Abstract:Are size and arrangement of valve mantle areolae in Aulacoseira Thwaites adapted to light intensity? To test one criterion demonstrating an adaptation, heritability experiments were run on isolates of Aulacoseira subarctica (Müller) Haworth. Several clones of A. subarctica were isolated from Yellowstone Lake (Wyoming, USA), Lewis Lake (Wyoming), and East Rosebud Lake (Montana, USA). Two to four clones from each lake were grown in batch cultures under three irradiance levels: 2, 11.4, and 115 lmol photons . m À… Show more
“…Experimental studies provide some support for this hypothesis. Provided sufficient genetic variation in phenotypic traits for selection to act on, a rapid evolutionary response can be predicted (Wood et al, 1987(Wood et al, , 2005Edgar and Theriot, 2003). Moreover, several authors have suggested that the seemingly cosmopolitan distribution and maintenance of relatively high abundances of many species of phytoplankton result from changes in genotype composition within species (cf.…”
Section: A D a P T I V E E V O L U T I O N I N R E S P O N S E T O E mentioning
Eukaryotic phytoplankton exhibit an enormous species richness, displaying a range of phylogenetic, morphological and physiological diversity. Yet, until recently, very little was known about the diversity, genetic variation and evolutionary processes within species and populations. An approach to explore this diversity and to understand evolution of phytoplankton is to use population genetics as a conceptual framework and methodology. Here, we discuss the patterns, processes and questions that population genetic studies have revealed in eukaryotic phytoplankton. First, we describe the main biological processes generating genetic variation. We specifically discuss the importance of life-cycle complexity for genetic and phenotypic diversity and consider how such diversity can be maintained during blooms when rapid asexual proliferation dominates. Next, we explore how genetic diversity is partitioned over time and space, with a focus on the processes shaping this structure, in particular selection and genetic exchange. Our aim is also to show how population genetics can be used to make inferences about realized dispersal and sexual recombination, as these processes are so difficult to study directly. Finally, we highlight important open questions and suggest promising avenues for future studies that will be made possible by new sequencing technologies.
“…Experimental studies provide some support for this hypothesis. Provided sufficient genetic variation in phenotypic traits for selection to act on, a rapid evolutionary response can be predicted (Wood et al, 1987(Wood et al, , 2005Edgar and Theriot, 2003). Moreover, several authors have suggested that the seemingly cosmopolitan distribution and maintenance of relatively high abundances of many species of phytoplankton result from changes in genotype composition within species (cf.…”
Section: A D a P T I V E E V O L U T I O N I N R E S P O N S E T O E mentioning
Eukaryotic phytoplankton exhibit an enormous species richness, displaying a range of phylogenetic, morphological and physiological diversity. Yet, until recently, very little was known about the diversity, genetic variation and evolutionary processes within species and populations. An approach to explore this diversity and to understand evolution of phytoplankton is to use population genetics as a conceptual framework and methodology. Here, we discuss the patterns, processes and questions that population genetic studies have revealed in eukaryotic phytoplankton. First, we describe the main biological processes generating genetic variation. We specifically discuss the importance of life-cycle complexity for genetic and phenotypic diversity and consider how such diversity can be maintained during blooms when rapid asexual proliferation dominates. Next, we explore how genetic diversity is partitioned over time and space, with a focus on the processes shaping this structure, in particular selection and genetic exchange. Our aim is also to show how population genetics can be used to make inferences about realized dispersal and sexual recombination, as these processes are so difficult to study directly. Finally, we highlight important open questions and suggest promising avenues for future studies that will be made possible by new sequencing technologies.
“…Since virtually every diatom species is inextricably linked to a morphological, character-based definition, candidates for mating experiments are chosen on the basis of their characters, which suggests some level of confidence in the character-based classification. Note also that classic heritability studies still provide an excellent way to explore the potential evolutionary importance of morphological characters in diatoms (Edgar and Theriot 2003;Wood et al 1987). A positive trend in BSC-based diatom research is the increasing number of studies that cite direct evidence from mating experiments (Amato et al 2007;Behnke et al 2004;Mann et al 2004;Vanormelingen et al 2007Vanormelingen et al , 2008, rather than indirect character-based evidence, to support species boundaries under the BSC.…”
“…The genus may extend back to the Late Cretaceous (Ambwani et al, 2003). Edgar and Theriot (2004) conducted a phylogenetic analysis of Aulacoseira using morphological and molecular data and studied the heritability of valve mantle features (Edgar and Theriot, 2003).…”
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