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Global Patterns (global + pattern)
Selected AbstractsGlobal pattern of NPP to GPP ratio derived from MODIS data: effects of ecosystem type, geographical location and climateGLOBAL ECOLOGY, Issue 3 2009Yangjian Zhang ABSTRACT Aim, To examine the global pattern of the net primary production (NPP)/gross primary production (GPP) ratio of the Earth's land area along geographical and climatic gradients. Location, The global planetary ecosystem. Methods, The 4-year average annual NPP/GPP ratio of the Earth's land area was calculated using 2000,03 Moderate Resolution Imaging Spectroradiometer (MODIS) data. The global pattern of the NPP/GPP ratio was investigated by comparing it among each typical terrestrial ecosystem and plotting it along a geographical and climatic gradient, including latitude, altitude, temperature and precipitation. Results, The global terrestrial ecosystem had an average NPP/GPP ratio value of 0.52 with minor variation from 2000 to 2003. However, the NPP/GPP ratio showed considerable spatial variation associated with ecosystem type, geographical location and climate. Densely vegetated ecosystems had a lower NPP/GPP ratio than sparsely vegetated ecosystems. Forest ecosystems had a lower NPP/GPP ratio than shrub and herbaceous ecosystems. Geographically, the NPP/GPP ratio increased with altitude. In the Southern Hemisphere, the NPP/GPP ratio decreased along latitude from 30° to 10° and it exhibited high fluctuation in the Northern Hemisphere. Climatically, the NPP/GPP ratio exhibited a decreasing trend along enhanced precipitation when it was less than 2300 mm year,1 and a static trend when the annual precipitation was over 2300 mm. The NPP/GPP ratio showed a decreasing trend along temperature when it was between ,20 °C and 10 °C, and showed an increasing trend along rising temperature when it was between ,10 °C and 20 °C. Within each ecosystem, the NPP/GPP ratio revealed a similar trend to the global trend along temperature and precipitation. Conclusions, The NPP/GPP ratio exhibited a pattern depending on the main climatic characteristics such as temperature and precipitation and geographical factors such as latitude and altitude. The findings of this research challenge the widely held assumption that the NPP/GPP ratio is consistent regardless of ecosystem type. [source] Global patterns of marine turtle bycatchCONSERVATION LETTERS, Issue 3 2010Bryan P. Wallace Abstract Fisheries bycatch is a primary driver of population declines in several species of marine megafauna (e.g., elasmobranchs, mammals, seabirds, turtles). Characterizing the global bycatch seascape using data on bycatch rates across fisheries is essential for highlighting conservation priorities. We compiled a comprehensive database of reported data on marine turtle bycatch in gillnet, longline, and trawl fisheries worldwide from 1990 to 2008. The total reported global marine turtle bycatch was ,85,000 turtles, but due to the small percentage of fishing effort observed and reported (typically <1% of total fleets), and to a global lack of bycatch information from small-scale fisheries, this likely underestimates the true total by at least two orders of magnitude. Our synthesis also highlights an apparently universal pattern across fishing gears and regions where high bycatch rates were associated with low observed effort, which emphasizes the need for strategic bycatch data collection and reporting. This study provides the first global perspective of fisheries bycatch for marine turtles and highlights region,gear combinations that warrant urgent conservation action (e.g., gillnets, longlines, and trawls in the Mediterranean Sea and eastern Pacific Ocean) and region,gear combinations in need of enhanced observation and reporting efforts (e.g., eastern Indian Ocean gillnets, West African trawls). [source] Global patterns of genetic variation in plant species along vertical and horizontal gradients on mountainsGLOBAL ECOLOGY, Issue 2 2008Takafumi Ohsawa ABSTRACT Aim To understand global patterns of genetic variation in plant species on mountains and to consider the significance of mountains for the genetic structure and evolution of plant species. Location Global. Methods We review published studies. Results Genetic diversity within populations can vary along altitudinal gradients in one of four patterns. Eleven of 42 cited studies (26% of the total) found that populations at intermediate altitudes have greater diversity than populations at lower and higher altitudes. This is because the geographically central populations are under optimal environmental conditions, whereas the peripheral populations are in suboptimal situations. The second pattern, indicating that higher populations have less diversity than lower populations, was found in eight studies (19%). The third pattern, indicating that lower populations have lower diversity than higher populations, was found in 10 studies (24%). In 12 studies (29%), the intrapopulation genetic variation was found to be unaffected by altitude. Evidence of altitudinal differentiation was found in more than half of these studies, based on measurements of a range of variables including genome size, number of chromosomes or a range of loci using molecular markers. Furthermore, great variation has been found in phenotypes among populations at different altitudes in situ and in common garden experiments, even in cases where there was no associated variation in molecular composition. Mountains can be genetic barriers for species that are distributed at low elevations, but they can also provide pathways for species that occupy high-elevation habitats. [Correction added after publication 9 October 2007: ,less diversity' changed to ,greater diversity' in the second sentence of the Results section of the Abstract] Main conclusions Genetic diversity within populations can vary along altitudinal gradients as a result of several factors. The results highlight the importance of phenotypic examinations in detecting altitudinal differences. The influence of mountain ridges on genetic differentiation varies depending, inter alia, on the elevation at which the species occurs. Based on these findings, zoning by altitudes or ridges would be helpful for the conservation of tree populations with the onset of global warming. [source] Global patterns of plant diversity and floristic knowledgeJOURNAL OF BIOGEOGRAPHY, Issue 7 2005Gerold Kier Abstract Aims, We present the first global map of vascular plant species richness by ecoregion and compare these results with the published literature on global priorities for plant conservation. In so doing, we assess the state of floristic knowledge across ecoregions as described in floras, checklists, and other published documents and pinpoint geographical gaps in our understanding of the global vascular plant flora. Finally, we explore the relationships between plant species richness by ecoregion and our knowledge of the flora, and between plant richness and the human footprint , a spatially explicit measure of the loss and degradation of natural habitats and ecosystems as a result of human activities. Location, Global. Methods, Richness estimates for the 867 terrestrial ecoregions of the world were derived from published richness data of c. 1800 geographical units. We applied one of four methods to assess richness, depending on data quality. These included collation and