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An evaluation of the Riparian Vegetation Index (RVI) in KwaZulu-Natal.Clarke, Simon. January 2003 (has links)
No abstract available. / Thesis (M.Sc.)-University of Natal, Pietermaritzburg, 2003.
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Modelling microbial utilisation of macrophyte organic matter inputs to rivers under different flow conditions /Bowen, Patricia Margaret. January 2006 (has links)
Thesis (PhD) - University of Canberra. / "March 2006" Submitted in accordance with assessment requirements for the Doctor of Philosophy degree of the University of Canberra. Bibliography: p. 228 - 250.
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Patterns of plant species richness in emergent and forestry wetlands of southeast Alaska /Pollock, Michael Moritz. January 1995 (has links)
Thesis (Ph.D.)--University of Washington, 1995. / Vita. Includes bibliographical references (leaves [135]-151).
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Impacts of flow augmentation on river channel processes and riparian vegetationBigelow, Sarah Grace, University of Lethbridge. Faculty of Arts and Science January 2006 (has links)
The Little Bow River Project was implemented in 2003 and includes Alberta’s newest dam. The Project involves tripling the diversion of water from the Highwood River to the Little Bow River and subsequently storing the water in the Twin Valley Reservoir. This MSc Thesis provided part of the environmental monitoring for that Project and particularly investigated the impacts of augmented flows on the river channel and riparian vegetation along the upper reach of the Little Bow River. An initial component of the long-term study was to determine the existing associations between fluvial geomorphic characteristics and riparian plant communities. Poplar (Populus balsamifera L.), willow (Salix bebbiana Sargent and S. exigua Nutt.) and wolf-willow (Elaeagnus commutata Bernh.) communities were located along the upper section of the river, where the channel had a steeper gradient and was narrower and more sinuous. Cattail (Typha latifolia L.) and grass (grasses and sedges) communities were generally located along the lower section of the river that was shallower in gradient, wider and straighter. Plant community distribution also reflected impacts from cattle grazing. Initial channel and vegetation responses in the first two years following the increase in flow augmentation were slight and included bank slumping, sediment scour and inundation of flooded zones. The initial responses are consistent with the primary prediction of channel widening and this will probably be associated with some changes in the adjacent riparian plant communities. / xiv, 139 leaves : ill. (some col.) ; 29 cm.
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Effects of invasive alien plants on riparian vegetation and their response to environmental factorsPattison, Zarah January 2016 (has links)
Biological invasions are reportedly one of the major contributory factors to biodiversity loss worldwide. The impacts of invasive alien plant (IAP) species on native communities are widely documented in the scientific literature, however, there is still a lack of detailed information on their impacts within the most vulnerable habitats. Riparian habitats are highly dynamic systems and naturally disturbed, making them particularly vulnerable to invasion. Climate change, directly or indirectly, is also predicted to adversely impact river systems, which may subsequently alter invasion rates and the impacts of IAPs. However, the interactions between climate and IAPs and their combined effects on vegetation have rarely been examined. To address these knowledge gaps, this thesis investigates: (1) the role of environmental variables, such as sediment loading or climate-related changes to river flow regime, on the abundance of IAPs within riparian zones; (2) how variation in IAP abundance impacts native vegetation, relative to the effects of native dominant plant species and (3) some of the mechanisms underlying the effects of IAPs in riparian habitats. Historic and recent field survey data were used to investigate changes in riparian vegetation on British rivers during the last 20 years. Analyses indicate that IAPs had a negative but small effect on native plant diversity. Overall, changes in land use and differences in flow regime between recording periods were the most important predictors of plant community change. Specifically, IAPs had a greater probability of being present along lowland rivers that experienced increased frequency of high flow events. On a local scale across rivers in Scotland, the abundance of IAPs was constrained by greater soil moisture in summer, whilst greater abundance was associated with tree-lined banks. Both native dominant species and IAPs negatively affected subordinate species abundance to a greater extent than species richness, although this effect varied spatially with bank elevation. Artificial turf mats were used to quantify viable propagules within riverine sediment deposited over-winter along invaded riverbanks. The data indicate that there is a legacy effect of IAP abundance, with the most invaded sites being associated with higher sediment loading the following year, though, contrary to the general pattern, 12 sediment associated propagules were scarcer at invaded sites. Moreover, lower above-ground native diversity was associated with sites which had been previously invaded. Plant species composition in the propagule bank and above-ground vegetation were highly dissimilar, particularly closest to the water’s edge at highly invaded sites. This suggests that mono-specific stands of IAPs proliferate best under less disturbed environmental conditions, although fluvial disturbance events may be required to create opportunities for initial establishment. The propagule bank contributed very little to the above-ground vegetation, nor did it limit invasion, suggesting that above-ground plant composition is largely dictated by competitive interactions. The findings presented in this thesis suggest that invasion by IAPs is an additional stressor for native vegetation within riparian habitats, modifying above-ground plant communities via competition and suppressing recruitment from the propagule bank. However, native dominant species common in riparian habitats also negatively impact, subordinate species via competition, in some cases equalling the effect of IAPs. Native dominant and IAP species are differently affected by environmental factors operating in the riparian zone, which may provide future opportunities for reducing and managing invasions.
