Apportioning sedimentary organic matter sources and its degradation state: Inferences based on aliphatic hydrocarbons, amino acids and δ15N.

The sources and state of sedimentary organic matter (SOM) in fresh water aquatic systems are important to understand the carbon cycling in terrestrial environments. The composition of organic matter in the lake sediments demonstrates the physical and chemical condition of the lake ecosystems. However, the systematic and structured investigations focussed on to understand the source and fate of organic matters within eutrophic lakes is still far from clear. The present study is focusing on the implications of amino acids (AA), aliphatic hydrocarbons and bulk geochemical (C/N, δ15N) proxies to understand the distribution, sources and state of sedimentary organic matter in Ahansar Lake from Kashmir valley, India. The relatively low C/N ratios along with high AA contents indicate enhanced aquatic productivity in the lake system. Likewise, the dominance of the mid-chain monomethyl alkanes (MMAs), highly branched isoprenoids (HBIs), botryococcenes, steroids and triterpenoids suggest OM sourced from periphyton remains. Furthermore, the presence of C27, C28 and C29 diagenetically altered steroids also reflects a major algal contribution. The spatial variability of Paq demonstrates their applicability as a proxy for the contribution of aquatic vegetation. The ratio of individual amino acids (oxic/anoxic ratio) and low Pr/Ph (pristane/phytane) values indicate anoxic nature of the current depositional environment. This also leads to significant organic matter preservation as revealed by amino acid indices (e.g., degradation index - DI and reactivity index - RI). These data collectively demonstrate the systematic investigation and comprehensive understanding of source of sedimentary organic matters and respective depositional condition via multiple indicators. Overall, understanding the OM molecular composition and its spatial heterogeneity in a lake system is important to better constrain the fate of organic carbon, and assess the pollution risks as well as adopt relevant management strategies.

Intensive nitrogen loss over the Omani Shelf due to anammox coupled with dissimilatory nitrite reduction to ammonium.

A combination of stable isotopes ((15)N) and molecular ecological approaches was used to investigate the vertical distribution and mechanisms of biological N(2) production along a transect from the Omani coast to the central-northeastern (NE) Arabian Sea. The Arabian Sea harbors the thickest oxygen minimum zone (OMZ) in the world's oceans, and is considered to be a major site of oceanic nitrogen (N) loss. Short (<48 h) anoxic incubations with (15)N-labeled substrates and functional gene expression analyses showed that the anammox process was highly active, whereas denitrification was hardly detectable in the OMZ over the Omani shelf at least at the time of our sampling. Anammox was coupled with dissimilatory nitrite reduction to ammonium (DNRA), resulting in the production of double-(15)N-labeled N(2) from (15)NO(2)(-), a signal often taken as the lone evidence for denitrification in the past. Although the central-NE Arabian Sea has conventionally been regarded as the primary N-loss region, low potential N-loss rates at sporadic depths were detected at best. N-loss activities in this region likely experience high spatiotemporal variabilities as linked to the availability of organic matter. Our finding of greater N-loss associated with the more productive Omani upwelling region is consistent with results from other major OMZs. The close reliance of anammox on DNRA also highlights the need to take into account the effects of coupling N-transformations on oceanic N-loss and subsequent N-balance estimates.