scholarly journals Changes in small mammal assemblage structure across a rain forest/open forest ecotone

1998 ◽  
Vol 14 (2) ◽  
pp. 187-198 ◽  
Author(s):  
STEPHEN E. WILLIAMS ◽  
HELENE MARSH

The effect of the change in vegetation structure from closed rain forest to tall open forest on the small mammal assemblage was studied by live trapping at three sites where the ecotone was very narrow (> 20 m) near the southern end of the Wet Tropics World Heritage Area of Australia. Habitat heterogeneity was significantly higher in the mixed open forest/ecotone area than in the adjacent rain forest. There was a large change in the struture of the small mammal assemblage coincident with the vegetation discontinuity. Although the species richness of small mammals was relatively constant across the gradient, the evenness and diversity of the assemblage declined across the transition from open forest into rain forest and biomass increased, largely due to the high abundance of Rattus fuscipes in the rain forest. The results suggest that the species richness of the small mammal assemblage was not determined by the spatial heterogeneity of the vegetation struture. The species composition of the rain forest is probably related to the historical biogeography of the area whereas the species richness of the wet sclerophyll forest is probably due to a mass-area effect from the adjcant large areas of rain forest and dry sclerophyll forest. However, the evenness, and therefore the diversity of the assemblage, was strongly affected by habitat heterogeneity.

2019 ◽  
Author(s):  
Monica T. Shilereyo ◽  
Flora J. Magige ◽  
Joseph O. Ogutu ◽  
Eivin Røskaft

AbstractLand use is an important factor influencing animal abundance, species richness and diversity in both protected and human-dominated landscapes. Increase in human population and activities intensify changes in habitat structure and hence abundance, species richness and diversity. We investigated the influences of land use and seasonality on small mammal abundance, species richness and diversity in 10 habitat types distributed over protected, agricultural and pastoral landscapes in the Serengeti ecosystem in Tanzania. We used live traps (n = 141) and capture-recapture methods in each of 10 fixed plots distributed across three landscapes for a total of 28,200 trap nights of effort. Trapping was carried out in the wet and dry seasons for two consecutive years (April 2017 to October 2018). Small mammal abundance was higher in the pastoral than in the protected and in the agricultural landscape. Abundance was higher in the dry than the wet season across all the three landscapes. Species richness and diversity were higher in the protected, middling in the agricultural and lowest in the pastoral landscape. The high abundance in the pastoral landscape was due to the numerical dominance of two species, namely A. niloticus in the shrubland and M. natalensis in the cropland habitat, resulting in low species richness and diversity. Abundance was more evenly distributed across all habitats in the protected area due to less disturbance. The low abundance in the agricultural landscape, likely reflects disturbance from cultivation. High species richness and diversity in the protected area indicate high habitat heterogeneity while high species diversity in the agricultural landscape was likely due to high food availability during and soon after harvests. These findings emphasize the importance of protection in maintaining habitat heterogeneity for wildlife. They also reaffirm the need for buffer zones around protected areas to cushion them from intensifying human activities.


1974 ◽  
Vol 50 (5) ◽  
pp. 181-185 ◽  
Author(s):  
Andrew Radvanyi

Live trapping and tagging methods were employed to assess small mammal populations within two hardwood plantations in southern Ontario. Excessive girdling damage in past years to young planted trees necessitated an evaluation of rodent populations and development of effective control measures. The application of an anticoagulant rodenticide to oat groats bait broadcast over the study area at an ingredient cost of approximately three dollars per acre virtually wiped out the small mammals. Reinvasion from surrounding areas was, however, fairly rapid, particularly during late summer. Further research on longer term control measures using poisoned bait feeder stations is recommended.


2014 ◽  
Vol 369 (1643) ◽  
pp. 20130197 ◽  
Author(s):  
Véronique St-Louis ◽  
Anna M. Pidgeon ◽  
Tobias Kuemmerle ◽  
Ruth Sonnenschein ◽  
Volker C. Radeloff ◽  
...  

Applications of remote sensing for biodiversity conservation typically rely on image classifications that do not capture variability within coarse land cover classes. Here, we compare two measures derived from unclassified remotely sensed data, a measure of habitat heterogeneity and a measure of habitat composition, for explaining bird species richness and the spatial distribution of 10 species in a semi-arid landscape of New Mexico. We surveyed bird abundance from 1996 to 1998 at 42 plots located in the McGregor Range of Fort Bliss Army Reserve. Normalized Difference Vegetation Index values of two May 1997 Landsat scenes were the basis for among-pixel habitat heterogeneity (image texture), and we used the raw imagery to decompose each pixel into different habitat components (spectral mixture analysis). We used model averaging to relate measures of avian biodiversity to measures of image texture and spectral mixture analysis fractions. Measures of habitat heterogeneity, particularly angular second moment and standard deviation, provide higher explanatory power for bird species richness and the abundance of most species than measures of habitat composition. Using image texture, alone or in combination with other classified imagery-based approaches, for monitoring statuses and trends in biological diversity can greatly improve conservation efforts and habitat management.