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Quantifying the interaction between riparian vegetation and flooding : from cross-section to catchment scale /Anderson, Brett Gordon. January 2006 (has links)
Thesis (Ph.D.)--University of Melbourne, School of Anthropology,Geography and Environmental Studies and the Dept. of Civil and Environmental Engineering, 2006. / Typescript. Includes bibliographical references.
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Using Landsat TM Imagery to Monitor Vegetation Change Following Flow Restoration to the Lower Owens River, CaliforniaBross, Lesley Crandell 15 December 2015 (has links)
Rehabilitating river corridors to restore valuable riparian habitat consumes significant resources from both governments and private companies. Given these considerable expenditures, it is important to monitor the progress of such projects. This study evaluated the utility of using Landsat Thematic Mapper remotely-sensed data from 2002 and 2009 to monitor vegetation change induced by instream flow restoration to the Lower Owens River in central California. This study compared the results of an unsupervised classification with an NDVI threshold classification to appraise the resources required and effectiveness of each analysis method. The results were inspected by creating standard remote sensing accuracy error matrices and by correlating landscape pattern metrics with bird indicator species. Both sets of classified maps show a noticeable increase in riparian vegetation in the study area following flow restoration in 2006, indicating an improvement of the quality of bird habitat. The study concluded that analyzing vegetation change using the unsupervised classification technique required more effort, expert knowledge, and supplementary data than using the NDVI threshold method. If these prerequisites are met, the output from the unsupervised classification process produces a more precise map of land cover change than the NDVI threshold method. However, if an analyst is lacking either resources or ground verification data, the NDVI threshold technique is capable of providing a generalized, but still valid evaluation of vegetation change. This conclusion is supported by higher correlations between indicator bird species under the unsupervised classification method than were found with the NDVI threshold method.
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The riparian vegetation of the Hottentots Holland Mountains, Western Cape, South AfricaSieben, E. J. J. 12 1900 (has links)
Dissertation (PhD)--University of Stellenbosch, 2003. / ENGLISH ABSTRACT: Riparian vegetation has received a lot of attention in South Africa recently, mainly
because of its importance in bank stabilization and its influence on flood regimes and
water conservation. The upper reaches have thus far received the least of this attention
because of their inaccessibility. This study mainly focuses on these reaches where
riparian vegetation is still mostly in a pristine state. The study area chosen for this
purpose is the Hottentots Holland Mountains in the Southwestern Cape, the area with
the highest rainfall in the Cape Floristic Region, which is very rich in species. Five
rivers originate in this area and the vegetation described around them covers a large
range of habitats, from high to low altitude, with different geological substrates and
different rainfall regimes.
All of these rivers are heavily disturbed in their lower reaches but are still
relatively pristine in their upper reaches. All of them are dammed in at least one place,
except for the Lourens River. An Interbasin Transfer Scheme connects the Eerste-,
Berg- and Riviersonderend Rivers. The water of this scheme is stored mainly in
Theewaterskloof Dam. Another big dam for water storage, Skuifraam Dam, will be
built on the Berg River near Franschhoek in the nearby future.
In order to study the vegetation around a river, a zonation pattern on the river
bank is described and several physical habitats are recognized. A primary distinction
is made between a Wet Bank (flooding at least once a year) and a Dry Bank (flooding
less than once a year). The Dry Bank is further subdivided into a Lower Dynamic, a
Shrub/Tree and a Back Dynamic Zone. In the lower reaches these zones are very
distinct, but in the upper reaches of a river they tend to blend into each other and some
zones can be absent or very narrow.
