Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threa (2024)

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Volume 51 Issue 10 October 2001

Article Contents

  • Area of current mangrove forest

  • Rates of mangrove forest loss

  • Mangrove habitat losses relative to human activity

  • The importance of mariculture for mangrove habitat losses

  • Comparisons with other tropical environments

  • Acknowledgments

  • References cited

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Ivan Valiela

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Jennifer L. Bowen

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Joanna K. York

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Oxford Academic

Ivan Valiela is a professor of biology, at the Boston University Marine Program, Marine Biological Laboratory, Woods Hole, MA 02543.

Jennifer L. Bowen and Joanna K. York are graduate students, at the Boston University Marine Program, Marine Biological Laboratory, Woods Hole, MA 02543.

Author Notes

BioScience, Volume 51, Issue 10, October 2001, Pages 807–815, https://doi.org/10.1641/0006-3568(2001)051[0807:MFOOTW]2.0.CO;2

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01 October 2001

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    Ivan Valiela, Jennifer L. Bowen, Joanna K. York, Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments, BioScience, Volume 51, Issue 10, October 2001, Pages 807–815, https://doi.org/10.1641/0006-3568(2001)051[0807:MFOOTW]2.0.CO;2

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The mass media and scientific press have widely reported losses of tropical environments, such as felling of rain forests and bleaching of coral reefs. This well-merited attention has created a worldwide constituency that supports conservation and restoration efforts in both of these threatened ecosystems. The remarkable degree of public awareness and support has been manifested in benefit rock concerts at Carnegie Hall and in the designation of ice cream flavors after rain forest products. Mangrove forests are another important tropical environment, but these have received much less publicity. Concern about the magnitude of losses of mangrove forests has been voiced mainly in the specialized literature (Saenger et al. 1983, Spalding et al. 1997).

Mangrove trees grow ubiquitously as a relatively narrow fringe between land and sea, between latitudes 25°N and 30°S. They form forests of salt-tolerant species, with complex food webs and ecosystem dynamics (Macnae 1968, Lugo and Snedaker 1974, Tomlinson 1986).

Destruction of mangrove forests is occurring globally. Global changes such as an increased sea level may affect mangroves (Ellison 1993, Field 1995), although accretion rates in mangrove forests may be large enough to compensate for the present-day rise in sea level (Field 1995). More important, it is human alterations created by conversion of mangroves to mariculture, agriculture, and urbanization, as well as forestry uses and the effects of warfare, that have led to the remarkable recent losses of mangrove habitats (Saenger et al. 1983, Fortes 1988, Marshall 1994, Primavera 1995, Twilley 1998).

New data on the magnitude of mangrove area and changes in it have become more readily available, especially with the advent of satellite imagery and the Internet. Moreover, information about the function of mangrove swamps, their importance in the sustainability of the coastal zone, and the effects of human uses of mangrove forests is growing. Some published regional assessments have viewed anthropogenic threats to mangrove forests with alarm (Ong 1982, Fortes 1988, Ellison and Farnsworth 1996), but reviews at the global scale are dated (Linden and Jernelov 1980, Saenger et al. 1983).

We collated and revised published information to review the status of mangrove swamps worldwide. To assess the status of this major coastal environment, we compiled and examined available data to quantify the extent of mangrove forest areas in different parts of the world, the losses of mangrove forest area recorded during recent decades, and the relative contributions by various human activities to these losses.

We first assessed current mangrove forest area in tropical countries of the world. It is difficult to judge the quality of these data in the published literature, because in many cases the methods used to obtain them were insufficiently described and the associated uncertainty was not indicated. Much information based on satellite imagery is summarized in the World Mangrove Atlas (Spalding et al. 1997). We compared and supplemented data from the atlas with data from local or regional publications, where available, to update estimates of the area covered by mangrove forests for as many countries as possible.

We then estimated long-term changes in mangrove habitat areas by compiling information on time courses of areas of mangrove forests. These data too were compiled for as many countries as published sources allowed. Few papers reported multiyear data; most of our compilation consists of data for a given country, published in different years (Table 1).

To examine linkages between human activities and losses of mangrove habitats, we compared overall economic activity by compiling data on per capita gross national product (GNP; data from the Central Intelligence Agency's World Factbook are available at Web site www.cia.gov). We also compared loss of mangrove habitat with absolute coastal population density (calculated as the length of coastline per country and estimating that 37% of the population lives within 100 km of the shore [Cohen et al. 1997]). Then, to identify the relative contribution of specific human activities responsible for losses of mangroves, we compiled published data on areas of mangrove that were lost or converted to other land covers through diverse human uses.

