The loss of seagrasses in Cockburn Sound, Western Australia. I. The time course and magnitude of seagrass decline in relation to industrial development

The areas of seagrass meadows in Cockburn Sound, a marine embayment in Western Australia, were estimated from historical aerial photographs supplemented by ground surveys, studies on meadows in adjoining areas, and coring for rhizome remains. Ten species of seagrasses with different habitat tolerances are recorded for the area, with Posidonia sinuosa Cambridge et Kuo forming the most extensive meadows. It is estimated that from 1954 to 1978 the meadow area was reduced from some 4200 to 900 ha. Based on measurements of aboveground productivity at several sites, this represents a reduction of leaf detritus production from 23 000 to 4000 t (dry wt.) y⁻¹. The major loss of seagrass occurred during a period of industrial development on the shore, and the discharge of effluents rich in plant nutrients.     

The loss of seagrass in cockburn sound,Western Australia. III. The effect of epiphytes on productivity of Posidonia australis Hook. F.

The hypothesis was examined that increased epiphyte growth was responsible for a reduction in seagrass meadows in Cockburn Sound during the discharge of nutrient-rich effluent. One study site was in a deteriorating meadow near an effluent outfall, the other at similar depth in an unaffected meadow in more oceanic water. Seagrass production at the first site was less than that at the second, with 33% lower growth per shoot and 29% less dense meadow. Water at the former site had higher mean concentrations of chlorophyll and phosphate than the latter, but light reaching the seagrass meadows was not significantly different. Epiphyte loads (as dry weight or chlorophyll per unit leaf area) were 2–8 times higher at the former site. Seasonal changes in epiphyte loads were well correlated with periphyton biomass on glass slides or plastic seagrass.Photosynthesis of leaf segments, with and without epiphytes, was measured using an oxygen meter in the laboratory; epiphyte photosynthetic rates were similar to those of periphyton on plastic, expressed per unit chlorophyll. The percentage reduction in light by known periphyton loads was measured, and used to calculate light reduction by epiphytes in the field, which was estimated to be 63% on average at the first site and 15% at the second. Pooling data for sites and seasons, there was a negative log-linear relationship between leaf production and epiphyte load. The observations provide support for the suggestion that seagrass loss in the Sound may be attributed to enhanced epiphyte loads following nutrient enrichment.     

Global seagrass distribution and diversity: A bioregional model

Seagrasses, marine flowering plants, are widely distributed along temperate and tropical coastlines of the world. Seagrasses have key ecological roles in coastal ecosystems and can form extensive meadows supporting high biodiversity. The global species diversity of seagrasses is low (< 60 species), but species can have ranges that extend for thousands of kilometers of coastline. Seagrass bioregions are defined here, based on species assemblages, species distributional ranges, and tropical and temperate influences. Six global bioregions are presented: four temperate and two tropical. The temperate bioregions include the Temperate North Atlantic, the Temperate North Pacific, the Mediterranean, and the Temperate Southern Oceans. The Temperate North Atlantic has low seagrass diversity, the major species being Zostera marina, typically occurring in estuaries and lagoons. The Temperate North Pacific has high seagrass diversity with Zostera spp. in estuaries and lagoons as well as Phyllospadix spp. in the surf zone. The Mediterranean region has clear water with vast meadows of moderate diversity of both temperate and tropical seagrasses, dominated by deep-growing Posidonia oceanica. The Temperate Southern Oceans bioregion includes the temperate southern coastlines of Australia, Africa and South America. Extensive meadows of low-to-high diversity temperate seagrasses are found in this bioregion, dominated by various species of Posidonia and Zostera. The tropical bioregions are the Tropical Atlantic and the Tropical Indo-Pacific, both supporting mega-herbivore grazers, including sea turtles and sirenia. The Tropical Atlantic bioregion has clear water with a high diversity of seagrasses on reefs and shallow banks, dominated by Thalassia testudinum. The vast Tropical Indo-Pacific has the highest seagrass diversity in the world, with as many as 14 species growing together on reef flats although seagrasses also occur in very deep waters. The global distribution of seagrass genera is remarkably consistent north and south of the equator; the northern and southern hemispheres share ten seagrass genera and only have one unique genus each. Some genera are much more speciose than others, with the genus Halophila having the most seagrass species. There are roughly the same number of temperate and tropical seagrass genera as well as species. The most widely distributed seagrass is Ruppia maritima, which occurs in tropical and temperate zones in a wide variety of habitats. Seagrass bioregions at the scale of ocean basins are identified based on species distributions which are supported by genetic patterns of diversity. Seagrass bioregions provide a useful framework for interpreting ecological, physiological and genetic results collected in specific locations or from particular species.     