interpretation of published data, use of species,area curves to extrapolate richness, use of taxon-based data, and estimates derived from other ecoregions within the same biome. Results, The highest estimate of plant species richness is in the Borneo lowlands ecoregion (10,000 species) followed by nine ecoregions located in Central and South America with , 8000 species; all are found within the Tropical and Subtropical Moist Broadleaf Forests biome. Among the 51 ecoregions with , 5000 species, only five are located in temperate regions. For 43% of the 867 ecoregions, data quality was considered good or moderate. Among biomes, adequate data are especially lacking for flooded grasslands and flooded savannas. We found a significant correlation between species richness and data quality for only a few biomes, and, in all of these cases, our results indicated that species-rich ecoregions are better studied than those poor in vascular plants. Similarly, only in a few biomes did we find significant correlations between species richness and the human footprint, all of which were positive. Main conclusions, The work presented here sets the stage for comparisons of degree of concordance of plant species richness with plant endemism and vertebrate species richness: important analyses for a comprehensive global biodiversity strategy. We suggest: (1) that current global plant conservation strategies be reviewed to check if they cover the most outstanding examples of regions from each of the world's major biomes, even if these examples are species-poor compared with other biomes; (2) that flooded grasslands and flooded savannas should become a global priority in collecting and compiling richness data for vascular plants; and (3) that future studies which rely upon species,area calculations do not use a uniform parameter value but instead use values derived separately for subregions. [source] Global patterns in plant heightJOURNAL OF ECOLOGY, Issue 5 2009Angela T. Moles Summary 1. ,Plant height is a central part of plant ecological strategy. It is strongly correlated with life span, seed mass and time to maturity, and is a major determinant of a species' ability to compete for light. Plant height is also related to critical ecosystem variables such as animal diversity and carbon storage capacity. However, remarkably little is known about global patterns in plant height. Here, we use maximum height data for 7084 plant Species × Site combinations to provide the first global, cross-species quantification of the latitudinal gradient in plant height. 2. ,The mean maximum height of species growing within 15° of the equator (7.8 m) was 29 times greater than the height of species between 60° and 75° N (27 cm), and 31 times greater than the height of species between 45° and 60° S (25 cm). There was no evidence that the latitudinal gradient in plant height was different in the northern hemisphere than in the southern hemisphere (P = 0.29). A 2.4-fold drop in plant height at the edge of the tropics (P = 0.006) supports the idea that there might be a switch in plant strategy between temperate and tropical zones. 3. ,We investigated 22 environmental variables to determine which factors underlie the latitudinal gradient in plant height. We found that species with a wide range of height strategies were present in cold, dry, low productivity systems, but there was a noticeable lack of very short species in wetter, warmer, more productive sites. Variables that capture information about growing conditions during the harsh times of the year were relatively poor predictors of height. The best model for global patterns in plant height included only one term: precipitation in the wettest month (R2 = 0.256). 4. ,Synthesis. We found a remarkably steep relationship between latitude and height, indicating a major difference in plant strategy between high and low latitude systems. We also provide new, surprising information about the correlations between plant height and environmental variables. [source] Growing supranational identities in a globalising world?EUROPEAN JOURNAL OF POLITICAL RESEARCH, Issue 5 2008A multilevel analysis of the World Values Surveys Using the World Values Surveys (WVS), this article shows that there is a global pattern in public attitudes toward supranational identity: the younger the respondent, the more supranational. Yet a life-cycle effect, as opposed to a generational one, underlies this pattern. A multilevel analysis confirms this age effect on supranational identification in 43 countries covered in the recent wave of the WVS, but provides little support for the idea that a country's integration into the global economy and world society promotes supranational attachments among mass publics, especially youths. Regional integration and globalisation appear either complementary or contradictory to this identity shift, depending upon how ordinary citizens perceive their country's involvement in the processes of regional integration and globalisation, respectively. [source] Regionalisation of chemical variability in European mountain lakesFRESHWATER BIOLOGY, Issue 12 2009LLUÍS CAMARERO Summary 1. We carried out a coordinated survey of mountain lakes covering the main ranges across Europe (including Greenland), sampling 379 lakes above the local tree line in 2000. The objectives were to identify the main sources of chemical variability in mountain lakes, define a chemical classification of lakes, and develop tools to extrapolate our results to regional lake populations through an empirical regionalisation or upscaling of chemical properties. 2. We investigated the main causes of chemical variability using factor analysis (FA) and empirical relationships between chemistry and several environmental variables. Weathering, sea salt inputs, atmospheric deposition of N and S, and biological activity in soils of the catchment were identified as the major drivers of lake chemistry. 3. We tested discriminant analysis (DA) to predict the lake chemistry. It was possible to use the lithology of the catchments to predict the range of Ca2+ and SO42, into which a lake of unknown chemistry will decrease. Lakes with lower SO42, concentrations have little geologically derived S, and better reflect the variations in atmospheric S loading. The influence of marine aerosols on lakewater chemistry could also be predicted from the minimum distance to the sea and altitude of the lakes. 4. The most remarkable result of FA was to reveal a factor correlated to DOC (positively) and NO3, (negatively). This inverse relationship might be the result either of independent processes active in the catchment soils and acting in an opposite sense, or a direct interaction, e.g. limitation of denitrification by DOC availability. Such a relationship has been reported in the recent literature in many sites and at all scales, appearing to be a global pattern that could reflect the link between the C and N cycles. 5. The concentration of NO3, is determined by both atmospheric N deposition and the processing capacity of the catchments (i.e. N uptake by plants and soil microbes). The fraction of the variability in NO3, because of atmospheric deposition is captured by an independent factor in the FA. This is the only factor showing a clear pattern when mapped over Europe, indicating lower N deposition in the northernmost areas. 