73 research outputs found

    Sea level and turbidity controls on mangrove soil surface elevation change

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    Increases in sea level are a threat to seaward fringing mangrove forests if levels of inundation exceed the physiological tolerance of the trees; however, tidal wetlands can keep pace with sea level rise if soil surface elevations can increase at the same pace as sea level rise. Sediment accretion on the soil surface and belowground production of roots are proposed to increase with increasing sea level, enabling intertidal habitats to maintain their position relative to mean sea level, but there are few tests of these predictions in mangrove forests. Here we used variation in sea level and the availability of sediments caused by seasonal and inter-annual variation in the intensity of La Nina-El Nino to assess the effects of increasing sea level on surface elevation gains and contributing processes (accretion on the surface, subsidence and root growth) in mangrove forests. We found that soil surface elevation increased with mean sea level (which varied over 250 mm during the study) and with turbidity at sites where fine sediment in the water column is abundant. In contrast, where sediments were sandy, rates of surface elevation gain were high, but not significantly related to variation in turbidity, and were likely to be influenced by other factors that deliver sand to the mangrove forest. Root growth was not linked to soil surface elevation gains, although it was associated with reduced shallow subsidence, and therefore may contribute to the capacity of mangroves to keep pace with sea level rise. Our results indicate both surface (sedimentation) and subsurface (root growth) processes can influence mangrove capacity to keep pace with sea level rise within the same geographic location, and that current models of tidal marsh responses to sea level rise capture the major feature of the response of mangroves where fine, but not coarse, sediments are abundant

    Mangrove dieback during fluctuating sea levels

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    Recent evidence indicates that climate change and intensification of the El Niño Southern Oscillation (ENSO) has increased variation in sea level. Although widespread impacts on intertidal ecosystems are anticipated to arise from the sea level seesaw associated with climate change, none have yet been demonstrated. Intertidal ecosystems, including mangrove forests are among those ecosystems that are highly vulnerable to sea level rise, but they may also be vulnerable to sea level variability and extreme low sea level events. During 16 years of monitoring of a mangrove forest in Mangrove Bay in north Western Australia, we documented two forest dieback events, the most recent one being coincident with the large-scale dieback of mangroves in the Gulf of Carpentaria in northern Australia. Diebacks in Mangrove Bay were coincident with periods of very low sea level, which were associated with increased soil salinization of 20–30% above pre-event levels, leading to canopy loss, reduced Normalized Difference Vegetation Index (NDVI) and reduced recruitment. Our study indicates that an intensification of ENSO will have negative effects on some mangrove forests in parts of the Indo-Pacific that will exacerbate other pressures.Data described in this paper are available in Supplementary Table S1. Funding was provided by the Johnston Fund of the Smithsonian Institution and the Australian Research Council, awards LP0561498, DP0774491, DP1096749 and DP150104437

    Reply to “Global coastal wetland expansion under accelerated sea-level rise is unlikely”

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    We thank Törnqvist et al. for engaging with our modelling study on the future response of global coastal wetlands to sea-level rise (SLR) and their careful and critical discussion of the presented methods and results. However, we disagree with their suggestion that our modelling approach is inadequate, a claim which relies on two arguments: (1) they argue that our results are inconsistent with the “A/S (accommodation versus sediment supply) theory”; (2) they refer to coastal Louisiana as a case example where our modelling results would deviate from historic observations and future projections of coastal wetland change. However, below we will demonstrate that Törnqvist et al.’s application of the A/S theory is not valid to predict changes in coastal wetland area, and that our global predictions are in line with regional observations and projections for coastal Louisiana and the wider region of the Gulf of Mexico. Taking coastal Louisiana as an example, Törnqvist et al. highlight that ca. 6000 km2 of land are expected to be lost over the coming 50 years due to RSLR and the erosion/drowning of coastal wetlands. However, this figure cannot directly be compared to our results, because it does not account for upland areas being converted to wetlands as sea level rises; it only accounts for seaward losses due to erosion and/or drowning with associated shoreline retreat and land loss3. Equivalent scenario runs of our model (i.e. only considering wetland accretion, but no inland migration) result in a comparable projected wetland loss in Louisiana of ca. 6,900 km2 until 2100, under the medium SLR scenario (RCP4.5). This loss is triggered by insufficient sediment availability for the marshes to keep pace with SLR in situ. Hence, Törnqvist et al.’s claim that our model underestimates future wetland loss on the US Gulf coast is incorrect. Rather, we demonstrate that our global-scale model predictions of wetland losses are comparable to regional estimates

    Future response of global coastal wetlands to sea-level rise.

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    The response of coastal wetlands to sea-level rise during the twenty-first century remains uncertain. Global-scale projections suggest that between 20 and 90 per cent (for low and high sea-level rise scenarios, respectively) of the present-day coastal wetland area will be lost, which will in turn result in the loss of biodiversity and highly valued ecosystem services1-3. These projections do not necessarily take into account all essential geomorphological4-7 and socio-economic system feedbacks8. Here we present an integrated global modelling approach that considers both the ability of coastal wetlands to build up vertically by sediment accretion, and the accommodation space, namely, the vertical and lateral space available for fine sediments to accumulate and be colonized by wetland vegetation. We use this approach to assess global-scale changes in coastal wetland area in response to global sea-level rise and anthropogenic coastal occupation during the twenty-first century. On the basis of our simulations, we find that, globally, rather than losses, wetland gains of up to 60 per cent of the current area are possible, if more than 37 per cent (our upper estimate for current accommodation space) of coastal wetlands have sufficient accommodation space, and sediment supply remains at present levels. In contrast to previous studies1-3, we project that until 2100, the loss of global coastal wetland area will range between 0 and 30 per cent, assuming no further accommodation space in addition to current levels. Our simulations suggest that the resilience of global wetlands is primarily driven by the availability of accommodation space, which is strongly influenced by the building of anthropogenic infrastructure in the coastal zone and such infrastructure is expected to change over the twenty-first century. Rather than being an inevitable consequence of global sea-level rise, our findings indicate that large-scale loss of coastal wetlands might be avoidable, if sufficient additional accommodation space can be created through careful nature-based adaptation solutions to coastal management.Personal research fellowship of Mark Schuerch (Project Number 272052902) and by the Cambridge Coastal Research Unit (Visiting Scholar Programme). Furthermore, this work has partly been supported by the EU research project RISES-AM- (FP7-ENV-693396)