Predicting the cumulative effect of multiple disturbances on seagrass connectivity

The rate of exchange, or connectivity, among populations effects their ability to recover after disturbance events. However, there is limited information on the extent to which populations are connected or how multiple disturbances affect connectivity, especially in coastal and marine ecosystems. We used network analysis and the outputs of a biophysical model to measure potential functional connectivity and predict the impact of multiple disturbances on seagrasses in the central Great Barrier Reef World Heritage Area (GBRWHA), Australia. The seagrass networks were densely connected, indicating that seagrasses are resilient to the random loss of meadows. Our analysis identified discrete meadows that are important sources of seagrass propagules and that serve as stepping stones connecting various different parts of the network. Several of these meadows were close to urban areas or ports and likely to be at risk from coastal development. Deep water meadows were highly connected to coastal meadows and may function as a refuge, but only for non‐foundation species. We evaluated changes to the structure and functioning of the seagrass networks when one or more discrete meadows were removed due to multiple disturbance events. The scale of disturbance required to disconnect the seagrass networks into two or more components was on average >245 km, about half the length of the metapopulation. The densely connected seagrass meadows of the central GBRWHA are not limited by the supply of propagules; therefore, management should focus on improving environmental conditions that support natural seagrass recruitment and recovery processes. Our study provides a new framework for assessing the impact of global change on the connectivity and persistence of coastal and marine ecosystems. Without this knowledge, management actions, including coastal restoration, may prove unnecessary and be unsuccessful.     

Satellite-based monitoring of tropical seagrass vegetation: current techniques and future developments

Decline of seagrasses has been documented in many parts of the world. Reduction in water clarity, through increased turbidity and increased nutrient concentrations, is considered to be the primary cause of seagrass loss. Recent studies have indicated the need for new methods that will enable early detection of decline in seagrass extent and productivity, over large areas. In this review of current literature on coastal remote sensing, we examine the ability of remote sensing to serve as an information provider for seagrass monitoring. Remote sensing offers the potential to map the extent of seagrass cover and monitor changes in these with high accuracy for shallow waters. The accuracy of mapping seagrasses in deeper waters is unclear. Recent advances in sensor technology and radiometric transfer modelling have resulted in the ability to map suspended sediment, sea surface temperature and below-surface irradiance. It is therefore potentially possible to monitor the factors that cause the decline in seagrass status. When the latest products in remote sensing are linked to seagrass production models, it may serve as an early-warning system for seagrass decline and ultimately allow a better management of these susceptible ecosystems.     

A genetic assessment of a successful seagrass meadow (Posidonia australis) restoration trial

Seagrass meadows are in decline globally. Although numerous experimental methods have been implemented to restore meadows, few have been successful in the long term. Poor decisions on the sourcing of transplants from donor sites, including poor genetic integration and/or low genetic diversity, may impact on restoration success. However, despite evidence to suggest a positive association between genetic diversity and ecological resilience, there is usually little or no input from genetic data to inform on the genetic management of ecological restoration. Cockburn Sound has seen a 77% decline in seagrass cover since 1967. A transplant trial was conducted between 2004 and 2008 with sprigs of Posidonia australis being planted into a bare sand area. Survival was monitored annually, and in 2012, we compared genetic diversity in this transplant area with the original donor site. Genetic diversity in the restored meadow was very high and comparable to the donor site, with no genetic differentiation detected. The high level of genetic diversity and choice of site may have played an important role in the success of this restoration trial. The observed natural recruits around the site after establishment of transplants suggest that local restoration efforts may improve seafloor habitat and facilitate natural expansion of the meadow.     

