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Provenance variation in Maesopsis eminii EnglNdeze, Michel January 1999 (has links)
No description available.
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The taxonomy, ecology and utilisation of African rattans (Palmae: Calamoideae)Sunderland, Terence Christopher Heesom January 2001 (has links)
No description available.
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Studies on the regeneration and growth characteristics of Brachylaena huillensis in semi-deciduous forests of KenyaKigomo, Bernard N. January 1989 (has links)
No description available.
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Cluster point sampling in moist tropical forests using large basal area factorsBanyard, Sydney G. January 1989 (has links)
No description available.
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Can Leaf Spectroscopy Predict Leaf and Forest Traits Along a Peruvian Tropical Forest Elevation Gradient?Doughty, Christopher E., Santos-Andrade, P. E., Goldsmith, G. R., Blonder, B., Shenkin, A., Bentley, L. P., Chavana-Bryant, C., Huaraca-Huasco, W., Díaz, S., Salinas, N., Enquist, B. J., Martin, R., Asner, G. P., Malhi, Y. 11 1900 (has links)
High-resolution spectroscopy can be used to measure leaf chemical and structural traits. Such leaf traits are often highly correlated to other traits, such as photosynthesis, through the leaf economics spectrum. We measured VNIR (visible-near infrared) leaf reflectance (400-1,075nm) of sunlit and shaded leaves in similar to 150 dominant species across ten, 1ha plots along a 3,300m elevation gradient in Peru (on 4,284 individual leaves). We used partial least squares (PLS) regression to compare leaf reflectance to chemical traits, such as nitrogen and phosphorus, structural traits, including leaf mass per area (LMA), branch wood density and leaf venation, and higher-level traits such as leaf photosynthetic capacity, leaf water repellency, and woody growth rates. Empirical models using leaf reflectance predicted leaf N and LMA (r(2)>30% and %RMSE<30%), weakly predicted leaf venation, photosynthesis, and branch density (r(2) between 10 and 35% and %RMSE between 10% and 65%), and did not predict leaf water repellency or woody growth rates (r(2)<5%). Prediction of higher-level traits such as photosynthesis and branch density is likely due to these traits correlations with LMA, a trait readily predicted with leaf spectroscopy.
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Exploring remotely sensed shadow in Amazonian regrowth forestsBailey, Philip January 1997 (has links)
No description available.
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Stand dynamics and regeneration of tropical dry forests in Nicaragua /Castro-Marín, Guillermo, January 2005 (has links) (PDF)
Diss. (sammanfattning) Umeå : Sveriges lantbruksuniversitet, 2005. / Härtill 4 uppsatser.
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Fire Ecology of a Seasonally Dry Tropical Forest in Southern IndiaMondal, Nandita January 2014 (has links) (PDF)
Fire ecology encompasses the study of the factors, biotic and abiotic, that influence the occurrence of fire in an area, as well as the effects fire has on the flora and fauna native and non-native to the region (Whelan 1995). Fire has had a major influence on shaping biomes as we see them today. Fire has had an effect on vegetation much before the evolution of Homo on Earth (Keeley and Rundel 2005, Pausas and Keeley 2009, Midgley and Bond 2011). With the evolution and expansion of Homo across Earth, fire has been tamed, and then generated and used over time to yield landscapes that were suitable for their existence (Pyne 1991, Bowman et al. 2009, Archibald et al. 2012). Thus, fire, vegetation and humans were, and still are, inextricably linked in certain biomes on Earth. The best examples are observed in tropical savannas and grasslands, biomes that experience distinct seasonality in climate and are thus prone to frequent fires caused either by lightning or by humans (Keeley and Rundel 2005, Archibald et al. 2012). At the other end of the spectrum of tropical vegetation types are rainforests where the occurrence of fires is constrained by a perpetually moist environment (Meyn et al. 2007, van der Werf et al. 2008), in the absence of manipulation of the forest landscape by humans. Frequent fires have been documented to alter structure and cause a decline in forest diversity in rainforests (Cochrane and Schulze 1999, Cochrane 2003), whereas fire exclusion in mesic savannas leads to increases in biomass and transition to forest ecosystems (Bond et al. 2003, Bond et al. 2005 and references therein).
A tropical biome that lies between these two extremes of vegetation types is the Seasonally Dry Tropical Forest (SDTF) where the occurrence of fire is common, but for which there are contrasting views on the effect of fire on this system (Saha and Howe 2003, Otterstrom et al. 2006 as examples). Current forest management policies in SDTF areas, especially in India, actively aim to exclude fire from these forests mostly because of the perception held by forest managers and the general public that fire has negative effects on forests. However, very few scientific studies have explored the ecology of fire in SDTFs. In order to formulate fire management policies, it is necessary to have a more comprehensive understanding of the ecology of fire in this tropical forest type.
