scholarly journals The association of Lantana camara with elephant (Elephas maximus), their food, habitat use and feeding behaviour in southern India

2021 ◽  
Author(s):  
◽  
Gaius Wilson

<p>Invasive exotic species pose an enormous threat to the world's biological diversity. Invasions can alter native communities, replacing local biotas with non-indigenous species introduced by humans. Exotic plant invasions can have negative effects on native flora, which can be in turn detrimental to the herbivores that depend on the vegetation. In this dissertation, I examined the association of an exotic invasive weed, Lantana camara L., with the Asian elephant (Elephas maximus), its food resources (grass and browse), habitat use and feeding behaviour in Mudumalai Tiger Reserve, southern India.  Exotic plant invasions are often associated with alterations or declines in native floral species. I first examined the association of L. camara and measured environmental covariates with floral species assemblage and richness, elephant browse plants, percentage grass cover and percentage grass occupancy. A multivariate analysis revealed a significant association of L. camara with floral species assemblage and richness, some elephant browse plants and grass cover within the moist deciduous forest (MDF) and dry deciduous forest (DDF), but not in the thorn forest (TF) of Mudumalai. My results suggest that L. camara appears to be capable of altering the floral community in some habitats. These results also suggest that changes in the floral community and a reduction in grass cover due to L. camara invasion could be detrimental to elephant and other herbivores that depend on grass in this reserve.   I then examined the association of L. camara with habitat use by elephant. Elephant dung density was used to assess elephant habitat use from 62 line transects, each 1-km in length. I found no evidence that L. camara was associated with elephant habitat use across habitats, although the interaction term between one habitat (DDF) and L. camara was significantly associated with elephant dung density suggesting that the effect of L. camara was different in different habitats. This indicates that L. camara is associated with elephant habitat use within certain habitats. Habitat and impact of human settlements were significantly associated with elephant habitat use across habitats within Mudumalai. In the DDF, however, only L. camara was associated with elephant habitat use. I conclude that while no significant effects of L. camara were seen across habitats, in specific habitats, negative associations of this invasive plant with elephant habitat use, possibly through the reduction of grass cover, are possible. These results indicate that L. camara appears detrimental to elephant in certain habitats and removal of L. camara in these habitats should be prioritised so as to facilitate growth of grass and native browse species, especially if elephant populations continue to expand.  Lastly, I examined the association of elephant behaviour, assessed from feeding and stepping rates, with variation in L. camara invasion. Fifty-seven elephants were observed for a total of 64.3 hours using the focal-animal sampling method. Elephant were never observed to feed on L. camara, but rather fed on grass and browse that were present within and around L. camara patches. Feeding rates (number of trunksful·min⁻¹) were negatively associated with L. camara invasion. A path analysis, which assesses both direct and indirect effects of independent variables, indicated that the total effect of L. camara on feeding rates was 11% less than the direct negative association owing to a positive indirect relationship between L. camara and feeding rates through grass cover and browse density. Lantana camara was not significantly associated with variation in stepping rates (number of steps·min⁻¹). Rather, stepping rates were negatively associated with grass cover and positively associated with browse density. My results indicate that L. camara is potentially capable of changing elephant feeding rates, likely through a loss of grass areas due to L. camara invasion.  Wild elephants do not eat L. camara, and this invasive plant appears to take the place of an important food source. My results indicate that managers should prioritize their focus on certain habitats to control the impact of L. camara on elephants and vegetation. However, this study was of a correlational nature based on observational data. Experimental work is therefore needed to test for causal relationships among the variables I measured, over multiple seasons and in different habitats. Experimental evidence will enhance our understanding of how invasive weeds modify floral communities, elephant habitat use and behaviour and help determine whether L. camara is a 'passenger' or 'driver' of these changes in this ecosystem.</p>

