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Books on the topic 'Species richness'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Adams, Jonathan. Species Richness. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-74278-4.

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2

Said, Mohamed Y. Multiscale perspectives of species richness in East Africa. ITC], 2003.

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3

Oliver, Caldecott Julian, and World Conservation Monitoring Centre, eds. Priorities for conserving global species richness and endemism. World Conservation Press, 1994.

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4

Schroeder, Richard L. Habitat suitability index models: Wildlife species richness in shelterbelts. National Ecology Center, Division of Wildlife and Contaminant Research, Fish and Wildlife Service, U.S. Dept. of Interior, 1986.

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5

Wade, Gary L. Species richness on five partially reclaimed Kentucky surface mines. s.n, 1993.

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6

Kleijn, David. Species richness and weed abundance in the vegetation of arable field boundaries. [s.n.], 1997.

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7

Eagleson, Peter S. Range and richness of vascular land plants: The role of variable light. American Geophysical Union, 2009.

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8

Eagleson, Peter S. Range and richness of vascular land plants: The role of variable light. American Geophysical Union, 2009.

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9

Carlsson, Diane Helene. Species diversity, richness and composition in jack pine communities after wildfire or clear-cut logging disturbance. Laurentian University, Department of Biology, 2000.

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10

McCrea, Alison R. Relationships between soil fertility and species-richness in created and semi-natural grassland in the English West Midlands. University of Wolverhampton, 1999.

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11

Keenan, Ted William G. Trembling aspen and balsam poplar stands in the Sudbury area: A study in species richness and inter-stand relationships. Laurentian University, Department of Biology, 1994.

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12

Houk, Peter. Rapid ecological assessment of Chuuk, Hall, and Mortlock Islands, Chuuk State, Federated States of Micronesia: Quantitative assessment of coral-reef assemblages and coral species richness. PMRI, 2008.

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13

Lindgren, Mariko. Polypore (Basidiomycetes) species richness and community structure in natural boreal forests of NW Russian Karelia and adjacent areas in Finland. Finnish Zoological and Botanical Publishing Board, 2001.

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14

Gujarat Ecological Education and Research Foundation. and World Wide Fund for Nature--India., eds. Ecological study of Thol Lake Wildlife (Bird) Sanctuary: A comprehensive study on waterfowl of Thol Wetland with emphasis on their species, richness, and abundance. GEER Foundation, 2002.

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15

Species richness in tropical forests. Academic Press, 1989.

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16

Effects of Spatial Heterogeneity on Species Richness. Simon & Schuster, 2008.

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17

Adams, Jonathan. Species Richness: Patterns in the Diversity of Life. Springer, 2010.

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18

Species richness: Patterns in the diversity of life. Springer, 2009.

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19

Sota, Teiji. Evolutionary Biology of Carabus Ground Beetles: How Species Richness Increases. Springer, 2022.

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20

Qadir, Mohammad F. Using percentile regression for estimating the maximum species richness line. 1993.

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21

Sota, Teiji. Evolutionary Biology of Carabus Ground Beetles: How Species Richness Increases. Springer Singapore Pte. Limited, 2022.

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22

Adams, Jonathan. Species Richness: Patterns in the Diversity of Life (Springer Praxis Books). Springer, 2010.

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23

Upton, Graham. Measuring Abundance: Methods for the Estimation of Population Size and Species Richness. Pelagic Publishing Ltd., 2020.

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24

Upton, Graham. Measuring Abundance: Methods for the Estimation of Population Size and Species Richness. Pelagic Publishing Ltd., 2020.

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25

Eagleson, Peter S. Range and Richness of Vascular Land Plants: The Role of Variable Light. American Geophysical Union, 2013.

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26

Eagleson, Peter S. Range and Richness of Vascular Land Plants: The Role of Variable Light. American Geophysical Union, 2013.

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27

Eagleson, Peter S. Range and Richness of Vascular Land Plants: The Role of Variable Light. American Geophysical Union, 2013.

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28

Eagleson, Peter S. Range and Richness of Vascular Land Plants: The Role of Variable Light. Wiley & Sons, Limited, John, 2013.

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29

Vesely, David G. Terrestrial amphibian abundance and species richness in headwater riparian buffer strips, Oregon Coast Range. 1996.

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30

The structure and dynamics of tropical rain forest in relation to tree species richness. Kluwer Academic Press, 1992.

