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Human Settlements (human + settlement)
Selected AbstractsOn the Rank-Size Distribution for Human SettlementsJOURNAL OF REGIONAL SCIENCE, Issue 1 2002William J. Reed An explanation for the rank-size distribution for human settlements based on simple stochastic models of settlement formation and growth is presented. Not only does the analysis of the model explain the rank-size phenomenon in the upper tail, it also predicts a reverse rank-size phenomenon in the lower tail. Furthermore it yields a parametric form (the double Pareto-lognormal distribution) for the complete distribution of settlement sizes. Settlement-size data for four regions (two in Spain and two in the U.S.) are used as examples. For these regions the lower tail rank-size property is seen to hold and the double Pareto-lognormal distribution shown to provide an excellent fit, lending support to the model and to the explanation for the rank-size law. [source] Human settlement and baobab distribution in south-western MaliJOURNAL OF BIOGEOGRAPHY, Issue 11 2007Chris S. Duvall Abstract Aim, Human settlement establishment and reproduction of the baobab tree (Adansonia digitata) appear spatially and temporally dependent because baobabs are abundant in many settlement sites in Africa. This paper tests the spatiotemporal relationship between baobab and settlement distribution. Location, South-western Mali. Methods, In an area of 183 km2, 1240 baobabs were located and mapped, their diameters measured, and habitat characteristics recorded for each individual. All occupied (n = 9) and abandoned (n = 84) settlements were located and mapped, and occupation dates were determined through interviews. Chi-squared analysis indicated baobab habitat preferences, and bivariate point-pattern analysis tested baobab,settlement spatiotemporal independence. Results, Baobabs and human settlements are positively spatially associated at most distances and for all baobab size-class,settlement age-class pairs. However, positive spatial association is significant only at distances < 500 m, and young settlements and large baobabs are not significantly associated. Positive association between small and large baobabs is marginally significant at <300 m, but observed significance is less than that for baobab,settlement positive association. Baobab abundance is not evenly distributed across the range of habitats it occupies; recruitment is strongest in settlements and fields, and on cliffs, while mortality is highest on cliffs. Ethnographic observations suggest that human settlement practices and fruit use are the main human factors contributing to baobab,settlement positive spatial association. Main conclusions, There are three main conclusions: (1) Human settlement and baobab recruitment are spatially dependant because settlement leads directly and indirectly to the development of baobab groves at settlement sites. (2) The lower than expected abundance of mature individuals in natural habitats, and the habitat preferences of the observed population, suggest that baobabs were introduced to south-western Mali, probably centuries ago. (3) Human mobility over decadal time-scales is necessary to maintain baobab population structure in landscapes dominated by shifting land use, where baobabs are not purposefully planted. Baobab population processes in such landscapes occur at the scale of human settlement. [source] Climatic influences and anthropogenic stressors: an integrated framework for streamflow management in Mediterranean-climate California, U.S.A.FRESHWATER BIOLOGY, Issue 2010THEODORE E. GRANTHAM Summary 1. In Mediterranean and other water-stressed climates, water management is critical to the conservation of freshwater ecosystems. To secure and maintain water allocations for the environment, integrated water management approaches are needed that consider ecosystem flow requirements, patterns of human water demands and the temporal and spatial dynamics of water availability. 2. Human settlements in Mediterranean climates have constructed water storage and conveyance projects at a scale and level of complexity far exceeding those in other, less seasonal climates. As a result, multiple ecological stressors associated with natural periods of flooding and drying are compounded by anthropogenic impacts resulting from water infrastructure development. 3. Despite substantial investments in freshwater ecosystem conservation, particularly in California, U.S.A., success has been limited because the scales at which river management and restoration are implemented are often discordant with the temporal and spatial scales at which ecosystem processes operate. Often, there is also strong social and political resistance to restricting water allocation to existing consumptive uses for environmental protection purposes. Furthermore, institutions rarely have the capacity to develop and implement integrated management programmes needed for freshwater ecosystem conservation. 4. We propose an integrated framework for streamflow management that explicitly considers the temporal and spatial dynamics of water supply and needs of both human and natural systems. This approach makes it possible to assess the effects of alternative management strategies to human water security and ecosystem conditions and facilitates integrated decision-making by water management institutions. 5. We illustrate the framework by applying a GIS-based hydrologic model in a Mediterranean-climate watershed in Sonoma County, California, U.S.A. The model is designed to assess the hydrologic impacts of multiple water users distributed throughout a stream network. We analyse the effects of vineyard water management on environmental flows to (i) evaluate streamflow impacts from small storage ponds designed to meet human water demands and reduce summer diversions, (ii) prioritise the placement of storage ponds to meet human water needs while optimising environmental flow benefits and (iii) examine the environmental and social consequences of flow management policies designed to regulate the timing of diversions to protect ecosystem functions. 6. Thematic implications: spatially explicit models that represent anthropogenic stressors (e.g. water diversions) and environmental flow needs are required to address persistent and growing threats to freshwater biodiversity. A coupled human,natural system approach to water management is particularly useful in Mediterranean climates, characterised by severe competition for water resources and high spatial and temporal variability in flow regimes. However, lessons learned from our analyses are applicable to other highly seasonal systems and those that are expected to have increased precipitation variability resulting from climate change. [source] Habitat-specific demography and source,sink dynamics in a population of Siberian jaysJOURNAL OF ANIMAL ECOLOGY, Issue 1 2010Magdalena Nystrand Summary 1.,There are a number of models describing population structure, many of which have the capacity to incorporate spatial habitat effects. One such model is the source,sink model, that describes a system where some habitats have a natality that is higher than mortality (source) and others have a mortality that exceeds natality (sink). A source can be maintained in the absence of migration, whereas a sink will go extinct. 2.,However, the interaction between population dynamics and habitat quality is complex, and concerns have been raised about the validity of published empirical studies addressing source,sink dynamics. In particular, some of these studies fail to provide data on survival, a significant component in disentangling a sink from a low quality source. Moreover, failing to account for a density-dependent increase in mortality, or decrease in fecundity, can result in a territory being falsely assigned as a sink, when in fact, this density-dependent suppression only decreases the population size to a lower level, hence indicating a ,pseudo-sink'. 