Area of current mangrove forest

We estimate, from our compilation of the most recent data for all countries where mangroves have been reported, that there are roughly 1.7×105 km2 of mangrove habitats along the shorelines of the world (Table 2). Our estimate of total mangrove area is similar to previous calculations of total mangrove area, 1.7×105 km2 (Saenger et al. 1983), and 1.8×105 km2 (Spalding et al. 1997). These compilations are based on near-complete coverage of current mangrove areas in countries around the world, but they include data collected across widely different times (1980s to present) through different methods, and there is large uncertainty in most of the numbers (Spalding et al. 1997). Even when the methods include modern remote sensing, uncertainty in remotely sensed data is greater for mangrove forests than terrestrial forests, because the translation of imagery to area is difficult in land parcels with the elongated linear shapes of mangrove forests (Muchoney et al. 2000).

To gain a notion of the uncertainty in estimates of mangrove area, for each country we compared two estimates from Spalding and colleagues (1997), who include both their estimate from vegetation maps and remote sensing and a recent estimate drawn from the literature. From these presumably independent estimates, we calculated that the mean difference between independent estimates of mangrove area per country was 36%; estimates of area are therefore relatively uncertain when considered for each country. We also calculated that, for the entire data set, the mean differences had an associated coefficient of variation of only 2.5%. This low value suggested that aggregating the data would yield more reliable results. For this calculation, we aggregated the country data on the basis of continents.

By far the largest proportions of mangroves occur in Asia and the Americas (Table 2). Countries with the largest area of mangroves are Indonesia (4.25×104 km2; Spalding et al. 1997), followed by Brazil (1.34×104 km2; Spalding et al. 1997), Nigeria (1.05×104 km2; Saenger and Bellan 1995), and Australia (1.00×104 km2; Robertson and Duke 1990).

Rates of mangrove forest loss

Mangrove acreage decreased during recent decades in most countries for which we found multiyear data in the literature (Figure 1). The rates of decline differ from country to country (Table 1), but the striking feature in Figure 1 is the dominant pattern of reduced acreage for nearly all countries, particularly those with large mangrove forest areas.

To evaluate losses of mangrove acreage within each continent, we pooled the country data from those countries with plausible multiyear records (Figure 1) and calculated losses per continent. We excluded data from some countries, however, because reported changes in area could reflect actual changes in area stemming from the combined effects of destruction, restoration efforts, and natural expansion of mangrove forests, as well as apparent increases derived from the improved quality of surveys. In practice, rates of increase from restoration and natural re-growth are slow (Roth 1992, Sherman et al. 2000), so that significant short-term (a few years) increases were most likely due to survey improvements. We did include data from Belize, Brunei, Cuba, Jamaica, Sierra Leone, and Yemen, where there were modest multiyear increases in area of mangroves (Table 1, Figure 1). In Cuba, for instance, there was a reported 257 km2 of planted mangroves (Spalding et al. 1997); this does not match the increases in Figure 1, but it shows that some increases were real rather than a result of better surveys.

To determine the change in mangrove area for each country with good multiyear data, we calculated the difference between the current and the “original” area of mangroves (by “original” we mean the earliest recorded area of mangrove forests in the literature). We then compiled the results by continent (Table 2). To obtain rates of change, we divided the change in area by the number of years spanned by the records. The span of years varied. For example, we found data for the Philippines and Madagascar beginning in the 1920s; for Vietnam, 1945; and for Thailand and India, 1965; the bulk of the data, however, were from the late 1970s to the early 1980s (Figure 1).

For all continents, present-day mangrove forest area is substantially smaller than the original area, with a world average loss of 35% (Table 2). On a worldwide scale, just under 3×103 km2 of mangroves have been lost each year since the early 1980s, which translates into an overall areal loss rate of 2.1% per year. On a continental basis, losses can be larger, as in the Americas, for example (Table 2). Published regional-scale surveys confirm high loss rates. For example, mangrove loss rates in Southeast Asia have been greater than 1% per year (Ong 1982). It is therefore evident that both the magnitude of mangrove loss and annual loss rates are considerable.

