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The west Antarctic Peninsula (WAP) is a region of marked climatic variability, exhibiting strong changes in sea ice extent, retreat of most of its glaciers, and shifts in the amount and form of precipitation. These changes can have significant impacts on the oceanic freshwater budget and marine biogeochemical processes; it is thus important to ascertain the relative balance of the drivers, and the spatial scales over which they operate. We present a novel 7‐year summer‐season (October to March; 2011 to 2018) series of oxygen isotopes in seawater (δ18O), augmented with some winter sampling, collected adjacent to Anvers Island at the WAP. These data are used to attribute oceanic freshwater changes to sea ice and meteoric sources, and to deduce information on the spatial scales over which the changes are driven. Sea ice melt shows significant seasonality (∼9% range) and marked interannual changes, with pronounced maxima in seasons 2013/14 and 2016/17. Both of these extrema are driven by anomalous winds, but reflect strongly contrasting dynamic and thermodynamic sea ice responses. Meteoric water also shows seasonality (∼7% range), with interannual variability reflecting changes in the input of accumulated precipitation and glacial melt to the ocean. Unlike sea ice melt, meteoric water extremes are especially pronounced in thin (

Although the oxygen isotope composition (δ18O) of calcite (δ18Ocalcite) and, to a lesser extent, diatom silica (δ18Odiatom) are widely used tracers of past hydroclimates (especially temperature and surface water hydrology), the degree to which these two hosts simultaneously acquire their isotope signals in modern lacustrine environments, or how these are altered during initial sedimentation, is poorly understood. Here, we present a unique dataset from a natural limnological laboratory to explore these issues. This study compares oxygen and hydrogen isotope data (δ18O, δ2H) of contemporary lake water samples at ~2-weekly intervals over a 2-year period (2010–12) with matching collections of diatoms (δ18Odiatom) and calcite (δ18Ocalcite) from sediment traps (at 10 m and 25 m) at Rostherne Mere (maximum depth 30 m), a well-monitored, eutrophic, seasonally stratified monomictic lake in the UK. The epilimnion shows a seasonal pattern of rising temperature and summer evaporative enrichment in 18O, and while there is a temperature imprint in both δ18Odiatom and δ18Ocalcite, there is significant inter-annual variability in both of these signals. The interpretation of δ18Odiatom and δ18Ocalcite values is complicated due to in-lake processes (e.g. non-equilibrium calcite precipitation, especially in spring, leading to significant 18Ocalcite depletion), and for δ18Odiatom, by post-mortem, depositional and possibly dissolution or diagenetic effects. For 2010 and 2011 respectively, there is a strong temperature dependence of δ18Ocalcite and δ18Odiatom in fresh trap material, with the fractionation slope for δ18Odiatom of ca. −0.2‰/°C, in agreement with several other studies. The δ18Odiatom data indicate the initiation of rapid post-mortem secondary alteration of fresh diatom silica (within ~6 months), with some trap material undergoing partial maturation in situ. Diatom δ18O of the trap material is also influenced by resuspension of diatom frustules from surface sediments (notably in summer 2011), with the net effect seen as an enrichment of deep-trap 18Odiatom by about +0.7‰ relative to shallow-trap values. Contact with anoxic water and anaerobic bacteria are potentially key to initiating this silica maturation process, as deep-trap samples that were removed prior to anoxia developing do not show enrichment. Dissolution (perhaps enhanced by anaerobic bacterial communities) may also be responsible for changes to δ18Odiatom that lead to increasing, but potentially predictable, error in inferred temperatures using this proxy. High resolution, multi-year monitoring can shed light on the complex dynamics affecting δ18Odiatom and δ18Ocalcite and supports the careful use of sedimentary δ18Odiatom and δ18Ocalcite as containing valuable hydroclimatic signals especially at a multi-annual resolution, although there remain substantial challenges to developing a reliable geothermometer on paired δ18Odiatom and δ18Ocalcite. In particular, δ18Odiatom needs cautious interpretation where silica post-mortem secondary alteration is incomplete and diatom preservation is not perfect, and we recommend dissolution be routinely assessed on diatom samples used for isotopic analyses.