3.,In this study, we investigate a long-term data set for key components of territory-specific demography (mortality and reproduction) and their relationship to habitat characteristics in the territorial, group-living Siberian jay (Perisoreus infaustus). We also assess territory-specific population growth rates (r), to test whether spatial population dynamics are consistent with the ideas of source,sink dynamics. 4.,Although average mortality did not differ between sexes, habitat-specific mortality did. Female mortality was higher in older forests, a pattern not observed in males. Male mortality only increased with an increasing amount of open areas. Moreover, reproductive success was higher further away from human settlement, indicating a strong effect of human-associated nest predators. 5.,Averaged over all years, 76% of the territories were sources. These territories generally consisted of less open areas, and were located further away from human settlement. 6.,The source,sink model provides a tool for modelling demography in distinct habitat patches of different quality, which can aid in identifying key habitats within the landscape, and thus, reduce the risk of implementing unsound management decisions. [source] Human settlement and baobab distribution in south-western MaliJOURNAL OF BIOGEOGRAPHY, Issue 11 2007Chris S. Duvall Abstract Aim, Human settlement establishment and reproduction of the baobab tree (Adansonia digitata) appear spatially and temporally dependent because baobabs are abundant in many settlement sites in Africa. This paper tests the spatiotemporal relationship between baobab and settlement distribution. Location, South-western Mali. Methods, In an area of 183 km2, 1240 baobabs were located and mapped, their diameters measured, and habitat characteristics recorded for each individual. All occupied (n = 9) and abandoned (n = 84) settlements were located and mapped, and occupation dates were determined through interviews. Chi-squared analysis indicated baobab habitat preferences, and bivariate point-pattern analysis tested baobab,settlement spatiotemporal independence. Results, Baobabs and human settlements are positively spatially associated at most distances and for all baobab size-class,settlement age-class pairs. However, positive spatial association is significant only at distances < 500 m, and young settlements and large baobabs are not significantly associated. Positive association between small and large baobabs is marginally significant at <300 m, but observed significance is less than that for baobab,settlement positive association. Baobab abundance is not evenly distributed across the range of habitats it occupies; recruitment is strongest in settlements and fields, and on cliffs, while mortality is highest on cliffs. Ethnographic observations suggest that human settlement practices and fruit use are the main human factors contributing to baobab,settlement positive spatial association. Main conclusions, There are three main conclusions: (1) Human settlement and baobab recruitment are spatially dependant because settlement leads directly and indirectly to the development of baobab groves at settlement sites. (2) The lower than expected abundance of mature individuals in natural habitats, and the habitat preferences of the observed population, suggest that baobabs were introduced to south-western Mali, probably centuries ago. (3) Human mobility over decadal time-scales is necessary to maintain baobab population structure in landscapes dominated by shifting land use, where baobabs are not purposefully planted. Baobab population processes in such landscapes occur at the scale of human settlement. [source] Historical and contemporary distributions of carnivores in forests of the Sierra Nevada, California, USAJOURNAL OF BIOGEOGRAPHY, Issue 8 2005William J. Zielinski Abstract Aim, Mammalian carnivores are considered particularly sensitive indicators of environmental change. Information on the distribution of carnivores from the early 1900s provides a unique opportunity to evaluate changes in their distributions over a 75-year period during which the influence of human uses of forest resources in California greatly increased. We present information on the distributions of forest carnivores in the context of two of the most significant changes in the Sierra Nevada during this period: the expansion of human settlement and the reduction in mature forests by timber harvest. Methods, We compare the historical and contemporary distributions of 10 taxa of mesocarnivores in the conifer forests of the Sierra Nevada and southern Cascade Range by contrasting the distribution of museum and fur harvest records from the early 1900s with the distribution of detections from baited track-plate and camera surveys conducted from 1996 to 2002. A total of 344 sample units (6 track plates and 1 camera each) were distributed systematically across c. 3,000,000 ha area over a 7-year period. Results, Two species, the wolverine (Gulo gulo) and the red fox (Vulpes vulpes), present in the historical record for our survey area, were not detected during the contemporary surveys. The distributions of 3 species (fisher [Martespennanti], American marten [M. americana], and Virginia opossum [Didelphisvirginiana]) have substantially changed since the early 1900s. The distributions of fishers and martens, mature-forest specialists, appeared to have decreased in the northern Sierra Nevada and southern Cascade region. A reputed gap in the current distribution of fishers was confirmed. We report for the first time evidence that the distribution of martens has become fragmented in the southern Cascades and northern Sierra Nevada. The opossum, an introduced marsupial, expanded its distribution in the Sierra Nevada significantly since it was introduced to the south-central coast region of California in the 1930s. There did not appear to be any changes in the distributions of the species that were considered habitat generalists: gray fox (Urocyon cinereoargenteus), striped skunk (Mephitis mephitis), western spotted skunk (Spilogale gracilis), or black bear (Ursus americanus). Detections of raccoons (Procyon lotor) and badgers (Taxidea taxus) were too rare to evaluate. Contemporary surveys indicated that weasels (M. frenata and M. erminea) were distributed throughout the study area, but historical data were not available for comparison. Main conclusions, Two species, the wolverine and Sierra Nevada red fox, were not detected in contemporary surveys and may be extirpated or in extremely low densities in the regions sampled. The distributions of the mature forest specialists (marten and fisher) appear to have changed more than the distributions of the forest generalists. This is most likely due to a combination of loss of mature forest habitat, residential development and the latent effects of commercial trapping. Biological characteristics of individual species, in combination with the effect of human activities, appear to have combined to affect the current distributions of carnivores in the Sierra Nevada. Periodic resampling of the distributions of carnivores in California, via remote detection methods, is an efficient means for monitoring the status of their populations. [source] Expansion of human settlement in Kenya's Maasai Mara: what future for pastoralism and wildlife?JOURNAL OF BIOGEOGRAPHY, Issue 6 2004Richard