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63 result(s) for "Forest microclimatology"
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Tropical Dry Forests in the Americas
This book provides a comprehensive overview of the most endangered ecosystem in the tropics: the tropical seasonal dry forests. Written by the best experts in studying these forests and leaders of the initiative on reducing emissions from deforestation and forest degradation, this reference will be the major synthesis of knowledge on the state of tropical dry forests of the Americas. It addresses new approaches for data sampling and analysis using remote sensing technology, and discusses new ecological and econometric methods to evaluate the effectiveness of the economic model used and to recognize ecosystem services at the continental level and at the national level.
Assessment of the risk of Amazon dieback
The Amazon basin is a key component of the global carbon cycle. The old-growth rainforests in the basin represent storage of ~ 120 petagrams of carbon (Pg C) in their biomass. Annually, these tropical forests process approximately 18 Pg C through respiration and photosynthesis. This is more than twice the rate of global anthropogenic fossil fuel emissions. The basin is also the largest global repository of biodiversity and produces about 20 percent of the world's flow of fresh water into the oceans. Despite the large carbon dioxide (CO2) efflux from recent deforestation, the Amazon rainforest ecosystem is still considered to be a net carbon sinks of 0.8-1.1 Pg C per year because growth on average exceeds mortality (Phillips et al. 2008). However, current climate trends and human-induced deforestation may be transforming forest structure and behavior (Phillips et al. 2009). Increasing temperatures may accelerate respiration rates and thus carbon emissions from soils (Malhi and Grace 2000). High probabilities for modification in rainfall patterns (Malhi et al. 2008) and prolonged drought stress may lead to reductions in biomass density. Resulting changes in evapo-transpiration and therefore convective precipitation could further accelerate drought conditions and destabilize the tropical ecosystem as a whole, causing a reduction in its biomass carrying capacity or dieback. In turn, changes in the structure of the Amazon and its associated water cycle will have implications for the many endemic species it contains and result in changes at a continental scale. Clearly, with much at stake, if climate-induced damage alters the state of the Amazon ecosystem, there is a need to better understand its risk, process, and dynamics. The objective of this study is to assist in understanding the risk, process, and dynamics of potential Amazon dieback and its implications.
Characterization of ozone deposition to a mixed oak–hornbeam forest – flux measurements at five levels above and inside the canopy and their interactions with nitric oxide
A 1-month field campaign of ozone (O3) flux measurements along a five-level vertical profile above, inside and below the canopy was run in a mature broadleaf forest of the Po Valley, northern Italy. The study aimed to characterize O3 flux dynamics and their interactions with nitrogen oxides (NOx) fluxes from the forest soil and the atmosphere above the canopy. Ozone fluxes measured at the levels above the canopy were in good agreement, thus confirming the validity of the constant flux hypothesis, while below-canopy O3 fluxes were lower than above. However, at the upper canopy edge O3 fluxes were surprisingly higher than above during the morning hours. This was attributed to a chemical O3 sink due to a reaction with the nitric oxide (NO) emitted from soil and deposited from the atmosphere, thus converging at the top of the canopy. Moreover, this mechanism was favored by the morning coupling between the forest and the atmosphere, while in the afternoon the fluxes at the upper canopy edge became similar to those of the levels above as a consequence of the in-canopy stratification. Nearly 80 % of the O3 deposited to the forest ecosystem was removed by the canopy by stomatal deposition, dry deposition on physical surfaces and by ambient chemistry reactions (33.3 % by the upper canopy layer and 46.3 % by the lower canopy layer). Only a minor part of O3 was removed by the understorey vegetation and the soil surface (2 %), while the remaining 18.2 % was consumed by chemical reaction with NO emitted from soil. The collected data could be used to improve the O3 risk assessment for forests and to test the predicting capability of O3 deposition models. Moreover, these data could help multilayer canopy models to separate the influence of ambient chemistry vs. O3 dry deposition on the observed fluxes.
Diurnal variation and size dependence of the hygroscopicity of organic aerosol at a forest site in Wakayama, Japan: their relationship to CCN concentrations
Formation of biogenic secondary organic aerosol (BSOA) and its subsequent evolution can modify the hygroscopicity of the organic aerosol component (OA) in the forest atmosphere, and affect the concentrations of cloud condensation nuclei (CCN) there. In this study, size-resolved aerosol hygroscopic growth at 85 % relative humidity and size-resolved aerosol composition were measured using a hygroscopic tandem differential mobility analyzer and an aerosol mass spectrometer, respectively, at a forest site in Wakayama, Japan, in August and September 2015. The hygroscopicity parameter of OA (κorg) presented daily minima in the afternoon hours, and it also showed an increase with the increase in particle dry diameter. The magnitudes of the diurnal variations in κorg for particles with dry diameters of 100 and 300 nm were on average 0.091 and 0.096, respectively, and the difference in κorg between particles with dry diameters of 100 and 300 nm was on average 0.056. The relative contributions of the estimated fresh BSOA and regional OA to total OA could explain 40 % of the observed diurnal variations and size dependence of κorg. The hygroscopicity parameter of fresh BSOA was estimated to range from 0.089 to 0.12 for particles with dry diameters from 100 to 300 nm. Compared with the use of time- and size-resolved κorg, the use of time- and size-averaged κorg leads to under- and over-estimation of the fractional contribution of OA to CCN number concentrations in the range from −5.0 % to 26 %. This indicates that the diurnal variations and size dependence of κorg strongly affect the overall contribution of OA to CCN concentrations. The fractional contribution of fresh BSOA to CCN number concentrations could reach 0.28 during the period of intensive BSOA formation. The aging of the fresh BSOA, if it occurs, increases the estimated contribution of BSOA to CCN number concentrations by 52 %–84 %.