Positive feedbacks in seagrass ecosystems--evidence from large-scale empirical data

Positive feedbacks cause a nonlinear response of ecosystems to environmental change and may even cause bistability. Even though the importance of feedback mechanisms has been demonstrated for many types of ecosystems, their identification and quantification is still difficult. Here, we investigated whether positive feedbacks between seagrasses and light conditions are likely in seagrass ecosystems dominated by the temperate seagrass Zostera marina. We applied a combination of multiple linear regression and structural equation modeling (SEM) on a dataset containing 83 sites scattered across Western Europe. Results confirmed that a positive feedback between sediment conditions, light conditions and seagrass density is likely to exist in seagrass ecosystems. This feedback indicated that seagrasses are able to trap and stabilize suspended sediments, which in turn improves water clarity and seagrass growth conditions. Furthermore, our analyses demonstrated that effects of eutrophication on light conditions, as indicated by surface water total nitrogen, were on average at least as important as sediment conditions. This suggests that in general, eutrophication might be the most important factor controlling seagrasses in sheltered estuaries, while the seagrass-sediment-light feedback is a dominant mechanism in more exposed areas. Our study demonstrates the potentials of SEM to identify and quantify positive feedbacks mechanisms for ecosystems and other complex systems.     

Cutting out the middle clam: lucinid endosymbiotic bacteria are also associated with seagrass roots worldwide

Seagrasses and lucinid bivalves inhabit highly reduced sediments with elevated sulphide concentrations. Lucinids house symbiotic bacteria (Ca. Thiodiazotropha) capable of oxidising sediment sulphide, and their presence in sediments has been proposed to promote seagrass growth by decreasing otherwise phytotoxic sulphide levels. However, vast and productive seagrass meadows are present in ecosystems where lucinids do not occur. Hence, we hypothesised that seagrasses themselves host these sulphur-oxidising Ca. Thiodiazotropha that could aid their survival when lucinids are absent. We analysed newly generated and publicly available 16S rRNA gene sequences from seagrass roots and sediments across 14 seagrass species and 10 countries and found that persistent and colonising seagrasses across the world harbour sulphur-oxidising Ca. Thiodiazotropha, regardless of the presence of lucinids. We used fluorescence in situ hybridisation to visually confirm the presence of Ca. Thiodiazotropha on roots of Halophila ovalis, a colonising seagrass species with wide geographical, water depth range, and sedimentary sulphide concentrations. We provide the first evidence that Ca. Thiodiazotropha are commonly present on seagrass roots, providing another mechanism for seagrasses to alleviate sulphide stress globally.Subject terms: Microbial ecology, Plant ecology, Soil microbiology     

Plant-herbivore interactions in seagrass meadows

During the past two decades we have gained much insight into the factors that regulate the productivity of seagrass dominated ecosystems, especially those at low latitudes. Here, we review and reassess the importance of plant-herbivore interactions in seagrass meadows, focusing on recent studies that have examined: 1) grazing on live seagrass leaves; 2) consumption of epiphytic algae growing on seagrass leaves; and 3) consumption of planktonic algae from the waters surrounding seagrass meadows. The major conclusion is that, in contrast to what has been reported in much of the literature on food webs in seagrass meadows, a diverse grazing pathway continues to represent an important conduit for the transfer of energy from the primary producers to higher order consumers. This remains true, although in many areas consumption of seagrasses is reduced in an historical context, owing to the overharvesting of many large species of herbivorous waterfowl, turtles and mammals.We also summarize our view of the important gaps in understanding the broadly defined topic of herbivory in seagrass-dominated ecosystems. We suggest that future studies should focus on: understanding the foraging strategies of seagrass herbivores; quantifying the impact of herbivory on seagrass demography, including effects on sexual reproduction, the fate of flowers, and the production of fruits and seeds; and documenting the commonness of compensatory responses to grazing. In addition, the role of chemical defenses in seagrass species remains inadequately investigated. Studies of the roles of nutritional content (as measured by C/N/P ratios) and chemical defenses are also fertile grounds for future studies of epiphytes and their grazers, as are additional experiments to quantify the relative roles of top-down and bottom-up factors as they determine algal growth and abundance. There is also a need to expand the geographical scope of studies of epiphyte-grazer interactions from cold temperate to sub-tropical and tropical waters. Suspension feeders also need to be studied more broadly, with additional experiments required to quantify their effects on water clarity and their ability to fertilize pore waters, and whether benefits from these activities balances the costs of shading and competition for space that can result from both epifaunal and infaunal suspension feeders.     

