Investigating the migration and transformation of carbonaceous and nitrogenous matter in the cryosphere areas is crucial for understanding global biogeochemical cycle and earth's climate system. However, water-soluble organic constituents and their transformation in multiple water bodies are barely investigated. Water-soluble organic carbon (WSOC) and organic nitrogen (WSON), and particulate black carbon (PBC) in multiple types of water bodies in eastern Tibetan Plateau (TP) cryosphere for the first time have been systematically investigated. Statistical results exhibited that from south to north and from east to west of this region, WSOC concentrations in alpine river runoff were gradually elevated. WSOC and nitrogenous matter in the alpine river runoff and precipitation in the glacier region presented distinct seasonal variations. WSON was the dominant component (63.4%) of water-soluble total nitrogen in precipitation over high-altitude southeastern TP cryosphere. Water-soluble carbonaceous matter dominated the carbon cycle in the TP cryosphere, but particulate carbonaceous matter in the alpine river runoff had a small fraction of the cryospheric carbon cycle. Analysis of optical properties illustrated that PBC had a much stronger light absorption ability (MAC-PBC: 2.28 ± 0.37 m² g⁻¹) than WSOC in the alpine river runoff (0.41 ± 0.26 m² g⁻¹). Ionic composition was dominated by SO₄²⁻, NO₃⁻, and NH₄⁺ (average: 45.13 ± 3.75%) in the snow of glaciers, implying important contribution of (fossil fuel) combustion sources over this region. The results of this study have essential implications for understanding the carbon and nitrogen cycles in high altitude cryosphere regions of the world. Future work should be performed based on more robust in-situ observations and measurements from multiple environmental medium over the cryosphere areas, to ensure ecological protection and high-quality development of the high mountain Asia.

The combined effects of emerging pollutants and ocean acidification (OA) on marine organisms and marine ecosystems have attracted increasing attention. However, the combined effects of tralopyril and OA on marine organisms and marine ecosystems remain unclear. In this study, Crassostrea gigas (C. gigas) were exposed to tralopyril (1 μg/L) and/or OA (PH = 7.7) for 21 days and a 14-day recovery acclimation. To investigate the stress response and potential molecular mechanisms of C. gigas to OA and tralopyril exposure alone or in combination, as well as the effects of OA and/or tralopyril on bivalve biomineralization and marine carbon cycling. The results showed that the combined toxicity was between that of acidification and tralopyril alone. Single or combined exposure activated the general stress defense responses of C. gigas mantle, affected energy metabolism and biomineralization of the organism and the carbon cycle of the marine ecosystem. Moreover, acidification-induced and tralopyril-induced toxicity showed potential recoverability at molecular and biochemical levels. This study provides a new perspective on the molecular mechanisms of tralopyril toxicity to bivalve shellfish and reveals the potential role of tralopyril and OA on marine carbon cycling.

Coastal wetland soils serve as a great C sink or source, which highly depends on soil carbon flux affected by complex hydrology in relation to salinity. We conducted a field experiment to investigate soil respiration of three coastal wetlands with different land covers (BL: bare land; SS: Suaeda salsa; PL: Phragmites australis) from May to October in 2012 and 2013 under three groundwater tables (deeper, medium, and shallower water tables) in the Yellow River Delta of China, and to characterize the spatial and temporal changes and the primary environmental drivers of soil respiration in coastal wetlands. Our results showed that the elevated groundwater table decreased soil CO₂ emissions, and the soil respiration rates at each groundwater table exhibited seasonal and diurnal dynamics, where significant differences were observed among coastal wetlands with different groundwater tables (p < 0.05), with the average CO₂ emission of 146.52 ± 13.66 μmol m⁻²s⁻¹ for deeper water table wetlands, 105.09 ± 13.48 μmol m⁻²s⁻¹ for medium water table wetlands and 54.32 ± 10.02 μmol m⁻²s⁻¹ for shallower water table wetlands. Compared with bare land and Suaeda salsa wetlands, higher soil respiration was observed in Phragmites australis wetlands. Generally, soil respiration was greatly affected by salinity and soil water content. There were significant correlations between groundwater tables, electrical conductivity and soil respiration (p < 0.05), indicating that soil respiration in coastal wetlands was limited by electrical conductivity and groundwater tables and soil C sink might be improved by regulating water and salt conditions. We have also observed that soil respiration and temperature showed an exponential relationship on a seasonal scale. Taking into consideration the changes in groundwater tables and salinity that might be caused by sea level rise in the context of global warming, we emphasize the importance of groundwater level and salinity in the carbon cycle process of estuarine wetlands in the future.

