitat provision), and (3) cultural
benefits (e.g., spiritual and religious beliefs, heritage
values).
However, for economists, the term ‘‘benefit’’ has a
specific meaning. Mendelsohn and Olmstead (2009:326)
summarize the standard definition as follows: ‘‘The
economic benefit provided by an environmental good or
service is the sum of what all members of society would
be willing to pay for it.’’ Thus, given this specific
meaning, some economists argue that it is misleading to
characterize all ecosystem services as ‘‘benefits.’’ As
explained by Boyd and Banzhaf (2007:619), ‘‘as endproducts of nature, final ecosystem services are not
benefits nor are they necessarily the final product
consumed. For example, recreation is often called an
ecosystem service. It is more appropriately considered a
benefit produced using both ecological services and
conventional goods and services.’’ To illustrate this
point, they consider recreational angling. It requires
certain ‘‘ecosystem services,’’ such as ‘‘surface waters
Ecological Monographs
Vol. 81, No. 2
and fish populations,’’ but also ‘‘other goods and
services including tackle, boats, time allocation, and
access’’ (Boyd and Banzhaf 2007:619). But other
economists still prefer a broader interpretation of
ecosystem services, along the lines of the Millennium
Ecosystem Assessment (MEA 2005), which equates
ecosystem services with benefits. For example, Polasky
and Segerson (2009:412) state: ‘‘We adopt a broad
definition of the term ecosystem services that includes
both intermediate and final services,’’ which they justify
by explaining that ‘‘supporting services, in economic
terms, are akin to the infrastructure that provides the
necessary conditions under which inputs can be usefully
combined to provide intermediate and final goods and
services of value to society.’’ Thus, unlike Boyd and
Banzhaf (2007), Polasky and Segerson (2009) consider
recreation to be an ecosystem service.
Economists do agree that, in order to determine
society’s willingness to pay for the benefits provided by
ecosystem goods and services, one needs to measure and
account for their various impacts on human welfare. Or,
as Freeman (2003:7) succinctly puts it: ‘‘The economic
value of resource–environmental systems resides in the
contributions that the ecosystem functions and services
make to human well-being,’’ and consequently, ‘‘the
basis for deriving measures of the economic value of
changes in resource–environmental systems is the effects
of the changes on human welfare.’’ Similarly, Bockstael
et al. (2000:1385) state: ‘‘In economics, valuation
concepts relate to human welfare. So the economic
value of an ecosystem function or service relates only to
the contribution it makes to human welfare, where
human welfare is measured in terms of each individual’s
own assessment of his or her well-being.’’ The key is
determining how changes in ecosystem goods and
services affect an individual’s well-being, and then
determining how much the individual is either willing
to pay for changes that have a positive welfare impact,
or conversely, how much the individual is willing to
accept as compensation to avoid a negative effect.
In our approach to identifying the key services of
estuarine and coastal ecosystem (ECEs) and their values,
we adopt this consensus economic view. That is, as long
as nature makes a contribution to human well-being,
either entirely on its own or through joint use with other
human inputs, then we can designate this contribution
as an ‘‘ecosystem service.’’ In other words, ‘‘ecosystem
services are the direct or indirect contributions that
ecosystems make to the well-being of human populations’’ (U.S. EPA 2009:12). In adopting this interpretation, (U.S. EPA 2009:12–13) ‘‘uses the term ecosystem
service to refer broadly to both intermediate and final
end services,’’ and as a result, the report maintains that
‘‘in specific valuation contexts. . .it is important to
identify whether the service being valued is an intermediate or a final service.’’
For example, following this approach, the tourism
and recreation benefits that arise through interacting
May 2011
ECOSYSTEM SERVICE VALUES
input from them, such as coastal protection, nutrient
cycling, erosion control, water purification, and carbon
sequestration. In recent years, substantial progress has
been made by economists working with ecologists and
other natural scientists in applying environmental
valuation methodologies to assess the welfare contribution of these services. The various nonmarket valuation
methods employed for ecosystem services are essentially
the standard techniques that are available to economists.
For example, Freeman (2003), Pagiola et al. (2004),
NRC (2005), Barbier (2007), U.S. EPA (2009), Mendelsohn and Olmstead (2009), and Hanley and Barbier
(2009) discuss how these standard valuation methods are
best applied to ecosystem services, emphasizing in
particular both the advantages and the shortcomings
of the different methods and their application. However,
what makes applying these methods especially difficult is
that they require three important, and interrelated, steps
(Barbier 1994, 2007, Freeman 2003, NRC 2005, Polasky
and Segerson 2009).
The first step involves determining how best to
characterize the change in ecosystem structure, functions, and processes that gives rise to the change in the
ecosystem service. For instance, the change could be in
the spatial area or quality of a particular type of ECE
habitat, such as a mangrove forest, marsh vegetation, or
sand dune extent. It could also be a change in a key
population, such as fish or main predator. Alternatively,
the change could be due to variation in the flow of
water, energy or nutrients through the system, such as
the variability in tidal surges due to coastal storm events
or the influx of organic waste from pollution upstream
from ECEs.
The second step requires tracing how the changes in
ecosystem structure, functions, and processes influence
the quantities and qualities of ecosystem service flows to
people. Underlying each ecosystem service is a range of
important energy flow, biogeochemical and biotic
processes and functions. For example, water purification
by seagrass beds is linked to the ecological processes of
nutrient uptake and suspended particle deposition
(Rybicki 1997, Koch et al. 2006). However, the key
ecological process and functions that generate an
ecosystem service are, in turn, controlled by certain
abiotic and biotic components that are unique to each
ecosystem’s structure. The various controlling components that may affect nutrient uptake and particle
deposition by seagrasses include seagrass species and
density, nutrient load, water residence time, hydrodynamic conditions, and light availability. Only when these
first two steps are completed is it possible to conduct the
final step, which involves using existing economic
valuation method to assess the changes in human wellbeing that result from the change in ecosystem services.
As summarized by NRC (2005:2) this three-step
approach implies that ‘‘the fundamental challenge of
valuing ecosystem services lies in providing an explicit
description and adequate assessment of the links
REVIEWS
with an ECE can be considered the product of a
‘‘service’’ provided by that ecosystem. But it should be
kept in mind, as pointed out by Boyd and Banzhaf
(2007:619), that the role of the ECE is really to provide
an ‘‘intermediate service’’ (along with ‘‘conventional
goods and services’’) in the production of the final
benefit of recreation and tourism. In selecting estimates
of the ‘‘value’’ of this ‘‘intermediate’’ ecosystem service
in producing recreational benefits, it is therefore
important to consider only those valuation estimates
that assess the effects of changes in the ECE habitat on
the tourism and recreation benefits, but not the
additional influence of any human inputs. The same
approach should be taken for those ‘‘final’’ ecosystem
services, such as coastal protection, erosion control,
nutrient cycling, water purification, and carbon sequestration, which may benefit human well-being without
any additional human-provided goods and services. But
if ‘‘final’’ services do involve any human inputs, the
appropriate valuation estimates should show how
changes in these services affect human welfare, after
controlling for the influence of these additional humanprovided goods and services. Although this approach to
selecting among valuation estimates of various ECE
services seems straightforward, in practice there are a
number of challenges to overcome. These difficulties are
key to understanding an important finding of our
review: Whereas considerable progress has been made
in valuing a handful of ECE services, there are still a
large number of these services that have either no or very
unreliable valuation estimates.
The most significant problem faced in valuing
ecosystem services, including those of ECEs, is that
very few are marketed. Some of the products arising
from ECEs, such as raw materials, food, and fish
harvests, are bought and sold in markets. Given that the
price and quantities of these marketed products are easy
to observe, there are many value estimates of the
contribution of the environmental input to this production. However, this valuation is more complicated than
it appears. Market conditions and regulatory policies for
the marketed output will influence the values imputed to
the environment input (Freeman 2003:259–296, McConnell and Bockstael 2005, Barbier 2007). For example,
one important service of many ECEs is the maintenance
of fisheries through providing coastal breeding and
nursery habitat. Although many fisheries are exploited
for commercial harvests sold in domestic and international markets, studies have shown that the inability to
control fishing access and the presence of production
subsidies and other market distortions can impact
harvests, the price of fish sold, and ultimately, the
estimated value of ECE habitats in supporting commercial fisheries (Freeman 1991, Barbier 2007, Smith 2007).
However, the majority of other key ECE services do
not lead to marketed outputs. These include many
services arising from ecosystem processes and functions
that benefit human beings largely without any additional
171
REVIEWS
172
EDWARD B. BARBIER ET AL.
between the structure and functions of natural systems,
the benefits (i.e., goods and services) derived by
humanity, and their subsequent values.’’ This approach
is summarized in Fig. 1. Human drivers of ecosystem
change affect important ecosystem processes and
functions and their controlling components. Assessing
this change is fundamental yet difficult. However,
‘‘making the translation from ecosystem structure and
function to ecosystem goods and services (i.e., the
ecological production) is even more difficult’’ and
‘‘probably the greatest challenge for successful valuation
of ecosystem services is to integrate studies of the
ecological production function with studies of the
economic valuation function’’ (NRC 2005:2–3). Similarly, Polasky and Segerson (2009:422) maintain that
‘‘among the more practical difficulties that arise in either
predicting changes in service flows or estimating the
associated value of ecosystem services’’ include the ‘‘lack
of multiproduct, ecological production functions to
quantitatively map ecosystem structure and function to
a flow of services that can then be valued.’’
We find that, for many key ECE services, the
integration of the ‘‘ecological production function’’ with
the ‘‘economic valuation function’’ is incomplete. In
many instances, how to go about making this linkage is
poorly understood. However, for a handful of services,
considerable progress has been made in estimating how
the structure and functions of ECEs generate economic
benefits. Thus, the main purpose of our review is to
illustrate the current state of identifying, assessing, and
valuing the key ecosystem services of ECEs, which is
motivated by an important question: What is the current
state of progress in integrating knowledge about the
‘‘ecological production function’’ underlying each important ECE service with economic methods to value
changes in this service in terms of impacts on human
welfare? To answer this important question, we adopt
the following approach.
First, for each of five critical ECEs, coral reefs,
seagrass beds, salt marshes, mangroves, and sand
beaches and dunes, we identified the main ecosystem
services associated with each habitat. Second, we
provided an overview of the ‘‘ecological production
function’’ underlying each service by assessing current
knowledge of the important ecosystem processes,
functions, and controlling components that are vital to
this service. Third, where possible, we cited estimates of
economic values arising from each service, and identified
those services where there is no reliable estimate of an
economic value. Fourth, we discussed briefly the main
human drivers of ecosystem change that are affecting
each ECE habitat. Finally, the results of our review are
summarized in a table for each ECE. This facilitates
comparison across all five habitats and also illustrates
the important ‘‘gaps’’ in the current state of valuing
some key ECE services. To keep the summary table
short, we selected only one valuation estimate as a
representative example. In some cases, it may be the only
Ecological Monographs
Vol. 81, No. 2
valuation estimate of a particular ecosystem service; in
others, we have tried to choose one of the best examples
from recent studies.
Note that our purpose in reviewing valuation
estimates of ECE services is, first, to determine which
services have at least one or more reliable estimate and
which do not, and, second, to identify future areas of
ecological and economic research to further progress in
valuing ECE services. We do not attempt to quantify the
total number of valuation studies for each ECE service,
nor do we analyze in detail the various valuation
methods used in assessing an ecosystem service. Instead,
we selected those examples of valuation studies that
conform to the standard and appropriate techniques
that are recommended for application to various
ecosystem services, as discussed in Freeman (2003),
Pagiola et al. (2004), NRC (2005), Barbier (2007),
Hanley and Barbier (2009), U.S. EPA (2009), and
Mendelsohn and Olmstead (2009). The interested reader
should consult these references for a comprehensive
discussion of economic nonmarket valuation methods
and their suitable application to ecosystem services.
Because our aim is to assess the extent to which
reliable valuation estimates exist for each identified ECE
service, we have reported each estimate as it appears in
the original valuation study. This is for two principal
reasons. First, many of the studies are for specific ECE
habitats in distinct locations at different time periods,
such as the recreation value of several coral reef marine
parks in the Seychelles (Mathieu et al. 2003), the value of
increased offshore fishery production from mangrove
habitat in Thailand (Barbier 2007), or the benefits of
beach restoration in the U.S. states of Maine and New
Hampshire (Huang et al. 2007). Each study also uses
specific measures and units of value appropriate for the
relevant study. For example, in the Seychelles study, the
value estimate was expressed in terms of the average
consumer surplus per tourist for a single year, the Maine
and New Hampshire study estimated each household’s
willingness to pay for an erosion control program to
preserve five miles of beach, and the Thailand study
calculated the capitalized value per hectare of mangrove
in terms of offshore fishery production. Although it is
possible to make assumptions to transform the valuation estimate of each study into the same physical units
(e.g., per hectare), temporal period (e.g., capitalized or
annual value), or currency (e.g., US$), we do not think
such a transformation is warranted for the purposes of
this study.
Second, we do not alter the original valuation
estimates into a common unit of measure (such as
US$ha1yr1 in 2010 prices) because of the concern
that such standardizing of values will be misused or
misinterpreted. For example, one might be tempted to
‘‘add up’’ all the ecosystem service values and come up
with a ‘‘total value’’ of a particular ECE habitat, such as
a salt marsh. Or, one might take the estimate for a
specific location, such as the recreation value of several
May 2011
FIG. 1.
ECOSYSTEM SERVICE VALUES
173
Key interrelated steps in the valuation of ecosystem goods and services. This figure is adapted from NRC (2005: Fig. 1-
3).
use values refer to those ecosystem services whose values
can only be measured indirectly, since they are derived
from supporting and protecting activities that have
directly measurable values.
As is apparent from Tables 1–5, the individual ECE
services that we identified and discuss contribute to
consumptive direct-use values (e.g., raw materials and
food), nonconsumptive direct-use values (e.g., tourism,
recreation, education, and research), and indirect-use
values (e.g., coastal protection, erosion control, water
catchment and purification, maintenance of beneficial
species, and carbon sequestration). When it comes to
valuing whether or not to create national parks from
ECEs, or to protect entire ecosystems, assessing nonusers’ willingness to pay is also important. For example,
Bateman and Langford (1997) assess the nonuse values
of households across Great Britain for preserving the
Norfolk and Suffolk Broads coastal wetlands in the
United Kingdom from salt water intrusion. Even poor
coastal communities in Malaysia, Micronesia, and Sri
Lanka show considerable existence and other nonuse
values for mangroves that can justify the creation of
national parks and other protection measures (Naylor
and Drew 1998, Othman et al. 2004, Wattage and
Mardle 2008). As our review highlights how ECEs
globally are endangered by a wide range of human
drivers of change, it will be important that future studies
assess all the use and nonuse values that arise from
ecosystem goods and services to determine whether it is
worth preserving or restoring critical ECEs.
RESULTS: THE KEY SERVICES
AND
VALUES
OF
ECES
In the following sections, we provide an overview of
the results of our review of the main ecological services
for five ECEs, arranged in order of most to least
submerged: coral reefs, seagrass beds, salt marshes,
mangroves, and sand beaches and dunes. To give an
indication of the ‘‘ecological production function’’
underlying the ecological services generated by each
REVIEWS
coral reef marine parks in the Seychelles (Mathieu et al.
2003), and ‘‘scale it up’’ by all the total hectares of coral
reefs in the Indian Ocean or even the world to come up
with a regional or global value of the recreational value
of coral reefs. As argued by Bockstael et al. (2000:1396),
when ‘‘the original studies valued small changes in
specific and localized components of individual ecosystems . . . it is incorrect to extrapolate the value estimates
obtained in any of these studies to a much larger scale,
let alone to suppose that the extrapolated estimates
could then be added together.’’