What lies beneath: Why knowledge of belowground biomass dynamics is crucial to effective seagrass management

Conservation of seagrasses meadows is important, because these habitats are ecologically important and under threat. Monitoring and modelling are essential tools for assessing seagrass condition and potential threats, however there are many seagrass indicators to choose from, and differentiating between natural variability and declining conditions poses a serious challenge. Tropical seagrass meadows in the Indo-Pacific, in contrast to most temperate meadows, are characterized by a multi-species composition and a year-round growth. Differences in characteristics between species growing within one meadow could induce uncertainty in the assessment of the dynamics of these meadows if variation in productivity and related biomass turnover timescales are not taken into consideration. We present data on biomass distribution, production and turnover timescales of above- and belowground tissues for three key tropical seagrass species (Thalassia hemprichii, Cymodocea rotundata and Halodule uninervis) in two mixed-species meadows in the Spermonde Archipelago, Indonesia. Seagrass leaf turnover time scales were comparable for the three studied seagrass species and varied between 25 and 30 days. Variation in leaf and rhizome turnover timescales were small (or insignificant) between the two meadows. In contrast, rhizome turnover time scales were around ten times longer than leaf turnover timescales, and large differences in rhizome turnover time scales (200–500 days) were observed between the species. The late-successional species T. hemprichii had much slower rhizome turnover compared to the two early successional species. Furthermore, since rhizome biomass has a much longer turnover time compared to leaf biomass, changes in rhizome biomass reflect effects on seagrass meadows on a much longer timescale compared to changes in leaf biomass for these tropical meadows. We conclude that belowground biomass dynamics are an important proxy to assess long-term effects of environmental stressors on seagrass ecosystems and should be included in tropical seagrass management programmes.     

Coastal retreat and improved water quality mitigate losses of seagrass from sea level rise

The distribution and abundance of seagrass ecosystems could change significantly over the coming century due to sea level rise (SLR). Coastal managers require mechanistic understanding of the processes affecting seagrass response to SLR to maximize their conservation and associated provision of ecosystem services. In Moreton Bay, Queensland, Australia, vast seagrass meadows supporting populations of sea turtles and dugongs are juxtaposed with the multiple stressors associated with a large and rapidly expanding human population. Here, the interactive effects of predicted SLR, changes in water clarity, and land use on future distributions of seagrass in Moreton Bay were quantified. A habitat distribution model of present day seagrass in relation to benthic irradiance and wave height was developed which correctly classified habitats in 83% of cases. Spatial predictions of seagrass and presence derived from the model and bathymetric data were used to initiate a SLR inundation model. Bathymetry was iteratively modified based on SLR and sedimentary accretion in seagrass to simulate potential seagrass habitat at 10 year time steps until 2100. The area of seagrass habitat was predicted to decline by 17% by 2100 under a scenario of SLR of 1.1 m. A scenario including the removal of impervious surfaces, such as roads and houses, from newly inundated regions, demonstrated that managed retreat of the shoreline could potentially reduce the overall decline in seagrass habitat to just 5%. The predicted reduction in area of seagrass habitat could be offset by an improvement in water clarity of 30%. Greater improvements in water clarity would be necessary for larger magnitudes of SLR. Management to improve water quality will provide present and future benefits to seagrasses under climate change and should be a priority for managers seeking to compensate for the effects of global change on these valuable habitats.     

