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71.
72.
1. The light climates of Darwin River Reservoir (DRR) and Manton River Reservoir (MRR), in northern Australia, are compared for an 8-year period. The reservoirs are subject to the same wet/dry tropical climate and have similar catchment characteristics, but differ in their basin morphology, retention time and trophic status.
2. Median euphotic depths in DRR and MRR were 9.7 and 4.4 m, respectively. Seasonal variation in each reservoir's euphotic depth was best explained by colour, based on a stepwise linear regression. Turbidity was excluded from the two regressions, while chlorophyll a concentration was significant only for the MRR regression.
3. Both reservoirs showed the same seasonal pattern for colour. Wet season inflow increased reservoir colour, and was followed by a reduction in colour due to photodegradation and microbial decomposition of humic material, reaching a minimum before the next wet seasons inflow.
4. Although the colour of catchment run-off into both reservoirs was similar, MRR colour was two to three times greater than that measured in DRR. The higher colour and greater light attenuation of MRR is attributed primarily to its shorter retention time, and therefore shorter time for colour removal. Annual retention time accounted for 97% of the variability of average annual colour (measured as absorption at 440 nm), based on a linear regression of log10 transformed data for both reservoirs.
5. Long retention times favour reduced colour, increasing water transparency, particularly in water bodies of low trophic state and inorganic turbidity. 相似文献
2. Median euphotic depths in DRR and MRR were 9.7 and 4.4 m, respectively. Seasonal variation in each reservoir's euphotic depth was best explained by colour, based on a stepwise linear regression. Turbidity was excluded from the two regressions, while chlorophyll a concentration was significant only for the MRR regression.
3. Both reservoirs showed the same seasonal pattern for colour. Wet season inflow increased reservoir colour, and was followed by a reduction in colour due to photodegradation and microbial decomposition of humic material, reaching a minimum before the next wet seasons inflow.
4. Although the colour of catchment run-off into both reservoirs was similar, MRR colour was two to three times greater than that measured in DRR. The higher colour and greater light attenuation of MRR is attributed primarily to its shorter retention time, and therefore shorter time for colour removal. Annual retention time accounted for 97% of the variability of average annual colour (measured as absorption at 440 nm), based on a linear regression of log
5. Long retention times favour reduced colour, increasing water transparency, particularly in water bodies of low trophic state and inorganic turbidity. 相似文献
73.
1. Slices of swede tissue placed under nitrogen produce carbondioxide and ethanol in equal amounts after an initial phaselasting about 1.5 hours. During this initial phase some 2 µM./g.fr. wt. of extra carbon dioxide is produced. The productionof such extra carbon dioxide is not affected by iodoacetate,fluoride, or arsenite which inhibit glycolysis or by dinitrophenolwhich stimulates glycolysis. Slices incubated in air in thepresence of cyanide also produce extra carbon dioxide. 2. A second extra burst of carbon dioxide can be induced aftersome hours of anaerobiosis by treating slices with methyleneblue, DPN, or TPN, or as a result of a short air experience. 3. Experiments with labelled sugars support the view that theextra carbon dioxide originates ultimately from carbohydrate,being released, it is proposed, in the oxidative decarboxylationof either pyruvate or 6-phosphogluconate. Carbon dioxide productionthen continues so long as oxidants are available in the cell,finally coming to a standstill when cell components reach theirreduced states. 相似文献
74.
J. PECCOUD C. C. FIGUEROA A. X. SILVA C. C. RAMIREZ L. MIEUZET J. BONHOMME S. STOECKEL M. PLANTEGENEST J.-C. SIMON 《Molecular ecology》2008,17(21):4608-4618
Asexuality confers demographic advantages to invasive taxa, but generally limits adaptive potential for colonizing of new habitats. Therefore, pre-existing adaptations and habitat tolerance are essential in the success of asexual invaders. We investigated these key factors of invasiveness by assessing reproductive modes and host-plant adaptations in the pea aphid, Acyrthosiphon pisum, a pest recently introduced into Chile. The pea aphid encompasses lineages differing in their reproductive mode, ranging from obligatory cyclical parthenogenesis to fully asexual reproduction. This species also shows variation in host use, with distinct biotypes specialized on different species of legumes as well as more polyphagous populations. In central Chile, microsatellite genotyping of pea aphids sampled on five crops and wild legumes revealed three main clonal genotypes, which showed striking associations with particular host plants rather than sampling locations. Phenotypic analyses confirmed their strong host specialization and demonstrated parthenogenesis as their sole reproductive mode. The genetic relatedness of these clonal genotypes with corresponding host-specialized populations from the Old World indicated that each clone descended from a particular Eurasian biotype, which involved at least three successful introduction events followed by spread on different crops. This study illustrates that multiple introductions of highly specialized clones, rather than local evolution in resource use and/or selection of generalist genotypes, can explain the demographic success of a strictly asexual invader. 相似文献
75.