Finally, because our efforts here focus on identifying
individual ECE services and any reliable estimates that
value changes in these specific services, we do not
emphasize valuation studies that estimate the value of
entire ecosystems to human beings or assessing broader
values, such as many nonuse existence and bequest
values, that relate to the protection of ecosystems.
However, we do recognize that such values are an
important motivation for the willingness to pay by many
members of society to protect ecosystems, including
ECEs.
For example, Fig. 2 is a more detailed version of Fig.
1, emphasizing the economic valuation component of
the latter diagram. As indicated in Fig. 2, there are a
number of different ways in which humans benefit from,
or value, ecosystem goods and services. The first
distinction is between the ‘‘use values’’ as opposed to
‘‘nonuse values’’ arising from these goods and services.
Typically, use values involve some human ‘‘interaction’’
with the environment, whereas nonuse values do not, as
they represent an individual valuing the pure ‘‘existence’’
of a natural habitat or ecosystem or wanting to
‘‘bequest’’ it to future generations. Direct-use values
refer to both consumptive and nonconsumptive uses
that involve some form of direct physical interaction
with environmental goods and services, such as recreational activities, resource harvesting, drinking clean
water, breathing unpolluted air, and so forth. Indirect-
REVIEWS
174
EDWARD B. BARBIER ET AL.
Ecological Monographs
Vol. 81, No. 2
FIG. 2. Economic valuation of ecosystem goods and services. UVB is ultraviolet-B radiation from sunlight, which can cause
skin cancer. This figure is adapted from NRC (2005: Fig. 4-1).
ECE (see Fig. 1), we outline briefly its key ecological
structure, processes and functions, and identify the main
controlling abiotic and biotic components. When
available, we cite estimates of economic values from
these services. The results give an indication as to the
level of progress in valuing key ECE services and,
equally important, where more integrated work on
ecological and economic assessment of ecosystem
services needs to be done.
Coral reefs
Coral reefs are structurally complex limestone habitats that form in shallow coastal waters of the tropics.
Reefs can form nearshore and extend hundreds of
kilometers in shallow offshore environments. Coral reefs
are created by sedentary cnidarians (corals) that accrete
calcium carbonate and feed on both zooplankton and
maintain a mutualistic symbiosis with photosynthetic
dinoflagellates. Thus, the majority of the reef structure is
dead coral skeleton laid down over millennia, covered by
a thin layer of live coral tissue that slowly accretes new
limestone. In addition, coralline algae play an important
role in stabilizing and cementing the coral reef structure.
The community composition of reefs depends on global,
regional, and local factors, which interact to produce the
wide variety of coral reefs present on earth (Connell et
al. 1997, Glynn 1997, Pandolfi 2002, Hughes et al. 2005).
As outlined in Table 1, coral reefs provide a number
of ecosystem services to humans including raw materi-
als, coastal protection, maintenance of fisheries, nutrient
cycling, and tourism, recreation, education, and research. The table indicates representative examples of
the values of some of these services, where they are
available.
Historically, live reefs have served as a source of lime,
which is an essential material in the manufacturing of
mortar and cement and road building, and is used to
control soil pH in agriculture (Dulvy et al. 1995).
Presently, excavation of live reefs for lime is uncommon
due to the obvious destructive nature of this resource
extraction. As there are no examples of such coral
mining being conducted sustainably, we have not
included any value estimates in Table 1.
An important ecosystem service provided by coral
reefs is coastal protection or the buffering of shorelines
from severe weather, thus protecting coastal human
populations, property, and economic activities. As
indicated in Table 1, this service is directly related to
the economic processes and functions of attenuating or
dissipating waves and facilitating beach and shoreline
retention. By altering the physical environment (i.e.,
reducing waves and currents), corals can engineer the
physical environment for entire ecosystems, making it
possible for other coastal ecosystems such as seagrass
beds and mangroves to develop, which in turn serve
their own suite of services to humans. Despite the
importance of this coastal protection service, very few
economic studies have estimated a value for it. Those
May 2011
ECOSYSTEM SERVICE VALUES
175
TABLE 1. Ecosystem services, processes and functions, important controlling components, examples of values, and human drivers
of ecosystem change for nearshore coral reefs.
Ecosystem services
Raw materials
Ecosystem processes
and functions
generates biological
productivity and
diversity
Important controlling
components
reef size and depth,
coral type, habitat
quality
Ecosystem service value
examples
estimates unavailable
wave height and length, US$174ha1yr1 for
Indian Ocean based
water depth above
on impacts from 1998
reef crest, reef length
bleaching event on
and distance from
property values
shore, coral species,
(Wilkinson et al.
wind climate
1999)
US$15–45 000km2yr1
coral species and
Maintenance of
provides suitable
in sustainable
density, habitat
fisheries
reproductive habitat
fishing for local
quality, food sources,
and nursery grounds,
consumption and $5–
hydrodynamic
sheltered living space
10 000km2yr1 for
conditions
live-fish export, the
Philippines (White et
al. 2000)
Nutrient cycling
provides
coral species and
estimates unavailable
biogeochemical
density, sediment
activity,
deposition,
sedimentation,
subsidence, coastal
biological
geomorphology
productivity
Tourism, recreation, provides unique and
lagoon size, beach area, US$88 000 total
education, and
aesthetic reefscapes,
wave height, habitat
consumer surplus for
research
suitable habitat for
quality, coral species
40 000 tourists to
diverse fauna and
and density, diversity
marine parks,
flora
Seychelles (Mathieu
et al. 2003) and metaanalysis of recreational
values (Brander et al.
2007)
Coastal protection
Human drivers of
ecosystem change
climate change, blast or
cyanide fishing, lime
mining, eutrophication,
sedimentation, coastal
development, dredging,
pollution, biological
invasion
attenuates and/or
dissipates waves,
sediment retention
reef fishes (e.g., jacks, snappers, groupers, and parrot
fishes), and large invertebrates (e.g., giant clams, conch,
lobsters, and crabs). The commercial value of these
fisheries can be significant for some economies. For
example, fish harvested from Hawaiian coral reefs are
estimated to contribute $1.3 million yearly to the
Hawaiian economy (Cesar and van Beukering 2004).
From 1982 to 2002, small-scale, predominantly coral
reef, fisheries contributed $54.7 million to the economies
of America Samoa and the Commonwealth of the
Northern Mariana Islands (Zeller et al. 2007).
Additional fishery harvests consist of the live-animal
aquarium trade, based on corals, small fishes, and
invertebrates collected from reefs. The aquarium trade
has substantially expanded in the past 20 years, listed in
1985 as making $20–40 million/yr as a world market
(Wood 1985) and expanding to an estimated $90–300
million/yr in 2002 (Sadovy and Vincent 2002). The
export and sale of shells and jewelry also makes up a
substantial portion of fisheries on reefs; giant clams,
conch shells, coral, and pearls are all among the many
heavily harvested byproducts.
REVIEWS
studies that do exist tend to use benefit transfer and
replacement cost methods of valuation in an ad hoc
manner, which undermine the reliability of the value
estimates (see Chong 2005 and Barbier 2007 for further
discussion). However, the widespread reef destruction
caused by catastrophic events and global change, such as
hurricanes, typhoons, and coral bleaching, gives some
indication of the value of the lost storm protection
services. For example, as a result of the 1998 bleaching
event in the Indian Ocean, the expected loss in property
values from declining reef protection was estimated to be
US$174ha1yr1 (hereafter all values in US$, unless
otherwise stated; Wilkinson et al. 1999).
Coral reefs also serve to maintain fisheries through the
enhancement of ecologically and economically important species by providing shelter space and substrate for
smaller organisms, and food sources for larger epibenthic and pelagic organisms. Increases in fishing
technology and transport have transformed reef fisheries
that initially functioned solely for subsistence into
commercial operations that serve international markets.
Coral reef fisheries consist of reef-associated pelagic
fisheries (e.g., tuna, mackerel, mahi-mahi, and sharks),
REVIEWS
176
EDWARD B. BARBIER ET AL.
Reliable values for the sustainable production of coral
reef fish for local consumption and the aquarium trade
are rare. White et al. (2000) provide some estimates for
the Philippines. The potential annual revenue for
sustainable fish production could be $15–45 000/km2
of healthy coral reef for local consumption and $5–
10 000/km2 for live fish export. Zhang and Smith (in
press) estimate the maximum sustainable yield to the
Gulf of Mexico reef fishery (mainly grouper and snapper
species, amberjack, and tilefish) to be ;1.30 million kg/
month (;2.86 million pounds/month). Though the reefs
in the Gulf of Mexico are generally exposed limestone or
sandstone and not coral, the habitats are similar in their
structural complexity, which is an important factor
in protecting young fish and smaller species from
predation.
Coral reef ecosystems also perform important services
by cycling organic and inorganic nutrients. Despite
housing a great deal of inorganic carbon in the limestone
skeleton that makes up the structure of the reef, coral
reefs may actually be a net source of atmospheric carbon
dioxide (Kawahata et al. 1997). Reefs do, however,
contribute significantly to the global calcium carbonate
(CaCO3) budget, estimated as 26% of coastal marine
CaCO3 and 11% of the total CaCO3 precipitation
(Hallock 1997, Gattuso et al. 1998). Reefs additionally
transfer excess nitrogen production from cyanobacteria
and benthic microbes on the reef to the pelagic (water
column) environment (Moberg and Folke 1999).
Though poorly quantified, the sequestering of CaCO3
to form the foundation or habitat of the reef is the
primary reason for such high abundance and diversity of
organisms. Unfortunately, as indicated in Table 1, there
are no reliable estimates of the economic value of the
nutrient cycling and transfer services of coral reefs.
Coral reefs and associated placid lagoons are also
economically valuable for the tourism and recreational
activities they support. Resorts depend on the aesthetically turquoise lagoons, white sandy beaches, and
underwater opportunities on the reef to attract tourists.
The high biological diversity and clear waters of tropical
reefs also support an abundance of recreational activities such as SCUBA diving, snorkeling, island tours,
and sport fishing. These activities can be highly lucrative
for individual economies; for example, in 2002, the
earnings of ;100 diver operators in Hawaii were
estimated at $50–60 million/year (van Beukering and
Cesar 2004). Revenues from coral reef tourism in the
Pulau Payar Marine Park, Malaysia, are estimated at
$390 000/year (Yeo 2002), and coral reef diving earns
gross revenue of $10 500–45 540/year in the Bohol
Marine Triangle, the Philippines (Samonte-Tan et al.
2007).
However, estimates of the recreational value of
individual reefs should be interpreted with caution as a
recent review of such studies found substantial bias in
the estimates of individual recreation values (Brander et
al. 2007). Reliable estimates can be made if such biases
Ecological Monographs
Vol. 81, No. 2
are controlled. For example, Mathieu et al. (2003) found
that the average consumer surplus per tourist visiting the
marine national parks in the Seychelles is $2.20, giving a
total consumer surplus estimate of $88 000 for the 40 000
tourists to the coral reefs in 1997. Tapsuwan and AsafuAdjaye (2008) were able to estimate the economic value
of scuba diving in the Similan Island coral reefs in
Thailand, controlling for diver’s attitude toward the
quality of the dive site, frequency of dive trips, and
socioeconomic characteristics, including whether divers
were Thai or foreign. The authors estimated a consumer
surplus value of $3233 per person per dive trip.
In addition to tourism and recreation, reefs also
provide substantial services through research opportunities for scientists, work that is essential to basic and
applied science (Greenstein and Pandolfi 2008). There
are no reliable estimates of this value for coral reefs. As
a rough indication of this value, expenditures for field
work, primary data gathering, boat/vessel rental,
supplies, and diving equipment amount to $32–
111ha1yr1 in Bohol Marine Triangle, the Philippines
(Samonte-Tan et al. 2007).
Despite the numerous economic benefits coral reefs
provide, reef ecosystems are under threat of irrevocable
decline worldwide from a suite of anthropogenic
stressors. Localized stressors (i.e., within reefs or
archipelagos) include overfishing, dynamite or cyanide
fishing, pollution, mining, eutrophication, coastal development, dredging, sedimentation, and biological invasion (e.g., Hoegh-Guldberg 1999, Gardner et al. 2003,
Bellwood et al. 2004, Hoegh-Guldberg et al. 2007). A
variety of reef ecosystem services may be affected by
coral degradation. For example, areas in Sumatra where
dynamite fishing had occurred suffered 70% greater
wave heights than undisturbed areas during the 2004
Indian Ocean Tsunami (Fernando et al. 2005). Blast
fishing can also have negative effects on local economies
by reducing the amount of available reef for tourisms; in
Indonesia, blast fishing led to the loss of a reef that was
valued at $306 800/km2 (Pet-Soede et al. 1999). Overfishing has important cascading consequences on both
reef ecosystem function and sustainable production by
inducing phase shifts (Mumby et al. 2006, 2007).
Overharvesting by the aquarium industry has also been
documented on local levels (Lubbock and Polunin 1975,
Warren-Rhodes et al. 2004). Moreover, eutrophicationinduced algal blooms led to millions of dollars of lost
tourism revenue in Hawaii (van Beukering and Cesar
2004).
Global-scale climate change is also threatening reefs
through coral bleaching, disease, and ocean acidification, leading to both reef destruction and structural
degradation (Graham et al. 2007, Hoegh-Guldberg et al.
2007, Carpenter et al. 2008). Several important reef
ecosystem services are likely to be affected. Though the
economic impacts of climate change on fisheries remain
somewhat unclear, the benthic composition of reefs is
likely to shift, thus affecting overall fish productivity and
May 2011
ECOSYSTEM SERVICE VALUES
177
TABLE 2. Ecosystem services, processes and functions, important controlling components, examples of values, and human drivers
of ecosystem change for seagrasses.
Ecosystem services
Ecosystem processes
and functions
Important controlling
components
Ecosystem service value
examples
Raw materials and
food
generates biological
productivity and
diversity
vegetation type and
density, habitat
quality
estimates unavailable
Coastal protection
attenuates and/or
dissipates waves
estimates unavailable
Erosion control
provides sediment
stabilization and soil
retention in
vegetation root
structure
Water purification
provides nutrient and
pollution uptake, as
well as retention,
particle deposition
Maintenance of
fisheries
provides suitable
reproductive habitat
and nursery grounds,
sheltered living space
wave height and length,
water depth above
canopy, seagrass bed
size and distance
from shore, wind
climate, beach slope,
seagrass species and
density, reproductive
stage
sea level rise,
subsidence, tidal
stage, wave climate,
coastal
geomorphology,
seagrass species and
density
seagrass species and
density, nutrient
load, water residence
time, hydrodynamic
conditions, light
availability
seagrass species and
density, habitat
quality, food sources,
hydrodynamic
conditions
generates
biogeochemical
activity,
sedimentation,
biological
productivity
Tourism, recreation, provides unique and
education, and
aesthetic submerged
research
vegetated landscape,
suitable habitat for
diverse flora and
fauna
seagrass species and
density, water depth,
light availability,
burial rates, biomass
export
biological productivity,
storm events, habitat
quality, seagrass
species and density,
diversity
harvests, as well as the availability of the most valued
fishes collected in the aquarium trade (Pratchett et al.
2008). Reductions in tourism due to recent climate
change-driven coral bleaching events are estimated in
the billions (Wilkinson et al. 1999, Pratchett et al. 2008).
The overall estimated economic damages from lost
fisheries production, tourism and recreation, coastal
protection, and other ecosystem services from the 1998
Indian Ocean coral bleaching event have ranged from
$706 million to $8.2 billion (Wilkinson et al. 1999).