H. Lamprey Abstract Aim, Wildlife and pastoral peoples have lived side-by-side in the Mara ecosystem of south-western Kenya for at least 2000 years. Recent changes in human population and landuse are jeopardizing this co-existence. The aim of the study is to determine the viability of pastoralism and wildlife conservation in Maasai ranches around the Maasai Mara National Reserve (MMNR). Location, A study area of 2250 km2 was selected in the northern part of the Serengeti-Mara ecosystem, encompassing group ranches adjoining the MMNR. Emphasis is placed on Koyake Group Ranch, a rangeland area owned by Maasai pastoralists, and one of Kenya's major wildlife tourism areas. Methods, Maasai settlement patterns, vegetation, livestock numbers and wildlife numbers were analysed over a 50-year period. Settlement distributions and vegetation changes were determined from aerial photography and aerial surveys of 1950, 1961, 1967, 1974, 1983 and 1999. Livestock and wildlife numbers were determined from re-analysis of systematic reconnaissance flights conducted by the Kenya Government from 1977 to 2000, and from ground counts in 2002. Corroborating data on livestock numbers were obtained from aerial photography of Maasai settlements in 2001. Trends in livestock were related to rainfall, and to vegetation production as indicated by the seasonal Normalized Difference Vegetation Index. With these data sets, per capita livestock holdings were determined for the period 1980,2000, a period of fluctuating rainfall and primary production. Results, For the first half of the twentieth century, the Mara was infested with tsetse-flies, and the Maasai were confined to the Lemek Valley area to the north of the MMNR. During the early 1960s, active tsetse-control measures by both government and the Maasai led to the destruction of woodlands across the Mara and the retreat of tsetse flies. The Maasai were then able to expand their settlement area south towards MMNR. Meanwhile, wildebeest (Connochaetes taurinus) from the increasing Serengeti population began to spill into the Mara rangelands each dry season, leading to direct competition between livestock and wildlife. Group ranches were established in the area in 1970 to formalize land tenure for the Maasai. By the late 1980s, with rapid population growth, new settlement areas had been established at Talek and other parts adjacent to the MMNR. Over the period 1983,99, the number of Maasai bomas in Koyake has increased at 6.4% per annum (pa), and the human population at 4.4% pa. Over the same period, cattle numbers on Koyake varied from 20,000 to 45,000 (average 25,000), in relation to total rainfall received over the previous 2 years. The rangelands of the Mara cannot support a greater cattle population under current pastoral practices. Conclusions, With the rapid increase in human settlement in the Mara, and with imminent land privatization, it is probable that wildlife populations on Koyake will decline significantly in the next 3,5 years. Per capita livestock holdings on the ranch have now fallen to three livestock units/reference adult, well below minimum pastoral subsistence requirements. During the 1980s and 90s the Maasai diversified their livelihoods to generate revenues from tourism, small-scale agriculture and land-leases for mechanized cultivation. However, there is a massive imbalance in tourism incomes in favour of a small elite. In 1999 the membership of Koyake voted to subdivide the ranch into individual holdings. In 2003 the subdivision survey allocated plots of 60 ha average size to 1020 ranch members. This land privatization may result in increased cultivation and fencing, the exclusion of wildlife, and the decline of tourism as a revenue generator. This unique pastoral/wildlife system will shortly be lost unless land holdings can be managed to maintain the free movement of livestock and wildlife. [source] Pastoralist's livestock and settlements influence game bird diversity and abundance in a savanna ecosystem of southern KenyaAFRICAN JOURNAL OF ECOLOGY, Issue 1 2009Dana L. Morris Abstract We investigated the vegetation structure and density of game birds along a successional gradient created by varying intensity of human settlement in a pastoral community in Shompole group ranch in southern Kenya. We examined four habitat types including heavily-grazed grass in currently occupied settlements, short grass in seasonal settlements, patches of bushed woodland in settlement sites that had been abandoned up to 30 years ago, and tall grass in a wildlife sanctuary. Vegetation biomass was the highest in the sanctuary where livestock are excluded and the lowest in the vicinity of currently occupied settlements. Abundance of doves (Oena spp. and Streptopelia spp.) was best associated with moderate grazing and per cent green grass, which provide good foraging opportunities. Francolin and spurfowl (Francolinus spp.) were positively associated with vegetation biomass. Quail (Coturnix spp.) were positively associated with tree cover. These data reflect the importance of maintaining a balance of wildlife and livestock grazing with patches of ungrazed grasslands and bushed woodlands in providing a mosaic of habitats that support a diverse population of game birds. The results have wide application for an integrated management approach to livestock, wildlife and game bird management in the savannas. Résumé Nous avons étudié la structure de la végétation et la densité du gibier à plume le long d'un gradient créé par la variation de l'intensité des installations humaines, dans une communauté pastorale dans un ranch de Shompole, dans le sud du Kenya. Nous avons examiné quatre types d'habitats: l'herbe fortement broutée dans les installations qui sont actuellement occupées, l'herbe courte des installations saisonnières, les îlots de broussailles dans les anciennes installations abandonnées parfois depuis 30 ans et les hautes herbes d'un sanctuaire de la faune. La biomasse de la végétation était la plus grande dans le sanctuaire d'où le bétail était exclu et la plus basse dans le voisinage des installations encore occupées. L'abondance des tourterelles (Oena spp. et Streptopelia spp.) était plutôt liée à un broutage modéré et à un pourcentage d'herbe verte qui donnent de bonnes possibilités de se nourrir. Les francolins (Francolinus spp.) étaient positivement liés à la biomasse de la végétation. Les cailles (Coturnix spp.) étaient positivement liées à la couverture arborée. Ces données reflètent l'importance de conserver un équilibre entre les pâturages de la faune sauvage et du bétail et des îlots non pâturés et des broussailles, pour créer une mosaïque d'habitats qui accueillent une population variée de gibier à plume. Les résultats peuvent largement trouver une application dans les approches intégrées de gestion du bétail, de la faune sauvage et du gibier à plume en savane. [source] Redating the onset of burning at Lynch's Crater (North Queensland): implications for human settlement in AustraliaJOURNAL OF QUATERNARY SCIENCE, Issue 8 2001C. S. M. Turney Abstract Lynch's Crater preserves a continuous, high-resolution record of environmental changes in north Queensland. This record suggests a marked increase in burning that appears to be independent of any known major climatic boundaries. This increase is accompanied, or closely followed, by the virtually complete replacement of rainforest by sclerophyll vegetation. The absence of any major climatic shift associated with this increase in fire frequency therefore has been interpreted as a result of early human impact in the area. The age for this increase in burning, on the basis of conventional radiocarbon dating, was previously thought to be