Carlos M. Duarte

Accelerating loss of seagrasses across the globe threatens coastal ecosystems

Coastal ecosystems and the services they provide are adversely affected by a wide variety of human activities. In particular, seagrass meadows are negatively affected by impacts accruing from the billion or more people who live within 50 km of them. Seagrass meadows provide important ecosystem services, including an estimated

A Global Crisis for Seagrass Ecosystems

1.9 trillion per year in the form of nutrient cycling; an order of magnitude enhancement of coral reef fish productivity; a habitat for thousands of fish, bird, and invertebrate species; and a major food source for endangered dugong, manatee, and green turtle. Although individual impacts from coastal development, degraded water quality, and climate change have been documented, there has been no quantitative global assessment of seagrass loss until now. Our comprehensive global assessment of 215 studies found that seagrasses have been disappearing at a rate of 110 km2 yr−1 since 1980 and that 29% of the known areal extent has disappeared since seagrass areas were initially recorded in 1879. Furthermore, rates of decline have accelerated from a median of 0.9% yr−1 before 1940 to 7% yr−1 since 1990. Seagrass loss rates are comparable to those reported for mangroves, coral reefs, and tropical rainforests and place seagrass meadows among the most threatened ecosystems on earth.

A blueprint for blue carbon: toward an improved understanding of the role of vegetated coastal habitats in sequestering CO2

ABSTRACT Seagrasses, marine flowering plants, have a long evolutionary history but are now challenged with rapid environmental changes as a result of coastal human population pressures. Seagrasses provide key ecological services, including organic carbon production and export, nutrient cycling, sediment stabilization, enhanced biodiversity, and trophic transfers to adjacent habitats in tropical and temperate regions. They also serve as “coastal canaries,” global biological sentinels of increasing anthropogenic influences in coastal ecosystems, with large-scale losses reported worldwide. Multiple stressors, including sediment and nutrient runoff, physical disturbance, invasive species, disease, commercial fishing practices, aquaculture, overgrazing, algal blooms, and global warming, cause seagrass declines at scales of square meters to hundreds of square kilometers. Reported seagrass losses have led to increased awareness of the need for seagrass protection, monitoring, management, and restoration. However, seagrass science, which has rapidly grown, is disconnected from public awareness of seagrasses, which has lagged behind awareness of other coastal ecosystems. There is a critical need for a targeted global conservation effort that includes a reduction of watershed nutrient and sediment inputs to seagrass habitats and a targeted educational program informing regulators and the public of the value of seagrass meadows.

Submerged aquatic vegetation in relation to different nutrient regimes

Recent research has highlighted the valuable role that coastal and marine ecosystems play in sequestering carbon dioxide (CO(2)). The carbon (C) sequestered in vegetated coastal ecosystems, specifically mangrove forests, seagrass beds, and salt marshes, has been termed blue carbon. Although their global area is one to two orders of magnitude smaller than that of terrestrial forests, the contribution of vegetated coastal habitats per unit area to long-term C sequestration is much greater, in part because of their efficiency in trapping suspended matter and associated organic C during tidal inundation. Despite the value of mangrove forests, seagrass beds, and salt marshes in sequestering C, and the other goods and services they provide, these systems are being lost at critical rates and action is urgently needed to prevent further degradation and loss. Recognition of the C sequestration value of vegetated coastal ecosystems provides a strong argument for their protection and restoration; however, it is necessary to improve scientific understanding of the underlying mechanisms that control C sequestration in these ecosystems. Here, we identify key areas of uncertainty and specific actions needed to address them.

The future of seagrass meadows

Abstract Submerged vegetation respond to increased nutrient loading through a shift from slow-growing seagrasses and large macroalgae to fast-growing macroalgae, and the ultimate dominance of phytoplankton at high nutrient loadings. This shift reflects a change from nutrient to light limitation along the eutrophication gradient. Slow-growing seagrasses and large macroalgae are good competitors when nutrients are limiting because they have relatively low nutrient requirements, are able of efficient internal nutrient recycling, and can access the elevated nutrient pools in the sediment. Fast-growing macroalgae and phytoplankton are superior competitors when light is limiting because they are positioned closer to the water surface, and capture and use light more efficiently. The important ecosystem consequences of altered nutrient regimes derive from the shift in dominant vegetation types. Slow-growing seagrasses and large macroalgae are longevous, decompose slowly, and experience only moderate grazing losse...

Thresholds of hypoxia for marine biodiversity.

