Proposed Ramsar Guidelines For Designating Salt Flats as Wetlands of International Importance Submitted by the Mangrove Action Project Salt flats are hypersaline flatlands partially or totally devoid of vascular vegetation. Salt flats come in many shapes and sizes, have diverse origins and may be associated with coastal or inland settings. In inland arid or semi-arid tropical and subtropical settings they develop in deserts where intermittent streams drain toward the center of a basin which is sometimes occupied by a temporary salt lake or lagoon where water evaporates and dissolved salts accumulate. Often these lakes dry up and only the salt beds of these remain. These are called Salinas. Coastal Salt Flats are most extensive, and become a dominant landscape feature on gently dipping coasts with marked tidal rhythms (macrotidal coastal margins) and dry climate where the Potential Evapotranspiration (PET) exceeds Precipitation throughout the year, or where there are prolonged dry seasons. They are characterized by very low gradient slopes (<1:1,000) and tidal flooding by Spring or Equinoctial Tides. These extensive floodable areas act as natural evaporating basins and high salinities develop in the substrate. Salinity levels rise beyond the physiological tolerance of most plant species (pore water salinity level above 100), and the substrate is bare. During the dry season these flats are also subject to extreme drying, and during any month may be affected by alternating periods of flooding by spring tides followed by drying. These salt flats are referred to as salt barrens, salt flats, salinas, salitrales, salares, sabkhas, sebkhas, and by various local names such as apicum, albinas, kavir, takir among many. Coastal salt flats usually develop between the Mean High Water Spring (MHWS) line and the upland tidal boundary. Coastal Salt flat sediments are mostly fine-grained mud (silt and clay) and fine sands. Extensive coastal salt flats are found on the west coast of Panama where salt flats (locally known as albinas, cover more than 19,000 ha. Extensive salt flats are also found on the Pacific coast of Ecuador particularly south of Bahia de Caraquez. Originally, and until about 1977 more than 130,000 ha of salt flats (salitrales) were found within the provinces of Guayas and El Oro Broad saltflats are associated with an extremely dry climate (<200 mm) and the macrotidal regime of the Gulf of Guayaquil. In recent years, extensive areas of salt flats have been eliminated for the construction of ponds for shrimp farming. By 1991 Ecuador had lost over 45,000 ha of salt flats. Sabkhas (sabkha is the Arabic word for a salt flat) are extensive salt flats found in arid and semiarid tectonically stable coastlines. Good examples are found in the Arabian Gulf, Baja California, Mexico and Sinai, Egypt. Salt flats are also found in King Sound (north western Australia) and near salt marshes in the Gulf of Gabes (Tunisia), and behind a barrier lagoon coast in Mediterranean Libya. There are Sabkhas on the Red Sea coast of the Yemen Arab Republic, with salt ponds in the lower margins. The Arabian Gulf is characterized by a series of sabkhas that stretch for some 320 km along the coast of the United Arab Emirates (UAE) reaching up to 24 km wide. These sabkhas have intertidal zones 1 to 2 km wide. The sediments are dominantly carbonate muds that have become colonized by blue-green algae that bind the sediment to form thick algal mats. These mats are subject to intense surface evaporation and heating. 