approximately 38 000 14C yr BP, supporting the traditional model for human arrival in Australia at 40 000 14C yr BP Here we have applied a more rigorous pre-treatment and graphitisation procedure for radiocarbon dating samples from the Lynch's Crater sequence. These new dates suggest that the increase in fire frequency occurred at 45 000 14C yr BP, supporting the alternative view that human occupation of Australia occurred by at least 45 000,55 000 cal. yr BP. Copyright © 2001 John Wiley & Sons, Ltd. [source] Tuberculosis and leprosy in perspectiveAMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue S49 2009Anne C. Stone Abstract Two of humankind's most socially and psychologically devastating diseases, tuberculosis and leprosy, have been the subject of intensive paleopathological research due to their antiquity, a presumed association with human settlement and subsistence patterns, and their propensity to leave characteristic lesions on skeletal and mummified remains. Despite a long history of medical research and the development of effective chemotherapy, these diseases remain global health threats even in the 21st century, and as such, their causative agents Mycobacterium tuberculosis and M. leprae, respectively, have recently been the subject of molecular genetics research. The new genome-level data for several mycobacterial species have informed extensive phylogenetic analyses that call into question previously accepted theories concerning the origins and antiquity of these diseases. Of special note is the fact that all new models are in broad agreement that human TB predated that in other animals, including cattle and other domesticates, and that this disease originated at least 35,000 years ago and probably closer to 2.6 million years ago. In this work, we review current phylogenetic and biogeographic models derived from molecular biology and explore their implications for the global development of TB and leprosy, past and present. In so doing, we also briefly review the skeletal evidence for TB and leprosy, explore the current status of these pathogens, critically consider current methods for identifying ancient mycobacterial DNA, and evaluate coevolutionary models. Yrbk Phys Anthropol 52:66,94, 2009. © 2009 Wiley-Liss, Inc. [source] Settlement history in the eastern Rub al-Khali: Preliminary Report of the Dubai Desert Survey (2006,2007)ARABIAN ARCHAEOLOGY AND EPIGRAPHY, Issue 1 2009Jesse Casana Regional archaeological survey in desert areas of Dubai, U.A.E., has identified numerous archaeological sites in this rapidly changing landscape. Subsurface geophysical surveys have been undertaken in concert with surface collection and test excavation to document the extent and chronology of each site. Contrary to expectations that deserts were permanently abandoned following the end of the mid-Holocene pluvial phase around 4000 BC, two sites, Al-Ashoosh and Saruq al-Hadid, show evidence of substantial occupation during the late third and early first millennia respectively. These findings suggest that the Rub al-Khali supported human settlement much later than is generally thought, challenging traditional understandings of the region's cultural and environmental histories. [source] Glechoma hederacea (Lamiaceae) in North America: invasion history and current distribution,FEDDES REPERTORIUM, Issue 1-2 2004M. Scholler Glechoma hederacea L. (Ground-ivy, Lamiaceae), a perennial mat-forming herb, is native to the temperate regions of Eurasia and was introduced elsewhere (South East Asia, New Zealand and North America). Based on data obtained from herbaria, literature, online and other data bases and field studies, we documented the invasion history and current distribution of this plant in North America. At present, the plant is recorded from all but two continental states of the USA and all southern provinces of Canada. There are two main ranges: the larger one covers mainly the eastern part of the U.S.A. and a smaller one stretches along the West Coast. While published records of Glechoma hederacea date from 1814, the oldest specimen is from 1829. During the 19th century the species spread westwards at a rate of approximately 30 km/year. The spread and present range of G. hederacea can only be explained by climatic factors (degree of oceanicity) and considering human activity. Especially long distance propagation of vegetative parts of the plants and the change of the environment that accompanies human settlements may have had a major influence on these processes. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) Glechoma hederacea L. (Lamiaceae) in Nordamerika: Invasionsgeschichte und derzeitige Verbreitung Glechoma hederacea (Gewöhnlicher Gundermann; Lamiaceae), eine im temperaten Eurasien beheimatete ausdauernde krautige Pflanze konnte sich als Neophyt in Südostasien, Neuseeland und Nordamerika etablieren. Basierend auf Daten aus der Literatur und Datenbanken, Belegdaten aus Herbarien und Felduntersuchungen werden die Ausbreitungsgeschichte der Art in Nordamerika und ihr gegenwärtiges Areal dokumentiert. Gegenwärtig ist die Art aus allen kanadischen Provinzen und mit Ausnahme von zwei Bundesstaaten auch von allen kontinentalen Bundesstaaten der USA dokumentiert. Es gibt zwei Hauptareale: ein großes, welches einen Großteil der östlichen USA einnimmt und ein kleineres an der Westküste. Der älteste Nachweis von 1814 von Glechoma hederacea stammt aus der Literatur, der älteste Beleg von 1829. Im Laufe des 19. Jahrhunderts breitete sich die Art mit einer Geschwindigkeit von etwa 30 km/Jahr nach Westen aus. Ausbreitungsgeschwindigkeit und das gegenwärtige Areal können nur mit Hilfe klimatischer (Ozeanität) und anthropogener Faktoren erklärt werden. Der Mensch trägt vor allem zur Verbreitung vegetativer Pflanzenteile bei und schafft in Siedlungen günstige Wachstumsbedingungen. [source] Teaching and Learning Guide for: The Geopolitics of Climate ChangeGEOGRAPHY COMPASS (ELECTRONIC), Issue 5 2008Jon Barnett Author's Introduction Climate change is a security problem in as much as the kinds of environmental changes that may result pose risks to peace and development. However, responsibilities for the causes of climate change, vulnerability to its effects, and capacity to solve the problem, are not equally distributed between countries, classes and cultures. There is no uniformity in the geopolitics of climate change, and this impedes solutions. Author Recommends 1.,Adger, W. N., et al. (eds) (2006). Fairness in adaptation to climate change. Cambridge, MA: MIT Press. A comprehensive collection of articles on the justice dimensions of adaptation to climate change. Chapters discuss potential points at which climate change becomes ,dangerous', the issue of adaptation under the United Nations Framework Convention on Climate Change (UNFCCC), the unequal outcomes of adaptation within a society, the effects of violent conflict on adaptation, the costs of adaptation, and examples from Bangladesh, Tanzania, Botswana, and Hungary. 2.,Leichenko, R., and O'Brien, K. (2008). Environmental change and globalization: double exposures. New York: Oxford University Press. This book uses examples from around the world to show the way global economic and political processes interact with environmental changes to create unequal outcomes within and across societies. A very clear demonstration of the way vulnerability to environmental change is as much driven by social processes as environmental ones, and how solutions lie within the realm of decisions about ,development' and ,environment'. 