Yihua Cai

Biomass offsets little or none of permafrost carbon release from soils, streams, and wildfire: an expert assessment

As the permafrost region warms, its large organic carbon pool will be increasingly vulnerable to decomposition, combustion, and hydrologic export. Models predict that some portion of this release w ...

Abundance, stable isotopic composition, and export fluxes of DOC, POC, and DIC from the Lower Mississippi River during 2006–2008

Sources, abundance, isotopic compositions, and export fluxes of dissolved inorganic carbon (DIC), dissolved and colloidal organic carbon (DOC and COC), and particulate organic carbon (POC), and their response to hydrologic regimes were examined through monthly sampling from the Lower Mississippi River during 2006–2008. DIC was the most abundant carbon species, followed by POC and DOC. Concentration and δ13C of DIC decreased with increasing river discharge, while those of DOC remained fairly stable. COC comprised 61 ± 3% of the bulk DOC with similar δ13C abundances but higher percentages of hydrophobic organic acids than DOC, suggesting its aromatic and diagenetically younger status. POC showed peak concentrations during medium flooding events and at the rising limb of large flooding events. While δ13C-POC increased, δ15N of particulate nitrogen decreased with increasing discharge. Overall, the differences in δ13C between DOC or DIC and POC show an inverse correlation with river discharge. The higher input of soil organic matter and respired CO2 during wet seasons was likely the main driver for the convergence of δ13C between DIC and DOC or POC, whereas enhanced in situ primary production and respiration during dry seasons might be responsible for their isotopic divergence. Carbon export fluxes from the Mississippi River were estimated to be 13.6 Tg C yr−1 for DIC, 1.88 Tg C yr−1 for DOC, and 2.30 Tg C yr−1 for POC during 2006–2008. The discharge-normalized DIC yield decreased during wet seasons, while those of POC and DOC increased and remained constant, respectively, implying variable responses in carbon export to the increasing discharge.

On the integrity of a commercial cassette ultrafiltration membrane: implications for marine colloidal biogeochemistry

The performance and integrity of a cassette cross-flow ultrafilter (Pellicon 2, Millipore) are examined with a suite of macromolecules of different molecular masses. The retention coefficient during the cross-flow ultrafiltration experiments increases with increasing molecular mass and reaches 90% with 10 kDa dextran in both milli-Q water and ultrafiltered seawater media. Based on a 90% retention coefficient, the molecular mass cut-off for the ultrafiltration membrane is defined at 10 kDa, which is ten times (1 kDa) that rated by the manufacturer. To further validate the accuracy of the laboratory calibration, the samples from the lower Zhujiang River and the Jiulong River Estuary are ultrafiltered with the cassette ultrafiltration membrane and the colloidal organic carbon abundances in these samples are quantified with the ultrafiltration permeation model based on time series permeation subsamples. The colloidal organic carbon abundances are 5.8%–21.1% in the Jiulong River Estuary and 5.6%–11.0% in the lower Zhujiang River. These are consistent with the reported values for both estuaries as well as with the colloidal organic carbon abundances in marine environments over the coastal and open oceans with 10 kDa cut-off membranes. Therefore, these field data support the laboratory calibration result and indicate the validity of the experimental and quantification procedure adopted. The discrepancy between the nominal molecular mass cut-off and the actual pore size of the ultrafiltration membrane should be of great concern for research in colloidal and nanoparticle biogeochemistry. Careful examination of the membrane integrity should be taken during ultrafiltration experiments in order to avoid misleading molecular mass cut-off information.

Floodplain Effects On the Transport of Dissolved and Colloidal Trace Elements in the East Pearl River, Mississippi

&NA; Substantial work suggests that floodplain wetlands could play a role in modifying fluvial fluxes of dissolved and colloidal trace elements. Yet, few studies have directly addressed this issue. We examined trace elements in the East Pearl River (Mississippi or Louisiana, USA), which is surrounded by wetlands that are temporally more or less connected to the river depending on river stage. Dissolved and colloidal trace element samples, along with ancillary data, including dissolved organic carbon and nutrients, were collected during eight surveys of this system at different flow stages from November 2007 to September 2008. Hydrology of the system is complex due to seasonal changes in water sources as well as potential inputs from the floodplain wetlands and the hyporheic zone. We therefore considered effects including nonconservative mixing of water sources, saltwater intrusion, and floodplain wetland flux requirements needed to support observed downstream concentration changes. During moderately high discharge, fluxes of many elements (e.g., Cd, Fe, Mn, and Zn) increased downstream by 20% or more, with inputs from the floodplain wetlands as the apparent source. At the highest discharge, however, wetland inputs to the river may have been rate‐limited (i.e., the wetland source was flushed faster than biogeochemical processes could regenerate dissolved or colloidal material). At low discharge, other effects, including saltwater intrusion and hyporheic zone interactions, are important. Both redox processes and organic ligands (or dissolved organic carbon), along with the supply of wetland inputs (or removal) relative to river fluxes, appear to be key factors determining floodplain wetland effects. While the behavior of some elements suggests they were dominantly affected by redox processes (Mn and V) or by organic complexation (dissolved Fe and light rare earths), other elements were affected by more than one process in ways that remain obscure (Cu). Overall our results are broadly consistent with previous field, laboratory, and modeling studies and suggest that a better understanding of the sources and transformations of Fe is a key area for future research.

Sources and conservative mixing of uranium in the Taiwan Strait

Seawater samples are collected in the spring of 2013 from the Taiwan Strait for the analysis of uranium (U) concentrations and isotopic compositions using MC-ICP-MS, and the geochemical behavior patterns of U in the Taiwan Strait are then investigated. Average concentrations of individual U isotopes are (3.23±0.14) μg/kg for 238U, (2.34±0.09)×10–2 μg/kg for 235U and (2.05±0.07)×10–4 μg/kg for 234U. Correspondingly, the U isotopic compositions are 155±18 for δ234U and 138±2 for 238U:235U. The U concentrations and isotopic ratios in the Taiwan Strait are similar to those of open ocean seawater, suggesting the dominance of the open ocean input to the strait’s U pool. However, river input, as suggested by the slightly lower salinity than that of the open ocean, also affected the U concentrations and isotopic compositions in the strait. From a compilation of U concentrations in the Taiwan Strait and adjacent areas, including the Jiulong Estuary and Zhujiang Estuary, the Xiamen Bay and the northern South China Sea, a strong and significant relationship between U concentration and salinity [U:S; U=(0.093 4±0.002 4)S+(0.092 0±0.061 5)] is revealed, suggesting conservative mixing of U in the Taiwan Strait. To better understand the U geochemistry in the Taiwan Strait, a multiple endmembers mixing model is applied to estimate the contributions of potential sources. The open ocean seawater contributed 69%–95% of U in the Taiwan Strait, with river water approximately 2%, and dust deposition only around 0.13%. Therefore, the model results supported the open ocean input source and the conservative mixing behavior of U derived from the observation of U concentrations and isotopic ratios and U:S ratios. The sediment interstitial water may be an important source of U to the Taiwan Strait with a possible contribution of 3%–29%, consistent with previous investigations based on radium isotopes. However, further investigations are warranted to examine the U concentration in the sediment interstitial water and its input to the overlying seawater in the Taiwan Strait.