Preconditioning of the Weddell Sea Polynya by the Ocean Mesoscale and Dense Water Overflows

The Weddell Sea polynya is a large opening in the open-ocean sea ice cover associated with intense deep convection in the ocean. A necessary condition to form and maintain a polynya is the presence of a strong subsurface heat reservoir. This study investigates the processes that control the stratification and hence the buildup of the subsurface heat reservoir in the Weddell Sea. To do so, a climate model run for 200 years under preindustrial forcing with two eddying resolutions in the ocean (0.25° CM2.5 and 0.10° CM2.6) is investigated. Over the course of the simulation, CM2.6 develops two polynyas in the Weddell Sea, while CM2.5 exhibits quasi-continuous deep convection but no polynyas, exemplifying that deep convection is not a sufficient condition for a polynya to occur. CM2.5 features a weaker subsurface heat reservoir than CM2.6 owing to weak stratification associated with episodes of gravitational instability and enhanced vertical mixing of heat, resulting in an erosion of the reservoir. In contrast, in CM2.6, the water column is more stably stratified, allowing the subsurface heat reservoir to build up. The enhanced stratification in CM2.6 arises from its refined horizontal grid spacing and resolution of topography, which allows, in particular, a better representation of the restratifying effect by transient mesoscale eddies and of the overflows of dense waters along the continental slope

Atlantic multi-decadal oscillation covaries with Agulhas leakage

The interoceanic transfer of seawater between the Indian Ocean and the Atlantic, ‘Agulhas leakage’, forms a choke point for the overturning circulation in the global ocean. Here, by combining output from a series of high-resolution ocean and climate models with in situ and satellite observations, we construct a time series of Agulhas leakage for the period 1870–2014. The time series demonstrates the impact of Southern Hemisphere westerlies on decadal timescales. Agulhas leakage shows a correlation with the Atlantic Multi-decadal Oscillation on multi-decadal timescales; the former leading by 15 years. This is relevant for climate in the North Atlanti

Antarctic Bottom Water Sensitivity to Spatio‐Temporal Variations in Antarctic Meltwater Fluxes

Ice sheet melting into the Southern Ocean can change the formation and properties of the Antarctic Bottom Water (AABW). Ocean models often mimic ice sheet melting by adding freshwater fluxes in the Southern Ocean under diverse spatial distributions. We use a global ocean and sea-ice model to explore whether the spatial distribution and magnitude of meltwater fluxes can alter AABW properties and formation. We find that a realistic spatially varying meltwater flux sustains AABW with higher salinities compared to simulations with uniform meltwater fluxes. Finally, we show that increases in ice sheet melting above 12% since 1958 can trigger AABW freshening rates similar to those observed in the Southern Ocean since 1990, suggesting that the increasing Antarctic meltwater discharge can drive the observed AABW freshening

Author Correction : Spiraling pathways of global deep waters to the surface of the Southern Ocean

© The Author(s), 2018. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Nature Communications 9 (2018): 209, doi:10.1038/s41467-017-02105-y.Correction to: Nature Communications 8:172 https://doi.org/10.1038/s41467-017-00197-0; Article published online: 2 August 201

Role of Mesoscale Eddies in Cross-Frontal Transport of Heat and Biogeochemical Tracers in the Southern Ocean

This study examines the role of processes transporting tracers across the Polar Front (PF) in the depth interval between the surface and major topographic sills, which this study refers to as the “PF core.” A preindustrial control simulation of an eddying climate model coupled to a biogeochemical model [GFDL Climate Model, version 2.6 (CM2.6)– simplified version of the Biogeochemistry with Light Iron Nutrients and Gas (miniBLING) 0.1° ocean model] is used to investigate the transport of heat, carbon, oxygen, and phosphate across the PF core, with a particular focus on the role of mesoscale eddies. The authors find that the total transport across the PF core results from a ubiquitous Ekman transport that drives the upwelled tracers to the north and a localized opposing eddy transport that induces tracer leakages to the south at major topographic obstacles. In the Ekman layer, the southward eddy transport only partially compensates the northward Ekman transport, while below the Ekman layer, the southward eddy transport dominates the total transport but remains much smaller in magnitude than the near-surface northward transport. Most of the southward branch of the total transport is achieved below the PF core, mainly through geostrophic currents. This study finds that the eddy-diffusive transport reinforces the southward eddy-advective transport for carbon and heat, and opposes it for oxygen and phosphate. Eddy-advective transport is likely to be the leading-order component of eddy-induced transport for all four tracers. However, eddy-diffusive transport may provide a significant contribution to the southward eddy heat transport due to strong along-isopycnal temperature gradients

Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

Ophthalmo-acromelic syndrome (OAS), also known as Waardenburg Anophthalmia syndrome, is defined by the combination of eye malformations, most commonly bilateral anophthalmia, with post-axial oligosyndactyly. Homozygosity mapping and subsequent targeted mutation analysis of a locus on 14q24.2 identified homozygous mutations in SMOC1 (SPARC-related modular calcium binding 1) in eight unrelated families. Four of these mutations are nonsense, two frame-shift, and two missense. The missense mutations are both in the second Thyroglobulin Type-1 (Tg1) domain of the protein. The orthologous gene in the mouse, Smoc1, shows site- and stage-specific expression during eye, limb, craniofacial, and somite development. We also report a targeted pre-conditional gene-trap mutation of Smoc1 (Smoc1tm1a) that reduces mRNA to ∼10% of wild-type levels. This gene-trap results in highly penetrant hindlimb post-axial oligosyndactyly in homozygous mutant animals (Smoc1tm1a/tm1a). Eye malformations, most commonly coloboma, and cleft palate occur in a significant proportion of Smoc1tm1a/tm1a embryos and pups. Thus partial loss of Smoc-1 results in a convincing phenocopy of the human disease. SMOC-1 is one of the two mammalian paralogs of Drosophila Pentagone, an inhibitor of decapentaplegic. The orthologous gene in Xenopus laevis, Smoc-1, also functions as a Bone Morphogenic Protein (BMP) antagonist in early embryogenesis. Loss of BMP antagonism during mammalian development provides a plausible explanation for both the limb and eye phenotype in humans and mice

Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

Correction to: Nature Geneticshttps://doi.org/10.1038/s41588-023-01314-0, published online 13 March 2023. In the version of the article initially published, the sample sizes in the main text and Supplementary Tables 1 and 2 were incorrect. In the abstract, the last paragraph of the Introduction, the first paragraph of the Results, the top box in Figure 1a and the Supplementary Information, the total sample size has been corrected from 580,869 to 588,452 participants and the size of the European cohort from 468,062 to 475,645. Some of the effect sizes in Supplementary Table 14 (columns W, Z, AC, AF) had the wrong sign. There was also an error in Supplementary Table 3 where the sample size instead of the variant count was shown for EXCEED. The errors do not affect the conclusions of the study. Additionally, two acknowledgments for use of INTERVAL pQTL and Lung eQTL consortium data were omitted from the Supplementary Information. These errors have been corrected in the Supplementary Information and HTML and PDF versions of the article