3.,Nordås, R., and Gleditsch, N. (2007). Climate conflict: common sense or nonsense? Political Geography 26 (6), pp. 627,638. doi:10.1016/j.polgeo.2007.06.003 An up-to-date, systematic and balanced review of research on the links between climate change and violent conflict. See also the other papers in this special issue of Political Geography. 4.,Parry, M., et al. (eds) (2007). Climate change 2007: impacts adaptation and vulnerability. Contribution of Working Group II to the fourth assessment report of the intergovernmental panel on climate change. Cambridge, UK: Cambridge University Press. The definitive review of all the peer-reviewed research on the way climate change may impact on places and sectors across the world. Includes chapters on ecosystems, health, human settlements, primary industries, water resources, and the major regions of the world. All chapters are available online at http://www.ipcc.ch/ipccreports/ar4-wg2.htm 5.,Salehyan, I. (2008). From climate change to conflict? No consensus yet. Journal of Peace Research 45 (3), pp. 315,326. doi:10.1177/0022343308088812 A balanced review of research on the links between climate change and conflict, with attention to existing evidence. 6.,Schwartz, P., and Randall, D. (2003). An abrupt climate change scenario and its implications for United States national security. San Francisco, CA: Global Business Network. Gives insight into how the US security policy community is framing the problem of climate change. This needs to be read critically. Available at http://www.gbn.com/ArticleDisplayServlet.srv?aid=26231 7.,German Advisory Council on Global Change. (2007). World in transition: climate change as a security risk. Berlin, Germany: WBGU. A major report from the German Advisory Council on Global Change on the risks climate changes poses to peace and stability. Needs to be read with caution. Summary and background studies are available online at http://www.wbgu.de/wbgu_jg2007_engl.html 8.,Yamin, F., and Depedge, J. (2004). The International climate change regime: a guide to rules, institutions and procedures. Cambridge, UK: Cambridge University Press. A clear and very detailed explanation of the UNFCCC's objectives, actors, history, and challenges. A must read for anyone seeking to understand the UNFCCC process, written by two scholars with practical experience in negotiations. Online Materials 1.,Environmental Change and Security Program at the Woodrow Wilson International Center for Scholars http://www.wilsoncenter.org/ecsp The major website for information about environmental security. From here, you can download many reports and studies, including the Environmental Change and Security Project Report. 2.,Global Environmental Change and Human Security Project http://www.gechs.org This website is a clearing house for work and events on environmental change and human security. 3.,Intergovernmental Panel on Climate Change (IPCC) http://www.ipcc.ch/ From this website, you can download all the chapters of all the IPCC's reports, including its comprehensive and highly influential assessment reports, the most recent of which was published in 2007. The IPCC were awarded of the Nobel Peace Prize ,for their efforts to build up and disseminate greater knowledge about man-made (sic) climate change, and to lay the foundations for the measures that are needed to counteract such change'. 4.,Tyndall Centre for Climate Change Research http://www.tyndall.ac.uk The website of a major centre for research on climate change, and probably the world's leading centre for social science based analysis of climate change. From this site, you can download many publications about mitigation of and adaptation to climate change, and about various issues in the UNFCCC. 5.,United Nations Framework Convention on Climate Change http://unfccc.int/ The website contains every major document relation to the UNFCCC and its Kyoto Protocol, including the text of the agreements, national communications, country submissions, negotiated outcomes, and background documents about most key issues. Sample Syllabus: The Geopolitics of Climate Change topics for lecture and discussion Week I: Introduction Barnett, J. (2007). The geopolitics of climate change. Geography Compass 1 (6), pp. 1361,1375. United Nations Secretary General, Kofi Annan, address to the 12th Conference of Parties to the United Nations Framework Convention on Climate Change, Nairobi, 15 November 2006. Available online at http://www.unep.org/Documents.Multilingual/Default.asp?DocumentID=495&ArticleID=5424&l=en Week II: The History and Geography of Greenhouse Gas Emissions Topic: The drivers of climate change in space and time Reading Baer, P. (2006). Adaptation: who pays whom? In: Adger, N., et al. (eds) Fairness in adaptation to climate change. Cambridge, MA: MIT Press, pp. 131,154. Boyden, S., and Dovers, S. (1992). Natural-resource consumption and its environmental impacts in the Western World: impacts of increasing per capita consumption. Ambio 21 (1), pp. 63,69. Week III: The Environmental Consequences of climate change Topic: The risks climate change poses to environmental systems Reading Intergovernmental Panel on Climate Change. (2007). Climate change 2007: climate change impacts, adaptation and vulnerability: summary for policymakers. Geneva, Switzerland: IPCC Secretariat. Watch: Al Gore. The Inconvenient Truth. Weeks IV and V: The Social Consequences of Climate Change Topic: The risks climate change poses to social systems Reading Adger, W. N. (1999). Social vulnerability to climate change and extremes in coastal Vietnam. World Development 27, pp. 249,269. Comrie, A. (2007). Climate change and human health. Geography Compass 1 (3), pp. 325,339. Leary, N., et al. (2006). For whom the bell tolls: vulnerability in a changing climate. A Synthesis from the AIACC project, AIACC Working Paper No. 21, International START Secretariat, Florida. Stern, N. (2007). Economics of climate change: the Stern review. Cambridge, UK: Cambridge University Press (Chapters 3,5). Week VI: Mitigation of Climate Change: The UNFCCC Topic: The UNFCCC and the Kyoto Protocol Reading Najam, A., Huq, S., and Sokona, Y. (2003). Climate negotiations beyond Kyoto: developing countries concerns and interests. Climate Policy 3 (3), pp. 221,231. UNFCCC Secretariat. (2005). Caring for climate: a guide to the climate change convention and the Kyoto Protocol. Bonn, Germany: UN Framework Convention on Climate Change Secretariat. Weeks VII and VIII: Adaptation to Climate Change Topic: What can be done to allow societies to adapt to avoid climate impacts? Reading Adger, N., et al. (2007). Assessment of adaptation practices, options, constraints and capacity. In: Parry, M., et al. (eds) Climate change 2007: impacts, adaptation and vulnerability. Contribution of Working Group II to the fourth assessment report of the intergovernmental panel on climate change. Cambridge, UK: Cambridge University Press, pp. 717,744. Burton, I., et al. (2002). From impacts assessment to adaptation priorities: the shaping of adaptation policy. Climate Policy 2 (2,3), pp. 145,159. Eakin, H., and Lemos, M. C. (2006). Adaptation and the state: Latin America and the challenge of capacity-building under globalization. Global Environmental Change: Human and Policy Dimensions 16 (1), pp. 7,18. Ziervogel, G., Bharwani, S., and Downing, T. (2006). Adapting to climate variability: pumpkins, people and policy. Natural Resources Forum 30, pp. 294,305. Weeks IX and X: Climate Change and Migration Topic: Will climate change force migration? Readings Gaim, K. (1997). Environmental causes and impact of refugee movements: a critique of the current debate. Disasters 21 (1), pp. 20,38. McLeman, R., and Smit, B. (2006). Migration as adaptation to climate change. Climatic Change 76 (1), pp. 31,53. Myers, N. (2002). Environmental refugees: a growing phenomenon