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Browsing by Subject "functional diversity"

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  • Yrjölä, Veikko (2023)
    While the effects of agricultural land use on biodiversity are beginning to unravel in Europe and North America, Africa remains poorly studied. Biodiversity in a broad sense provides ecosystem functioning and services, whose importance has become obvious to humankind in the quickly changing modern world. In Ghana, the practice of mango farming continues to grow in popularity due to suitable climate and potential source of livelihood. With increased demand and production of mango, natural habitats, namely savannahs, are being converted to plantations. The effects of such habitat conversion on local biodiversity are unknown for most taxa, thus providing an interesting study system for biodiversity research. Given the direct relation between functional diversity and ecosystem services, in this work I compare the taxonomic and functional diversity of ground-living spiders between mango orchards and savannah. I chose spiders (Arthropoda; Araneae) as model organisms as they critically contribute to several ecosystem services, such as biological pest control and nitrogen cycling, while being ubiquitous and abundant, thus easy to collect in the field. Spiders were captured with pitfall traps from six mango and four savannah areas in the Northern region of Ghana. A total of 424 individuals and 53 (morpho)species were identified and counted. Additionally, six morphological and four ecological traits were quantified for each (morpho)species. With these data, I calculated taxonomic richness and evenness, functional richness, dispersion, and evenness, and beta diversity of the different assemblages in the R environment. These metrics were then compared between spiders collected from mango orchards and savannah. Mango orchards showed lower taxonomic and functional evenness than savannah, contrary to all other alpha diversity measures. The two habitat types share many of the same diversity of ground-living spiders, but species and traits are distributed less evenly in mango orchards due to incomplete niche differentiation between species. Both taxonomic and functional beta diversity were significantly different between habitat types indicating that mango orchards sustain a similar richness of species as savannah, but the species composition is different. In conclusion, mango orchards have the potential to conserve some aspects of the original diversity, but species composition and the way species interact are substantially different. We should strive to find the best practices to produce mango without radically changing the natural biodiversity patterns.
  • Rikberg, Jon (2018)
    The Red List Index (RLI) has widely been recognized as a useful tool in keeping track of extinction risk trends of large taxa. The RLI is an index based on IUCN’s threat categories. Functional diversity (FD) is a way of measuring biodiversity that describes species´ traits that are linked to species´ ecological roles. In this work I have mapped the spatial distribution of the RLI and functional diversity for Finnish vascular plants. I first produced species distribution models (SDMs) for all 1194 species of vascular plants in the Finnish Red List 2010 based on records from the Kastikka and Hertta databases and environmental data. A functional tree incorporating 971 of those species was calculated using seven functional traits. The traits that I used were life form, maximum plant height, seed mass, seedbank longevity, life span, specific leaf area (SLA), and leaf dry matter content (LDMC). The trait data was gained from the databases Leda and TRY. Based on the SDMs, the functional tree, and the Finnish Red List, taxonomic and functional diversity and RLI were mapped for the whole of Finland using 10 x 10 km cells. This was the first time FD and RLI were mapped for vascular plant species across Finland. Null models were used to compare observed values with the ones expected if species (and consequently traits) distributions were random accross the country. Taxonomic diversity (TD) was higher than expected in southern Finland and lowest in northern Finland, suggesting a strong latitudinal gradient. TD correlated with the same environmental variables as FD. Thus, it is likely that both TD and FD are dirven by the same environmental variables. FD was higher than expected in southern and western Finland and lower in the northern and eastern parts of the country. A strong environmental filtering in the north might cause low FD by limiting species´ distributions within many clades and favouring species with similar traits that allow them to survive in extreme conditions. In southern Finland, competitive exclusion might limit the co-existence of species with similar traits, thus increasing trait divergence. The RLI values were lowest in the Åland islands, along the southern coast, in a few sites in eastern Finland (e.g. Koli and Kuusamo areas), around Kemi and the Gulf of Bothnia and in Kilpisjärvi. Thus, these sites have high concentrations of threatened species. The low RLI sites correspond well with areas with either limestone or dolomite deposits, which explains why many of these areas are floristically unique and present high concentrations of threatened species. In addition, many of the sites with low RLI are geographical extreme areas in Finland, corresponding to the distribution limits of many species. The RLI was high in Ostrobothnia and in large parts of Lapland. In Ostrobothnia, centuries of forest management and a homogenous bedrock and topography have resulted in a vascular plant community based mostly on common species. It is possible, that regional extinctions have happened in Ostrobothnia already before red listing measures began, thus explaining the high RLI values today. On sites with more variety among habitats and bedrock, the RLI values were significantly lower than in the rest of Lapland, suggesting that the high RLI values for parts of Lapland are due to homogeneous plant communities in the northern boreal forests that host only few threatened species. The spatial distribution of the RLI and functional diversity for vascular plants in Finland were mapped for the first time. A strong latitudinal gradient was found for TD and FD. Low RLI values were found on calcareous soils and on geographic extremes in Finland. To track possible changes in the RLI it would be crucial to remap the RLI in 2019 when the next Finnish Red List is published. A comparision between this work and the remapping based on the 2019 assessment would track changes in the extinction risk across Finland. The current limitation with RLI is that it only considers taxonomic diversity. However, in future work it is possible to incorporate the functional tree used in this thesis into RLI to calculate a functionally weighted RLI.