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1.
This paper estimates the difference in stand biomass due to shorter and lighter trees in southwest (SW) and southern Amazonia (SA) compared to trees in dense forests in central Amazonia (CA). Forest biomass values used to estimate carbon emissions from deforestation throughout, Brazilian Amazonia will be affected by any differences between CA forests and those in the “arc of deforestation” where clearing activity is concentrated along the southern edge of the Amazon forest. At 12 sites (in the Brazilian states of Amazonas, Acre, Mato Grosso and Pará) 763 trees were felled and measurements were made of total height and of stem diameter. In CA dense forest, trees are taller at any given diameter than those in SW bamboo-dominated open, SW bamboo-free dense forest and SA open forests. Compared to CA, the three forest types in the arc of deforestation occur on more fertile soils, experience a longer dry season and/or are disturbed by climbing bamboos that cause frequent crown damage. Observed relationships between diameter and height were consistent with the argument that allometric scaling exponents vary in forests on different substrates or with different levels of natural disturbance. Using biomass equations based only on diameter, the reductions in stand biomass due to shorter tree height alone were 11.0, 6.2 and 3.6%, respectively, in the three forest types in the arc of deforestation. A prior study had shown these forest types to have less dense wood than CA dense forest. When tree height and wood density effects were considered jointly, total downward corrections to estimates of stand biomass were 39, 22 and 16%, respectively. Downward corrections to biomass in these forests were 76 Mg ha−1 (∼21.5 Mg ha−1 from the height effect alone), 65 Mg ha−1 (18.5 Mg ha−1 from height), and 45 Mg. ha−1 (10.3 Mg ha−1 from height). Hence, biomass stock and carbon emissions are overestimated when allometric relationships from dense forest are applied to SW or SA forest types. Biomass and emissions estimates in Brazil's National Communication under the United Nations Framework Convention on Climate Change require downward corrections for both wood density and tree height.  相似文献   

2.
Efforts are needed in order to increase confidence for carbon accounts in the land use sector, especially in tropical forest ecosystems that often need to turn to default values given the lack of precise and reliable site specific data to quantify their carbon sequestration and storage capacity. The aim of this study was then to estimate biomass and carbon accumulation in young secondary forests, from 4 and up to 20 years of age, as well as its distribution among the different pools (tree including roots, herbaceous understory, dead wood, litter and soil), in humid tropical forests of Costa Rica. Carbon fraction for the different pools and tree components (stem, branches, leaves and roots) was estimated and varies between 37.3% (±3.3) and 50.3% (±2.9). Average carbon content in the soil was 4.1% (±2.1). Average forest plant biomass was 82.2 (±47.9) Mg ha−1 and the mean annual increment for carbon in the biomass was 4.2 Mg ha−1 yr−1. Approximately 65.2% of total biomass was found in the aboveground tree components, while 14.2% was found in structural roots and the rest in the herbaceous vegetation and necromass. Carbon in the soil increased by 1.1 Mg ha−1 yr−1. Total stored carbon in the forest was 180.4 Mg ha−1 at the age of 20 years. In these forests, most of the carbon (51-83%) was stored in the soil. Models selected to estimate biomass and carbon in trees as predicted by basal area had R2 adjustments above 95%. Results from this study were then compared with those obtained for a variety of secondary and primary forests in different Latin-American tropical ecosystems and in tree plantations in the same study area.  相似文献   