Seagrasses cover about 0.1–0.2% of the global ocean, and develop highly productive ecosystems which fulfil a key role in the coastal ecosystem. Widespread seagrass loss results from direct human impacts, including mechanical damage (by dredging, fishing, and anchoring), eutrophication, aquaculture, siltation, effects of coastal constructions, and food web alterations; and indirect human impacts, including negative effects of climate change (erosion by rising sea level, increased storms, increased ultraviolet irradiance), as well as from natural causes, such as cyclones and floods. The present review summarizes such threats and trends and considers likely changes to the 2025 time horizon. Present losses are expected to accelerate, particularly in South-east Asia and the Caribbean, as human pressure on the coastal zone grows. Positive human effects include increased legislation to protect seagrass, increased protection of coastal ecosystems, and enhanced efforts to monitor and restore the marine ecosystem. However, these positive effects are unlikely to balance the negative impacts, which are expected to be particularly prominent in developing tropical regions, where the capacity to implement conservation policies is limited. Uncertainties as to the present loss rate, derived from the paucity of coherent monitoring programmes, and the present inability to formulate reliable predictions as to the future rate of loss, represent a major barrier to the formulation of global conservation policies. Three key actions are needed to ensure the effective conservation of seagrass ecosystems: (1) the development of a coherent worldwide monitoring network, (2) the development of quantitative models predicting the responses of seagrasses to disturbance, and (3) the education of the public on the functions of seagrass meadows and the impacts of human activity.

Patterns in decomposition rates among photosynthetic organisms : the importance of detritus C:N:P content

Hypoxia is a mounting problem affecting the worlds coastal waters, with severe consequences for marine life, including death and catastrophic changes. Hypoxia is forecast to increase owing to the combined effects of the continued spread of coastal eutrophication and global warming. A broad comparative analysis across a range of contrasting marine benthic organisms showed that hypoxia thresholds vary greatly across marine benthic organisms and that the conventional definition of 2 mg O2/liter to designate waters as hypoxic is below the empirical sublethal and lethal O2 thresholds for half of the species tested. These results imply that the number and area of coastal ecosystems affected by hypoxia and the future extent of hypoxia impacts on marine life have been generally underestimated.

Seagrass depth limits

The strength and generality of the relationship between decomposition rates and detritus carbon, nitrogen, and phosphorus concentrations was assessed by comparing published reports of decomposition rates of detritus of photosynthetic organisms, from unicellular algae to trees. The results obtained demonstrated the existence of a general positive, linear relationship between plant decomposition rates and nitrogen and phosphorus concentrations. Differences in the carbon, nitrogen, and phosphorus concentrations of plant detritus accounted for 89% of the variance in plant decomposition rates of detritus orginating from photosynthetic organisms ranging from unicellular microalgae to trees. The results also demonstrate that moist plant material decomposes substantially faster than dry material with similar nutrient concentrations. Consideration of lignin, instead of carbon, concentrations did not improve the relationships obtained. These results reflect the coupling of phosphorus and nitrogen in the basic biochemical processes of both plants and their microbial decomposers, and stress the importance of this coupling for carbon and nutrient flow in ecosystems.

The Pace of Shifting Climate in Marine and Terrestrial Ecosystems

Abstract Examination of the depth limit of seagrass communities distributed worldwide showed that sea-grasses may extend from mean sea level down to a depth of 90 m, and that differences in seagrass depth limit (Zc) are largely attributable to differences in light attenuation underwater (K). This relationship is best described by the equation log Z c (m ) = 0.26 − 1.07 log K ( m − ) that holds for a large number of marine angiosperm species, although differences in seagrass growth strategy and architecture also appear to contribute to explain differences in their depth limits. The equation relating seagrass depth limit and light attenuation coefficient is qualitatively similar to previous equations developed for freshwater angiosperms, but predicts that seagrasses will colonize greater depths than freshwater angiosperms in clear (transparency greater than 10 m) waters. Further, the reduction in seagrass biomass from the depth of maximum biomass towards the depth limit is also closely related to the light attenuation coefficient. The finding that seagrasses can extend to depths receiving, on average, about 11% of the irradiance at the surface, together with the use of the equation described, may prove useful in the identification of seagrass meadows that have not reached their potential extension.

Major role of marine vegetation on the oceanic carbon cycle

Ecologically relevant measures of contemporary global climate change can predict species distributions and vulnerabilities. Climate change challenges organisms to adapt or move to track changes in environments in space and time. We used two measures of thermal shifts from analyses of global temperatures over the past 50 years to describe the pace of climate change that species should track: the velocity of climate change (geographic shifts of isotherms over time) and the shift in seasonal timing of temperatures. Both measures are higher in the ocean than on land at some latitudes, despite slower ocean warming. These indices give a complex mosaic of predicted range shifts and phenology changes that deviate from simple poleward migration and earlier springs or later falls. They also emphasize potential conservation concerns, because areas of high marine biodiversity often have greater velocities of climate change and seasonal shifts.