2021 ◽  
Author(s):  
◽  
Gaius Wilson

<p>Invasive exotic species pose an enormous threat to the world's biological diversity. Invasions can alter native communities, replacing local biotas with non-indigenous species introduced by humans. Exotic plant invasions can have negative effects on native flora, which can be in turn detrimental to the herbivores that depend on the vegetation. In this dissertation, I examined the association of an exotic invasive weed, Lantana camara L., with the Asian elephant (Elephas maximus), its food resources (grass and browse), habitat use and feeding behaviour in Mudumalai Tiger Reserve, southern India.  Exotic plant invasions are often associated with alterations or declines in native floral species. I first examined the association of L. camara and measured environmental covariates with floral species assemblage and richness, elephant browse plants, percentage grass cover and percentage grass occupancy. A multivariate analysis revealed a significant association of L. camara with floral species assemblage and richness, some elephant browse plants and grass cover within the moist deciduous forest (MDF) and dry deciduous forest (DDF), but not in the thorn forest (TF) of Mudumalai. My results suggest that L. camara appears to be capable of altering the floral community in some habitats. These results also suggest that changes in the floral community and a reduction in grass cover due to L. camara invasion could be detrimental to elephant and other herbivores that depend on grass in this reserve.   I then examined the association of L. camara with habitat use by elephant. Elephant dung density was used to assess elephant habitat use from 62 line transects, each 1-km in length. I found no evidence that L. camara was associated with elephant habitat use across habitats, although the interaction term between one habitat (DDF) and L. camara was significantly associated with elephant dung density suggesting that the effect of L. camara was different in different habitats. This indicates that L. camara is associated with elephant habitat use within certain habitats. Habitat and impact of human settlements were significantly associated with elephant habitat use across habitats within Mudumalai. In the DDF, however, only L. camara was associated with elephant habitat use. I conclude that while no significant effects of L. camara were seen across habitats, in specific habitats, negative associations of this invasive plant with elephant habitat use, possibly through the reduction of grass cover, are possible. These results indicate that L. camara appears detrimental to elephant in certain habitats and removal of L. camara in these habitats should be prioritised so as to facilitate growth of grass and native browse species, especially if elephant populations continue to expand.  Lastly, I examined the association of elephant behaviour, assessed from feeding and stepping rates, with variation in L. camara invasion. Fifty-seven elephants were observed for a total of 64.3 hours using the focal-animal sampling method. Elephant were never observed to feed on L. camara, but rather fed on grass and browse that were present within and around L. camara patches. Feeding rates (number of trunksful·min⁻¹) were negatively associated with L. camara invasion. A path analysis, which assesses both direct and indirect effects of independent variables, indicated that the total effect of L. camara on feeding rates was 11% less than the direct negative association owing to a positive indirect relationship between L. camara and feeding rates through grass cover and browse density. Lantana camara was not significantly associated with variation in stepping rates (number of steps·min⁻¹). Rather, stepping rates were negatively associated with grass cover and positively associated with browse density. My results indicate that L. camara is potentially capable of changing elephant feeding rates, likely through a loss of grass areas due to L. camara invasion.  Wild elephants do not eat L. camara, and this invasive plant appears to take the place of an important food source. My results indicate that managers should prioritize their focus on certain habitats to control the impact of L. camara on elephants and vegetation. However, this study was of a correlational nature based on observational data. Experimental work is therefore needed to test for causal relationships among the variables I measured, over multiple seasons and in different habitats. Experimental evidence will enhance our understanding of how invasive weeds modify floral communities, elephant habitat use and behaviour and help determine whether L. camara is a 'passenger' or 'driver' of these changes in this ecosystem.</p>


2014 ◽  
Vol 30 (6) ◽  
pp. 551-563 ◽  
Author(s):  
Gaius Wilson ◽  
Ajay A. Desai ◽  
Dalice A. Sim ◽  
Monica A. M. Gruber ◽  
Philip J. Lester

Abstract:We examined changes in a community of seedlings/saplings 10–150 cm tall associated with the presence of a widely invasive plant, Lantana camara and environmental covariates along 67 randomly located transects, in Mudumalai, India. We compared plant species assemblage and grass cover in L. camara-invaded and uninvaded plots in three habitats. Multivariate analyses revealed a significant association of all environmental covariates with plant species assemblage. Pairwise tests indicated that L. camara was significantly associated with changes in plant species assemblage and grass cover within the moist and dry deciduous forest, but not in the thorn forest. The relationship between L. camara and that of elephant browse plants varied with species. A linear regression analysis indicated that L. camara invasion was the only significant predictor of grass occupancy. Our results indicate that in addition to other factors, L. camara was associated with altering plant species assemblage, some elephant browse plants and grass cover in the moist and dry deciduous forest. It appears that L. camara can have a major effect on diversity within this reserve, but whether this effect is by L. camara driving the change or being associated with other habitat change requires further experimental evidence.


2013 ◽  
Vol 29 (3) ◽  
pp. 199-207 ◽  
Author(s):  
Gaius Wilson ◽  
Ajay A. Desai ◽  
Dalice A. Sim ◽  
Wayne L. Linklater

Abstract:Invasive weeds like Lantana camara have a range of effects on animals such as elephant. These plants are not edible by the Asian elephant (Elephas maximus). They also compete for space with elephant food plants and take over large areas of elephant habitat. We tested whether the addition of L. camara to a model consisting of measured environmental variables improved predictions of habitat use by elephant in Mudumalai Tiger Reserve, India. Elephant dung density was used to assess elephant habitat use from 62 line transects 1-km in length. Results indicated that habitat and impact of human settlements significantly influenced elephant habitat use at a landscape scale. However, we found no evidence for the hypothesis that the addition of L. camara significantly predicted elephant habitat use at the landscape level. We then tested the association of L. camara on elephant habitat use in the dry deciduous forest (DDF) where there was a significant interaction between DDF and L. camara. In the DDF, L. camara significantly predicted elephant habitat use. We conclude that while no significant effects of L. camara were seen at the level of an entire reserve, at a finer scale and in specific habitats negative effects of this invasive plant on elephant habitat use were observed.