Vegetation has been sampled in transects across the riverbed, following the
Braun-Blanquet method. Additional vegetation samples have been recorded in the
bogs and mires at the sources of the rivers. Vegetation structure and physical habitat
has been described to contribute to the description of the vegetation types. In order to
understand the environmental processes that determine the vegetation, environmental
parameters were recorded in every vegetation sample, such as, slope, aspect,
rockiness and soil variables.
The classification of the vegetation samples resulted in the identification and
subsequent description of 26 riverine and 11 mire communities. The riverinecommunities have been subdivided into ten Community Groups, including a group of
Aquatic communities and three groups of Wet Bank communities. The main
distinction within the Wet Bank Zone is the importance of erosion or deposition as a
driving force of the ecosystem. Three groups of Fynbos communities are identified in
the Back Dynamic Zone, with Asteraceous Fynbos occurring on shales and granites,
Ericaceous Fynbos occurring on Table Mountain Group sandstones and Transitional
Fynbos on a variety of substrates. One community group is characterized by the
dominance of Cliffortia odorata, which shows affinity with some renosterveld
communities known from literature. The two final groups contain the Afromontane
Forests and Riparian Scrub communities, respectively.
Discharges are calculated from data recorded at existing gauging weirs. The
recurrence intervals, inundation levels and stream power of several flood events are
derived from these data and are extrapolated to upstream sites. It appears that most
vegetation types in the zonation pattern on the riverbank can be explained by these
flood events, except for the Afromontane Forests, which are dependent on other sitespecific
factors including protection from fire.
Constrained and unconstrained ordinations are used to relate vegetation
patterns to the environment. The vegetation is determined by three environmental
gradients, operating at different scales. The lateral gradient across the riverbed is
mainly determined by inundation frequency and stream power, which are difficult to
measure in rocky mountain situations, although variables like distance from the
water’s edge, elevation above the water level and rockiness are correlated to them.
The longitudinal gradient is the gradient along the length of the river, from high to
low altitude. This gradient has the least influence on the riparian vegetation. The
geographical gradient reflects the large-scale climatic processes across the mountain
range. This gradient accounts for the biggest part of the total explained variation.
Important variables are especially the ratio between the summer and winter rainfall
and the geological substrate. In the Fynbos Biome, where gamma diversity is
extremely high, large-scale environmental processes are important in azonal
vegetation as well. The most species-rich vegetation associated with the rivers is
found furthest from the water’s edge at intermediate altitudes.
Knowledge about the vegetation types and environmental processes in
Western Cape rivers is essential for monitoring and maintaining these special
ecosystems. Specific threats are related to possible abstraction of water from theTable Mountain Group aquifer and from climate change, which might result in an
overall drying of the ecosystem. / AFRIKAANSE OPSOMMING: Riviere se oewerplantegroei kry die laaste tyd baie aandag in Suid-Afrika,
hoofsaaklik vanweë die belang vir die beheer van vloede, stabilisasie van die oewers
en die bewaring van drinkwater. Die hoë-liggende dele van die riviere het tot dusver
die minste aandag geniet omdat hulle tot ’n groot mate ontoeganklik is weens die
onherbergsame terrein waarin hulle geleë is. In hierdie studie is daar veral na
bergstrome gekyk waar die plantegroei nog taamlik natuurlik en onversteur is. Die
studiegebied wat vir hierdie doel gekies is, is die Hottentots-Holland berge in die
Wes-Kaap. Die gebied het die hoogste reënval in die Kaapse Floristiese Ryk en is ook
baie ryk aan spesies. Vyf riviere het in hierdie gebied hulle oorsprong. Die plantegroei
wat hier voorkom sluit ‘n wye reeks habitatte in: van hoog tot laag in hoogte bo
seespieël, verskeie geologiese substrate asook verskillende reënval patrone.
Al die vyf riviere wat ondersoek is, is baie versteur in hul onderlope, maar is
nog grotendeels natuurlik in hul hoë-liggende dele. Almal is reeds opgedam deur een
of meer damme, behalwe die Lourensrivier. ’n Tussenopvanggebied-oordragskema
verbind tans die Eerste-, Berg- en Riviersonderendriviere met mekaar. Die water uit
hierdie riviere word tans hoofsaaklik in die Theewaterskloofdam opgegaar. ’n
Verdere groot opgaardam, die sogenaamde Skuifraamdam, word binnekort in die
Bergrivier te Franschhoek gebou.
