Storage and release of fossil organic carbon related to weathering of sedimentary rocks

International audienceThe biogeochemical carbon cycle, which plays an undeniable role in global climate change, is defined both by the size of carbon reservoirs (such as the atmosphere, biomass, soil and bedrock) and the exchange between them of various mineral and organic carbon forms. Among these carbon forms, fossil organic carbon (FOC) (i.e., the ancient organic matter stored in sedimentary rocks) is widely observed in modern environments but is not included in the supergene carbon budget. Using a digitized map of the world and an existing model of CO2 consumption associated with rock weathering, we establish the global distribution of FOC stored in the first meter of sedimentary rocks and a first estimation of annual FOC delivery to the modern environment resulting from chemical weathering of these rocks. Results are given for the world's 40 major river basins and extended to the entire continental surface. With a mean value of 1100 109 t, mainly controlled by shale distribution, the global FOC stock is significant and comparable to that of soil organic carbon (1500 109 t). The annual chemical delivery of FOC, estimated at 43 106 t yr− 1 and controlled by the areal distribution of shales and runoff, is of the same order of magnitude as the FOC output flux to oceans. Chemical weathering of bedrock within the Amazon basin produces one-quarter of the total global flux of FOC derived from chemical weathering, and thus is expected to govern FOC release on a global scale. These results raise important questions concerning the role of FOC in the modern carbon cycle as well as the origin and the budget of carbon in soils and river

Evidence and effects of fluid circulation on organic matter in intramontane coalfields (Massif Central, France)

Recent evidence for a Late Carboniferous hydrothermal event responsible for Au-As mineralization within the Variscan belt of the French Massif Central adds a supplementary episode to the already rather complex thermal history of this area. To better understand this history, 45 coal samples from various sites in the Massif Central were studied petrographically (reflectance analysis) and geochemically (Rock-Eval pyrolysis). The results of this study suggest that the studied coal was buried to 1500 m and that the coalification took place within 25 Ma, probably ending at the boundary between the Early and Late Permian (marked by the Saalic orogeny). Two thermal end-members basins were identified: (i) the Carboniferous of Bosmoreau-les-Mines (Limousin) and West Graissessac (Montagne Noire) showing geothermal paleoflow values between 150 and 180 mW m−2, and (ii) the Stephanian of Argentat and Détroit de Rodez (SW Massif Central) with values estimated at between 100 and 120 mW m−2. By plotting the Tmax and Ro values on a diagram, the samples were grouped into two populations, the first showing a positive correlation between Ro and Tmax and the second with higher Tmax values than expected after Ro values. Selected samples of the second group are also characterized by a high Oxygen Index (OI) that increases with Tmax. These divergence between Ro and Tmax associated with a high OI may be the result of the circulation of slightly oxidizing hot fluids subsequent to coalification. The other kind of Ro-Tmax divergence seems to be linked to local, particularly high thermal activity, especially in Graissessac and Bosmoreau basins. It is interpreted as being due to a difference in response of these two maturity indicators, respectively to the intensity and duration of the thermal events (e.g., short-lived hydrothermal circulation and thermal domes of regional extent)

Using Rock-Eval 6 pyrolysis for tracking fossil organic carbon in modern environments: implications for the roles of erosion and weathering.