1 In inland settings extensive salt flats are found associated with beds of former salt lakes and intermontane and endoreic drainage systems (systems that do not drain to the sea) and basins such as those in the Altiplano basin that extends for approximately 1000 km from southern Peru, across Bolivia and into Argentina and Chile. The floor of this basin lies at an elevation of 3750 ?4000 m asl. and is some 200 km wide. The floor of the altiplano contains the sediments of shrunken or extinct lakes. Several large salt flats and salt lakes and lagoons (salares) occur here, including the Salar de Uyani and Salar de Coinasa. On a more limited spatial scale, but locally important, salt flats (salinas) are linked to shallow salt ponds in the insular Caribbean (a microtidal environment), salt ponds are formed where mangroves or fringing coral reefs grow across inlets, or where active alongshore transport deposits sand that blocks the entrance to a coastal lagoon. Evaporation in the closed basin is high and fresh water flows from the small watersheds are very reduced and sporadic. As a result the ponds dry up completely forming a salt flat with crystallized salt on the surface. The ecology of these pond and salt flat complexes is very complex and dynamic. Occasionally the berms blocking the ponds are breached by waves or are overtopped by storm water outflows from the land. This allows reinvasion by marine animals, usually crabs and fish. These die off as the pond recloses and salinity increases again. These alternating cycles of life and death result in the release of large amounts of nutrients that become available following breaching and reinvasion. Saline lagoons and salt flats are important to migratory shorebirds such as plovers and sandpipers and migratory waterfowl such as blue-winged teal and several waders. The mangroves that line these saline ponds and salt flats provide a habitat for nesting populations of herons, pigeons and many songbirds. Salt flats are threatened by the disruption of processes that maintain their ecological character and integrity. This includes water diversions that reduce fluvial inputs of water and the direct and indirect effects of urban, and industrial expansion, and coastal development and infrastructure such as roads marinas, harbors, airports, as well as reclamation for agriculture and aquaculture (fish and shrimp farms). Possible climate change as a result of the greenhouse effect poses a particularly important threat to salt flats and associated ecosystems by changing water budgets and hydrologic regimes. In designating salt flats as Wetlands of International Importance, the administrative authority should concentrate on the guidance provided by Ramsar's Handbook # 7 "Strategic Framework and Guidelines for the Future Development of the List of Wetlands of International Importance". The designation of wetland sites for their international importance should be based on their "international significance in terms of biology, botany, zoology, limnology or hydrology". Special consideration should be given to the listing of sites where there is a threat of degradation, and where listing can lead to comprehensive management or internationally coordinated actions that preserve the system's integrity and ecological character. In applying Criterion 1, in terms of hydrology, Contracting Parties are urged to give priority to salt flats that play a substantial role in the functioning of a major coastal landform system such as a delta, coastal lagoon or embayment, and that contribute to the maintenance and stability of these systems by providing protection from coastal erosion, and sediment sinks that compensate for land subsidence. In applying Criterion 5, Convention signatories should give priority to the designation of tidal flats that are part of migratory routes, such as the Australasian Flyway, the West Pacific Flyway, the Central Asian-Indian Flyway, the African-Eurasian Migratory Flyway, or the Atlantic Flyway. In selecting sites, the designating authority should consider those areas that: (a) have remained largely intact and have suffered the least human-induced change, including physical habitat alteration and pollution; (b) have the highest habitat diversity; (c) contain the greatest 2 number of rare critical habitats, such as breeding and feeding areas, and sheltering areas for juveniles; and (d) have the best habitats for endangered, threatened, rare or sensitive species, or biological assemblages. Designating authorities must also consider the need to protect selected sites against external land-use changes and land-based sources of pollutants. A Coastal Wetland site is unlikely to succeed unless it is established within an integrated management