The estimates of losses of mangrove area shown in Table 2 are based on information from countries that in aggregate hold 54% of the world's mangrove acreage (Table 2). We can surmise that the remaining 46% of the world's mangroves are exposed to similar losses. Two countries with large areas of mangrove were not included in our calculations. We found no plausible multiyear record of mangrove areas for Indonesia (26% of the world total), where losses in some regions are said to reach 50% to 80% (Wolanski et al. 2000). Estimates of Nigerian mangrove areas (6.3% of the world total) from the 1980s to 1997 exist (Saenger et al. 1983, Adegbehin and Nwaigbo 1990, Diop 1993, Saenger and Bellan 1995), but differences in the estimates make it difficult to find a convincing time course. Research and surveys to assess destruction of Indonesian and Nigerian mangroves should be a priority. We expect that, given the many published citations of damage in parts of the world for which we could find no documented losses, the reductions in total mangrove areas that we report are underestimates.

Do losses of mangrove forests matter? Mangrove ecosystems support essential ecological functions, so significant losses of mangrove forests will have important consequences. Mangrove forests intercept land-derived nutrients, pollutants, and suspended matter before these contaminants reach deeper water (Marshall 1994, Rivera-Monroy and Twilley 1996, Tam and Wong 1999), and they export materials that support near-shore food webs, including shrimp and prawns (Rodelli et al. 1984, Twilley 1988, Sasekumar et al. 1992). These natural subsidies are provided in addition to various extractive benefits, including wood, lumber, honey, tannins, mariculture crops, salt, and so on (Saenger et al. 1983, Spalding et al. 1997).

Because mangroves are strategically located between land and sea and are biogeochemically important, the effects of losses of their area are magnified. Nutrient transport from land to estuaries is the principal agent of ecological change in many coastal areas (GESAMP 1990, Goldberg 1995); land-derived nutrients thus have to traverse fringing coastal wetlands—including mangrove forests—on their way to receiving estuaries. In fact, nutrient processing down-estuary from mariculture facilities might mitigate eutrophication caused by effluent from the mariculture ponds (Wolanski et al. 2000). Burial and denitrification within mangrove forests significantly lower the export of terrigenous nutrients to the estuaries (Rivera-Monroy et al. 1995, Robertson and Phillips 1995, Rivera-Monroy and Twilley 1996). This fortuitous location means that the role of mangrove forests is far more important biogeochemically than their relatively small area (compared with terrestrial tropical forests, for example) might suggest.

Mangroves also perform other important services, such as preventing coastal erosion by stabilizing sediments (Marshall 1994, Tam and Wong 1999), furnishing nursery and spawning areas for commercially important coastal fish and shellfish species (Rodelli et al. 1984, Sasekumar et al. 1992), and providing stopover sites for migratory birds, fish, and mammals (Saenger et al. 1983). Mangrove forests are also habitats for a diversity of species that have considerable importance, both economically and ecologically. The fauna of mangroves includes fish and shellfish taxa that support subsistence fishing, as well as rare endemic proboscis monkeys in Borneo, scarlet ibis, the vulnerable straight-billed woodcreeper in Trinidad, threatened Bengal tigers in India and Bangladesh, rare Bulbophyllum and other orchids in Singapore, endangered manatees in Florida, and many other key species (Saenger et al. 1983). Any loss of mangrove forest therefore means a loss of important subsidies to subsistence uses and ecological, economic, and conservation functions.

Mangrove habitat losses relative to human activity

To identify the general anthropogenic effects on mangrove losses, we first stratified the loss data into countries with losses (filled circles in Figure 2) and countries with no losses or with gains (open circles in Figure 2). In countries with reductions in area of mangrove forests, the percentage loss of mangrove forests increased as per capita GNP increased (Figure 2a). The scatter of the data was considerable, so the relationship, although significant, is not particularly predictive (Prairie 1996). This scatter may be attributable in part to foreign rather than national investment, reflecting substantial international monetary subsidies in industrial-level mari cultural and wood-chip exploitation (Wolanski et al. 2000). There was no evident relationship between human population density and percentage change in mangrove area (Figure 2b). We conclude that the relative wealth of a country, more than the concentration of humans, may establish the potential for loss of this coastal environment, but this effect may be broadly altered by foreign financial involvement.

Many specific human activities at various levels (subsistence, artisanal, and industrial) reduce the area of mangroves (Wolanski et al. 2000). Humans harvest fish, crabs, shellfish, reptile skins, and honey at subsistence and artisanal levels from most of the world's mangroves (Nurkin 1994). People also harvest forest products for local consumption of wood, charcoal, and tannins; at industrial levels, they harvest wood chips and lumber (Ong 1982). They cut and fill mangroves for agricultural, industrial, and urban development (Linden and Jernelov 1980); they convert mangroves to salt flats for salt production, and to shallow diked ponds for maricultural purposes (Nurkin 1994, Primavera 1995). In addition, other activities on land diminish the area of mangroves, including interception of freshwater in Bangladesh, Thailand, and Taiwan and wartime use of herbicides in Vietnam and “mangrove control” in Africa (Linden and Jernelov 1980).