This thesis addresses two components of fire ecology as applied to SDTFs. The first is how fire is influenced by the environment, and the second, how fires influence the biotic community particular to SDTFs. The study was carried out in an SDTF in southern India where fire is a common occurrence -the forests of Mudumalai – a protected area that exhibits a range of SDTF vegetation types, from moist deciduous to dry thorn forest, corresponding to a rainfall gradient.
Fire influenced by the environment:
For this section, the influence of fuel load, fuel moisture and ambient weather on area burnt, fire occurrence and fire temperatures were studied in the SDTF vegetation types of Mudumalai.
The extent of fire (area burnt) in an ecosystem differs according to the relative contribution of fuel load and fuel moisture available (Meyn et al. 2007). At a global scale, these factors vary along a spatial gradient of climatic conditions and are thus “varying constraints” (Krawchuk and Moritz 2011) on fire activity in natural ecosystems (Meyn et al. 2007, Krawchuk and Moritz 2011). Moist ecosystems such as tropical rainforests are at one end of the spectrum where fire activity is constrained by fuel moisture. At the other end are arid ecosystems, such as deserts, where fire activity is limited by the presence of fuels. The potential for the globally widespread seasonally dry tropical forests (SDTFs) to be placed as a single entity in this framework was examined by analyzing the interacting effects of fuel load and fuel moisture on the extent of fire in Mudumalai. Logistic regression was used to model proportion area burnt in a given year with factors that would influence fuel load and fuel moisture – these were proportion area burnt the previous year, wet season rainfall the previous year and early dry season rainfall. Modelling was conducted at two levels
– the overall landscape and within four defined moisture regimes (between 700 and 1700 mm yr-1) – using a dataset of area burnt and seasonal rainfall from 1990 to 2010. The landscape scale model showed that the extent of fire in a given year within this SDTF is dependent on the combined interaction of seasonal rainfall and extent burnt the previous year. However, within individual moisture regimes the relative contribution of these factors to the annual extent burnt varied – early dry season rainfall (i.e. a moderator of fuel moisture) was the predominant factor in the wettest regime, while the previous year’s wet season rainfall (i.e. a proxy for fuel load) had a large influence on fire extent in the driest regime. Thus, the diverse structural vegetation types associated with SDTFs across a wide range of rainfall regimes would have to be examined at finer regional or local scales to understand the specific environmental drivers of fire.
While the extent burnt in SDTFs is largely dependent on climatic influences, the probability of ignition has not been characterized for SDTFs. Anthropogenic fires are a regular occurrence during the dry season in SDTFs (Stott et al. 1990). We investigated if the occurrences of anthropogenic fire in Mudumalai were associated with any particular weather conditions during the dry season. Logistic regression between probability of a fire day and weather variables -seasonal rainfall, ambient relative humidity and temperature -was examined during the dry seasons of 20042010 in Mudumalai. Fire incidence data was obtained from the Fire Information for Resource Management System (FIRMS; NASA 2002) and weather data from two automatic weather stations within Mudumalai. The analysis showed that days with high probabilities of fire occurrence were associated with low levels of early dry season rainfall, low daily average relative humidity, and high daily average temperatures. These weather conditions are known to influence moisture levels of fine fuels (Viney 1991, Archibald et al. 2009). In Mudumalai as well as other SDTFs the primary fuels for fires are fine fuels such as litter and dried grass that accumulate on the forest floor during the dry season. Our results suggest that the occurrence of fire is moderated by environmental conditions that reduce or enhance the flammability of fine fuels in the dry tropics. A quantitative framework for assessing risk of a fire day has been proposed as an outcome of this analysis to assist forest managers in anticipating fire occurrences in this SDTF, and possibly for those across south Asia.
