papers Flashcards

1
Q

Hurtado et al
What is it about?

A
  • study about the introduction of the Japanese carpet shell into European marine ecosystems
  • and study about the resulting hybridization
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2
Q

Hurtado et al
What did they do?

A
  • used length differences in major ribosomal RNA gene and minor ribosomal RNA gene for genetic identification
  • they did FISH-experiment (=fluorescent in situ hybridization)
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3
Q

Hurtado et al
results?

A

length differences on RNA genes:
- showed evidence that morphological identification was not right in some cases
- genetic identification could identify hybrids that before were morphologically identified as European carpet shell
- FISH-experiment confirmed hybrid nature

–> cytological and genetic evidence for hybrids

  • suggest further experiments with species-specific molecular markers to
    (1) detect degree of interspecific hybridization
    (2) detect existence of introgression
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4
Q

Farrell et al
What did he do?

A
  • study about recent demographic events and gene flow
  • about boarfish-pop.
  • why have the boarfish pop. increased?
    –> migration?
    –> local expansion?
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5
Q

Farrell et al.
how did he do it?

A
  • he used microsatellites in combination with NGS and GBS (genotyping by sequencing)
  • they sampled from
  • good study that highlights the combination of different molecular markers
  • highlights the use of microsats due to their high allelic richness, mutation rate and statistical power
  • detected 40 loci that they used
  • they calculated Fit and expected He
  • they did cluster-analysis from STRUCTURE analysis and AMOVA
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6
Q

Farrell et al.
what are the results?

A
  • there were 7 distinct populations
  • there was a lack of migration –> lack of gene flow
  • pop. increase was NO result of recent influx
  • increase was probably a demographic process (local expansion)
  • he emphasizes microsats as generic, cost-effective and rapid method for large-scale studies
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7
Q

Cordero et al
what did they do?

A
  • study with microsats and mtDNA
  • to assess genetic structure of Manila clam pop.
    –> unraveled their population structure (North America, Japan, Europe)
    –> unraveled history of clam introduction
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8
Q

Cordero et al.
what did they find out?

A

with microsats:
- small overall differentiation
- suggests recent introduction of Manila clam in North America and Europe
- evidence that Japanese Manila clam is ancestor of North American’s and Europe’s

mtDNA
- suggests a strong founder event in European pops
–> because higher differentiation between North American and European clams
than
differentiation between North American and Japanese clams
- reduction in genetic variability in Europe attributed to that founder effect

  • study suggests: maybe concealed introduction (especially concerning European pops.) due to recent hatchery practices
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9
Q

what does the Manila clam study show in terms of use of genetic markers?

A

it’s a good study that shows the combination of two diff. markers to understand genetic patterns
(1) in unraveling pop. structure
(2) in unraveling history of clam introduction

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