New and compiled Na/Ca measurements of the planktonic foraminifera Globigerinoides ruber. The dataset contains data from foraminiferal samples 1) collected from plankton tows and sediment traps which span a wide salinity range (32.5 - 40.7 salinity units) across the Bay-of-Bengal, Arabian Sea, and Red Sea, 2) cultured in the laboratory under varying carbonate chemistry, and 3) a globally-distributed suite of core-top samples. Na/Ca was measured using both solution and laser ablation ICP-MS. The foraminiferal Na/Ca data are provided alongside environmental parameters for each sample (e.g. temperature, salinity, pH, bottom water Omega calcite), in order to assess the environmental controls on Na/Ca in foraminifera. The data accompany the following manuscript: Gray et al. (2023, doi:10.1016/j.gca.2023.03.011).
LA-ICP-MS data from three different experiments including five foraminiferal species: Ammonia confertitesta (Bourgenuf, France), Bulimina marginata, Cassidulina laevigata (Gullmard Fjord, Sweden), Amphistegina lessonii and Operculina ammonoides (Eilat, Israel). Foraminifera were cultured at different oxygen concentrations (30% and 100% oxygen saturation). Element to calcium ratio (E/Ca) and partition coefficients (D) of Mg, Mn and Sr are noted for individual laser ablation measurements per specimen.
About 30% of the anthropogenically released CO2 is taken up by the oceans; such uptake causes surface ocean pH to decrease and is commonly referred to as ocean acidification (OA). Foraminifera are one of the most abundant groups of marine calcifiers, estimated to precipitate ca. 50 % of biogenic calcium carbonate in the open oceans. We have compiled the state of the art literature on OA effects on foraminifera, because the majority of OA research on this group was published within the last three years. Disparate responses of this important group of marine calcifiers to OA were reported, highlighting the importance of a process-based understanding of OA effects on foraminifera. We cultured the benthic foraminifer Ammonia sp. under a range of carbonate chemistry manipulation treatments to identify the parameter of the carbonate system causing the observed effects. This parameter identification is the first step towards a process-based understanding. We argue that CO3 is the parameter affecting foraminiferal size-normalized weights (SNWs) and growth rates. Based on the presented data, we can confirm the strong potential of Ammonia sp. foraminiferal SNW as a CO3 proxy.
The chemical and isotopic composition of foraminiferal shells (so-called proxies) reflects the physico-chemical properties of the seawater. In current day paleoclimate research, the reconstruction of past seawater carbonate system to infer atmospheric CO2 concentrations is one of the most pressing challenges and a variety of proxies have been investigated, such as foraminiferal U/Ca. Since in natural seawater and traditional CO2 perturbation experiments, the carbonate system parameters co-vary, it is not possible to determine the parameter of the carbonate system causing e.g. changes in U/Ca, complicating the use of the latter as a carbonate system proxy. We overcome this problem, by culturing the benthic foraminifer Ammonia sp. at a range of carbonate chemistry manipulation treatments. Shell U/Ca values were determined to test sensitivity of U incorporation to various parameters of the carbonate system. We argue that CO3 is the parameter affecting the U/Ca ratio and consequently, the partitioning coefficient for U in Ammonia sp DU. We can confirm the strong potential of foraminiferal U/Ca as a CO3 proxy.
Metabarcoding has become the workhorse of community ecology. Sequencing a taxonomically informative DNA fragment from environmental samples gives fast access to community composition across taxonomic groups, but it relies on the assumption that the number of sequences for each taxon correlates with its abundance in the sampled community. However, gene copy number varies among and within taxa, and the extent of this variability must therefore be considered when interpreting community composition data derived from environmental sequencing. Here we measured with single-cell qPCR the SSU rDNA gene copy number of 139 specimens of five species of planktonic foraminifera. We found that the average gene copy number varied between of ~4 000 to ~50 000 gene copies between species, and individuals of the same species can carry between ~300 to more than 350 000 gene copies. This variability cannot be explained by differences in cell size and considering all plausible sources of bias, we conclude that this variability likely reflects dynamic genomic processes acting during the life cycle. We used the observed variability to model its impact on metabarcoding and found that the application of a correcting factor at species level may correct the derived relative abundances, provided sufficiently large populations have been sampled.