570 Biowissenschaften; Biologie
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- Auchenorrhyncha (1)
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- Institut für Integrierte Naturwissenschaften, Abt. Biologie (4) (entfernen)
Nandi forests (South and North Nandi forests) are situated in the Rift Valley Province of Kenya very close to Kakamega forest. From previous documents it has been seen that Kakamega and Nandi forests were connected to each other forming one big "U" shaped forest block till the beginnings of 1900s. Due to human pressures, currently there are three different forests form the previous one block forest. Although they were one forest, information on Nandi forests is very scanty when it is compared to that of Kakamega forest. The species composition and diversity as well as plant communities and population structure of Nandi forests have not been studied. Information is not available about the similarity status of South and North Nandi forests. Furthermore the natural regeneration potential (seedling bank) of these forests is not well studied and documented. Hence this study aims to fill these gaps.
In this study totally 76 quadrates (49 from South Nandi and 27 from North Nandi) were used to collect data. In the South Nandi forests 27 of the quadrates were laid in the better side of the forest (at Kobujoi) and the remaining 22 were in the heavily disturbed part of this forest (Bonjoge). The quadrates were arranged on transects that have one to one and half km which were parallel to the slope. The distance between the quadrates was 100 meter and transects are 500 m apart. The size of the main quadrate was 400 m2 (20 X 20 m) which also had five small plots (3 X 3 m) distributed on the four corners and in the center. Each woody plants (climbers, shrubs and trees) having more than one meter and greater than two centimeter diameter at breast height (dbh) were measured and recorded. Seedlings and herbaceous plants were sampled in the smaller plots. Individual plants were identified at species level and when it was not possible to identify in the field voucher specimen were prepared and latter identified at the East African Herbarium, National Museum of Kenya, and Nairobi. Clustering and ordination were performed using PC-ORD and CANOCO ecological softwares, respectively. For both clustering and ordination abundance data of the species was used. Shannon diversity index and evenness were computed using PC-ORD while similarity indices, Fisher alpha, rarefaction, species richness estimation (nonparametric species richness estimators) were conducted using EstimateS. Indicator species analysis was undertaken using PC-ORD. Basal area and height class distribution at forests level or site level (Bonjoge and Kobujoi) and diameter (dbh) class distribution for selected trees species were performed to evaluate population structure.
Furthermore importance value (IV) of woody plant species was calculated. SPSS version 16 was used to undertake both parametric (when data assume normal distribution) and nonparametric (when data are not assuming normal distribution) comparison of means, correlation and regression analysis.
In this study totally 321 vascular plant species comprising 92 families and 243 genera were identified in Nandi forests (both South and North Nandi forests). In South Nandi forest 253 plant species form 82 families and 201 genera were recorded while in North Nandi 181 species comprising 67 families and 155 genera were recorded. Jackknife second order estimators gave the highest species richness estimate for both South and North Nandi forests i.e. 284 and 209, respectively. In the case of highly disturbed and less disturbed parts of South Nandi forest 138 and 172 vascular plant species were recorded, respectively. Asteraceae, Rubiaceae and Euphorbiaceae are the top three species rich families of Nandi forests. In terms of different diversity measures (i.e. alpha and beta diversity, Fisher alpha, Shannon diversity and evenness indices) South Nandi is more diverse than North Nandi forest. Sörensen and Jaccard (classic) as well as their respective abundance based similarities showed that there is a low species similarity between South and Nandi forests. The cluster analysis resulted in three different plant communities and this result is supported by the ordination result.
South and North Nandi forest has inverted "J" height class distribution showing that larger proportion of woody plant individuals are found in the lower height classes. Similar pattern is observed when the diameters of all woody plants were considered together. However, different diameter class distributions (seven types) were identified when selected tree species were analyzed separately. It has been observed that the basal area of South Nandi forest is significantly lower than that of North Nandi forest (Mann-Whitney U =358, p < 0.001). Similarly Bonjoge has significantly lower basal area (t-value=3.77, p<0.01) than that of Kobujoi. Number of woody plat seedlings in South Nandi forest is significantly higher than that of North Nandi (Mann-Whitney U = 362.5, p<0.001). In the same way Bonjoge has significantly smaller number of ssedlings than Kobujoi (t-value 4.24, p<0.001). Most of species in both forests are able to resprout from stumps after physical damage; hence this helps the regeneration of the forests in addition to seedling banks. This study enables to fill some of the information gaps about Nandi forests especially of floristic composition, population structure, natural regeneration and human impacts on this ecosystem.
Foliicolous lichens are one of the most abundant epiphytes in tropical rainforests and one of the few groups of organisms that characterize these forests. Tropical rainforests are increasingly affected by anthropogenic disturbance resulting in forest destruction and degradation. However, not much is known on the effects of anthropogenic disturbance on the diversity of foliicolous lichens. Understanding such effects is crucial for the development of appropriate measures for the conservation of such organisms. In this study, foliicolous lichens diversity was investigated in three tropical rainforests in East Africa. Godere Forest in Southwest Ethiopia is a transitional rainforest with a mixture of Afromontane and Guineo-Congolian species. The forest is secondary and has been affected by shifting cultivation, semi-forest coffee management and commercial coffee plantation. Budongo Forest in West Uganda is a Guineo-Congolian rainforest consisting of primary and secondary forests. Kakamega Forest in western Kenya is a transitional rainforest with a mixture of Guineo-Congolian and Afromontane species. The forest is a mosaic of near-primary forest, secondary forests of different seral stages, grasslands, plantations, and natural glades.