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31

Species richness and species occurrence of five taxonomic groups in relation to pH and other lake characteristics in southeastern Canada. Dept. of Fisheries and Oceans, 1997.

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32

Applied Hierarchical Modeling in Ecology: Analysis of Distribution, Abundance and Species Richness in R and BUGS. Elsevier, 2021. http://dx.doi.org/10.1016/c2015-0-04070-9.

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33

Cerletti, Gianpietro. Soil water conditions and root growth of seedlings and their importance for species richness in limestone grasslands. 1997.

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34

Krell, Frank-Thorsten. Pleistocene Dung Beetles from MIS 5 at Ziegler Reservoir, Snowmass Village, Colorado (Coleoptera: Scarabaeidae: Aphodiinae). Denver Museum of Nature & Science, 2014. http://dx.doi.org/10.55485/inyl3767.

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Nine aphodiine dung beetle species are recorded from Pleistocene sediments of the Ziegler Reservoir near Snowmass Village, Colorado, U.S.A. Insect remains from this deposit range from 125,000 to 77,000 yr BP, and are unique in their species richness and in their occurrence at high elevation (2720 meters). Three extant species occur: Aphodius (Dialytodius) decipiens Horn, A. (Planolinellus) vittatus Say, and A. (Planolinoides) duplex LeConte. Six unidentified species are also described, belonging to the genus Aphodius. All species are relatively small coprophagous dwellers known as endocoprids.

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35

Ebert, Kathryn M. The effects of wilderness recreation on avian species richness and distribution in the Eagle Cap Wilderness area, northeastern Oregon. 1987.

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36

Royle, J. Andrew, and Marc Kery. Applied Hierarchical Modeling in Ecology: Analysis of Distribution, Abundance and Species Richness in R and Bugs - Prelude and Static Models. Elsevier Science & Technology Books, 2015.

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37

Royle, J. Andrew, and Marc Kery. Applied Hierarchical Modeling in Ecology : Analysis of Distribution, Abundance and Species Richness in R and BUGS : Volume 2: Dynamic and Advanced Models. Elsevier Science & Technology, 2020.

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38

Royle, J. Andrew, and Marc Kery. Applied Hierarchical Modeling in Ecology : Analysis of Distribution, Abundance and Species Richness in R and BUGS : Volume 2: Dynamic and Advanced Models. Elsevier Science & Technology Books, 2020.

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39

Applied Hierarchical Modeling in Ecology : Analysis of Distribution, Abundance and Species Richness in R and BUGS : Volume 2: Dynamic and Advanced Models. Elsevier Science & Technology, 2020.

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40

Clarke, Andrew. Temperature and diversity. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780199551668.003.0015.

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The diversity (species richness) of plants and animals is typically highest in the tropics and the strongest environmental correlate of species richness is often climate. The energy for plant production is sunlight, but the rate is governed jointly by temperature and the availability of water (as captured by actual evapotranspiration, AET). Greater production is then linked to higher diversity because larger population size protects against stochastic extinction (the more individuals mechanism). A greater biomass and diversity of plants allows for a greater diversity of herbivores and so on th

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41

Esler, Karen J., Anna L. Jacobsen, and R. Brandon Pratt. Introduction. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198739135.003.0001.

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Mediterranean-type climate (MTC) regions have long been of interest to scientists and they formed the basis for many early ecological studies. This has included comparisons of the vegetation within these regions (mediterranean-type vegetation) as well as other functional, climatic, and historical studies and comparisons. Comparing MTC regions and the species that occur within them has been used to test the evolutionary convergence hypothesis. Continuing scientific interest in MTC regions is linked to their unusually high levels of species richness and biodiversity. These regions have the highe

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42

Royle, J. Andrew, and Marc Kery. Applied Hierarchical Modeling in Ecology : Analysis of Distribution, Abundance and Species Richness in R and BUGS Vol. 1 : Volume 1: Prelude and Static Models. Elsevier Science & Technology Books, 2015.

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43

Jacobsen, Dean, and Olivier Dangles. Organisms and diversity patterns at high altitudes. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198736868.003.0004.

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Chapter 4 gives a group-by-group treatment from amphibians and fish to algae and microbes of what is known about altitudinal diversity patterns, dominant groups, and prominent species from high altitude waters around the world. This is accompanied by biogeographical considerations on dispersal, immigration, and local speciation processes. The general and well-known decrease in species richness with increasing altitude observed in the terrestrial environment is also the rule in aquatic systems. Yet, while some groups of organisms show very clear altitudinal patterns, others do not. Some groups

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44

Worm, Boris, and Derek P. Tittensor. A Theory of Global Biodiversity (MPB-60). Princeton University Press, 2018. http://dx.doi.org/10.23943/princeton/9780691154831.001.0001.