6. A classification has been derived which takes into account all the major chemical features of the mountain lakes in Europe. FA provided the criteria to establish the most important factors influencing lake water chemistry, define classes within them, and classify the surveyed lakes into each class. DA can be used as a tool to scale up the classification to unsurveyed lakes, regarding sensitivity to acidification, marine influence and sources of S. [source] Global pattern of NPP to GPP ratio derived from MODIS data: effects of ecosystem type, geographical location and climateGLOBAL ECOLOGY, Issue 3 2009Yangjian Zhang ABSTRACT Aim, To examine the global pattern of the net primary production (NPP)/gross primary production (GPP) ratio of the Earth's land area along geographical and climatic gradients. Location, The global planetary ecosystem. Methods, The 4-year average annual NPP/GPP ratio of the Earth's land area was calculated using 2000,03 Moderate Resolution Imaging Spectroradiometer (MODIS) data. The global pattern of the NPP/GPP ratio was investigated by comparing it among each typical terrestrial ecosystem and plotting it along a geographical and climatic gradient, including latitude, altitude, temperature and precipitation. Results, The global terrestrial ecosystem had an average NPP/GPP ratio value of 0.52 with minor variation from 2000 to 2003. However, the NPP/GPP ratio showed considerable spatial variation associated with ecosystem type, geographical location and climate. Densely vegetated ecosystems had a lower NPP/GPP ratio than sparsely vegetated ecosystems. Forest ecosystems had a lower NPP/GPP ratio than shrub and herbaceous ecosystems. Geographically, the NPP/GPP ratio increased with altitude. In the Southern Hemisphere, the NPP/GPP ratio decreased along latitude from 30° to 10° and it exhibited high fluctuation in the Northern Hemisphere. Climatically, the NPP/GPP ratio exhibited a decreasing trend along enhanced precipitation when it was less than 2300 mm year,1 and a static trend when the annual precipitation was over 2300 mm. The NPP/GPP ratio showed a decreasing trend along temperature when it was between ,20 °C and 10 °C, and showed an increasing trend along rising temperature when it was between ,10 °C and 20 °C. Within each ecosystem, the NPP/GPP ratio revealed a similar trend to the global trend along temperature and precipitation. Conclusions, The NPP/GPP ratio exhibited a pattern depending on the main climatic characteristics such as temperature and precipitation and geographical factors such as latitude and altitude. The findings of this research challenge the widely held assumption that the NPP/GPP ratio is consistent regardless of ecosystem type. [source] Investor Protection and International Investment Positions: An Empirical Analysis,INTERNATIONAL FINANCE, Issue 2 2006Teresa L. Cyrus Given the recent revival of interest in the institutional determinants of global capital flows, we investigate the relationship between investor protection and international investment positions, using data on 40 countries for the period 1970,98. We find that strong shareholder protection is an important predictor of gross foreign direct investment liabilities, while countries with strong creditor protection tend to have positive stocks of net foreign assets. We conclude that the global pattern of investor protection is a significant determinant of international investment positions. [source] Explaining the global pattern of protected area coverage: relative importance of vertebrate biodiversity, human activities and agricultural suitabilityJOURNAL OF BIOGEOGRAPHY, Issue 8 2008Colby Loucks Abstract Aim, Twelve per cent of the Earth's terrestrial surface is covered by protected areas, but neither these areas nor the biodiversity they contain are evenly distributed spatially. To guide future establishment of protected areas, it is important to understand the factors that have shaped the spatial arrangement of the current protected area system. We used an information-theoretic approach to assess the ability of vertebrate biodiversity measures, resource consumption and agricultural potential to explain the global coverage pattern of protected areas. Location, Global. Methods, For each of 762 World Wildlife Fund terrestrial ecoregions of the world, we measured protected area coverage, resource consumption, terrestrial vertebrate species richness, number of endemic species, number of threatened species, net primary production, elevation and topographic heterogeneity. We combined these variables into 39 a priori models to describe protected area coverage at the global scale, and for six biogeographical realms. Using the Akaike information criterion and Akaike weights, we identified the relative importance and influence of each variable in describing protected area coverage. Results, Globally, the number of endemic species was the best variable describing protected area coverage, followed by the number of threatened species. Species richness and resource consumption were of moderate importance and agricultural potential had weak support for describing protected area coverage at a global scale. Yet, the relative importance of these factors varied among biogeographical realms. Measures of vertebrate biodiversity (species richness, endemism and threatened species) were among the most important variables in all realms, except the Indo-Malayan, but had a wide range of relative importance and influence. Resource consumption was inversely related to protected area coverage across all but one realm (the Palearctic), most strongly in the Nearctic realm. Agricultural potential, despite having little support in describing protected area coverage globally, was strongly and positively related to protection in the Palearctic and Neotropical realms, as well as in the Indo-Malayan realm. The Afrotropical, Indo-Malayan and Australasian realms showed no clear, strong relationships between protected area coverage and the independent variables. Main conclusions, Globally, the existing protected area network is more strongly related to biodiversity measures than to patterns of resource consumption or agricultural potential. However, the relative importance of these factors varies widely among the world's biogeographical realms. Understanding the biases of the current protected area system may help to correct for them as future protected areas are added to the global network. [source] Dermoscopic observation of Bowen's diseaseJOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY & VENEREOLOGY, Issue 5 2004L Bugatti ABSTRACT Background, In the literature no specific dermoscopic criteria have been described for the diagnosis of Bowen's disease (BD). Objective/aim, To assess the morphological findings of BD seen under dermoscopic observation. Methods, Clinical and dermoscopic images of 14 patients affected by BD with various amount of pigmentation were obtained by means of Heine Dermaphot. Dermoscopic images were analysed by experienced observers applying the modified pattern analysis. Results, The most frequently occurring dermoscopic features were found to be: multicomponent pattern (100%); atypical vascular structures (86.6%); absence of pigmented network (64.3%) or presence of pseudo-network (35.7%); irregular diffuse pigmentation or blotches of pigment (64.2%); irregularly distributed dots and globules (64.2%); focal/multifocal hypopigmentation (78.5%), scaly surface (64.2%) and haemorrages (26.6%). Conclusions, Dermoscopically, BD is mainly characterized