Recent IPCC projections suggest that Africa will be subject to particularly severe changes in atmospheric conditions. How the vegetation of Africa and particularly the grassland–savanna–forest complex will respond to these changes has rarely been investigated. Most studies on global carbon cycles use vegetation models that do not adequately account for the complexity of the interactions that shape the distribution of tropical grasslands, savannas and forests. This casts doubt on their ability to reliably simulate the future vegetation of Africa. We present a new vegetation model, the adaptive dynamic global vegetation model (aDGVM) that was specifically developed for tropical vegetation. The aDGVM combines established components from existing DGVMs with novel process‐based and adaptive modules for phenology, carbon allocation and fire within an individual‐based framework. Thus, the model allows vegetation to adapt phenology, allocation and physiology to changing environmental conditions and disturbances in a way not possible in models based on fixed functional types. We used the model to simulate the current vegetation patterns of Africa and found good agreement between model projections and vegetation maps. We simulated vegetation in absence of fire and found that fire suppression strongly influences tree dominance at the regional scale while at a continental scale fire suppression increases biomass in vegetation by a more modest 13%. Simulations under elevated temperature and atmospheric CO2 concentrations predicted longer growing periods, higher allocation to roots, higher fecundity, more biomass and a dramatic shift toward tree dominated biomes. Our analyses suggest that the CO2 fertilization effect is not saturated at ambient CO2 levels and will strongly increase in response to further increases in CO2 levels. The model provides a general and flexible framework for describing vegetation response to the interactive effects of climate and disturbances. 相似文献
76.
Live trapping to monitor small mammals in Britain 总被引:1,自引:0,他引:1
JOHN R. FLOWERDEW RICHARD F. SHORE† SIMON M. C. POULTON‡ TIMOTHY H. SPARKS† 《Mammal Review》2004,34(1-2):31-50
77.
MATTHEW L. BUFFINGTON SEÁN G. BRADY SHELAH I. MORITA SIMON VAN NOORT 《Systematic Entomology》2012,37(2):287-304
We examine the phylogenetic relationships of Figitidae and discuss host use within this group in light of our own and previously published divergence time data. Our results suggest Figitidae, as currently defined, is not monophyletic. Furthermore, Mikeiinae and Pycnostigminae are sister‐groups, nested adjacent to Thrasorinae, Plectocynipinae and Euceroptrinae. The recovery of Pycnostigminae as sister‐group to Mikeiinae suggests two major patterns of evolution: (i) early Figitidae lineages demonstrate a Gondawanan origin (Plectocynipinae: Neotropical; Mikeiinae and Thrasorinae: Australia; Pycnostigminae: Africa); and (ii) based on host records for Mikeiinae, Thrasorinae and Plectocynipinae, Pycnostigminae are predicted to be parasitic on gall‐inducing Hymenoptera. The phylogenetic position of Parnips (Parnipinae) was unstable, and various analyses were conducted to determine the impact of this uncertainty on both the recovery of other clades and inferred divergence times; when Parnips was excluded from the total evidence analysis, Cynipidae was found to be sister‐group to [Euceroptrinae + (Plectocynipinae (Thrasorinae + (Mikeiinae + Pycnostigminae)))], with low support. Divergence dating analyses using BEAST indicate the stem‐group node of Figitidae to be c. 126 Ma; the dipteran parasitoids (Eucoilinae and Figitinae), were estimated to have a median age of 80 and 88 Ma, respectively; the neuropteran parasitoids (Anacharitinae), were estimated to have a median age of 97 Ma; sternorrhynchan hyperparasitoids (Charipinae), were estimated to have a median age of 110 Ma; the Hymenoptera‐parasitic subfamilies (Euceroptinae, Plectocynipinae, Trasorinae, Mikeiinae, Pycnostigminae, and Parnipinae), ranged in median ages from 48 to 108 Ma. Rapid radiation of Eucoilinae subclades appears chronologically synchronized with the origin of their hosts, Schizophora (Diptera). Overall, the exclusion of Parnips from the BEAST analysis did not result in significant changes to divergence estimates. Finally, though sparsely represented in the analysis, our data suggest Cynipidae have a median age of 54 Ma, which is somewhat older than the age of Quercus spp (30–50 Ma), their most common host. 相似文献
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