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Diameter Increments (diameter + increment)
Selected AbstractsEffects of Season, Rainfall, and Hydrogeomorphic Setting on Mangrove Tree Growth in MicronesiaBIOTROPICA, Issue 2 2007Ken W. Krauss ABSTRACT Seasonal patterns of tree growth are often related to rainfall, temperature, and relative moisture regimes. We asked whether diameter growth of mangrove trees in Micronesia, where seasonal changes are minimal, is continuous throughout a year or conforms to an annual cycle. We installed dendrometer bands on Sonneratia alba and Bruguiera gymnorrhiza trees growing naturally within mangrove swamps on the islands of Kosrae, Federated States of Micronesia (FSM), Pohnpei, FSM, and Butaritari, Republic of Kiribati, in the eastern Caroline Islands of the western Pacific Ocean. Trees were remeasured monthly or quarterly for as long as 6 yr. Annual mean individual tree basal area increments ranged from 7.0 to 79.6 cm2/yr for all S. alba trees and from 4.8 to 27.4 cm2/yr for all B. gymnorrhiza trees from Micronesian high islands. Diameter increment for S. alba on Butaritari Atoll was lower at 7.8 cm2/yr for the one year measured. Growth rates differed significantly by hydrogeomorphic zone. Riverine and interior zones maintained up to seven times the annual diameter growth rate of fringe forests, though not on Pohnpei, where basal area increments for both S. alba and B. gymnorrhiza were approximately 1.5 times greater in the fringe zone than in the interior zone. Time-series modeling indicated that there were no consistent and statistically significant annual diameter growth patterns. Although rainfall has some seasonality in some years on Kosrae and Pohnpei and overall growth of mangroves was sometimes related positively to quarterly rainfall depths, seasonal diameter growth patterns were not distinctive. A reduced chance of moisture-related stress in high-rainfall, wetland environments may serve to buffer growth of Micronesian mangroves from climatic extremes. [source] Tree growth in an African woodland savanna affected by disturbanceJOURNAL OF VEGETATION SCIENCE, Issue 3 2006R.M. Holdo Abstract: Questions: How does tree growth in a tropical woodland savanna vary as a function of size, and how is it affected by competition from neighbours, site attributes, and damage caused by disturbance? Location: western Zimbabwe. Methods: Trees of common species were tagged, mapped, and measured annually between 2001 and 2003 in a Kalahari sand woodland savanna. Diameter increments were analysed with mixed model regressions for the largest ramet in each genet. Stem diameter and damage, soil texture, and indices of competition at multiple spatial scales were used as covariates. Results: Stem diameter increased initially and then declined as a function of size in undamaged trees, which grew faster than damaged trees. Growth in damaged trees declined with size. No site differences were detected, and there was evidence for between-tree competition on growth only in the fastest-growing species, Brachystegia spiciformis. In several species the growth rate of the largest ramet increased as a function of the basal area of secondary ramets, contrary to expectations. For many species, the growth models showed poor explanatory power. Conclusions: Growth in Kalahari sand savanna trees varies as a function of size and changes in tree architecture caused by disturbance agents such as fire, frost, and elephant browsing. Disturbance may thus play an important role on vegetation dynamics through its effects on growth in the post-disturbance phase. Growth is highly stochastic for some species in this system, and more deterministic in others. It is hypothesized that this dichotomy may be driven by differences in rooting depth among species. [source] Influence of canopy tree size on stand basal area may reflect uncoupling of crown expansion and trunk diameter growthAUSTRAL ECOLOGY, Issue 2 2003Christopher H. Lusk Abstract A recent article by Midgley and colleagues suggests that large trees give rise to inordinately high stand basal areas because they pack canopy space more efficiently than smaller trees. We argue that this phenomenon bears more relation to the fact that diameter increment is not necessarily accompanied by significant crown expansion during all stages of a tree's life. Using data from a canopy tree population in an old-growth temperate forest, we found that crown area scaled as roughly the 3/5 power of trunk basal area. Rather than reflecting fixed scaling laws, we suggest that this pattern arises because of limited opportunities for crown expansion in dense stands. Old canopy trees in dense stands can thus accumulate large basal areas without occupying a commensurately large canopy area. [source] Testing