Of the various components of a fire regime, fire intensity is an important aspect. High fire temperatures (one measure of fire intensity, Keeley 2009) and resulting soil temperatures would have an effect on soil properties as well as plant species demography and community structure (Moreno and Oechel 1991, Neary et al. 1999, Morrison 2002). Fires that occur frequently in a region could vary in their intensity and severity depending upon the amount of fuel available and ambient weather conditions (Stinson and Wright 1969, Stott 1986, Stronach and McNaughton 1989, Ansley et al. 1998, Wotton et al. 2012). However, this relationship has not been examined in a multiple regression framework for SDTFs. Fire temperature was recorded and its relationship with ambient weather and fuel load was studied in two SDTFs of southern India -Mudumalai and Biligiri Rangaswamy Temple (BRT) Wildlife Sanctuary in Karnataka. During “controlled burns” conducted by the forest department staff in these reserves in February and March 2010, temperature indicating lacquers on mica sheets were used to measure fire temperature at several points at ground level and one cm below the ground. Biomass was harvested close to the temperature measurement points to estimate fuel load and fuel moisture. Ambient weather conditions were recorded during the controlled burn when the flame passed over the indicators. Temperatures recorded at ground level ranged from <79oC to 760oC, with the most frequently recorded temperatures between 343-399 oC and 510566 oC. Temperatures measured one cm below the ground ranged from <79oC to 302oC, with a majority of the indicators recording temperatures in the <79oC category. Ground-level temperatures increased with increasing biomass. A linear regression of ground-level temperatures with fuel load and ambient weather conditions of relative humidity and temperature was found to explain most of the variation in the data. Ground-level fire temperatures increased with increasing fuel load, but were also found to be lower at higher relative humidities at a given temperature. In order to reduce the intensity of forest fires that occur accidentally during the dry season, we recommend that fuel loads be reduced in the forest by prescribed burning early in the dry season. This applies especially to areas where there is accumulation of biomass over years, such as that of the tall grass Themeda cymbaria found predominantly in dry deciduous forest types.
If prescribed burning is incorporated in fire management policies for these forests, then the season of burning will be important to consider. It is known from ecosystems where prescribed burning is regularly applied that early dry season fires are less intense than late dry season fires (Williams et al. 1998). However, this has not been systematically investigated for SDTFs. Through a burning experiment carried out in private land with vegetation type similar to tropical dry thorn forest, we investigated differences in area burnt, ground-level fire temperatures and soil temperatures one cm below the ground in the early dry season in January, late dry season in April and and early wet season in June. We also examined differences in fuel load, fuel moisture, soil moisture and weather conditions of ambient relative humidity (RH), temperature and wind speed in these phases; these factors could be responsible for observed differences in fire and soil temperatures or area burnt. Although area burnt was not significantly different between the early and late phases of the dry season, fire and soil temperatures were significantly lower in the former. The late dry season was characterized by distinctly higher fuel loads, lower fuel moisture, lower relative humidity, higher ambient temperatures and higher wind speeds compared that measured in the early dry season. Differences in soil temperature between these months may be attributed to the increase in fuel load since there were no significant differences in soil moisture. Fire spread was limited in the experimental plots in the early wet season in June, probably due to significantly higher levels of fuel moisture in this month; the resultant fire and soil temperatures recorded were low. Forest management should, therefore, consider early dry season burns in the month of January for prescribed burns in the sanctuary, although this would have to be tested in other SDTF vegetation types with more variable fuel load, fuel moisture and weather conditions.
Fire’s influence on the biotic community:
Concerns regarding the regeneration capacity of woody species in SDTFs have been voiced with respect to increasing frequencies of fire (Saha and Howe 2006, Kodandapani et al. 2008). Fire is known to cause high mortality of individuals of small size (Swaine et al. 1990, Suresh et al. 2010). However, mortality has been examined for large size classes, and not for seedlings. It is essential to understand the dynamics of seedlings and their contribution to the regeneration potential of SDTFs.
Woody species in SDTFs are known to have traits that help them recover from recurring disturbances, such as sprouting from underground root stocks (Vieira and Scariot 2006). Another trait may relate to growth rates of seedlings. Growth rates of seedlings (defined in this study as established individuals between 10 and 100cm height) after dry season (February-March) fires were compared between adjacent pairs of burnt and unburnt transects established at eight sites in Mudumalai across vegetation types of moist deciduous, dry deciduous and dry thorn forest. The growth of grasses, a possible competitor for resources, was also monitored at each site. Seedling and grass heights were monitored at 3-month intervals between August 2009 and August 2010. A second fire in March 2010 affected transects at two sites in Mudumalai. Seedling and grass heights were monitored for two enumerations till August 2010 subsequent to the second fire at these two sites. A total of 1032 individuals across 58 woody species were enumerated. High seedling survivorship (>95%) was observed in both burnt and unburnt areas. Although seedling heights were significantly different between burnt and unburnt areas at the start of the enumeration in August 2009, heights were comparable within a year and a half of the fire. Comparable seedling heights in such a short time span were because of distinctly higher growth rates of seedlings in burnt areas compared to unburnt areas after the fire event, particularly during the pre-monsoon season. Grass biomass (volume), on the other hand, was significantly different between burnt and unburnt areas at both the first and last enumerations. Grass growth (change in volume) did not differ between burnt and unburnt areas. Rapid growth by seedlings after a fire implies adaptation through the use of stored resources for growth, possibly aided by lower competition from grasses, in order to attain a certain size before the subsequent return of unfavourable factors such as a recurrent fire event.