This work relates to the debate on the fossil organic carbon (FOC) input in modern environments and its possible implication for the carbon cycle, and suggests the use of Rock-Eval 6 pyrolysis as a relevant tool for tracking FOC in such environments. Considering that such a delivery is mainly due to supergene processes affecting the continental surface, we studied organic matter in different reservoirs such as bedrocks, alterites, soils and rivers in two experimental catchments at Draix (Alpes de Haute Provence, France). Samples were subjected to geochemical (Rock-Eval 6 pyrolysis) investigations and artificial bacterial degradations. After comparing the geochemical fingerprint of samples, geochemical markers of FOC were defined and tracked in the different reservoirs. Our results confirm the contribution of FOC in modern soils and rivers and display the various influences of weathering and erosional processes on the fate of FOC during its exchange between these pools. In addition, the contrasting behaviour of these markers upon the supergene processes has also highlighted the refractory or labile characters of the fossil organic matter (FOM). Bedrock to river fluxes, controlled by gully erosion, are characterized by a qualitative and quantitative preservation of FOM. Bedrock to alterite fluxes, governed by chemical weathering, are characterized by FOC mineralization without qualitative changes in deeper alterites. Alterite to soils fluxes, controlled by (bio)chemical weathering, are characterized by strong FOC mineralization and qualitative changes of FOM. Thus weathering and erosional processes induce different FOM evolution and affect the fate of FOC towards the global carbon cycle. In this study, gully erosion would involve maintenance of an ancient sink for the global carbon cycle, while (bio)chemical processes provide a source of CO2. Finally, this study suggests that Rock-Eval 6 pyrolysis can be considered as a relevant tool for tracking FOC in modern environments

Annual fossil organic carbon delivery due to mechanical and chemical weathering of marly badlands areas

International audienceA key issue in the study of the carbon cycle is constraining the stocks and fluxes in and between C-reservoirs. Among these, the role and importance of fossil organic carbon (FOC) release by weathering of outcropping sedimentary rocks on continental surfaces is still debated and remains poorly constrained. Our work focuses on FOC fluxes due to chemical and mechanical weathering of marls in two experimental watersheds with typical badlands geomorphology (Draix watersheds, Laval and Moulin, Alpes de Haute Provence, France). Organic matter from bedrock, soil litter and riverine particles are characterized by Rock-Eval 6 pyrolysis. FOC fluxes due to mechanical weathering are then estimated by monitoring the annual particulate solid exports at the outlets of the watersheds (1985-2005 period). FOC fluxes from chemical weathering were calculated using Ca2+ concentrations in dissolved loads (year 2002) to assess the amount of FOC released by the dissolution of the carbonate matrix. Results show that FOC delivery is mainly driven by mechanical weathering, with a yield ranging from 30 to 59 t km-2 yr-1 in the Moulin (0.08 km2) and Laval (0.86 km2) catchments, respectively, (1985-2005 average). The release of FOC attributed to chemical weathering was 2.2 to 4.2 t km-2 for the year 2002. These high FOC fluxes from badlands are similar to those observed in tectonically active mountain catchments. At a regional scale, badland outcropping within the Durance watershed does not exceed 0.25% in area of the Rhone catchment, but could annually deliver 12 000 t yr-1 of FOC. This flux could correspond to 27% of the total particulate organic carbon (POC) load exported by the Rhone River to the Mediterranean Sea. At a global scale, our findings suggest that erosion of badlands may contribute significantly to the transfer of FOC from continental surfaces to depositional environments

Quantitative palynofacies analysis as a new tool to study transfers of fossil organic matter in recent terrestrial environments

International audienceClassical palynofacies method, which consists in an organic concentrate microscopic qualitative observation after mineral phase dissolution, is commonly used in order to study sedimentary organic matter. In the present study we develop a new quantitative palynofacies method that allows organic particles mass concentrations to be determined in studied samples. This method was developed to help quantify the input of fossil organic matter (FOM) into modern environments as a result of sedimentary rocks weathering. Studied samples were collected from different pools, like bedrocks, weathering profiles, soils and riverine particles in an experimental watershed "Le Laval". This watershed overlying Callovo-Oxfordian marls (1 km² in area) is located near Digne, Alpes-de-Haute-Provence, in France. In addition to palynofacies techniques, Rock-Eval 6 pyrolysis and Al2O3 content measurements (inductively coupled plasma emission spectrometry) were carried out on the samples. Obtained results show that this quantitative palynofacies method is suitable for FOM studies in modern environments, and FOM particles are quantified in the different pools. Results also give evidence that FOM alteration depends on the type of weathering, but also on the kind of organic particles. Soil formation under vegetation, resulting from the (bio)chemical weathering, lead to fossil organic particles concentration losses that do not exceed 30%. Elsewhere, mechanical weathering appears extremely fast and has no qualitative or quantitative influence on the observed FOM particles, which feeds directly into riverine stocks. FOM appears to be very resistant to weathering processes, this highlights its occurrence into supergene pools and then into carbon cycle. Quantitative palynofacies analysis is a new method adapted to a such study, but can also be applied to other palynological, paleoenvironmental or archeological studies

