Southern Cross University ePublications@SCU School of Environment, Science and Engineering Papers School of Environment, Science and Engineering 2009 Mangrove islands Peter Saenger Southern Cross University Publication details Saenger, P 2009, 'Mangrove islands', in RG Gillespie & DA Clague (eds), Encyclopedia of Islands, University of California Press, Berkeley, CA, pp. 591-593. ISBN: 9780520256491 ePublications@SCU is an electronic repository administered by Southern Cross University Library. Its goal is to capture and preserve the intellectual output of Southern Cross University authors and researchers, and to increase visibility and impact through open access to researchers around the world. For further information please contact [email protected]. understanding the evolutionary history of mammalian radiations, as well as new information on how we may conserve these remarkable fauna. SEE ALSO THE FOLLOWING ARTICLES Convergence / Endemism / Lemurs and Tarsiers / Madagascar / Philippines, Biology / Radiation Zone / Rodents FURTHER READING Burney, D. A., L. P. Burney, L. R. Godfrey, W. L. Jungers, S. M. Goodman, H. T. Wright, and A. J. T. Jull. . A chronology for late Prehistoric Madagascar. Journal of Human Evolution : –. Goodman, S. M., ed. . Paysages naturels et biodiversité de Madagascar. Paris: Muséum national d’Histoire Naturelle. Goodman, S. M., and J. P. Benstead, eds. . The natural history of Madagascar. Chicago: The University of Chicago Press. Heaney, L. R. . Dynamic disequilibrium: a long-term, large-scale perspective on the equilibrium model of island biogeography. Global Ecology and Biogeography : –. Jansa, S., K. Barker, and L. R. Heaney. . Molecular phylogenetics and divergence time estimates for the endemic rodents of the Philippine Islands: evidence from mitochondrial and nuclear gene sequences. Systematic Biology : –. Steppan, S., C. Zawadski, and L. R. Heaney. . Molecular phylogeny of the endemic Philippine rodent Apomys and the dynamics of diversification in an oceanic archipelago. Biological Journal of the Linnean Society : –. Woods, C. A., and Florence E. Sergile, eds. . Biogeography of the West Indies: patterns and perspectives, nd ed. Boca Raton, FL: CRC Press. MANGROVE ISLANDS mangroves form a part of the island vegetation. Those mangrove islands consisting only of mangroves commonly occur where sediments have built up sufficiently to form an island at low tide, which has then been colonized by mangroves (Fig. ). These are known as overwash mangroves as the islands are completely submerged at high tide, and only the mangroves are visible. Such overwash forests are commonly associated with deltas of rivers carrying high terrigenous silt loads (e.g., the Meghna–Brahmaputra delta of Bangladesh or the Fly River delta of Papua New Guinea) or in shallow waters where abundant sediments of biogenic carbonates accumulate (e.g., the overwash mangrove islands of the Florida Keys). Clearly, however, the mangrove vegetation will differ structurally and functionally in the deltaic, terrigenous setting from that of the carbonate setting. FIGURE 1 Overwash mangroves on carbonate shoals in the Ras Mohammed National Park in the northern Red Sea, Egypt. These man- PETER SAENGER Southern Cross University, Lismore, Australia Mangrove islands are islands composed entirely or partially of mangrove vegetation and comprise microcosms of generally high productivity, high biodiversity, and structurally complex habitats in the nearshore environment. Such mangrove islands are largely confined to the tropics, with their latitudinal limits occurring in those regions where water temperatures never exceed °C throughout the year. In comparison to shoreline mangroves, the vegetation of mangrove islands is subjected to much greater fluctuations in hydrological and meteorological conditions, resulting in its high dynamism and leading to its enhanced susceptibility to drastic change. MANGROVE ISLAND TYPES Mangrove islands can be subdivided into two broad types: islands consisting only of mangroves and islands where groves consist of only one species, Avicennia marina, whose pneumatophores form a 20–30-cm-high dense fringe to the stand. The second type of mangrove islands, where mangroves form a significant but non-exclusive part of the island vegetation, are usually associated with coral reef islands. There mangroves may grow directly over a reef flat or a fossil reefal platform, or in the lee of shingle ramparts, which provide protection from trade winds. Mangrove islands on reef flats are common off the coast of Central America (e.g., Belize) and on many islands of the Pacific (e.g., Palau and Ponape), where low energy conditions and relatively low tidal ranges occur. Although such mangroves are generally more extensive on “high islands”—which are not included here as mangrove islands—they are also common on “low islands” (e.g., the