Detection of inconspicuous epiphytic algae supporting food webs in seagrass meadows

Summary Detritus from common seagrasses and other marine angiosperms may often be a less important basis for estuarine food webs than previously believed. In NW Gulf of Mexico seagrass meadows, epiphytic algae have high productivities, palatability, and a more important trophic role than common large plants have. Interdisciplinary field experiments show (1) intensive night-time ingestion of epiphytes by various invertebrate detritivores, (2) very high productivity of epiphytic algae on seagrasses, and (3) assimilation of epiphytes rather than seagrasses, as measured by ¹³C comparisons. These combined data show that many naturally concentrated and potentially competing invertebrates in Gulf of Mexico seagrass meadows feed largely on the algal overgrowth on seagrass blades, even when such algae appear to be sparse. Primary productivity of these epiphytic algae can equal that of the seagrasses, per blade or per unit biomass. Animal ¹³C values tracked epiphytic values rather than seagrass values when comparisons were made over six sites. These measurements reinforce the view that epiphytic algae can be the primary basis of the food web in seagrass meadows.Contribution No. 608 of The University of Texas Marine Science Institute     

Evaluation of aboveground and belowground biomass recovery in physically disturbed seagrass beds

Several studies addressed aboveground biomass recovery in tropical and subtropical seagrass systems following physical disturbance. However, there are few studies documenting belowground biomass recovery despite the important functional and ecological role of roots and rhizomes for seagrass ecosystems. In this study, we compared the recovery of biomass (g dry weight m(-2)) as well as the biomass recovery rates in ten severely disturbed multi-species seagrass meadows, after the sediments were excavated and the seagrasses removed. Three sites were located in the tropics (Puerto Rico) and seven in the subtropics (Florida Keys), and all were originally dominated by Thalassia testudinum. Total aboveground biomass reached reference values at four out of ten sites studied, two in the Florida Keys and two in Puerto Rico. Total belowground biomass was lower at the disturbed locations compared to the references at all sites, apart from two sites in the Florida Keys where the compensatory effect of opportunistic species (Syringodium filiforme and Halodule wrightii) was observed. The results revealed large variation among sites in aboveground and belowground biomass for all species, with higher aboveground recovery than belowground for T. testudinum. Recovery rates for T. testudinum were highly variable across sites, but a general trend of faster aboveground than belowground recovery was observed. Equal rates between aboveground and belowground biomass were found for opportunistic species at several sites in the Florida Keys. These results indicate the importance of belowground biomass when assessing seagrass recovery and suggest that the appropriate metric to assess seagrass recovery should address belowground biomass as well as aboveground biomass in order to evaluate the full recovery of ecological services and functions performed by seagrasses. We point out regional differences in species composition and species shifts following severe disturbance events and discuss ecological implications of gap dynamics in multi-species seagrass meadows.     

Against the odds: complete outcrossing in a monoecious clonal seagrass Posidonia australis (Posidoniaceae)

Background and Aims

Seagrasses are marine, flowering plants with a hydrophilous pollination strategy. In these plants, successful mating requires dispersal of filamentous pollen grains through the water column to receptive stigmas. Approximately 40 % of seagrass species are monoecious, and therefore little pollen movement is required if inbreeding is tolerated. Outcrossing in these species is further impacted by clonality, which is variable, but can be extensive in large, dense meadows. Despite this, little is known about the interaction between clonal structure, genetic diversity and mating systems in hydrophilous taxa.

Methods

Polymorphic microsatellite DNA markers were used to characterize genetic diversity, clonal structure, mating system and realized pollen dispersal in two meadows of the temperate, monoecious seagrass, Posidonia australis, in Cockburn Sound, Western Australia.