framework, such as that provided by an Integrated Coastal Zone Management (ICZM) regime. Salt flats can form, or be essential elements of landscapes that cover extensive regions (>1,000 km2), therefore the designated site must be large enough to encompass an entire selfperpetuating system or complex of salt flats and associated systems. To maintain the integrity of the system it may be desirable to designate a network of sites that define an ecologically functional unit. The ideal management unit consists of an integrated system that includes highly protected areas that are managed for the highest level of protection, as well as a suite of controls in other less sensitive areas to promote ecologically sustainable development. The concept of protected landscapes (IUCN categories V and VI) is a relevant management model for the conservation and sustainable use of tidal flats because these categories encompass larger areas and a wider range of interdependent ecosystems than other IUCN categories (6). These IUCN categories of management also allow the greatest flexibility in terms of meeting the necessary conservation and social objectives. National governments have many obligations on the environmental front. These mechanisms interlock, and should be mutually reinforcing. When designating salt flats as Wetlands of International Importance, Contracting Parties are urged to consult IUCN's publication "A Global Representative System of Marine Protected Areas" and to consider, as specified in Objective 4.2, the opportunities that the designation provides for supporting established or developing flywaywide conservation initiatives under international or regional environment conventions and programs, as well as supporting biodiversity conservation strategies, and regional intergovernmental and non-governmental initiatives and projects that provide a framework for international cooperation on issues related to the conservation of migratory waterbirds and their habitats following an integrated flyway/ecosystem approach, such as: working with the Convention on Biological Diversity (CBD); the International Waterfowl and Wetlands Research Bureau (IWWRB now Wetlands International), the Agreement on the Conservation of AfricanEurasian Migratory Waterbirds (AEWA), The Pacific Waterbird Flyway Conservation Program (Wetlands International), the North American Waterfowl Management Plan (NAWMP); the AsiaPacific Migratory Waterbird Conservation Strategy (APMWCS); the Council for Arctic Flora and Fauna (CAFF); the Western Hemisphere Shorebird Reserve Network (WHSRN); and its bilateral and "site twinning" examples. REFERENCES Abbeykalio, N.J.. 1992. A pilot study of mangrove litter production in the Bonny Estuary of southern Nigeria. Discov Innovat., 4:71-78 Alongi, D.M.. 1990. Abundances of Benthic Microfauna in Relation to Outwelling of Mangrove Detritus in a Tropical Coastal Region. MAR ECOL-PR 63: 53-63 Altenburg, W., & T. Van Spanje.. 1989. Utilization of mangroves by birds in Guinea-Bissau.. Ardea 77: 57-74. 3 Bhuva, V.J., & V.C. Soni.. 1998. Wintering population of four migratory species of waders in the Gulf of Kachchh and human pressures.. Wader Study Group Bull. 86: 48-51. Burns, K.A., Garrity, S.D., Levings, S.C.. 1993 How many years until mangrove ecosystems recover from catastrophic oil spills. Mar Pollut Bull 26:239-248 Butler, R. W., R.I.G. Morrison, F. Delgado, R.K. Ross, &G.E.J. Smith.. 1997. Habitat assosiations of coastal birds in Panama.. Colonial Waterbirds 20: 518-524. Carmona, R., and G. D. Danemann.. 1998. Statiotemporal distribution of birds at the Guerrero Negro saltworks, Baja California Sur, Mexico. Ciencias Marinas 24: 389-408. Collazo, J.A., Harrington, B.A., Grear, J.S., Colon, J.A.. 1995. Abundance and distribution of shorebirds at the Cabo Rojo salt flats, Puerto Rico. J Field Ornithol, 66: 424-438 daSilva, E.M., PesoAguiar, M.C., Navarro, M.D.T., Chastinet, C.D.E.A.. 1997. Impact of petroleum pollution on aquatic coastal ecosystems in Brazil. Environmental Toxicology and Chemistry 16; 112-118. Edwards, P. J., & D. Parish.. 