A landscape perspective of Holocene organic carbon cycling in coastal SW Greenland lake-catchments

Arctic organic carbon (OC) stores are substantial and have accumulated over millennia as a function of changes in climate and terrestrial vegetation. Arctic lakes are also important components of the regional C-cycle as they are sites of OC production and CO2emissions but also store large amounts of OC in their sediments. This sediment OC pool is a mixture derived from terrestrial and aquatic sources, and sediment cores can therefore provide a long-term record of the changing interactions between lakes and their catchments in terms of nutrient and C transfer. Sediment carbon isotope composition (δ13C), C/N ratio and organic C accumulation rates (C AR) of14C-dated cores covering the last ∼10,000 years from six lakes close to Sisimiut (SW Greenland) are used to determine the extent to which OC dynamics reflect climate relative to lake or catchment characteristics. Sediment δ13C ranges from −19 to −32‰ across all lakes, while C/N ratios are 20 (mean = 12), values that indicate a high proportion of the organic matter is from autochthonous production but with a variable terrestrial component. Temporal trends in δ13C are variable among lakes, with neighbouring lakes showing contrasting profiles, indicative of site-specific OC processing. The response of an individual lake reflects its morphometry (which influences benthic primary production), the catchment:lake ratio, and catchment relief, lakes with steeper catchments sequester more carbon. The multi-site, landscape approach used here highlights the complex response of individual lakes to climate and catchment disturbance, but broad generalisations are possible. Regional Neoglacial cooling (from ∼5000 cal yr BP) influenced the lateral transfer of terrestrial OC to lakes, with three lakes showing clear increases in OC accumulation rate. The lakes likely switched from being autotrophic (i.e. net ecosystem production > ecosystem respiration) in the early Holocene to being heterotrophic after 5000 cal yr BP as terrestrial OC transfer increased

Mid Pleistocene foraminiferal mass extinction coupled with phytoplankton evolution

Understanding the interaction between climate and biotic evolution is crucial for deciphering the sensitivity of life. An enigmatic mass extinction occurred in the deep oceans during the Mid Pleistocene, with a loss of over 100 species (20%) of sea floor calcareous foraminifera. An evolutionarily conservative group, benthic foraminifera often comprise >50% of eukaryote biomass on the deep-ocean floor. Here we test extinction hypotheses (temperature, corrosiveness and productivity) in the Tasman Sea, using geochemistry and micropalaeontology, and find evidence from several globally distributed sites that the extinction was caused by a change in phytoplankton food source. Coccolithophore evolution may have enhanced the seasonal ‘bloom’ nature of primary productivity and fundamentally shifted it towards a more intra-annually variable state at ∼0.8 Ma. Our results highlight intra-annual variability as a potential new consideration for Mid Pleistocene global biogeochemical climate models, and imply that deep-sea biota may be sensitive to future changes in productivity

Linking land and lake: Using novel geochemical techniques to understand biological response to environmental change

The exploitation of lakes has led to large-scale contemporary impacts on freshwater systems, largely in response to catchment clearance. Such clearance is causing changes to carbon dynamics in tropical lakes which may have significance for wider carbon budgets, depending on the changes in carbon sequestration and mineralisation driven by changing roles of terrestrial and aquatic carbon in lakes over time. Despite increasing awareness of the pivotal role of carbon source in carbon dynamics, discriminating the source of carbon from a palaeolimnological record is rarely undertaken. Here we use novel geochemical techniques (brGDGTs, n-alkanes, Rock-Eval pyrolysis), paired with traditional analyses (diatoms, pollen), to elucidate changing sources of carbon through time and ecosystem response. Environmental changes at Lake Nyamogusingiri can be divided into three phases: Phase I (CE 1150-1275), a shallow and productive lake, where a diverse terrestrial environment is, initially, the main carbon source, before switching to an aquatic source; Phase II (CE 1275-1900), variable lake levels (generally in decline) with increasing productivity, and carbon is autochthonous in source; Phase III (CE 1900-2007), lake level declines, and the carbon is of a mixed source, though the terrestrially derived carbon is from a less diverse source. The organic geochemical analyses provide a wealth of data regarding the complexity of aquatic response to catchment and with-in lake changes. These data demonstrate show that small, tropical lake systems have the potential to bury high quantities of carbon, which has implications for the disruption of local biogeochemical cycles (C, P, N, and Si) both in the past, and the future as human and climate pressures increase

Assessing human impact on Rostherne Mere, UK, using the geochemistry of organic matter

