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Seagrass meadows provide valuable socio-ecological ecosystem services, including a key role in climate change mitigation and adaption. Understanding the natural history of seagrass meadows across environmental gradients is crucial to deciphering the role of seagrasses in the global ocean. In this data collation, spatial and temporal patterns in seagrass meadow structure, biomass and production data are presented as a function of biotic and abiotic habitat characteristics. The biological traits compiled include measures of meadow structure (e.g. percent cover and shoot density), biomass (e.g. above-ground biomass) and production (e.g. shoot production). Categorical factors include bioregion, geotype (coastal or estuarine), genera and year of sampling. This dataset contains data extracted from peer-reviewed publications published between 1975 and 2020 based on a Web of Science search and includes 11 data variables across 12 seagrass genera. The dataset excludes data from mesocosm and field experiments, contains 14 271 data points extracted from 390 publications and is publicly available on the PANGAEA® data repository (10.1594/PANGAEA.929968; Strydom et al., 2021). The top five most studied genera are Zostera, Thalassia, Cymodocea, Halodule and Halophila (84 % of data), and the least studied genera are Phyllospadix, Amphibolis and Thalassodendron (2.3 % of data). The data hotspot bioregion is the Tropical Indo-Pacific (25 % of data) followed by the Tropical Atlantic (21 %), whereas data for the other four bioregions are evenly spread (ranging between 13 and 15 % of total data within each bioregion). From the data compiled, 57 % related to seagrass biomass and 33 % to seagrass structure, while the least number of data were related to seagrass production (11 % of data). This data collation can inform several research fields beyond seagrass ecology, such as the development of nature-based solutions for climate change mitigation, which include readership interested in blue carbon, engineering, fisheries, global change, conservation and policy. [ABSTRACT FROM AUTHOR]

Herbivore distributions and abundance are shifting because of climate change, leading to intensified grazing pressure on foundation species such as seagrasses. This, combined with rapidly increasing magnitudes of change in estuarine ecosystems, may affect seagrass resilience. While the overall resilience of seagrasses is generally well-studied, the timeframes of recovery has received comparatively little attention, particularly in temperate estuaries. We investigated how the recovery time (RT) of seagrass is affected by simulated grazing in a southwestern Australian estuary. Whilst excluding swans, we simulated different grazing intensities (25, 50, 75, and 100% removal from 1 m2 plots) at four locations in the Swan-Canning Estuary, Western Australia during summer and tracked the recovery of seagrass over 3 months, using seagrass cover as the main measure of recovery.We found that seagrass recovered within 4--6 weeks from the lower grazing intensities (25 and 50%) and 7--19 weeks from the higher grazing intensities (75 and 100%) across the estuary. Increased grazing intensity led to not only longer recovery times (RTs), but also greater variability in the RT among experimental locations. The RT from the higher grazing intensities at one location in particular was more than double other locations. Seagrass recovery was through vegetative mechanisms and not through sexual reproduction. There was a significant grazing treatment effect on seagrass meadow characteristics, particularly belowground biomass which had not recovered 3 months following grazing. As the pressure of climate change on estuarine environments increases, these quantified RTs for seagrass provide a baseline for understanding grazing pressure as a singular disturbance. Future work can now examine how grazing and other potentially interacting pressures in our changing climate could impact seagrass recovery even further. [ABSTRACT FROM AUTHOR]

Seagrass meadows provide valuable socio-ecological ecosystem services, including a key role in climate change mitigation and adaption. Understanding the natural history of seagrass meadows across environmental gradients is crucial to decipher the role of seagrasses in the global ocean. In this data collation, spatial and temporal patterns in seagrass meadow structure, biomass, production and reproduction data are presented as a function of biotic and abiotic habitat characteristics. The biological traits compiled include measures of meadow structure (e.g., percent cover and shoot density), biomass (e.g., above-ground biomass), production (e.g., shoot production), and reproduction effort (e.g., flowering intensity and seed bank density). Categorical factors include bioregion, geotype (coastal or estuarine), genera and year of sampling. This dataset contains data extracted from peer-reviewed publications published between 1975 and 2020 based on a Web of Science search, and includes 15 data variables across 12 seagrass genera. The top four most studied genera are Zostera, Thalassia, Halophila and Cymodocea (80% of data), and the least studied genera are Phyllospadix, Amphibolis and Thalassodendron (2.3% of data). The data hotspot bioregion is the Tropical Indo Pacific (25% of data), whereas data for the other five bioregions are evenly spread (ranging between 13 and 16% of total data within each bioregion). From the data compiled, 39% related to seagrass biomass, while the least number of data were related to seagrass production (10% of data). This data collation can inform several research fields beyond seagrass ecology, such as the development of nature-based solutions for climate change mitigation, which include readership interested in blue carbon, engineering, fisheries, global change, conservation and policy. [ABSTRACT FROM AUTHOR]

Extreme climate events are predicted to alter estuarine salinity gradients exposing habitat‐forming species to more frequent salinity variations. The intensity and duration of these variations, rather than the mean salinity values ecosystems are exposed to, may be more important in influencing resilience but requires further investigation.Precipitation, including the frequency, intensity and timing of occurrence, is shifting due to climate change. A global analysis on the timing of rainfall in estuarine catchments was conducted. In 80% of the case studies, the maximum daily rainfall occurred in the dry season at least once over the 40‐year period and could be classified as an extreme event.We selected an estuary in southwestern Australia and investigated the effects of an extreme rainfall event in 2017 resulting in an excess discharge of freshwater on seagrass Halophila ovalis. Adapting an approach applied for marine heatwaves using salinity data, we quantified metrics and characterised the event along the estuarine gradient. We assessed seagrass resilience by calculating resistance times based on the comparisons of biomass and leaf density data prior to, and during the event, and recovery times through assessment against historical condition.Where salinity is historically more variable, reductions in biomass were lower (higher resistance via plasticity in salinity tolerance) and meadows recovered within 9–11 months. Where salinity is historically more stable, loss of biomass was greatest (low resistance) post‐event and recovery may exceed 22 months, and potentially due to the rapid decline in salinity (−3 PSU/day).As estuaries become more hydrologically variable, these metrics provide a baseline for retrospective and future comparisons. Our results suggest seagrass resilience to hyposalinity is population specific. This understanding enables more accurate predictions about ecological responses to climate change and identifies which populations may 'future proof' ecosystem resilience.Synthesis. Following an extreme rainfall event, we found seagrass populations that are exposed to variable salinities recovered while those from a stable salinity environment were unable to recover within the study time frame. These findings expand upon existing evidence, derived primarily from other ecosystems, that show new sources of resilience may be uncovered by accounting for between‐population variation. [ABSTRACT FROM AUTHOR]