Department of Environmental Studies, Davidson College, Davidson, NC, 28035, USA; Department of Biology, University of North Carolina at Greensboro, Greensboro, NC, 27402, USA.
Department of Biology, University of North Carolina at Greensboro, Greensboro, NC, 27402, USA; School of Life Sciences, Earth and Environmental Sciences Programme, State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Chemosphere. 2022 Dec;308(Pt 2):136310. doi: 10.1016/j.chemosphere.2022.136310. Epub 2022 Sep 8.
Wetlands are widely regarded as biogeochemical hotspots of highly toxic methylmercury (MeHg), mainly mediated by sulfate-reducing bacteria. In low-lying coastal wetlands, sea level rise, a phenomenon caused by global climate change, is slowly degrading numerous healthy freshwater forested wetlands into salt-degraded counterparts with a nickname "ghost forests", and eventually converting them to saltmarshes. However, little is known about the changes of mercury (Hg) methylation, bioaccumulation, and biomagnification along the forest-to-saltmarsh gradient. Here, we conducted extensive field sampling in three wetland states (healthy forested wetlands, salt-degraded forested wetlands, and saltmarsh) along a salinity gradient (from 0 to 9.4 ppt) in Winyah Bay, South Carolina, USA. We found that in our study wetland systems the saltmarshes had the lowest levels of both total Hg and MeHg in sediments and biota, as compared to healthy forested wetlands and saltwater-degraded ghost forests. Our results suggest that the slow conversion of forested wetland to saltmarsh could reduce net MeHg production in our study wetland systems, which we hypothesized that could be attributed to increased sulfate reduction and excessive buildup of sulfide in sediment that inhibits microbial Hg methylation, and/or reduced canopy density and increased photodegradation of MeHg. However, it should be noted that biogeochemical MeHg responses to salinity changes may be site-specific and we urge more similar studies in other wetland systems along a salinity gradient. Therefore, long-term salinization of coastal wetlands and the slow conversion of forests to marshes could decrease long-term exposure of toxic MeHg levels in coastal food webs that are similar to our system, and ultimately reduce human exposure to this neurotoxin.
湿地被广泛认为是高度有毒的甲基汞(MeHg)的生物地球化学热点区域,主要由硫酸盐还原菌介导。在地势低洼的沿海湿地,海平面上升——这一由全球气候变化引起的现象,正慢慢地将众多健康的淡水森林湿地降级为带有“鬼林”别名的盐化湿地,并最终将其转化为盐沼。然而,人们对汞(Hg)甲基化、生物累积和生物放大沿森林到盐沼梯度的变化知之甚少。在这里,我们在美国南卡罗来纳州的威亚湾(Winyah Bay)沿着盐度梯度(从 0 到 9.4 ppt)在三个湿地状态(健康的森林湿地、盐化森林湿地和盐沼)进行了广泛的实地采样。我们发现,与健康的森林湿地和盐水退化的鬼林相比,我们研究的湿地系统中的盐沼在沉积物和生物群中总汞和 MeHg 的含量最低。我们的结果表明,森林湿地向盐沼的缓慢转化可能会减少我们研究的湿地系统中净 MeHg 的产生,我们假设这可能归因于硫酸盐还原的增加和沉积物中硫化物的过度积累抑制了微生物的 Hg 甲基化,和/或冠层密度降低和 MeHg 的光降解增加。然而,应该注意的是,生物地球化学 MeHg 对盐度变化的响应可能是特定地点的,我们敦促在其他盐度梯度的湿地系统中进行更多类似的研究。因此,沿海湿地的长期盐化和森林向沼泽的缓慢转化可能会降低与我们的系统类似的沿海食物网中有毒 MeHg 水平的长期暴露,并最终减少人类对这种神经毒素的暴露。