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Raleigh 1973.pdf
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Raley et al 2006.pdf
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Ramification of stream networks
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The geometric complexity of stream networks has been a source of fascination for centuries. However, a comprehensive understanding of ramification—the mechanism of branching by which such networks grow—remains elusive. Here we show that streams incised by groundwater seepage branch at a characteristic angle of 2π/5 = 72°. Our theory represents streams as a collection of paths growing and bifurcating in a diffusing field. Our observations of nearly 5,000 bifurcated streams growing in a 100 km2 groundwater field on the Florida Panhandle yield a mean bifurcation angle of 71.9° ± 0.8°. This good accord between theory and observation suggests that the network geometry is determined by the external flow field but not, as classical theories imply, by the flow within the streams themselves.
river networks | network growth | Laplacian growth
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Rand Wiles 1982.pdf
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Rapid deposition of oxidized biogenic compounds to a temperate forest
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We report fluxes and dry deposition velocities for 16 atmospheric compounds above a southeastern United States forest, including: hydrogen peroxide (H2O2), nitric acid (HNO3), hydrogen cyanide (HCN), hydroxymethyl hydroperoxide, peroxyacetic acid, organic hydroxy nitrates, and other multifunctional species derived from the oxidation of isoprene and monoterpenes. The data suggest that dry deposition is the dominant daytime sink for small, satu- rated oxygenates. Greater than 6 wt %C emitted as isoprene by the forest was returned by dry deposition of its oxidized products. Peroxides account for a large fraction of the oxidant flux, possibly eclipsing ozone in more pristine regions. The measured organic nitrates comprise a sizable portion (15%) of the oxidized nitrogen input into the canopy, with HNO3 making up the balance. We ob- serve that water-soluble compounds (e.g., strong acids and hydro- peroxides) deposit with low surface resistance whereas compounds with moderate solubility (e.g., organic nitrates and hydroxycarbon- yls) or poor solubility (e.g., HCN) exhibited reduced uptake at the surface of plants. To first order, the relative deposition velocities of water-soluble compounds are constrained by their molecular diffu- sivity. From resistance modeling, we infer a substantial emission flux of formic acid at the canopy level (∼1 nmol m−2·s−1). GEOS−Chem, a widely used atmospheric chemical transport model, currently under- estimates dry deposition for most molecules studied in this work. Reconciling GEOS−Chem deposition velocities with observations resulted in up to a 45% decrease in the simulated surface con- centration of trace gases.
biosphere−atmosphere exchange | isoprene | dry deposition | OVOCs | fluxes
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Rapid evolution of flowering time by an annual plant in response to a climate fluctuation
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Ongoing climate change has affected the ecological dynamics of many species and is expected to impose natural selection on ecologically important traits. Droughts and other anticipated changes in precipitation may be particularly potent selective fac- tors, especially in arid regions. Here we demonstrate the evolutionary response of an annual plant, Brassica rapa, to a recent climate fluctuation resulting in a multiyear drought. Ancestral (predrought) genotypes were recovered from stored seed and raised under a set of common environments with descendant (postdrought) genotypes and with ancestordescendant hybrids. As predicted, the abbreviated growing seasons caused by drought led to the evolution of earlier onset of flowering. Descendants bloomed earlier than ancestors, advancing first flowering by 1.9 days in one study population and 8.6 days in another. The inter- mediate flowering time of ancestordescendant hybrids supports an additive genetic basis for divergence. Experiments confirmed that summer drought selected for early flowering, that flowering time was heritable, and that selection intensities in the field were more than sufficient to account for the observed evolutionary change. Natural selection for drought escape thus appears to have caused adaptive evolution in just a few generations. A systematic effort to collect and store propagules from suitable species would provide biologists with materials to detect and elucidate the genetic basis of further evolutionary shifts driven by climate change.
contemporary evolution global climate change life history theory local adaptation plant phenology
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Rapid growth in CO2 emissions after the 2008–2009 global financial crisis.pdf
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1st paragraph: Global carbon dioxide emissions from fossil-fuel combustion and cement production grew 5.9% in 2010, surpassed 9 Pg of carbon (Pg C) for the first time, and more than offset the 1.4% decrease in 2009. The impact of the 2008–2009 global financial crisis (GFC) on emissions has
been short-lived owing to strong emissions growth in emerging economies, a return to emissions growth in developed economies, and an increase in the fossil-fuel intensity of the world economy.
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Rapid Range Shifts of Species Associated with High Levels of Climate Warming
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The distributions of many terrestrial organisms are currently shifting in latitude or elevation in responseto changing climate. Using a meta-analysis, we estimated that the distributions of species haverecently shifted to higher elevations at a median rate of 11.0 meters per decade, and to higher latitudes
at a median rate of 16.9 kilometers per decade. These rates are approximately two and three times faster than previously reported. The distances moved by species are greatest in studies showing thehighest levels of warming, with average latitudinal shifts being generally sufficient to track temperature
changes. However, individual species vary greatly in their rates of change, suggesting that the range shift of each species depends on multiple internal species traits and external drivers of change. Rapid average shifts derive from a wide diversity of responses by individual species.
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Rapid shifts in plant distribution with recent climate change
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A change in climate would be expected to shift plant distribution as species expand in newly favorable areas and decline in increas- ingly hostile locations. We compared surveys of plant cover that were made in 1977 and 2006–2007 along a 2,314-m elevation gradient in Southern California’s Santa Rosa Mountains. Southern California’s climate warmed at the surface, the precipitation vari- ability increased, and the amount of snow decreased during the 30-year period preceding the second survey. We found that the average elevation of the dominant plant species rose by 65 m between the surveys. This shift cannot be attributed to changes in air pollution or fire frequency and appears to be a consequence of changes in regional climate.
plant migration range shift
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Rashleigh 2008.pdf
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