of the 21st century. Philosophical Transactions of the Royal Society 357 (1420), pp. 609,613. Perch-Nielsen, S., Bättig, M., and Imboden, D. (2008). Exploring the link between climate change and migration. Climatic Change (online first, forthcoming); doi:10.1007/s10584-008-9416-y Weeks XI and XII: Climate Change and Violent Conflict Topic: Will Climate change cause violent conflict? Readings Barnett, J., and Adger, N. (2007). Climate change, human security and violent conflict. Political Geography 26 (6), pp. 639,655. Centre for Strategic and International Studies. (2007). The age of consequences: the foreign policy and national security implications of global climate change. Washington, DC: CSIS. Nordås, R., and Gleditsch, N. (2007). Climate conflict: common sense or nonsense? Political Geography 26 (6), pp. 627,638. Schwartz, P., and Randall, D. (2003). An abrupt climate change scenario and its implications for United States national security. San Francisco, CA: Global Business Network. [online]. Retrieved on 8 April 2007 from http://www.gbn.com/ArticleDisplayServlet.srv?aid=26231 Focus Questions 1Who is most responsible for climate change? 2Who is most vulnerable to climate change? 3Does everyone have equal power in the UNFCCC process? 4Will climate change force people to migrate? Who? 5What is the relationship between adaptation to climate change and violent conflict? [source] Carbon stored in human settlements: the conterminous United StatesGLOBAL CHANGE BIOLOGY, Issue 1 2010GALINA CHURKINA Abstract Urban areas are home to more than half of the world's people, responsible for >70% of anthropogenic release of carbon dioxide and 76% of wood used for industrial purposes. By 2050 the proportion of the urban population is expected to increase to 70% worldwide. Despite fast rates of change and potential value for mitigation of carbon dioxide emissions, the organic carbon storage in human settlements has not been well quantified. Here, we show that human settlements can store as much carbon per unit area (23,42 kg C m,2 urban areas and 7,16 kg C m,2exurban areas) as tropical forests, which have the highest carbon density of natural ecosystems (4,25 kg C m,2). By the year 2000 carbon storage attributed to human settlements of the conterminous United States was 18 Pg of carbon or 10% of its total land carbon storage. Sixty-four percent of this carbon was attributed to soil, 20% to vegetation, 11% to landfills, and 5% to buildings. To offset rising urban emissions of carbon, regional and national governments should consider how to protect or even to increase carbon storage of human-dominated landscapes. Rigorous studies addressing carbon budgets of human settlements and vulnerability of their carbon storage are needed. [source] The triggering of debris flow due to channel-bed failure in some alpine headwater basins of the Dolomites: analyses of critical runoffHYDROLOGICAL PROCESSES, Issue 13 2008C. Gregoretti Abstract The debris deposits at the bottom of very steep natural channels and streams in high mountain areas can be mobilized by runoff, triggering a water,sediment mixture flow known as debris flow. The routing of debris flow through human settlements can cause damage to civil structures and loss of human lives. The prediction of such an event, or the runoff discharge that triggers it, assumes an interest in risk analyses and the planning of defence measures. The object of this study is to find a method to determine the critical runoff value that triggers debris flow as a result of channel-bed failure. Historical and rainfall data on 30 debris flows that occurred in six watersheds of the Dolomites (north-eastern Italian Alps) were collected from different sources. Field investigations at the six sites, together with the hydrologic response to the rainfalls that triggered the events, were performed to obtain a realistic scenario of the formation of the debris flow there occurred. Field observations include a survey along the channel of the triggering reach of debris flow, with measurements of the channel slope and cross-section and sampling of debris deposits for grain size distribution. Simulated runoff discharge values based on the rainfall recorded by pluviometers were then compared with values obtained through experimental criteria on the initiation and formation of debris flow by bed failure. The results are discussed to provide a plausible physical-based method for the prediction of the triggering of debris flow by channel-bed failure. Copyright © 2007 John Wiley & Sons, Ltd. [source] Remote sensing and GIS-based flood vulnerability assessment of human settlements: a case study of Gangetic West Bengal, IndiaHYDROLOGICAL PROCESSES, Issue 18 2005Joy Sanyal Abstract Flooding due to excessive rainfall in a short period of time is a frequent hazard in the flood plains of monsoon Asia. In late September 2000, a devastating flood stuck Gangetic West Bengal, India. This particular event has been selected for this study. Instead of following the conventional approach of flooded area delineation and overall damage estimation, this paper seeks to identify the rural settlements that are vulnerable to floods of a given magnitude. Vulnerability of a rural settlement is perceived as a function of two factors: the presence of deep flood water in and around the settlement and its proximity to an elevated area for temporary shelter during an extreme hydrological event. Landsat ETM+ images acquired on 30 September 2000 have been used to identify the non-flooded areas within the flooded zone. Particular effort has been made to differentiate land from water under cloud shadow. ASTER digital elevation data have been used to assess accuracy and rectify the classified image. The presence of large numbers of trees around rural settlements made it particularly difficult to extract the flooded areas from their spectral signatures in the visible and infrared bands. ERS-1 synthetic aperture radar data are found particularly useful for extracting the settlement areas surrounded by trees. Finally, all information extracted from satellite imageries are imported into ArcGIS, and spatial analysis is carried out to identify the settlements vulnerable to river inundation. Copyright © 2005 John Wiley & Sons, Ltd. [source] A Late Neolithic vertebrate food web based on stable isotope analysesINTERNATIONAL JOURNAL OF OSTEOARCHAEOLOGY, Issue 4 2006C. Bösl Abstract Stable carbon and nitrogen isotope analyses of bone collagen, and stable carbon and oxygen isotope analyses of the bone's structural carbonate, were performed on 120 individuals representing 33 vertebrate species, including a single human bone find, collected from the Late Neolithic settlement at Pestenacker, Bavaria, Germany. We were thus capable of reconstructing a rather complex food web and could also address particular issues, such as whether humans influenced the diet of their domestic animals as opposed to their wild relatives, or whether humans perhaps had to compete over food with their domesticates. A rather unexpected result was that freshwater fish, which could be captured in the nearby river Lech, a major tributary of the Danube, contributed to the human diet only occasionally. As for mammals, it was also possible to recognise different trophic levels for birds and aquatic vertebrates, applying stable isotope analyses to both bone collagen and structural carbonate. In the case of fish, ,18O values at least revealed a physiological regularity in terms of temperature preference, besides diet. Conceivably, variability of ,18O in surface water as reflected, for example, by species that avoided human settlements, may help to characterise past ecosystems and to define