Seagrass beds
Seagrasses are flowering plants that colonize shallow
marine and estuarine habitats. With only one exception
eutrophication,
overharvesting, coastal
development, vegetation
disturbance, dredging,
aquaculture, climate
change, sea level rise
estimates unavailable
estimates unavailable
loss of 12 700 ha of
seagrasses in
Australia; associated
with lost fishery
production of
AU$235 000
(McArthur and
Boland 2006)
estimates unavailable
estimates unavailable
(the genus Phyllospadix), seagrasses colonize soft
substrates (e.g., mud, sand, cobble) and grow to depths
where ;11% of surface light reaches the bottom (Duarte
1991). Seagrasses prefer wave-sheltered conditions as
sediments disturbed by currents and/or waves lead to
patchy beds or their absence (Koch et al. 2006). Despite
being among the most productive ecosystems on the
planet, fulfilling a key role in the coastal zone (Duarte
2002) and being lost at an alarming rate (Orth et al.
2006, Waycott et al. 2009), seagrasses receive little
attention when compared to other ECEs (Duarte et al.
2008).
As indicated in Table 2, seagrass beds provide a wide
range of ecosystem services, including raw materials and
REVIEWS
Carbon
sequestration
Human drivers of
ecosystem change
REVIEWS
178
Ecological Monographs
Vol. 81, No. 2
EDWARD B. BARBIER ET AL.
food, coastal protection, erosion control, water purification, maintenance of fisheries, carbon sequestration,
and tourism, recreation, education, and research, yet
reliable estimates of the economic values of most of
these services are lacking.
Although in the past seagrasses were highly valued as
raw materials and food, modern direct uses of seagrasses
are rather limited. For example, seagrasses are still
harvested in Tanzania, Portugal, and Australia, where
they are used as fertilizer (Hemminga and Duarte 2000,
de la Torre-Castro and Rönnbäck 2004). In the
Chesapeake Bay, USA, seagrass by-catch or beach-cast
is used to keep crabs moist during transport. In East
Africa, some species are served as salad, while others are
used in potions and rituals (de la Torre-Castro and
Rönnbäck 2004). In the Solomon Islands, roots of the
seagrass Enhalus acoroides are sometimes used as food,
while leaf fibers are used to make necklaces and to
provide spiritual benefits such as a gift to a newborn
child, for fishing luck, and to remove an aphrodisiac
spell (Lauer and Aswani 2010). However, currently there
are no reliable estimates of the values of these food and
raw material uses of harvested seagrasses.
Coastal protection and erosion control are often listed
as important ecosystem services provided by seagrasses
(Hemminga and Duarte 2000, Spalding et al. 2003,
Koch et al. 2009). Seagrasses can attenuate waves and,
as a result, smaller waves reach the adjacent shoreline
(Fonseca and Cahalan 1992, Koch 1996, Prager and
Halley 1999). Coastal protection is highest when the
plants occupy the entire water column, such as at low
tide, or when plants produce long reproductive stems
(Koch et al. 2006). When small seagrasses colonize
deeper waters, their contribution to wave attenuation
and coastal protection is more limited. Sediment
stabilization by seagrass roots and rhizomes, as well as
by their beach-casted debris is important for controlling
coastal erosion (Hemminga and Nieuwenhuize 1990).
The benefits seagrasses provide in terms of coastal
protection and erosion control via sediment stabilization
and wave attenuation are yet to be valued satisfactorily.
Water purification, or the increase in water clarity, by
seagrasses occurs via two processes: nutrient uptake and
suspended particle deposition. Seagrasses not only
remove nutrients from the sediments and water column
(Lee and Dunton 1999), but also their leaves are
colonized by algae (epiphytes), which further remove
nutrients from the water column (Cornelisen and
Thomas 2006). The nutrients incorporated into the
tissue of seagrasses and algae are slowly released back
into the water column once the plants decompose or are
removed from the nutrient cycle when buried in the
sediment (Romero et al. 2006). In addition to reducing
nutrients, seagrass beds also decrease the concentration
of suspended particles (e.g., sediment and microalgae)
from the water (Gacia et al. 1999). Leaves in the water
column provide an obstruction to water flow and, as a
result, currents and waves are reduced within seagrass
canopies causing particles to be deposited (Koch et al.
2006). This water purification effect can be quite
dramatic with clearer water in vegetated areas compared
to those without vegetation (Rybicki 1997). No reliable
economic estimates exist for the water purification
service provided by seagrass beds.
Seagrasses also generate value as habitat for ecologically and economically important species such as
scallops, shrimp, crabs, and juvenile fish. Seagrasses
protect these species from predators and provide food in
the form of leaves, detritus, and epiphytes. The market
value of the potential shrimp yield in seagrass beds in
Western Australia is estimated to be between $684 and
$2511ha1yr1 (Watson et al. 1993). In Bohol Marine
Triangle, the Philippines, the annual net revenue from
gleaning mollusks and echinoderms (e.g., starfish, sea
urchins, sea cucumbers, etc.) from seagrass beds
at low tide ranges from $12–120/ha and from fishing
$8–84/ha (Samonte-Tan et al. 2007). The fish, shrimp,
and crab yield in southern Australia is valued at
US$1436ha1yr1 (McArthur and Boland 2006). Based
on the latter estimate, a loss of 2700 ha of seagrass
beds results in lost fishery production of AU$235 000
(Table 2).
Seagrasses are involved in carbon sequestration by
using carbon dissolved in the seawater (mostly in the
form of CO2, but also HCO3) to grow. Once the plants
complete their life cycle, a portion of these materials is
then buried in the sediment in the form of refractory
detritus. It has been estimated that detritus burial from
vegetated coastal habitats contributes about half of the
total carbon burial in the ocean (Duarte et al. 2005).
Therefore, the decline in seagrasses could lead to an
important loss in the global CO2 sequestration capacity,
although this effect has yet to be valued.
Anthropogenic influences such as eutrophication,
overharvesting, sediment runoff, algal blooms, commercial fisheries and aquaculture practices, vegetation
disturbance, global warming, and sea level rise are
among the causes for the decline of seagrasses worldwide (Orth et al. 2006, Waycott et al. 2009). With the
disappearance of seagrasses, valuable ecosystem services
are also lost (McArthur and Boland 2006). Yet, as very
few of these benefits have been estimated reliably (see
Table 2), we have only historical and anecdotal evidence
of the likely economic impacts. For example, the
disappearance of most seagrasses in Long Island,
USA, in the 1930s due to wasting disease led to the
collapse of the scallop industry (Orth et al. 2006).
Salt marshes
Salt marshes are intertidal grasslands that form in
low-energy, wave-protected shorelines along continental
margins. Extensive salt marshes (.2 km in width)
establish and grow both behind barrier-island systems
and along the wave-protected shorelines of bays and
estuaries. Salt marshes are characterized by sharp
zonation of plants and low species diversity, but
May 2011
ECOSYSTEM SERVICE VALUES
which may be degraded by nutrients and pollutants. In
southern Louisiana, USA, treatment of wastewater by
predominantly marsh swamps achieved capitalized cost
savings of $785 to $15 000/acre (1 acre ¼ 0.4 ha)
compared to conventional municipal treatment (Breaux
et al. 1995).
Salt marsh ecosystems also serve to maintain fisheries
by boosting the production of economically and
ecologically important fishery species, such as shrimp,
oysters, clams, and fishes (Boesch and Turner 1984,
MacKenzie and Dionne 2008). For example, salt
marshes may account for 66% of the shrimp and 25%
of the blue crab production in the Gulf of Mexico
(Zimmerman et al. 2000). Because of their complex and
tightly packed plant structure, marshes provide habitat
that is mostly inaccessible to large fishes, thus providing
protection and shelter for the increased growth and
survival of young fishes, shrimp, and shellfish (Boesch
and Turner 1984). For example, the capitalized value of
an acre of salt marsh in terms of recreational fishing is
estimated to be $6471 and $981 for the east and west
coasts of Florida, USA, respectively (Bell 1997). The
contribution of an additional acre of salt marsh to the
value of the Gulf Coast blue crab fishery ranges from
$0.19 to $1.89/acre (Freeman 1991).
As one of the most productive ecosystems in the world
(up to 3900 g Cm2yr1), salt marshes sequester
millions of tons of carbon annually (Mitsch and
Gosselink 2008). Because of the anoxic nature of the
marsh soils (as in most wetlands), carbon sequestered by
salt marsh plants during photosynthesis is often shifted
from the short-term carbon cycle (10–100 years) to the
long-term carbon cycle (1000 years) as buried, slowly
decaying biomass in the form of peat (Mitsch and
Gosselink 2008, Mayor and Hicks 2009). This cycleshifting capability is unique among many of the world’s
ecosystems, where carbon is mostly turned over quickly
and does not often move into the long-term carbon
cycle. However, to our knowledge, there is no valuation
estimation of this carbon sequestration service. Based on
an estimate of permanent carbon sequestration by
global salt marshes of 2.1 Mg C/ha by Chmura et al.
(2003), and employing the 23 September 2009 Carbon
Emission Reduction (CER) price of the European
Emission Trading System (ETS) of €12.38/Mg converted
to $2000, we calculated a value of $30.50ha1yr1 as an
approximate indicator of this benefit, but this is likely to
vary greatly depending on latitude, as warmer marshes
do not accumulate peat like their colder counterparts.
Salt marshes provide important habitat for many
other beneficial species, which are important for
tourism, recreation, education, and research. For
example, estimates from land sales and leases for
marshes in England suggest prices in the range of
£150–493/acre for bird shooting and wildfowling (King
and Lester 1995). Respondents were willing to pay
£31.60/person to create otter habitat and £1.20 to
REVIEWS
extremely high primary and secondary production. The
structure and function of salt marsh plant communities
(and thus their services) were long thought to be
regulated by physical processes, such as elevation,
salinity, flooding, and nutrient availability (Mitsch and
Gosselink 2008). Over the past 25 years, however,
experiments have shown that competition (Bertness
1991) and facilitation (Hacker and Bertness 1995)
among marsh plants is also critically important in
controlling community structure. More recently, research has revealed the presence of strong trophic
cascades driven by habitat-destroying herbivorous
grazers (Silliman and Bertness 2002, Silliman and
Bortolus 2003, Silliman et al. 2005, Henry and Jefferies
2009).
Among coastal ecosystems, salt marshes provide a
high number of valuable benefits to humans, including
raw materials and food, coastal protection, erosion
control, water purification, maintenance of fisheries,
carbon sequestration, and tourism, recreation, education, and research. Some of these important values have
been estimated (Table 3).
For over 8000 years, humans have relied on salt
marshes for direct provisioning of raw materials and
food (Davy et al. 2009). Although harvesting of marsh
grasses and use of salt marshes as pasture lands has
decreased today, these services are still important locally
in both developed and developing areas of the world
(Bromberg-Gedan et al. 2009). For example, in the
Ribble estuary on England’s west coast, annual net
income from grazing in a salt marsh nature reserve is:
£15.27ha1yr1 (King and Lester 1995).
For thousands of years, salt marshes have provided
coastal protection from waves and storm surge, as well
as from coastal erosion, for humans (Davy et al. 2009).
By stabilizing sediment, increasing the intertidal height,
and providing baffling vertical structures (grass), salt
marshes reduce impacts of incoming waves by reducing
their velocity, height, and duration (Morgan et al. 2009;
Bromberg-Gedan et al., in press). Marshes are also likely
to reduce storm surge duration and height by providing
extra water uptake and holding capacity in comparison
to the sediments of unvegetated mudflats. This storm
protection value can be substantial, as a study of the
protection against hurricanes by coastal wetlands along
the U.S. Atlantic and Gulf coasts reveals (Table 3;
Costanza et al. 2008). However, there are no reliable
estimates of the economic value of salt marshes in
controlling coastal erosion.
Salt marshes act as natural filters that purify water
entering the estuary (Mitsch and Gosselink 2008). As
water (e.g., from rivers, terrestrial runoff, groundwater,
or rain) passes through marshes, it slows due to the
baffling and friction effect of upright grasses (Morgan et
al. 2009). Suspended sediments are then deposited on the
marsh surface, facilitating nutrient uptake by salt marsh
grasses. This water filtration service benefits human
health, but also adjacent ecosystems, such as seagrasses,
179
180
EDWARD B. BARBIER ET AL.
Ecological Monographs
Vol. 81, No. 2
TABLE 3. Ecosystem services, processes and functions, important controlling components, examples of values, and human drivers
of ecosystem change for salt marshes.
REVIEWS
Ecosystem services
Ecosystem processes
and functions
Important controlling
components
Ecosystem service value
examples
Raw materials and
food
generates biological
productivity and
diversity
vegetation type and
density, habitat quality,
inundation depth,
habitat quality, healthy
predator populations
£15.27 ha1yr1 net
income from livestock
grazing, UK (King and
Lester 1995)
Coastal protection
attenuates and/or
dissipates waves
US$8236ha1yr1 in
reduced hurricane
damages, USA (Costanza et al. 2008)
Erosion control
provides sediment
stabilization and soil
retention in
vegetation root
structure
Water purification
provides nutrient and
pollution uptake, as
well as retention,
particle deposition
Maintenance of
fisheries
provides suitable
reproductive habitat
and nursery grounds,
sheltered living space
tidal height, wave height
and length, water depth
in or above canopy,
marsh area and width,
wind climate, marsh
species and density, local
geomorphology
sea level rise, tidal stage,
coastal geomorphology,
subsidence, fluvial
sediment deposition and
load, marsh grass species
and density, distance
from sea edge
marsh grass species and
density, marsh quality
and area, nutrient and
sediment load, water
supply and quality,
healthy predator
populations
marsh grass species and
density, marsh quality
and area, primary
productivity, healthy
predator populations
Carbon
sequestration
generates
biogeochemical
activity,
sedimentation,
biological
productivity
Tourism, recreation, provides unique and
education, and
aesthetic landscape,
research
suitable habitat for
diverse fauna and
flora
marsh grass species and
density, sediment type,
primary productivity,
healthy predator
populations
marsh grass species and
density, habitat quality
and area, prey species
availability, healthy
predator populations
Human drivers of
ecosystem change
marsh reclamation,
vegetation
disturbance,
climate change,
sea level rise,
pollution, altered
hydrological
regimes, biological
invasion
estimates unavailable
US$785–15 000/acre
capitalized cost savings
over traditional waste
treatment, USA (Breaux
et al. 1995)
US$6471/acre and $981/
acre capitalized value for
recreational fishing for
the east and west coasts,
respectively, of Florida,
USA (Bell 1997) and
$0.19–1.89/acre marginal
value product in Gulf
Coast blue crab fishery,
USA (Freeman 1991)
US$30.50ha1yr1à
£31.60/person for otter
habitat creation and
£1.20/person for
protecting birds, UK
(Birl and Cox 2007)
One acre ¼ 0.4 ha.
à Based on Chumra et al. (2003) estimate of permanent carbon sequestration by global salt marshes of 2.1 Mg Cha1yr1 and
23 September 2009 Carbon Emission Reduction (CER) price of the European Emission Trading System (ETS) of €12.38/Mg, which
was converted to US$2000.
protect birds in the Severn Estuary Wetlands bordering
England and Wales (Birol and Cox 2007).
Current human threats to salt marshes include
biological invasions, eutrophication, climate change
and sea level rise, increasing air and sea surface
temperatures, increasing CO2 concentrations, altered
hydrologic regimes, marsh reclamation, vegetation
disturbance, and pollution (Silliman et al. 2009). As
indicated in Table 3, a growing number of valuable
marsh services are lost with the destruction of this
habitat. Approximately 50% of the original salt marsh
ecosystems have been degraded or lost globally, and in
some areas, such as the West Coast of the USA, the loss
is .90% (Bromberg and Silliman 2009, BrombergGedan et al. 2009). This is likely to be exacerbated by
the recent Gulf of Mexico oil spill in 2010.