liana cutting and controlled burning as silvicultural treatments for a logged forest in the eastern AmazonJOURNAL OF APPLIED ECOLOGY, Issue 6 2001Jeffrey J. Gerwing Summary 1In the eastern Brazilian Amazon, logged forests frequently include patches where liana density is particularly high. In these so-called liana tangles, competition from lianas is predicted to reduce tree growth significantly, thus effectively impeding future timber production. To begin to develop a silvicultural strategy for these patches, the impact of liana cutting and controlled burning on liana density, tree growth and tree regeneration in liana-dominated patches was investigated in a logged forest in the eastern Brazilian Amazon. 2The two treatments (liana cutting and controlled burning) and a control were installed in 40 × 40-m plots in a randomized complete block design of six blocks. Treatments were conducted during October 1997, and tree diameter growth and mortality, canopy cover, regeneration and liana density were monitored over 2 years. 3Mean mortality following burning was significantly higher for lianas (79%) than for trees (48%), as was the mean coppicing rate of top-killed stems (42% for lianas vs. 20% for trees). Coppicing combined with some recruitment from seed resulted in liana densities in the burned plots returning to 70% of the values in the control plots only 2 years post-treatment. 4Canopy light transmittance, estimated from hemispherical canopy photographs taken at 1 m above the ground, increased significantly from c. 4% in controls to 8% in cut and 12% in burned treatments, and these differences persisted over the 2-year study period. 5In the absence of silvicultural intervention, mean tree diameter increments were low (1·3 mm year,1), suggesting that the successional transition to higher stature forest was occurring very slowly. Each of the treatments resulted in a more than doubling of mean annual tree growth (3 and 2·8 mm year,1 for liana-cut and burned treatments, respectively). The treatments also significantly reduced the occurrence of trees that showed no growth over the study period, from 56% in controls to 30% in cut and 32% in burned treatments. 6The results of this study suggest that although burning resulted in increased tree growth, rapid recolonization of surviving trees by lianas and the high vulnerability of burned stands to unwanted repeat burns are likely to cancel out any of the possible benefits of controlled burning as a silvicultural treatment for liana-dominated patches. Liana cutting, on the other hand, showed promise and its adoption as part of a larger strategy for the recuperation of the timber production potential of logged tropical forests seems warranted. [source] Natural regeneration and population dynamics of the tree Afzelia quanzensis in woodlands in Southern AfricaAFRICAN JOURNAL OF ECOLOGY, Issue 4 2009Karin Gerhardt Abstract The logging of tree species of high commercial value is increasing throughout the African continent, yet the ecology of these species is generally poorly known. We studied the regeneration pattern and size class distribution of Afzelia quanzensis populations in northern South Africa over a 5-year period. Recruitment was low as the annual seedling mortality was >65%. Seedlings were located under the canopy and were affected by drought and browsing. The adults were scattered or were in a clump-dispersed pattern, which would result in higher recruitment of offspring near parents. Individuals of 0,10 cm diameter at breast height (DBH) were few, while there were 32 trees ha,1 at >10 cm DBH with an annual mortality of 0.8%. Annual diameter increments varied between 0.06 and 0.28 cm. It appears that the transition from the sapling into the juvenile stage could be a bottleneck in the regeneration of the species. A longer study, including more rainfall cycles, may reveal other patterns as dry and wet years have different impacts on dynamics. Résumé La coupe d'espèces d'arbres de grande valeur commerciale augmente dans tout le continent africain, pourtant l'écologie de ces espèces est généralement mal connue. Nous avons étudié le schéma de régénération et la distribution des classes d'âge des populations d'Afzelia quanzensis dans le nord de l'Afrique du Sud pendant cinq ans. Le recrutement était faible car la mortalité annuelle des jeunes plants était de plus de 65%. Les jeunes plans se trouvaient sous la canopée et étaient affectés par la sécheresse et par le broutage des animaux. Les adultes étaient dispersés ou se trouvaient en un schéma en bosquet, qui résulte en un plus fort recrutement de la progéniture près des parents. Les individus de 0,10 cm DBH étaient rares, alors qu'il y avait32 arbres ha,1à >10 cm DBH, avec une mortalité annuelle de 0,8%. L'incrément