As Table 3 shows, mariculture plays a major role in the reduction of mangrove forest area. Shrimp culture is, by a considerable margin, the greatest cause of mangrove loss; including losses attributable to fish culture, maricultural endeavors are responsible for more than half (52%) of the losses of mangroves.

Although fish culture is ancient, with records of tambak fish culture in Java and bangos culture in the Philippines going back to 1400 (Herre and Mendoza 1929), the practice has proliferated recently, supported by national and international subsidies (Wolanski et al. 2000). Diverse forest uses (mainly industrial-level lumber and wood-chip production, with minor effects from artisanal making of charcoal and extraction of tannin) also lead to significant losses of mangroves (Table 3). Other activities, such as salt production, cause losses of lesser magnitude, but these are nonetheless important locally.

We estimated the mangrove loss due to mariculture by compiling data on the areas of maricultural ponds reported in each country (Jory 1997, Primavera 1995). We assumed that the entire area of the ponds was built on land previously occupied by mangroves. Therefore, if ponds were built on upland areas, our assumption would overestimate mangrove losses. However, for intensive maricultural practices, it is important to be as close to water as possible because flushing is important to maintain high water quality (Primavera 1991). Moreover, dry land can be used for agriculture and is thus considered more valuable than mangroves.

In addition, the area of mariculture ponds is most likely underreported, and the industry is growing quickly. For example, the percentage of commercial shrimp yield that was farm raised increased from 3% to almost 30% between 1981 and 1995 (Lucien-Brun 1997). Our estimates, based largely on data reported in the mid-1990s, almost certainly underestimate the area of coastal habitat converted to mariculture. Because of these considerations, and lacking any more concrete data, we simply assumed that culture ponds were built on mangrove habitats.

The sum of losses from all the various human activities, across all continents, reached 36×103 km2(Table 3). This sum was obtained from data from countries that hold 66% of the area of mangrove forests. The prorated, aggregate loss from various human uses amounts to 64% of the total loss of mangrove forest area that we report (Table 2, the difference between the original 136,914 km2 and the present 89,568 km2). Losses estimated by summing areas altered by specific activities (Table 3) were smaller than total world mangrove loss (Table 2) because losses have increased in many countries in recent years, and, unfortunately, the data on uses tend to be older than the data on total area. The 64% accounted for by summing the effects of various activities, however, seems to be a sufficiently large portion of losses of mangrove forests to warrant evaluating the relative importance of the various human activities.

The importance of mariculture for mangrove habitat losses

It is apparent that maricultural practices are responsible for the bulk of the increasing losses of mangrove swamps worldwide. This mirrors, at a larger, global scale, what has been said for specific sites. For example, pond culture has been reported to be responsible for 50% of the loss of mangrove environments in the Philippines (Primavera 1991), and 50%–80% in Southeast Asia (Wolanski et al. 2000). Most of the damage is attributable to the direct loss of habitat from conversion of “cheap” mangrove land to valuable shrimp, prawn, and fish ponds (Figure 3).

Intensive mariculture has many other, indirect ecological effects. Shrimp culture demands supplies of juveniles, a demand that has decimated natural stocks (Sasekumar et al. 1992, DeWalt et al. 1996). Intensive shrimp farming demands intensive use of fish meal as shrimp food, which puts pressure on offshore stocks (Primavera 1991). Because the conversion of food to shrimp is incomplete, considerable amounts of organic matter and nutrients pass through the ponds, and the effluent may cause or exacerbate the eutrophication of downstream estuaries and mangrove forests (Wolanski et al. 2000). There is too little substantive information on the intensity or extensiveness of these critical effects, but flow rates and concentrations in the effluents suggest that there must be significant impacts.

The problems associated with maricultural practices in ponds established in areas previously occupied by mangroves are exacerbated by the short life span of such ponds. Attendant problems of eutrophication, accumulation of toxins, sulfide-related acidification, and crop diseases limit use of a pond to a 5–10-year span, after which growers move on to a new area of mangrove (DeSilva 1998, Wolanski et al. 2000). This shifting cultivation pattern accelerates loss of mangrove environments, because the rate of recovery from spent ponds to mangrove forests is much slower than the rate of habitat loss (Primavera 1991). Fuller assessment of the combined effects of direct losses of habitat and the potentially major consequences of indirect effects of maricultural practices should therefore be a high priority for understanding what is taking place in one of the world's major coastal habitats.