atoll islands of Nui, Vaitupu, and Nanumanga of Tuvalu). On the Great Barrier Reef of Australia, persistent southeasterly trade winds occur during April to November, resulting in shingle ramparts on the windward, southeastern shores of these “low islands” and leeward sand cays with MANGROVE ISLANDS Gillespie08_M.indd 591 591 4/21/09 5:28:49 PM 592 Gillespie08_M.indd 592 intervening mangroves in the lee of the shingle. These are referred to as “low wooded islands” and occur commonly in northeastern Queensland, north of ° S. Low wooded islands display a complex range of features, which occupy around –% of the reef flat. The windward shingle banks are often partially colonized by mangrove scrub (e.g., Avicennia marina, Aegialitis annulata, Pemphis acidula) and other halophytes (e.g., Sarcocornia, Sesuvium, Suaeda), and moats form to the leeward of the shingle ramparts, which retain water at low tide and allow micro-atoll growth (commonly of Porites andrewsi) to occur. The micro-atolls grow upward to mean low water level, and provide a convenient platform for the anchoring of drifting propagules and the subsequent growth of mangroves, which ultimately cover the entire moat with a closed canopy mangrove forest. On the Great Barrier Reef, the primary colonizing species is Rhizophora stylosa, although other species, such as Avicennia marina and Lumnitzera racemosa, quickly follow. In the northern Great Barrier Reef, closed canopy mangroves on low wooded islands consist of around species. Because of the small catchment areas of these islands, freshwater availability is restricted, and mangrove communities on low wooded islands are restricted to regions where the annual rainfall exceeds mm. Low Isles, off Cooktown in North Queensland, is the most studied low wooded island on the Great Barrier Reef, being originally surveyed by the – Great Barrier Reef Expedition, which spent a year surveying the biota of this island. The island and its mangroves have been resurveyed in , , , and , and over that period, the Rhizophora woodland has increased markedly. Some, but not all, other low wooded islands also showed mangrove expansion, and it seems that reef-top topography and the extent of micro-atoll formation appear to be the major factors in the extent of mangrove development. Cyclones are an annual occurrence in this area, and destructive winds can arrest or even reverse mangrove expansion on low wooded islands for considerable periods. flocculate and are deposited when mixed with seawater. As a result, nutrient-rich sediments are deposited around mangrove pneumatophores and stiltroots on mangrove islands, and luxuriant and diverse mangrove communities rapidly develop. Organic-matter production is generally washed out of the system (strongly outwelling) and replenished by the river-borne nutrient supply. In turn, the outwelling of organic matter trophically supports nearshore food webs, particularly for molluscs, penaeid shrimp, and juvenile fish. By way of contrast, reefal settings bear the brunt of the tides, which are generally full-strength seawater. Only biogenic sediments are available, brought in by daily tides (bidirectional flux), and nutrients are generally deficient. As a consequence, mangroves are slowed in terms of their organic-matter production, nutrient coupling is usually tight, and organic matter tends to accumulate amongst the vegetation. Reefal mangrove islands are susceptible to erosion, particularly around their periphery, and tend to have less luxuriant mangrove vegetation, often wind-pruned and limited in species richness to those species capable of growing in full-strength seawater. The tendency toward erosion, however, may be offset in this setting, as root material does not break down as rapidly as in deltaic systems and may accumulate as mangrove peat, which facilitates vertical accretion and habitat stability. In Central America, in particular, wherever coring of reefal mangrove islands has been undertaken, peat layers of up to m in depth have been found, and carbon dating suggests that the mangrove communities were initiated through rising sea levels around years ago and have accumulated peat at a rate that allowed them to keep pace with the rising sea levels of the late Holocene. On the Great Barrier Reef, the mangrove communities of low wooded islands, less reliant on peat accumulation than on micro-atoll growth, were initiated around years ago. ENVIRONMENTAL SETTINGS OF MANGROVE ISLANDS ECOLOGICAL SERVICES PROVIDED BY MANGROVE ISLANDS As outlined above, mangrove islands occur in two contrasting settings: in river mouth deltas and on reefal platforms. Clearly, the deltaic setting is river-dominated, and the reefal setting is tide-dominated. These dominating factors result in significant differences in the structure and functioning of mangrove islands. In the deltaic setting, mangrove islands