Conclusions:
The results from the study point to climatically driven fire regimes in an SDTF in southern India, with daily influences of weather conditions during the dry season on fire occurrences. Fire intensities increase with increasing fuel loads in these forests, moderated by weather conditions such as RH and temperature. Since fires are an anthropogenic phenomenon in these forests, active management with the use of prescribed fires in the early phase of the dry season is a possible option to control late dry season fires that would be higher in intensity. The current woody tree species assemblage in this southern Indian SDTF is resilient to fires at the seedling stage, with established individuals exhibiting high survivorship and rapid growth after a fire. However, the effects of fires of varying intensities on the regenerative capacity of the seedlings are not known. The effect of fire on habitat utilisation by large herbivores, or the impact of fire on the faunal community in general has not been studied for vegetation types that comprise SDTFs. The effect of fire exclusion on the ecology of SDTFs will provide useful information that can feed into management policies for this ecosystem type. These are potential areas of research for the future. Fire, if managed wisely, can be an effective tool for the conservation of SDTFs across south and southeast Asia.
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Light Spectra Distributions in Temperate Conifer-Forest Canopy Gaps, Oregon and in Tropical Cloud-Forest Canopy, VenezuelaMonteleone, Susan Elaine 12 1900 (has links)
Light spectra distributions were measured in two different montane forests: temperate and tropical. Spectral light measurements were made in different sized canopy gaps in the conifer forest at H. J. Andrews Experimental Forest in Oregon, USA. Researchers at Oregon State University created these
gaps of 20 m, 30 m, and 50 m in diameter. In the tropical cloud forest, spectral light measurements were made in two plots that were permanently established at La Mucuy Parque Nacional in Venezuela, in collaboration with researchers at Universidad de Los Andes. In both studies, spectra and distributions of physiologically active light were analyzed: red, far-red, R/FR ratio, and blue light.
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A composição isotópica do CO2 respirado e sua variabilidade sazonal na Amazônia Oriental / Isotopic composition of respired CO2 and seasonal variability in the Amazon tropical ForestIshida, Françoise Yoko 24 September 2007 (has links)
O presente estudo foi conduzido na Floresta Nacional do Tapajós (FLONA) (2°51'S 54°58'W) localizado no km 67 nos anos de 2003 e 2004. O objetivo foi avaliar as mudanças na composição isotópica do carbono respirado por uma floresta e seus componentes (δ13CR), além da composição isotópica do material orgânico (δ13C) de folhas, solo, serapilheira e madeira morta. A técnica da reta de Keeling e a equação de Farquhar foram utilizadas para determinar o valor de δ13CR e para estimar o valor de ci/ca, respectivamente. De acordo com os resultados, o δ13C respirado pelo ecossistema foi significativamente influenciado pela sazonalidade em 2003. O δ13C das folhas apresentou uma estratificação significativa ao longo do perfil vertical, apresentando valores mais enriquecidos no topo de dossel. O valor médio de ci/ca apresentou um aumento vertical no sentido do sub-bosque. As correlações encontradas entre os valores de δ13C respirado com temperatura, DPV, RFA e precipitação indicam uma estreita relação entre as trocas gasosas e variabilidade climática local, onde a intensificação nas amostragens ao longo de dois anos consecutivos confirmou as diferenças sazonais observadas anteriormente. A definição dos padrões isotópicos de um ecossistema em diferentes condições climáticas é de fundamental importância para a melhor compreensão do ciclo do carbono, desde uma folha até o ecossistema; especialmente na região Amazônica onde as atividades antrópicas têm aumentado significativamente, fortalecendo o cenário de mudanças no clima. / This study was conducted in 2003 and 2004 at the km 67 old growth forest in the Tapajós National Forest (2 ° 51'S 54 ° 58'W). The objective was measure the carbon isotope ratio (13C/12C) of respired CO2 from the entire ecosystem and isotope composition of organic components leaves, soil, litter and dead wood. The Keeling plot technique and Farquhar's leaf model was used to examine the physiological drivers of the isotopic composition of these components as well as the seasonal response for them. A variation of respired δ13CR - CO2 by the ecosystem was well related with precipitation variation, VPD and PAR, and a significant seasonal difference was found in 2003. The δ13C of leaf organic matter showed a clear stratification along the vertical profile. The estimated ci/ca ratio values showed significant differences between heights and seasons. The results indicated that the isotopic composition of respired CO2 and organic matter was sensitive to microclimatic variations; so far the δ13C values can be used to understand how environmental changes can affect the carbon cycle at ecosystem scale.
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