2014 ◽  
Vol 128 (3) ◽  
pp. 272 ◽  
Author(s):  
Gilbert Proulx

Late-winter habitat use by the Fisher, Pekania pennanti (Erxleben, 1777) in northwestern Saskatchewan was assessed in February 2009, 2011, and 2012. A total of 78 Fisher tracks were recorded over 60 300 m of snowshoe surveys. Fisher tracks were significantly less frequent than expected in Tamarack (Larix laricina [Du Roi] K. Koch) stands with > 40% crown closure and mainly 0–10 m trees (P < 0.05) and in open areas. Fishers used other habitat types equal to availability, including muskeg and coniferous, mixed, and deciduous forest stands. Maintaining mosaics of forest stands of different seral stages interspersed with muskeg would meet the late-winter habitat needs of Fishers in the Boreal Plains Ecozone of northwestern Saskatchewan.


Author(s):  
JAVIER A. FIGUEROA ◽  
SERGIO A. CASTRO ◽  
PABLO A. MARQUET ◽  
FABIAN M. JAKSIC

2018 ◽  
Vol 220 ◽  
pp. 50-59 ◽  
Author(s):  
Christie Sampson ◽  
Peter Leimgruber ◽  
David Tonkyn ◽  
Jennifer Pastorini ◽  
H.K. Janaka ◽  
...  

2021 ◽  
Author(s):  
Jiang Wang ◽  
Yuan Ge ◽  
J. Hans C. Cornelissen ◽  
Xiaoyan Wang ◽  
Song Gao ◽  
...  

Abstract Biodiversity loss, exotic plant invasions and climatic change are currently the three major challenges to our globe and can each affect various ecological processes, including litter composition. To gain a better understanding of global change impacts on ecological processes, these three global change components need to be considered simultaneously. Here we assembled experimental plant communities with species richness levels (1, 2, 4, 8 or 16) and subjected them to drought (no, moderate or intensive drought) and invasion (invasion by the exotic annual plant Symphyotrichum subulatum or not). We collected litter of the native plant communities and let it decompose for nine months within the communities. Drought decreased litter decomposition, while the exotic plant invasion had no impact. Increasing species richness decreased litter decomposition under the mesic condition (no drought), but had little impact under moderate and intensive drought. A structural equation model showed that drought and species richness affected litter decomposition mainly via influencing litter nitrogen concentration, but not via altering the quantity and diversity of soil meso-fauna or soil physio-chemical properties. The negative impact of species diversity on litter decomposition under the mesic condition was mainly ascribed to a sampling effect, i.e. via particularly low litter nitrogen concentrations in the two dominant species. Our results indicate that species richness can interact with drought to affect litter decomposition via effect on litter nitrogen. We conclude that nitrogen-dependent litter decomposition should be a mechanism to predict integrated effects of plant diversity loss, exotic plant invasions and climatic change on litter decomposition.


2021 ◽  
Author(s):  
Muriel Deparis ◽  
Nicolas Legay ◽  
Francis Isselin-Nondedeu ◽  
Sébastien Bonthoux

Abstract ContextCities are high sources of plant invasions. To understand mechanisms of introduction and dispersion of invasive alien species (IAS) in city, we need a thoroughly description of the social and structural components of urban landscapes. ObjectivesWe assessed the effects of neighborhood types and their associated human activities and structural linear elements on the distributions of IAS in a French medium city (Blois). We examined how the relative contributions of these variables varied between scales of analysis. MethodsWe recorded the presence of seven IAS species in the entire city (22 km²), at three spatial resolutions: 100×100m, 200×200m and 400×400m. We characterized neighborhoods through their main covers, human uses, and ages and structural elements through impervious soil, area of and distance to roads and railways.ResultsNeighborhood type was the most important variable in explaining IAS distributions. This variable was especially important at the finest scale which allowed a fine urban classification. B. davidii and B. aquifolium were found in individual residential neighborhoods, whereas R. pseudoacacia and A. altissima were most encountered in industrial areas. The effects of the structural elements differed between species and were lower. ConclusionsCharacterizing the high spatial and functional heterogeneity of urban landscapes at fine scale is critical to understand IAS distribution patterns. We show that considering human uses and planting practices is determinant to understand IAS introduction patterns. Then, linear transport corridors and ruderal conditions explain the dispersion and establishment of IAS across the city and potentially to the surrounding natural spaces.


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