2021 ◽  
pp. 175815592110660
Author(s):  
Jenő J Purger ◽  
Dávid Szép

The relative abundance of small mammal species detected from Common Barn-owl pellets reflects the landscape structure and habitat pattern of the owl’s hunting area, but it is also affected by the size of the collected pellet sample and the size of the supposed hunting area. The questions arise: how many pellets should be collected and analyzed as well as how large hunting area should be taken into consideration in order to reach the best correspondence between the owl’s prey composition and the distribution of habitats preferred by small mammals preyed in supposed hunting areas? For this study, we collected 1045 Common Barn-owl pellets in a village in southern Hungary. All detected small mammal species were classified into functional groups (guilds) preferring urban, open, forest and wetland habitats. The proportion of functional groups was compared to the proportion of these habitats around the pellet collection site within circles of one, two, and three km radius. Saturation curves showed that at least 300 pellets or ca. 600 mammalian remains are required for the detection of the 19 small mammal species. The share of small mammals detected in the prey and their functional groups according to their habitat preference showed an increasing consistency with the distribution of real habitats in the potential hunting area of a radius of 3 km around the owl’s breeding or resting place.


Koedoe ◽  
2006 ◽  
Vol 49 (1) ◽  
Author(s):  
M. Van Deventer ◽  
J.A.J. Nel

The effect of habitat differences and food availability on small mammal (rodent and elephant shrew) species richness, diversity, density and biomass was investigated in Namaqualand, South Africa. Species richness in the three habitats sampled, namely Upland Succulent Karoo, Dry Riverine Shrub and North-western Mountain Renosterveld was low, with only 2–4 species per habitat. Rodents trapped were predominantly Gerbillurus paeba and Aethomys namaquensis, with fewer Mus minutoides and Petromyscus sp. The only non-rodent was the elephant shrew Elephantulus edwardii. Ten habitat features, the percentage of total plant cover, tree cover, shrub cover, grass cover, plant litter, total basal cover, sand, gravel or rock cover, and the dominant plant height were recorded at 30 randomly chosen points on five sampling grids in each habitat. Small mammal density and biomass was significantly correlated with food availability (green foliage cover, seeds, and relative density and biomass of insects). Species richness and diversity of small mammals were significantly correlated with shrub cover. Numbers and biomass of specific species correlated significantly with different habitat features in each case.


1999 ◽  
Vol 15 (4) ◽  
pp. 399-413 ◽  
Author(s):  
T. Ganesh ◽  
Priya Davidar

Fruit biomass and frugivore abundance were quantified over 3 y in a rain forest of the south Western Ghats, India. Fruit biomass was estimated by sampling fruit fall in the primary forest, and frugivore abundance by a 2.5-km transect. A total of 645 kg ha−1 of fruit was produced annually in the forest. Only 49% of this is edible to the frugivores and the remaining 51% is in the form of non-edible husks. Mammalian frugivores outnumbered avian frugivores and the majority of the mammals were seed predators. The total fruit biomass produced at Kakachi is lower than in the lowland forest and mountain forests in the neotropics but higher than in the wet sclerophyll forest of Australia. Lower diversity of trees and edaphic factors at Kakachi could be some of the reasons for these differences. On the other hand, paucity of fleshy fruits, low density of trees producing fleshy fruits and irregular fruiting of these species, account for the low number of obligate avian frugivores at Kakachi.


2012 ◽  
Vol 18 (4) ◽  
pp. 263 ◽  
Author(s):  
Tom Lewis ◽  
David Taylor ◽  
Scott Swift ◽  
Valerie Debuse

We monitored an area that was revegetated with the goal of restoring a Eucalyptus tereticornis open forest on former agricultural land in central, eastern Queensland. Revegetation involved: (1) planting 60 ha of previously cleared and heavily grazed land with eight local trees species; and (2) removing cattle grazing to encourage natural regeneration in areas where some mature trees remained. We compared the revegetation site to native pasture that had also been previously cleared, with only scattered paddock trees remaining, and continued to be managed for livestock production (an area similar to the revegetation site, prior to planting) and a remnant forest (reference area). Nine years since revegetation began there was some evidence that the revegetated site was diverging from pasture in terms of understorey plant composition, sapling density and topsoil C and N. There was little divergence in terms of plant species richness (native, introduced, grass, forb and woody plant richness), herbaceous biomass and woody plant regeneration. Some monitoring plots were subject to fire (prescribed fire and or wildfire) over the period of monitoring. With increasing time since fire, the richness of native species, introduced species and grass species (both native and introduced) declined, and forb and grass species richness declined with increasing litter biomass, suggesting that the occurrence of fire and the associated removal of litter biomass has a positive influence on herbaceous diversity in this ecosystem. Woody plant regeneration persisted through lignotubers at the revegetation site and at the pasture, but this regeneration was stunted at the pasture presumably due to livestock grazing. Hence areas of former E. tereticornis forest showed promising regenerative capacity where mature trees remained and where livestock grazing was removed.


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