Comparisons with other tropical environments

Losses of terrestrial tropical forests have justifiably received much attention recently. By the end of the 20th century, human activities converted up to 30% of the original pristine acreage of terrestrial tropical forests to other land covers (Houghton 1995). Estimates by the Food and Agriculture Organization of the United Nations (FAO 1997) suggest that 1.54×107 ha y–1 of terrestrial tropical forest were lost during the 1980s, and 1.37×107 ha y–1 during 1990–1995. These losses translate into an annual loss of 0.8% of the area of terrestrial tropical forests. Losses of coral reefs have also received considerable press and scientific attention. Best estimates are that about 10% of the world's coral reefs have been lost and perhaps up to 30% will be degraded in 10–20 years (Wilkinson 1992).

For comparison, the world's area of mangrove forests has been reduced by about 35% on a worldwide scale since the 1980s, and 2.1% of the existing worldwide mangrove area is lost each year. The rate is as high as 3.6% in the Americas (Table 2). Such losses of mangrove forests are alarming rates of loss of a major coastal environment.

These comparisons speak to the enormous pressures being exerted on tropical environments by anthropogenic processes. The losses of rain forests and reefs are, rightly, widely acknowledged, and a measure of concern and response to the changes has been manifested. The information compiled here supports the alarm felt by those in the research and management communities with firsthand knowledge of what is happening in the boundary between land and sea, where mangroves grow. Although mangrove forests, especially in the Americas and Asia, are among the most threatened major environments on earth, this major transformation in the coastal tropics has received scant public or political recognition. Comprehensive research aimed at assessing the status of mangroves in many countries must be undertaken, as must restoration or conservation efforts that impel public and political notice of the dimensions of the problem. Although the data reviewed in this article are in many ways incomplete, they do demonstrate the significant global losses of mangrove forests and suggest the need for conservation of this valuable coastal environment.

Acknowledgments

Resources from the National Center for Environmental Assessment Office of the US Environmental Protection Agency, and from the National Oceanographic and Atmospheric Administration's Sea Grant Program at the Woods Hole Oceanographic Institution, were helpful in the preparation of this article. We acknowledge the assistance of S. Brunelle, J. Champagne, E. Koenig, L. McInerney, C. Watkins, and D. Weisbaum, students in the 1999 Marine Pollution course at the Boston University Marine Program, who first started collecting the information reported here. We thank Robert Twilley and two anonymous referees for useful critiques of an earlier version of the manuscript.

References cited

Adegbehin

J. O.

Nwaigbo

L. C.

.

1990

.

Mangrove resources in Nigeria: Use and management perspectives.

Nature and Resources

26

:

13

21

.

Google Scholar

OpenURL Placeholder Text

Alvarez-Leon

R.

1993. Mangrove ecosystems of Colombia: Utilization, impacts, conservation and recuperation. Pages 8–9 in Lacerda LD, Field CD, eds. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part I: Latin America. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Azariah

J.

Azariah

H.

Gunasekaran

S.

Selvam

V.

.

1992

.

Structure and species distribution in Coringa mangrove forest, Godavari Delta, Andhra Pradesh, India.

Hydrobiologia

247

:

11

16

.

Chou

L. M.

1990

.

Assessing the coastal living resources of Singapore: A study in the ASEAN-Australia Resources Project.

Wallaceana

59

:

7

9

.

Google Scholar

OpenURL Placeholder Text

[CIA] Central Intelligence Agency

2000. World Factbook. Washington (DC): Central Intelligence Agency. (24 September 2001; www.cia.gov)

.

Cohen

J. E.

Small

C.

Mellinger

A.

Gallup

J.

Sachs

J. D.

.

1997

.

Estimates of coastal populations.

Science

278

:

1211

.

Google Scholar

OpenURL Placeholder Text

Conde

J. E.

Alarcon

C.

.

1993. The status of mangroves from the coast of Venezuela. Pages 10–11 in Lacerda LD, Field CD, eds. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions Part I: Latin America. Okinawa (Japan): International Society for Mangrove Ecosystems

.

D'croz

L.

1993. Mangrove uses and conservation in Panama. Page 8in Lacerda LD, Field CD, eds. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part I: Latin America. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Desilva

S. S.

ed. 1998. Tropical Mariculture. San Diego (CA): Academic Press

.

Dewalt

B. R.

Vergne

P.

Harding

M.

.

1996

.

Shrimp aquaculture development and the environment: People, mangroves and fisheries on the Gulf of Fonseca, Honduras.

World Development

24

:

1193

1208

.

Diop

E. S.

Field

C. D.

.

eds. 1993. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part II: Africa. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Ellison

J. C.

1993

.

