Ecology the Study of the Relationships Between Living Organisms and Their Environment Biosphere: Levels of Organization
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Biogeography, Community Structure and Biological Habitat Types of Subtidal Reefs on the South Island West Coast, New Zealand
Biogeography, community structure and biological habitat types of subtidal reefs on the South Island West Coast, New Zealand SCIENCE FOR CONSERVATION 281 Biogeography, community structure and biological habitat types of subtidal reefs on the South Island West Coast, New Zealand Nick T. Shears SCIENCE FOR CONSERVATION 281 Published by Science & Technical Publishing Department of Conservation PO Box 10420, The Terrace Wellington 6143, New Zealand Cover: Shallow mixed turfing algal assemblage near Moeraki River, South Westland (2 m depth). Dominant species include Plocamium spp. (yellow-red), Echinothamnium sp. (dark brown), Lophurella hookeriana (green), and Glossophora kunthii (top right). Photo: N.T. Shears Science for Conservation is a scientific monograph series presenting research funded by New Zealand Department of Conservation (DOC). Manuscripts are internally and externally peer-reviewed; resulting publications are considered part of the formal international scientific literature. Individual copies are printed, and are also available from the departmental website in pdf form. Titles are listed in our catalogue on the website, refer www.doc.govt.nz under Publications, then Science & technical. © Copyright December 2007, New Zealand Department of Conservation ISSN 1173–2946 (hardcopy) ISSN 1177–9241 (web PDF) ISBN 978–0–478–14354–6 (hardcopy) ISBN 978–0–478–14355–3 (web PDF) This report was prepared for publication by Science & Technical Publishing; editing and layout by Lynette Clelland. Publication was approved by the Chief Scientist (Research, Development & Improvement Division), Department of Conservation, Wellington, New Zealand. In the interest of forest conservation, we support paperless electronic publishing. When printing, recycled paper is used wherever possible. CONTENTS Abstract 5 1. Introduction 6 2. -
Genetic Methods for Estimating the Effective Size of Cetacean Populations
Genetic Methods for Estimating the Effective Size of Cetacean Populations Robin S. Waples Northwest Fisheries Center, National Marine Fisheries Service, 2725 Montlake Boulevard East, Seattle, Washington 98112, USA ABSTRACT Some indirect (genetic) methods for estimating effective population size (N,) are evaluated for their suitability in studyingcetacean populations. The methodscan be grouped into those that (1) estimate current N,, (2) estimate long-term N, and (3) provide information about recent genetic bottlenecks. The methods that estimate current effective size are best suited for the analysis of small populations. and nonrandom sampling and population subdivision are probably the most serious sources of potential bias. Methods that estimate long-term N, are best suited to the analysis of large populations or entire species, may be more strongly influenced by natural selection and depend on accurate estimates of mutation or DNA base substitution rates. Precision of the estimates of N, is likely to be a limiting factor in many applications of the indirect methods. Keywords: genetics; assessment: cetaceans - general: evolution. INTRODUCTION Population size is one of the most important factors that determine the rate of various evolutionary processes, and it appears as a parameter in many of the fundamental equations of population genetics. However, knowledge merely of the total number of individuals (N) in a population is not sufficient for an accurate description of these evolutionary processes. Because of the influence of demographic parameters, two populations of the same total size may experience very different rates of genetic change. Wright (1931; 1938) developed the concept of effective population size (N,) as a way of summarising relevant demographic information so that one can predict the evolutionary consequences of finite population size (see Fig. -
Ecological Principles and Function of Natural Ecosystems by Professor Michel RICARD
Intensive Programme on Education for sustainable development in Protected Areas Amfissa, Greece, July 2014 ------------------------------------------------------------------------ Ecological principles and function of natural ecosystems By Professor Michel RICARD Summary 1. Hierarchy of living world 2. What is Ecology 3. The Biosphere - Lithosphere - Hydrosphere - Atmosphere 4. What is an ecosystem - Ecozone - Biome - Ecosystem - Ecological community - Habitat/biotope - Ecotone - Niche 5. Biological classification 6. Ecosystem processes - Radiation: heat, temperature and light - Primary production - Secondary production - Food web and trophic levels - Trophic cascade and ecology flow 7. Population ecology and population dynamics 8. Disturbance and resilience - Human impacts on resilience 9. Nutrient cycle, decomposition and mineralization - Nutrient cycle - Decomposition 10. Ecological amplitude 11. Ecology, environmental influences, biological interactions 12. Biodiversity 13. Environmental degradation - Water resources degradation - Climate change - Nutrient pollution - Eutrophication - Other examples of environmental degradation M. Ricard: Summer courses, Amfissa July 2014 1 1. Hierarchy of living world The larger objective of ecology is to understand the nature of environmental influences on individual organisms, populations, communities and ultimately at the level of the biosphere. If ecologists can achieve an understanding of these relationships, they will be well placed to contribute to the development of systems by which humans -