Key Results

Within the two sampled meadows, genetic diversity was moderate among the maternal shoots (R = 0·45 and 0·64) and extremely high in the embryos (R = 0·93–0·97). Both meadows exhibited a highly clumping (or phalanx) structure among clones, with spatial autocorrelation analysis showing significant genetic structure among shoots and embryos up to 10–15 m. Outcrossing rates were not significantly different from one. Pollen dispersal distances inferred from paternity assignment averaged 30·8 and 26·8 m, which was larger than the mean clone size (12·8 and 13·8 m).

Conclusions

These results suggest highly effective movement of pollen in the water column. Despite strong clonal structure and moderate genetic diversity within meadows, hydrophilous pollination is an effective vector for completely outcrossed offspring. The different localized water conditions at each site (highly exposed conditions vs. weak directional flow) appear to have little influence on the success and pattern of successful pollination in the two meadows.     

Seagrass losses since mid‐20th century fuelled CO2 emissions from soil carbon stocks

Seagrass meadows store globally significant organic carbon (C_org) stocks which, if disturbed, can lead to CO₂ emissions, contributing to climate change. Eutrophication and thermal stress continue to be a major cause of seagrass decline worldwide, but the associated CO₂ emissions remain poorly understood. This study presents comprehensive estimates of seagrass soil C_org erosion following eutrophication‐driven seagrass loss in Cockburn Sound (23 km² between 1960s and 1990s) and identifies the main drivers. We estimate that shallow seagrass meadows (<5 m depth) had significantly higher C_org stocks in 50 cm thick soils (4.5 ± 0.7 kg C_org/m²) than previously vegetated counterparts (0.5 ± 0.1 kg C_org/m²). In deeper areas (>5 m), however, soil C_org stocks in seagrass and bare but previously vegetated areas were not significantly different (2.6 ± 0.3 and 3.0 ± 0.6 kg C_org/m², respectively). The soil C_org sequestration capacity prevailed in shallow and deep vegetated areas (55 ± 11 and 21 ± 7 g C_org m^?2 year^?1, respectively), but was lost in bare areas. We identified that seagrass canopy loss alone does not necessarily drive changes in soil C_org but, when combined with high hydrodynamic energy, significant erosion occurred. Our estimates point at ~0.20 m/s as the critical shear velocity threshold causing soil C_org erosion. We estimate, from field studies and satellite imagery, that soil C_org erosion (within the top 50 cm) following seagrass loss likely resulted in cumulative emissions of 0.06–0.14 Tg CO_2‐eq over the last 40 years in Cockburn Sound. We estimated that indirect impacts (i.e. eutrophication, thermal stress and light stress) causing the loss of ~161,150 ha of seagrasses in Australia, likely resulted in the release of 11–21 Tg CO_2‐eq since the 1950s, increasing cumulative CO₂ emissions from land‐use change in Australia by 1.1%–2.3% per annum. The patterns described serve as a baseline to estimate potential CO₂ emissions following disturbance of seagrass meadows.     

Seagrasses of south–west Australia: A conceptual synthesis of the world's most diverse and extensive seagrass meadows