by a multicomponent global pattern associated with a prominent vascular pattern (mainly dotted vessels) and a scaly surface. Although no specific dermoscopic criteria can be given for BD, epiluminescence can be a valuable aid in the diagnosis of such a mimicker lesion. [source] The global pattern of gene identity variation reveals a history of long-range migrations, bottlenecks, and local mate exchange: Implications for biological raceAMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 1 2009Keith L. Hunley Abstract Several recent studies have argued that human genetic variation conforms to a model of isolation by distance, whereas others see a predominant role for long-range migrations and bottlenecks. It is unclear whether either of these views fully describes the global pattern of human genetic variation. In this article, we use a coalescent-based simulation approach to compare the pattern of neutral genetic variation predicted by these views to the observed pattern estimated from neutral autosomal microsatellites assayed in 1,032 individuals from 53 globally-distributed populations. We find that neither view predicts every aspect of the observed pattern of variation on its own, but that a combination of the two does. Specifically, we demonstrate that the observed pattern of global gene identity variation is consistent with a history of serial population fissions, bottlenecks and long-range migrations associated with the peopling of major geographic regions, and gene flow between local populations. This history has produced a nested pattern of genetic structure that is inconsistent with the existence of independently evolving biological races. We consider the implications of our findings for methods that apportion variation into within- and between-group components and for medical genetics. Am J Phys Anthropol 2009. © 2009 Wiley-Liss, Inc. [source] Distance, power and ideology: diplomatic representation in a world of nation-statesAREA, Issue 2 2008Eric Neumayer Sending diplomatic missions abroad and receiving foreign missions at home is in the political and economic interests of countries. But such missions depend on domestic and foreign political will and they also cost scarce resources. This article demonstrates that the global pattern of diplomatic representation is significantly determined by geographical distance between countries, by the power of both sending and recipient countries and by the degree of their ideological affinity. The pattern of diplomatic representation is both a reflection of and a contributor to a world of nation-states dominated by geographical distance, unequal power and ideological division. [source] Does habitat use explain large scale species richness patterns of aquatic beetles in Europe?ECOGRAPHY, Issue 2 2003Ignacio Ribera Regularities in species richness are widely observed but controversy continues over its mechanistic explanation. Because richness patterns are usually a compound measure derived from taxonomically diverse species with different ecological requirements, these analyses may confound diverse causes of species numbers. Here we investigate species richness in the aquatic beetle fauna of Europe, separating major taxonomic groups and two major ecological types, species occurring in standing and running water bodies. We collated species distributions for 800+ species of water beetles in 15 regions across western Europe. Species number in any of these regions was related to three variables: total area size, geographic connectedness of the area, and latitude. Pooled species numbers were accurately predicted, but correlations were different for species associated with either running or standing water. The former were mostly correlated with latitude, while the latter were only correlated with the measure of connectedness or with area size. These differences were generally also observed in each of the four phylogenetically independent lineages of aquatic Coleoptera when analysed separately. We propose that effects of habitat, in this case possibly mediated by different long term persistence of running and standing water bodies, impose constraints at the population or local level which, if effective over larger temporal and spatial scales, determine global patterns of species richness. [source] A comprehensive framework for global patterns in biodiversityECOLOGY LETTERS, Issue 1 2004Robert E. Ricklefs Abstract The present study proposes to reconcile the different spatial and temporal scales of regional species production and local constraint on species richness. Although interactions between populations rapidly achieve equilibrium and limit membership in ecological communities locally, these interactions occur over heterogeneous environments within large regions, where the populations of species are stably regulated through competition and habitat selection. Consequently, exclusion of species from a region depends on long-term regional-scale environmental change or evolutionary change among interacting populations, bringing species production and extinction onto the same scale and establishing a link between local and regional processes. [source] Self-Assembled Heteroepitaxial Oxide Nanocomposite Thin Film Structures: Designing Interface-Induced Functionality in Electronic MaterialsADVANCED FUNCTIONAL MATERIALS, Issue 13 2010Judith L. MacManus-Driscoll Abstract Achieving self-assembling/self-organizing systems is the holy grail of nanotechnology. Spontaneous organization is not unique to the physical sciences since nature has been producing such systems for millions of years. In biological systems global patterns emerge from numerous interactions among lower-level components of the system. The same is true for physical systems. In this review, the self-assembly mechanisms of oxide nanocomposite films, as well as the advantageous functionalities that arise from such ordered structures, are explored. [source] Below-ground carbon flux and partitioning: global patterns and response to temperatureFUNCTIONAL ECOLOGY, Issue 6 2008C. M. Litton Summary 1The fraction of gross primary production (GPP) that is total below-ground carbon flux (TBCF) and the fraction of TBCF that is below-ground net primary production (BNPP) represent globally significant C fluxes that are fundamental in regulating ecosystem C balance. However, global estimates of the partitioning of GPP to TBCF and of TBCF to BNPP, as well as the absolute size of these fluxes, remain highly uncertain. 2Efforts to model below-ground processes are hindered by methodological difficulties for estimating below-ground C cycling, the complexity of below-ground interactions, and an incomplete understanding of the response of GPP, TBCF and BNPP to climate change. Due to a paucity of available data, many terrestrial ecosystem models and ecosystem-level studies of whole stand C use efficiency rely on assumptions that: (i) C allocation patterns across large geographic, climatic and taxonomic scales are fixed; and (ii) c. 50% of TBCF is BNPP. 3Here, we examine available information on GPP, TBCF, BNPP, TBCF : GPP and BNPP : TBCF from a diverse global data base of forest ecosystems to understand patterns in below-ground C flux and partitioning, and their response to mean annual temperature (MAT). 4MAT and mean annual precipitation (MAP) covaried strongly across the global forest data base (37 mm increase in MAP for every 1 °C increase in MAT). In all analyses, however, MAT was the most important variable explaining observed patterns in below-ground C processes. 