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The number of species found at a given point on the planet varies by orders of magnitude, yet large-scale gradients in biodiversity appear to follow some very general patterns. Little mechanistic theory has been formulated to explain the emergence of observed gradients of biodiversity both on land and in the oceans. Based on a comprehensive empirical synthesis of global patterns of species diversity and their drivers, this book develops and applies a new theory that can predict such patterns from few underlying processes. The book shows that global patterns of biodiversity fall into four consi

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45

Wilsey, Brian J. Biodiversity and Ecosystem Functioning in Grasslands. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198744511.003.0006.

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Biodiversity is a measure of variety of life forms, and can be assessed at the genetic, species, and landscape levels. Species diversity can be partitioned into its basic components of richness (number of species) and evenness, and into spatial components (alpha, beta, gamma). Local extinction rates are often higher in situations where evenness is low due to low abundances in rare species. Many experimental and observational studies have been done on how ecosystem process rates will be impacted by reductions in biodiversity. The mechanism behind observed positive relationships between diversit

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46

Vellend, Mark. Are local losses of biodiversity causing degraded ecosystem function? Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198808978.003.0004.

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This chapter highlights the scale dependence of biodiversity change over time and its consequences for arguments about the instrumental value of biodiversity. While biodiversity is in decline on a global scale, the temporal trends on regional and local scales include cases of biodiversity increase, no change, and decline. Environmental change, anthropogenic or otherwise, causes both local extirpation and colonization of species, and thus turnover in species composition, but not necessarily declines in biodiversity. In some situations, such as plants at the regional scale, human-mediated coloni

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47

James, Philip. Spatial patterns. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198827238.003.0008.

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In this chapter, the discussion focuses on the spatial variation of species within urban environment. Studies on urban–rural gradients are discussed. These are studies along gradients of disturbance and environmental stress. The extreme heterogeneity of urban environments, where contrasting urban forms are juxtaposed, is recognized as an issue in drawing generalities. Despite this, some limited generalities in the patterns of species richness and density can be detected. The intermediate disturbance hypothesis is discussed and its limitations identified. Examples are presented from a number of

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48

Kaila, Lauri. Elachistine Moths of Australia. CSIRO Publishing, 2011. http://dx.doi.org/10.1071/9780643103481.

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Elachistine moths are the World’s most species-rich group of Lepidoptera that specialise on monocotyledon plants, especially grasses and sedges. This volume is the first reference to describe the so-far unknown diversity of these leaf-mining moths in Australia. It provides a new generic classification for the group on a worldwide basis, and describes in detail the genera and species that occur in Australia. Keys to genera and species, as well as generic, subgeneric and species group descriptions are given, richly supplied with illustrations of larvae, pupae and adult moths. In addition,

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49

Simonsen, Thomas. Splendid Ghost Moths and Their Allies. CSIRO Publishing, 2018. http://dx.doi.org/10.1071/9781486307487.

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The Hepialidae (Ghost Moths) are a family of often spectacular micro-moths. The Australian region is one of the hot spots for hepialid diversity and the fauna is divided into three groups: primitive Hepialidae with small, often overlooked species; oxycanine Hepialidae, containing the large and poorly known genus Oxycanus and its allies; and finally the hepialine Hepialidae, which span from stunning, green Splendid Ghost Moths in the genus Aenetus, to the enormous moths in the genera Zelotypia and Abantiades (which include some of the most impressive insects in the world), to smaller, drab pest

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50

Stahl, Peter W. Zooarchaeological approaches to Pre-Columbian archaeology in the neotropics of northwestern South America. Edited by Umberto Albarella, Mauro Rizzetto, Hannah Russ, Kim Vickers, and Sarah Viner-Daniels. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199686476.013.43.

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Despite various problems associated with the practice of zooarchaeology in the neotropics, archaeologists have recovered impressive evidence from caves and open air sites for early landscape management and food production in northwestern South America, a region renowned for harbouring elevated species richness and high rates of endemism. The trajectory for subsequent pre-Columbian cultural developments in the area was established very early through the precocious achievements of its earliest Holocene human occupations. Archaeobiological evidence is used to outline the subsequent development an

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