We caught the adults of a secondary wood-boring insect, Callidiellum rufipenne (Motschulsky), on Japanese cedar, Cryptomeria japonica D. Don., trees and logs with manipulated bark water contents to clarify the mechanism of host selection by C. rufipenne. More C. rufipenne were trapped when the bark water content range was ca. 120–200%. Fewer C. rufipenne were trapped at higher and lower bark water contents. These findings indicate that C. rufipenne adults do not simply select weakened or dying trees. Bark water content is one of important factors for C. rufipenne choosing their host for oviposition. 相似文献
The coastal forest of Gabon abounds in monospecific secondary Aucoumea klaineana stands derived from natural regeneration after shifting cultivation. This paper aims to describe the changes in the structure and dynamics of these stands with age. It then assesses the impact of selective thinning in the upper storey on both structural and dynamic parameters.
The experiment consisted of 34 Permanent Plots in stands from establishment to more mature stages (ca. 50 years old). Thirteen plots (17–45 years old) were thinned. More than 80% of the removal came from supernumerary dominant A. klaineana.
A. klaineana represented 60% of the total density in stands ca. 15 years old but >90% of the dominant trees in older stands. The changes with age in the floristic composition of the unthinned stands showed three successional stages during which pioneer species associated with A. klaineana (from establishment to ca. 15 years) were progressively replaced by mature forest species.
Basal area increased and density decreased with age before reaching stable values at ca. 40–45 years. Mortality was very high in young stands but decreased in the older ones. Mortality generally affected small diameter individuals in the dominated storey. Diameter and basal area increments showed that the stand growth resulted from the growth of dominant A. klaineana. Diameter increments of A. klaineana were elevated during the first years of colonisation (1.9 cm/year) and were still ca. 0.7 cm/year for 50-year-old dominant trees.
Thinning did not increase the mortality of the dominant population. It favoured the individual growth of A. klaineana. The gain was substantial for dominated trees and small dominant trees (from 60 to 100%) but was lower for large dominant trees (ca. 25–30%). Therefore, stimulation of individual growth did not compensate for the loss of basal area at the stand level. 相似文献
In July 1992 the Rondônia Agroforestry Pilot Project (RAPP) was launched in two agricultural municipalities (Nova União and Alto Paraiso) in the western Brazilian Amazon State of Rondônia. The purpose of the RAPP was to assess the conditions under which colonist farmers in the western Amazon would integrate agroforestry plantings into their small-scale farming systems and to assess the performance of those plantings over time. An experimental group consisting of 50 small-scale farmers was selected to participate. Plots were designed to accommodate between 3 and 25 different species, each producing one or more commodities with local market potential (hardwood, fruits, nuts, latexes, oils). Farmers planted seedlings typically on a 1-ha plot, located and designed by each farmer with the advice of a professional Brazilian extensionist. During the first phase of the project (1992–1998), the growth performance of the seedlings and changes in household characteristics were monitored on an annual basis. By 2002, 32 (64.0%) of the original 50 agroforest plots were found in place. This paper updates the research findings based on a 2002 follow-up visit to these 32 farms. In addition to growth performance, the authors’ found that 17.95% of the farms in the neighboring control group had planted trees and other agroforest crops between 1992 and 2002, compared to only 5.38% of farms outside the project area, suggesting spontaneous diffusion. The authors also found a potentially synergistic relationship between agroforestry and secondary forest regeneration with the use of satellite image analysis. The experience of the RAPP indicates that colonist farmers in Amazonia can be successful managers of agroforest plots with minimal external inputs over the long-term (10 years). 相似文献
In order to infer successional changes in structure, species composition and diversity of warm-temperate forest, we compared secondary stands regenerating after clear-felling (41–64-years old) with old-growth stands at altitudes between 300 and 800 m on Yakushima Island, southern Japan. Stem density and maximum stem diameter differed between secondary and old-growth stands, but basal area and aboveground biomass did not. At lower altitudes, the dominant species in old-growth stands with a strong sprouting capacity (Castanopsiscuspidata) also dominated secondary stands, and species composition of secondary and old-growth stands was similar. At higher altitudes, by contrast, the dominant species in old-growth stands (Distyliumracemosum) had little sprouting capacity and was poorly represented in diverse secondary stands, which were dominated by Castanopsis or other less abundant species. Secondary stands had greater species diversity (Shannon–Wiener index) than old-growth stands, particularly at higher altitudes. This was due to greater species richness resulting from higher stem density per area, but not to greater evenness. We grouped the component species that share ecologically similar traits into four guilds (fagaceous, primary evergreen, secondary evergreen and deciduous species). Secondary stands were characterized by greater numbers of deciduous and secondary evergreen species. We concluded that different sprouting capacities of dominant species and different regeneration traits among guilds are responsible for the change in species composition and diversity during succession. 相似文献
Recent studies have remarked on differences in the life cycles of individual fine roots. However, the dynamics of individual roots with different life cycles, such as ephemeral and perennial, during root system development are still unknown. We examined individual roots during fine root system development in a mature stand of Chamaecyparis obtusa Sieb. et Zucc. (Cupressaceae) using the sequential ingrowth core method and an anatomical method. The visual classification, i.e., orange, red, brown, intact dead, and fragmented dead, of fine roots corresponded well with the anatomical classification. Orange and red roots contained passage cells, and brown roots contained cork cambium. The proportions of protoxylem groups differed among visual classes. Brown secondary roots were mainly triarch (43%) and tetrarch (40%) and rarely diarch (12%), whereas fragmented dead roots, which constituted more than 95% of the dead roots, were mainly diarch (67%). These results imply that triarch and tetrarch roots tend to form secondary roots, whereas diarch roots tend to become dead roots without secondary growth. Using the numbers of root tips and clusters, root system development could be classified into three stages: colonization, branching within the root system, and maintenance. During the colonization stage, mainly triarch and tetrarch roots, which tend to be secondary growth, invaded ingrowth cores. During the branching stage, primarily diarch roots, which tend to be ephemeral, emerged. Fine root system development involved the recruitment of different individual roots during the life cycle depending on the growth stage. 相似文献
Carbon stocks in vegetation replacing forest in Brazilian Amazonia affect net emissions of greenhouse gases from land-use change. A Markov matrix of annual transition probabilities was constructed to estimate landscape composition in 1990 and to project future changes, assuming behavior of farmers and ranchers remains unchanged. The estimated 1990 landscape was 5.4% farmland, 44.8% productive pasture, 2.2% degraded pasture, 2.1% ‘young’ (1970 or later) secondary forest derived from agriculture, 28.1% ‘young’ secondary forest derived from pasture, and 17.4% ‘old’ (pre-1970) secondary forest. The landscape would eventually approach an equilibrium of 4.0% farmland, 43.8% productive pasture, 5.2% degraded pasture, 2.0% secondary forest derived from agriculture, and 44.9% secondary forest derived from pasture. An insignificant amount is regenerated ‘forest’ (defined as secondary forest over 100 years old). Average total biomass (dry matter, including below-ground and dead components) was 43.5 t ha−1 in 1990 in the 410 × 103 km2 deforested by that year for uses other than hydroelectric dams. At equilibrium, average biomass would be 28.5 t ha−1 over all deforested areas (excluding dams). These biomass values are more than double those forming the basis of deforestation emission estimates currently used by the Intergovernmental Panel on Climate Change (IPCC). Although higher replacement landscape biomass decreases net emissions from deforestation, these estimates still imply large net releases. 相似文献