5GPP, TBCF and BNPP all increased linearly across the global scale range of MAT. TBCF : GPP increased significantly with MAT for temperate and tropical ecosystems (> 5 °C), but variability was high across the data set. BNPP : TBCF varied from 0·26 to 0·53 across the entire MAT gradient (,5 to 30 °C), with a much narrower range of 0·42 to 0·53 for temperate and tropical ecosystems (5 to 30 °C). 6Variability in the data sets was moderate and clear exceptions to the general patterns exist that likely relate to other factors important for determining below-ground C flux and partitioning, in particular water availability and nutrient supply. Still, our results highlight global patterns in below-ground C flux and partitioning in forests in response to MAT that in part confirm previously held assumptions. [source] Shifts in leaf N : P ratio during resorption reflect soil P in temperate rainforestFUNCTIONAL ECOLOGY, Issue 4 2008Sarah J. Richardson Summary 1Large-scale syntheses of leaf and litter N and P concentrations have demonstrated that leaf and litter N : P ratios both decline with latitude, that litter N : P ratios are generally greater than those of fresh leaves, and that the difference between these two ratios increases towards the tropics. These patterns have been ascribed to either a direct effect of temperature on plant growth rates and leaf-level physiology, or a decline in soil P towards the tropics. We test the hypothesis that global patterns of leaf and litter N : P ratios reflect a soil-P gradient by examining leaf and litter N : P in all species from a temperate rainforest along a soil-P gradient. 2The soil P gradient followed a toposequence of 20 plots. There was > 50-fold variation in soil total P from ridges (23,136 mg kg,1), through faces and terraces (32,744 mg kg,1), to gullies (440,1214 mg kg,1). 3The N : P ratios of leaves and litter both declined as soil total P increased, and the N : P ratio of litter was greater than that of fresh leaves. The difference between litter N : P and fresh leaf N : P declined with increasing soil total P supporting the hypothesis that global patterns of N : P ratios reflect gradients of soil P. 4Compositional turnover with soil P partly contributed to the total plant community leaf and litter nutrient concentration responses. However, consistent within-species responses pointed to a soil-based mechanism for determining responses by the total plant community. 5Comparisons of our litter data to global data sets suggest that the vegetation was well adapted to low soil nutrient concentrations with 37% of litter N and 24% of litter P samples being below published thresholds for highly proficient nutrient resorption. 6The range of leaf N and leaf P concentrations at our site captured a large portion of the range reported in global leaf trait data sets. 7Highly proficient P resorption was responsible for the divergence in leaf and litter N : P ratios on P-poor soils. These results emphasize the significance of proficient nutrient resorption as an advantageous plant trait for nutrient conservation on P-poor soils. [source] Geostatistical Simulation for the Assessment of Regional Soil PollutionGEOGRAPHICAL ANALYSIS, Issue 2 2010Marc Van Meirvenne Regional scale inventories of heavy metal concentrations in soil increasingly are being done to evaluate their global patterns of variation. Sometimes these global pattern evaluations reveal information that is not identified by more detailed studies. Geostatistical methods, such as stochastic simulation, have not yet been used routinely for this purpose in spite of their potential. To investigate such a use of geostatistical methods, we analyzed a data set of 14,674 copper and 12,441 cadmium observations in the topsoil of Flanders, Belgium, covering 13,522 km2. Outliers were identified and removed, and the distributions were spatially declustered. Copper was analyzed using sequential Gaussian simulation, whereas for cadmium we used sequential indicator simulation because of the large proportion (43%) of censored data. We complemented maps of the estimated values with maps of the probability of exceeding a critical sanitation threshold for agricultural land use. These sets of maps allowed the identification of regional patterns of increased metal concentrations and provided insight into their potential causes. Mostly areas with known industrial activities (such as lead and zinc smelters) could be delineated, but the effects of shells fired during the First World War were also identified. En los estudios de contaminación de suelos as escala regional, es práctica común la implementación de inventarios de concentraciones de metales pesados en el suelo con el fin de evaluar sus patrones globales de variación espacial. A veces dichas evaluaciones de patrones globales proporcionan información que no son aparentes en estudios realizados a escalas más detalladas. En este contexto, a pesar del potencial analítico que poseen, los métodos geostadísticos como la simulación estocástica han recibido poca atención. Los autores del presente artículo proponen llenar este vacío aplicando métodos geostadísticos para el análisis de dos bases de datos: 14,674 observaciones de cobre (Cu) y 12,441 observaciones de cadmio (Cd). Los datos corresponden a la capa superior de suelo en un área de 13,522 km2 en Flandes, Belgica. Tras la remoción de los valores extremos (outliers) y la desaglomeración de las distribuciones, los autores analizan los datos vía dos procedimientos: a) una Simulación Secuencial Gausiana (SGS) para los datos de cobre, y b) una Simulación Secuencial Indicador (SIS). La diferencia en el tratamiento analítico para ambos metales obedece a la considerable proporción (43%) de datos censurados de cadmio. Los mapas resultantes de valores estimados fueron complementados con mapas que ilustran la probabilidad de exceder los umbrales críticos para uso agrícola de la tierra. Esta serie de mapas permitió la identificación de patrones regionales de concentraciones crecientes de metales y proporciono claves importantes acerca de sus posibles causas. Los patrones hallados coinciden con áreas donde se realizan actividades industriales (como fundiciones de plomo y zinc), pero también con la distribución espacial de casquillos de balas disparadas durante la Primera Guerra Mundial. [source] Interplay between global patterns of environmental temperature and variation in nonshivering thermogenesis of rodent species across large spatial scalesGLOBAL CHANGE BIOLOGY, Issue 9 2009ENRIQUE RODRÍGUEZ-SERRANO Abstract The purpose of this study was to test for correlations of mass-independent nonshivering thermogenesis (NST) in rodent species with climatic factors such as maximum and minimum geographic temperature. We first analyzed whether the responses of rodents show a phylogenetic signal. If so, and if the NST over a broad geographical range is similar, then such responses probably reflect physiological evolutionary adaptation. Our results show that NST did not show phylogenetic signal, appears to be evolutionary labile and is negatively correlated with environmental temperature. We predicted that species evolved in cold climates will exhibit higher mass-independent NST than species from warmer habitats. Indeed, we observed that the relationships between mass-independent NST and minimum temperature (rs=,0.411, P=0.009) as