Mangrove retreat with rising sea level, Bermuda.

Estuarine, Coastal and Shelf Science

37

:

75

87

.

Ellison

A. M.

Farnsworth

E. J.

.

1996

.

Anthropogenic disturbance of Caribbean mangrove ecosystems: Past impacts, present trends and future predictions.

Biotropica

28

:

549

565

.

[FAO] Food and Agriculture Organization of the United Nations

1997. State of the World's Forests. London: Oxford Words and Publications

.

Fortes

M.

1988

.

Mangrove and seagrass beds of East Asia: Habitats under stress.

Ambio

17

:

207

213

.

Google Scholar

OpenURL Placeholder Text

Funes

C. A.

1994. Situación de la bosques salados en El Salvador. Pages 115–124 in Suman DO, ed. El Ecosistema de Manglar en América Latina y la Cuenca del Caribe: Su Manejo y Conservación. Miami (FL): University of Miami

.

[GESAMP] Joint

Group of Experts on the Scientific Aspects of Marine Pollution. 1990. State of the Marine Environment. United Nations Environment Programme. Reports and Studies no. 39

.

Goldberg

E. D.

1995

.

Emerging problems in the coastal zone for the twenty-first century.

Marine Pollution Bulletin

31

:

152

158

.

Herre

A. W.

Mendoza

J.

.

1929

.

Bangos culture in the Philippine Islands.

Philippine Journal of Science

38

:

451

505

.

Google Scholar

OpenURL Placeholder Text

Houghton

R. A.

1995

.

Land use change and the carbon cycle.

Global Change Biology

1

:

257

287

.

Htay

U. A. S.

1994. Re-afforestation of mangrove forests in Myanmar. In Proceedings of the workshop on ITTO Project: Development and Dissemination of Re-afforestation Techniques of Mangrove Forests. Bangkok (Thailand): Japan Association for Mangroves and Thai National Mangrove Committee

.

Jimenez

J. A.

1993. Status of mangrove ecosystems in Central America. Pages 5–7 in Lacerda LD, Field CD, eds. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part I: Latin America. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Johnson

R.

Johnson

R.

.

1993. Mangroves of Sierra Leone. Pages 7–9 in Diop ES, Field CD, eds. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part II: Africa. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Jory

D. E.

1997

.

Status of marine shrimp farming.

Aquaculture Magazine

26

:

39

46

.

Google Scholar

OpenURL Placeholder Text

Li

M. S.

Lee

S. Y.

.

1997

.

Mangroves of China: A brief review.

Forest Ecology and Management

96

:

243

260

.

Linden

O.

Jernelov

A.

.

1980

.

The mangrove swamps: An ecosystem in danger.

Ambio

9

:

81

88

.

Google Scholar

OpenURL Placeholder Text

Lucien-Brun

H.

1997

.

Evolution of world shrimp production: Fisheries and aquaculture.

World Aquaculture

28

:

21

33

.

Google Scholar

OpenURL Placeholder Text

Lugo

A. E.

Snedaker

S. C.

.

1974

.

The ecology of mangroves.

Annual Review of Ecology and Systematics

5

:

39

64

.

Macnae

W.

1968

.

A general account of fauna and flora of mangrove swamps in the Indo-West Pacific region.

Advances in Marine Biology

6

:

73

270

.

Marguerite

R. V.

1993. Mangroves of Madagascar. Pages 245–260 in Diop ES, Field CD eds. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part II: Africa. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Marshall

N.

1994

.

Mangrove conservation in relation to overall environmental consideration.

Hydrobiologia

285

:

303

309

.

Menesveta

P.

1997

.

Mangrove destruction and shrimp culture systems.

World Aquaculture

12

:

36

42

.

Google Scholar

OpenURL Placeholder Text

Muchoney

D.

Borak

J.

Chi

H.

Friedl

M.

Gopal

S.

Hodges

J.

Morrow

N.

Strahler

A.

.

2000

.

Application of the MODIS global supervised classification model to vegetation and land cover mapping of Central America.

Journal of Remote Sensing

21

:

1115

1138

.

Nurkin

B.

1994

.

Degradation of mangrove forest in South Sulawesi, Indonesia.

Hydrobiologia

285

:

271

276

.

Odum

W. E.

Rosze

L. P.

Mcivor

C. C.

.

1982. The Ecology of the Mangroves of South Florida: A Community Profile. Washington (DC): US Fish and Wildlife Service. FWS/OBS-83/17

.

Ong

J. E.

1982

.

Mangroves and aquaculture in Malaysia.

