Description: Long-chain diols (LCDs) occur widespread in marine environments and also in lakes and rivers. Transport of LCDs from rivers may impact the distribution of LCDs in coastal environments, however relatively little is known about the distribution and biological sources of LCDs in river systems. In this study, we investigated the distribution of LCDs in suspended particulate matter (SPM) of three river systems (Godavari, Danube, and Rhine) in relation with precipitation, temperature, and source catchments. The dominant long-chain diol is the C32 1,15-diol followed by the C30 1,15-diol in all studied river systems. In regions influenced by marine waters, such as delta systems, the fractional abundance of the C30 1,15-diol is substantially higher than in the river itself, suggesting different LCD producers in marine and freshwater environments. A change in the LCD distribution along the downstream transects of the rivers studied was not observed. However, an effect of river flow is observed; i.e., the concentration of the C32 1,15-diol is higher in stagnant waters such as reservoirs and during seasons with river low stands. A seasonal change in the LCD distribution was observed in the Rhine, likely due to a change in the producers. Eukaryotic diversity analysis by 18S rRNA gene sequencing of SPM from the Rhine showed extremely low abundances of sequences (i.e., 〈0.32% of total reads) related to known algal LCD producers. Furthermore, incubation of the river water with 13C-labeled bicarbonate did not result in 13C incorporation into LCDs. This indicates that the LCDs present are mainly of fossil origin in the fast-flowing part of the Rhine. Overall, our results suggest that the LCD producers in rivers predominantly reside in lakes or side ponds that are part of the river system.

Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Lattaud, J., Broder, L., Haghipour, N., Rickli, J., Giosan, L., & Eglinton, T., I. Influence of hydraulic connectivity on carbon burial efficiency in Mackenzie Delta lake sediments. Journal of Geophysical Research: Biogeosciences, 126(3), (2021): e2020JG006054, https://doi.org/10.1029/2020JG006054.

Description: The Arctic is undergoing accelerated changes in response to ongoing modifications to the climate system, and there is a need for local to regional scale records of past climate variability in order to put these changes into context. The Mackenzie Delta region in northern Canada is populated by numerous small shallow lakes. They are classified as no-, low-, and high-closure (NC, LC, and HC, respectively) lakes, reflecting varying degrees of connection to the river main stem, and have different sedimentation characteristics. This study examines sedimentological (mineral surface area, grain size), carbon isotopic (bulk and molecular-level) and inorganic isotopic (neodymium) characteristics of sediment cores from three lakes representing each class. We find that HC lake sediments exhibit strikingly different properties from the other lake sediments. Specifically, they are characterized by higher organic carbon loadings per unit mineral surface area and with relatively minor influence from allochthonous, petrogenic (rock-derived) organic carbon. In contrast, LC and NC lakes have the potential to record basin-scale climatic changes at a high resolution by virtue of enhanced detrital sedimentation. Overall the delta lakes have the capacity to bury about 2 MtC year−1, with little changes in the last 200 years. However, in the (near) future, an increased number of high closure lakes might change the carbon burial efficiency of the Mackenzie Delta as they seem to retain less carbon than NC and LC lakes.

Description: J. Lattaud was funded by a Rubicon grant (019.183EN.002) from NWO, Netherlands Organization for scientific research.

Description: The Canadian Beaufort Sea receives large quantities of sediment, organic carbon and nutrients from rapid coastal erosion and permafrost degradation. In addition, the Mackenzie River, the largest North American Arctic river, discharges great amounts of freshwater, dissolved solids and suspended sediments to the Beaufort Sea. Current changes in these fluxes in response to the warming climate have uncertain consequences for the carbon budget on the shelf and in the deep ocean. To investigate the movement and transformation of organic matter along the land-ocean continuum, we collected water and surface sediment samples along five major transects across the Beaufort Sea during the 2021 expedition of the Canadian Coast Guard Ship Amundsen. Sampling locations span from shallow, coastal, sites with water depths ≤ 20 m, to shelf-break and deep-water settings on the continental slope (water depths of ≥1000 m). For this study, we use stable and radiocarbon isotopic (δ13C and Δ14C) analyses of dissolved inorganic (DIC), dissolved organic (DOC) and particulate organic carbon (POC) for surface and bottom waters, as well as surface sediments, in order to compare, contrast and constrain the relative source contributions and ages of these different forms of carbon. Our results will help to better understand the fate of permafrost organic matter in the marine environment and to ultimately improve assessments of the Canadian Beaufort Sea shelf as a carbon source or sink and its potential trajectory with ongoing environmental changes.