Highlights • Novel multi-disciplinary approach to tracing freshwater and particle transport into boundary currents; • Significant glacial inputs reach coastal waters and are transported rapidly offshore; • Low surface water dissolved silicon concentrations maintained by diatom activity despite strong glacial and benthic supplies. Abstract Biogeochemical cycling in high-latitude regions has a disproportionate impact on global nutrient budgets. Here, we introduce a holistic, multi-disciplinary framework for elucidating the influence of glacial meltwaters, shelf currents, and biological production on biogeochemical cycling in high-latitude continental margins, with a focus on the silica cycle. Our findings highlight the impact of significant glacial discharge on nutrient supply to shelf and slope waters, as well as surface and benthic production in these regions, over a range of timescales from days to thousands of years. Whilst biological uptake in fjords and strong diatom activity in coastal waters maintains low dissolved silicon concentrations in surface waters, we find important but spatially heterogeneous additions of particulates into the system, which are transported rapidly away from the shore. We expect the glacially-derived particles – together with biogenic silica tests – to be cycled rapidly through shallow sediments, resulting in a strong benthic flux of dissolved silicon. Entrainment of this benthic silicon into boundary currents may supply an important source of this key nutrient into the Labrador Sea, and is also likely to recirculate back into the deep fjords inshore. This study illustrates how geochemical and oceanographic analyses can be used together to probe further into modern nutrient cycling in this region, as well as the palaeoclimatological approaches to investigating changes in glacial meltwater discharge through time, especially during periods of rapid climatic change in the Late Quaternary.

Stable isotope analyses of ostracod shells are a commonly-used proxy for palaeoenvironmental reconstruction. Although the fundamental controls on isotope composition of ostracod shells are well understood and, in some instances, quantifiable, the paleoclimatic and palaeoenvironmental interpretation of records from lake sediments depends strongly on the characteristics of individual lakes including the climatic setting, depth, volume, hydrology, aquatic vegetation and catchment properties. This is particularly important for coastal lakes where physio-chemical variations may occur on diurnal timescales. Here, we combine variations in δ18Owater, δ18Oostracod and δ13Costracod, hourly water temperature, and Mg/Caostracod inferred water temperatures (constraining calcification temperature) to improve palaeoenvironmental interpretation and provide insights into lake carbon cycle. The dataset improves understanding of complex coastal lake site systematics and downcore interpretation of stable isotopes from C. torosa, a geographically widespread brackish water ostracod. The δ18Oostracod values show a complex relationship with temperature and suggest, in most circumstances, that δ18Owater is the dominant control on δ18Oostracod. During times of fresher water, δ13Costracod increases, suggesting increasing aquatic productivity. Above a certain δ18Owater threshold however, aquatic productivity begins to decline. The interpretation of δ13Costracod in some coastal lakes, may therefore be dependent on understanding of the range of expected δ18Owater. Due to short-term (diurnal to seasonal) variations that cause large ranges in δ18Owater and δ18Oostracod, stable isotope analyses of C. torosa should be: (1) undertaken on multiple single shells (2) where carapaces are preserved, paired with trace-element/Ca analyses on the same individual; and (3) undertaken alongside a study of the modern lake system.

Understanding the modern day relationship between climate and the oxygen isotopic composition of precipitation (δ18OP) is crucial for obtaining rigorous palaeoclimate reconstructions from a variety of archives. To date, the majority of empirical studies into the meteorological controls over δ18OP rely upon daily, event scale, or monthly time series from individual locations, resulting in uncertainties concerning the representativeness of statistical models and the mechanisms behind those relationships. Here, we take an alternative approach by analysing daily patterns in δ18OP from multiple stations across the British Isles (n = 10–70 stations). We use these data to examine the spatial and seasonal heterogeneity of regression statistics between δ18OP and common predictors (temperature, precipitation amount and the North Atlantic Oscillation index; NAO). Temperature and NAO are poor predictors of daily δ18OP in the British Isles, exhibiting weak and/or inconsistent effects both spatially and between seasons. By contrast δ18OP and rainfall amount consistently correlate at most locations, and for all months analysed, with spatial and temporal variability in the regression coefficients. The maps also allow comparison with daily synoptic weather types, and suggest characteristic δ18OP patterns, particularly associated with Cylonic Lamb Weather Types. Mapping daily δ18OP across the British Isles therefore provides a more coherent picture of the patterns in δ18OP, which will ultimately lead to a better understanding of the climatic controls. These observations are another step forward towards developing a more detailed, mechanistic framework for interpreting stable isotopes in rainfall as a palaeoclimate and hydrological tracer.

