TY - JOUR A1 - Dulanya, Zuze A1 - Croudace, Ian A1 - Reed, Jane M. A1 - Trauth, Martin H. T1 - Palaeolimnological reconstruction of recent environmental change in Lake Malombe (S. Malawi) using multiple proxies JF - Water SA N2 - Shallow inland water bodies in Malawi continue to be threatened by various environmental challenges despite their importance to the fisheries industry. Due to the complex interaction between natural and anthropogenic disturbances, disentangling the effect of the two may be a complicated process. The littoral zone of most water bodies is important in environmental reconstructions including pollution and lake level monitoring. This study used a littoral zone, transect-based approach employing multi-proxy palaeolimnological techniques to reconstruct recent environmental change (ca. 100 yrs.) in Lake Malombe in the Malawi Rift, East Africa. The results of the study could inform fisheries management in Lake Malombe, which experienced a catastrophic decline in fish stocks. Results support documentary evidence for the complete desiccation of the lake less than 100 years ago. Subsequently, there is evidence for accelerated eutrophication in the recent past. In light of these results, it is concluded that transect sampling approaches rather than relying on single core measurements, and the need for careful consideration of the types of proxy, are significant considerations in palaeoenvironmental reconstructions. KW - littoral zone KW - palaeolimnology KW - diatoms KW - Lake Malombe Y1 - 2014 U6 - https://doi.org/10.4314/wsa.v40i4.17 SN - 0378-4738 SN - 1816-7950 VL - 40 IS - 4 SP - 717 EP - 727 PB - Water Research Commission CY - Pretoria ER - TY - JOUR A1 - Epp, Laura Saskia A1 - Stoof-Leichsenring, Kathleen Rosemarie A1 - Trauth, Martin H. A1 - Tiedemann, Ralph T1 - Molecular profiling of diatom assemblages in tropical lake sediments using taxon-specific PCR and Denaturing High-Performance Liquid Chromatography (PCR-DHPLC) JF - Molecular ecology resources N2 - Here we present a protocol to genetically detect diatoms in sediments of the Kenyan tropical Lake Naivasha, based on taxon-specific PCR amplification of short fragments (approximately 100 bp) of the small subunit ribosomal (SSU) gene and subsequent separation of species-specific PCR products by PCR-based denaturing high-performance liquid chromatography (DHPLC). An evaluation of amplicons differing in primer specificity to diatoms and length of the fragments amplified demonstrated that the number of different diatom sequence types detected after cloning of the PCR products critically depended on the specificity of the primers to diatoms and the length of the amplified fragments whereby shorter fragments yielded more species of diatoms. The DHPLC was able to discriminate between very short amplicons based on the sequence difference, even if the fragments were of identical length and if the amplicons differed only in a small number of nucleotides. Generally, the method identified the dominant sequence types from mixed amplifications. A comparison with microscopic analysis of the sediment samples revealed that the sequence types identified in the molecular assessment corresponded well with the most dominant species. In summary, the PCR-based DHPLC protocol offers a fast, reliable and cost-efficient possibility to study DNA from sediments and other environmental samples with unknown organismic content, even for very short DNA fragments. KW - diatoms KW - environmental DNA KW - lake sediments KW - PCR-DHPLC Y1 - 2011 U6 - https://doi.org/10.1111/j.1755-0998.2011.03022.x SN - 1755-098X VL - 11 IS - 5 SP - 842 EP - 853 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Stoof-Leichsenring, Kathleen Rosemarie A1 - Epp, Laura Saskia A1 - Trauth, Martin H. A1 - Tiedemann, Ralph T1 - Hidden diversity in diatoms of Kenyan Lake Naivasha a genetic approach detects temporal variation JF - Molecular ecology N2 - This study provides insights into the morphological and genetic diversity in diatoms occurring in core sediments from tropical lakes in Kenya. We developed a genetic survey technique specific for diatoms utilizing a short region (7667 bp) of the ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit (rbcL) gene as genetic barcode. Our analyses (i) validated the use of rbcL as a barcoding marker for diatoms, applied to sediment samples, (ii) showed a significant correlation between the results obtained by morphological and molecular data and (iii) indicated temporal variation in diatom assemblages on the inter- and intra-specific level. Diatom assemblages from a short core from Lake Naivasha show a drastic shift over the last 200 years, as littoral species (e.g. Navicula) are replaced by more planktonic ones (e.g. Aulacoseira). Within that same period, we detected periodic changes in the respective frequencies of distinct haplotype groups of Navicula, which coincide with wet and dry periods of Lake Naivasha between 1820 and 1938 AD. Our genetic analyses on historical lake sediments revealed inter- and intra-specific variation in diatoms, which is partially hidden behind single morphotypes. The occurrence of particular genetic lineages is probably correlated with environmental factors. KW - diatoms KW - DNA barcoding KW - historical DNA KW - intra-specific variation KW - rbcL KW - tropical lake sediments Y1 - 2012 U6 - https://doi.org/10.1111/j.1365-294X.2011.05412.x SN - 0962-1083 VL - 21 IS - 8 SP - 1918 EP - 1930 PB - Wiley-Blackwell CY - Malden ER -