South–west Australia contains extensive seagrass meadows along 2,500 km of coastline from the shallow subtidal to 50+ m water depths, and in many of the 51 bar-built estuaries along the coast. There are geomorphological differences between the south and west coasts that result in different patterns of swell exposure influencing the processes that structure seagrass habitats. In this paper, ‘sheltered’, ‘exposed’ and ‘estuarine’ seagrass habitat types are defined for south–west Australia to synthesize processes influencing seagrass communities. Sheltered habitats in south–west Australia are characterized by high light, low to moderate water motion and sporadic disturbance from storms, making them ideal habitats for a diversity of seagrass assemblages. Exposed seagrass habitats are characterized by the presence of strong and consistent ocean swells (3–8 m), predominantly from the south or south–west and seagrasses exhibit a suite of adaptive traits to survive the effects of exposure to ocean swell and associated sand movement. These include morphological features such as heavy fiber reinforcement to strengthen the aboveground stems or leaves, deep vertical rhizomes and life history traits such as rapid growth and high seed set. Within estuarine habitats highly dynamic seagrass communities are the result of fluctuating annual cycles in temperature, light and salinity. Compared to global seagrass meadows, coastal south–west Australian seagrass habitats experience high light, low nutrients and high water movement. Despite these differences, similarities with other regions do exist and here we place the habitats of south–west Australia into a global context using comparative data. The wide array of morphology and life history traits displayed among seagrass species of south–west Australia are presented in a conceptual model including habitat type, physical stressors and seagrass responses. The combination of adaptations to the habitats and processes that define them make south–west Australia a region where there is an unusually high number of co-occurring seagrass species, the highest in the world for a temperate environment (19 species), and approaching the species diversity of many tropical environments. Linking aspects of seagrass habitat, physical aspects of the environment and seagrass life history provides a context for applying knowledge gained from seagrasses in south–west Australia to other coastal ecosystems throughout the world.     

Seagrasses and eutrophication

This review summarizes the historic, correlative field evidence and experimental research that implicate cultural eutrophication as a major cause of seagrass disappearance. We summarize the underlying physiological responses of seagrass species, the potential utility of various parameters as indicators of nutrient enrichment in seagrasses, the relatively sparse available information about environmental conditions that exacerbate eutrophication effects, and the better known array of indirect stressors imposed by nutrient over-enrichment that influence seagrass growth and survival. Seagrass recovery following nutrient reductions is examined, as well as the status of modeling efforts to predict seagrass response to changing nutrient regimes.The most common mechanism invoked or demonstrated for seagrass decline under nutrient over-enrichment is light reduction through stimulation of high-biomass algal overgrowth as epiphytes and macroalgae in shallow coastal areas, and as phytoplankton in deeper coastal waters. Direct physiological responses such as ammonium toxicity and water-column nitrate inhibition through internal carbon limitation may also contribute. Seagrass decline under nutrient enrichment appears to involve indirect and feedback mechanisms, and is manifested as sudden shifts in seagrass abundance rather than continuous, gradual changes in parallel with rates of increased nutrient additions. Depending on the species, interactions of high salinity, high temperature, and low light have been shown to exacerbate the adverse effects of nutrient over-enrichment. An array of indirect effects of nutrient enrichment can accelerate seagrass disappearance, including sediment re-suspension from seagrass loss, increased system respiration and resulting oxygen stress, depressed advective water exchange from thick macroalgal growth, biogeochemical alterations such as sediment anoxia with increased hydrogen sulfide concentrations, and internal nutrient loading via enhanced nutrient fluxes from sediments to the overlying water. Indirect effects on trophic structure can also be critically important, for example, the loss of herbivores, through increased hypoxia/anoxia and other habitat shifts, that would have acted as “ecological engineers” in promoting seagrass survival by controlling algal overgrowth; and shifts favoring exotic grazers that out-compete seagrasses for space. Evidence suggests that natural seagrass population shifts are disrupted, slowed or indefinitely blocked by cultural eutrophication, and there are relatively few known examples of seagrass meadow recovery following nutrient reductions.Reliable biomarkers as early indicators of nutrient over-enriched seagrass meadows would benefit coastal resource managers in improving protective measures. Seagrasses can be considered as “long-term" integrators (days to weeks) of nutrient availability, especially through analyses of their tissue content, and of activities of enzymes such as nitrate reductase and alkaline phosphatase. The ratio of leaf nitrogen content to leaf mass has also shown promise as a “nutrient pollution indicator” for the seagrass Zostera marina, with potential application to other species. In modeling efforts, seagrass response to nutrient loading has proven difficult to quantify beyond localized areas because long-term data consistent in quality are generally lacking, and high inter-annual variability in abundance and productivity depending upon stochastic meteorological and hydrographic conditions.Efforts to protect remaining seagrass meadows from damage and loss under eutrophication, within countries and across regions, are generally lacking or weak and ineffective. Research needs to further understand about seagrasses and eutrophication should emphasize experimental studies to assess the response of a wider range of species to chronic, low-level as well as acute, pulsed nutrient enrichment. These experiments should be conducted in the field or in large-scale mesocosms following appropriate acclimation, and should emphasize factor interactions (N, P, C; turbidity; temperature; herbivory) to more closely simulate reality in seagrass ecosystems. They should scale up to address processes that occur over larger scales, including food-web dynamics that involve highly mobile predators and herbivores. Without any further research, however, one point is presently very clear: Concerted local and national actions, thus far mostly lacking, are needed worldwide to protect remaining seagrass meadows from accelerating cultural eutrophication in rapidly urbanizing coastal zones.     