3.
An accurate characterization of tree carbon (TC), forest floor carbon (FFC) and soil organic carbon (SOC) in tropical forest plantations is important to estimate their contribution to global carbon stocks. This information, however, is poor and fragmented. Carbon contents were assessed in patula pine (Pinus patula) and teak (Tectona grandis) stands in tropical forest plantations of different development stages in combination with inventory assessments and soil survey information. Growth models were used to associate TOC to tree normal diameter (D) with average basal area and total tree height (HT), with D and HT parameters that can be used in 6–26 years old patula pine and teak in commercial tropical forests as indicators of carbon stocks. The information was obtained from individual trees in different development stages in 54 patula pine plots and 42 teak plots. The obtained TC was 99.6 Mg ha−1 in patula pine and 85.7 Mg ha−1 in teak forests. FFC was 2.3 and 1.2 Mg ha−1, SOC in the surface layer (0–25 cm) was 92.6 and 35.8 Mg ha−1, 76.1 and 19 Mg ha−1 in deep layers (25–50 cm) in patula pine and teak, respectively. Carbon storage in trees was similar between patula pine and teak plantations, but patula pine had higher levels of forest floor carbon and soil organic carbon. Carbon storage in trees represents 37 and 60% of the total carbon content in patula pine and teak plantations, respectively. Even so, the remaining percentage corresponds to SOC, whereas FFC content is less than 1%. In summary, differences in carbon stocks between patula pine and teak trees were not significant, but the distribution of carbon differed between the plantation types. The low FFC does not explain the SOC stocks; however, current variability of SOC stocks could be related to variation in land use history.  相似文献   

4.
The recovery process of fallow stands in the mountainous region of Northwestern Vietnam was studied, based on a chronosequence of 1–26-year-old secondary forests after intensive shifting cultivation. The number of species present in a 26-year-old secondary forest attained 49% of the 72 species present in an old-growth forest. Total stem density decreased gradually from 172,500 ha−1 in a 3-year-old forest to 24,600 ha−1 in the 26-year-old stand, but stem density of larger trees (diameter at breast height (D) ≥ 5 cm) increased from 60 ha−1 in a 7-year-old to 960 ha−1 in the 26-year-old forests, which was similar to that of an old-growth forest. Annual biomass increment of the 26-year-old stand was 4.2 Mg ha−1 year−1. A saturation curve was fitted to biomass accumulation in secondary forests. After an estimated time of 60 years, a secondary forest can achieve 80% of the biomass of old-growth forests (240 Mg ha−1). Species diversity expressed by Shannon Index shows that it takes 60 years for a secondary forest in fallow to achieve a plant species diversity similar to that of old-growth forests.  相似文献   

5.
With increasing CO2 in the atmosphere, there is an urgent need of reliable estimates of biomass and carbon pools in tropical forests, most especially in Africa where there is a serious lack of data. Information on current annual increment (CAI) of carbon biomass resulting from direct field measurements is crucial in this context, to know how forest ecosystems will affect the carbon cycle and also to validate eddy covariance flux measurements. Biomass data were collected from 25 plots of 13 ha spread over the different vegetation types and land uses of a moist evergreen forest of 772,066 ha in Cameroon. With site-specific allometric equations, we estimated biomass and aboveground and belowground carbon pools. We used GIS technology to develop a carbon biomass map of our study area. The CAI was estimated using the growth rates obtained from tree rings analysis. The carbon biomass was on average 264 ± 48 Mg ha−1. This estimate includes aboveground carbon, root carbon and soil organic carbon down to 30 cm depth. This value varied from 231 ± 45 Mg ha−1 of carbon in Agro-Forests to 283 ± 51 Mg ha−1 of carbon in Managed Forests and to 278 ± 56 Mg ha−1 of carbon in National Park. The carbon CAI varied from 2.54 ± 0.65 Mg ha−1 year−1 in Agro-Forests to 2.79 ± 0.72 Mg ha−1 year−1 in Managed Forests and to 2.85 ± 0.72 Mg ha−1 year−1 in National Park. This study provides estimates of biomass, carbon pools and CAI of carbon biomass from a forest landscape in Cameroon as well as an appropriate methodology to estimate these components and the related uncertainty.  相似文献   