1988. The distribution of migratory waders in south-west Sarawak.. Wader Study Group Bull. 54: 36-40. Evans, P. R.. 1974. Exploratory investigation of feeding ecology and behaviour of shorebirds in Westenport Bay. Report on project w 38/74, Westenport Bay Environmental Study, Victoria, Australia.. Report, see above Gajardo, G.M., & J.A. Beardmore.. 1989. Ability to switch reproductive mode in Artemia is related to maternity heterozygosity.. Marine Ecol. Prog. Ser. 55: 191-195. Garrity, S.D., Levings, S.C., Burns, K.A.. 1994 The Galeta Oil Spill .1. Long-Term Effects on the Physical Structure of the Mangrove Fringe. Estuar Coast Shelf Sci 38:327-348 Grant, D.L., Clarke, P.J., Allaway, W.G.. 1993. The Response of Grey Mangrove (Avicennia marina (Forsk) Vierh) Seedlings to Spills of Crude Oil. J Exp Mar Biol Ecol 171:273-295 Grear, J. S.. 1992. Habitat use by migratory shorebirds at the Cabo Rojo salt flats, Puerto Rico.. MSc. Thesis, U. of Florida, 99pp. Grear, J., & J.A. Collazo.. 1994. Macroinvertebrates used by migratory calidrid shorebirds and physical patterns associated with their abundance and distribution at the Cabo Rojo salt flats, Puerto Rico.. Research File # 23 Guillou, J.-J.. 1988. Open mud flats in mangrove: their influence on the distribution of gulls and waders in West Africa. Alauda 56: 411-412. Haase, B.. 1996. Status of waders in southwest Ecuador.. Manuscript. Research file # 121. Hazevoet, C. J.. 1992. Migrant and resident waders in the Cape Verde Islands.. WSG Group Bull., 64:46-50. Herbst, D. B., F. P. Conte, & V. J. Brookes.. 1983. Ephydra hians ecology at Mono Lake, Ca. and Abert lake, Or.. Final Report to the U.S. Fish & Wildlife Service, mimeo, 24 pp. Hogarth, P. J., J. Jinxiang, C. Erxi, A.R.G. Price, & R.F.G. Ormond.. 1989. Mangroves and development around Xiamen, China.. Coastal Zone89: 4832-4846. 4 Jacobi, C.M., Schaeffernovelli, Y.. 1990. Oil Spills in Mangroves - A Conceptual Model Based on Long-Term Field Observations. Ecol Model 52: 53-59 Jehl, J. R., Jr.. 1988. Biology of the Eared Grebe and Wilson's Phalarope in the nonbreeding season: a study of adaptations to saline lakes.. Stud. in Avian Biology, 12: 1-74. Jelgersma, S., Vanderzijp, M., Brinkman, R.. 1993. Sea level rise and the coastal lowlands in the developing world.. J Coastal Res., 9:958-972 Kalejita, B.. 1994. Palearctic shorebird research in South Africa- past, present and future.. Wader Study Group Bull. 74: 24-26. Laegdsgaard, P., & C. R. Johnson.. 1995. Mangrove habitats as nurseries: unique assemblages of juvenile fish in subtropical mangroves in eastern Australia.. Mar. Ecol. Prog. Ser., 126: 67-81. Lee, G. C.. 1989. Breeding ecology and habitat use patterns of Snowy and Wilson's Plovers at the Cabo Rojo Salt Flats, Puerto Rico.. MS Thesis, Clemson University, 76 pp. Lefebvre, G., Poulin, B.. 1996. Seasonal abundance of migrant birds and food resources in Panamanian mangrove forests. Wilson Bulletin 108; 748-759. Lensink, R. and P.L. Meininger.. 1990. Measurements, weights and moult of waders on the Bank D'Arguin, Mauritania, October 1988.. Wader Study Group Bull. 58:35-48. Lenz, R. H., S. D. Cooper, J. M. Melack, & D. W. Winkler. 1986. Spatial and temporal distribution patterns of three trophic levels in a saline lake.. J. Phytoplankton Res. 8: 1051-1064 Levings, S.C., Garrity, S.D., Burns, K.A.. 1994 The Galeta Oil Spill .3. Chronic Reoiling, LongTerm Toxicity of Hydrocarbon Residues and Effects on Epibiota in the Mangrove Fringe. Estuar Coast Shelf Sci 38:365-395 Linsley, R. H., & L. H. Carpelan.. 1961. Invertebrate fauna. Pp. 43-47 in B. W. Walker (Ed.). The ecology of the Salton Sea, California in relation to the sports fishery.. Calif. Dept. Fish & Game Bull. 113. Lonzarich, D.G., Smith, J.J.. 1997. Water chemistry and community structure of saline and hypersaline salt evaporation ponds in San Francisco Bay, California. Calif. Fish and Game, 83: 89-104 Lopez-Portillo, J., & E. Ezcurra.. 1989. Responses of three mangroves to salinity in two geoforms.. Functional Ecol. 3: 355-362. Martin, A. P., & R. M. Randall.. 