Community Ecology
Schueller 509: Lecture 12 Community ecology 1. The birds of Guam – e.g. of community interactions 2. What is a community? 3. What can we measure about whole communities? An ecology mystery story If birds on Guam are declining due to… • hunting, then bird populations will be larger on military land where hunting is strictly prohibited. • habitat loss, then the amount of land cleared should be negatively correlated with bird numbers. • competition with introduced black drongo birds, then….prediction? • ……. come up with a different hypothesis and matching prediction! $3 million/yr Why not profitable hunting instead? (Worked for the passenger pigeon: “It was the demographic nightmare of overkill and impaired reproduction. If you’re killing a species far faster than they can reproduce, the end is a mathematical certainty.” http://www.audubon.org/magazine/may-june- 2014/why-passenger-pigeon-went-extinct) Community-wide effects of loss of birds Schueller 509: Lecture 12 Community ecology 1. The birds of Guam – e.g. of community interactions 2. What is a community? 3. What can we measure about whole communities? What is an ecological community? Community Ecology • Collection of populations of different species that occupy a given area. What is a community? e.g. Microbial community of one human “YOUR SKIN HARBORS whole swarming civilizations. Your lips are a zoo teeming with well- fed creatures. In your mouth lives a microbiome so dense —that if you decided to name one organism every second (You’re Barbara, You’re Bob, You’re Brenda), you’d likely need fifty lifetimes to name them all. -
Can More K-Selected Species Be Better Invaders?
Diversity and Distributions, (Diversity Distrib.) (2007) 13, 535–543 Blackwell Publishing Ltd BIODIVERSITY Can more K-selected species be better RESEARCH invaders? A case study of fruit flies in La Réunion Pierre-François Duyck1*, Patrice David2 and Serge Quilici1 1UMR 53 Ӷ Peuplements Végétaux et ABSTRACT Bio-agresseurs en Milieu Tropical ӷ CIRAD Invasive species are often said to be r-selected. However, invaders must sometimes Pôle de Protection des Plantes (3P), 7 chemin de l’IRAT, 97410 St Pierre, La Réunion, France, compete with related resident species. In this case invaders should present combina- 2UMR 5175, CNRS Centre d’Ecologie tions of life-history traits that give them higher competitive ability than residents, Fonctionnelle et Evolutive (CEFE), 1919 route de even at the expense of lower colonization ability. We test this prediction by compar- Mende, 34293 Montpellier Cedex, France ing life-history traits among four fruit fly species, one endemic and three successive invaders, in La Réunion Island. Recent invaders tend to produce fewer, but larger, juveniles, delay the onset but increase the duration of reproduction, survive longer, and senesce more slowly than earlier ones. These traits are associated with higher ranks in a competitive hierarchy established in a previous study. However, the endemic species, now nearly extinct in the island, is inferior to the other three with respect to both competition and colonization traits, violating the trade-off assumption. Our results overall suggest that the key traits for invasion in this system were those that *Correspondence: Pierre-François Duyck, favoured competition rather than colonization. CIRAD 3P, 7, chemin de l’IRAT, 97410, Keywords St Pierre, La Réunion Island, France. -
To What Degree Are Philosophy and the Ecological Niche Concept Necessary in the Ecological Theory and Conservation?
EUROPEAN JOURNAL OF ECOLOGY EJE 2017, 3(1): 42-54, doi: 10.1515/eje-2017-0005 To what degree are philosophy and the ecological niche concept necessary in the ecological theory and conservation? Universidade Federal Rogério Parentoni Martins* do Ceará, Programa de Pós-Graduação em Ecologia e Recursos Naturais, Departamento ABSTRACT de Biologia, Centro de Ecology as a field produces philosophical anxiety, largely because it differs in scientific structure from classical Ciências, Brazil physics. The hypothetical deductive models of classical physics are simple and predictive; general ecological *Corresponding author, models are predictably limited, as they refer to complex, multi-causal processes. Inattention to the conceptual E-mail: rpmartins917@ structure of ecology usually imposes difficulties for the application of ecological models. Imprecise descrip- gmail.com tions of ecological niche have obstructed the development of collective definitions, causing confusion in the literature and complicating communication between theoretical ecologists, conservationists and decision and policy-makers. Intense, unprecedented erosion of biodiversity is typical of the Anthropocene, and knowledge of ecology may provide solutions to lessen the intensification of species losses. Concerned philosophers and ecolo- gists have characterised ecological niche theory as less useful in practice; however, some theorists maintain that is has relevant applications for conservation. Species niche modelling, for instance, has gained traction in the literature; however, there are few examples of its successful application. Philosophical analysis of the structure, precision and constraints upon the definition of a ‘niche’ may minimise the anxiety surrounding ecology, poten- tially facilitating communication between policy-makers and scientists within the various ecological subcultures. The results may enhance the success of conservation applications at both small and large scales. -
COULD R SELECTION ACCOUNT for the AFRICAN PERSONALITY and LIFE CYCLE?