well as between NST and maximum temperature (rs=,0.443, P=0.004) were both negatively and significantly correlated, thus supporting our predictions. Thus, thermal physiology may be a significant factor underlying the ecological and evolutionary success of animals. Finally we suggest that due to the pressing need to explain and predict the likely biological impact of climatic change, advances in this field are necessary. [source] Crop planting dates: an analysis of global patternsGLOBAL ECOLOGY, Issue 5 2010William J. Sacks ABSTRACT Aim, To assemble a data set of global crop planting and harvesting dates for 19 major crops, explore spatial relationships between planting date and climate for two of them, and compare our analysis with a review of the literature on factors that drive decisions on planting dates. Location, Global. Methods, We digitized and georeferenced existing data on crop planting and harvesting dates from six sources. We then examined relationships between planting dates and temperature, precipitation and potential evapotranspiration using 30-year average climatologies from the Climatic Research Unit, University of East Anglia (CRU CL 2.0). Results, We present global planting date patterns for maize, spring wheat and winter wheat (our full, publicly available data set contains planting and harvesting dates for 19 major crops). Maize planting in the northern mid-latitudes generally occurs in April and May. Daily average air temperatures are usually c. 12,17 °C at the time of maize planting in these regions, although soil moisture often determines planting date more directly than does temperature. Maize planting dates vary more widely in tropical regions. Spring wheat is usually planted at cooler temperatures than maize, between c. 8 and 14 °C in temperate regions. Winter wheat is generally planted in September and October in the northern mid-latitudes. Main conclusions, In temperate regions, spatial patterns of maize and spring wheat planting dates can be predicted reasonably well by assuming a fixed temperature at planting. However, planting dates in lower latitudes and planting dates of winter wheat are more difficult to predict from climate alone. In part this is because planting dates may be chosen to ensure a favourable climate during a critical growth stage, such as flowering, rather than to ensure an optimal climate early in the crop's growth. The lack of predictability is also due to the pervasive influence of technological and socio-economic factors on planting dates. [source] New insights into global patterns of ocean temperature anomalies: implications for coral reef health and managementGLOBAL ECOLOGY, Issue 3 2010Elizabeth R. Selig ABSTRACT Aim, Coral reefs are widely considered to be particularly vulnerable to changes in ocean temperatures, yet we understand little about the broad-scale spatio-temporal patterns that may cause coral mortality from bleaching and disease. Our study aimed to characterize these ocean temperature patterns at biologically relevant scales. Location, Global, with a focus on coral reefs. Methods, We created a 4-km resolution, 21-year global ocean temperature anomaly (deviations from long-term means) database to quantify the spatial and temporal characteristics of temperature anomalies related to both coral bleaching and disease. Then we tested how patterns varied in several key metrics of disturbance severity, including anomaly frequency, magnitude, duration and size. Results, Our analyses found both global variation in temperature anomalies and fine-grained spatial variability in the frequency, duration and magnitude of temperature anomalies. However, we discovered that even during major climatic events with strong spatial signatures, like the El Niño,Southern Oscillation, areas that had high numbers of anomalies varied between years. In addition, we found that 48% of bleaching-related anomalies and 44% of disease-related anomalies were less than 50 km2, much smaller than the resolution of most models used to forecast climate changes. Main conclusions, The fine-scale variability in temperature anomalies has several key implications for understanding spatial patterns in coral bleaching- and disease-related anomalies as well as for designing protected areas to conserve coral reefs in a changing climate. Spatial heterogeneity in temperature anomalies suggests that certain reefs could be targeted for protection because they exhibit differences in thermal stress. However, temporal variability in anomalies could complicate efforts to protect reefs, because high anomalies in one year are not necessarily predictive of future patterns of stress. Together, our results suggest that temperature anomalies related to coral bleaching and disease are likely to be highly heterogeneous and could produce more localized impacts of climate change. [source] Global trends in senesced-leaf nitrogen and phosphorusGLOBAL ECOLOGY, Issue 5 2009Zhiyou Yuan ABSTRACT Aim, Senesced-leaf litter plays an important role in the functioning of terrestrial ecosystems. While green-leaf nutrients have been reported to be affected by climatic factors at the global scale, the global patterns of senesced-leaf nutrients are not well understood. Location, Global. Methods, Here, bringing together a global dataset of senesced-leaf N and P spanning 1253 observations and 638 plant species at 365 sites and of associated mean climatic indices, we describe the world-wide trends in senesced-leaf N and P and their stoichiometric ratios. Results, Concentration of senesced-leaf N was highest in tropical forests, intermediate in boreal, temperate, and mediterranean forests and grasslands, and lowest in tundra, whereas P concentration was highest in grasslands, lowest in tropical forests and intermediate in other ecosystems. Tropical forests had the highest N : P and C : P ratios in senesced leaves. When all data were pooled, N concentration significantly increased, but senesced-leaf P concentration decreased with increasing mean annual temperature (MAT) and mean annual precipitation (MAP). The N : P and C : P ratios also increased with MAT and MAP, but C : N ratios decreased. Plant functional type (PFT), i.e. life-form (grass, herb, shrub or tree), phylogeny (angiosperm versus gymnosperm) and leaf habit (deciduous versus evergreen), affected senesced-leaf N, P, N : P, C : N and C : P with a ranking of senesced-leaf N from high to low: forbs , shrubs , trees > grasses, while the ranking of P was forbs , shrubs , trees < grasses. The climatic trends of senesced-leaf N and P and their stoichiometric ratios were similar between PFTs. Main conclusions, Globally, senesced-leaf N and P concentrations differed among ecosystem types, from tropical forest to tundra. Differences were significantly related to global climate variables such as MAT and MAP and also related to plant functional types. These results at the global scale suggest that nutrient feedback to soil through leaf senescence depends on both the climatic conditions and the plant composition of an ecosystem. [source] Richness patterns, species distributions and the principle of extreme deconstructionGLOBAL ECOLOGY, Issue 2 2009Levi Carina Terribile ABSTRACT Aim, To analyse the global patterns in species richness of Viperidae snakes through the deconstruction of richness into sets of species according to their distribution models, range size, body size and phylogenetic structure, and to test if