Spectrocolorimetric interpretation of sedimentary dynamics: The new "Q7/4 diagram"

International audienceColour is a fundamental property of sediment and is often used for lithographic description to determine sedimentological structures, facies etc. However, the sedimentary information contained in this parameter is difficult to extract because it is difficult to quantify. Colour can be quantified by spectrocolorimetry which provides very high resolution data quickly and non-destructively. When adapted to sedimentology, spectrocolorimeters prove to be powerful tools due to their low purchase and maintenance costs, and some are portable and easily used in-the-field. Several methods have been used to extract sedimentological data from colorimetric spectra (first derivatives, factorial analysis, etc.). In the present study, we first provide a review of the sedimentological application of spectrophotometers and, after having described these methods, their advantages and disadvantages, we then describe a new tool called the Q7/4 diagram (abscissa L*; Ordinates 700/400 ratio). This new technique permits sedimentological units to be defined, allows the identification of different sediment components and provides 5 distinct poles: Clayey deposits, organic rich deposits (chlorophyll a and by products), altered organic matter deposits, iron rich deposits, carbonated deposits. Coupled with the analysis of first derivative spectra, it is possible to distinguish different pigments linked to the degradation and/or nature of the organic material (Chlorophyll a, melanoidin, etc.), the state of iron oxidation (for example, hematite and goethite-like signatures) and the nature of clays. The Q7/4 diagram permits rapid acquisition of high resolution data on changes of sediment dynamics in geosystems that have been subjected to highly varied climatic/environmental conditions. The instrument is non destructive, easy to use and maintain, portable for use in the field, fast to implement, is capable of high resolution, and has a vast range of possible applications. Spectrocolorimetry appears to provide many advantages and could become an essential and robust tool for preliminary sedimentological studies

Apport de la matière organique dans l'étude de la dynamique sédimentaire lacustre en zone sahélienne (exemples de deux complexes limniques, SW Niger)

International audienceLe remplissage sédimentaire des mares de Bangou-Bi et de Tankalawal (SW Niger) a fait l'objet d'une étude de son contenu organique qui fournit des informations sur l'origine et les conditions de dépôt du matériel sédimentaire. Deux carottes mesurant respectivement 140 cm (carotte BB2) et 60 cm (carotte TK1) ont été étudiées. Les échantillons ont été soumis à une pyrolyse Rock-Eval 6 renseignant sur la géochimie globale de la Matière Organique (MO) et le signal S2 de la pyrolyse a été exploité afin de mieux préciser la nature de ces MO. Le niveau argilo-limoneux de la carotte BB2 contient une MO aquatique et terrestre dont la composition en composés hydrocarbonés se répartit entre les biopolymères (F1+F2), et les géopolymères matures (F3) et immatures (F4). Cette MO serait déposée dans un environnement calme. En revanche le niveau inférieur sableux renferme une MO terrestre très altérée et enrichie en géopolymères matures qui serait amenée par des pulses détritiques grossiers (colluvionnement) issus du bassin versant. Les valeurs des paramètres géochimiques et leur évolution avec la profondeur indiquent que la MO de la carotte TK1 est aquatique et a enregistré une dégradation en milieu anoxique. Cette MO contenant majoritairement des géopolymères matures (F4) riches en lipides se révèle étonnamment plus résistante face à l'altération que celle présente dans la carotte BB2