6.
The efficiency with which trees convert photosynthetically active radiation (PAR) to biomass has been shown to be consistent within stands of an individual species, which is useful for estimating biomass production and carbon accumulation. However, radiation use efficiency (?) has rarely been measured in mixed-species forests, and it is unclear how species diversity may affect the consistency of ?, particularly across environmental gradients. We compared aboveground net primary productivity (ANPP), intercepted photosynthetically active solar radiation (IPAR), and radiation use efficiency (? = ANPP/IPAR) between a mixed deciduous forest and a 50-year-old white pine (Pinus strobus L.) plantation in the southern Appalachian Mountains. Average ANPP was similar in the deciduous forest (11.5 Mg ha−1 y−1) and pine plantation (10.2 Mg ha−1 y−1), while ? was significantly greater in the deciduous forest (1.25 g MJ−1) than in the white pine plantation (0.63 g MJ−1). Our results demonstrate that late-secondary hardwood forests can attain similar ANPP as mature P. strobus plantations in the southern Appalachians, despite substantially less annual IPAR and mineral-nitrogen availability, suggesting greater resource-use efficiency and potential for long-term carbon accumulation in biomass. Along a 260 m elevation gradient within each forest there was not significant variation in ?. Radiation use efficiency may be stable for specific forest types across a range of environmental conditions in the southern Appalachian Mountains, and thus useful for generating estimates of ANPP at the scale of individual watersheds.  相似文献   

7.
This paper presents a synthesis of experiments conducted in a tropical tree plantation established in 2001 and consisting of 22 plots of 45 m × 45 m with either one, three or six native tree species. We examined the changes in carbon (C) pools (trees, herbaceous vegetation, litter, coarse woody debris (CWD), and mineral topsoil at 0-10 cm depth) and fluxes (decomposition of CWD and litter, as well as soil respiration) both through time and among diversity levels. Between 2001 and 2009 the aboveground C pools increased, driven by trees. Across diversity levels, the mean observed aboveground C pool was 7.9 ± 2.5 Mg ha−1 in 2006 and 20.4 ± 7.4 Mg ha−1 in 2009, a 158% increase. There was no significant diversity effect on the observed aboveground C pool, but we found a significant decrease in the topsoil C pool, with a mean value of 34.5 ± 2.4 Mg ha−1 in 2001 and of 25.7 ± 5.7 Mg ha−1 in 2009 (F1,36 = 52.12, p < 0.001). Assuming that the biomass C pool in 2001 was negligible (<1 Mg ha−1), then the plantation gained in C, on average, ∼20 and lost ∼9 Mg ha−1 in biomass and soil respectively, for an overall gain of ∼11 Mg ha−1 over 8 years. Across the entire data set, we uncovered significant effects of diversity on CWD decomposition (diversity: F2,393 = 15.93, p < 0.001) and soil respiration (monocultures vs mixtures: t = 15.35, df = 11, p < 0.05) and a marginally significant time × diversity interaction on the loss of total C from the mineral topsoil pool (see above). Monthly CWD decomposition was significantly faster in monocultures (35.0 ± 24.1%) compared with triplets (31.3 ± 21.0%) and six-species mixtures (31.9 ± 26.8%), while soil respiration was higher in monocultures than in mixtures (t = 15.35, df = 11, p < 0.001). Path analyses showed that, as diversity increases, the links among the C pools and fluxes strengthen significantly. Our results demonstrate that tree diversity influences the processes governing the changes in C pools and fluxes following establishment of a tree plantation on a former pasture. We conclude that the choice of tree mixtures for afforestation in the tropics can have a marked influence on C pools and dynamics.  相似文献   

8.
Selective logging is an important socio-economic activity in the Congo Basin but one with associated environmental costs, some of which are avoidable through the use of reduced-impact logging (RIL) practices. With increased global concerns about biodiversity losses and emissions of carbon from forest in the region, more information is needed about the effects of logging on forest structure, composition, and carbon balance. We assessed the consequences of low-intensity RIL on above-ground biomass and tree species richness in a 50 ha area in northwestern Gabon. We assessed logging impacts principally in 10 randomly located 1-ha plots in which all trees ?10 cm dbh were measured, identified to species, marked, and tagged prior to harvesting. After logging, damage to these trees was recorded as being due to felling or skidding (i.e., log yarding) and skid trails were mapped in the entire 50-ha study area. Allometric equations based on tree diameter and wood density were used to transform tree diameter into biomass.Logging was light with only 0.82 trees (8.11 m3) per hectare extracted. For each tree felled, an average of 11 trees ?10 cm dbh suffered crown, bole, or root damage. Skid trails covered 2.8% of the soil surface and skidding logs to the roadside caused damage to an average of 15.6 trees ?10 cm dbh per hectare. No effect of logging was observed on tree species richness and pre-logging above-ground forest biomass (420.4 Mg ha−1) declined by only 8.1% (34.2 Mg ha−1). We conclude from these data that with harvest planning, worker training in RIL techniques, and low logging intensities, substantial carbon stocks and tree species richness were retained in this selectively logged forest in Gabon.  相似文献   