annuel du diamètre variait entre 0,06 et 0,28 cm. Il semble que la transition entre le stade de jeune arbre et celui de juvénile pourrait bien constituer un étranglement dans la régénération de l'espèce. Une étude plus longue, comprenant plus de cycles de pluies, pourrait révéler un autre schéma étant donné que les années sèches et humides ont des impacts différents sur cette dynamique. [source] Effects of selective logging on tree diversity, composition and plant functional type patterns in a Bornean rain forestJOURNAL OF VEGETATION SCIENCE, Issue 1 2003René Verburg Sidiyasa et al. (1999); Anon. (1955,1994) Abstract. The effects of selective logging on tree diversity, changes in tree species composition and plant functional types were studied with the use of seven permanent plots in virgin and in logged forest. All plots were located in a lowland dipterocarp rain forest in East Kalimantan on the island of Borneo. Just after logging and during the following 20 yr tree diversity measured as Fishers', was not significantly affected in logged forest plots. Temporal shifts in tree species composition were analysed with Principal Component Analysis (PCA). Logged forest plots had much larger changes over time than virgin forest plots. In the smallest diameter class, some logged forest plots showed a distinct trajectory in PCA space compared to virgin forest plots, while in larger diameter classes movement of logged plots in PCA space was random. This suggests that there is no predetermined community to which logged forest plots tend to shift when recovering from logging. We found a significant negative correlation between diameter increments and the species-specific wood densities of tree species. Species-specific wood density and potential tree height were used to assign species to five PFTs. As expected, logging increased the fraction of softwood stems in small diameter classes. In the largest diameter classes (, 50 cm DBH) a strong decrease of softwood emergent stems was found in logged forest plots. After more than 20 yr no recruitment was found of softwood emergent stems in selectively logged forest. [source] The microclimate under coloured hailnets affects leaf and fruit temperature, leaf anatomy, vegetative and reproductive growth as well as fruit colouration in appleANNALS OF APPLIED BIOLOGY, Issue 1 2010A. Solomakhin The purpose of this study was to investigate supposedly positive biological effects of coloured hailnets on microclimate, including photosynthetically active radiation (PAR), UV-B, air, soil, fruit and leaf temperature as well as humidity, which in turn may affect leaf anatomy, tree growth and fruit quality; apple was chosen as a model crop at Klein-Altendorf near Bonn, Germany; adjacent uncovered trees served as control. Red and green hailnets transmitted 3,6% more red or green light, without alteration of the red:far red (R,666 nm:FR,730 nm) ratio (0.99,1.01:1) and hence without affecting the phytochrome system. The microclimate was changed with a reduction by 12,23% in PAR and, to a larger extent, by 20,28% in UV, viz. shading. Light measurements at a 45° angle, to mimic the fruit or leaf position, showed that PAR was 90,210 µmol m,2 s,1 larger outside on a sunny summer day than under the white or red-white and 150,340 µmol m,2 s,1 larger than under red-black and green-black hailnets. Air temperature and relative humidity under coloured hailnets decreased by ca. 1.3°C and by ca 2% rh (cloudy) to 5% rh (sunny day), respectively, compared with outside; leaf temperature was decreased by up to 3°C and fruit temperature by up to 6°C. Soil temperatures at 5 cm depth were 0.5,1°C colder under red-black and green-black hailnets, but up to 0.9°C warmer under white and red-white hailnets compared with the uncovered control outside. Alternate bearing had a larger impact on vegetative growth in the affected year than the coloured hailnets; annual trunk diameter increments in cv. ,Fuji', i.e. the variety susceptible to alternate bearing, showed a larger variation than cv. ,Pinova' without alternate bearing. Reproductive growth, viz. return bloom and leaf anatomy were impaired by the coloured hailnets. Apple trees under dark hailnets developed thinner leaves with a thinner epidermis and fewer layers of palisade cells. These leaves were 3.5°C (dark hailnets) and 2.5°C (white hailnets) cooler than outside on a sunny day compared with ca. 1.5°C (dark hailnets) and 0.85°C (white hailnets) on a cloudy day. Transpirational cooling of cv. ,Fuji' leaves was 0.3,0.6°C outside and 1.4,1.6°C under the green-black hailnet on sunny days compared to <0.1°C on cloudy days. As a practical application, apple fruit colouration was dependent on light (PAR and UV-B) transmission of the respective hailnet colour. [source] | ||||||||||