Al die riviere se onderlope is tot ’n mindere of meerdere mate vervuil met
landbou- en rioolafvoerprodukte. Uitheemse indringerplante, wat die natuurlike
oewerplantegroei verdring, skep veral probleme stroomaf van plantasies en dorpe.
Om die plantegroei van die rivieroewers na te vors, te klassifiseer en te
beskryf, is variasies in die fisiese omgewing bepaal en korrelasies gesoek om die
verspreiding van die plantegroei te verklaar. Die belangrikste verdeling in die
oewerplantegroei wat gevind is, is tussen die Nat-oewersone (dit word meer as een
keer per jaar oorstroom) en die Droë-oewersone (dit word minder as een keer per jaar
oorstroom). Die Droë-oewersone word verder onderverdeel in die Laerdinamiesesone,
die Boom/Struiksone en die Agter-dinamiesesone. In die laer dele van
die rivier is hierdie soneringspatrone baie duidelik, maar in die boonste dele van die
rivier kan die onderverdelings dikwels nie van mekaar onderskei word nie omdat
hulle gemeng is, of kan die sones baie smal wees of selfs heeltemal afwesig wees.Die plantegroei is gemonster in transekte wat dwarsoor die rivierloop uitgelê
is. Die Braun-Blanquet monstertegniek is gevolg. Bykomende monsterpersele is
opgemeet in die moerasse in die boonste dele van die berg-opvanggebiede. Om die
omgewingsprosesse wat die plantegroei bepaal te verstaan, is ’n aantal
omgewingsfaktore in elke monsterperseel aangeteken, wat, onder andere, helling,
aspek en bedekking van rotse ingesluit het, terwyl die variasie in samestelling van die
bodem ook aangeteken is.
Die klassifikasie van die plantegroei het tot die beskrywing van 26
plantgemeenskappe in die riviere en 11 gemeenskappe in die moerasse gelei. Die
struktuur van die plantegroei asook kenmerke van die fisiese habitat is in die
beskrywing van die plantegroei-eenhede ingesluit. Die gemeenskappe in die riviere is
onderverdeel in tien gemeenskapsgroepe. Daar is een gemeenskapsgroep wat die
akwatiese gemeenskappe en drie wat die Nat-oewersone gemeenskappe insluit. Die
belangrikste verskille tussen die verskillende Nat-oewersone gemeenskappe word
bepaal deur die mate waartoe erosie of deposisie voorkom. Daar is ook drie
gemeenskapsgroepe van Fynbos onderskei wat in die Agter-dinamiesesone voorkom.
Dit sluit in die Aster-fynbos op die skalies en graniete, die Erica-fynbos op die
sandstene en die Oorgangs-fynbos op gemengde substrate. Een gemeenskapsgroep is
deur die dominansie van Cliffortia odorata gekenmerk. Dit toon verwantskap met
renosterveld gemeenskappe wat reeds in die literatuur beskryf is. Die laaste twee
groepe sluit die Afromontane woude en Oewerstruikbosse in.
Die waterafloop is bereken deur middel van data verkry vanaf bestaande
keerwal meetstasies. Die herhalings-intervalle, oorstromingsdiepte en vloei-sterkte
van verskillende vloedtipes word vanaf hierdie data afgelei en stroomop
geekstrapoleer. Die meeste plantegroeivariasie op die oewers kan deur die vloede
verklaar word, behalwe in die geval van die Afromontane woude, wat deur ander
omgewingsfaktore bepaal is.
Beperkte en onbeperkte ordinasie is gebruik om die verband tussen die
plantegroeipatrone en die omgewing te bepaal. Die plantegroei se verspreiding is
bepaal deur drie omgewingsgradiënte, wat op verskillende skale ‘n uitwerking het.
Die laterale gradiënt oor die rivierbedding is hoofsaaklik bepaal deur
oorstromingsfrekwensie en stroomvloeisterkte. Hierdie veranderlikes is moeilik
bepaalbaar, alhoewel ander soos, afstand vanaf die rivier, hoogte bo watervlak en
bedekking van rotse, wat hieraan gekorreleer is, wel meetbaar is. Die lengte gradiënt,dit is die gradiënt wat van oorsprong na einde langs die lengte van die rivier
teenwoordig is, het die minste invloed op die plantegroei. Die geografiese gradiënt
weerspieel die grootskaalse klimaatsveranderinge oor die bergreeks. Deur hierdie
gradiënt word die grootste deel van die totale variasie tussen die monsters verklaar.