9.
Changes in above-ground biomass (AGB) of 17 1 ha logged plots of terra firme rain forest in the eastern Amazon (Brazil, Paragominas) were monitored for four years (2004–2008) after reduced-impact logging. Over the same time period, we also monitored two 0.5 ha plots in adjacent unlogged forest. While AGB in the control plots changed little over the observation period (increased on average 1.4 Mg ha−1), logging resulted in immediate reductions in ABG that averaged 94.5 Mg ha−1 (±42.0), which represented 23% of the 410 Mg ha−1 (±64.9) present just prior to harvesting. Felled trees (dbh > 55 cm) accounted for 73% (±15) of these immediate losses but only 18.9 Mg ha−1 (±8.1) of biomass was removed in the extracted logs. During the first year after logging, the annual AGB balance (annual AGB gain by recruitment and growth − annual AGB loss by mortality) remained negative (−31.1 Mg ha−1 year−1; ±16.7), mainly due to continued high mortality rates of damaged trees. During the following three years (2005–2008), average net AGB accumulation in the logged plots was 2.6 Mg ha−1 year−1 (±4.6). Post-logging biomass recovery was mostly through growth (4.3 ± 1.5 Mg ha−1 year1 for 2004–2005 and 6.8 ± 0.9 Mg ha−1 year1 for 2005–2008), particularly of large trees. In contrast, tree recruitment contributed little to the observed increases in AGB (1.1 ± 0.6 Mg ha−1 year−1 for 2004–2005 and 3.1 ± 1.3 Mg ha−1 year−1 for 2005–2008). Plots with the lowest residual basal area after logging generally continued to lose more large trees (dbh ≥70 cm), and consequently showed the greatest AGB losses and the slowest overall AGB gains. If 100% AGB recovery is desired and the 30-year minimum cutting cycle defined by Brazilian law is adhered to, current logging intensities (6 trees ha−1) need to be reduced by 40–50%. Such a reduction in logging intensity will reduce financial incomes to loggers, but might be compensated for by the payment of environmental services through the proposed REDD (reduced emissions from deforestation and forest degradation) mechanism of the United Nations Framework Convention on Climate Change.  相似文献   

10.
Four forest stands each of twenty major forest types in sub-tropical to temperate zones (350 m asl–3100 m asl) of Garhwal Himalaya were studied. The aim of the study was to assess the stem density, tree diversity, biomass and carbon stocks in these forests and make recommendations for forest management based on priorities for biodiversity protection and carbon sequestration. Stem density ranged between 295 and 850 N ha−1, while total biomass ranged from 129 to 533 Mg ha−1. Total carbon storage ranged between 59 and 245 Mg ha−1. The range of Shannon–Wiener diversity index was between 0.28 and 1.75. Most of the conifer-dominated forest types had higher carbon storage than broadleaf-dominated forest types. Protecting conifer-dominated stands, especially those dominated by Abies pindrow and Cedrus deodara, would have the largest impact, per unit area, on reducing carbon emissions from deforestation.  相似文献   