May 2011
ECOSYSTEM SERVICE VALUES
181
TABLE 4. Ecosystem services, processes and functions, important controlling components, examples of values, and human drivers
of ecosystem change for mangroves.
Ecosystem services
Ecosystem processes
and functions
Important controlling
components
generates biological
productivity and
diversity
vegetation type and
density, habitat
quality
Coastal protection
attenuates and/or
dissipates waves
and wind energy
Erosion control
provides sediment
stabilization and
soil retention in
vegetation root
structure
Water purification
provides nutrient
and pollution
uptake, as well as
particle retention
and deposition
provides suitable
reproductive
habitat and
nursery grounds,
sheltered living
space
tidal height, wave
height and length,
wind velocity, beach
slope, tide height,
vegetation type and
density, distance
from sea edge
sea level rise, tidal
stage, fluvial
sediment deposition,
subsidence, coastal
geomorphology,
vegetation type and
density, distance
from sea edge
mangrove root length
and density,
mangrove quality and
area
Maintenance of
fisheries
Carbon
sequestration
Tourism, recreation,
education, and
research
generates biological
productivity,
biogeochemical
activity,
sedimentation
provides unique and
aesthetic
landscape,
suitable habitat
for diverse fauna
and flora
mangrove species and
density, habitat
quality and area,
primary productivity
vegetation type and
density, fluvial
sediment deposition,
subsidence, coastal
geomorphology
mangrove species and
density, habitat
quality and area,
prey species
availability, healthy
predator populations
Human drivers of
ecosystem change
US$484–585ha1yr1
capitalized value
of collected
products,
Thailand (Barbier
2007)
US$8966–10 821/ha
capitalized value for
storm protection,
Thailand (Barbier
2007)
mangrove disturbance,
degradation, conversion;
coastline disturbance;
pollution; upstream soil
loss; overharvesting of
resources
US$3679ha1yr1
annualized
replacement cost,
Thailand
(Sathirathai and
Barbier 2001)
estimates unavailable
US$708-$987/ha
capitalized value
of increased
offshore fishery
production,
Thailand (Barbier
2007)
US$30.50ha1yr1
estimates unavailable
Based on Chumra et al. (2003) estimate of permanent carbon sequestration by global salt marshes of 2.1 Mg Cha1yr1and 23
September 2009 Carbon Emission Reduction (CER) price of the European Emission Trading System (ETS) of €12.38/Mg, which
was converted to US$2000.
Mangroves
Mangroves are coastal forests that inhabit saline tidal
areas along sheltered bays, estuaries, and inlets in the
tropics and subtropics throughout the world. Around
50–75 woody species are designated as ‘‘mangrove,’’
which is a term that describes both the ecosystem and
the plant families (Ellison and Farnsworth 2001). In the
1970s, mangroves may have covered as much as 200 000
km2, or 75% of the world’s coastlines (Spalding et al.
1997). But since then, at least 35% of global mangrove
area has been lost, and mangroves are currently
disappearing at the rate of 1–2% annually (Valiela et
al. 2001, Alongi 2002, FAO 2007).
The worldwide destruction of mangroves is of concern
because they provide a number of highly valued
ecosystems services, including raw materials and food,
coastal protection, erosion control, water purification,
maintenance of fisheries, carbon sequestration, and
tourism, recreation, education, and research (Table 4).
For many coastal communities, their traditional use of
mangrove resources is often closely connected with the
health and functioning of the system, and thus this use is
often intimately tied to local culture, heritage, and
traditional knowledge (Walters et al. 2008).
Of the ecosystem services listed, three have received
most attention in terms of determining their value to
coastal populations. These include (1) their use by local
coastal communities for a variety of products, such as
fuel wood, timber, raw materials, honey and resins, and
crabs and shellfish; (2) their role as nursery and breeding
REVIEWS
Raw materials and
food
Ecosystem service
value examples
REVIEWS
182
EDWARD B. BARBIER ET AL.
habitats for offshore fisheries; and (3) their propensity to
serve as natural ‘‘coastal storm barriers’’ to periodic
wind and wave or storm surge events, such as tropical
storms, coastal floods, typhoons, and tsunamis. Assigning a value to these three mangrove ecosystem services
has been conducted for Thailand by Barbier (2007), who
compared the net economic returns per hectare to
shrimp farming, the costs of mangrove rehabilitation,
and the value of mangrove services. All land uses were
assumed to be instigated over a nine-year period (1996
to 2004), and the net present value (NPV) of each land
use or ecosystem service was estimated in 1996 US$ per
hectare. The NPV arising from the net income to local
communities from collected forest and other products
and shellfish was $484 to $584/ha. In addition, the NPV
of mangroves as breeding and nursery habitat in support
of offshore artisanal fisheries ranged from $708 to $987/
ha, and the storm protection service was $8966 to
$10 821/ha.
Such benefits are considerable when compared to the
average incomes of coastal households; a survey
conducted in July 2000 of four mangrove-dependent
communities in two different coastal provinces of
Thailand indicates that the average household income
per village ranged from $2606 to $6623/yr, and the
overall incidence of poverty (corresponding to an annual
income of $180 or lower) in all but three villages
exceeded the average incidence rate of 8% found across
all rural areas of Thailand (Sarntisart and Sathirathai
2004). The authors also found that excluding the income
from collecting mangrove forest products would have
raised the incidence of poverty to 55.3% and 48.1% in
two of the villages, and to 20.7% and 13.64% in the other
two communities.
The Thailand example is not unusual; coastal
households across the world typically benefit from the
mangrove services, indicated in Table 4 (Ruitenbeek
1994, Bandaranayake 1998, Barbier and Strand 1998,
Naylor and Drew 1998, Janssen and Padilla 1999,
Rönnbäck 1999, Badola and Hussain 2005, Chong 2005,
Brander et al. 2006, Walton et al. 2006, Rönnbäck et al.
2007, Aburto-Oropeza et al. 2008, Walters et al. 2008,
Lange and Jiddawi 2009, Nfotabong Atheull et al. 2009).
Mangroves also provide important cultural benefits to
coastal inhabitants. A study in Micronesia finds that the
communities ‘‘place some value on the existence and
ecosystem functions of mangroves over and above the
value of mangroves’ marketable products’’ (Naylor and
Drew 1998:488).
Since the 2004 Indian Ocean Tsunami, there has been
considerable global interest in one particular service of
mangroves: their role as natural barriers that protect the
lives and properties of coastal communities from
periodic storm events and flooding. Eco-hydrological
evidence indicates that this protection service is based on
the ability of mangroves to attenuate waves and thus
reduce storm surges (Mazda et al. 1997, 2006, Massel et
al. 1999, Wolanski 2007, Barbier et al. 2008, Koch et al.
Ecological Monographs
Vol. 81, No. 2
2009). Comprehensive reviews of all the field assessments in the aftermath of the Indian Ocean Tsunami
suggest that some areas were more protected by the
presence of healthy mangroves, provided that the tidal
wave was not too extreme in magnitude (Montgomery
2006, Braatz et al. 2007, Forbes and Broadhead 2007,
Alongi 2008, Cochard et al. 2008). For other major
storm events, there is more economic evidence of the
protective role of mangroves. For example, during the
1999 cyclone that struck Orissa, India, mangroves
significantly reduced the number of deaths as well as
damages to property, livestock, agriculture, fisheries,
and other assets (Badola and Hussain 2005, Das and
Vincent 2009). Das and Vincent estimated that there
could have been 1.72 additional deaths per village within
10 km of the coast if the mangrove width along
shorelines had been reduced to zero. Losses incurred
per household were greatest ($154) in a village that was
protected by an embankment but had no mangroves
compared to losses per household ($33) in a village
protected only by mangrove forests (Badola and
Hussain 2005).
The ability of mangroves to stabilize sediment and
retain soil in their root structure reduces shoreline
erosion and deterioration (Daehler and Strong 1996,
Sathirathai and Barbier 2001, Thampanya et al. 2006,
Wolanski 2007). But despite the importance of this
erosion control service, very few economic studies have
been conducted to value it. Existing studies tend to use
the replacement cost methods of valuation, due to lack
of data, which can undermine the reliability of the value
estimates (Chong 2005, Barbier 2007). In Thailand, the
annualized replacement cost of using artificial barriers
instead of mangroves is estimated to be $3679ha1yr1
(Sathirathai and Barbier 2001).
Mangroves also serve as barriers in the other
direction; their water purification functions protect coral
reefs, seagrass beds, and important navigation waters
against siltation and pollution (Wolanski 2007). In
southern China, field experiments have been conducted
to determine the feasibility of using mangrove wetlands
for wastewater treatment (Chen et al. 2009). Mangrove
roots may also serve as a sensitive bio-indicator for
metal pollution in estuarine systems (MacFarlane et al.
2003). The economic value of the pollution control
service of mangroves has not been reliably estimated,
however.
Because mangroves are among the most productive
and biogeochemically active ecosystems, they are
important sources of global carbon sequestration. To
date, the value of mangroves as a carbon sink has not
been estimated. Based on an estimate of permanent
carbon sequestration by all mangroves globally (Chumra et al. 2003), following the same approach described
above for salt marshes (see Salt marshes), we calculate a
value of $30.50ha1yr1 as an approximate indicator of
this benefit for mangroves.
May 2011
ECOSYSTEM SERVICE VALUES
Although many factors contribute to global mangrove
deforestation, a major cause is aquaculture expansion in
coastal areas, especially the establishment of shrimp
farms (Barbier and Cox 2003). Aquaculture accounts for
52% of mangrove loss globally, with shrimp farming
alone accounting for 38%. Forest use, mainly from
industrial lumber and woodchip operations, causes 26%
of mangrove loss globally. Freshwater diversion accounts for 11% of deforestation, and reclamation of land
for other uses causes 5% of decline. The remaining
sources of mangrove deforestation consist of herbicide
impacts, agriculture, salt ponds, and other coastal
developments (Valiela et al. 2001). The extensive and
rapid loss of mangroves globally reinforces the importance of measuring the value of such ecological services,
and employing these values appropriately in coastal
management and planning.
Sand beaches and dunes
(Carter 1991, Hesp and Short 1999, Short 1999).
Foredunes can vary in height and width, and thus
their ability to attenuate waves, depending on the
presence of vegetation and sand supply from the beach
(Hesp 1989; Hacker et al., in press). Measuring the
coastal protective properties of sand shoreline systems
involves understanding the relationship between beach
and foredune shape and wave attenuation, especially in
the aftermath of storms, hurricanes, or tsunamis
(Leatherman 1979, Lui et al. 2005, Sallenger et al.
2006, Morton et al. 2007, Stockdon et al. 2007,
Ruggiero et al. 2010). The economic value, although
not calculated previously, is likely to be substantial.
For example, Liu et al. (2005) report that, after the
2004 Indian Ocean Tsunami, there was total devastation and loss of 150 lives in a resort located directly
behind where a foredune was removed to improve the
scenic view of the beach and ocean.
Beaches and sand dunes provide sediment stabilization and soil retention in vegetation root structure, thus
controlling coastal erosion and protecting recreational
beaches, tourist-related business, ocean front properties,
land for aquaculture and agriculture, and wildlife
habitat. Although this service has not been valued
directly, there have been a growing number of studies
that value the benefits gained from erosion control
programs that either preserve or ‘‘nourish’’ existing
beaches and dunes (Landry et al. 2003, Kriesel and
Landry 2004, Huang et al. 2007, Whitehead et al. 2008,
Morgan and Hamilton 2010). Such programs often
substitute for property owners building their own
erosion protection structures, such as seawalls and
groins, which can inadvertently accelerate the degradation of the coastal environment (Landry et al. 2003,
Kriesel and Landry 2004). However, erosion control
programs can also have negative effects on the
surrounding environment, including affecting recreational beach use and views, displacing coastal erosion
elsewhere, and disturbing wildlife habitat. For example,
in the U.S. states of New Hampshire and Maine, a
coastal erosion program that preserves five miles of
beach is estimated to have net benefits, adjusted for the
costs associated with the risk of injury to swimmers from
the control measures, disturbance to wildlife habitat,
and deterioration of water quality, of $4.45/household
(Huang et al. 2007). Landry et al. (2003) find that a onemeter increase in beach width, or equivalently, the
prevention of one meter of beach erosion, increased
oceanfront and inlet-front property values by $233 on
Tybee Island in the U.S. state of Georgia.
Another important service of coastal sand ecosystems
is water catchment. Sand dunes are able to store
significant amounts of water that can serve as aquifers
for coastal populations (Carter 1990). For example, in
the Meijendel dunes in The Netherlands, dune aquifers
have been used as a source of drinking water for
centuries (van der Meulen et al. 2004). The aquifer still
supplies enough water for 1.5 million people in
REVIEWS
Coastal sand beaches and dunes are important but
understudied arbiters of coastal ecosystem services.
They form at low-lying coastal margins where sand
transported by oceanic waves and wind combine with
vegetation to produce dynamic geomorphic structures.
Thus, sandy-shore ecosystems include both marine and
terrestrial components and vary, depending on sand
supply, in the extent to which the beach vs. the dune
dominates (Short and Hesp 1982). Sandy beaches and
dunes occur at all latitudes on earth and cover roughly
34% of the world’s ice-free coastlines (Hardisty 1994).
For centuries, due to their unique position between
ocean and land, coastal beaches and dunes have
provided humans with important services such as raw
materials, coastal protection, erosion control, water
catchment and purification, maintenance of wildlife,
carbon sequestration, and tourism, recreation, education, and research (Table 5; Carter 1990, Pye and Tsoar
1990). However, very few of these services have been
valued, with the exception of erosion control and
recreation and tourism (Table 5).
Beaches and dunes provide raw materials in the form
of sand that has been mined for centuries for multiple
uses, including extraction of minerals such silica and
feldspar for glass and ceramic production, infill for
development, amendments for agriculture, and base
material for construction products. Although sand is a
valuable resource, its extraction through mining can
have obvious negative effects, especially on coastal
protection and aquifers.
Coastal protection is arguably one of the most
valuable services provided by sand shore ecosystems
especially in the face of extreme storms, tsunamis, and
sea level rise. As waves reach the shoreline they are
attenuated by the beach slope and, at high tide, also by
the foredune, a structure immediately behind the beach
where sand accumulates in hills or ridges parallel to the
shoreline. Beaches vary in their ability to attenuate
waves depending on a continuum in their morphology
183
184
EDWARD B. BARBIER ET AL.
Ecological Monographs
Vol. 81, No. 2
TABLE 5. Ecosystem services, processes and functions, important controlling components, examples of values, and human drivers
of ecosystem change for sand beaches and dunes.
Ecosystem services
Important controlling
components
Ecosystem service value
examples
Raw materials
provides sand of
particular grain
size, proportion
of minerals
dune and beach area,
estimates unavailable
sand supply, grain
for sustainable
size, proportion of
extraction
desired minerals (e.g.,
silica, feldspar)
Coastal protection
attenuates and/or
dissipates waves
and reduces
flooding and
spray from sea
provides sediment
stabilization and
soil retention in
vegetation root
structure
wave height and length, estimates unavailable
beach slope, tidal
height, dune height,
vegetation type and
density, sand supply
sea level rise,
US$4.45/household for
subsidence, tidal
an erosion control
stage, wave climate,
program to preserve
coastal
8 km of beach, for
geomorphology,
Maine and New
beach grass species
Hampshire beaches,
and density
USA (Huang et al.