Person. individ.Diff. Vol. 15, No. 6, pp. 665-675, 1993 0191-8869/93 S6.OOf0.00 Printedin Great Britain.All rightsreserved Copyright0 1993Pergamon Press Ltd COULD r SELECTION ACCOUNT FOR THE AFRICAN PERSONALITY AND LIFE CYCLE? EDWARD M. MILLER Department of Economics and Finance, University of New Orleans, New Orleans, LA 70148, U.S.A. (Received I7 November 1992; received for publication 27 April 1993) Summary-Rushton has shown that Negroids exhibit many characteristics that biologists argue result from r selection. However, the area of their origin, the African Savanna, while a highly variable environment, would not select for r characteristics. Savanna humans have not adopted the dispersal and colonization strategy to which r characteristics are suited. While r characteristics may be selected for when adult mortality is highly variable, biologists argue that where juvenile mortality is variable, K character- istics are selected for. Human variable birth rates are mathematically similar to variable juvenile birth rates. Food shortage caused by African drought induce competition, just as food shortages caused by high population. Both should select for K characteristics, which by definition contribute to success at competition. Occasional long term droughts are likely to select for long lives, late menopause, high paternal investment, high anxiety, and intelligence. These appear to be the opposite to Rushton’s r characteristics, and opposite to the traits he attributes to Negroids. Rushton (1985, 1987, 1988) has argued that Negroids (i.e. Negroes) were r selected. This idea has produced considerable scientific (Flynn, 1989; Leslie, 1990; Lynn, 1989; Roberts & Gabor, 1990; Silverman, 1990) and popular controversy (Gross, 1990; Pearson, 1991, Chapter 5), which Rushton (1989a, 1990, 1991) has responded to. -
Ecological Niche Theory: a Brief Review
The International Journal of Indian Psychology ISSN 2348-5396 (e) | ISSN: 2349-3429 (p) Volume 3, Issue 2, No.2, DIP: 18.01.022/20160302 ISBN: 978-1-329-81573-5 http://www.ijip.in | January - March, 2016 Ecological Niche Theory: A Brief Review Mina Khatibi1*, Razieh Sheikholeslami2 ABSTRACT In ecology, a niche is a term with a variety of meanings related to the behavior of a species living under specific environmental conditions. The ecological niche describes how an organism or population responds to the distribution of resources and competitors. The ecological niche concept expresses the relationship of an individual or a population to all aspects of its environment. Studies on the relationship between human population and environmental resources have employed niche concept. Ecological niche comprehends all conditions necessary for an organism to exist. Keywords: Niche, Ecology, Environment, Organism What is ecological niche? 1. The position or function of an organism or a population within a biological and physical environment. 2. The area within a habitat occupied by an organism. The ecological niche is an organism position in the habitat (Online Psychology Dictionary, 2014). The ecological niche concept, as proposed by Hutchinson (1957), expresses the relationship of an individual or a population to all aspects of its environment. Studies on the relationship between human population and environmental resources have employed niche concept (Adams, 2002; Hanazaki and Begossi, 2004; Cavallini and Nordi, 2005; Silva and Begossi, 2009). According to Hardesty (1972), ecological niche comprehends all conditions necessary for an organism to exist. Considering the ecological niche, it can analyze each one of all interactions. -
The Role of Nearshore Ecosystems As Fish and Shellfish Nurseries
l About Issues in Ecology Issues in Ecology is designed to report, in language understandable by non-scientists, the consensus of a panel of scientific experts on issues relevant to the environment. Issues in Ecology is supported by the Pew Scholars in Conservation Biology program and by the Ecological Society of America. It is published at irregular intervals, as reports are com- pleted. All reports undergo peer review and must be approved by the Editorial Board before publication. No responsibility for the views expressed by authors in ESA publica- tions is assumed by the editors or the publisher, the Ecological Society of America. Issues in Ecology is an official publication of the Ecological Society of America, the nation’s leading professional society of ecologists. Founded in 1915, ESA seeks to promote the responsible application of ecological principles to the solution of environmental problems. For more information, contact the Ecological Society of America, 1707 H Street, NW, Suite 400, Washington, DC, 20006. ISSN 1092-8987 PublishedIssues by the Ecological Society of America in Eco Number 11, lSpringogy 2003 The RoleofNearshoreEcosystems as Fish andShellfishNurseries as Fish Issues in Ecology Number 11 Spring 2003 The Role of Nearshore Ecosystems as Fish and Shellfish Nurseries SUMMARY Coastal ecosystems provide many vital ecological and economic services, including shoreline protection, productive commercial and sport fisheries, and nutrient cycling. Key nearshore ecosystems such as seagrass meadows, marshes, and mangrove forests -
National Wildlife Federation's Community Wildlife Habitat
