Many of the world's wetlands may be profoundly affected by climate change over the coming decades. Although wetland managers may have little control over the causes of climate change, they can help to counteract its effects through local measures. This is because direct anthropogenic impacts, such as water extraction and nutrient loading, work in concert with climate change to damage wetlands. Control of these local stressors may therefore ameliorate undesired effects of climate change, such as a shift towards dominance by invasive floating plants, increasingly frequent cyanobacteria blooms, or extinction of key species. Using the iconic Doñana wetlands in Spain as a case study, we illustrate how the concept of creating a “safe operating space” may be implemented to better ensure that ecosystems do not surpass thresholds for collapse during an era of global change.
The widespread decline of seagrass beds within the Mediterranean often results in the replacement of seagrasses by opportunistic green algae of the Caulerpa family. Because Caulerpa beds have a different height, stiffness and density compared to seagrasses, these changes in habitat type modify the interaction of the seafloor with hydrodynamics, influencing key processes such as sediment resuspension and particle trapping. Here, we compare the effects on hydrodynamics and particle trapping of Caulerpa taxifolia, C. racemosa, and C. prolifera with the Mediterranean seagrasses Cymodocea nodosa and Posidonia oceanica. All macrophyte canopies reduced near-bed volumetric flow rates compared to bare sediment, vertical profiles of turbulent kinetic energy revealed peak values around the top of the canopies, and maximum values of Reynolds stress increased by a factor of between 1.4 (C. nodosa) and 324.1 (P. oceanica) when vegetation was present. All canopies enhanced particle retention rates compared to bare sediment. The experimental C. prolifera canopy was the most effective at particle retention (m2 habitat); however, C. racemosa had the largest particle retention capacity per structure surface area. Hence, in terms of enhancing particle trapping and reducing hydrodynamic forces at the sediment surface, Caulerpa beds provided a similar or enhanced function compared to P.oceanica and C. nodosa. However, strong seasonality in the leaf area index of C. racemosa and C. taxifolia within the Mediterranean, combined with a weak rhizome structure, suggests that sediments maybe unprotected during winter storms, when most erosion occurs. Hence, replacement of seagrass beds with Caulerpa is likely to have a major influence on annual sediment dynamics at ecosystem scales.
In this paper we investigate the temperature sensitivity of the photosynthetic process of the benthic diatom Cylindrotheca closterium grown in light-limited turbidostat cultures at two different growth rates. Photosynthesis was measured as the rate of oxygen evolution and as the photosystem II (PSII) electron transport rate (ETR). The photosynthetic efficiency (a), as measured by both methods, was rather insensitive to temperature, and decreased significantly only at the extreme temperatures used (5 and 35°C). The maximum PSII quantum efficiency (Fv/Fm) showed a small but significant trend of reduction with increasing temperature. However, the maximum rate of photosynthesis (PBmax and ETRmax) was extremely temperature sensitive. The effect of temperature on the relationship between PB and ETR was limited to the most extreme temperatures investigated; deviations from linearity were most extreme at 5°C and different conversion factors were observed at 5 and 35°C. A short-term change in temperature (10–30°C), as might be experienced during emersion on a European tidal flat, will not significantly affect the relationship between PB and ETR. However, care should be taken when using a single conversion factor between PB and ETR at the extremes of the temperature range. We have also shown that algal absorption measurements are important for correct calculation of ETR. The facts that different species seem to have different conversion factors and that changing environmental conditions will affect the absorption capacity and growth rate of the microphytobenthos (MPB) community suggest that it is wise to perform further calibrations of the relationship in the field before use in primary production modelling. Variable fluorescence measurements are quick and non-invasive and, with knowledge of the absorption properties of the MPB community, allow the quantification of photosynthetic parameters across large areas. Hence they are potentially useful for improving our estimates of ecosystem scale primary production.
The hypotheses that (1) different seagrass morphologies may facilitate different nutrient uptake rates under similar hydrodynamic forcing and (2) this effect on nutrient uptake rates is spatially explicit, with the highest uptake rates at edges of patches, where currents and turbulence are highest, were examined under unidirectional flow conditions. Homogeneous patches (2 m long) of two seagrass species (Cymodocea nodosa and Zostera noltii) with contrasting shoot size and density were placed in a race track flume. 15NH4+ uptake and hydrodynamic properties along a gradient from outside to inside the patch were measured at a range of current velocities (0.05 to 0.3 m s‐1). For each velocity we also determined the height and bending of the canopy. Water velocity affected the ammonium uptake rate of both species. The almost double uptake rates of C. nodosa shoots, compared to those of Z. noltii, were mainly attributed to a twofold difference in the within‐canopy water flow (Qc, m3 s‐1). Spatial patterns in canopy water flow were highly correlated with spatial patterns in NH4+ uptake, thereby explaining the 20% higher uptake rates at the leading edge of both canopies. The correlation between spatial patterns in canopy water flow and ammonium uptake rates underlines the role of canopy and patch configuration in determining the functioning of seagrass landscapes and their associated ecosystem services, such as nitrogen assimilation.