2007)
dune area, dune height, estimates unavailable
sand and water
supply
Erosion control
Water catchment and
purification
Maintenance of wildlife
REVIEWS
Ecosystem processes
and functions
Carbon sequestration
Tourism, recreation,
education, and research
stores and filters
water through
sand; raises water
table
biological
productivity and
diversity, habitat
for wild and
cultivated animal
and plant species
generates biological
productivity,
biogeochemical
activity
dune and beach area,
water and nutrient
supply, vegetation
and prey biomass
and density
vegetative type and
density, fluvial
sediment deposition,
subsidence, coastal
geomorphology
provides unique and dune and beach area,
aesthetic
sand supply, wave
landscapes,
height, grain size,
suitable habitat
habitat quality,
for diverse fauna
wildlife species,
and flora
density and diversity,
desirable shells and
rocks
surrounding cities. Because of the importance of this
water source, the Meijendel dune is managed as a nature
reserve that serves both drinking water and recreation
needs. In 1999, the cost of management was $3.8
million/year, while the yearly income of the reserve
was $99.2 million/year.
Coastal dunes can provide maintenance of wildlife in
the form of habitat for fish, shellfish, birds, rodents, and
ungulates, which have been captured or cultivated for
food since humans first colonized the coast (Carter 1990,
Pye and Tsoar 1990). In Europe, protection and
restoration of dune wildlife and habitat has become a
priority (Baeyens and Martı́nez 2004). In other regions
of the world, dunes have been used for agricultural
purposes (Pye and Tsoar 1990). However, there are no
reliable estimates on the value of beaches and dunes as a
source of habitat for wildlife.
Human drivers of
ecosystem change
loss of sand through
mining, development
and coastal structures
(e.g., jetties),
vegetation
disturbance, overuse
of water, pollution,
biological invasion
estimates unavailable
estimates unavailable
US$166/trip or $1574
per visiting
household per year
for North Carolina
beaches, USA
(Landry and Liu
2009)
Dunes that encourage vegetation growth and productivity will also assist in carbon sequestration, although
this process is likely to vary with the type of vegetation,
sediment deposition and subsidence, and coastal geomorphology. There are currently no estimates of the
value of this service provided by dunes, however.
Beaches and dunes also supply important recreational
benefits. Boating, fishing, swimming, scuba diving,
walking, beachcombing, and sunbathing are among the
numerous recreational and scenic opportunities that are
provided by beach and dune access. In the USA alone,
70% of the population visits the beach on vacation, and
85% of total tourism dollars come from beach visits
(Houston 2008). An analysis of North Carolina beaches
shows that implementation of a beach replenishment
policy to improve beach width by an average of 100 feet
would increase the average number of trips by visitors in
May 2011
ECOSYSTEM SERVICE VALUES
DISCUSSION: ISSUES
FOR
FUTURE RESEARCH
Our review of economic values of key ecosystem
services for five estuarine and coastal ecosystems (coral
reefs, seagrass beds, salt marshes, mangroves, and sand
beaches and dunes) reveals that progress has been made
in estimating these benefits for some systems and
services, but much work remains. For example, reliable
valuation estimates are beginning to emerge for the key
services of some ECEs, such as coral reefs, salt marshes,
and mangroves, but many of the important benefits of
seagrass beds and sand dunes and beaches have not been
assessed properly. Even for coral reefs, marshes, and
mangroves, important ecological services have yet to be
valued reliably, such as cross-ecosystem nutrient transfer
(coral reefs), erosion control (marshes), and pollution
control (mangroves). Although more studies valuing
ECE services have been conducted recently, our review
shows that the number of reliable estimates is still
relatively small.
Measurement issues, data availability, and other
limitations continue to prevent the application of
standard valuation methods to many ecosystem services.
In circumstances where an ecological service is unique to
a specific ecosystem and is difficult to value, often the
cost of replacing the service or treating the damages
arising from the loss of the service is used as a valuation
approach. Such methods have been employed frequently
to measure coastal protection, erosion control, and
water purification services by ECEs (Ellis and Fisher
1987, Chong 2005, Barbier 2007). However, economists
recommend that the replacement cost approach should
be used with caution because, first, one is essentially
estimating a benefit (e.g., storm protection) by a cost
(e.g., the costs of constructing seawalls, groins, and
other structures), and second, the human-built alternative is rarely the most cost-effective means of providing
the service (Ellis and Fisher 1987, Barbier 1994, 2007,
Freeman 2003, NRC 2005).
As summarized in our tables, ECE habitats tend to
generate multiple ecosystem services. These typically
range from tourism and recreation benefits to coastal
protection, erosion control, nutrient cycling, water
purification, and carbon sequestration to food and
raw-material products. Where studies are aware of such
multiple benefits, the current approach is still to value
each service as if it is independent, as was done for
coastal protection, habitat–fishery linkages, and raw
materials for mangroves in Thailand (Barbier 2007).
However, as our tables indicate, similar ecological
processes and functions, as well as controlling components, may influence more than one ecosystem service.
Such ecological interactions are bound to affect the
value of multiple services arising from a single habitat,
which is an important direction for future research in
valuing ECE services.
For a growing number of services, there is evidence
that ecological functions vary spatially or temporally,
and thus influence the economic benefits that they
provide (Peterson and Turner 1994, Petersen et al. 2003,
Rountree and Able 2007, Aburto-Oropeza et al. 2008,
Aguilar-Perera and Appeldoorn 2008, Barbier et al.
2008, Meynecke et al. 2008, Koch et al. 2009). For
example, wave attenuation by coral reefs, seagrass beds,
salt marshes, mangroves, and sand dunes provides
protection against wind and wave damage caused by
coastal storm and surge events, but the magnitude of
protection will vary spatially across the extent of these
habitats (Barbier et al. 2008, Koch et al. 2009). In
particular, ecological and hydrological field studies
suggest that mangroves are unlikely to stop storm waves
that are greater than 6 m in height (Forbes and
Broadhead 2007, Wolanski 2007, Alongi 2008, Cochard
et al. 2008). On the other hand, where mangroves are
effective as ‘‘natural barriers’’ against storms that
generate waves less than 6 m in height, the wave height
of a storm decreases quadratically for each 100 m that a
mangrove forest extends out to sea (Mazda et al. 1997,
Barbier et al. 2008). In other words, wave attenuation is
greatest for the first 100 m of mangroves, but declines as
more mangroves are added to the seaward edge.
Valuation of coastal habitat support for offshore
fisheries increasingly indicates that the value of this
service varies spatially because the quality of the habitat
is greater at the seaward edge or ‘‘fringe’’ of the coastal
ecosystem than further inland (Peterson and Turner
1994, Manson et al. 2005, Aburto-Oropeza et al. 2008,
REVIEWS
the subsequent year from 11 to 14, with beach-goers
willing to pay $166/trip or $1574 per visiting household
per year (Landry and Liu 2009). Another study of North
Carolina beaches found that widening beach width
increases the consumer surplus of visitors by $7/trip
(Whitehead et al. 2008). However, overuse of dune
habitat due to beach recreation can also cause significant
damages. The impacts to beach and dune function have
been mostly in the form of changes in sand stabilization
and distribution. Trampling of native vegetation by
pedestrians or vehicles can destabilize sand and result in
the loss of foredunes and thus coastal protection.
Therefore, as with all coastal systems, reducing the
damages caused by overuse of certain services such as
the recreation and tourism benefits provided by beaches
and dunes, requires thoughtful management and planning (e.g., Heslenfeld et al. 2004, Moreno-Casasola
2004).
Many of the services provided by sand beaches and
dunes are threatened by human use, species invasions,
and climate change (Brown and McLachlan 2002,
Zarnetske et al. 2010; Hacker et al., in press). In
particular, the removal or disruption of sand and
vegetation coupled with increased storm intensity and
sea level rise threaten critical services provided by this
ecosystem, specifically those of coastal protection
(Ruggiero et al. 2010) and coastal freshwater catchment.
The fact that no reliable estimates of these services are
currently available is worrisome.
185
REVIEWS
186
EDWARD B. BARBIER ET AL.
Aguilar-Perera and Appeldoorn 2008). In the case of
mangroves and salt marshes, the evidence suggests that
both storm protection and habitat–fishery linkage
benefits tend to decline with the distance inshore from
the seaward edge of most coastal wetland habitats, such
as mangroves and salt marshes. For example, Peterson
and Turner (1994) found that densities of most fish and
crustaceans were highest in salt marshes in Louisiana
within 3 m of the water’s edge compared to the interior
marshes. In the Gulf of California, Mexico, the
mangrove fringe with a width of 5–10 m has the most
influence on the productivity of nearshore fisheries, with
a median value of $37 500/ha. Fishery landings also
increased positively with the length of the mangrove
fringe in a given location (Aburto-Oropeza et al. 2008).
The tendency for these services to vary unidirectionally
across such coastal landscapes has implications for
modeling the provision of these services and valuing
their benefits (Barbier 2008).
Coastal protection can also vary if damaging storm
events occur when plant biomass and/or density are low
(Koch et al. 2009). This is particularly important in
temperate regions, where seasonal fluctuations of
biomass may differ from the seasonal occurrence of
storms. For example, along the U.S. Atlantic coast, the
biomass of seagrass peaks in the summer (April–June),
yet decreases in the fall (July–September) when storm
events usually strike. In tropical areas, vegetation in
coastal systems, such as mangroves but also seagrasses,
has relatively constant biomass throughout the year, so
the coastal protection service is relatively unaffected by
seasonal or temporal variability.
The value of some ECE services can also vary
spatially (i.e., distance from the shoreline) and temporally (i.e., seasonality). This is of particular importance
for recreational and property-related benefits (Coombes
et al. 2010, Morgan and Hamilton 2010). A study of
home values near Pensacola Beach, Florida, found that
Gulf-front property owners were willing to pay an
annual tax of $5807 for a five-year beach nourishment
project that would improve access and shoreline views;
however, the tax payment declines to $2770 for a
property in the next block, $2540 for a property two
blocks away, and $1684 for a property three blocks
away (Morgan and Hamilton 2010). Models of beach
visitors in East Anglia, UK, reveal that seasonal
differences are important. For example, school holidays
and temperatures have the greatest influence on visitor
numbers, and the visitors’ propensity to visit the coast
increases rapidly at temperatures exceeding 158C
(Coombes et al. 2010). Spatial characteristics that were
also associated with more visitors included wide and
sandy beaches, beach cleanliness, the presence of a
nature reserve, pier, or an urban area behind the beach,
and close proximity of an entrance point, car park, and
toilet facilities.
Another unique feature of ECEs is that they occur at
the interface between the coast, land, and watersheds,
Ecological Monographs
Vol. 81, No. 2
which also make them especially valuable. The location
of ECEs in the land–sea interface suggests a high degree
of ‘‘interconnectedness’’ or ‘‘connectivity’’ across these
systems, leading to the linked provision of one or
multiple services by more than one ECE.
As Moberg and Rönnbäck (2003) describe for tropical
regions, numerous physical and biogeochemical interactions have been identified among mangroves, seagrass
beds, and coral reefs that effectively create interconnected systems, or a single ‘‘seascape.’’ By dissipating the
force of currents and waves, coral reefs are instrumental
for the evolution of lagoons and sheltered bays that are
suitable environments for seagrass beds and mangroves.
In turn, the control of sedimentation, nutrients, and
pollutants by mangroves and seagrasses create the
coastal water conditions that favor the growth of coral
reefs. This synergistic relationship between coral reefs,
seagrasses, mangroves, and even sand dunes, suggests
that the presence of these interlinked habitats in a
seascape may considerably enhance the ecosystem
service provided by one single habitat.
For example, Alongi (2008) suggests that the extent to
which mangroves offer protection against catastrophic
storm events, such as tsunamis, may depend not only on
the relevant features and conditions within the mangrove ecosystem, such as width of forest, slope of forest
floor, forest density, tree diameter and height, proportion of aboveground biomass in the roots, soil texture,
and forest location (open coast vs. lagoon), but also on
the presence of foreshore habitats, such as coral reefs,
seagrass beds, and dunes. Similar cumulative effects of
wave attenuation are noted for seascapes containing
coral reefs, seagrasses, and marshes (Koch et al. 2009).
As can be seen from Tables 1–5, each ECE habitat has
considerable ability to attenuate waves, and thus the
presence of foreshore habitats, such as coral reefs and
seagrasses, can reduce significantly the wave energy
reaching the seaward edge of mangroves, salt marshes,
and sand beaches and dunes. For instance, evidence
from the Seychelles documents how rising coral reef
mortality and deterioration have increased significantly
the wave energy reaching shores that are normally
protected from erosion and storm surges by these reefs
(Sheppard et al. 2005). In the Caribbean, mangroves
appear not only to protect shorelines from coastal
storms, but may also enhance the recovery of coral reef
fish populations from disturbances due to hurricanes
and other violent storms (Mumby and Hastings 2008).
ECE habitats are also linked biologically. Many fish
and shellfish species utilize mangroves and seagrass beds
as nursery grounds, and eventually migrate to coral reefs
as adults, only to return to the mangroves and seagrasses
to spawn (Layman and Silliman 2002, Nagelkerken et al.
2002, Mumby et al. 2004, Rountree and Able 2007,
Meynecke et al. 2008). In addition, the high biological
productivity of mangroves, marshes, and seagrasses also
produce significant amounts of organic matter that is
used directly or indirectly by marine fishes, shrimps,
May 2011
ECOSYSTEM SERVICE VALUES
mangroves and seagrasses enhance considerably the
biomass of coral reef fish communities. A key finding is
that mangroves become more important as nursery
habitat when excessive fishing effort levels are applied to
the reef, because the mangroves can directly offset the
negative impacts of fishing effort. Such results support
the development of ‘‘ecosystem-based’’ fishery management and the design of integrated coastal-marine
reserves that emphasize the importance of conserving
and restoring coastal mangroves as nursery sites for reef
fisheries (Mumby 2006).
In sum, allowing for the connectivity of ECE habitats
may have important implications for assessing the
ecological functions underling key ecosystems services,
such as coastal protection, control of erosion, and
habitat–fishery linkages. Only recently have studies of
ECEs begun to assess the cumulative implications for
these services, or to model this connectivity. This is one
important area for future direction of research into ECE
services that requires close collaboration between
economists, ecologists and other environmental scientists.
CONCLUSION: TOWARD
A
MANAGEMENT ACTION PLAN
Given the rate and scale at which ECEs are
disappearing worldwide, assessing and valuing the
ecological services of these systems are critically
important for improving their management and for
designing better policies. Certainly, the various economic values of ECEs should be incorporated into policy
decisions that are currently determining the major
human drivers of ecological change, such as ecosystem
conversion and degradation, resource overexploitation,
pollution, and water diversion. As indicated in Figs. 1
and 2, valuation of ECE services is a key step in
demonstrating how these human drivers of change alter
ecosystem structure and functions, and thus the
ecological production of important ecosystem goods
and services that benefit human beings.
Yet, as this review has shown, many ECE values are
non-marketed. If the aggregate willingness to pay for
these benefits is not revealed through market outcomes,
then efficient management of such ecosystem services
requires explicit methods to measure this social value.
Thus, it should not be surprising that the failure to
consider the values provided by key ECE services in
current policy and management decisions is a major
reason for the widespread disappearance of many of
these ecosystems and habitats across the globe. Improving the assessment and valuation of ECE services should
therefore be a top policy priority for any global
management plan for these ecosystems (Granek et al.
2010).
Such a priority is urgent. Our review of five ECEs (i.e.,
nearshore coral reefs, seagrass beds, salt marshes,
mangroves, and sand beaches and dunes) reveals that
many of the important benefits of these habitats have
not been estimated reliably, and even for those services
REVIEWS
crabs, and other species (Chong 2007). The consequence
is that interconnected seascapes contribute significantly
to supporting fisheries via a number of ecosystem
functions including nursery and breeding habitat,
trophic interactions, and predator-free habitat.
