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Biodiversity, redundancy and resilience of riparian vegetation under different land management regimes.Kotschy, Karen Ann 05 March 2014 (has links)
Biodiversity is widely thought to enhance resilience in ecosystems by providing ‘insurance’ which
buffers the effects of disturbances on ecosystem functioning. However, little empirical evidence is
available to support this assumption. Biodiversity and resilience are both complex, multifaceted
concepts, and the mechanisms underlying the relationship between them are far from clear.
However, understanding this relationship is important because resilience underpins the ability
of ecosystems to continue to provide essential ‘goods and services’ in the face of increasing human
pressure and an uncertain future.
In this thesis I address two properties thought to be important in determining the resilience
of ecological assemblages, namely functional redundancy (similarities in ecological functioning
between species) and response disparity (differences in species’ responses to disturbance). Both
are related to biodiversity, being determined by the degree of similarity or difference among the
species in an assemblage. After developing a conceptual framework for understanding the relationship
between biodiversity and resilience, I provide a critical evaluation of existing methods
for measuring redundancy and response disparity, and develop measures of these two properties
that better reflect the continuous, multidimensional nature of differences between species. A
key element of my approach is the use of different sets of functional traits to describe individual
species’ contributions to different ecological functions. This is valuable because it explicitly
recognises that species have multiple functional roles, an obvious fact that is often overlooked and
a source of much misunderstanding about redundancy and disparity. I then use these methods to
measure redundancy and response disparity in riparian plant assemblages from different–sized
streams and under different land management regimes, providing some of the first empirical
evidence for these aspects of resilience in real, species–rich assemblages. In particular, I provide
the first empirical confirmation of two hypotheses about the roles of redundancy and response
disparity in the resilience of plant assemblages, namely (1) that minor species in the tail of the
abundance distribution provide redundancy for functions performed by the dominant species,
and (2) that groups of species that provide redundancy for each others’ functioning differ in
their response traits, thus providing response disparity (Walker et al., 1999, Ecosyst. 2:95–113).
This thesis also contributes to our understanding of the effects of land management practices on
the resilience of riparian systems, something which is poorly understood but of critical interest to
conservation and land managers. Ecosystem–based approaches to management place emphasis
on maintaining desirable functioning in ecosystems. However, often it is very difficult for managers
to assess whether this is being achieved (the ‘manager’s dilemma’). The resilience measures
developed here are valuable because they provide a measure of the long–term sustainability of
the various functions performed by species assemblages.
Both redundancy and response disparity were present in the riparian assemblages studied.
Species in the tail of the abundance distribution were particularly important providers of redundancy.
These tail species, often inadequately sampled or left out of functional diversity
analyses, provided 53–100% (mean 82%) of the redundancy for the functioning of the more
abundant species. For most functions performed by a particular species, between 5 and 20 other
species were potentially able to perform that function in a similar way, thus providing redundancy.
However, all assemblages also had species (1–40%) with low redundancy for one or more
functions, suggesting that certain particular aspects of functioning may lack resilience, even in
assemblages with high overall resilience.
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Species providing redundancy for a particular function were seldom very similar in their contributions
to other functions. Functional ‘analogues’ (species identical or very similar in all
functions) were relatively uncommon (42–71% of species across different management regimes
and stream sizes had no analogues for the small number of functions studied, and this number
was shown to increase with the number of functions considered). Redundancy was usually
provided by a large number of partially similar species rather than by a few identical species. Redundancy
and disparity were therefore simultaneously present in each assemblage, because each
species contributed both to redundancy (for some functions) and disparity (for others). This
suggests that the commonly held view of redundancy provided by ‘identical copies’ is far too
one–dimensional, and successfully lays to rest the debates about its existence and the concerns
that promoting redundancy will somehow be detrimental to diversity. I therefore propose that
it is time to put redundancy back on the research agenda as an important aspect of functional
organisation which leads to resilience.
The highly distributed nature of redundancy, involving many partially similar species, also has
important implications for our understanding of change in ecosystems. It means that functional
compensation will seldom be a simple matter of species replacing each other as ‘drop–in replacements’.
Rather, compensatory changes in species composition or abundance will have knock–on
effects that affect many other species and lead to many ‘readjustments’ in species’ functioning,
responses to disturbance, interactions and abundances. The results of this study have shown
that the way changes in species composition or diversity affect resilience are often idiosyncratic,
depending on which particular species are involved. It is therefore not appropriate to try to
model the impacts of changes in biodiversity on ecosystem resilience deterministically.