11.
Data on the biomass and productivity of southeast Asian tropical forests are rare, making it difficult to evaluate the role of these forest ecosystems in the global carbon cycle and the effects of increasing deforestation rates in this region. In particular, more precise information on size and dynamics of the root system is needed. In six natural forest stands at pre-montane elevation (c. 1000 m a.s.l.) on Sulawesi (Indonesia), we determined above-ground biomass and the distribution of fine (d < 2 mm) and coarse roots (d > 2 mm), estimated above- and below-ground net production, and compared the results to literature data from other pre-montane paleo- and neotropical forests. The mean total biomass of the stands was 303 Mg ha−1 (or 128 Mg C ha−1), with the largest biomass fraction being recorded for the above-ground components (286 Mg ha−1) and 11.2 and 5.6 Mg ha−1 of coarse and fine root biomass (down to 300 cm in the soil profile), resulting in a remarkably high shoot:root ratio of c. 17. Fine root density in the soil profile showed an exponential decrease with soil depth that was closely related to the concentrations of base cations, soil pH and in particular of total P and N. The above-ground biomass of these stands was found to be much higher than that of pre-montane forests in the Neotropics, on average, but lower compared to other pre-montane forests in the Paleotropics, in particular when compared with dipterocarp forests in Malesia. The total above- and below-ground net primary production was estimated at 15.2 Mg ha−1 yr−1 (or 6.7 Mg C ha−1 yr−1) with 14% of this stand total being invested below-ground and 86% representing above-ground net primary production. Leaf production was found to exceed net primary production of stem wood. The estimated above-ground production was high in relation to the mean calculated for pre-montane forests on a global scale, but it was markedly lower compared to data on dipterocarp forests in South-east Asia. We conclude that the studied forest plots on Sulawesi follow the general trend of higher biomasses and productivity found for paleotropical pre-montane forest compared to neotropical ones. However, biomass stocks and productivity appear to be lower in these Fagaceae-rich forests on Sulawesi than in dipterocarp forests of Malesia.  相似文献   

12.
The net primary productivity of Bruguiera parviflora dominated mangrove forest at Kuala Selangor, Malaysia was estimated from the average yearly biomass increment and litter production. The average yearly biomass increment in saplings and trees was 0.58 and 16.51 t ha−1, respectively, and the annual amount of total litter production was 10.35 t ha−1. The biomass increment in saplings and trees was not significantly different (t-test, p > 0.05) in 2 successive years and the estimated net primary productivity was 27.44 t ha−1 year−1. The ratio (2.65:1) of net primary productivity and litterfall suggests that this mangrove forest is at a juvenile stage.  相似文献   

13.
Allometric equations were developed and applied to forest inventory data to estimate biomass and carbon stocks for temperate species and forests of Durango and Chihuahua and for tropical dry forests of Sinaloa, Mexico. A total of 872 trees were harvested and dissected into their component parts: leaves and branches, boles, and coarse roots. Coarse roots of 40 temperate trees ranging in diameter at breast height (DBH) from 6.0 to 52.9 cm were excavated in their entirety (i.e., >0.5 cm diameter). The species sampled (number of trees) in tropical dry forests (39) were Lysiloma divaricata (Jacq) Macbr. (10), Haematoxylon brasiletto Karst. (10), Cochlospermum vitifolium (Wild.) (5), Ceiba acuminata (S. Watson) Rose (5), Bursera penicillata (B. inopinnata) (5), and Jatropha angustifolia Mull. Arg. (4) and in temperate forests (833) were Quercus spp. (118) (Q. rugosa Neé, 15, Quercus sideroxylla Humb. & Bonpl, 51, Quercus spp., 52), Pinus herrerae Martinez 1940 (19), Pinus oocarpa Schiede ex Schlectendal 1838 (31), Pinus engelmannii Carriere 1854 (7), Psudotsuga menziesii (Mirb.) Franco (19), Pinus leiophylla Schiede ex Schlectendal et Chamisso 1831 (27), Pinus teocote Schiede ex Schlectendal et Chamisso (55), Pinus ayacahuite Ehrenb. ex Schltdl. (58), Pinus cooperi Blanco (48), Pinus durangensis Martinez 1942 (385), and Pinus arizonica Engelmann 1879 (66). Allometric equations having only DBH as an independent variable were developed for each component of each species. Since Pinus herrerae, Pinus engelmannii, Pinus oocarpa and Pseudotsuga menziensii had a small number of trees, an individual allometric equation was developed for these species. We used non-linear regression to fit parameters of the typical allometric power equation. The resulting 31 equations (10 species or groups of species, three biomass components; bole, branch and leaves, and total aerial; and the generalized equation for coarse roots) fit the data well and enable the user to predict biomass by component for each of the 10 different groups of species or each of six temperate species. A single allometric equation that incorporates the basic specific gravity for aboveground biomass of all temperate tree species also fit the data well, and this equation provides both the detail and the accuracy supplied by species-specific, plant-part-specific equations. Biomass equations coupled with forest inventory data for temperate (637 circular, 1/10 ha plots) and tropical dry forests (166 20 m × 20 m-quadrats) of northwestern Mexico predict a mean (confidence intervals) of 130 Mg ha−1 (4.2 Mg ha−1) and 73 Mg ha−1 (7.1 Mg ha−1) for total tree and total aboveground biomass, respectively. Large sample sizes and the economic and ecological importance of the species studied make this data set uniquely useful for biomass estimations and for understanding the inherent heterogeneity of tree structure in dynamic tropical and temperate environments of northwestern Mexico.  相似文献   