For example, studies in the Caribbean show that the
presence of mangroves and seagrasses enhance considerably the biomass of coral reef fish communities
(Nagelkerken et al. 2002, Mumby et al. 2004, Mumby
2006). In Malaysia, it is estimated that mangrove forests
sustain more than half of the annual offshore fish
landings, much of which are from reef fisheries (Chong
2007). In Puerto Rico, maps show fish distributions to
be controlled by the spatial arrangement of mangroves,
seagrasses, and coral reefs and the relative value of these
habitats as nurseries (Aguilar-Perera and Appeldoorn
2008). Stratification of environmental conditions along a
marsh habitat gradient, stretching from intertidal
vegetated salt marshes, to subtidal marsh creeks, to
marsh–bay fringe, and then to open water channels,
indicates large spatial and temporal variability in fish
migration, nursery habitats, and food webs (Rountree
and Able 2007). Finally, indices representing the
connectivity of mangroves, salt marshes, and channels
explained 30% to 70% of the catch-per-unit effort
harvesting yields for commercially caught species in
Queensland, Australia (Meynecke et al. 2008).
There are two ways in which current economic studies
of ECE services are incorporating such synergies. One
approach is to assess the multiple benefits arising from
entire interconnected habitats, such as estuaries. A
second method is to allow for the biological connectivity
of habitats, food webs, and migration and life-cycle
patterns across specific seascapes, such as mangrove–
seagrass–reef systems and large marine systems.
For example, Johnston et al. (2002) estimate the
benefits arising from a wide range of ecosystem services
provided by the Peconic Estuary in Long Island, New
York, USA. The tidal mudflats, salt marshes, and
seagrass (eelgrass) beds of the estuary support the
shellfish and demersal fisheries. In addition, birdwatching and waterfowl hunting are popular activities.
Incorporating production function methods, the authors
simulate the biological and food web interactions of the
ecosystems to assess the marginal value per acre in terms
of gains in commercial value for fish and shellfish, birdwatching, and waterfowl hunting. The aggregate annual
benefits are estimated to be $67 per acre for intertidal
mud flats, $338 for salt marsh, and $1065 for seagrass
across the estuary system. Using these estimates, the
authors calculate that the asset value per acre of
protecting existing habits to be $12 412 per acre for
seagrass, $4291 for salt marsh, and $786 for mudflats; in
comparison, the asset value of restored habitats is $9996
per acre for seagrass, $3454 for marsh, and $626 for
mudflats.
Sanchirico and Mumby (2009) developed an integrated seascape model to illustrate how the presence of
187
REVIEWS
188
EDWARD B. BARBIER ET AL.
that have been valued, only a few dependable studies
have been conducted. Without more efforts to value the
key services of ECEs, and to employ these values
appropriately in coastal management and planning,
slowing the worldwide degradation of coastal and
estuarine landscapes will be difficult. Assessing the
values of ECE services is critical, as all coastal interface
habitats are facing increasing pressure for conversion to
other economic activities, while at the same time, in
many coastal areas where ECEs have been degraded or
lost, there is often keen interest in restoring these
habitats.
Our review also points to other important policy
challenges for improving global management of ECEs.
For example, there is now sufficient evidence to suggest
that some services, such as coastal protection and
habitat–fishery linkages, are not uniform across a
coastal seascape. Maintaining ECEs for their multiple
and synergistic ecosystem services will also invariably
involve managing coastal landscapes across different
spatial and temporal scales. Incorporating nonlinear and
synergistic characteristics of ECEs into management
scenarios is likely to result in the most ecologically and
economically sustainable management plan possible
(Granek et al. 2010). How an ecological function, and
thus the ecosystem service it supports, varies nonlinearly
across a coastal landscape can have important implications for management at the landscape scale for all
ECEs (Koch et al. 2009).
Because the connectivity of ECEs across land–sea
gradients also influences the provision of certain
ecosystem services, management of the entire seascape
will be necessary to preserve such synergistic effects. For
example, Mumby (2006) argues that the management of
ECE habitats in the Caribbean should take into account
the life cycle migration of fish between mangroves,
seagrass beds, and coral reefs. He recommends that
management planning should focus on connected
corridors of these habitats and emphasize four key
priorities: (1) the relative importance of mangrove
nursery sites, (2) the connectivity of individual reefs to
mangrove nurseries, (3) areas of nursery habitat that
have an unusually large importance to specific reefs, and
(4) priority sites for mangrove restoration projects.
Similarly, Meynecke et al. (2008) emphasize that to
improve marine protected areas, it is important to
understand the role of connectivity in the life history of
fishes that likely utilize different ECEs.
Given the perilous state of many ECEs globally and
their critically important benefits, there is clearly a need
for a global action plan for protecting and/or enhancing
the immediate and longer term values of important ECE
services. Such a plan should contain the following
features.
First, more interdisciplinary studies involving economists, ecologists, and environmental scientists are
required to assess the values of the various ECE services
identified in this review for coral reefs, seagrasses, salt
Ecological Monographs
Vol. 81, No. 2
marshes, mangroves, and sand beaches and dunes
(Tables 1–5). A key priority is to value those services
identified in this review for which estimates are currently
unavailable or unreliable. Although we know less about
the economic benefits of seagrasses and sand beaches
and dunes compared to the other ECEs, the number of
reliable estimates of almost all services remains woefully
inadequate.
Second, destruction of these five critical ECEs for
coastal economic development can no longer be viewed
as ‘‘costless’’ by those responsible for managing and
approving such developments. In particular, the widespread global practice of giving away mangroves, salt
marshes, and other ECEs as ‘‘free land’’ for coastal
aquaculture, agricultural, and residential development
needs to be halted. Especially destructive economic
activities, such as dynamite fishing of coral reefs, clearcutting mangroves for wood chips or shrimp farming,
mining of sand dunes, extracting seagrasses for shellfish
beds, and using salt marshes for landfills, should be
banned and the bans enforced. Coastal pollution from
aquaculture, tourism activities and infrastructure, agriculture, urban areas and industry need to be monitored,
regulated, and where appropriate, taxed.
Third, in many developing countries, the current legal
framework and formal institutional structures of ECEs
and resource management do not allow local coastal
communities any legal rights to establish and enforce
control over the ECE goods and services on which the
livelihoods of these communities depend. Establishing
an improved institutional framework does not necessarily require transferring full ownership of ECE resources
to local communities, but could involve co-management
by governments and local communities that would
allow, for example, the participation of the communities
in decisions concerning the long-term management,
development and utilization of these resources.
Finally, where appropriate, ecological restoration of
key ECEs should be encouraged. However, ecological
restoration of these systems is difficult and costly, and
requires the right incentives. For example, in Thailand,
the full costs of replanting and restoring mangroves in
abandoned shrimp ponds is estimated to be around
$9318/ha, which nearly accounts for the entire capitalized value of the restored services of $12 392/ha (Barbier
2007). This suggests that investors in shrimp farms and
other coastal developments that cause widespread
mangrove destruction should have the legal requirement
to replant mangroves and finance the costs, rather than
leaving mangrove restoration solely to governments and
local communities. It should be recognized, however,
that ex post ecological restoration is no panacea for
failed conservation. Such investments are not only costly
but risky, and in many cases fall short of recovering the
full suite of ecosystem services (Palmer and Filoso 2009).
For example, as discussed in the previous section, the
Johnston et al. (2002) study of the Peconic Estuary of
Long Island found that the asset value of restored salt
May 2011
ECOSYSTEM SERVICE VALUES
marsh and seagrass and tidal mudflats in terms of
nursery habitat and recreational services were much
lower than for conserving the original habitats.
In sum, the more we learn about ECEs and their
services, it is apparent that ignoring these benefits is
detrimental to coastal management and planning. In
addition, more attention needs to be paid to how these
services vary across seascapes, as these considerations
clearly matter to managing estuarine, coastal, and
inshore marine environments (Granek et al. 2010).
Coasts and small islands may comprise just 4% of the
Earth’s total land area, but as this review has shown, the
ECEs that dominate these geographic areas provide
some of the most important global benefits for
humankind.
ACKNOWLEDGMENTS
We are grateful to two anonymous referees for helpful
comments and suggestions on this paper.
LITERATURE CITED
Bellwood, D. R., T. P. Hughes, C. Folke, and M. Nystrom.
2004. Confronting the coral reef crisis. Nature 429:827–833.
Bertness, M. D. 1991. Zonation of Spartina spp. in New
England salt marshes. Ecology 72:138–148.
Birol, K., and V. Cox. 2007. Using choice experiments to design
wetland management programmes: the case of the Severn
Estuary Wetland, UK. Journal of Environmental Planning
and Management 50:363–380.
Bockstael, N. E., A. M. Freeman III, R. J. Kopp, P. R.
Portney, and V. K. Smith. 2000. On measuring economic
values for nature. Environmental Science and Technology
34:1384–1389.
Boesch, D. F., and R. E. Turner. 1984. Dependency of fishery
species on salt marshes: the role of food and refuge. Estuaries
and Coasts 7:460–468.
Boyd, J., and S. Banzhaf. 2007. What are ecosystem services?
The need for standardized environmental accounting units.
Ecological Economics 63:616–626.
Braatz, S., S. Fortuna, J. Broadhead, and R. Leslie. 2007.
Coastal protection in the aftermath of the Indian Ocean
Tsunami. What role for forests and trees? Proceedings of the
Regional Technical Workshop, Khao Lak, Thailand, 28–31
August 2006. FAO, Bangkok, Thailand.
Brander, L. M., R. J. G. M. Florax, and J. E. Vermaat. 2006.
The empirics of wetland valuation: a comprehensive summary and a meta-analysis of the literature. Environmental and
Resource Economics 33:223–250.
Brander, L. M., P. Van Beukering, and H. S. J. Cesar. 2007.
The recreational value of coral reefs: a meta-analysis.
Ecological Economics 63:209–218.
Breaux, A., S. Farber, and J. Day. 1995. Using natural coastal
wetlands systems for wastewater treatment: an economic
benefit analysis. Journal of Environmental Management
44:285–291.
Bromberg, K., and B. R. Silliman. 2009. Patterns of salt marsh
loss within coastal regions of North America: pre-settlement
to present. Pages 253–266 in B. R. Silliman, T. Grosholz, and
M. D. Bertness, editors. Human impacts on salt marshes: a
global perspective. University of California Press, Berkeley,
California, USA.
Bromberg-Gedan, K., M. Kirwan, E. Barbier, E. Wolinksi, and
B. R. Silliman. In press. Coastal vegetations present and
future role in protecting shorelines: An answer to recent
challenges to the paradigm. Journal of Climate Change.
Bromberg-Gedan, K., B. R. Silliman, and M. D. Bertness.
2009. Centuries of human-driven change in salt marsh
ecosystems. Annual Review of Marine Science 1:117–141.
Brown, A. C., and A. McLachlan. 2002. Sandy shore
ecosystems and the threats facing them: some predictions
for the year 2025. Environmental Conservation 29:62–77.
Carpenter, K. E., et al. 2008. One-third of reef-building coral
face elevated extinction risk from climate change and local
impacts. Science 321:560–563.
Carter, R. W. G. 1990. Coastal environments: an introduction
to the physical, ecological and cultural systems of coastlines.
Academic Press, London, UK.
Carter, R. W. G. 1991. Near-future sea level impacts on coastal
dune landscapes. Landscape Ecology 6:29–39.
Cesar, H. S. J., and P. J. H. van Beukering. 2004. Economic
valuation of the coral reefs of Hawai’i. Pacific Science
58:231–242.
Chen, L., W. Wang, Y. Zhang, and G. Lin. 2009. Recent
progresses in mangrove conservation, restoration and research in China. Journal of Plant Ecology 2:45–54.
Chmura, G. L., S. C. Anisfeld, D. R. Cahoon, and J. C. Lynch.
2003. Global carbon sequestration in tidal, saline wetland
soils. Global Biogeochemical Cycles 17:1111.
Chong, J. 2005. Protective values of mangrove and coral
ecosystems: a review of methods and evidence. IUCN,
Gland, Switzerland.
REVIEWS
Aburto-Oropeza, O., E. Ezcurra, G. Danemann, V. Valdez, J.
Murray, and E. Sala. 2008. Mangroves in the Gulf of
California increase fishery yields. Proceedings of the National
Academy of Sciences USA 105:10456–10459.
Aguilar-Perera, A., and R. S. Appeldoorn. 2008. Spatial
distribution of marine fishes along a cross-shelf gradient
containing a continuum of mangrove-seagrass-coral reefs off
southwestern Puerto Rico. Estuarine, Coastal and Shelf
Science 76:378–394.
Alongi, D. M. 2002. Present state and future of the world’s
mangrove forests. Environmental Conservation 29:331–349.
Alongi, D. M. 2008. Mangrove forests: resilience, protection
from tsunamis, and responses to global climate change.
Estuarine, Coastal and Shelf Science 76:1–13.
Badola, R., and S. A. Hussain. 2005. Valuing ecosystems
functions: an empirical study on the storm protection
function of Bhitarkanika mangrove ecosystem, India. Environmental Conservation 32:85–92.
Baeyens, G., and M. L. Martı́nez. 2004. Animal life on coastal
dunes: from exploitation and prosecution to protection and
monitoring. Pages 279–296 in M. L. Martı́nez, and N. P.
Psuty, editors. Coastal dunes: ecology and conservation.
Springer-Verlag, Heidelberg, Germany.
Bandaranayake, W. M. 1998. Traditional and medicinal uses of
mangroves. Mangroves and Salt Marsh 2:133–148.
Barbier, E. B. 1994. Valuing environmental functions: tropical
wetlands. Land Economics 70:155–173.
Barbier, E. B. 2007. Valuing ecosystem services as productive
inputs. Economic Policy 22:177–229.
Barbier, E. B. 2008. Ecosystems as natural assets. Foundations
and Trends in Microeconomics 4:611–681.
Barbier, E. B., and M. Cox. 2003. Does economic development
lead to mangrove loss? A cross-country analysis. Contemporary Economic Policy 21:418–432.
Barbier, E. B., et al. 2008. Coastal ecosystem-based management with nonlinear ecological functions and values. Science
319:321–323.
Barbier, E. B., and I. Strand. 1998. Valuing mangrove-fishery
linkages: a case study of Campeche, Mexico. Environmental
and Resource Economics 12:151–166.
Bateman, I. J., and I. H. Langford. 1997. Non-users willingness
to pay for a national park: an application of the contingent
valuation method. Regional Studies 31:571–582.
Bell, F. W. 1997. The economic valuation of saltwater marsh
supporting marine recreational fishing in the southeastern
United States. Ecological Economics 21:243–254.
189
REVIEWS
190
EDWARD B. BARBIER ET AL.
Chong, V. C. 2007. Mangrove-fishery linkages: the Malaysian
perspective. Bulletin of Marine Science 80:755–772.
Cochard, R., S. L. Ranamukhaarachchi, G. P. Shivakotib,
O. V. Shipin, P. J. Edwards, and K. T. Seeland. 2008. The
2004 tsunami in Aceh and Southern Thailand: a review on
coastal ecosystems, wave hazards and vulnerability. Perspectives in Plant Ecology, Evolution and Systematics 10:3–40.
Connell, J., T. Hughes, and C. Wallace. 1997. A 30-year study
of coral abundance, recruitment, and disturbance at several
scales in space and time. Ecological Monographs 67:461–488.
Coombes, E. G., A. P. Jones, I. J. Bateman, J. A. Tratalos, J. A.
Gill, D. A. Showler, A. R. Watkinson, and W. J. Sutherland.
2010. Spatial and temporal modeling of beach use: a case
study of East Anglia, U.K. Coastal Management 37:94–115.
Cornelisen, C. D., and F. I. Thomas. 2006. Water flow enhances
ammonium and nitrate uptake in a seagrass community.