Ambio

11

:

252

257

.

Google Scholar

OpenURL Placeholder Text

Ong

J. E.

1995

.

The ecology of mangrove conservation and management.

Hydrobiologia

298

:

343

351

.

Google Scholar

OpenURL Placeholder Text

Parks

P. J.

Bonifaz

M.

.

1994

.

Nonsustainable use of renewable resources: Mangrove deforestation and mariculture in Ecuador.

Marine Resources Economics

9

:

1

18

.

Prairie

Y. T.

1996

.

Evaluating the predictive power of regression models.

Canadian Journal of Fisheries and Aquatic Sciences

53

:

490

492

.

Primavera

J. H.

1991

.

Intensive prawn farming in the Philippines: Ecological, social, and economic implications.

Ambio

20

:

28

33

.

Google Scholar

OpenURL Placeholder Text

Primavera

J. H.

1995

.

Mangroves and brackish water pond culture in the Philippines.

Hydrobiologia

295

:

303

309

.

Rivera-Monroy

V. H.

Twilley

R. R.

Boustany

R. G.

Day

J. W.

Vera-Herrera

F.

Ramirez

M. C.

.

1995

.

Direct denitrification in mangrove sediments in Terminos Lagoon, Mexico.

Marine Ecology Progress Series

126

:

97

109

.

Rivera-Monroy

V. H.

Twilley

R. R.

.

1996

.

The relative role of denitrification and immobilization in the fate of inorganic nitrogen in mangrove sediments.

Limnology and Oceanography

41

:

284

296

.

Robertson

A. I.

Duke

N. C.

.

1990

.

Recruitment, growth and residence time of fishes in a tropical Australian mangrove system.

Estuarine, Coastal and Shelf Science

31

:

723

743

.

Robertson

A. I.

Phillips

M. J.

.

1995

.

Mangroves as filters of shrimp pond effluent: Predictions and biogeochemical research needs.

Hydrobiologia

295

:

311

321

.

Rodelli

M. R.

Gearing

J. N.

Gearing

P. J.

Marshall

N.

Sasekumar

A.

.

1984

.

Stable isotope ratio as a tracer of mangrove carbon in Malaysian ecosystems.

Oecologia

61

:

326

333

.

Roth

L. C.

1992

.

Hurricanes and mangrove regeneration: Effects of Hurricane Joan, October 1988, on the vegetation of Isla de Venado, Bluefields, Nicaragua.

Biotropica

24

:

375

384

.

Saenger

P.

Hegerl

E. J.

Davie

J. D. S.

.

1983. Global status of mangrove ecosystems. The Environmentalist 3 (supplement 3)

.

Saenger

P.

Bellan

M. F.

.

1995. The Mangrove Vegetation of the Atlantic Coast of Africa. Toulouse (France): University of Toulouse Press

.

Sasekumar

A.

Chong

V. C.

Leh

M. U.

D'cruz

R.

.

1992

.

Mangroves as a habitat for fish prawns.

Hydrobiologia

247

:

195

207

.

Sheppard

C.

Price

A.

Roberts

C.

.

1992. Marine Ecology of the Arabian Region: Patterns and Processes in Extreme Tropical Environments. London: Academic Press

.

Sherman

R. E.

Fahey

T. J.

Battles

J. J.

.

2000

.

Small-scale disturbance and regeneration dynamics in a neo-tropical mangrove forest.

Journal of Ecology

88

:

165

178

.

Sidhu

S. S.

1963

.

Studies on the mangrove of India.

Indian Forester

89

:

337

351

.

Google Scholar

OpenURL Placeholder Text

Simao

A.

1993. The mangrove swamps of Guinea Bissau. Pages 3–5 in Diop ES, Field CD, eds. Proceedings of a workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part II: Africa. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Spalding

M. D.

Blasco

F.

Field

C. D.

.

1997. World Mangrove Atlas. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Stonich

S. C.

Bort

J. R.

Ovares

L. L.

.

1999. Challenges to sustainability: The Central American shrimp mariculture industry. Pages 212–221 in Hatch LU, Swisher ME, eds. Managed Ecosystems: The Mesoamerican Experience. New York: Oxford University Press

.

Tam

N. F. Y.

Wong

Y. S.

.

1999

.

Mangrove soils in removing pollutants from municipal wastewater of different salinities.

Journal of Environmental Quality

28

:

556

564

.

Tomlinson

P. B.

1986. The Botany of Mangroves. Cambridge (UK): Cambridge University Press

.

Turner

R. K.

Adger

W. N.

Lorenzoni

I.

.