Dissolved organic carbon (DOC) is not only a critical component of global and regional carbon budgets, but also an important precursor for carcinogenic disinfection byproducts (DBP) generated during drinking water disinfection process. The lack of process based watershed scale model for carbon cycling has been a limiting factor impeding effective watershed management to control DOC fluxes to source waters. Here, we integrated terrestrial and aquatic carbon processes into the widely tested Soil and Water Assessment Tool (SWAT) watershed model to enable watershed-scale DOC modeling (referred to as SWAT-DOC hereafter). The modifications to SWAT mainly fall into two groups: (1) DOC production in soils and its transport to aquatic environment by different hydrologic processes, and (2) riverine transformation of DOC and their interactions with particular organic carbon (POC), inorganic carbon and algae (floating and bottom). We tested the new SWAT-DOC model in the Cannonsville watershed, which is part of the New York City (NYC) water supply system, using long-term DOC load data (from 1998 to 2012) derived from 1399 DOC samplings. The calibration and verification results indicate that SWAT-DOC achieved satisfactory performance for both streamflow and DOC at daily and monthly temporal scales. The parameter sensitivity analysis indicates that DOC loads in the Cannonsville watershed are controlled by the DOC production in soils and its transport in both terrestrial and aquatic environments. Further model uncertainty analysis indicates high uncertainties associated with peak DOC loads, which are attributed to underestimation of high streamflows. Therefore, future efforts to enhance SWAT-DOC to better represent runoff generation processes hold promise to further improve DOC load simulation. Overall, the wide use of SWAT and the satisfactory performance of SWAT-DOC make it a useful tool for DOC modeling and mitigation at the watershed scale.

Organic aerosol (OA) are always the most abundant species in terms of relative proportion to PM₂.₅ concentration in Beijing, while in previous studies, poor link between carbonaceous particles and their gaseous precursors were established based on field observation results. Through this study, we provided a comprehensive analysis of critical carbonaceous species in the atmosphere. The concentrations, diurnal variations, conversions, and gas-particle partitioning (F-factor) of 8 carbonaceous species, carbon dioxide (CO₂), carbon monoxide (CO), methane (CH₄), volatile organic compounds (VOCs), non-methane hydrocarbon (NMHC), organic carbon (OC), elemental carbon (EC), and water soluble organic compounds (WSOCs), in Beijing were analyzed synthetically. Carbonaceous gases (CO, CO₂, VOCs, and CH₄) and OC/EC ratios exhibited double-peak diurnal patterns with a pronounced midnight peak, especially in winter. High correlation between VOCs and OC during winter nighttime indicated that OC was formed from VOCs precursors via an unknown mechanism at relative humidity greater than 50% and 80%, thereby promoting WSOC formation in PM₁ and PM₂.₅ respectively. The established F-factor method was effective to describe gas-to-particle transformation of carbonaceous species and was a good indicator for haze events since high F-factors corresponded with enhanced PM₂.₅ level. Moreover, higher F-factors in winter indicated carbonaceous species were more likely to exist as particles in Beijing. These results can help gain a comprehensive understanding of carbon cycle and formation of secondary organic aerosols from gaseous precursors in the atmosphere.

Anthropogenic activities, such as mining and agriculture, have resulted in many freshwater systems having elevated concentrations of copper. Despite the prevalence of this contamination, and the vital ecological function of prokaryotes, just three studies have investigated prokaryote community responses to copper concentration in freshwater sediments. To address this, the current study investigated these communities in outdoor mesocosms spiked with varying copper concentrations. We profiled the prokaryotic communities at the taxonomic level, using next-generation high-throughput sequencing techniques, as well as their function, using baiting with leaf analogues, and Biolog Ecoplates for community-level physiological profiling. Sediments containing just 46 mg kg⁻¹ of copper, had distinctly different microbial communities compared with controls, as determined by both DNA and RNA 16S ribosomal RNA gene (rRNA) profiling. In addition to this, sediment communities displayed a greatly reduced utilisation of carbon substrates under elevated copper, while the communities recruited onto leaf analogues were also disparate from those of control ponds. Given the vital role of prokaryotes in ecosystem processes, including carbon cycling, these changes are potentially of great ecological relevance, and are seen to occur well below the ‘low risk’ sediment quality guideline values (SQGV) used by regulatory bodies internationally.

