Alan Grainger

Bio: Alan Grainger is an academic researcher from University of Leeds. The author has contributed to research in topic(s): Deforestation & Global warming. The author has an hindex of 31, co-authored 65 publication(s) receiving 10358 citation(s).

Extinction risk from climate change

Abstract: Climate change over the past approximately 30 years has produced numerous shifts in the distributions and abundances of species and has been implicated in one species-level extinction. Using projections of species' distributions for future climate scenarios, we assess extinction risks for sample regions that cover some 20% of the Earth's terrestrial surface. Exploring three approaches in which the estimated probability of extinction shows a power-law relationship with geographical range size, we predict, on the basis of mid-range climate-warming scenarios for 2050, that 15-37% of species in our sample of regions and taxa will be 'committed to extinction'. When the average of the three methods and two dispersal scenarios is taken, minimal climate-warming scenarios produce lower projections of species committed to extinction ( approximately 18%) than mid-range ( approximately 24%) and maximum-change ( approximately 35%) scenarios. These estimates show the importance of rapid implementation of technologies to decrease greenhouse gas emissions and strategies for carbon sequestration.

Dynamics of global forest area: Results from the FAO Global Forest Resources Assessment 2015

Abstract: The area of land covered by forest and trees is an important indicator of environmental condition This study presents and analyses results from the Global Forest Resources Assessment 2015 (FRA 2015) of the Food and Agriculture Organization of the United Nations FRA 2015 was based on responses to surveys by individual countries using a common reporting framework, agreed definitions and reporting standards Results indicated that total forest area declined by 3%, from 4128Mha in 1990 to 3999Mha in 2015 The annual rate of net forest loss halved from 73Mhay−1 in the 1990s to 33Mhay−1 between 2010 and 2015 Natural forest area declined from 3961Mha to 3721Mha between 1990 and 2015, while planted forest (including rubber plantations) increased from 168Mha to 278Mha From 2010 to 2015, tropical forest area declined at a rate of 55Mhay−1 – only 58% of the rate in the 1990s – while temperate forest area expanded at a rate of 22Mhay−1 Boreal and sub-tropical forest areas showed little net change Forest area expanded in Europe, North America, the Caribbean, East Asia, and Western-Central Asia, but declined in Central America, South America, South and Southeast Asia and all three regions in Africa Analysis indicates that, between 1990 and 2015, 13 tropical countries may have either passed through their forest transitions from net forest loss to net forest expansion, or continued along the path of forest expansion that follows these transitions Comparing FRA 2015 statistics with the findings of global and pan-tropical remote-sensing forest area surveys was challenging, due to differences in assessment periods, the definitions of forest and remote sensing methods More investment in national and global forest monitoring is needed to provide better support for international initiatives to increase sustainable forest management and reduce forest loss, particularly in tropical countries

Difficulties in tracking the long-term global trend in tropical forest area

Abstract: The long-term trend in tropical forest area receives less scrutiny than the tropical deforestation rate. We show that constructing a reliable trend is difficult and evidence for decline is unclear, within the limits of errors involved in making global estimates. A time series for all tropical forest area, using data from Forest Resources Assessments (FRAs) of the United Nations Food and Agriculture Organization, is dominated by three successively corrected declining trends. Inconsistencies between these trends raise questions about their reliability, especially because differences seem to result as much from errors as from changes in statistical design and use of new data. A second time series for tropical moist forest area shows no apparent decline. The latter may be masked by the errors involved, but a "forest return" effect may also be operating, in which forest regeneration in some areas offsets deforestation (but not biodiversity loss) elsewhere. A better monitoring program is needed to give a more reliable trend. Scientists who use FRA data should check how the accuracy of their findings depends on errors in the data.

The forest transition: Towards a more comprehensive theoretical framework☆

Abstract: Building on the contributions of Mather and others, this paper offers an approach for developing a more comprehensive theory of the forest transition. We argue that long-run changes in forest cover in a country or region cannot be separated from the overall pattern of land use changes. Moreover, this pattern is determined by relative land values; forest cover changes over time as the value of one land use relative to the value of its competing use changes over time. However, the actual values that are used to allocate land may be far from optimal; that is, the presence of market, policy and institutional failures can distort economic and political incentives that can lead to bias in favour of one type of land use over the other, and may ultimately explain why a forest transition may be delayed unnecessarily in some countries and regions.

The extent of forest in dryland biomes

Abstract: Dryland biomes cover two-fifths of Earth’s land surface, but their forest area is poorly known. Here, we report an estimate of global forest extent in dryland biomes, based on analyzing more than 210,000 0.5-hectare sample plots through a photo-interpretation approach using large databases of satellite imagery at (i) very high spatial resolution and (ii) very high temporal resolution, which are available through the Google Earth platform. We show that in 2015, 1327 million hectares of drylands had more than 10% tree-cover, and 1079 million hectares comprised forest. Our estimate is 40 to 47% higher than previous estimates, corresponding to 467 million hectares of forest that have never been reported before. This increases current estimates of global forest cover by at least 9%.