14.
Roots, stems, branches and needles of 160 Norway spruce trees younger than 10 years were sampled in seven forest stands in central Slovakia in order to establish their biomass functions (BFs) and biomass expansion factors (BEFs). We tested three models for each biomass pool based on the stem base diameter, tree height and the two parameters combined. BEF values decreased for all spruce components with increasing height and diameter, which was most evident in very young trees under 1 m in height. In older trees, the values of BEFs did tend to stabilise at the height of 3–4 m. We subsequently used the BEFs to calculate dry biomass of the stands based on average stem base diameter and tree height. Total stand biomass grew with increasing age of the stands from about 1.0 Mg ha−1 at 1.5 years to 44.3 Mg ha−1 at 9.5 years. The proportion of stem and branch biomass was found to increase with age, while that of needles was fairly constant and the proportion of root biomass did decrease as the stands grew older.  相似文献   

15.
As in many other developing countries, the state government of Acre, Brazil, is developing a program for compensating forest holders (such as communities of rubber tappers and indigenous peoples as well as small, medium and large private land holders) reducing their emission of atmospheric heat-trapping gases by not deforesting. We describe and then apply to Acre a method for estimating carbon stocks by land cover type. We then compare the results of our simple method, which is based on vegetation mapping and ground-based samples, with other more technically demanding methods based on remote sensing. We estimated total biomass carbon stocks by multiplying the measured above-ground biomass of trees >10 cm DBH in each of 18 forest types and published estimates for non-forest areas, as determined by measurement of 44 plots throughout the state (ranging from 1 to 10 ha each), by land-cover area estimated using a geographical information system. State-wide, we estimated average above-ground biomass in forested areas to be 246 ± 90 Mg ha−1; dense forest showed highest (322 ± 20 Mg ha−1) and oligotrophic dwarf forest (campinarana) the lowest biomass (20 ± 30 Mg ha−1). The two most widespread forest types in Acre, open canopy forests dominated by either palms and bamboo (for which ground-based data are scant), support an estimated 246 ± 44 and 224 ± 50 Mg ha−1 of above-ground biomass, respectively. We calculate the total above-ground biomass of the 163,000 km2 State of Acre to be 3.6 ± 0.8 Pg (non-forest biomass included). This estimate is very similar to two others generated using much more technologically demanding methods, but all three methods, regardless of sophistication, suffer from lack of field data.  相似文献   

16.
Despite widespread use of intensive vegetation control (VC) in forest management, the effects of VC on allocation of biomass and nutrients between young trees and competing vegetation are not well understood. On three Pacific Northwest sites differing in productivity, soil parent material, and understory vegetation community, we evaluated year-5 effects of presence/absence of 5 years of VC on allocation of aboveground biomass and nitrogen (N) between planted Douglas-fir (Pseudotsuga menziesii var. menziesii) and competing vegetation. Equations for predicting bole, branch, foliar, and total dry weights based on stem diameter at a height of 15 cm and total tree height did not differ significantly among sites or by presence or absence of VC. This contrasts with previous research, using diameter at breast height rather than at 15 cm, which found that separate equations were warranted for trees with and without competing vegetation. Estimated whole-tree biomass among the six site/VC combinations ranged from 0.8 to 7.5 Mg ha−1, and increases in tree biomass associated with VC ranged from 62% to 173% among sites. Among the three sites, there were positive, linear relationships between soil total N content to a depth of 60 cm and both N content of aboveground vegetation (trees plus competing vegetation) and Douglas-fir foliar N concentration. Tree N content increased by 8.4, 8.2, and 40.0 kg N ha−1 with VC at the three sites, whereas competing vegetation N content decreased with VC by 0.9, 18.8, and 32.0 kg N ha−1, respectively, at the same sites. Thus, VC did not lead to a direct compensatory tradeoff between aboveground N content of trees and other vegetation. However, soil N content was linearly related to N accumulation and plant growth across the three sites. In addition to differences in N availability among sites, the effect of VC on the redistribution of resources among trees and competing vegetation also was influenced by vegetation community composition and efficacy of VC treatments.  相似文献   

