Biodegradability of unheated and laboratory heated dissolved organic matter†

IF 4.3 3区 环境科学与生态学 Q1 CHEMISTRY, ANALYTICAL Environmental Science: Processes & Impacts Pub Date : 2024-07-12 DOI:10.1039/D3EM00383C
Saraf Islam Promi, Courtney M. Gardner and Amanda K. Hohner
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Abstract

Following wildfires, partially combusted biomass remains on the forest floor and erosion from the landscape can release dissolved pyrogenic organic matter (dPyOM) to surface waters. Therefore, post-fire alterations to dissolved organic matter (DOM) in aquatic systems may play a vital role in DOM stability and biogeochemical cycles. Dissolved PyOM biodegradation remains poorly understood and is expected to vary with combustion temperature and fuel source. In this study laboratory heating and leaching of forest floor materials (soil and litter) were used to compare the biodegradability of unheated, low (250 °C), and moderate (450 °C) temperature leachates. Inoculation experiments were performed with river microbes. Dissolved organic carbon (DOC) and nitrogen (DON), inorganic nitrogen, and DOM optical properties were monitored for 38 days. Inoculation experiments showed significantly greater DOC biodegradation of low and moderate temperature samples (64% and 71%, respectively) compared to unheated samples (32%). The greater DOC biodegradation may be explained by lower molecular weight DOM composition of heated leachates which was supported by higher initial E2/E3 ratios (absorbance at 250 nm/365 nm). Further, the observed decrease in the E2/E3 ratio after incubation suggests biodegradation of smaller compounds. This trend was greater for heated samples than unheated DOM. Specific ultraviolet absorbance increased after incubation, suggesting biodegradation of aliphatic compounds. Inoculated moderate temperature samples showed the greatest DON degradation (74%), followed by low temperature (58%) and unheated (51%) samples. Overall, results suggest that low and moderate temperature dPyOM was more biodegradable than unheated DOM, which may have implications for aquatic biogeochemical cycling, ecosystem function, and water quality in fire-impacted watersheds.

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未加热和实验室加热的溶解有机物的生物降解性
野火发生后,部分燃烧的生物质会残留在森林地面上,而地表的侵蚀会向地表水释放溶解热原有机物(dPyOM)。因此,火灾后水生系统中溶解有机物(DOM)的变化可能对 DOM 的稳定性和生物地球化学循环起着至关重要的作用。人们对溶解 PyOM 的生物降解仍然知之甚少,而且预计它会随燃烧温度和燃料来源的不同而变化。本研究采用实验室加热和浸出林地材料(土壤和垃圾)的方法,比较未加热、低温(250°C)和中温(450°C)浸出液的生物降解性。对河流微生物进行了接种实验。对溶解有机碳(DOC)、溶解有机氮(DON)、无机氮和 DOM 光学特性进行了长达 38 天的监测。接种实验表明,与未加热的样本(32%)相比,低温和中温样本的 DOC 生物降解率明显更高(分别为 64% 和 71%)。DOC 生物降解能力更强的原因可能是加热浸出液中的 DOM 分子重量较低,而较高的初始 E2/E3 比率(250 纳米/365 纳米吸光度)也证明了这一点。此外,培养后观察到的 E2/E3 比率下降表明,生物降解的是较小的化合物。与未加热的 DOM 相比,加热样品的这一趋势更为明显。特定紫外线吸光度在培养后增加,表明脂肪族化合物发生了生物降解。接种温度适中的样本显示出最大的 DON 降解率(74%),其次是低温样本(58%)和未加热样本(51%)。总之,研究结果表明,低温和中温 dPyOM 比未加热的 DOM 更容易生物降解,这可能会对受火灾影响流域的水生生物地球化学循环、生态系统功能和水质产生影响。
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来源期刊
Environmental Science: Processes & Impacts
Environmental Science: Processes & Impacts CHEMISTRY, ANALYTICAL-ENVIRONMENTAL SCIENCES
CiteScore
9.50
自引率
3.60%
发文量
202
审稿时长
1 months
期刊介绍: Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.
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