environmental drivers explaining the geographical ranges of species are similar to those explaining richness patterns, something we called the extreme deconstruction principle. Location, Global. Methods, We generated a global dataset of 228 terrestrial viperid snakes, which included geographical ranges (mapped at 1° resolution, for a grid with 7331 cells world-wide), body sizes and phylogenetic relationships among species. We used logistic regression (generalized linear model; GLM) to model species geographical ranges with five environmental predictors. Sets of species richness were also generated for large and small-bodied species, for basal and derived species and for four classes of geographical range sizes. Richness patterns were also modelled against the five environmental variables through standard ordinary least squares (OLS) multiple regressions. These subsets are replications to test if environmental factors driving species geographical ranges can be directly associated with those explaining richness patterns. Results, Around 48% of the total variance in viperid richness was explained by the environmental model, but richness sets revealed different patterns across the world. The similarity between OLS coefficients and the primacy of variables across species geographical range GLMs was equal to 0.645 when analysing all viperid snakes. Thus, in general, when an environmental predictor it is important to model species geographical ranges, this predictor is also important when modelling richness, so that the extreme deconstruction principle holds. However, replicating this correlation using subsets of species within different categories in body size, range size and phylogenetic structure gave more variable results, with correlations between GLM and OLS coefficients varying from ,0.46 up to 0.83. Despite this, there is a relatively high correspondence (r = 0.73) between the similarity of GLM-OLS coefficients and R2 values of richness models, indicating that when richness is well explained by the environment, the relative importance of environmental drivers is similar in the richness OLS and its corresponding set of GLMs. Main conclusions, The deconstruction of species richness based on macroecological traits revealed that, at least for range size and phylogenetic level, the causes underlying patterns in viperid richness differ for the various sets of species. On the other hand, our analyses of extreme deconstruction using GLM for species geographical range support the idea that, if environmental drivers determine the geographical distribution of species by establishing niche boundaries, it is expected, at least in theory, that the overlap among ranges (i.e. richness) will reveal similar effects of these environmental drivers. Richness patterns may be indeed viewed as macroecological consequences of population-level processes acting on species geographical ranges. [source] Global patterns of genetic variation in plant species along vertical and horizontal gradients on mountainsGLOBAL ECOLOGY, Issue 2 2008Takafumi Ohsawa ABSTRACT Aim To understand global patterns of genetic variation in plant species on mountains and to consider the significance of mountains for the genetic structure and evolution of plant species. Location Global. Methods We review published studies. Results Genetic diversity within populations can vary along altitudinal gradients in one of four patterns. Eleven of 42 cited studies (26% of the total) found that populations at intermediate altitudes have greater diversity than populations at lower and higher altitudes. This is because the geographically central populations are under optimal environmental conditions, whereas the peripheral populations are in suboptimal situations. The second pattern, indicating that higher populations have less diversity than lower populations, was found in eight studies (19%). The third pattern, indicating that lower populations have lower diversity than higher populations, was found in 10 studies (24%). In 12 studies (29%), the intrapopulation genetic variation was found to be unaffected by altitude. Evidence of altitudinal differentiation was found in more than half of these studies, based on measurements of a range of variables including genome size, number of chromosomes or a range of loci using molecular markers. Furthermore, great variation has been found in phenotypes among populations at different altitudes in situ and in common garden experiments, even in cases where there was no associated variation in molecular composition. Mountains can be genetic barriers for species that are distributed at low elevations, but they can also provide pathways for species that occupy high-elevation habitats. [Correction added after publication 9 October 2007: ,less diversity' changed to ,greater diversity' in the second sentence of the Results section of the Abstract] Main conclusions Genetic diversity within populations can vary along altitudinal gradients as a result of several factors. The results highlight the importance of phenotypic examinations in detecting altitudinal differences. The influence of mountain ridges on genetic differentiation varies depending, inter alia, on the elevation at which the species occurs. Based on these findings, zoning by altitudes or ridges would be helpful for the conservation of tree populations with the onset of global warming. [source] Political Consequences of the New InequalityINTERNATIONAL STUDIES QUARTERLY, Issue 3 2001Craig N. Murphy This article proposes agendas for teaching and research about shifting global patterns of equality and inequality, a very different agenda than was appropriate when the last undergraduate professor was president of ISA, almost forty years ago. Today, unlike in that Cold War world, formal democracy is flourishing, state power is diminishing, gender inequality has diminished, and income inequality has risen. Consequences of these new patterns that demand our attention as teachers and scholars include: (1) more frequent protracted social conflicts, (2) a newly politicized sphere of international public health, (3) the new global gender politics, (4) the new global politics of the super-rich, and (5) the new politics and ethics of the world's privileged, a group that includes most ISA members and most of our students. Our responsibilities as teachers have grown, in part, because popular media present a decreasingly coherent picture of each of these patterns; and that incoherence, itself, may help sustain global inequalities. [source] Long-standing environmental conditions, geographic isolation and host,symbiont specificity influence the relative ecological dominance and genetic diversification of coral endosymbionts in the genus SymbiodiniumJOURNAL OF BIOGEOGRAPHY, Issue 5 2010Todd C. LaJeunesse Abstract Aim, This study examines the importance of geographic proximity, host life history and regional and local differences in environment (temperature and water clarity) in driving the ecological and evolutionary processes underpinning the global patterns of diversity and distribution of symbiotic dinoflagellates. By comparing and contrasting coral,algal symbioses from isolated regions with differing environmental conditions, we may assess the potential of coral communities to respond to significant changes in climate. Location, Indian Ocean. Methods, Community assemblages of obligate symbiotic invertebrates were sampled at numerous sites from