Marine Ecology Progress Series 312:1–13.
Costanza, R., O. Pérez-Maqueo, M. L. Martinez, P. Sutton,
S. J. Anderson, and K. Mulder. 2008. The value of coastal
wetlands for hurricane protection. Ambio 37:241–248.
Daehler, C. C., and D. R. Strong. 1996. Status, prediction and
prevention of introduced cordgrass Spartina spp. invasions in
Pacific estuaries, USA. Biological Conservation 78:51–58.
Das, S., and J. R. Vincent. 2009. Mangroves protected villages
and reduced death toll during Indian super cyclone.
Proceedings of the National Academy of Sciences USA
106:7357–7360.
Davy, A., E. Figueroa, and J. Bakker. 2009. Human
modification European salt marshes. Pages 311–336 in
B. R. Silliman, T. Grosholz, and M. D. Bertness, editors.
Human impacts on salt marshes: a global perspective.
University of California Press, Berkeley, California, USA.
de la Torre-Castro, M., and P. Rönnbäck. 2004. Links between
humans and seagrasses: an example from tropical East
Africa. Ocean and Coastal Management 47:361–387.
Duarte, C. M. 1991. Seagrass depth limits. Aquatic Botany
40:363–377.
Duarte, C. M. 2002. The future of seagrass meadows.
Environmental Conservation 29:192–206.
Duarte, C. M., W. C. Dennison, R. J. Orth, and T. J. B.
Carruthers. 2008. The charisma of coastal ecosystems:
addressing the imbalance. Estuaries and Coasts 31:233–238.
Duarte, C. M., J. J. Middleburg, and N. Caraco. 2005. Major
role of marine vegetation on the oceanic carbon cycle.
Biogeosciences 2:1–8.
Dulvy, N. K., D. Stanwellsmith, W. R. T. Darwall, and C. J.
Horrill. 1995. Coral mining at Mafia-island, Tanzania: a
management dilemma. Ambio 24:358–365.
Ellis, G. M., and A. C. Fisher. 1987. Valuing the environment
as input. Journal of Environmental Management 25:149–156.
Ellison, A. M., and E. J. Farnsworth. 2001. Mangrove
communities. Pages 423–442 in M. D. Bertness, S. D. Gaines,
and M. E. Hay, editors. Marine community ecology. Sinauer,
Sunderland, Massachusetts, USA.
FAO [Food and Agricultural Organization of the United
Nations]. 2007. The world’s mangroves 1980–2005. FAO
Forestry Paper 153. Food and Agricultural Organization of
the United Nations, Rome, Italy.
Fernando, H. J. S., J. L. McCulley, S. G. Mendis, and K.
Perera. 2005. Coral poaching worsens tsunami destruction in
Sri Lanka. EOS, Transactions American Geophysical Union
86(33):301304.
Fonseca, M. S., and J. A. Cahalan. 1992. A preliminary
evaluation of wave attenuation for four species of seagrass.
Estuarine, Coastal and Shelf Science 35:565–576.
Forbes, K., and J. Broadhead. 2007. The role of coastal forests
in the mitigation of tsunami impacts. RAP Publication 2007/
1. Food and Agricultural Organization of the United
Nations, Regional Office for Asia and the Pacific, Bangkok,
Thailand.
Ecological Monographs
Vol. 81, No. 2
Freeman, A. M., III. 1991. Valuing environmental resources
under alternative management regimes. Ecological Economics 3:247–256.
Freeman, A. M., III. 2003. The measurement of environmental
and resource values: theory and methods. Second edition.
Resources for the Future, Washington, D.C., USA.
Gacia, E., T. C. Granata, and C. M. Duarte. 1999. An
approach to the measurements of particle flux and sediment
retention within seagrass (Posidonia oceanica) meadows.
Aquatic Botany 65:255–269.
Gardner, T. A., I. M. Cote, J. A. Gill, A. Grant, and A. R.
Watkinson. 2003. Long-term region-wide declines in Caribbean corals. Science 301:958–960.
Gattuso, J. P., M. Frankignoulle, and R. Wollast. 1998. Carbon
and carbonate metabolism in coastal aquatic ecosystems.
Annual Review of Ecology and Systematics 405–434.
Glynn, P. W. 1997. Bioerosion and coral-reef growth: a
dynamic balance. Pages 68–95 in C. Birkeland, editor. Life
and death of coral reefs. Chapman and Hall, New York, New
York, USA.
Graham, N. A. J., S. K. Wilson, S. Jennings, N. V. C. Polunin,
J. Robinson, J. P. Bijoux, and T. M. Daw. 2007. Lag effects
in the impacts of mass coral bleaching on coral reef fish,
fisheries, and ecosystems. Conservation Biology 21:1291–
1300.
Granek, E. F., et al. 2010. Ecosystem services as a common
language for coastal ecosystem-based management. Conservation Biology 24:207–216.
Greenstein, B. J., and J. M. Pandolfi. 2008. Escaping the heat:
range shifts of reef coral taxa in coastal Western Australia.
Global Change Biology 14:513–528.
Hacker, S. D., and M. D. Bertness. 1995. Morphological and
physiological consequences of a positive plant interaction.
Ecology 76:2165–2175.
Hacker, S. D., P. Zarnetske, E. Seabloom, P. Ruggiero, J. Mull,
S. Gerrity, and C. Jones. In press. Subtle differences in two
non-native congeneric beach grasses significantly affect their
colonization, spread, and impact. Oikos.
Hallock, P. 1997. Reefs and reef limestones in earth history.
Pages 13–42 in C. Birlelund, editor. Life and death of coral
reefs. Chapman and Hall, New York, New York, USA.
Halpern, B. S., et al. 2008. A global map of human impacts on
marine ecosystems. Science 319:948–952.
Hanley, N., and E. B. Barbier. 2009. Pricing nature: cost-benefit
analysis and environmental policy-making. Edward Elgar,
London, UK.
Hardisty, J. 1994. Beach and nearshore sediment transport.
Pages 216–255 in K. Pye, editor. Sediment transport and
depositional processes. Blackwell, London, UK.
Hemminga, M. A., and C. M. Duarte. 2000. Seagrass ecology.
Cambridge University Press, Cambridge, UK.
Hemminga, M. A., and J. Nieuwenhuize. 1990. Seagrass wrackinduced dune formation on a tropical coast (Banc-Darguin,
Mauritania). Estuarine Coastal and Shelf Science 31:499–
502.
Henry, H., and R. L. Jefferies. 2009. Opportunistic herbivores,
migratory connectivity, and catastrophic shifts in Arctic
coastal ecosystems. Pages 85–102 in B. R. Silliman, T.
Grosholz, and M. D. Bertness, editors. Human impacts on
salt marshes: a global perspective. University of California
Press, Berkeley, California, USA.
Heslenfeld, P., P. D. Jungerius, and J. A. Klijn. 2004. European
coastal dunes: ecological values, threats, opportunities, and
policy development. Pages 335–351 in M. L. Martı́nez and
N. P. Psuty, editors. Coastal dunes: ecology and conservation. Springer-Verlag, Heidelberg, Germany.
Hesp, P. A. 1989. A review of biological and geomorphological
processes involved in the initiation and development of
incipient foredunes. Proceedings of the Royal Society of
Edinburgh 96B:181–201.
May 2011
ECOSYSTEM SERVICE VALUES
Leatherman, S. P. 1979. Beach and dune interactions during
storm conditions. Quarterly Journal of Engineering Geology
and Hydrogeology 12:281–290.
Lee, K. S., and K. H. Dunton. 1999. Inorganic nitrogen
acquisition in the seagrass Thalassia testudinum: development
of a whole plant nitrogen budget. Limnology and Oceanography 44:1404–1215.
Lotze, H. K., H. S. Lenihan, B. J. Bourque, R. H. Bradbury,
R. G. Cooke, M. C. Kay, S. M. Kidwell, M. X. Kirby, C. H.
Peterson, and J. B. C. Jackson. 2006. Depletion, degradation,
and recovery potential of estuaries and coastal seas. Science
312:1806–1809.
Lubbock, H. R., and N. V. C. Polunin. 1975. Conservation and
the tropical marine aquarium trade. Environmental Conservation 2:229–232.
Lui, P. L.-F., P. Lynett, H. Fernando, B. E. Jaffe, F. Fritz, B.
Higman, R. Morton, J. Goff, and C. Synolakis. 2005.
Observations by the International Tsunami Survey Team in
Sri Lanka. Science 308:1595.
MacFarlane, G. R., A. Pulkownik, and M. D. Burchett. 2003.
Accumulation and distribution of heavy metals in the grey
mangrove, Avicennia marina (Forsk.) Vierh.: biological
indication potential. Environmental Pollution 123:139–151.
MacKenzie, R. A., and M. Dionne. 2008. Habitat heterogeneity: importance of salt marsh pools and high marsh surfaces
to fish production in two Gulf of Maine salt marshes. Marine
Ecology Progress Series 368:217–230.
Manson, F. J., N. R. Loneragan, G. A. Skilleter, and S. R.
Phinn. 2005. An evaluation of the evidence for linkages
between mangroves and fisheries: a synthesis of the literature
and identification of research directions. Oceanography and
Marine Biology: An Annual Review 43:483–513.
Massel, S. R., K. Furukawa, and R. M. Brinkman. 1999.
Surface wave propagation in mangrove forests. Fluid
Dynamics Research 24:219–249.
Mathieu, L. F., I. H. Langford, and W. Kenyon. 2003. Valuing
marine parks in a developing country: a case study of the
Seychelles. Environment and Development Economics
8:373–390.
Mayor, J., and C. Hicks. 2009. Potential impacts of elevated
CO2 on plant interactions, sustained growth, and carbon
cycling in salt marsh ecosystems. Pages 207–230 in B. R.
Silliman, T. Grosholz, and M. D. Bertness, editors. Human
impacts on salt marshes: a global perspective. University of
California Press, Berkeley, California, USA.
Mazda, Y., M. Magi, Y. Ikeda, T. Kurokawa, and T. Asano.
2006. Wave reduction in a mangrove forest dominated by
Sonneratia sp. Wetlands Ecology and Management 14:365–
378.
Mazda, Y., M. Magi, M. Kogo, and P. N. Hong. 1997.
Mangroves as a coastal protection from waves in the Tong
King Delta, Vietnam. Mangroves and Salt Marshes 1:127–
135.
McArthur, L. C., and J. W. Boland. 2006. The economic
contribution of seagrass to secondary production in South
Australia. Ecological Modeling 196:163–172.
McConnell, K. E., and N. E. Bockstael. 2005. Valuing the
environment as a factor of production. Pages 621–669 in
K.-G. Mäler and J. R. Vincent, editors. Handbook of
environmental economics. Volume 2. Elsevier, Amsterdam,
The Netherlands.
MEA [Millennium Ecosystem Assessment]. 2005. Ecosystems
and human well-being: current state and trends. Coastal
systems. Island Press, Washington, D.C., USA.
Mendelsohn, R., and S. Olmstead. 2009. The economic
valuation of environmental amenities and disamenities:
methods and applications. Annual Review of Environment
and Resources 34:325–347.
Meynecke, J.-O., S. Y. Lee, and N. C. Duke. 2008. Linking
spatial metrics and fish catch reveals the importance of
REVIEWS
Hesp, P. A., and A. D. Short. 1999. Barrier morphodynamics.
Pages 307–333 in A. D. Short, editor. Handbook of beach
and shoreface morphodynamics. Wiley and Sons, Chichester,
UK.
Hoegh-Guldberg, O. 1999. Climate change, coral bleaching and
the future of the world’s coral reefs. Marine and Freshwater
Research 50:839–866.
Hoegh-Guldberg, O., et al. 2007. Coral reefs under rapid
climate change and ocean acidification. Science 318:1737–
1742.
Houston, J. R. 2008. The economic value of beaches: a 2008
update. Shore and Beach 76:22–26.
Huang, J.-C., P. J. Poor, and M. Q. Zhao. 2007. Economic
valuation of beach erosion control. Marine Resource
Economics 32:221–238.
Hughes, T. P., D. R. Bellwood, C. Folke, R. S. Steneck, and J.
Wilson. 2005. New paradigms for supporting resilience of
marine ecosystems. Trends in Ecology and Evolution 20:380–
386.
Janssen, R., and J. E. Padilla. 1999. Preservation or conservation? Valuation and evaluation of a mangrove forest in the
Philippines. Environmental and Resource Economics 14:297–
331.
Johnston, R. J., T. A. Grigalunas, J. J. Opaluch, M. Mazzotta,
and J. Diamantedes. 2002. Valuing estuarine resource
services using economic and ecological models: the Peconic
Estuary System. Coastal Management 30:47–65.
Kawahata, H., A. Suzuki, and K. Goto. 1997. Coral reef
ecosystems as a source of atmospheric CO2: evidence from
PCO2 measurements of surface waters. Coral Reefs 16:261–
266.
King, S. E., and J. N. Lester. 1995. The value of salt marsh as a
sea defence. Marine Pollution Bulletin 30:180–189.
Koch, E. W. 1996. Hydrodynamics of a shallow Thalassia
testudinum bed in Florida, USA. Pages 105–110 in J. Kuo,
R. C. Phillips, D. I. Walker, and H. Kirkman, editors.
Seagrass biology: proceedings of an international workshop.
Western Australia Museum, Perth, Australia.
Koch, E. W., J. Ackerman, M. van Keulen, and J. Verduin.
2006. Fluid dynamics in seagrass ecology: from molecules to
ecosystems. Pages 193–225 in A. W. D. Larkum, R. J. Orth,
and C. M. Duarte, editors. Seagrasses: biology, ecology and
conservation. Springer-Verlag, Heidelberg, Germany.
Koch, E. W., et al. 2009. Non-linearity in ecosystem services:
temporal and spatial variability in coastal protection.
Frontiers in Ecology and the Environment 7:29–37.
Kriesel, W., and C. E. Landry. 2004. Participation in the
National Flood Insurance Program: an empirical analysis for
coastal properties. Journal of Risk and Insurance 71:405–
420.
Landry, C. E., A. G. Keeler, and W. Kriesel. 2003. An
economic evaluation of beach erosion management alternatives. Marine Resource Economics 18:105–127.
Landry, C. E., and H. Liu. 2009. A semi-parametric estimator
for revealed and stated preference application to recreational
beach visitation. Journal of Environmental Economics and
Management 57:205–218.
Lange, G.-M., and N. Jiddawi. 2009. Economic value of marine
ecosystem services in Zanzibar: implications for marine
conservation and sustainable development. Ocean and
Coastal Management 52:521–532.
Lauer, M., and S. Aswani. 2010. Indigenous knowledge and
long-term ecological change: detection, interpretation, and
responses to changing ecological conditions in pacific Island
Communities. Environmental Management 45:985–997.
hhttp://www.springerlink.com/content/g6u604k241n57646/
fulltext.pdf i
Layman, C. A., and B. R. Silliman. 2002. Preliminary survey of
the fish fauna in Fresh Creek, Andros, Bahamas. Bulletin of
Marine Science 70:199–210.
191
REVIEWS
192
EDWARD B. BARBIER ET AL.
coastal wetland connectivity to inshore fisheries in Queensland, Australia. Biological Conservation 141:981–996.
Mitsch, W. J., and J. G. Gosselink. 2008. Wetlands. Van
Nostrand Reinhold, New York, New York, USA.
Moberg, F., and C. Folke. 1999. Ecological goods and services
of coral reef ecosystems. Ecological Economics 29:215–233.
Moberg, F., and P. Rönnbäck. 2003. Ecosystem services of the
tropical seascape: interactions, substitutions and restoration.
Ocean and Coastal Management 46:27–46.