Two medium-depth ice cores were retrieved from Berkner Island by a joint project between the Alfred-Wegener-Institut and the British Antarctic Survey in the 1994/95 field season. A 151m deep core from the northern dome (Reinwarthhöhe) of Berkner Island spans 700 years, while a 181 m deep core from the southern dome (Thyssenhöhe) spans approximately 1200 years. Both cores display clear seasonal cycles in electrical conductivity measurements, allowing dating by annual-layer counting and the calculation of accumulation profiles. Stable-isotope measurements (both δ18O and δD), together with the accumulation data, allow us to estimate changes in climate for most of the past millennium: the data show multi-decadal variability around a generally stable long-termmean. In addition, a full suite of major chemistry measurements is available to define the history of aerosol deposition at these sites: again, there is little evidence that the chemistry of the sites has changed over the past six centuries. Finally, we suggest that the southern dome, with an ice thickness of 950 m, is an ideal site from which to gain a climate history of the late stages of the last glacial and the deglaciation for comparison with the records from the deep Antarctic ice cores, and with other intermediate-depth cores such as Taylor Dome and Siple Dome.

Over the past 50 years, warming of the Antarctic Peninsula has been accompanied by accelerating glacier mass loss and the retreat and collapse of ice shelves. A key driver of ice loss is summer melting; however, it is not usually possible to specifically reconstruct the summer conditions that are critical for determining ice melt in Antarctic. Here we reconstruct changes in ice-melt intensity and mean temperature on the northern Antarctic Peninsula since AD 1000 based on the identification of visible melt layers in the James Ross Island ice core and local mean annual temperature estimates from the deuterium content of the ice. During the past millennium, the coolest conditions and lowest melt occurred from about AD 1410 to 1460, when mean temperature was 1.6 degrees C lower than that of 1981-2000. Since the late 1400s, there has been a nearly tenfold increase in melt intensity from 0.5 to 4.9%. The warming has occurred in progressive phases since about AD 1460, but intensification of melt is nonlinear, and has largely occurred since the mid-twentieth century. Summer melting is now at a level that is unprecedented over the past 1,000 years. We conclude that ice on the Antarctic Peninsula is now particularly susceptible to rapid increases in melting and loss in response to relatively small increases in mean temperature.

[1] The accumulation, isotopic and chemical signals of an ice core from James Ross Island, Antarctica, are investigated for the interval from 1967 to 2008. Over this interval, comparison with station, satellite and reanalysis data allows for a detailed assessment of the environmental information preserved in the ice. Accumulation at James Ross Island is enhanced during years when the circumpolar westerlies are weak, allowing more precipitation events to reach the northeastern Antarctic Peninsula. The stable water isotope composition of the ice core has an interannual temperature dependence consistent with the spatial isotope-temperature gradient across Antarctica, and preserves information about both summer and winter temperature variability in the region. Sea salts in the ice core are derived from open water sources in the marginal sea ice zone to the north of James Ross Island and transported to the site by strengthened northerly and westerly winds in the winter. A strong covariance with temperature means that the sea salt record may be able to be utilized, in conjunction with the isotope signal, as an indicator of winter temperature. Marine biogenic compounds in the ice core are derived from summer productivity within the sea ice zone to the south of James Ross Island. This source region may have become significant only in recent decades, when the collapse of nearby ice shelves established new sites of open water with high summer productivity. These findings provide a foundation for interpreting the environmental signals in the James Ross Island ice core, which extends though the whole Holocene and represents the oldest ice core that has been recovered from the Antarctic Peninsula region.

The relationship between isotope ratios in precipitation and lake waters was monitored by bi-weekly measurements taken over a five and a half year period between May 2000 and September 2005 (a period of 1964 days) at Lochnagar, a remote mountain lake in eastern Scotland. Short-term changes in the oxygen isotope composition of lake water (δ18OL) at Lochnagar follow a seasonal pattern similar to isotopes in local precipitation (δ18OP), however changes in catchment residence time, snow accumulation, lake ice cover and lake stratification modify the temporal structure of δ18OL over the seasonal cycle. Of particular importance is precipitation amount, which controls catchment and lake residence times, and determines the degree of phase lag and amplitude change between δ18OL and δ18OP. A simple mass balance model replicates these effects and demonstrates that the degree of phase lag and amplitude reduction is predictable given known input/volume ratio. The implications of these observations for the use of δ18O records in palaeoclimatology are important, since it is rare that authigenic and biogenic minerals or organic compounds (from which δ18O and/or δ2H can be measured) are produced in a lake evenly throughout the year.