Die belangrikste veranderlikes is die verhouding van somer- teenoor winter-reënval
en die geologiese substraat.
Soortgelyk aan die fynbos in die Fynbosbioom, waar gammadiversiteit
buitegewoon hoog is, is die grootskaalse omgewingsprosesse, ook vir asonale
oewerplantegroei, baie belangrik. Die spesierykste plantegroei rondom die rivier word
die verste van die oewer op gemiddelde hoogtes bo seespieël gevind.
Kennis oor die plantegroei en die omgewingsprosesse in die riviere in die
Wes-Kaap is belangrik vir die monitering en effektiewe beheer van hierdie besondere
ekosisteem. Spesifieke bedreigings is gekoppel aan die potensiële ontginning van
water uit die akwifer in die Tafelberggroep-sedimente asook deur grootskaalse
klimaatsveranderinge waartydens die hoeveelheid water, volgens voorspellings,
waarskynlik sal afneem in hierdie ekosisteem.
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The effect of cattle grazing in riparian areas on winter biodiversity and ecologyFranz, Simone, University of Lethbridge. Faculty of Arts and Science January 2009 (has links)
Livestock grazing in riparian habitats alters the vegetation structure, which has a detrimental effect on wildlife. This study examined the effect of cattle grazing in riparian habitats on winter bird biodiversity, small mammal biodiversity, and microclimate. Study sites were ungrazed, moderately grazed, and heavily grazed riparian habitats along the Oldman River, Alberta during winter 2005 and 2006. Bird species richness, individual abundance, and diversity indices were higher in ungrazed habitats than in grazed habitats. Deer mouse population sizes were not different except during spring 2006, when populations were larger in ungrazed sites. Microclimate data were collected in riparian sites and upland sites in winter 2006. Temperatures were higher and wind speeds were slower in riparian sites than in upland sites. Wind speeds were faster in heavily grazed riparian sites than in lightly grazed sites. Faster winds in heavily grazed sites may account for the decreased winter biodiversity in these habitats. / x, 118 leaves ; 29 cm
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Vegetation, Environmental Characteristics, and their Relationships: Variation within the Annually Flooded Riparian Zones of the John Day River Basin, OregonHartsfield, Samuel J. 13 February 2009 (has links)
I hypothesized that vegetation and physical environmental characteristics would differ between the upper and lower extents of the annually flooded riparian zone on the John Day River, and that relationships between species and environmental variables would display differences between these two zones. Vegetation, environmental variables, and relationships between them were assessed for the entire annually flooded riparian zone, and for the proposed upper and lower zones. Data were collected from 60 one-square-meter quadrats: 30 in each the upper and lower zones. Sites were randomly selected and located so that flood duration was roughly equal at all sites within each zone.
34 plant species were encountered: 25 in the upper zone, 27 in the lower zone. Wetland obligate and facultative wetland species groups and eight individual species accounted for statistically different percentages ofquadrat cover between zones. ANOSIM analysis identified two statistically distinct vegetation communities between the two zones.
Soil texture averaged 75.85% sand and 20.81% fines. Sand ranged between 36.69% and 95.55%. Fines ranged between 2.54% and 58.84%. A horizon depths and fine soil particle concentrations were greater in the upper zone. Coarser soils with more sand and gravel dominated the lower zone. All enviromnental variables studied, except pH, were highly variable throughout the study area. ANOSIM analysis results suggest that the upper and lower zones have distinct, statistically different physical environments from each other.
Regression analyses relating species quadrat cover to physical environmental variables were performed for the total, upper, and lower riparian zones. Numerous differences were identified between the upper and lower riparian zones that the riparian scale analyses did not represent accurately. There were ten instances in which the zone scale analyses identified a relationship in either the upper or lower zone, while the corresponding riparian scale analysis failed to identify any relationship.
The results of this study indicate that vegetation and the physical environment are statistically different between the upper and lower zones on this river, and that relationships between a given plant species and environmental variable can vary between zones. Future research and management efforts should consider and address the potential for such between-zone variation.
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