1987. Numbers of waterbirds at a commercial saltpan, and suggestions for management.. S. African J. Wildl. Res. 17: 75-81. Masero JA, Perez-Hurtado A, Castro M, Arroyo GM. 2000. Complementary use of intertidal mudflats and adjacent salinas by foraging waders. ARDEA 88: 177-191. Masero, J. A.. 2000. Diet, foraging behavior and intake rate of Red Knot feeding in saltworks during sapring migration.. Research file # 89 Masero, J. A., A. Perez-Hurtado, M. Castro, and G. M. Arroyo.. 2000. Complementary use of intertidal mudflats and adjacent salinas by foraging waders. Ardea 88: 177-191 5 Masero, J. A., and A. P‚rez-Hurtado. 2001. Importance of supratidal habitats for maintaining overwintering shorebird populations.. Condor 103: 21-30. Mcguinness, K.A.. 19?? Effects of Oil Spills on Macro-Invertebrates of Saltmarshes and Mangrove Forests in Botany Bay, New-South-Wales, Australia. J. Exp. Mar. Biol. Ecol. 142: 121135 Neves, R., & R. Rufino.. 1994. Import ncia ornitol¢gica das salinas; o caso particular do Estu rio do Sado.. Estudos de biologia y conserva‡ao da naturaleza No. 15. Lisboa: Instituto da Conserva‡ao ICN, 37pp. Nogueira, H.C., E.L. Carrique, J.S.G. Romero, J.C.N. Ariza, & P.A. Aquilera. 1996. Management of avocet breeding islands.. Wader Study Group Bull. 81: 46-49. Parish, D.. 1987. Conservation of wader habitats in East Asia.. Wader Study Group Bull. 49, Suppl.:132-134. Rashid, S. M. A., & D. A. Scott.. 1988. Some waders of the Sunderbans mangrove forest, Bangladesh. Stilt 12: 51-52. Robertson, A. I., & P. A. Daniel.. 1989. The influence of crabs on liter processing in high intertidal mangrove forests in tropical Australia. Oecologia 78: 191-198. Robertson, A.I., Daniel, P.A., Dixon, P.. 1991. Mangrove Forest Structure and Productivity in the Fly River Estuary, Papua-New-Guinea. Mar Biol., 111:147-155 Salvig, J.C., et al.. 1997. Coastal waders in Guinea-Bissau -- aerial survey results and seasonal occurrence on selected low water plots.. WSG Bull. 84:33-38. Sampath, K., & K. Krishnamurthy.. 1990. Shorebirds (Charadriiformes) of the Pichavaram mangroves, Tamil Nadu, India.. Wader Study Group Bull. 58: 24-27. Sheridan, P.F.. 1992 Comparative Habitat Utilization by Estuarine Macrofauna Within the Mangrove Ecosystem of Rookery Bay, Florida. Bull Mar Sci 50:21-39 Shuford, W. D., G.W. Page, & J.E. Kjelmyr.. 1998. Patterns and dynamics of shorebird use of California's Central Valley.. Condor 100: 227-244. Smith, T.J., Boto, K.G., Frusher, S.D., Giddins, R.L.. 1991 Keystone Species and Mangrove Forest Dynamics - The Influence of Burrowing by Crabs on Soil Nutrient Status and Forest Productivity.. Estuar Coast Shelf Sci 33: 419-432. Stevenson, N.J.. 1997. Disused shrimp ponds: Options for redevelopment of mangroves. Coastal Management, 25 : 425-435 Thiyagesan, K., & R. Nagarajan.. 1997. Effects of a cyclone on waterbird populations at the Pichavaram mangroves, southern India.. WSG Bull. 84:47-51. Tripp, K.J.. 1996. Prey Availability and Behavioral Dynamics of Foraging Small Calidrid Sandpipers at the Cabo Rojo Salt Flats, Puerto Rico. MS North Carolina State University, 1996: 66pp. Velasquez, C.R.. 1992. Managing artificial saltpans as a waterbird habitat - species responses to water level manipulation. Colon Waterbird., 15:43-55 6 Verheugt, W.J.M., F. Danielsen, H. Skov, A. Purwoko, R. Kadarisman et al.. 1990. Seasonal variations in the wader populations of the Banyuasin Delta, South Sumatra, Indonesia.. Wader Study Group Bull. 58:28-35. Verkuil, Y., A. Koolhaas, and J. van der Winden.. 1993. Wind effects on prey availability: how northward migrating waders use brackish and hypersaline lagoons in the Sivash, Ukrane.. Neth, J. Sea Res. 31: 359-374. Warnock, N., G.W. Page, T.D. Ruhlen, N. Nur, J.Y. Takekawa, & J.T. Hanson.. 2002. Management and conservation of San Francisco Bay salt ponds: effects of pond salinity, area, tide, and season on Pacific flyway waterbirds.. Waterbirds 25: 79-92. Warnock, S. E., and J. Y. Takekawa.. 1995. Habitat preference of wintering shorebirds in a temporally changing environment: Western Sandpipers in the San Francisco Bay estuary.. Auk 112: 920-930. Zwarts, L.. 1988. Numbers and distribution of coastal waders in Guinea-Bissau.. Ardea 76, 4255. 7