Recent climate change may be enhancing mercury fluxes to Arctic lake sediments, confounding the use of sediment cores to reconstruct histories of atmospheric deposition. Assessing the independent effects of climate warming on mercury sequestration is challenging due to temporal overlap between warming temperatures and increased long-range transport of atmospheric mercury following the Industrial Revolution. We address this challenge by examining mercury trends in short cores (the last several hundred years) from eight lakes centered on Cape Herschel (Canadian High Arctic) that span a gradient in microclimates, including two lakes that have not yet been significantly altered by climate warming due to continued ice cover. Previous research on subfossil diatoms and inferred primary production indicated the timing of limnological responses to climate warming, which, due to prevailing ice cover conditions, varied from ∼1850 to ∼1990 for lakes that have undergone changes. We show that climate warming may have enhanced mercury deposition to lake sediments in one lake (Moraine Pond), while another (West Lake) showed a strong signal of post-industrial mercury enrichment without any corresponding limnological changes associated with warming. Our results provide insights into the role of climate warming and organic carbon cycling as drivers of mercury deposition to Arctic lake sediments.

Nitrogen (N) deposition in China has increased greatly, but the general impact of elevated N deposition on carbon (C) dynamics in Chinese terrestrial ecosystems is not well documented. In this study we used a meta-analysis method to compile 88 studies on the effects of N deposition C cycling on Chinese terrestrial ecosystems. Our results showed that N addition did not change soil C pools but increased above-ground plant C pool. A large decrease in below-ground plant C pool was observed. Our result also showed that the impacts of N addition on ecosystem C dynamics depend on ecosystem type and rate of N addition. Overall, our findings suggest that 1) decreased below-ground plant C pool may limit long-term soil C sequestration; and 2) it is better to treat N-rich and N-limited ecosystems differently in modeling effects of N deposition on ecosystem C cycle.

We present a new formulation of the acidification model MAGIC that uses decomposer dynamics to link nitrogen (N) cycling to carbon (C) turnover in soils. The new model is evaluated by application to 15–30 years of water chemistry data at three coniferous-forested sites in the Czech Republic where deposition of sulphur (S) and N have decreased by >80% and 40%, respectively. Sulphate concentrations in waters have declined commensurately with S deposition, but nitrate concentrations have shown much larger decreases relative to N deposition. This behaviour is inconsistent with most conceptual models of N saturation, and with earlier versions of MAGIC which assume N retention to be a first-order function of N deposition and/or controlled by the soil C/N ratio. In comparison with earlier versions, the new formulation more correctly simulates observed short-term changes in nitrate leaching, as well as long-term retention of N in soils. The model suggests that, despite recent deposition reductions and recovery, progressive N saturation will lead to increased future nitrate leaching, ecosystem eutrophication and re-acidification.

Using a process-based Dynamic Land Ecosystem Model, we assessed carbon dynamics of urbanized/developed lands in the Southern United States during 1945–2007. The results indicated that approximately 1.72 (1.69–1.77) Pg (1P = 10¹⁵) carbon was stored in urban/developed lands, comparable to the storage of shrubland or cropland in the region. Urbanization resulted in a release of 0.21 Pg carbon to the atmosphere during 1945–2007. Pre-urbanization vegetation type and time since land conversion were two primary factors determining the extent of urbanization impacts on carbon dynamics. After a rapid decline of carbon storage during land conversion, an urban ecosystem gradually accumulates carbon and may compensate for the initial carbon loss in 70–100 years. The carbon sequestration rate of urban ecosystem diminishes with time, nearly disappearing in two centuries after land conversion. This study implied that it is important to take urbanization effect into account for assessing regional carbon balance.