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A taxonomic revision of the genus Pteris in tropical Africa revealed 26 species. An identification key to the species is provided. Morphological characters were used to prepare a cladistic analysis of the relevant taxa. Each species was evaluated concerning the IUCN red list status. Only Pteris mkomaziensis was considered as Near Threatened, and all other species only as Least Concern. An inventory of the ferns of Kakamega Forest / Kenya and Budongo Forest / Uganda revealed 85 species in Kakamega and 66 species in Budongo. Life form spectra were analysed and the ferns were studied for their value for bioindication.
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.
The first group that was revised within my study is Ochralea Clark, 1865 (Hazmi & Wagner 2010a). I have checked the type specimen of most species that were originally described in Ochralea and there is no doubt that this genus is clearly distinct from Monolepta. Weise (1924) has synonymised Galeruca nigripes (Olivier, 1808) with O. nigricornis Clark, 1865 and the valid name of the species is O. nigripes (Olivier, 1808). Out of ten species originally described in this genus, only this species remain valid and O. pectoralis is a new synonym of O. nigripes. Additionally, Monolepta wangkliana Mohamedsaid, 2000 is very closely related to O. nigripes and need to be transferred to Ochralea. The second genus where the revision is still published is Arcastes Baly, 1865 (Hazmi & Wagner 2010b). I have checked the genitalic characters of A. biplagiata, and most of the type species of other Arcastes. Arcastes biplagiata possesses a peculiar shape of the median lobe and asymmetrically arranged endophallic structures. These peculiar characters are very useful to delimit this genus from the others. Therefore, only three valid species remain in Arcastes, while two new synonyms are found and fourrnother species need to be transferred to other genera. While checking the genitalic characteristics of type species of Arcastes sanguinea, thernmedian lobe as well as the spermatheca of this species possesses strong differences to A. biplagiata. The species was redescribed and transferred in a monotypic new genus Rubrarcastes Hazmi & Wagner, 2010c. The fourth genus that was already revised is Neolepta Jacoby, 1884. It was originally described on base of only two species by that time, N. biplagiata and N. fulvipennis. Jacoby has not designated a type species of the genus, and Maulik (1936) did it later, with the designation of N. biplagiata. Jacoby in his original description has only commented that Neolepta is very close and similar to Monolepta Chevrolat, 1837 and Candezea Chapuis, 1879. Subsequent authors have described further eight species, and transferred one species from Luperodes to it, summing up the total number of eleven described species in Neolepta. I have checked the genitalic characters of the type, N. biplagiata and have found out that the median lobe is not incised apically and stronger sclerotised ventral carinae with an apical hook close to the apex occur. Out of all described species, only two are closely related to the genero-type, N. sumatrensis (Jacoby, 1884) new combination and N. quadriplagiata Jacoby, 1886 that will remain in this group after the revision. All other species need to be transferred to other genera, including the newly described Paraneolepta and Orthoneolepta. The last distinct paper of this thesis presented the results on Monolepta Chevrolat, 1837. The massive number of Monolepta from the entire Oriental Region, with about 260 described species names is a more long-life project and not practicable within a PhD-study. Thus I have focused on the species of Monolepta known from the Sundaland area in this work. A comprehensive revision including the study of the primary types of the described species, has never been done for Monolepta from this sub-region, while new species have also been described in the last decade (e. g. Mohamedsaid 1993, 1997, 1998, 1999, 2000a,b, 2001, 2002, 2005).
On base of the most current species lists of Mohamedsaid (2001, 2004, 2005) and Kimoto (1990), the number of valid species described from this region is about 72. After my revision, only thirteen valid species can remain in Monolepta in the sense of the generotype M. bioculata (Wagner 2007), while seven species have been found as new synonyms, three have been already transferred to other genera and further 49 species need to be transferred to other genera.