Linkage of Arctic atmospheric circulation and Siberian shelf hydrography: a proxy validation using δ18O records of bivalve shells

High resolution oxygen isotope profiles of aragonitic bivalve shells (Astarte borealis) collected alive in different years are used to trace hydrographical changes on the Laptev Sea shelf, which are mainly forced by changes in riverine freshwater discharge and arctic atmospheric circulation patterns. By merging individual isotope profiles, a high resolution time series of relative changes in bivalve δ18O is obtained for the eastern Laptev Sea for the period 1969 to 1998. The resulting pattern in the δ18O time series reflects seasonal bottom-water salinity changes in the Laptev Sea, which is dominated by the peak input of freshwater discharged by the Lena River onto the Laptev Sea shelf during summer. The relative changes in summer bottom-water salinity, deduced from the δ18O values in the bivalves and the discharge anomaly of the Lena River, show a significant negative correlation. It is therefore suggested that the annual and subdecadal variations of the riverine freshwater and its influence on the shelf hydrography are imprinted in the bivalve shells. Moreover, we note that extreme summer precipitation anomalies in the Lena River catchment area affect the river discharge characteristics, events which are detectable in the δ18O time series. This all implies that δ18O records of bivalve shells have the potential to build long-term records of atmospheric-forced changes in arctic circulation

Stable oxygen and carbon isotopes in modern benthic foraminifera from the Laptev Sea shelf: implications for reconstructing proglacial and profluvial environments in the Arctic

Measurements of δ18O and δ13C isotopes in three benthic foraminiferal species from surface sediments of the eastern Laptev Sea are compared to water δ18O values and δ13C values of dissolved inorganic carbon (DIC). Samples investigated originate from two environmentally contrasting core locations, which are influenced by riverine freshwater runoff to a varying degree. At the river-distal site, located within relatively stable marine conditions on the outer shelf, Elphidiella groenlandica, Haynesina orbiculare and Elphidium excavatum forma clavata show a positive specific offset of 1.4‰, 1.5‰ and 1‰, respectively, in their δ18O values relative to the expected value for inorganic calcite precipitated under equilibrium conditions. At the site close to the Lena River confluence, with enhanced seasonal hydrographic contrasts, calculated δ18O offsets in E. groenlandica and in H. orbiculare remain about the same whereas E. e. clavata displays a distinctly negative offset of −1.8‰. The δ18O variation in E. e. clavata is interpreted as a vital effect, a finding which limits the potential of this species for reconstructing freshwater-influenced shelf paleoenvironments on the basis of oxygen isotopes. This interpretation gains support when comparing foraminiferal δ13C with the δ13CDIC of the water. While some of the difference in the carbonate δ13C seems to be controlled by a riverine-related admixture of DIC, clearly defined δ13C ranges in each of the three foraminifera at the river-proximal site shows that also the carbon isotopic signature in E. e. clavata is particularly affected by environmental factors

The Concise Guide to PHARMACOLOGY 2023/24: G protein-coupled receptors.

The Concise Guide to PHARMACOLOGY 2023/24 is the sixth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of approximately 1800 drug targets, and about 6000 interactions with about 3900 ligands. There is an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (https://www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes almost 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.16177. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2023, and supersedes data presented in the 2021/22, 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: G protein-coupled receptors.

The Concise Guide to PHARMACOLOGY 2021/22 is the fifth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of nearly 1900 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes over 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.15538. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2021, and supersedes data presented in the 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate