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Semiarid Areas (semiarid + area)
Selected AbstractsLivelihood diversification and implications on dryland resources of central TanzaniaAFRICAN JOURNAL OF ECOLOGY, Issue 2009Emma T. Liwenga Abstract The concern over sustainable livelihoods in African drylands is an issue that has received considerable attention from researchers and policy makers alike. Over the past two decades African rural areas have undergone rapid changes, whereby, rural income diversification has become the most salient feature. With a particular focus on dryland ecosystems, among the major challenges facing communities in these areas is recurrent drought leading to conditions of food insecurity. This paper draws on experience on coping mechanisms for food insecurity from an agro-pastoral community in Mvumi, located in the semiarid areas of central Tanzania. An understanding of livelihoods of people in this area has involved examining how communities have managed to adjust their livelihood in the midst of challenges resulting not only from drought but also from various forces such as socio,economic, political and ecological factors. It has been found out that, despite profound food crisis in this area, people are not always desperate and that there are possibilities for realizing some hidden potentials of dryland resources for livelihood diversification. The issue of sustainable natural resource management in such areas is, however, questionable because of some adverse environmental effects associated with some of the coping mechanisms. [source] Inferring ancient Agave cultivation practices from contemporary genetic patternsMOLECULAR ECOLOGY, Issue 8 2010KATHLEEN C. PARKER Abstract Several Agave species have played an important ethnobotanical role since prehistory in Mesoamerica and semiarid areas to the north, including central Arizona. We examined genetic variation in relict Agave parryi populations northeast of the Mogollon Rim in Arizona, remnants from anthropogenic manipulation over 600 years ago. We used both allozymes and microsatellites to compare genetic variability and structure in anthropogenically manipulated populations with putative wild populations, to assess whether they were actively cultivated or the result of inadvertent manipulation, and to determine probable source locations for anthropogenic populations. Wild populations were more genetically diverse than anthropogenic populations, with greater expected heterozygosity, polymorphic loci, effective number of alleles and allelic richness. Anthropogenic populations exhibited many traits indicative of past active cultivation: fixed heterozygosity for several loci in all populations (nonexistent in wild populations); fewer multilocus genotypes, which differed by fewer alleles; and greater differentiation among populations than was characteristic of wild populations. Furthermore, manipulated populations date from a period when changes in the cultural context may have favoured active cultivation near dwellings. Patterns of genetic similarity among populations suggest a complex anthropogenic history. Anthropogenic populations were not simply derived from the closest wild A. parryi stock; instead they evidently came from more distant, often more diverse, wild populations, perhaps obtained through trade networks in existence at the time of cultivation. [source] Light rings in Chinese pine (Pinus tabulaeformis) in semiarid areas of north China and their palaeo-climatological potentialNEW PHYTOLOGIST, Issue 4 2006Eryuan Liang Summary ,,Light rings in conifer trees are characterized by a light-coloured, narrow latewood band of thin-walled tracheids. Most reports on light rings have been for subarctic and subalpine regions, and little is known about their occurrence in semiarid areas. ,,Dendrochronological methods were used to date the occurrence of light rings in Chinese pine (Pinus tabulaeformis) in the semiarid region of north China. The anatomical and chemical characteristics and the potential environmental controls of their formation were investigated. ,,Light rings in Chinese pine were dated to the year of their formation. The wall thickness and lumen diameter of the wood cells of light rings and reference rings were distinctly different. However, the configuration of the light-ring latewood cell walls was normal, although they were thinner than average, and their lignification had been completed normally. ,,The climate characteristics that result in light-ring formation appear to be ongoing severe drought from the previous autumn to July of the current year in conjunction with a warm summer, suggesting that light rings can be used as indicators for past drought events. [source] The Influence of Historical Land Use and Water Availability on Grassland RestorationRESTORATION ECOLOGY, Issue 2010Zhuwen Xu The ecological role of historical land use has rarely been explored in the context of grassland restoration. We conducted a 4-year field experiment in a steppe and an old field in Inner Mongolia in northern China to examine the influence of historical land use and water availability on ecosystem restoration. Species richness, evenness, and plant cover were higher in the steppe than in the old field. The steppe was more temporally stable compared with the old field in terms of species richness, evenness, plant density, and cover. Water addition increased peak aboveground biomass, belowground net primary productivity, species richness, plant density, and cover in both the steppe and the old field. Water addition also enhanced the stability of ecosystems and the restoration of grassland. Our findings suggested that historical land use determines community structure and influences the process of grassland restoration. Converting grasslands to farmland in semiarid areas can cause the long-term loss of biodiversity and instability of ecosystem with consequent impacts on ecosystem services. The amendment of limited resources is an effective practice to increase the success of ecosystem restoration. [source] | ||||||||||