Description: Long chain alkyl diols are lipids that occur ubiquitously in marine sediments and are used as a proxy for sea surface temperature (SST), using the Long chain Diol Index (LDI), and for upwelling intensity/high nutrient conditions. The distribution of 1,13- and 1,15-diols has been documented in open marine and lacustrine sediments and suspended particulate matter, but rarely in coastal seas receiving a significant riverine, and thus continental organic matter, input. Here we studied the distribution of diols in four shelf seas with major river outflows: the Gulf of Lion, the Kara Sea, the Amazon shelf and the Berau delta, covering a wide range of climate conditions. The relative abundance of the C32 1,15-diol is consistently higher close to the river mouth and particularly in the suspended particulate matter of the rivers suggesting a terrigenous source. This is supported by statistical analysis which points out a significant positive correlation between the C32 1,15-diol and the Branched and Isoprenoid Tetraether index, a proxy reflecting soil and riverine input in marine environments. However, the C32 1,15-diol was not detected in soils and is unlikely to be derived from vegetation, suggesting that the C32 1,15-diol is mainly produced in rivers. This agrees with the observation that it is a dominant diol in most cultivated freshwater eustigmatophyte algae. We, therefore, suggest that the relative abundance of the C32 1,15-diol can potentially be used as a proxy for riverine organic matter input in shelf seas. Our results also show that long chain alkyl diols delivered by rivers can substantially affect LDI-reconstructed SSTs in coastal regions close to river mouths.

Description: The study of past sedimentary records from coastal margins allows us to reconstruct variations in terrestrial input into the marine realm and to gain insight into continental climatic variability. There are numerous organic proxies for tracing terrestrial input into marine environments but none that strictly reflect the input of river-produced organic matter. Here, we test the fractional abundance of the C32 alkane 1,15-diol relative to all 1,13- and 1,15-long-chain diols (FC32 1, 15) as a tracer of input of river-produced organic matter in the marine realm in surface and Quaternary (0-45 ka) sediments on the shelf off the Zambezi and nearby smaller rivers in the Mozambique Channel (western Indian Ocean). A Quaternary (0-22 ka) sediment record off the Nile River mouth in the eastern Mediterranean was also studied for long-chain diols. For the Mozambique Channel, surface sediments of sites most proximal to Mozambique rivers showed the highest F1, 15 - C32 (up to 10 k%). The sedimentary record shows high (15-35 k%) pre-Holocene F1, 15 - C32 and low (〈 10 k%) Holocene F1, 15 - C32 values, with a major decrease between 18 and 12 ka. F1, 15 - C32 is significantly correlated (r2 = 0.83, p 〈 0.001) with the branched and isoprenoid tetraether (BIT) index, a proxy for the input of soil and river-produced organic matter in the marine environment, which declines from 0.25 to 0.60 for the pre-Holocene to 〈 0.10 for the Holocene. This decrease in both FC32 1, 15 and the BIT is interpreted to be mainly due to rising sea level, which caused the Zambezi River mouth to become more distal to our study site, thereby decreasing riverine input at the core location. Some small discrepancies are observed between the records of the BIT index and FC32 1, 15 for Heinrich Event 1 (H1) and the Younger Dryas (YD), which may be explained by a change in soil sources in the catchment area rather than a change in river influx. Like for the Mozambique Channel, a significant correlation between FC32 1, 15 and the BIT index (r2 = 0.38, p 〈 0.001) is observed for the eastern Mediterranean Nile record. Here also, the BIT index and FC32 1, 15 are lower in the Holocene than in the pre-Holocene, which is likely due to the sea level rise. In general, the differences between the BIT index and FC32 1, 15 eastern Mediterranean Nile records can be explained by the fact that the BIT index is not only affected by riverine runoff but also by vegetation cover with increasing cover leading to lower soil erosion. Our results confirm that FC32 1, 15 is a complementary proxy for tracing riverine input of organic matter into marine shelf settings, and, in comparison with other proxies, it seems not to be affected by soil and vegetation changes in the catchment area.

Description: Long-chain diols (LCDs) have been measured on suspended particulate matter from the surface of Lake Geneva (France/Switzerland) during a year (August 2017 to June 2018). LCD have been extracted from the filter (~20L of water) by acid and base hydrolysis followed by an aluminum oxide column (eluted with dichloromethane:methanol, 1:1, v/v). They have been quantified on a GC-MS (gas chromatograph mass spectrometer) on single ion monitoring mode. In addition, 40L of water have been incubated with 13C-labeled bicarbonate and the LCD have been extracted as above plus their 13C-ratio has been determined after silylation using a gas chromatograph isotope ratio mass spectrometer.