Regional precipitation trends since 1500 CE reconstructed from calcite sublayers of a varved Mediterranean lake record (Central Pyrenees).

The Mediterranean region is expected to be highly impacted by global warming, although the uncertainty of future scenarios, particularly about precipitation patterns remains quite large. To better predict shifts in its current climate system and to test models, more regional climate records are needed spanning longer than the instrumental period. Here we provide a high-resolution reconstruction of autumn precipitation for the Central Pyrenees since 1500 CE based on annual calcite sublayer widths from Montcortès Lake (Central southern Pyrenees) varved sediments. The 500-yr calcite data series was detrended and calibrated with instrumental climate records by applying correlations and cross-correlations to regional precipitation anomalies. Highest relationships were obtained between a composite calcite series and autumn precipitation anomalies for the complete calibration period (1900-2002) and for the two halves of the full period. Applied statistical tests were significant, evidencing that the climatic signal could be reconstructed. The reconstructed precipitation anomalies show interdecadal shifts, and rainfall decrease within the coldest period of the LIA and during the second half of the 20th century, probably associated to current Global Warming. Neither increasing nor decreasing linear trends or periods of extreme precipitation events were identified. Our results are coherent with other palaeohydrological reconstructions for northern Iberian Peninsula. Correlations between the predicted autumn precipitation and the main teleconnections -NAO, ENSO and WEMO- were weak, although a potential relationship with the Atlantic Multidecadal Oscillation (AMO) pattern is suggested. The obtained reconstruction provides the first estimations of regional autumn precipitation shifts in the Central Pyrenees and is one of the few reconstructions that cover annual-to-century scale climate variability of precipitation in the Mediterranean region from the end of the Litte Ice Age (LIA) to the current period of Global Warming.

Climate changes modulated the history of Arctic iodine during the Last Glacial Cycle.

Iodine has a significant impact on promoting the formation of new ultrafine aerosol particles and accelerating tropospheric ozone loss, thereby affecting radiative forcing and climate. Therefore, understanding the long-term natural evolution of iodine, and its coupling with climate variability, is key to adequately assess its effect on climate on centennial to millennial timescales. Here, using two Greenland ice cores (NEEM and RECAP), we report the Arctic iodine variability during the last 127,000 years. We find the highest and lowest iodine levels recorded during interglacial and glacial periods, respectively, modulated by ocean bioproductivity and sea ice dynamics. Our sub-decadal resolution measurements reveal that high frequency iodine emission variability occurred in pace with Dansgaard/Oeschger events, highlighting the rapid Arctic ocean-ice-atmosphere iodine exchange response to abrupt climate changes. Finally, we discuss if iodine levels during past warmer-than-present climate phases can serve as analogues of future scenarios under an expected ice-free Arctic Ocean. We argue that the combination of natural biogenic ocean iodine release (boosted by ongoing Arctic warming and sea ice retreat) and anthropogenic ozone-induced iodine emissions may lead to a near future scenario with the highest iodine levels of the last 127,000 years.

Antarctic ozone hole modifies iodine geochemistry on the Antarctic Plateau.

Polar stratospheric ozone has decreased since the 1970s due to anthropogenic emissions of chlorofluorocarbons and halons, resulting in the formation of an ozone hole over Antarctica. The effects of the ozone hole and the associated increase in incoming UV radiation on terrestrial and marine ecosystems are well established; however, the impact on geochemical cycles of ice photoactive elements, such as iodine, remains mostly unexplored. Here, we present the first iodine record from the inner Antarctic Plateau (Dome C) that covers approximately the last 212 years (1800-2012 CE). Our results show that the iodine concentration in ice remained constant during the pre-ozone hole period (1800-1974 CE) but has declined twofold since the onset of the ozone hole era (~1975 CE), closely tracking the total ozone evolution over Antarctica. Based on ice core observations, laboratory measurements and chemistry-climate model simulations, we propose that the iodine decrease since ~1975 is caused by enhanced iodine re-emission from snowpack due to the ozone hole-driven increase in UV radiation reaching the Antarctic Plateau. These findings suggest the potential for ice core iodine records from the inner Antarctic Plateau to be as an archive for past stratospheric ozone trends.

Rapid increase in atmospheric iodine levels in the North Atlantic since the mid-20th century.