site catchment exploited by Neolithic man in the course of food acquisition. Copyright © 2006 John Wiley & Sons, Ltd. [source] Space allocation in Melanophila knoteki knoteki (Reitt.) var. hellenica (Obenberger) (Col., Buprestidae) in the attack of Greek fir [Abies cephalonica Loud. var. graeca (Fraas) Liu]: a pattern to process approachJOURNAL OF APPLIED ENTOMOLOGY, Issue 1 2004P. V. Petrakis Abstract: The phloeo-cambiophagous buprestid Melanophila knoteki knoteki (Reitt.) var. hellenica (Obenberger.) is not a primary factor of fir decline problem although the beetle substantially contributes to Greek fir Abies cephalonica Loud. var. graeca (Fraas) Liu mortality. By using mapping depiction of the exit holes of the insect on a set of fir trees located on a line transect in a randomized point-centred quarter scheme and employing pattern analysis techniques we were able to reveal various scales of the infestation pattern. Four scales were recognized, two of them corresponding to the pattern of microsite selection on the bark of a fir tree. While the dispersed exit holes exhibited a statistically significant random dispersion on the bark, within each aggregation the pattern was uniform. The area of compartments created by Dirichlet partition approximated very well the sizes of the actual larval galleries. The Dirichlet tessellation of the bark space and the analysis of the parameter of the resulting partitions showed the predominance of the hexagonal conformation of the larval spaces when space was limited. When some exit holes were positioned close together it was found that they were directed away from each other so the resulting galleries were well separated. Several hypotheses are presented as to the mechanisms underpinning the observed patterns. The allocation of space is in accordance with the widely accepted ,central place theory' of W. Christaller, a general theory of pattern generated in the geographical dispersion of human settlements. The revealed pattern was also in accordance with the predictions of the theory of ,central place foraging' of R. H. MacArthur and the theory of ,resource concentration hypothesis' of R. Root. [source] Human settlement and baobab distribution in south-western MaliJOURNAL OF BIOGEOGRAPHY, Issue 11 2007Chris S. Duvall Abstract Aim, Human settlement establishment and reproduction of the baobab tree (Adansonia digitata) appear spatially and temporally dependent because baobabs are abundant in many settlement sites in Africa. This paper tests the spatiotemporal relationship between baobab and settlement distribution. Location, South-western Mali. Methods, In an area of 183 km2, 1240 baobabs were located and mapped, their diameters measured, and habitat characteristics recorded for each individual. All occupied (n = 9) and abandoned (n = 84) settlements were located and mapped, and occupation dates were determined through interviews. Chi-squared analysis indicated baobab habitat preferences, and bivariate point-pattern analysis tested baobab,settlement spatiotemporal independence. Results, Baobabs and human settlements are positively spatially associated at most distances and for all baobab size-class,settlement age-class pairs. However, positive spatial association is significant only at distances < 500 m, and young settlements and large baobabs are not significantly associated. Positive association between small and large baobabs is marginally significant at <300 m, but observed significance is less than that for baobab,settlement positive association. Baobab abundance is not evenly distributed across the range of habitats it occupies; recruitment is strongest in settlements and fields, and on cliffs, while mortality is highest on cliffs. Ethnographic observations suggest that human settlement practices and fruit use are the main human factors contributing to baobab,settlement positive spatial association. Main conclusions, There are three main conclusions: (1) Human settlement and baobab recruitment are spatially dependant because settlement leads directly and indirectly to the development of baobab groves at settlement sites. (2) The lower than expected abundance of mature individuals in natural habitats, and the habitat preferences of the observed population, suggest that baobabs were introduced to south-western Mali, probably centuries ago. (3) Human mobility over decadal time-scales is necessary to maintain baobab population structure in landscapes dominated by shifting land use, where baobabs are not purposefully planted. Baobab population processes in such landscapes occur at the scale of human settlement. [source] Hermit crabs, humans and Mozambique mangrovesAFRICAN JOURNAL OF ECOLOGY, Issue 3 2001David K. A. Barnes Abstract There is a complex interrelationship between upper shore hermit crabs (such as Coenobita sp. and Clibanarius sp.), coastal human populations and mangrove forests in Mozambique. The abundance, activity, shell selection and behaviour of three species of hermit crab are related to the level of mangrove cover. With increased density of mangrove trees, the study species of hermit crab changed in abundance, tended to become diurnal, spent more time feeding and were clustered in larger groups when doing so, and selected longer spired shells. All five of the same variables are also linked to the proximity and activity of humans through both direct and indirect actions. Direct effects included a tendency to nocturnal activity with proximity to human activity; indirect effects included increased and more clumped food supplies, and shell middens from intertidal harvesting and deforestation. Mangroves are important to local human populations as well as to hermit crabs, for a wide variety of (similar) reasons. Mangroves provide storm shelter, fisheries and fishery nursery grounds for adjacent human settlements, but they also harbour mosquito populations and their removal provides valuable building materials and fuel. Hermit crabs may be useful (indirectly) to coastal human populations by being a source of food to certain commercial species, and by quickly consuming rotting/discarded food and faeces (thereby reducing disease and pests). They can also cause minor problems to coastal human populations because they use shells of (fisheries) target mollusc species and can be more abundant than the living molluscs, thereby slowing down effective hand collection through confusion over identification. The mixture of positive and negative attributes that the three groups impart to each other in the Quirimba Archipelago, northern Mozambique, is discussed. Résumé Il existe des interrelations complexes entre les Bernard-l'Ermite du haut littoral (tels que Coenobita sp. Et Clibanarius sp.), les populations humaines côtières et les forêts de mangroves au Mozambique. L'abondance, l'activité, le choix de la coquille et le comportement de trois espèces de Bernard-l'Ermite sont liés au degré de couverture de la mangrove. Lorsque la densité des arbres de la mangrove augmente, l'abondance des espèces étudiées de Bernard-l'Ermite change, ils ont tendance à devenir diurnes, passent plus de temps à se nourrir et se rassemblent à ces moments-là en plus grands groupes, et ils choisissent aussi de plus longues coquilles. Les cinq mêmes variables sont aussi liées à la proximité et à l'activité des hommes, directement et indirectement. Parmi les effets directs, on compte une tendance à une activité nocturne lorsque les activités humaines sont proches ; les effets indirects incluent des apports de nourriture et de débris de coquilles accrus et plus regroupés résultant des marées et de la déforestation. Les mangroves sont aussi importantes pour les populations locales que pour les