National Wildlife Federation’s Community Wildlife Habitat Certification Requirements To achieve certification through the National Wildlife Federation’s Community Wildlife Habitat program, you must create or restore wildlife habitat in your community and do education and outreach. First, a certain number of homes, schools and common areas must become National Wildlife Federation Certified Wildlife Habitats by providing the four basic elements that all wildlife need: food, water, cover and places to raise young. The NWF Certified Wildlife Habitat program also requires sustainable gardening practices such as using rain barrels, reducing water usage, removing invasive plants, using native plants and eliminating pesticides. These requirements are based on population – see chart below. Second, communities earn education and outreach points through a flexible checklist that includes educating citizens at community events, hosting a native plant sale, organizing a stream clean up, bringing new partners to the effort and hosting workshops – see pages 2 and 3. Property Certification Requirements: Minimum Habitat Sliding Scale Based on Activity / Type of Certification Points Certification Points Population Size For each home certified, including townhomes and apartments 1 20 500 or Less For each common area certified, including public parks, HOA common 40 501-1,000 areas, businesses, places of worship, farms, universities and municipal 3 100 1,001-5000 buildings 150 5,001-10,000 For each school certified as an NWF Schoolyard Habitat - Pre-K - 12 or 175 10,001-15,000 5 nature center 200 15,001-20,000 225 20,001-25,000 250 25,001-50,000 VERIFICATION: Each home or common area must be certified within 15 300 50,001-100,000 years of a community's registration date to count for points. -
Integrating Community and Ecosystem-Based Approaches in Climate
Integrating Community and Ecosystem-Based Approaches in Climate Change Adaptation i Responses This paper is the result of extensive discussions led by adaptation professionals coming from different backgrounds and facilitated by the Ecosystem and Livelihoods Adaptation Network (ELAN).ii ELAN is an innovative alliance between two conservation organisations (International Union for the Conservation of Nature [IUCN] and WWF) and two development organisations (CARE International and the International Institute for Environment and Development [IIED]). The objective of ELAN is to establish a global network to develop, evaluate, synthesize and share successful strategies for adapting to climate change, build capacity for such strategies to be assessed and implemented at national and sub-national levels, and advance policies and knowledge sharing platforms that will facilitate the scaling up of effective strategies. Two emerging approaches to adaptation have gained currency over the past few years, namely Community-based Adaptation (CBA) and Ecosystem-based Adaptation (EBA). Each has its specific emphasis, the first on empowering local communities to reduce their vulnerabilities, and the latter on harnessing the management of ecosystems as a means to provide goods and services in the face of climate change. In this paper, ELAN argues for a more truly “integrated approach” to adaptation that addresses and seeks to reconcile differences between CBA and EBA. ELAN has developed a conceptual framework for an approach to adaptation, which empowers -
Effective Size of Populations with Heritable Variation in Fitness
Heredity (2002) 89, 413–416 2002 Nature Publishing Group All rights reserved 0018-067X/02 $25.00 www.nature.com/hdy SHORT REVIEW Effective size of populations with heritable variation in fitness T Nomura Department of Biotechnology, Faculty of Engineering, Kyoto Sangyo University, Kyoto 603–8555, Japan The effective size of monogamous populations with heritable zygotes are produced by random union of gametes, each variation in fitness is formulated, and the expression from conceptual male and female gametic pools. A con- obtained is compared with a published equation. It is shown venient equation for practical use is proposed, and the appli- that the published equation for dioecious populations is inap- cation is illustrated with the estimation of the effective size propriate for most animal and human populations, because of a rural human community in Japan. the derivation is implicitly based on the assumption that Heredity (2002) 89, 413–416. doi:10.1038/sj.hdy.6800169 Keywords: effective population size; random genetic drift; fitness; heritability; human population; animal population Introduction situations have been developed (Santiago and Caballero, 1995; Nomura, 1996, 1997; Wang, 1998; Bijma et al, 2000, The effective size of a population is a parameter central 2001). Only one extension to directional selection on fit- to understanding evolution in small populations, because ness was given by Nei and Murata (1966). Based on the the magnitude of this parameter determines the genetic approach of Robertson (1961), they worked out an equ- effects of both inbreeding and genetic drift (Falconer, ation for monoecious populations. They also extended 1989; Caballero, 1994). This parameter is also important their derivation to dioecious populations.