Atmospheric iodine causes tropospheric ozone depletion and aerosol formation, both of which have significant climate impacts, and is an essential dietary element for humans. However, the evolution of atmospheric iodine levels at decadal and centennial scales is unknown. Here, we report iodine concentrations in the RECAP ice-core (coastal East Greenland) to investigate how atmospheric iodine levels in the North Atlantic have evolved over the past 260 years (1750-2011), this being the longest record of atmospheric iodine in the Northern Hemisphere. The levels of iodine tripled from 1950 to 2010. Our results suggest that this increase is driven by anthropogenic ozone pollution and enhanced sub-ice phytoplankton production associated with the recent thinning of Arctic sea ice. Increasing atmospheric iodine has accelerated ozone loss and has considerably enhanced iodine transport and deposition to the Northern Hemisphere continents. Future climate and anthropogenic forcing may continue to amplify oceanic iodine emissions with potentially significant health and environmental impacts at global scale.

Historical shifts in oxygenation regime as recorded in the laminated sediments of lake Montcortès (Central Pyrenees) support hypoxia as a continental-scale phenomenon.

Recent expansion of anoxia has become a global issue and there is potential for worsening under global warming. At the same time, obtaining proper long-term instrumental oxygen records is difficult, thus reducing the possibility of recording long-term changes in oxygen shifts that can be related with climate or human influence. Varved lake sediments provide the better time frame to study this phenomenon at high resolution. We tracked the oxic/anoxic shifts of the varved Lake Montcortès since 1500CE, and tried to recognise anthropogenic and climatic influences combining biological and geochemical proxies. Four main scenarios emerged: 1) years with abrupt sediment inputs (A); 2) years with outstanding mixing and oxygenation of the water column (B); 3) years with strong stratification, anoxia, intense sulfur bacterial activity and increased biomass production (C); 4) years with stratification and anoxia, but relatively less biomass production (D). In line with current limnologic trends, high supra-annual variability in the occurrence of oxygenation events was observed. Interestingly, at least 45.3% of the years were mixing years and, like the meromictic ones, were mostly clustered into groups of consecutive years, thus alternating years of monomixis with years of meromixis. Most years of D belong to the period 1500-1820CE, when human activities were the most intense. Most years of A belonged to the climatic unstable period of 1850-1899CE. Years of B were irregularly distributed but were best represented in the period 1820-1849CE. Most years of C belonged to the 20th century. More than 90% of the years with climatic instrumental records belonged to B and C. Current climate warming seems to be taking control over the oxygenation capacity of the lake, especially since the second half of the 20th century. Our results support recent findings related to hypoxia spreading at the global scale.

Mineralization pathways of organic matter deposited in a river-lake transition of the Rhone River Delta, Lake Geneva.

During the éLEMO endeavour (a research project in which the Russian MIR submersibles were used for studying Lake Geneva) four sediment cores were retrieved on a transect from the delta of the Rhone River towards the profundal part of the lake. The degradation pathways of organic material (OM) were investigated considering different electron acceptors. Essentially, OM at the delta sites had a higher fraction of terrestrial material than the lake sites indicated by higher C/N ratios, and higher long-chain n-alkane and alcohol concentrations. The concentrations of chlorins were higher at the distant sites indicating more easily degradable OM in the sediments. However, the chlorin index that was used to determine the degradation state of the OM material indicated that pigment derived OM of deltaic sediments was less degraded than that of the profundal sediments. The fluxes of reduced species from the sediments decreased from the delta to the profundal for CH4 (from 2.3 to 0.5 mmol m(-2) d(-1)) and NH4(+) (from 0.31 to 0.13 mmol m(-2) d(-1)). Fluxes of Fe(ii) and Mn(ii), however, increased although they were generally very low (between 9 × 10(-5) and 7.6 × 10(-3) mmol m(-2) d(-1)). Oxygen concentration profiles in the pore waters revealed lower fluxes close to the river inflow with 4.3 and 4.1 mmol m(-2) d(-1) compared to two times higher fluxes at the profundal sites (8.8 and 8.2 mmol m(-2) d(-1)). The rates for totally mineralized OM (Rtotal) at the shallower sites (4.7 mmol C m(-2) d(-1)) were only half of those of the deeper sites (9.7 mmol C m(-2) d(-1)). Accordingly, not only the rates but also the mineralization pathways differed between the shallow and profundal sites. Whereas only 0-6% of the OM was mineralized aerobically at the shallow sites (since almost all O2 was used to oxidize the large flux of CH4 from below) the situation was reversed at the deeper sites and the fraction of aerobically degraded OM was 72-78%. We found a better efficiency in CH4 production per carbon equivalent deposited at the deeper sites as a result of the higher degradability of the mainly autochthonous OM in spite of the lower deposition rate and the higher degradation state of the OM compared to the delta sites.