17.
Anthropogenic understory fires have affected large areas of tropical forest in recent decades, particularly during severe droughts. Yet, the mechanisms that control fire-induced mortality of tropical trees and lianas remain ambiguous due to the challenges associated with documenting mortality given variation in fire behavior and forest heterogeneity. In a seasonally dry Amazon forest, we conducted a burn experiment to quantify how increasing understory fires alter patterns of stem mortality. From 2004 to 2007, tree and liana mortality was measured in adjacent 50-ha plots that were intact (B0 - control), burned once (B1), and burned annually for 3 years (B3). After 3 years, cumulative tree and liana mortality (≥1 cm dbh) in the B1 (5.8% yr−1) and B3 (7.0% yr−1) plots significantly exceeded mortality in the control (3.2% yr−1). However, these fire-induced mortality rates are substantially lower than those reported from more humid Amazonian forests. Small stems were highly vulnerable to fire-induced death, contrasting with drought-induced mortality (measured in other studies) that increases with tree size. For example, one low-intensity burn killed >50% of stems <10 cm within a year. Independent of stem size, species-specific mortality rates varied substantially from 0% to 17% yr−1 in the control, 0% to 26% yr−1 in B1, and 1% to 23% yr−1 in B3, with several species displaying high variation in their vulnerability to fire-induced mortality. Protium guianense (Burseraceae) exhibited the highest fire-induced mortality rates in B1 and B3, which were 10- and 9-fold greater than the baseline rate. In contrast, Aspidosperma excelsum (Apocynaceae), appeared relatively unaffected by fire (0.3% to 1.0% mortality yr−1 across plots), which may be explained by fenestration that protects the inner concave trunk portions from fire. For stems ≥10 cm, both char height (approximating fire intensity) and number of successive burns were significant predictors of fire-induced mortality, whereas only the number of consecutive annual burns was a strong predictor for stems <10 cm. Three years after the initial burn, 62 ± 26 Mg ha−1 (s.e.) of live biomass, predominantly stems <30 cm, was transferred to the dead biomass pool, compared with 8 ± 3 Mg ha−1 in the control. This biomass loss from fire represents ∼30% of this forest's aboveground live biomass (192 (±3) Mg ha−1; >1 cm DBH). Although forest transition to savanna has been predicted based on future climate scenarios, our results indicate that wildfires from agricultural expansion pose a more immediate threat to the current carbon stocks in Amazonian forests.  相似文献   

18.
The above- and belowground biomass and nutrient content (N, P, K, Ca, S and Mg) of pure deciduous Nothofagus antarctica (Forster f.) Oersted stands grown in a marginal site and aged from 8 to 180 years were measured in Southern Patagonia. The total biomass accumulated ranged from 60.8 to 70.8 Mg ha−1 for regeneration and final growth stand, respectively. The proportions of belowground components were 51.6, 47.2, 43.9 and 46.7% for regeneration, initial growth, final growth and mature stand, respectively. Also, crown classes affected the biomass accumulation where dominant trees had 38.4 Mg ha−1 and suppressed trees 2.6 Mg ha−1 to the stand biomass in mature stand. Nutrient concentrations varied according to tree component, crown class and stand age. Total nutrient concentration graded in the fallowing order: leaves > bark > middle roots > small branches > fine roots > sapwood > coarse roots > heartwood. While N and K concentrations increased with age in leaves and fine roots, concentration of Ca increased with stand age in all components. Dominant trees had higher N, K and Ca concentrations in leaves, and higher P, K and S concentrations in roots, compared with suppressed trees. Although the stands had similar biomass at different ages, there were important differences in nutrient accumulation per hectare from 979.8 kg ha−1 at the initial growth phase to 665.5 kg ha−1 at mature stands. Nutrient storage for mature and final growth stands was in the order Ca > N > K > P > Mg > S, and for regeneration stand was Ca > N > K > Mg > P > S. Belowground biomass represented an important budget of all nutrients. At early ages, N, K, S, Ca and Mg were about 50% in the belowground components. However, P was 60% in belowground biomass and then increased to 70% in mature stands. These data can assist to quantify the impact of different silviculture practices which should aim to leave material (mainly leaves, small branches and bark) on the site to ameliorate nutrient removal and to avoid a decline of long-term yields.  相似文献   

