Testing the link between terrestrial climate change and Galactic spiral arm transit

We re-examine past suggestions of a close link between terrestrial climate change and the Sun's transit of spiral arms in its path through the Milky Way galaxy. These links produced concrete fits, deriving the unknown spiral pattern speed from terrestrial climate correlations. We test these fits against new data on spiral structure based on CO data that does not make simplifying assumptions about symmetry and circular rotation. If we compare the times of these transits to changes in the climate of Earth, not only do the claimed correlations disappear, but also we find that they cannot be resurrected for any reasonable pattern speed.Comment: Accepted for publication in ApJ Letters. Moderate revisions with clarification, no change in conclusion

A visão brasileira da futura ordem global Brazil's vision of the future global order

Este artigo visa desdobrar a concepção brasileira da futura ordem global localizada entre os polos extremos de um concerto de grandes potências e de uma ordem mundial multirregional. O autor demonstra como os formuladores de política externa brasileira contribuem para um tipo de ordem global que oferece espaço de manobra para a potência emergente. As opções de política externa do Brasil são limitadas, diante do superior poder material (hard power) das grandes potências estabelecidas. A estratégia de soft balancing do Brasil envolve estratégias institucionais, como a formação de coalizões diplomáticas limitadas ou alianças para restringir o poder das grandes potências estabelecidas. O Brasil tem estado entre os mais poderosos condutores de mudança incremental na diplomacia mundial e é beneficiado em grande parte pelas conectadas mudanças de poder global. Em uma ordem global moldada por grandes potências por meio de arranjos e instituições internacionais, esses jogadores que efetivamente operam em ambos como inovadores, construtores de coalizões e porta-vozes, ao mesmo tempo em que preservam grande parcela de soberania e autonomia, têm o potencial de influenciar substancialmente os resultados da futura política global.<br>This article aims to unfold the Brazilian conception of the future global order located between the extreme poles of a concert of great powers and a multiregional world order. The author demonstrates how Brazilian foreign policy makers contribute to the kind of global order, which offers most room to manoeuvre to the rising power. The foreign policy options of Brazil are limited in view of the superior hard power of the established great powers. Brazil's soft balancing strategy involves institutional strategies such as the formation of limited diplomatic coalitions or ententes to constrain the power of the established great powers. Brazil has been amongst the most powerful drivers of incremental change in world diplomacy and it benefits most from the connected global power shifts. In a global order shaped by great powers through international groupings and institutions, those players who effectively operate within them as innovators, coalition builders and spokesmen while preserving great amounts of sovereignty and autonomy have the potential to substantially influence the outcomes of future global politics

Permanent Genetic Resources added to Molecular Ecology Resources Database 1 May 2009-31 July 2009

This article documents the addition of 512 microsatellite marker loci and nine pairs of Single Nucleotide Polymorphism (SNP) sequencing primers to the Molecular Ecology Resources Database. Loci were developed for the following species: Alcippe morrisonia morrisonia, Bashania fangiana, Bashania fargesii, Chaetodon vagabundus, Colletes floralis, Coluber constrictor flaviventris, Coptotermes gestroi, Crotophaga major, Cyprinella lutrensis, Danaus plexippus, Fagus grandifolia, Falco tinnunculus, Fletcherimyia fletcheri, Hydrilla verticillata, Laterallus jamaicensis coturniculus, Leavenworthia alabamica, Marmosops incanus, Miichthys miiuy, Nasua nasua, Noturus exilis, Odontesthes bonariensis, Quadrula fragosa, Pinctada maxima, Pseudaletia separata, Pseudoperonospora cubensis, Podocarpus elatus, Portunus trituberculatus, Rhagoletis cerasi, Rhinella schneideri, Sarracenia alata, Skeletonema marinoi, Sminthurus viridis, Syngnathus abaster, Uroteuthis (Photololigo) chinensis, Verticillium dahliae, Wasmannia auropunctata, and Zygochlamys patagonica. These loci were cross-tested on the following species: Chaetodon baronessa, Falco columbarius, Falco eleonorae, Falco naumanni, Falco peregrinus, Falco subbuteo, Didelphis aurita, Gracilinanus microtarsus, Marmosops paulensis, Monodelphis Americana, Odontesthes hatcheri, Podocarpus grayi, Podocarpus lawrencei, Podocarpus smithii, Portunus pelagicus, Syngnathus acus, Syngnathus typhle, Uroteuthis (Photololigo) edulis, Uroteuthis (Photololigo) duvauceli and Verticillium alboatrum. This article also documents the addition of nine sequencing primer pairs and sixteen allele specific primers or probes for Oncorhynchus mykiss and Oncorhynchus tshawytscha; these primers and assays were cross-tested in both species.Glenn R. Almany...Rohan Mellick...Maurizio Rossetto...et al

Permanent Genetic Resources added to Molecular Ecology Resources Database 1 May 2009–31 July 2009

This article documents the addition of 512 microsatellite marker loci and nine pairs of Single Nucleotide Polymorphism (SNP) sequencing primers to the Molecular Ecology Resources Database. Loci were developed for the following species: Alcippe morrisonia morrisonia, Bashania fangiana, Bashania fargesii, Chaetodon vagabundus, Colletes floralis, Coluber constrictor flaviventris, Coptotermes gestroi, Crotophaga major, Cyprinella lutrensis, Danaus plexippus, Fagus grandifolia, Falco tinnunculus, Fletcherimyia fletcheri, Hydrilla verticillata, Laterallus jamaicensis coturniculus, Leavenworthia alabamica, Marmosops incanus, Miichthys miiuy, Nasua nasua, Noturus exilis, Odontesthes bonariensis, Quadrula fragosa, Pinctada maxima, Pseudaletia separata, Pseudoperonospora cubensis, Podocarpus elatus, Portunus trituberculatus, Rhagoletis cerasi, Rhinella schneideri, Sarracenia alata, Skeletonema marinoi, Sminthurus viridis, Syngnathus abaster, Uroteuthis (Photololigo) chinensis, Verticillium dahliae, Wasmannia auropunctata, and Zygochlamys patagonica. These loci were cross-tested on the following species: Chaetodon baronessa, Falco columbarius, Falco eleonorae, Falco naumanni, Falco peregrinus, Falco subbuteo, Didelphis aurita, Gracilinanus microtarsus, Marmosops paulensis, Monodelphis Americana, Odontesthes hatcheri, Podocarpus grayi, Podocarpus lawrencei, Podocarpus smithii, Portunus pelagicus, Syngnathus acus, Syngnathus typhle,Uroteuthis (Photololigo) edulis, Uroteuthis (Photololigo) duvauceli and Verticillium albo-atrum. This article also documents the addition of nine sequencing primer pairs and sixteen allele specific primers or probes for Oncorhynchus mykiss and Oncorhynchus tshawytscha; these primers and assays were cross-tested in both species.This article is from Molecular Ecology Resources 9 (2009): 1460, doi:10.1111/j.1755-0998.2009.02759.x.</p