    Effect of temperature on the accumulation and repair of UV damage in Symbiodinium and corals

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    Variable impacts of climate change on blue carbon

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    Blue carbon provides opportunities to mitigate climate change while increasing ecosystem services for coastal communities, including climate change adaptation; however, blue carbon ecosystems are vulnerable to climate change, leading to uncertainties in the future efficacy of these ecosystems. In this review, we assess the potential impacts of climate change on blue carbon. Despite uncertainties, carbon sequestration in coastal ecosystems is enhanced by landward migration of blue carbon habitats, maintenance of sediment supply, restoration, and improved water quality. As an example, landward migration of mangroves could result in carbon sequestration of 1.5 Pg by 2100. Mudflats, seaweed beds, and coastal swamp forests could also contribute to climate change mitigation, although there are large data gaps. Achieving the full potential of blue carbon requires protection and restoration of ecosystems and facilitation of changes in ecosystem distributions with climate change, actions that will also deliver adaptation benefits. Conversely, in the worst-case coastal squeeze scenario, losses of 3.4 Pg of sequestered carbon by 2100 could occur

    Quantification of Coastal Change and Preliminary Sediment Budget Calculation Using SfM Photogrammetry and Archival Aerial Imagery

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    A preliminary sediment budget for the sandy shores flanking the entrance to Western Port, a large bay in Australia, was formulated using a comparison between two Digital Surface Models (DSMs) with a 30-year interval and auxiliary shoreline data. The 1977 DSM was generated from ten aerial photographs using Structure-from-Motion (SfM) photogrammetry. Assessment of its accuracy obtained an RMSE of 0.48 m with most of the independent points overpredicting or underpredicting elevations by less than 0.5 m following manual point cloud cleaning. This technique created a 7.5 km2 surface with a Ground Sampling Distance of 34.3 cm between two coastal towns separated by a narrow channel. Comparison of the 1977 DSM to a second, light detection and ranging (LiDAR)-derived DSM from 2007 showed that a volume of ~200,000 m3 of sediment (above Mean Sea Level) was deposited at Newhaven Beach on Phillip Island, while, during the same period, ~40,000 m3 of sediment was lost from the mainland beaches of San Remo, on the eastern side of the channel. Shoreline positions extracted from aerial photographs taken in 1960 and a nautical chart published one century earlier indicate that the progradation experienced at Newhaven Beach has been possible due to provision of sediment via destabilisation of the vegetation covering the updrift Woolamai isthmus on the southeast coast of Phillip Island, whereas the retreat observed at San Remo Beach since 1960 can be attributed to the natural dynamics of the entrance, which appears to favour flood-dominance on the western side and ebb-dominance on the eastern side. While a more comprehensive balance of volumes entering and exiting the area would specifically benefit from volumetric assessments of the subaqueous part of the entrance, the general usefulness of quantifying coastal change using SfM and historical photographs is demonstrated

    Regulation of water balance in Mangroves

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    Background Mangroves are a group of highly salt-tolerant woody plants. The high water use efficiency of mangroves under saline conditions suggests that regulation of water transport is a crucial component of their salinity tolerance

    Potential Pollution Sources from Agricultural Activities on Tropical Forested Floodplain Wetlands Revealed by Soil eDNA

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    Tropical floodplain wetlands are found in low-lying areas that are periodically inundated. During wet periods, these wetlands can receive large amounts of suspended and dissolved material from the catchment, including many potential pollutants. In this study, we use traditional isotope tracers (δ15N and δ13C) along with soil eDNA to investigate the sources of transported materials and potential contaminants in seven forested floodplain wetlands in tropical Australia. We hypothesised that eDNA and isotope tracers in the soil would reflect the land use of the catchment. Our goal was to test whether eDNA could be used as a potential tool to identify and monitor pollutants in floodplain wetlands. The sampling sites were located within catchments that have a mosaic of land types, from well-conserved rainforests to intensive agricultural land uses, such as grazing, sugar cane, wood production, and horticulture. The soil eDNA was comprised of a mix of plant species consistent with the land use of the catchments. Most of the eDNA pool was derived from native trees, accounting for 46.2 ± 6.5% of the total; while cultivated species associated with agricultural activities contributed to 1–24% of the total. From the cultivated species, highest contributions (>5%) were from Sorghum sp. used for grazing, banana (Musa ornata), melons (Cucumis melo), and Pinus radiata and Juniperus sp. grown for wood production. Interestingly, tropical wetlands on sites 15 km offshore had soil eDNA from agricultural activities of the mainland, highlighting the connectivity of these wetlands, probably during extensive floods. Overall, soil eDNA, more than isotopic tracers, showed promising results for tracing and monitoring potential pollutants in tropical floodplain wetlands that are highly connected and susceptible to environmental degradation
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