two regions, the north-eastern Indian Ocean (Andaman Sea, western Thailand) and the western Indian Ocean (Zanzibar, Tanzania). Molecular genetic methods, including denaturing gradient gel electrophoresis analysis of the ribosomal internal transcribed spacers, DNA sequencing and microsatellite genotyping, were used to characterize the ,species' diversity and evolutionary relationships of symbiotic dinoflagellates (genus Symbiodinium). Host,symbiont specificity, geographic isolation and local and regional environmental factors were evaluated in terms of their importance in governing the distribution and prevalence of certain symbiont taxa. Results, Host-generalist symbionts (C3u and D1-4, formerly D1a now designated Symbiodinium trenchi) frequently occurred alone and sometimes together in hosts with horizontal modes of symbiont acquisition. However, the majority of Symbiodinium diversity consisted of apparently host-specific ,species'. Clade C Symbiodinium were diverse and dominated host assemblages from sites sampled in the western Indian Ocean, a pattern analogous to symbiont communities on the Great Barrier Reef with similar environmental conditions. Clade D Symbiodinium were diverse and occurred frequently in hosts from the north-eastern Indian Ocean, especially at inshore locations, where temperatures are warmer, water turbidity is high and large tidal exchanges commonly expose coral populations to aerial desiccation. Main conclusions, Regional and local differences in cnidarian,algal combinations indicate that these symbioses are ecologically and evolutionarily responsive and can thrive under various environmental conditions. The high temperatures and turbid conditions of the north-eastern Indian Ocean partly explain the ecological success of Clade D Symbiodinium relative to Clade C. Phylogenetic, ecological and population genetic data further indicate that Clade D has undergone an adaptive radiation, especially in regions around Southeast Asia, during the Pleistocene. [source] Global patterns in plant heightJOURNAL OF ECOLOGY, Issue 5 2009Angela T. Moles Summary 1. ,Plant height is a central part of plant ecological strategy. It is strongly correlated with life span, seed mass and time to maturity, and is a major determinant of a species' ability to compete for light. Plant height is also related to critical ecosystem variables such as animal diversity and carbon storage capacity. However, remarkably little is known about global patterns in plant height. Here, we use maximum height data for 7084 plant Species × Site combinations to provide the first global, cross-species quantification of the latitudinal gradient in plant height. 2. ,The mean maximum height of species growing within 15° of the equator (7.8 m) was 29 times greater than the height of species between 60° and 75° N (27 cm), and 31 times greater than the height of species between 45° and 60° S (25 cm). There was no evidence that the latitudinal gradient in plant height was different in the northern hemisphere than in the southern hemisphere (P = 0.29). A 2.4-fold drop in plant height at the edge of the tropics (P = 0.006) supports the idea that there might be a switch in plant strategy between temperate and tropical zones. 3. ,We investigated 22 environmental variables to determine which factors underlie the latitudinal gradient in plant height. We found that species with a wide range of height strategies were present in cold, dry, low productivity systems, but there was a noticeable lack of very short species in wetter, warmer, more productive sites. Variables that capture information about growing conditions during the harsh times of the year were relatively poor predictors of height. The best model for global patterns in plant height included only one term: precipitation in the wettest month (R2 = 0.256). 4. ,Synthesis. We found a remarkably steep relationship between latitude and height, indicating a major difference in plant strategy between high and low latitude systems. We also provide new, surprising information about the correlations between plant height and environmental variables. [source] Tobacco use, cancer causation and public health impactJOURNAL OF INTERNAL MEDICINE, Issue 6 2002H. Kuper Abstract.,Kuper H, Adami H-O, Boffetta P (University College London, Torrington Place, London, UK; Karolinska Institutet, Stockholm, Sweden; and International Agency for Research on Cancer, Lyon, France). Tobacco use, cancer causation and public health impact. J Intern Med 2002; 251: 455,466. This review describes global patterns of tobacco use and the mechanisms by which tobacco use is involved in carcinogenesis. A second part will discuss the association between tobacco use and risk of specific cancer types. To bacco use has traditionally been a practice of high-income countries, but it has recently been taken up in low-income countries and it is particularly common in men. A wide variety of tobacco products exist, of which cigarettes are most frequently consumed. Tobacco products contain more than 50 established or identified carcinogens and these may increase risk of cancer by causing mutations that disrupt cell cycle regulation, or through their effect on the immune or endocrine systems. Certain factors such as genes, diet and environmental exposures may alter susceptibility to cancer in tobacco users. Today at least 15% of all cancers are estimated to be attributable to smoking, but this figure is expected to increase because of the uptake of tobacco use in low-income countries. [source] Global map of the prevalence of symptoms of rhinoconjunctivitis in children: The International Study of Asthma and Allergies in Childhood (ISAAC) Phase ThreeALLERGY, Issue 1 2009N. Aït-Khaled Background:, Phase One of the International Study of Asthma and Allergies in Childhood (ISAAC) measured the global patterns of prevalence and severity of symptoms of rhinoconjunctivitis in children in 1993,1997. Methods:, International Study of Asthma and Allergies in Childhood Phase Three was a cross-sectional survey performed 5,10 years after Phase One using the same methodology. Phase Three covered all of the major regions of the world and involved 1 059 053 children of 2 age groups from 236 centres in 98 countries. Results:, The average overall prevalence of current rhinoconjunctivitis symptoms was 14.6% for the 13- to 14-year old children (range 1.0,45%). Variation in the prevalence of severe rhinoconjunctivitis symptoms was observed between centres (range 0.0,5.1%) and regions (range 0.4% in western Europe to 2.3% in Africa), with the highest prevalence being observed mainly in the centres from middle and low income countries, particularly in Africa and Latin America. Co-morbidity with asthma and eczema varied from 1.6% in the Indian sub-continent to 4.7% in North America. For 6- to 7-year old children, the average prevalence of rhinoconjunctivitis symptoms was 8.5%, and large variations in symptom prevalence were also observed between regions, countries and centres. Discussion:, Wide global variations exist in the prevalence of current rhinoconjunctivitis symptoms, being higher in high vs low income countries, but the prevalence of severe symptoms was greater in less affluent countries. Co-morbidity with asthma is high particularly in Africa, North America and Oceania. This global map of symptom prevalence is of clinical importance for health professionals. [source] | ||||||||||||||||||||||||||||||||||