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Woodland Savanna (woodland + savanna)
Selected AbstractsRain forest invasion of eucalypt-dominated woodland savanna, Iron Range, north-eastern Australia: II.JOURNAL OF BIOGEOGRAPHY, Issue 8 2004Rates of landscape change Abstract Aim, To explore rates of rain forest expansion and associated ecological correlates in Eucalyptus -dominated woodland savanna vegetation in north-eastern Australia, over the period 1943,91. Location, Iron Range National Park and environs, north-east Queensland, Australia. This remote region supports probably the largest extent of lowland (< 300 m) rain forest extant in Australia. Rainfall (c. 1700 mm p.a.) occurs mostly between November and June, with some rain typically occurring even in the driest months July,October. Methods, Interpretation of change in lowland rain forest vegetation cover was undertaken for a 140 km2 area comprising complex vegetation, geology and physiography using available air photos (1943, 1970 and 1991). A GIS database was assembled comprising rain forest extent for the three time periods, geology, elevation, slope, aspect, proximity to streams and roads. Using standard GIS procedures, a sample of 6996 10 × 10 m cells (0.5% of study area) was selected randomly and attributed for vegetation structure (rain forest and non-rain forest), and landscape features. Associations of rain forest expansion with landscape features were examined with logistic regression using the subset of cells that had changed from other vegetation types to rain forest, and remained rain forest over the assessment period, and comparing them with cells that showed no change from their original, non-rain forest condition. Results, Rain forest in the air photo study area increased from 45 km2 in 1943 to 78.1 km2 by 1970, and to 82.6 km2 by 1991. Rainfall (and atmospheric CO2 concentration) was markedly lower in the first assessment period (1943,70). Modelled rates of rain forest invasion differed predominantly with respect to substrate type, occurring faster on substrates possessing better moisture retention properties, and across all elevation classes. Greatest expansion, at least in the first assessment period, occurred on the most inherently infertile substrates. Expansion was little constrained by slope, aspect and proximity to streams and roads. On schist substrates, probability of invasion remained high (> 60%) over distances up to 1500 m from mature rain forest margins; on less favourable substrates (diorite, granites), probability of expansion was negligible at sites more than 400 m from mature margins. Main conclusions, (i) Rain forest expansion was associated primarily with release from burning pressure from c. the 1920s, following major disruption of customary Aboriginal lifestyles including hunting and burning practices. (ii) Decadal-scale expansion of rain forest at Iron Range supports extensive observations from the palaeoecological literature concerning rapid rain forest invasion under conducive environmental conditions. (iii) The generality of these substrate-mediated observations requires further testing, especially given that landscape-scale rain forest invasion of sclerophyll-dominated communities is reported from other regions of north-eastern Australia. [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] Historical biogeography of Androcymbium Willd. (Colchicaceae) in Africa: evidence from cpDNA RFLPsBOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2001JULI CAUJAPÉ-CASTELLS The cpDNA restriction variation in 39 populations representing a geographical sampling of 18 species of Androcymbium in southwestern and northern Africa was examined to assess the historical biogeography of the genus. The cpDNA phylogeny indicates that the disjunction between South and North Africa is best explained by the dispersal of southern African ancestors into North Africa. Divergence time estimates suggest that the geographic range of the genus may have extended considerably north (perhaps to Tanzania and Kenya) prior to the global desiccation of Africa in the Miocene. Further expansion of the genus northward was probably stalled until climatic changes in the late Miocene brought about the gradual replacement of a subtropical woodland savanna with the arid landscape that gave rise to the Sahara. Aridification of the northern quarter of the continent provided the ecological conditions for fostering the expansion of Androcymbium along the Mediterranean fringe (probably east to west) and its introduction into the Canary Islands. Unlike their South African congeners, the northern species have experienced expansions, fragmentations, and local extinctions in response to the severe climatic shifts in this area during the Pliocene-Pleistocene. According to our divergence time estimates, the arid track may have already existed as a continuous area connecting southern and northern Africa in the late Miocene. [source] Season of grazing and stocking rate interactively affect fuel loads in Baikiaea plurijuga Harms woodland in northwestern ZimbabweAFRICAN JOURNAL OF ECOLOGY, Issue 4 2008J. Gambiza Abstract Wildfire is a major disturbance in Baikiaea plurijuga Harms woodland savannas. We tested the hypothesis that the timing and intensity of herbivory influence fuel loads. We used three stocking rates namely light (three cows and four goats ha,1), medium (six cows and eight goats ha,1) and heavy (eleven cows and sixteen goats ha,1) and three times of grazing namely early-, middle- and late-growing seasons. Season of grazing and stocking rate influenced herbaceous phytomass. Phytomass was generally the highest (53.5 g DM m,2) in paddocks grazed during the early growing season and the lowest (27.8 g DM m,2) in those grazed during the late growing season. Phytomass was also generally the highest (40.4 g DM m,2) in lightly stocked paddocks and the lowest (32.7 g DM m,2) in heavily stocked ones. Litter mass was the lowest (160.8 g DM m,2) in paddocks grazed during the early season whereas there were no differences in ungrazed paddocks and those grazed during either mid- or late growing seasons (205.4 g DM m,2). There was a negative relationship between litter mass and stocking rate. Baikiaea Benth. woodlands should be grazed during either the mid- or late-growing season at stocking rates greater than 0.1 LU ha,1 to reduce grass fuel loads. Résumé Les feux de brousse sont une perturbation majeure dans les savanes arborées àBaikiaea plurijuga Harms. Nous avons testé l'hypothèse selon laquelle le timing et l'intensité de la consommation par les herbivores influenceraient la quantité de combustible. Nous avons utilisé trois taux de pâturage: léger (trois vaches et quatre chèvres par hectare), moyen (six vaches et huit chèvres par hectare) et élevé (11 vaches et 16 chèvres par hectare), et trois périodes de pâturage, à savoir au début, au milieu et à la fin de la période de croissance. La période de pâturage et le taux de pâturage influençaient la phytomasse herbacée. La phytomasse était généralement la plus élevée (53.5 g MS m,2) dans les enclos pâturés au début de la saison de croissance, et la plus faible (27.8 g MS m,2) dans ceux qui sont pâturés en fin de période de croissance. La phytomasse était aussi généralement la plus grande (40.4 g MS m,2) dans les enclos légèrement pâturés et la plus basse (32.7 g MS m,2) dans les enclos très pâturés. La biomasse végétale (litière) était la plus faible (160.8 g MS m,2) dans les enclos pâturés au début de la saison, alors qu'il n'y avait pas de différence entre les enclos non pâturés et ceux qui l'étaient au milieu ou à la fin de la période de croissance (205.4 g MS m,2). Il y avait une relation négative entre la masse de litière et le taux de pâturage. Les forêts àBaikiaea Benth. devraient être pâturés en milieu ou en fin de période de croissance, et à des taux plus élevés que 0.1 UFL ha,1, pour réduire la quantité de combustible herbacé. [source] | ||||||||||