Department of Civil and Environmental Engineering, Washington State University, Pullman, WA, USA.
Maseeh Department of Civil, Architectural and Environmental Engineering, University of Texas at Austin, TX, USA.
Environ Sci Process Impacts. 2024 Aug 14;26(8):1429-1439. doi: 10.1039/d3em00383c.
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 / ratios (absorbance at 250 nm/365 nm). Further, the observed decrease in the / 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.
野火过后,部分燃烧的生物质残留在森林地面上,景观的侵蚀会将溶解的热成因有机物质(dPyOM)释放到地表水中。因此,水生系统中溶解有机物质(DOM)的火灾后变化可能在 DOM 稳定性和生物地球化学循环中发挥重要作用。溶解的 PyOM 生物降解仍然知之甚少,预计会随燃烧温度和燃料源而变化。在这项研究中,实验室加热和林地材料(土壤和凋落物)的浸提用于比较未加热、低(250°C)和中(450°C)温浸提物的生物降解性。使用河流微生物进行接种实验。监测溶解有机碳(DOC)和氮(DON)、无机氮和 DOM 光学性质 38 天。接种实验表明,与未加热样品相比,低温和中温样品的 DOC 生物降解率分别显著更高(分别为 64%和 71%)。加热浸提物中 DOM 组成的分子量较低可能解释了更大的 DOC 生物降解,这得到了更高的初始/比值(250nm 处的吸光度/365nm 处的吸光度)的支持。此外,孵育后观察到/比值下降表明较小化合物的生物降解。这种趋势在加热样品中比未加热 DOM 中更为明显。特定紫外吸收在孵育后增加,表明脂肪族化合物的生物降解。接种中温样品显示最大的 DON 降解(74%),其次是低温(58%)和未加热(51%)样品。总体而言,结果表明,低温和中温 dPyOM 比未加热的 DOM 更具生物降解性,这可能对受火灾影响的流域中的水生生物地球化学循环、生态系统功能和水质产生影响。