Bernard-l'Ermite, pour toute une série de raisons (semblables). Les mangroves constituent un abri en cas de tempête, un terrain de pêche et de frai dont bénéficient les populations humaines voisines, mais elles renferment aussi beaucoup de moustiques, et leur bois fournit un bon matériau de construction et du combustible. Les Bernard-l'Ermite peuvent être (indirectement) utiles aux populations côtières car certaines espèces commerciales sont comestibles et que tous consomment rapidement les restes de nourriture en décomposition et les excréments (réduisant ainsi les risques de maladie et d'animaux nuisibles). Ils peuvent aussi causer des problèmes mineurs aux populations côtières parce qu'ils utilisent la coquille d'espèces de mollusques qui font l'objet de la pêche et qu'ils peuvent être plus abondants que les mollusques eux-mêmes, ce qui ralentit la pêche manuelle à cause du besoin d'identification. On discute le mélange de qualités négatives et positives que les trois groupes représentent les uns pour les autres dans l'Archipel de Quirimba, au nord du Mozambique. [source] Grassland diversity related to the Late Iron Age human population densityJOURNAL OF ECOLOGY, Issue 3 2007MEELIS PÄRTEL Summary 1Species-rich semi-natural grasslands in Europe developed during prehistoric times and have endured due to human activity. At the same time, intensive grassland management or changes in land use may result in species extinction. As a consequence, plant diversity in semi-natural calcareous grasslands may be related to both historical and current human population density. 2We hypothesize that current vascular plant diversity in semi-natural calcareous grasslands is positively correlated with the Late Iron Age (c. 800,1000 years ago) density of human settlements (indicated by Late Iron Age fortresses and villages) due to enhancement of grassland extent and species dispersal, and negatively correlated with current human population density due to habitat loss and deterioration. 3We described the size of the community vascular plant species pool, species richness per 1 m2 and the relative richness (richness divided by the size of the species pool) in 45 thin soil, calcareous (alvar) grasslands in Estonia. In addition to historical and current human population density we considered simultaneously the effects of grassland area, connectivity to other alvar grasslands, elevation above sea level (indicating grassland age), soil pH, soil N, soil P, soil depth, soil depth heterogeneity, geographical east,west gradient, precipitation and spatial autocorrelation. 4Both the size of the community species pool and the species richness are significantly correlated with the Late Iron Age human population density. In addition, species richness was unimodally related to the current human population density. The relative richness (species ,packing density') was highest in the intermediate current human population densities, indicative of moderate land-use intensity. 5Community species pool size decreased non-linearly with increasing soil N, and was highest at intermediate elevation. Small-scale richness was greater when sites were well connected and when the elevation was intermediate. Spatial autocorrelation was also significant for both species pool size and small-scale richness. 6In summary, human land-use legacy from prehistoric times is an important aspect in plant ecology, which could be an important contributor to the current variation in biodiversity. [source] On the Rank-Size Distribution for Human SettlementsJOURNAL OF REGIONAL SCIENCE, Issue 1 2002William J. Reed An explanation for the rank-size distribution for human settlements based on simple stochastic models of settlement formation and growth is presented. Not only does the analysis of the model explain the rank-size phenomenon in the upper tail, it also predicts a reverse rank-size phenomenon in the lower tail. Furthermore it yields a parametric form (the double Pareto-lognormal distribution) for the complete distribution of settlement sizes. Settlement-size data for four regions (two in Spain and two in the U.S.) are used as examples. For these regions the lower tail rank-size property is seen to hold and the double Pareto-lognormal distribution shown to provide an excellent fit, lending support to the model and to the explanation for the rank-size law. [source] Ecology of the gastrointestinal parasites of Colobus vellerosus at Boabeng-Fiema, Ghana: Possible anthropozoonotic transmissionAMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 3 2009Julie A. Teichroeb Abstract Parasite richness and prevalence in wild animals can be used as indicators of population and ecosystem health. In this study, the gastrointestinal parasites of ursine colobus monkeys (Colobus vellerosus) at the Boabeng-Fiema Monkey Sanctuary (BFMS), Ghana, were investigated. BFMS is a sacred grove where monkeys and humans have long lived in relatively peaceful proximity. Fecal samples (n = 109) were collected opportunistically from >27 adult and subadult males in six bisexual groups and one all-male band from July 2004 to August 2005. Using fecal floatation, we detected three protozoans (two Entamoeba sp., Isospora sp.), five nematodes (Ascaris sp., Enterobius sp., Trichuris sp., two strongyle sp.), and one digenean trematode. Using fluorescein labeled antibodies, we detected an additional protozoan (Giardia sp.), and with PCR techniques, we characterized this as G. duodenalis Assemblage B and also identified a protistan (Blastocystis sp., subtype 2). The most prevalent parasite species were G. duodenalis and Trichuris sp. Parasites were more prevalent in the long wet season than the long dry. Parasite prevalence did not vary by age, and average parasite richness did not differ by rank for males whose status remained unchanged. However, males that changed rank tended to show higher average parasite richness when they were lower ranked. Individuals that spent more time near human settlements had a higher prevalence of Isospora sp. that morphologically resembled the human species I. belli. The presence of this parasite and G. duodenalis Assemblage B indicates possible anthropozoonotic and/or zoonotic transmission between humans and colobus monkeys at this site. Am J Phys Anthropol, 2009. © 2009 Wiley-Liss, Inc. [source] Status of diurnal primate populations at the former settlement of a displaced village in CameroonAMERICAN JOURNAL OF PRIMATOLOGY, Issue 7 2010Lawrence Baya Abstract To understand whether or not primate populations recover in areas of abandoned human settlements, data are required that allow for site-specific comparison over time. Here, we present baseline information on the presence/absence and relative abundance of primate species at the abandoned settlement of the Ekundukundu village, relocated out of the Korup National Park in 2000. Between July 2007 and March 2008, 62,km of transects was surveyed for sightings and calls of primates. All eight species of diurnal primates reported in the KNP were confirmed: Cercopithecus nictitans ludio, C. mona, C. erythrotis camerunensis, C. pogonias, Procolobus pennantii preussi, Cercocebus torquatus, Mandrillus leucophaeus leucophaeus, and Pan troglodytes vellerosus. At old Ekundukundu, C. nictitans accounted for 65% of all primate group sightings. Overall, sighting frequency of primates (0.55,groups/km) was not significantly different from other park sectors surveyed by a previous observer (J. Linder) in 2004,2005. The data reported here will be useful in the long-term monitoring of primate populations in regenerating forest habitats of earlier human settlements. Am. J. Primatol. 72:645,652, 2010. © 2010 Wiley-Liss, Inc. [source] | |||||||||||||