Native plant diversity in tropical savannas decreases when exotic pasture grass cover increases

2012 ◽  
Vol 34 (2) ◽  
pp. 183 ◽  
Author(s):  
A. S. Kutt ◽  
J. E. Kemp

The invasion of exotic plants into savanna ecosystems can disrupt the natural pattern of vegetation. Indian couch Bothriochloa pertusa was introduced into Australia as a species for rehabilitation of degraded grazing land. In this study the effect of increasing B. pertusa cover on native plant diversity and possible mechanisms of its spread were examined. Forty sites were sampled in uncleared Queensland rangelands with a range of B. pertusa and Bothriochloa ewartiana (a native species) cover. The mean number of native species per quadrat declined with increasing B. pertusa cover but remained stable over sites with increasing B. ewartiana cover. Mean species richness accumulated at a significantly lower rate for sites with B. pertusa present. Canonical analysis of principle coordinates suggested that three groups of sites, ranging from low to high species richness and cover of native plants, were correlated along gradients of B. pertusa cover, grazing intensity and basal area of dead trees. Generalised linear modelling indicated significant negative relationships between B. pertusa cover and total ground cover, forbs and perennial grass richness and cover, and cover of nine native perennial tussock grasses (Aristida leptopoda, B. decipiens, B. ewartiana, Chrysopogon fallax, Dichanthium fecundum, D. sericeum, Heteropogon contortus, H. triticeus and Themeda triandra). This study suggests that an increase in B. pertusa is associated with a substantial change in the cover and species richness of native plant communities. This was considered to occur via competitive effects as well as a result of cattle grazing, rainfall deficit and tree death. Regardless of the mechanism, continued spread of exotic pasture species has the potential to cause significant changes to rangeland biodiversity.

2022 ◽  
Vol 80 ◽  
pp. 87-95
Author(s):  
C.W. Sherrill ◽  
S.D. Fuhlendorf ◽  
L.E. Goodman ◽  
R.D. Elmore ◽  
R.G. Hamilton

2010 ◽  
Vol 19 (4) ◽  
pp. 490 ◽  
Author(s):  
Erich K. Dodson ◽  
David W. Peterson ◽  
Richy J. Harrod

Slope stabilisation treatments like mulching and seeding are used to increase soil cover and reduce runoff and erosion following severe wildfires, but may also retard native vegetation recovery. We evaluated the effects of seeding and fertilisation on the cover and richness of native and exotic plants and on individual plant species following the 2004 Pot Peak wildfire in Washington State, USA. We applied four seeding and three fertilisation treatments to experimental plots at eight burned sites in spring 2005 and surveyed vegetation during the first two growing seasons after fire. Seeding significantly reduced native non-seeded species richness and cover by the second year. Fertilisation increased native plant cover in both years, but did not affect plant species richness. Seeding and fertilisation significantly increased exotic cover, especially when applied in combination. However, exotic cover and richness were low and treatment effects were greatest in the first year. Seeding suppressed several native plant species, especially disturbance-adapted forbs. Fertilisation, in contrast, favoured several native understorey plant species but reduced tree regeneration. Seeding, even with native species, appears to interfere with the natural recovery of native vegetation whereas fertilisation increases total plant cover, primarily by facilitating native vegetation recovery.


1998 ◽  
Vol 4 (2) ◽  
pp. 132 ◽  
Author(s):  
Gabriel M. Crowley ◽  
Stephen T. Garnett

The vegetation of 64 grassland and grassy woodland sites in east-central Cape York Peninsula, surveyed by CSIRO in 1966, was re-surveyed in 1995. While the original vegetation communities had persisted at most sites, a change in species dominance was recorded at 14% of sites. Melaleuca viridiflora (ti-tree) had invaded eight sites, and increased in abundance in at least 16 of the 35 sites in which it had occurred in 1966. This had led to four out of 13 grassland sites, and three out of four mixed evergreen sites being re-classified as ti-tree woodlands. Analysis of aerial photographs covering 415 km2 showed a 10% net loss of grasslands between 1969 and 1988. These changes are attributed to a reduction in the use of fire as a management tool since European settlement. Changes were also found in perennial grass composition consistent with grazing or over-grazing, particularly in the eucalypt/ironwood communities. A shift from Themeda triandra to Heteropogon contortus parallels earlier, grazing-related changes in southern Queensland. Evidence of a decline in Heteropogon triticeus and isolated losses of Sorghum plumosum are more suggestive of localized, unsustainable overgrazing. An increase in Sorghum plumosum in wet habitats appears to be associated with recent lack of burning. These changes suggest that further intensification of cattle grazing in the area may not be possible without significantly reducing both conservation values and pasture condition.


2015 ◽  
Vol 40 (1) ◽  
pp. 112-134 ◽  
Author(s):  
Sébastien Larrue ◽  
Jean-François Butaud ◽  
Pascal Dumas ◽  
Stéphane Ballet