are flooded by river water as well as by tides, so salinity remains moderate. Silt and nutrients are carried by the river water, but they Mangrove islands play an important role in stabilizing and protecting shoaling sand and mud flats. Their roots bind the sediments, and their stiltroots and pneumatophores reduce the water velocity around them, leading to the further deposition of sediments. Mangrove islands, particularly those associated with deltas, tend to be strongly outwelling. Organic matter is broken down by various biotic and physical process into small particles, and this detritus supports a range of dependent MANGROVE ISLANDS 4/21/09 5:28:50 PM Stoddart, D. R. . Mangroves as successional stages, inner reefs of the northern Great Barrier Reef. Journal of Biogeography : –. Woodroffe, C. D. . Pacific Island mangroves: distribution and environmental settings. Pacific Science : –. MARIANAS, BIOLOGY GORDON H. RODDA U. S. Geological Survey, Fort Collins, Colorado FIGURE 2 Brown pelicans and darters roost in the canopy of Avicennia germinans on reefal mangrove islands in Quintana Roo, Mexico. Although such roosting aggregations may provide significant nutrient enrichment, it does not offset the physical damage they do to the upper canopy. nearshore species, including penaeid shrimp (prawns) and detritivorous fish, such as mullet (family Mugilidae) and bream (family Sparidae). Many commercial and subsistence fisheries are focused in and around such mangrove islands. Finally, mangrove islands constitute structurally complex habitats that provide roosting and nesting sites, particularly for bats and seabirds. The surrounding waters, the mangrove vegetation, and the mangrove-associated invertebrates provide a diverse source of food for such nesting and roosting aggregations. On the Great Barrier Reef, around species of seabirds nest on low wooded islands; one species, the Torres Strait pigeon (Myristicivora spilorrhoa), relies on such mangrove islands in its annual migrations between Australia and Papua New Guinea. Although such nesting aggregations in the reefal setting bring much needed nutrients, this comes at a physical cost in that dense aggregations of seabirds damage the mangroves (Fig. ). SEE ALSO THE FOLLOWING ARTICLES Climate on Islands / Coral / Great Barrier Reef Islands, Biology / Hurricanes and Typhoons / Hydrology / Tides FURTHER READING Cintrón, G., A. E. Lugo, D. J. Pool, and G. Morris. . Mangroves of arid environments in Puerto Rico and adjacent islands. Biotropica : –. Hopley, D. . The geomorphology of the Great Barrier Reef: Quaternary development of coral reefs. New York: John Wiley & Sons Inc. Macintyre, I. G., M. A. Toscano, R. G. Lighty, and G. B. Bond. . Holocene history of the Mangrove Islands of Twin Cays, Belize, Central America. Atoll Research Bulletin : –. Saenger, P. . Mangrove ecology, silviculture and conservation. Dordrecht, Netherlands: Kluwer Academic Publishers. The Mariana archipelago is a line of small oceanic islands in the tropical northern Pacific Ocean about km east of the Philippine Islands. Because of its remoteness from Melanesian and Asian source areas, its small land area, its limited elevational range, and the sparse opportunities for faunal exchange among islands, the native biota of the Mariana Islands is relatively depauperate (species-poor), and native vertebrates are limited to species that can fly (birds, bats) or raft on floating vegetation and withstand contact with seawater (small lizards). Many of these vertebrates have been extirpated, and all but one of the Mariana endemic vertebrates have experienced range reductions consequent to the arrival of humans and human-introduced species. BIOGEOGRAPHY The Mariana island chain consists of primary islands stretching km from north to south and ranging in size from -km Guam (.° N) to -km Farallon de Pajaros (.° N). Guam is more than four times the size of the next larger Mariana island (Saipan, at km) and by itself makes up over half the land area of the Marianas. Guam is also the largest island in Micronesia, the cluster of mostly tiny islands (hence the “micro” in Micronesia) stretching more than km east–west across the vast area of tropical northern Pacific Ocean west of the International Date Line. The Mariana Islands arose from the depths of the ocean, in response to melting of the Pacific plate as it pushed under the Philippine plate. Accordingly, none of the islands has ever been connected to a continental land mass or to its neighboring islands. The southern arc of islands (Guam to Farallon de Medinilla) arose at about the same time, during a land-building period that occurred from to million years ago. Although seismically active, the southern arc has experienced no volcanism in the modern era. MARIANAS, BIOLOGY Gillespie08_M.indd 593 593 4/21/09 5:28:50 PM
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