19.
Hurricane disturbance has the potential to markedly affect coastal forest structure and ecosystem processes. This study focused on the impacts of Hurricane Katrina in Louisiana's Pearl River basin, which lies just west of Katrina's final landfall at the Louisiana–Mississippi border. Prior to landfall, composition and structure of bottomland hardwood forests in this region were studied with permanent forest inventory plots sampled in 1989, 1998, 2005 and following the storm in 2006. This enabled a direct comparison of forest structure and dynamics before and after the disturbance, including species-specific tree mortality and damage rates, biomass production, and differences among forest types having varied hydrologic regimes. Background tree mortality rate before Hurricane Katrina was 1.9%, while average annual mortality was 20.5% for the census interval including the disturbance. Change in live tree biomass estimated from allometric models demonstrated a shift from an average annual production of 3.5 Mg ha−1 before the disturbance, to an average loss of 77.6 Mg ha−1 from the storm. Damage associated with Hurricane Katrina varied significantly with tree species but not tree size. Flooded cypress-tupelo swamp forests sustained the least damage and frequently flooded bottomland hardwood forests sustained the highest damage. Hurricane disturbance influenced the structure and composition of these coastal forests through species-specific differences in damage and mortality rates, and varied impacts dependent on forest flooding regime.  相似文献   

20.
Land-use and land cover strongly influence carbon (C) storage and distribution within ecosystems. We studied the effects of land-use on: (i) above- and belowground biomass C, (ii) soil organic C (SOC) in bulk soil, coarse- (250–2000 μm), medium- (53–250 μm) and fine-size fractions (<53 μm), and (iii) 13C and 15N abundance in plant litter, bulk soil, coarse-, and medium- and fine-size fractions in the 0–50 cm soil layer in Linaria AB, Canada between May and October of 2006. Five adjacent land-uses were sampled: (i) agriculture since 1930s, (ii) 2-year-old hybrid poplar (Populusdeltoides × Populus × petrowskyana var. Walker) plantation, (iii) 9-year-old Walker hybrid poplar plantation, (iv) grassland since 1997, and (v) an 80-year-old native aspen (Populus tremuloides Michx.) stand. Total ecosystem C stock in the native aspen stand (223 Mg C ha−1) was similar to that of the 9-year-old hybrid poplar plantation (174 Mg C ha−1) but was significantly greater than in the agriculture (132 Mg C ha−1), 2-year-old hybrid poplar plantation (110 Mg C ha−1), and grassland (121 Mg C ha−1). Differences in ecosystem C stocks between the land-uses were primarily the result of different plant biomass as SOC in the 0–50 cm soil layer was unaffected by land-use change. The general trend for C stocks in soil particle-size fractions decreased in the order of: fine > medium > coarse for all land-uses, except in the native aspen stand where C was uniformly distributed among soil particle-size fractions. The C stock in the coarse-size fraction was most affected by land-use change whilst the fine fractions the least. Enrichment of the natural abundances of 13C and 15N across the land-uses since time of disturbance, i.e., from agriculture to 2- and then 9-year-old hybrid poplar plantations or to grassland, suggests shifts from more labile forms of C to more humified forms of C following those land-use changes.  相似文献   

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