Coastal populations are often connected by unidirectional current systems, but the biological effects of such asymmetric oceanographic connectivity remain relatively unstudied. We used mtDNA analysis to determine the phylogeographic origins of beach-cast bull-kelp (Durvillaea antarctica) adults in the Canterbury Bight, a 180 km coastal region devoid of rocky-reef habitat in southern New Zealand. A multi-year, quantitative analysis supports the oceanographically derived hypothesis of asymmetric dispersal mediated by the north-flowing Southland Current. Specifically, 92% of beach-cast specimens examined had originated south of the Bight, many drifting north for hundreds of kilometres, and some traversing at least 500 km of ocean from subantarctic sources. In contrast, only 8% of specimens had dispersed south against the prevailing current, and these counter-current dispersers likely travelled relatively small distances (tens of kilometres). These data show that oceanographic connectivity models can provide robust estimates of passive biological dispersal, even for highly buoyant taxa. The results also indicate that there are no oceanographic barriers to kelp dispersal across the Canterbury Bight, indicating that other ecological factors explain the phylogeographic disjunction across this kelp-free zone. The large number of long-distance dispersal events detected suggests drifting macroalgae have potential to facilitate ongoing connectivity between otherwise isolated benthic populations.
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http://dx.doi.org/10.1111/j.1365-294X.2010.04842.x | DOI Listing |
Chem Sci
December 2024
Department of Chemistry, Biology and Biotechnology, University of Perugia Via Elce di Sotto, 8 06123 Perugia Italy
The majority of enantioselective organocatalytic reactions occur in apolar or weakly polar organic solvents. Nevertheless, the influence of solute-solvent van der Waals forces on the relative kinetics of competitive pathways remains poorly understood. In this study, we provide a first insight into the nature and strength of these interactions at the transition state level using advanced computational tools, shedding light into their influence on the selectivity.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Materials Science, Fudan University, Shanghai 200433, China.
Borohydrides, known for ultrahigh hydrogen density, are promising hydrogen storage materials but typically require high operating temperatures due to their strong thermodynamic stability. Here we introduce a novel light-induced destabilization mechanism for hydrogen storage reaction of borohydrides under ambient conditions photogenerated vacancies in LiH. These vacancies thermodynamically destabilize B-H bonds through the spontaneous "strong adsorption" of BH groups, which trigger an asymmetric redistribution of electrons, enabling hydrogen release at near room temperature, approximately 300 °C lower than the corresponding thermal process.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Chemical and Petroleum Engineering, University of Calgary, 2500 University Drive, NW, Calgary, AB, Canada.
Solar-driven CO reduction to value-added C chemicals is thermodynamically challenging due to multiple complicated steps. The design of active sites and structures for photocatalysts is necessary to improve solar energy efficiency. In this work, atomically dispersed Ru-O sites in RuInO are constructed by interior lattice anchoring of Ru.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
IISER Kolkata: Indian Institute of Science Education and Research Kolkata, Department of Chemical Sciences, Mohanpur, 741246, Nadia, INDIA.
Chiral allyl amines are important structural components in natural products, pharmaceuticals, and chiral catalysts. Herein, we report a cobalt-catalyzed enantioselective reductive coupling of imines with internal alkynes to synthesize chiral allyl amines. The reaction is catalyzed by a cobalt complex derived from commercially available bisphosphine ligand utilizing zinc as the electron donor.
View Article and Find Full Text PDFIUCrdata
December 2024
Nelson Mandela University, Summerstrand Campus, Department of Chemistry, University Way, Summerstrand, PO Box 77000, Port Elizabeth, 6031, South Africa.
The title compound, CHIN, is the -iodinated derivative of aniline. The asymmetric unit contains two mol-ecules. The structure was refined as a two-component inversion twin with a volume ratio of 55.
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