Diversity indices and species abundance models

Author(s):  
Anne E. Magurran
2021 ◽  
Vol 13 (10) ◽  
pp. 5747
Author(s):  
Dehuan Li ◽  
Wei Sun ◽  
Fan Xia ◽  
Yixuan Yang ◽  
Yujing Xie

Biodiversity maintenance is a crucial ecosystem service. Due to time limits and data availability, assessing biodiversity using indicators or models has become a hot topic in recent decades. However, whether some proposed indicators can explain biodiversity well at the local scale is still unclear. This study attempted to test whether the habitat quality index (HQI) as measured using the integrated valuation of ecosystem services and trade-offs (InVEST) model could explain variations in bird diversity in New Jiangwan Town, a rapidly urbanized region of Shanghai, China. The relationships from 2002 to 2013 among HQI and the two diversity indices, species richness and species abundance, were analyzed using Fisher’s exact test and gray correlation analysis. No significant association was found. Habitat connectivity was then integrated to develop a new combined indicator of habitat quality and connectivity index (HQCI). The associations between HQCI and the two diversity indices were improved significantly. The results indicated that connectivity may be an important factor explaining the diversity of certain species at a local scale. More empirical studies should be conducted to provide scientific evidence relating habitat quality to biodiversity.


2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Hellen K. Mandela ◽  
Mugatsia H. Tsingalia ◽  
Mary Gikungu ◽  
Wilbur M. Lwande

Pollination is an important ecosystem service in the maintenance of biodiversity and most importantly in food production. Pollination is on the decline due to habitat loss, exotic species invasions, pollution, overharvesting, and land use changes. This study analyzed the abundance and diversity of flower visitors’ of Ocimum kilimandscharicum in Kakamega forest with increasing distance from the forest edge. Data were collected through direct observation and sweep netting. Six study sites were identified along two transects each 2.5 km long and labeled A to F. Distance in metres from the forest edge to each site was A=221, B=72, C=83, D=198, E=113, and F=50. Sampling was done from 7:30 am to 4:00 pm, three days in a week for five months consecutively. Diversity indices of different flower visitors were calculated using the Shannon-Wiener diversity index. One-way analysis of variance was used to compare differences between sites and a two-sample t-test was used to identify mean significant differences in species diversity between the closest and the furthest sites. A total of 645 individuals belonging to 35 species were captured from 4 families. The highest diversity was at site F (H’= 2.38) which was closest to the forest edge and the lowest diversity was from site A (H’=1.44) which was furthest from the forest edge. Distance from the forest edge significantly influenced species diversity (F(3, 20)=14.67, p=0.024). Distance from the forest edge also significantly influenced species abundance between the furthest sites A, D, and E and the nearest sites F, B, and C to the forest edge (t=4.177; p=0.0312) and species richness (t=3.2893; p=0.0187). This study clearly demonstrates that Ocimum kilimandscharicum flower visitors play essential roles in pollination and their higher number of visits translates into higher numbers of seeds set. Many of these pollinators are associated with the forest and hence the need to conserve the Kakamega forest as a source pool for pollinators.


2002 ◽  
Vol 32 (1) ◽  
pp. 38-51 ◽  
Author(s):  
Steven G Newmaster ◽  
F Wayne Bell

In northern forests, cryptogams (spore producing plants) occupy a key position in forest ecosystem diversity and function. Forest harvesting and silvicultural practices have the potential to reduce cryptogam diversity. This project uses four blocks that were mechanically site prepared, planted with a single conifer species, and subsequently subjected to five conifer release treatments: (1) motor-manual cleaning, (2) mechanical brush cutting, (3) aerial application of triclopyr, (4) aerial application of glyphosate, and (5) control (untreated clearcut). Five 10 × 10 m subplots were installed in each of the five treatment plots and the uncut forest on the four blocks. Botanical surveys were conducted before and 1–5 years after treatments. Species richness and abundance, Shannon's and Heip's indices, and rank abundance diagrams clearly show that richness and abundance were affected by silvicultural treatments. Vegetation management treatments resulted in significant reductions in cryptogam diversity, to the point that only a few colonists and drought-tolerant species remained. Cryptogam diversity was ranked in the following order: forest > clearcut > mechanical clearing > herbicide treatment. Herbicide treatments had the greatest initial effect on species richness, species abundance, and diversity indices. Cryptogam diversity showed signs of recovery 5 years after treatments. Missed strips (untreated areas) within a clearcut provided a refuge for remnant communities of forest cryptogams that could play a key role in the rehabilitation forest diversity.


1997 ◽  
Vol 8 (1) ◽  
pp. 19-26 ◽  
Author(s):  
Ola Atlegrim ◽  
Kjell Sjöberg ◽  
John Ball

To compare the effects of two tree harvesting methods (clear-cutting and single tree selection felling), spring-occurring ground beetles (Carabidae) were studied by pitfall trapping in northern Sweden. Species abundance, total abundance and Hill's diversity indices were used to compare the ground beetle community in clear-cuts to selectively-logged and to uncut control forests. In addition, to highlight the importance of site replication when evaluating a spatially-variable ecosystem like the boreal forest, we consider how our conclusions might have differed with and without site replication. Results from the two analyses differed considerably, highlighting the importance of site replication in studies offorestry effects in order to increase confidence in the conclusions. Overall, no significant harvest effects were found on the ground beetle community except for a significantly higher abundance of the open habitat species P. assimilis in clear-cuts than in uncut control forests. Our results thus do not support suggestions of an increase in diversity following clear-cutting, but are consistent with previous findings regarding increased abundances of open habitat species and no changes in abundance of forest generalists in clear-cuts. In general, the carabid community in the selection loggings resembled that in the uncut control forest, indicating a low effect of this harvesting method. Based on our analysis, we suggest that future studies of forestry impacts on invertebrates attempt to increase the number of sites evaluated rather than increase the number of samples from a given area.


2009 ◽  
Vol 69 (4) ◽  
pp. 1015-1025 ◽  
Author(s):  
WS. Smith ◽  
M. Petrere Jr. ◽  
W. Barrella

A fish assemblage study was accomplished in different habitats of the Sorocaba River Basin. Fish were caught with gillnets, were weighed (weight total - g) and measured (standard length - mm). Several abiotic variables of selected sampling sites were measured in order to characterise their habitats in order to attempt establishing correlations with fish community traits. Fish numbers per species were adjusted to the lognormal and logseries species/abundance models The fish community totaled 38 species, distributed in 28 genera, 14 families and 4 orders. Diversity was calculated both in number and in weight and both presented higher values in better preserved sites. We did not detect any statistical differences between dry and rainy seasons. We also concluded that the abundance distribution was not influenced by abiotic variables.


Oikos ◽  
2006 ◽  
Vol 114 (1) ◽  
pp. 27-36 ◽  
Author(s):  
Frank Johansson ◽  
Göran Englund ◽  
Tomas Brodin ◽  
Hans Gardfjell

Author(s):  
A. V. Matsyura

<p>Here we presented some theoretical conclusions about the nonlinear links in island bird communities. It is proved, that the relations between the specific biodiversity, structure and entropy of biogeocenosis are nonlinear. The optimal level of diversity in island bird communities does not depend on the carrying capacity. The optimal level of species diversity and the corresponding value of the total population (biomass) increases with carrying capacity and available ecological niches. The population diversity is the basis for community adaptation towards the unstable environment. Species diversity allows the community as a whole to be more efficient and to use the resources of environment more efficient by differentiating of ecological niches. The species diversity indices do not strive to stable constant, they increase along with species abundance but these dependences are rather nonlinear.</p><p> </p>


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