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The duration and maximum combustion temperature of vegetation fires are important fire properties with implications for ecology, hydrology, hazard potential, and many other processes. Directly measuring maximum combustion temperature during vegetation fires is difficult. However, chemical transformations associated with temperature are reflected in the chemical properties of charcoals (a by-product of fire). Therefore, charcoal could be used indirectly to determine the maximum combustion temperature of vegetation fires with application to palaeoecological charcoal records. To evaluate the reliability of charcoal chemistry as an indicator of maximum combustion temperature, we studied the chemical properties of charcoal formed through two laboratory methods at measured temperatures. Using a muffle furnace, we generated charcoal from the woody material of ten different tree and shrub species at seven distinct peak temperatures (from 200°C to 800°C in 100°C increments). Additionally, we simulated more natural combustion conditions by burning woody material and leaves of four tree species in a combustion facility instrumented with thermocouples, including thermocouples inside and outside of tree branches. Charcoal samples generated in these controlled settings were analyzed using Fourier Transform Infrared (FTIR) spectroscopy to characterize their chemical properties. The Modern Analogue Technique (MAT) was employed on FTIR spectra of muffle furnace charcoal to assess the accuracy of inferring maximum pyrolysis temperature. The MAT model temperature matching accuracy improved from 46% for all analogues to 81% when including ±100°C. Furthermore, we used MAT to compare charcoal created in the combustion facility with muffle furnace charcoal. Our findings indicate that the spectra of charcoals generated in a combustion facility can be accurately matched with muffle furnace-created charcoals of similar temperatures using MAT, and the accuracy improved when comparing the maximum pyrolysis temperature from muffle furnace charcoal with the maximum inner temperature of the combustion facility charcoal. This suggests that charcoal produced in a muffle furnace may be representative of the inner maximum temperatures for vegetation fire-produced charcoals. 

Monitoring plastic litter in the environment is critical to understanding the amount, sources, transport, fate, and environmental impact of this pollutant. However, few studies have monitored plastic litter on lakebeds which are potentially important environments for determining the fate and transport of plastic litter in freshwater basins. In this study, a self-contained underwater breathing apparatus was used for litter collection at the lakebed along five transects in Lake Tahoe, United States. Litter was brought to the surface and characterized by litter type. Plastic litter was subsampled, and polymer composition was determined using attenuated total reflection Fourier transform infrared spectroscopy. The average plastic litter from the lakebed for the five dive transects was 83 ± 49 items per kilometer. The top plastic litter categories were other plastic litter (plastic litter that did not fall in another category), followed by food containers, bottles <2 L, plastic bags, and toys. These results are in line with prior studies on submerged litter, and intervention approaches or ongoing education are needed. The six polymers most frequently detected in the subsamples were polyvinyl chloride, polystyrene/expanded polystyrene, polyethylene terephthalate/polyester, polyethylene, polypropylene, and polyamide. These observations reflect global plastic production and microplastic studies from lake surface water and sediments. We found that some litter subcategories were primarily comprised of a single polymer type, therefore, in studies where the polymer type cannot be measured but litter is categorized, these results could provide an estimate of the total polymer composition for select litter categories. 

Anthropogenic climate change—combined with increased human-caused ignitions—is leading to increased wildfire frequency, carbon dioxide emissions, and refractory black carbon (rBC) aerosol emissions. This is particularly evident in the Amazon rainforest, where fire activity has been complicated by the synchronicity of natural and anthropogenic drivers of ecological change, coupled with spatial and temporal heterogeneity in past and present land use. One approach to elucidating these factors is through long-term regional fire histories. Using a novel method for rBC determinations, we measured an approximately 3500-year sediment core record from Lake Caranã in the eastern Amazon for rBC influx, a proxy of biomass burning and fossil fuel combustion. Through comparisons with previously published records from Lake Caranã and regional evidence, we distinguished between local and regional rBC emission sources demonstrating increased local emissions of rBC from ~1250 to 500 calendar years before present (cal yr BP), coinciding with increased local-scale fire management during the apex of pre-Columbian activity. This was followed by a regional decline in biomass burning coincident with European contact, pre-Columbian population decline, and regional fire suppression associated with the rubber boom (1850–1910 CE), supporting the minimal influence of climate on regional burning at this time. During the past century, rBC influx has rapidly increased. Our results can serve to validate rBC modeling results, aiding with future predictions of rBC emissions and associated impacts to the climate system.