However, ecosystem managers require information about resilience to implement ecosystem–
based management. This information needs to be simple enough to be useful, but flexible anough
to account for the fact that idiosyncratic species effects frequently make considering the details of
a particular situation unavoidable. In this thesis I outline an approach that involves the judicious
use of generalisations together with a flexible means of combining compositional, functional and
resilience perspectives on species assemblages, allowing exploration of the relationship between
diversity and resilience in a particular system. This approach is more flexible, and allows a wider
range of questions to be addressed, than commonly used approaches using indices of diversity or
ecosystem health. Rather than summarising a large amount of detailed information in the form
of an index, my approach retains the detail but concentrates on making it easier to interpret.
This provides a flexible way of using the detail to answer specific management questions, thus
increasing its usefulness to managers.
The finding of a generally positive relationship between redundancy and species richness in this
study is a useful generalisation for managers trying to implement an ecosystem–based approach
to conservation and land management. It suggests that, in general, maintaining species–rich
assemblages will tend to maintain redundancy. However, this relationship varied with growth
form (woody vs herbaceous), stream order (small streams vs main river) and the function being
considered. The amount of redundancy and response disparity associated with each species for
each function were also highly variable, pointing to the need to use generalisations with care.
Comparison of assemblages under the different land management regimes (Kruger National
Park, privately–owned reserves and communal rangeland) suggested that management practices
in river catchments do affect the resilience of riparian vegetation, but not always in the manner
expected. Management practices in the conservation areas did not necessarily promote higher
diversity or resilience than management practices in the communal area, which may come as a
surprise to many conservationists. While assemblages from the main river were less resilient in
the communal area than in the reserves, assemblages from the small streams were more diverse
and resilient than those in the reserves, even though communal rangeland areas are not managed
specifically for biodiversity conservation. Far from being ‘degraded’ as is usually assumed, small
streams within these communally managed areas are in fact valuable as biodiversity hotspots,
and this should be reflected in conservation planning and ecosystem service assessments in the
region.
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Correlation of riparian vegetation and stream attributes /Miller, Rachel Ann, January 1993 (has links)
Thesis (M.S.)--Oregon State University, 1994. / Typescript (photocopy). Includes bibliographical references (leaves 37-41). Also available on the World Wide Web.
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Development and evaluation of a technique for evaluating riparian vegetation change in the tallgrass prairieMacKay, Mark Andrew. January 2004 (has links)
Thesis (M.S.) University of Missouri-Columbia, 2004. / The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file viewed on (June 30, 2006) Vita. Includes bibliographical references.
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Habitat parameters associated with the distribution of seven willow species on a stream in southeastern Oregon /Gilbert, Griffith J. January 1900 (has links)
Thesis (M.S.)--Oregon State University, 2007. / Printout. Includes bibliographical references (leaves 94-99). Also available on the World Wide Web.
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Riparian vegetation and forest structure of two unregulated tributaries, compared to the regulated Snake River, Grand Teton NP, WYFoy, Elizabeth Christina. January 2008 (has links) (PDF)
Thesis (MS)--Montana State University--Bozeman, 2008. / Typescript. Chairperson, Graduate Committee: David Roberts. Includes bibliographical references.
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Modeling water temperature in small agricultural drainage watercoursesShepard, Dawn Joy, January 2005 (has links) (PDF)
Thesis (M.S. in engineering)--Washington State University. / Includes bibliographical references.
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Sources, transport, and fate of terrestrial organic matter inputs to small Puget Lowland streams : effects of urbanization, floods, and salmon /Roberts, Mindy. January 2007 (has links)
Thesis (Ph. D.)--University of Washington, 2007. / Vita. Includes bibliographical references (leaves 119-130).
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The response of riparian vegetation to PL-566 flood control structuresDuke, Jacquelyn R. White, Joseph Daniel. January 2006 (has links)
Thesis (Ph.D.)--Baylor University, 2006. / Includes bibliographical references (p. 112-129).
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Production of cutthroat trout (Salmo clarki) in relation to riparian vegetation in Bear Creek, Washington /Martin, Douglas J. January 1985 (has links)
Thesis (Ph. D.)--University of Washington, 1985. / Vita. Includes bibliographical references (leaves [98]-105).
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Biotechnical engineering on alluvial riverbanks of southeastern Australia a quantified model of the earth-reinforcing properties of some native riparian trees /Docker, Benjamin Brougham. January 2003 (has links)
Thesis (Ph. D.)--School of Geosciences, Faculty of Science, University of Sydney, 2004. / Degree awarded 2004; thesis submitted 2003. Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy to the School of Geosciences, Faculty of Science. Title from title screen (viewed 13 January 2009). Includes bibliographical references. Also available in print form.
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