Effects of pesticides on seagrass beds

In the German Wadden Sea there has been a remarkable decline in seagrass beds. It was the aim of this study to test whether herbicide contamination could be a reason for this. Concentrations of triazine herbicides such as atrazine, simazine and terbutylazine as well as phenylurea herbicides were measured in Wadden Sea sediments within or in the neighbourhood of seagrass meadows. Sediments were thus used as a marker for medium-term contamination of the Wadden Sea. The respective concentrations were examined in relation to the density and status of the seagrass meadows. Preliminary results show that there may be a connection between seagrass decline and herbicide contamination in the parts of the Wadden Sea sampled. A comparison with other contamination is also given. Received: 11 January 1999 / Received in revised form: 1 December 1999 / Accepted: 8 December 1999     

Overexpression of seagrass DnaJ gene ZjDjB1 enhances the thermotolerance of transgenic arabidopsis thaliana

Seagrass meadows are one of the most important marine resources that grow along the coast. They provide habitat and a food source for animals. They also protect the coast, fix sediment and purify seawater. In the current period of global climate change, anomalies in coastal water temperatures are increasing. A sudden increase in water temperature owing to a heat wave can have a profound effect on seagrass. Zostera japonica is a type of intertidal seagrasses, which is exposed to the air at low tide. High temperatures in the summer often lead to a decline in seagrass meadows. DnaJ proteins, also known as J proteins, are a family of conserved chaperone proteins. They are designated as J proteins because they contain a highly conserved J domain. They function as chaperones of heat shock proteins in organisms. In this study, the role of DnaJ protein (ZjDjB1) of Z. japonica under heat stress was studied. ZjDjB1 was localized to the cytoplasm and nucleus. The overexpression of ZjDjB1 in Arabidopsis thaliana results in an increase in thermotolerance and a decrease in the accumulation of reactive oxygen species and also a reduction in membrane damage. ZjDjB1 may achieve this goal by maintaining a low activity of proteolytic enzymes.     

Trophic Transfers from Seagrass Meadows Subsidize Diverse Marine and Terrestrial Consumers

In many coastal locations, seagrass meadows are part of a greater seascape that includes both marine and terrestrial elements, each linked to the other via the foraging patterns of consumers (both predators and herbivores), and the passive drift of seagrass propagules, leaves, roots and rhizomes, and seagrass-associated macroalgal detritus. With seagrasses declining in many regions, the linkages between seagrass meadows and other habitats are being altered and diminished. Thus, it is timely to summarize what is known about the prevalence and magnitude of cross-habitat exchanges of seagrass-derived energy and materials, and to increase awareness of the importance of seagrasses to adjacent and even distant habitats. To do so we examined the literature on the extent and importance of exchanges of biomass between seagrass meadows and other habitats, both in the form of exported seagrass biomass as well as transfers of animal biomass via migration. Data were most abundant for Caribbean coral reefs and Australian beaches, and organisms for which there were quantitative estimates included Caribbean fishes and North American migratory waterfowl. Overall, data from the studies we reviewed clearly showed that seagrass ecosystems provide a large subsidy to both near and distant locations through the export of particulate organic matter and living plant and animal biomass. The consequences of continuing seagrass decline thus extend far beyond the areas where seagrasses grow.