This study investigates recent changes in the geochemistry of organic material from a hypereutrophic lake (Rostherne Mere, United Kingdom) using the geochemical and molecular composition of radiometrically dated sediment cores. Modern samples suggest that recent sedimentation is dominated by algal production; however, a minor component of allochthonous organic material is present. Sediment cores reveal that absolute proxy values and the magnitude of observed changes are broadly homogenous across the lake basin. A transition to environmental conditions favouring enhanced algal productivity in recent sediments is suggested by higher total organic carbon (TOC) and lower carbon to nitrogen ratio (C/N), carbon isotope composition of organic matter (δ 13 C org ), and average n-alkane chain length. A strong covariance between TOC and Rock-Eval Hydrogen Index implies this transition is driven by an increasing algal contribution rather than being a response to variations in the source of organic matter. Decadal trends and abrupt shifts in organic geochemical proxies are suggested to be directly related to changes in external anthropogenic nutrient loading following the construction and decommissioning of sewage treatment plants. The development of hypereutrophic conditions likely occurred in stages, where rapid transitions are associated with the commencement of sewage effluent input in the 1930s, population increases in the 1980s, and a dramatic reduction in external nutrient loads in the 1990s. Recovery of the lake ecosystem is limited by internal nutrient recycling, and organic proxies indicate that the geochemistry of sediments has remained relatively constant since effluent diversion. This study highlights the utility of organic geochemical parameters in tracing recent eutrophication processes in lakes to provide evidence for the timing and scale of anthropogenic environmental change

Stream and slope weathering effects on organic-rich mudstone geochemistry and implications for hydrocarbon source rock assessment: A Bowland Shale case study

This study contributes to the exploration and quantification of the weathering of organic-rich mudstones under temperate climatic conditions. Bowland Shales, exposed by a stream and slope, were sampled in order to develop a model for the effects of weathering on the mudstone geochemistry, including major and trace element geochemistry, Rock-Eval pyrolysis and δ13Corg. Four weathering grades (I – IV) are defined using a visual classification scheme; visually fresh and unaltered (I), chemically altered (II, III) and ‘paper shale’ that typifies weathered mudstone on slopes (IV). Bedload abrasion in the stream exposes of visually fresh and geochemically unaltered mudstone. Natural fractures are conduits for oxidising meteoric waters that promote leaching at the millimetre scale and/or precipitation of iron oxide coatings along fracture surfaces. On the slope, bedding-parallel fractures formed (and may continue to form) in response to chemical and/or physical weathering processes. These fractures develop along planes of weakness, typically along laminae comprising detrital grains, and exhibit millimetre- and centimetre-scale leached layers and iron oxide coatings. Fracture surfaces are progressively exposed to physical weathering processes towards the outcrop surface, and results in disintegration of the altered material along fracture surfaces. Grade IV, ‘paper shale’ mudstone is chemically unaltered but represents a biased record driven by initial heterogeneity in the sedimentary fabric. Chemically weathered outcrop samples exhibit lower concentrations of both ‘free’ (S1) (up to 0.6 mgHC/g rock) and ‘bound’ (S2) (up to 3.2 mgHC/g rock) hydrocarbon, reduced total organic carbon content (up to 0.34 wt%), reduced hydrogen index (up to 58 mgHC/gTOC), increased oxygen index (up to 19 mgCO + CO2/gTOC) and increased Tmax (up to 11 °C) compared with unaltered samples. If analysis of chemically weathered samples is unavoidable, back-extrapolation of Rock-Eval parameters can assist in the estimation of pre-weathering organic compositions. Combining Cs/Cu with oxygen index is a proxy for identifying the weathering progression from fresh material (I) to ‘paper shale’ (IV). This study demonstrates that outcrop samples in temperate climates can provide information for assessing hydrocarbon potential of organic-rich mudstones

Mid-Holocene sea surface conditions and riverine influence on the inshore Great Barrier Reef

We present measurements of Sr/Ca, δ18O, and spectral luminescence ratios (G/B) from a mid-Holocene Porites sp. microatoll recovered from the nearshore Great Barrier Reef (GBR). These records were used as proxies to reconstruct sea surface temperature (SST), the δ18O of surrounding seawater (δ18Osw), and riverine influence, respectively, and compared with records from a modern Porites sp. microatoll growing in the same environment. Strong riverine influence in the mid-Holocene record is indicated by (1) an increased annual δ18Osw range in the mid-Holocene record, (2) negative peaks in δ18O characteristic of flood events, and (3) a higher G/B luminescence ratio. Seasonal cycles in G/B suggest that humic acid inputs were elevated for a longer portion of the year during the mid-Holocene. The seasonal cycle of δ18Osw peaked earlier in the year in the mid-Holocene record relative to the modern, while mean δ18Osw values from the mid-Holocene record were similar to modern values. These records provide an insight into the oceanographic conditions the nearshore GBR experienced during mid-Holocene climatic shifts and are consistent with a strong Australian–Indonesian Summer Monsoon (AISM) system at ~ 4700 cal. yr BP