Anthropogenic perturbation of the carbon fluxes from land to ocean

A substantial amount of the atmospheric carbon taken up on land through photosynthesis and chemical weathering is transported laterally along the aquatic continuum from upland terrestrial ecosystems to the ocean. So far, global carbon budget estimates have implicitly assumed that the transformation and lateral transport of carbon along this aquatic continuum has remained unchanged since pre-industrial times. A synthesis of published work reveals the magnitude of present-day lateral carbon fluxes from land to ocean, and the extent to which human activities have altered these fluxes. We show that anthropogenic perturbation may have increased the flux of carbon to inland waters by as much as 1.0 Pg C yr-1 since pre-industrial times, mainly owing to enhanced carbon export from soils. Most of this additional carbon input to upstream rivers is either emitted back to the atmosphere as carbon dioxide (~0.4 Pg C yr-1) or sequestered in sediments (~0.5 Pg C yr-1) along the continuum of freshwater bodies, estuaries and coastal waters, leaving only a perturbation carbon input of ~0.1 Pg C yr-1 to the open ocean. According to our analysis, terrestrial ecosystems store ~0.9 Pg C yr-1 at present, which is in agreement with results from forest inventories but significantly differs from the figure of 1.5 Pg C yr-1 previously estimated when ignoring changes in lateral carbon fluxes. We suggest that carbon fluxes along the land–ocean aquatic continuum need to be included in global carbon dioxide budgets.Peer reviewe

A remote input of African dust to Last Glacial Europe

During the Last Glacial Maximum global surface air temperatures were up to 6 °C lower than pre-industrial levels and the mineral dust cycle was highly active, with global dust loading two to four times higher than during the Holocene. Loess deposits and Greenland ice cores show peak dust concentrations during this time. While Asian sources were traditionally seen as the main contributors to dust transported to Greenland, recent studies using geochemical methods suggest a mix of Asian, North African, and European sources. Europe experienced intense dust activity, with mineral particles largely emitted from regional sources. Here we present the trace elements, and strontium and lead isotopes from Last-Glacial Maximum samples collected at 15 sites across Europe. The results reveal that fine dust originated from remote sources, potentially northern Africa. Earth System model simulations support this finding, highlighting Northern Africa’s substantial role in dust deposition during glacial periods across the Northern Hemisphere

The origin of the 1500-year climate cycles in Holocene North-Atlantic records

© 2007 Author(s) et al. This is an open-access article distributed under a Creative Commons License. The definitive version was published in Climate of the Past 3 (2007): 569-575, doi:10.5194/cp-3-569-2007Since the first suggestion of 1500-year cycles in the advance and retreat of glaciers (Denton and Karlen, 1973), many studies have uncovered evidence of repeated climate oscillations of 2500, 1500, and 1000 years. During last glacial period, natural climate cycles of 1500 years appear to be persistent (Bond and Lotti, 1995) and remarkably regular (Mayewski et al., 1997; Rahmstorf, 2003), yet the origin of this pacing during the Holocene remains a mystery (Rahmstorf, 2003), making it one of the outstanding puzzles of climate variability. Solar variability is often considered likely to be responsible for such cyclicities, but the evidence for solar forcing is difficult to evaluate within available data series due to the shortcomings of conventional time-series analyses. However, the wavelets analysis method is appropriate when considering non-stationary variability. Here we show by the use of wavelets analysis that it is possible to distinguish solar forcing of 1000- and 2500- year oscillations from oceanic forcing of 1500-year cycles. Using this method, the relative contribution of solar-related and ocean-related climate influences can be distinguished throughout the 10 000 yr Holocene intervals since the last ice age. These results reveal that the 1500-year climate cycles are linked with the oceanic circulation and not with variations in solar output as previously argued (Bond et al., 2001). In this light, previously studied marine sediment (Bianchi and McCave, 1999; Chapman and Shackleton, 2000; Giraudeau et al., 2000), ice core (O'Brien et al., 1995; Vonmoos et al., 2006) and dust records (Jackson et al., 2005) can be seen to contain the evidence of combined forcing mechanisms, whose relative influences varied during the course of the Holocene. Circum-Atlantic climate records cannot be explained exclusively by solar forcing, but require changes in ocean circulation, as suggested previously (Broecker et al., 2001; McManus et al., 1999).This work is supported by ANR project: “Integration des contraintes Paleoclimatiques pour reduire les Incertitudes sur l’evolution du Climat pendant les periodes Chaudes”- PICC (ANR-05-BLAN- 0312-02)