Montgomery, R. D. 2006. The next Sumatera tsunami: Who
will live and who will die? Asian Affairs 37:50–71.
Moreno-Casasola, P. 2004. A case study of conservation and
management of tropical sand dune systems: La Mancha–El
Llano. Pages 319–333 in M. L. Martı́nez, N. P. Psuty, editors.
Coastal dunes: ecology and conservation. Springer-Verlag,
Heidelberg, Germany.
Morgan, O. A., and S. E. Hamilton. 2010. Estimating a
payment vehicle for financing nourishment of residential
beaches using a spatial-lag hedonic property price model.
Coastal Management 38:65–75.
Morgan, P. A., D. M. Burdick, and F. T. Short. 2009. The
functions and values of fringing salt marshes in Northern
New England, USA. Estuaries and Coasts 32:483–495.
Morton, R. A., G. Gelfenbaum, and B. E. Jaffe. 2007. Physical
criteria for distinguishing sandy tsunami and storm deposits
using modern examples. Sedimentary Geology. [doi: 10.1016/
j.sedgeo.2007.01.003]
Mumby, P. J. 2006. Connectivity of reef fish between
mangroves and coral reefs: algorithms for the design of
marine reserves at seascape scales. Biological Conservation
128:215–222.
Mumby, P. J., et al. 2006. Fishing, trophic cascades, and the
process of grazing on coral reefs. Science 311:98–101.
Mumby, P. J., A. J. Edwards, J. E. Arias-Gonzalez, K. C.
Lindeman, P. G. Blackwell, A. Gall, M. I. Gorczynska, A. R.
Harborne, C. L. Pescod, H. Renken, C. C. C. Wabnitz, and
G. Llewellyn. 2004. Mangroves enhance the biomass of reef
fisheries in the Caribbean. Nature 427:533–536.
Mumby, P. J., A. R. Harborne, J. Williams, C. V. Kappel,
D. R. Brumbaugh, F. Micheli, K. E. Holmes, C. P. Dahlgren,
C. B. Paris, and P. G. Blackwell. 2007. Trophic cascade
facilitates coral recruitment in a marine reserve. Proceedings
of the National Academy of Sciences USA 104:8362–8367.
Mumby, P. J., and A. Hastings. 2008. The impact of ecosystem
connectivity on coral reef resilience. Journal of Applied
Ecology 45:854–862.
Nagelkerken, I., C. M. Roberts, G. van der Velde, M.
Dorenbosch, M. C. van Riel, E. Cocheret de la Morinière,
and P. H. Nienhuis. 2002. How important are mangroves and
seagrass beds for coral-reef fish? The nursery hypothesis
tested on an island scale. Marine Ecology Progress Series
244:299–305.
Naylor, R., and M. Drew. 1998. Valuing mangrove resources in
Kosrae, Micronesia. Environment and Development Economics 3:471–490.
Nfotabong Atheull, A., N. Din, S. N. Longonje, N. Koedam,
and F. Dahdouh-Guebas. 2009. Commercial activities and
subsistence utilization of mangrove forests around the Wouri
estuary and the Douala-Edea reserve (Cameroon). Journal of
Ethnobiology and Ethnomedicine 5:35–49.
NRC [National Research Council]. 2005. Valuing ecosystem
services: toward better environmental decision making.
National Academies Press, Washington, D.C., USA.
Orth, R. J., et al. 2006. A global crisis for seagrass ecosystems.
BioScience 56:987–996.
Othman, J., J. Bennett, and R. Blamey. 2004. Environmental
management and resource management options: a choice
modelling experiment in Malaysia. Environment and Development Economics 9:803–824.
Ecological Monographs
Vol. 81, No. 2
Pagiola, S., K. von Ritter, and J. Bishop. 2004. How much is an
ecosystem worth? Assessing the economic value of conservation. World Bank, Washington, D.C., USA.
Palmer, M. A., and S. Filoso. 2009. Restoration of ecosystem
services for environmental markets. Science 31:575–576.
Pandolfi, J. M. 2002. Coral community dynamics at multiple
scales. Coral Reefs 21:12–23.
Peterson, G. W., and R. E. Turner. 1994. The value of salt
marsh edge versus interior as habitat for fish and decapods
crustaceans in a Louisiana tidal marsh. Estuaries 17:235–262.
Petersen, J. E., et al. 2003. Multiscale experiments in coastal
ecology: improving realism and advancing theory. BioScience
53:1181–1197.
Pet-Soede, C. H., S. J. Cesar, and J. S. Pet. 1999. An economic
analysis of blast fishing on Indonesian coral reefs. Environmental Conservation 26:83–93.
Polasky, S., and K. Segerson. 2009. Integrating ecology and
economics in the study of ecosystem services: some lessons
learned. Annual Review of Resource Economics 1:409–434.
Prager, E. J., and R. B. Halley. 1999. The influence of seagrass
on shell layers and Florida Bay mudbanks. Journal of
Coastal Research 15:1151–1162.
Pratchett, M. S., M. S. Munday, S. K. Wilson, N. A. J.
Graham, J. E. Cinner, D. R. Bellwood, G. P. Jones, N. V. C.
Polunin, and T. R. McClanahan. 2008. Effects of climateinduced coral bleaching on coral-reef fishes: ecological and
economic consequences. Oceanography and Marine Biology
46:251–296.
Pye, K., and H. Tsoar. 1990. Aeolian sand and sand dunes.
Unwin Hyman, London, UK.
Romero, J., K.-S. Lee, M. Perez, M. A. Mateo, and T.
Alcoverro. 2006. Nutrient dynamics in seagrass ecosystems.
Pages 227–254 in A. W. D. Larkum, R. J. Orth, and C. M.
Duarte, editors. Seagrass biology, ecology and conservation.
Springer-Verlag, Amsterdam, The Netherlands.
Rönnbäck, P. 1999. The ecological basis for economic value of
seafood production supported by mangrove ecosystems.
Ecological Economics 29:235–252.
Rönnbäck, P., B. Crona, and L. Ingwall. 2007. The return of
ecosystem goods and services in replanted mangrove forests:
perspectives from local communities in Gazi Bay, Kenya.
Environmental Conservation 34:313–324.
Rountree, R. A., and K. W. Able. 2007. Spatial and temporal
habitat use patterns for salt marsh nekton: implications for
ecological functions. Aquatic Ecology 41:25–45.
Ruggiero, P., M. C. Buijsman, G. M. Kaminsky, and G. B.
Gelfenbaum. 2010. Modeling the effect of wave climate and
sediment supply variability on large scale shoreline change.
Marine Geology 273:127–140.
Ruitenbeek, H. J. 1994. Modeling economy–ecology linkages in
mangroves: economic evidence for promoting conservation in
Bintuni Bay, Indonesia. Ecological Economics 10:233–247.
Rybicki, N. B. 1997. Observations of tidal flux between
submersed aquatic plant stand and the adjacent channel in
the Potomac River near Washington, D.C. Limnology and
Oceanography 42:307–317.
Sadovy, Y. J., and A. C. J. Vincent. 2002. Ecological issues and
the trades in live reef fishes. Pages 391–420 in P. F. Sale,
editor. Coral reef fishes: dynamics and diversity in a complex
ecosystem. Academic Press, San Diego, California., USA.
Sallenger, A. H., H. F. Stockdon, L. Fauver, M. Hansen, D.
Thompson, C. W. Wright, and J. Lillycrop. 2006. Hurricanes
2004: an overview of their characteristics and coastal change.
Estuaries and Coasts 29:880–888.
Samonte-Tan, G. P. B., A. T. White, M. T. J. Diviva, E.
Tabara, and C. Caballes. 2007. Economic valuation of
coastal and marine resources: Bohol Marine Triangle,
Philippines. Coastal Management 35:319–338.
Sanchirico, J. N., and P. Mumby. 2009. Mapping ecosystem
functions to the valuation of ecosystem services: implications
May 2011
ECOSYSTEM SERVICE VALUES
van der Meulen, F., T. W. M. Bakker, and J. A. Houston. 2004.
The costs of our coasts: examples of dynamic dune
management from Western Europe. Pages 259–277 in M. L.
Martı́nez, and N. P. Psuty, editors. Coastal dunes: ecology
and conservation. Springer-Verlag, Heidelberg, Germany.
Walters, B. B., P. Rönnbäck, J. M. Kovacs, B. Crona, S. A.
Hussain, R. Badola, J. H. Primavera, E. B. Barbier, and F.
Dahdouh-Guebas. 2008. Ethnobiology, socio-economics and
management of mangrove forests: a review. Aquatic Botany
89:220–236.
Walton, M. E. M., G. P. B. Samonte-Tan, J. H. Primavera, G.
Edwards-Jones, and L. Le Vay. 2006. Are mangroves worth
replanting? The direct economic benefits of a communitybased reforestation project. Environmental Conservation
33:335–343.
Warren-Rhodes, K., Y. Sadovy, and H. Cesar. 2004. Marine
ecosystem appropriation in the Indo-Pacific: A case study of
the live reef fish food trade. Ambio 33:116–119.
Watson, R. A., R. G. Coles, and W. L. L. Long. 1993.
Simulation estimates of annual yield and landed value for
commercial Panaeid prawns from a tropical seagrass habitat,
Northern Queensland, Australia. Australian Journal of
Marine and Freshwater Research 44:211–219.
Wattage, P., and S. Mardle. 2008. Total economic value of
wetland conservation in Sri Lanka: identifying use and nonuse value. Wetlands Ecology and Management 16:359–369.
Waycott, M., et al. 2009. Accelerating loss of seagrasses across
the globe threatens coastal ecosystems. Proceedings of the
National Academy of Sciences USA 106:12377–12381.
White, A. T., H. P. Vogt, and T. Arin. 2000. Philippine coral
reefs under threat: the economic losses caused by reef
destruction. Marine Pollution Bulletin 40:598–605.
Whitehead, J. C., C. F. Dumas, J. Herstine, J. Hill, and B.
Buerger. 2008. Valuing beach access and width with revealed
and stated preference data. Marine Resource Economics
23:119–135.
Wilkinson, C., O. Linden, H. Cesar, G. Hodgson, J. Rubens,
and A. E. Strong. 1999. Ecological and socioeconomic
impacts of 1998 coral mortality in the Indian Ocean: an
ENSO impact and a warning of future change? Ambio
28:188–196.
Wolanski, E. 2007. Estuarine ecohydrology. Elsevier, Amsterdam, The Netherlands.
Wood, E. M. 1985. Exploitation of coral reef fishes for the
aquarium fish trade. Marine Conservation Society, RossonWye, UK.
Worm, B., et al. 2006. Impacts of biodiversity loss on ocean
ecosystem services. Science 314:787–790.
Yeo, B. 2002. Valuing a marine park in Malaysia. Pages 311–
326 in David Pearce, editor. Valuing the environment in
developing countries: case studies. Edward Elgar Publishing,
Cheltenham, UK.
Zarnetske, P. L., E. W. Seabloom, and S. D. Hacker. 2010.
Non-target effects of invasive species management: beachgrass, birds, and bulldozers in coastal dunes. Ecosphere 1:
art13.
Zeller, D., S. Booth, and D. Pauly. 2007. Fisheries contributions to the gross domestic product: underestimating smallscale fisheries in the Pacific. Marine Resource Economics
21:355–374.
Zhang, J., and M. D. Smith. In press. Estimation of a
generalized fishery model: a two-stage approach. Review of
Economics and Statistics.
Zimmerman, R. J., T. J. Minnillo, and L. P. Rozas. 2000. Salt
marsh linkages to productivity of Penaeid shrimps and blue
crabs in the Northern Gulf of Mexico. Pages 293–314 in
M. P. Weinstein and D. A. Kreeger, editors. Concepts and
controversies in marsh ecology. Kluwer Academic, Amsterdam, The Netherlands.
REVIEWS
of species-habitat associations for coastal land-use decisions.
Theoretical Ecology 2:67–77.
Sarntisart, I., and S. Sathirathai. 2004. Mangrove dependency,
income distribution and conservation. Pages 96–114 in E. B.
Barbier, and S. Sathirathai, editors. Shrimp farming and
mangrove loss in Thailand. Edward Elgar, London, UK.
Sathirathai, S., and E. B. Barbier. 2001. Valuing mangrove
conservation, Southern Thailand. Contemporary Economic
Policy 19:109–122.
Sheppard, C., D. J. Dixon, M. Gourlay, A. Sheppard, and R.
Payet. 2005. Coral mortality increases wave energy reaching
shores protected by reef flats: examples from the Seychelles.
Estuarine, Coastal and Shelf Science 64:223–234.
Short, A. D. 1999. Wave-dominated beaches. Pages 173–203 in
A. D. Short, editor. Handbook of beach and shoreface
morphodynamics. Wiley and Sons, Chichester, UK.
Short, A. D., and P. A. Hesp. 1982. Wave, beach and dune
interactions in southeast Australia. Marine Geology 48:259–
284.
Silliman, B. R., and M. D. Bertness. 2002. A trophic cascade
regulates salt marsh primary production. Proceedings of the
National Academy of Sciences USA 99:10500–10505.
Silliman, B. R., and A. Bortolus. 2003. Underestimation of
Spartina alterniflora production in Western Atlantic salt
marshes. Oikos 143:549–555.
Silliman, B. R., T. Grosholz, and M. D. Bertness. 2009. Salt
marshes under global siege. Pages 103–114 in B. R. Silliman,
T. Grosholz, and M. D. Bertness, editors. Human impacts on
salt marshes: a global perspective. University of California
Press, Berkeley, California, USA.
Silliman, B. R., J. van de Koppel, M. D. Bertness, L. Stanton,
and I. Mendelsohn. 2005. Drought, snails, and large-scale
die-off of southern U.S. salt marshes. Science 310:1803–1806.
Smith, M. D. 2007. Generating value in habitat-dependent
fisheries: the importance of fishery management institutions.
Land Economics 83:59–73.
Spalding, M. D., F. Blasco, and C. D. Field. 1997. World
mangrove atlas. International Society for Mangrove Ecosystems, Okinawa, Japan.
Spalding, M. D., M. Taylor, C. Ravilious, F. Short, and E.
Green. 2003. The distribution and status of seagrasses. Pages
5–26 in E. P. Green and F. T. Short, editors. World atlas of
seagrasses. University of California Press, Berkeley, California, USA.
Stockdon, H. F., H. A. Sallenger, R. A. Holman, and P. A.
Howd. 2007. A simple model for the spatially-variable
coastal response to hurricanes. Marine Geology 238:1–20.
Tapsuwan, S., and J. Asafu-Adjaye. 2008. Estimating the
economic benefit of SCUBA diving in the Similan Islands,
Thailand. Coastal Management 36:431–442.
Thampanya, U., J. E. Vermaat, S. Sinsakul, and N. Panapitukkul. 2006. Coastal erosion and mangrove progradation of
Southern Thailand. Estuarine, Coastal and Shelf Science
68:75–85.
UNEP [United Nations Environment Programme]. 2006.
Marine and coastal ecosystems and human wellbeing: A
synthesis report based on the findings of the Millennium
Ecosystem Assessment. UNEP, Nairobi, Kenya.
U.S. EPA [U.S. Environmental Protection Agency]. 2009.
Valuing the protection of ecological systems and services. A
report of the EPA Science Advisory Board. EPA, Washington, D.C., USA.
Valiela, I., J. L. Bowen, and J. K. York. 2001. Mangrove
forests: one of the world’s threatened major tropical
environments. BioScience 51:807–815.
van Beukering, P. J. H., and H. S. J. Cesar. 2004. Ecological
economic modeling of coral reefs: evaluating tourist overuse
at Hanauma Bay and algae blooms at the Kihei coast,
Hawai’i. Pacific Science 58:243–260.
193