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The chemical composition of mollusk shells is a useful tool in (paleo)climatology since it captures inter- and intra-annual variability in environmental conditions. Trace element and stable isotope analysis with improved sampling resolution now allows in situ determination of the composition of mollusk shell volumes precipitated at daily to sub-daily time intervals. Here, we discuss hourly resolved Mg / Ca, Mn / Ca, Sr / Ca, and Ba / Ca profiles measured by laser ablation inductively coupled plasma – mass spectrometry (ICP-MS) through shells of the photosymbiotic giant clams (Tridacna maxima, T. squamosa, and T. squamosina) and the non-photosymbiotic scallop Pecten maximus. Precise sclerochronological age models and spectral analysis allowed us to extract daily and tidal rhythms in the trace element composition of these shells. We find weak but statistically significant expressions of these periods and conclude that this cyclicity explains less than 10 % of the sub-annual variance in trace element profiles. Tidal and diurnal rhythms explain variability of, at most, 0.2 mmol mol−1 (∼ 10 % of mean value) in Mg / Ca and Sr / Ca, while ultradian Mn / Ca and Ba / Ca cyclicity has a median amplitude of less than 2 µmol mol−1 mol mol−1 (∼ 40 % and 80 % of the mean of Mn / Ca and Ba / Ca, respectively). Daily periodicity in Sr / Ca and Ba / Ca is stronger in Tridacna than in Pecten, with Pecten showing stronger tidal periodicity. One T. squamosa specimen which grew under a sunshade exhibits among the strongest diurnal cyclicity. Daily cycles in the trace element composition of giant clams are therefore unlikely to be driven by variations in direct insolation but rather reflect an inherent biological rhythmic process affecting element incorporation. Finally, the large amount of short-term trace element variability unexplained by tidal and daily rhythms highlights the dominance of aperiodic processes in mollusk physiology and/or environmental conditions over shell composition at the sub-daily scale. Future studies should aim to investigate whether this remaining variability in shell chemistry reliably records weather patterns or circulation changes in the animals' environment.

Coral cores provide vital climate reconstructions for site-specific temporal variability in river flow and sediment load. Yet, their ability to record spatial differences across multiple catchments is relatively unknown. Here, we investigate spatial linkages between four coral proxies of terrestrial runoff and their relationships between sites. Coral cores were drilled in and around Antongil Bay, the largest bay in Madagascar, and individually analysed for fifteen years of continuous luminescence (G / B), Ba / Ca, δ18Osw and δ13C data. Each coral core was drilled close to individual river mouths (≥ 7 km), and proxy data were compared to modelled river discharge and sediment runoff data for the three corresponding catchments. A reasonable agreement between terrestrial runoff proxies with modelled river discharge and sediment yield was observed. Some inconsistencies between proxy and modelled data are likely linked to proxy behaviour, watershed size and local environmental physiochemical parameters. In general, the further a coral resided from its river source, the weaker the proxy relationship was with modelled data and other corals, due to mixing gradients and currents. Nevertheless, we demonstrate that two coral Ba / Ca and luminescence (G / B) records influenced by the same watershed are reproducible. Furthermore, a strong Ba / Ca relationship was observed between two cores from distant watersheds, with baseline averages in agreement with modelled sediment runoff data. As humic acids behave conservatively in the water column, luminescence (G / B) data gave the highest regional correlations between cores, and showed the most consistent relationship with site specific modelled discharge. No statistical relationship was observed between cores in terms of interannual δ18Osw and δ13C, meaning corals were recording a localised signal at their respective sites, confounded by vital effects. Comparing proxy baseline averages and mean seasonal cycles provided a good overview of the runoff dynamics of the bay system.

Patterns of regeneration and burial of phosphorus (P) in the Baltic Sea are strongly dependent on redox conditions. Redox varies spatially along water depth gradients and temporally in response to the seasonal cycle and multidecadal hydrographic variability. Alongside the well-documented link between iron oxyhydroxide dissolution and release of P from Baltic Sea sediments, we show that preferential remineralization of P with respect to carbon (C) and nitrogen (N) during degradation of organic matter plays a key role in determining the surplus of bioavailable P in the water column. Preferential remineralization of P takes place both in the water column and upper sediments and its rate is shown to be redox-dependent, increasing as reducing conditions become more severe at greater water-depth in the deep basins. Existing Redfield-based biogeochemical models of the Baltic may therefore underestimate the imbalance between N and P availability for primary production, and hence the vulnerability of the Baltic to sustained eutrophication via the fixation of atmospheric N. However, burial of organic P is also shown to increase during multidecadal intervals of expanded hypoxia, due to higher net burial rates of organic matter around the margins of the deep basins. Such intervals may be characterized by basin-scale acceleration of all fluxes within the P cycle, including productivity, regeneration and burial, sustained by the relative accessibility of the water column P pool beneath a shallow halocline.