Hidden diversity in diatoms of Kenyan Lake Naivasha: a genetic approach detects temporal variation

Mol Ecol. 2012 Apr;21(8):1918-30. doi: 10.1111/j.1365-294X.2011.05412.x. Epub 2012 Jan 4.

Abstract

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 (76-67 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.

Publication types

  • Historical Article
  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Barcoding, Taxonomic / methods*
  • DNA Primers
  • Diatoms / classification
  • Diatoms / genetics*
  • Diatoms / isolation & purification
  • Diatoms / physiology
  • Genetic Variation*
  • Geologic Sediments / microbiology*
  • Haplotypes
  • History, 19th Century
  • History, 20th Century
  • History, 21st Century
  • Kenya
  • Lakes / microbiology*
  • Lead Radioisotopes / analysis
  • Phylogeny
  • Polymerase Chain Reaction / methods
  • Ribulose-Bisphosphate Carboxylase / genetics*
  • Sequence Analysis, DNA
  • Species Specificity

Substances

  • DNA Primers
  • Lead Radioisotopes
  • Ribulose-Bisphosphate Carboxylase