Which abiotic factors influence the number of native plant species on remote atolls is an important question to understand better the spatial pattern of the species observed on these low and vulnerable coral islands. However, this issue is still very poorly documented, often due to human degradation, partial botanical surveys or the difficult geographic access of remote atolls for researchers. The remote atolls of Eastern Polynesia, which are among the most isolated in the world, are of great interest for studies of native species’ distribution due to their isolation, low human density and urbanisation. In this study, we selected 49 remote atolls of Eastern Polynesia with complete botanical surveys to test the relative influence of eight abiotic factors on native plant species richness (i.e. indigenous and endemic species). Abiotic factors used as potential predictors included atoll area (km2), shoreline length (km), atoll elevation (m) and index of isolation (UNEP), but also the coastal index of the atoll ( Ic), the distance to the nearest similar atoll (km), the distance to the nearest large volcanic island ≥ 1000 km2 (here, Tahiti as a potential stepping-stone island) and the distance to the nearest raised atoll ≥ 15 m a.s.l. (here, Makatea or Henderson as a potential refugium during sea-level highstands). Spearman’s rank correlation, linear regression analysis and frequency diagrams were used to assess the relative influence of these factors on native species richness. No relationship was found between the species richness and the index of isolation or the distance to the nearest similar atoll. Atoll area and distance to the nearest raised atoll of Makatea explained 47.1% and 40%, respectively, of the native species richness variation observed on the remote atolls. The distance to the volcanic island of Tahiti and the coastal index explained 36.9% and 27.3% of the variation, while elevation and shoreline length explained 23.3% and 18.4% of the variation, respectively. Native species richness on the atolls surveyed increased with the increasing atoll area, elevation and shoreline length, but decreased with the increasing distance to the nearest raised atoll of Makatea and the large volcanic island of Tahiti. This supports the view that the spatial pattern of native species richness observed on the remote atolls was strongly influenced by (i) atoll area but also by (ii) the distance to the raised atoll of Makatea, and (iii) the distance to the volcanic island of Tahiti. This finding suggests that the raised atoll may be viewed as a refugium during sea-level highstands while the large volcanic island played the role of stepping-stone island, both islands influencing the dispersal of native species on remote atolls and attenuating the isolation effect in the study area.


2004 ◽  
Vol 52 (5) ◽  
pp. 597 ◽  
Author(s):  
J. B. Kirkpatrick

Few temporal studies document vegetation change in Australian temperate grassy woodlands. Floristic and structural data were collected from 68 randomly located sites in the Queens Domain, an urban grassy woodland remnant, in 1974, 1984, 1994 and 2000 and a search made for rare species. Species of conservation significance were concentrated at highly disturbed sites, whereas vegetation types of conservation significance decreased in area as a result of increases in the numbers of Allocasuarina verticillata, which caused a change in many unmown areas from Eucalyptus viminalis grassy woodland to E. viminalis–A. verticillata woodland/forest or A. verticillata open/closed forest. Structural changes were associated with changes in species composition and an increase in native-species richness. Increases in tree cover occurred where fires were most frequent, possibly as a result of the lack of mammalian herbivores. The frequencies of herbs and annual grasses were strongly affected by precipitation in the month of sampling. Half of the species that showed a consistent rise or fall through time were woody plants, approximately twice the number expected. In the dataset as a whole, species-richness variables were largely explained by varying combinations of variables related to moisture availability, altitude and the incidence of mowing. The strongest influences on species composition were the same, although slope and time since the last fire also contributed to multiple regression and generalised linear models. Compositional stability was positively related to native-species richness, whereas high levels of exotic-species richness occurred at both low and high levels of native-species richness. The maintenance of native-plant biodiversity on the Domain requires such counterintuitive measures as the maintenance of exotic trees and the control of native trees, demonstrating the contingencies of conservation management in fragmented vegetation that consists of a mixture of native and exotic species.


2014 ◽  
Vol 281 (1794) ◽  
pp. 20141841 ◽  
Author(s):  
Ian S. Pearse ◽  
Andrew L. Hipp

There is often an inverse relationship between the diversity of a plant community and the invasibility of that community by non-native plants. Native herbivores that colonize novel plants may contribute to diversity–invasibility relationships by limiting the relative success of non-native plants. Here, we show that, in large collections of non-native oak trees at sites across the USA, non-native oaks introduced to regions with greater oak species richness accumulated greater leaf damage than in regions with low oak richness. Underlying this trend was the ability of herbivores to exploit non-native plants that were close relatives to their native host. In diverse oak communities, non-native trees were on average more closely related to native trees and received greater leaf damage than those in depauperate oak communities. Because insect herbivores colonize non-native plants that are similar to their native hosts, in communities with greater native plant diversity, non-natives experience greater herbivory.


2006 ◽  
Vol 28 (1) ◽  
pp. 27 ◽  
Author(s):  
A. C. Grice

Most parts of the Australian rangelands are at risk of invasion by one or more species of non-native plants. The severity of current problems varies greatly across the rangelands with more non-native plant species in more intensively settled regions, in climatic zones that have higher and more reliable rainfall, and in wetter and more fertile parts of rangeland landscapes. Although there is quantitative evidence of impacts on either particular taxonomic groups or specific ecological processes in Australian rangelands, a comprehensive picture of responses of rangeland ecosystems to plant invasions is not available. Research has been focused on invasive species that are perceived to have important effects. This is likely to down play the significance of species that have visually less dramatic influences and ignore the possibility that some species could invade and yet have negligible consequences. It is conceivable that most of the overall impact will come from a relatively small proportion of invasive species. Impacts have most commonly been assessed in terms of plant species richness or the abundance of certain groups of vertebrates to the almost complete exclusion of other faunal groups. All scientific studies of the impacts of invasive species in Australian rangelands have focused on the effects of individual invasive species although in many situations native communities are under threat from a complex of interacting weed species. Invasion by non-native species is generally associated with declines in native plant species richness, but faunal responses are more complex and individual invasions may be associated with increase, decrease and no-change scenarios for different faunal groups. Some invasive species may remain minor components of the vegetation that they invade while others completely dominate one stratum or the vegetation overall.


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