Wetlands are the largest natural source of atmospheric methane 1 , the second most important greenhouse gas 2 . Methane flux to the atmosphere depends strongly on the climate 3 ; however, by far the largest part of the methane formed in wetland ecosystems is recycled and does not reach the atmosphere 4,5 . The biogeochemical controls on the efficient oxidation of methane are still poorly understood. Here we show that submerged Sphagnum mosses, the dominant plants in some of these habitats, consume methane through symbiosis with partly endophytic methanotrophic bacteria, leading to highly effective in situ methane recycling. Molecular probes revealed the presence of the bacteria in the hyaline cells of the plant and on stem leaves. Incubation with 13 C-methane showed rapid in situ oxidation by these bacteria to carbon dioxide, which was subsequently fixed by Sphagnum, as shown by incorporation of 13 C-methane into plant sterols. In this way, methane acts as a significant (10-15%) carbon source for Sphagnum. The symbiosis explains both the efficient recycling of methane and the high organic carbon burial in these wetland ecosystems.Peat bogs alternate between lawns and pools. Lawns are dominated by species that grow up to several decimetres above the water table. Pools are dominated by aquatic species, such as Sphagnum cuspidatum, that form layers of living plants below the water table. We investigated the methane-oxidizing activity of submerged S. cuspidatum from peat bog pools at different field locations in the Netherlands, and compared it to the activity of S. magellanicum and S. papillosum growing in lawns. The potential methane-oxidizing activity was substantially higher in the submerged mosses (Fig. 1). In control experiments with bog water, methane was not oxidized, indicating that the methanotrophic bacteria were mainly present on or in the living Sphagnum tissue.The identity and location of these methanotrophs was determined in a molecular approach. Total genomic DNA from washed Sphagnum plants was isolated and bacterial 16S ribosomal RNA genes were amplified, cloned into Escherichia coli, sequenced and analysed phylogenetically. One of the 16S rRNA gene sequences of the clone library was affiliated to a cluster of type II methanotrophs that contained acidophilic methanotrophs isolated from Sphagnum bogs, such as Methylocella palustris (identity 93%) 6 and Methylocapsa acidiphila (identity 93%) 7 .The full 16S rRNA gene sequence was used to design two specific oligonucleotide probes for fluorescence in situ hybridization (FISH). FISH was combined with serial sectioning of the stems and the stem leaves of multiple individuals of submerged S. cuspidatum. The methanotrophic bacterium targeted by the probes was the dominant methanotroph in S. cuspidatum sections, accounting for over 75% of
In the 1980s and 1990s, it became increasingly clear that changes in external nutrient loads alone could not entirely explain the severe eutrophication of surface waters in the Netherlands. Nowadays, 'internal eutrophication' has become a widely accepted term in Dutch water management practice to describe the eutrophication of an ecosystem without additional external input of nutrients (N, P, K). This review surveys the principal mechanisms involved in this process. It also discusses possible remedies to combat internal eutrophication.
In wetland soils and underwater sediments of marine, brackish and freshwater systems, the strong phytotoxin sulfide may accumulate as a result of microbial reduction of sulfate during anaerobiosis, its level depending on prevailing edaphic conditions. In this review, we compare an extensive body of literature on phytotoxic effects of this reduced sulfur compound in different ecosystem types, and review the effects of sulfide at multiple ecosystem levels: the ecophysiological functioning of individual plants, plant-microbe associations, and community effects including competition and facilitation interactions. Recent publications on multi-species interactions in the rhizosphere show even more complex mechanisms explaining sulfide resistance. It is concluded that sulfide is a potent phytotoxin, profoundly affecting plant fitness and ecosystem functioning in the full range of wetland types including coastal systems, and at several levels. Traditional toxicity testing including hydroponic approaches generally neglect rhizospheric effects, which makes it difficult to extrapolate results to real ecosystem processes. To explain the differential effects of sulfide at the different organizational levels, profound knowledge about the biogeochemical, plant physiological and ecological rhizosphere processes is vital. This information is even more important, as anthropogenic inputs of sulfur into freshwater ecosystems and organic loads into freshwater and marine systems are still much higher than natural levels, and are steeply increasing in Asia. In addition, higher temperatures as a result of global climate change may lead to higher sulfide production rates in shallow waters.
Seagrasses evolved from terrestrial plants into marine foundation species around 100 million years ago. Their ecological success, however, remains a mystery because natural organic matter accumulation within the beds should result in toxic sediment sulfide levels. Using a meta-analysis, a field study, and a laboratory experiment, we reveal how an ancient three-stage symbiosis between seagrass, lucinid bivalves, and their sulfide-oxidizing gill bacteria reduces sulfide stress for seagrasses. We found that the bivalve-sulfide-oxidizer symbiosis reduced sulfide levels and enhanced seagrass production as measured in biomass. In turn, the bivalves and their endosymbionts profit from organic matter accumulation and radial oxygen release from the seagrass roots. These findings elucidate the long-term success of seagrasses in warm waters and offer new prospects for seagrass ecosystem conservation.
Fens represent a large array of ecosystem services, including the highest biodiversity found among wetlands, hydrological services, water purification and carbon sequestration. Land-use change and drainage has severely damaged or annihilated these services in many parts of North America and Europe; restoration plans are urgently needed at the landscape level. We review the major constraints on the restoration of rich fens and fen water bodies in agricultural areas in Europe and disturbed landscapes in North America: (i) habitat quality problems: drought, eutrophication, acidification, and toxicity, and (ii) recolonization problems: species pools, ecosystem fragmentation and connectivity, genetic variability, and invasive species; and here provide possible solutions. We discuss both positive and negative consequences of restoration measures, and their causes. The restoration of wetland ecosystem functioning and services has, for a long time, been based on a trial-and-error approach. By presenting research and practice on the restoration of rich fen ecosystems within agricultural areas, we demonstrate the importance of biogeochemical and ecological knowledge at different spatial scales for the management and restoration of biodiversity, water quality, carbon sequestration and other ecosystem services, especially in a changing climate. We define target processes that enable scientists, nature managers, water managers and policy makers to choose between different measures and to predict restoration prospects for different types of deteriorated fens and their starting conditions.
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