Due to their confinement to specific host plants or restricted habitat types, Auchenorrhyncha are suitable biological indicators to measure the quality of chalk grassland under different management practices for nature conservation. They can especially be used as a tool to assess the success of restoring chalk grassland on ex-arable land. One objective of this study was to identify the factors which most effectively conserve and enhance biological diversity of existing chalk grasslands or allow the creation of new areas of such species-rich grassland on ex-arable land. A second objective was to link Auchenorrhyncha communities to the different grassland communities occurring on chalk according to the NVC (National Vegetation Classification). Altogether 100 chalk grassland and arable reversion sites were sampled between 1998 and 2002. Some of the arable reversion sites had been under certain grazing or mowing regimes for up to ten years by 2002. Vegetation structure and composition were recorded, and Auchenorrhyncha were sampled three times during the summer of each year using a "vortis" suction sampler. Altogether 110 leafhopper species were recorded during the study. Two of the species, Kelisia occirrega and Psammotettix helvolus, although widespread within the area studied, had not previously been recognized as part of the British fauna. By displaying insect frequency and dominance as it is commonly done for vegetation communities, it was possible to classify preferential and differential species of distinct Auchenorrhyncha communities. The linking of the entomological data with vegetation communities defined by the NVC showed that different vegetation communities were reflected by distinct Auchenorrhyncha communities. Significant differences were observed down to the level of sub-communities. The data revealed a strong positive relationship between the diversity of leafhoppers species and the vegetation height. There was also a positive correlation between the species richness of Auchenorrhyncha and the diversity of plant species. In that context it is remarkable that there was no correlation between vegetation height and botanical diversity. There is a substantial decrease in Auchenorrhyncha species richness from unimproved grassland to improved grassland and arable reversion. The decline of typical chalk grassland and general dry grassland species is especially notable. Consequently, the number of stenotopic Auchenorrhyncha species which are confined to only a few habitat types, are drastically reduced with the improvement of chalk grassland. Improved grassland and arable reversion fields are almost exclusively inhabited by common habitat generalists. The decrease in typical chalk grassland plants due to improvement is mirrored in the decline of Auchenorrhyncha species, which rely monophagously or oligophagously on specific host plants. But even where suitable host plants re-colonize arable reversion sites quickly, there is a considerable delay before leafhoppers follow. That becomes especially obvious with polyphagous leafhoppers like Turrutus socialis or Mocydia crocea, which occur on improved grassland or arable reversion sites only in low frequency and abundance, despite wide appearance or even increased dominance of their host plants. These species can be considered as the most suitable indicators to measure success or failure of long term grassland restoration. A time period of ten years is not sufficient to restore species-rich invertebrate communities on grassland, even if the flora indicates an early success.
In the present study the flora and vegetation of Kakamega Forest, an East African rainforest in Western Kenya, was investigated. Kakamega Forest is highly degraded and fragmented and is an ideal model to study the anthropogenic influence on the forest inventory. The main focus was to analyse the influence of human impact on the vascular plant species composition. During five field phases in the years 2001 to 2004 a total of 19 study sites scattered over the whole forest including all fragments were investigated regarding forest structure, species composition and plant communities. The different forest sites were analysed by three different methods, phytosociological relevés, line-transect and with the variable-area transect method. The forest survey revealed about 400 taxa of vascular plant species, among them 112 trees, 62 shrubs, 58 climbers and 114 herbs. Several species are restricted to this forest in Kenya, but only one endemic species, the herb Commelina albiflora, could be discovered. About 15 species were recorded as new for Kenya and probably at least one species is new to science. Kakamega Forest is a unique mixture of Guineo-Congolian and Afromontane floral elements. About one half of the vascular plant species has its origin in the lowland forests of the Congo basin and one third originates from Afromontane habitats. The present study represents the first description of plant communities of Kakamega Forest. An analysis of different forest sites and plantations resulted in 17 different vegetation units. For the mature forest sites eleven plant communities were described. The young succession stage consists of two plant communities. Since the disturbance history and the age of the different plant communities could be estimated, their chronology was also described. An exception are the study sites within the plantations and afforested sites. The four defined vegetation units were not described as plant communities, because they are highly affected by man and do not belong to the natural succession of Kakamega Forest. Nevertheless, the regeneration potential of such forests was investigated. Due to the different succession stages the changing species composition along a disturbance gradient could be analysed. Most of Kakamega Forest consists of middle-aged secondary forest often surrounded by very young secondary forest. A true primary rainforest could not be found due the massive influence by over-exploitation. In all parts of the forest the anthropogenic influence could be observed. The forest develops towards a climax stage, but a 2 Abstract comparison with former surveys shows that the regeneration is much slower than expected. Human impact has to be avoided to allow the forest to develop into a primary-like rainforest. But several climax tree species might be missing anyway, because after the broad logging activities in the past there are not enough seed trees remaining. Species richness was highest in disturbed forest sites. A mixture of pioneer, climax and bushland species could be recorded there. Therefore, a high species richness is not a suitable indicator for forest quality. The proportion of climax species typical for Kakamega Forest would be a better measure. Compared to the main forest block the forest fragments do not lack in diversity as expected due to fragmentation processes. Instead, the only near primary forest could be recorded in Kisere, a northern fragment. The high amount of climax species and the more or less undisturbed forest structure is a result of the strict protection by the Kenya Wildlife Service and due to low logging activities. Differences in species composition between the studied forest sites are either a result of the different logging history or management regime rather than due to different edaphic or climatic conditions.