1998. Towards integrated modelling and analysis in coastal zones: Principles and practices. Texel (Netherlands): Land-Ocean Interactions in the Coastal Zone Project, Reports and Studies no. 11

.

Twilley

R. R.

1988. Coupling of mangroves to the productivity of estuarine and coastal waters. Pages 155–180 in Coastal-Offshore Ecosystems Interactions: Lecture Notes on Coastal and Estuarine Studies 22. Berlin: Springer-Verlag

.

Twilley

R. R.

1998. Mangroves. Pages 445–473 in Messina MG, Conner WH, eds. Southern Forested Wetlands: Ecology and Management. Boca Raton (FL): Lewis Publishers

.

Wilkinson

C. R.

1993. Coral Reefs of the world are facing widespread devastation: Can we prevent this through sustainable management practices? Pages 11–21 in the Proceedings of the Seventh International Coral Reef Symposium; 22–27 June 1992; Guam, Micronesia

.

Wolanski

E.

Spagnol

S.

Thomas

S.

Moore

K.

Alongi

D. M.

Trott

L.

Davidson

A.

.

2000

.

Modelling and visualizing the fate of shrimp pond effluent in a mangrove-fringed tidal creek.

Estuarine, Coastal and Shelf Science

50

:

85

97

.

YañArancibia

A.

Lara-Dominguez

A. L.

Zapata

G. J. V.

Arriaga

E. R.

Seijo

J. C.

.

1993. Mangrove ecosystems of Mexico: Ecological function, economic value, and sustainable development. Pages 2–3 in Lacerda LD, Field CD, eds. Proceedings of a Workshop on Conservation and Sustainable Utilization of Mangrove Forests in Latin America and Africa Regions, Part I: Latin America. Okinawa (Japan): International Society for Mangrove Ecosystems

.

Figure 1.

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (3)

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Change in area of mangrove forest for countries in Africa, Asia, and the Americas (data sources are listed in Table 1). Data from Angola, Cambodia, Dominican Republic, Fiji, French Guyana, Gabon, Indonesia, Iran, Nicaragua, and Papua New Guinea were not used because there were unrealistic changes in mangrove area across only a few years. Such large changes in short time periods must result from different mapping techniques rather than from real areal changes. Data from Guinea Bissau (4760 km2 in 1953), Madagascar (4000 km2 in 1921), Philippines (5000 km2 in 1920), and Vietnam (4000 km2 in 1945) extend to the left of the y-axis. Unlabeled countries have less than 500 km2, and include Benin in Africa, Brunei, Singapore, and Yemen in Asia, and Anguilla, Antigua-Barbuda, Cayman Islands, El Salvador, Grenada, Guadaloupe, Guatemala, Honduras, Jamaica, Peru, St. Kitts, St. Lucia, St. Vincent, and Turks and Caicos in the Americas. All other countries with mangroves had insufficient data to calculate a time course

Figure 2.

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (4)

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Annual percentage change in mangrove area for each country, as a function of the per capita GNP (a) and the coastal population density (b)

Figure 3.

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (5)

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Oblique aerial view of a mangrove forest in Borneo, showing dikes and enclosed shrimp ponds carved out of the mangrove habitat. Photo: Frans Lanting, Minden Pictures

Table 1.

Mangrove areas in all the countries for which multiyear data are available

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (6)

Open in new tab

Table 1.

Mangrove areas in all the countries for which multiyear data are available

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (7)

Open in new tab

Table 2.

Current area of mangrove forests, total known losses, and percentage loss compared with initial value of acreage for Asia, Africa, Australia, and the Americas, as well as totals for the world

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (8)

Open in new tab

Table 2.

Current area of mangrove forests, total known losses, and percentage loss compared with initial value of acreage for Asia, Africa, Australia, and the Americas, as well as totals for the world

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (9)

Open in new tab

Table 3.

Human use of mangrove area leading to loss of habitat, by continent

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (10)

Open in new tab

Table 3.

Human use of mangrove area leading to loss of habitat, by continent

Mangrove Forests: One of the World's Threatened Major Tropical Environments: At least 35% of the area of mangrove forests has been lost in the past two decades, losses that exceed those for tropical rain forests and coral reefs, two other well-known threatened environments (11)

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Author notes

Ivan Valiela is a professor of biology, at the Boston University Marine Program, Marine Biological Laboratory, Woods Hole, MA 02543.

Jennifer L. Bowen and Joanna K. York are graduate students, at the Boston University Marine Program, Marine Biological Laboratory, Woods Hole, MA 02543.

© 2001 American Institute of Biological Sciences

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