The Theory of Island Biogeography

Abstract: Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols Used xiii 1. The Importance of Islands 3 2. Area and Number of Speicies 8 3. Further Explanations of the Area-Diversity Pattern 19 4. The Strategy of Colonization 68 5. Invasibility and the Variable Niche 94 6. Stepping Stones and Biotic Exchange 123 7. Evolutionary Changes Following Colonization 145 8. Prospect 181 Glossary 185 References 193 Index 201

Maximum entropy modeling of species geographic distributions

Abstract: The availability of detailed environmental data, together with inexpensive and powerful computers, has fueled a rapid increase in predictive modeling of species environmental requirements and geographic distributions. For some species, detailed presence/absence occurrence data are available, allowing the use of a variety of standard statistical techniques. However, absence data are not available for most species. In this paper, we introduce the use of the maximum entropy method (Maxent) for modeling species geographic distributions with presence-only data. Maxent is a general-purpose machine learning method with a simple and precise mathematical formulation, and it has a number of aspects that make it well-suited for species distribution modeling. In order to investigate the efficacy of the method, here we perform a continental-scale case study using two Neotropical mammals: a lowland species of sloth, Bradypus variegatus, and a small montane murid rodent, Microryzomys minutus. We compared Maxent predictions with those of a commonly used presence-only modeling method, the Genetic Algorithm for Rule-Set Prediction (GARP). We made predictions on 10 random subsets of the occurrence records for both species, and then used the remaining localities for testing. Both algorithms provided reasonable estimates of the species’ range, far superior to the shaded outline maps available in field guides. All models were significantly better than random in both binomial tests of omission and receiver operating characteristic (ROC) analyses. The area under the ROC curve (AUC) was almost always higher for Maxent, indicating better discrimination of suitable versus unsuitable areas for the species. The Maxent modeling approach can be used in its present form for many applications with presence-only datasets, and merits further research and development. © 2005 Elsevier B.V. All rights reserved.

Novel methods improve prediction of species' distributions from occurrence data

Abstract: Prediction of species' distributions is central to diverse applications in ecology, evolution and conservation science. There is increasing electronic access to vast sets of occurrence records in museums and herbaria, yet little effective guidance on how best to use this information in the context of numerous approaches for modelling distributions. To meet this need, we compared 16 modelling methods over 226 species from 6 regions of the world, creating the most comprehensive set of model comparisons to date. We used presence-only data to fit models, and independent presence-absence data to evaluate the predictions. Along with well-established modelling methods such as generalised additive models and GARP and BIOCLIM, we explored methods that either have been developed recently or have rarely been applied to modelling species' distributions. These include machine-learning methods and community models, both of which have features that may make them particularly well suited to noisy or sparse information, as is typical of species' occurrence data. Presence-only data were effective for modelling species' distributions for many species and regions. The novel methods consistently outperformed more established methods. The results of our analysis are promising for the use of data from museums and herbaria, especially as methods suited to the noise inherent in such data improve.

High-Resolution Global Maps of 21st-Century Forest Cover Change

Abstract: Quantification of global forest change has been lacking despite the recognized importance of forest ecosystem services. In this study, Earth observation satellite data were used to map global forest loss (2.3 million square kilometers) and gain (0.8 million square kilometers) from 2000 to 2012 at a spatial resolution of 30 meters. The tropics were the only climate domain to exhibit a trend, with forest loss increasing by 2101 square kilometers per year. Brazil's well-documented reduction in deforestation was offset by increasing forest loss in Indonesia, Malaysia, Paraguay, Bolivia, Zambia, Angola, and elsewhere. Intensive forestry practiced within subtropical forests resulted in the highest rates of forest change globally. Boreal forest loss due largely to fire and forestry was second to that in the tropics in absolute and proportional terms. These results depict a globally consistent and locally relevant record of forest change.

Predicting species distribution: offering more than simple habitat models.

Abstract: In the last two decades, interest in species distribution models (SDMs) of plants and animals has grown dramatically. Recent advances in SDMs allow us to potentially forecast anthropogenic effects on patterns of biodiversity at different spatial scales. However, some limitations still preclude the use of SDMs in many theoretical and practical applications. Here, we provide an overview of recent advances in this field, discuss the ecological principles and assumptions underpinning SDMs, and highlight critical limitations and decisions inherent in the construction and evaluation of SDMs. Particular emphasis is given to the use of SDMs for the assessment of climate change impacts and conservation management issues. We suggest new avenues for incorporating species migration, population dynamics, biotic interactions and community ecology into SDMs at multiple spatial scales. Addressing all these issues requires a better integration of SDMs with ecological theory.