MESTRE · MESTRE . Title: locandina mestre Created Date: 10/21/2019 5:09:32 PM
Ivan Gomez-mestre and Miguel Tejedo 2005
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Transcript of Ivan Gomez-mestre and Miguel Tejedo 2005
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Adaptation or Exaptation?An experimental test of hypotheses on
the origin of salinity tolerance in Bufo calamita
Ivan Gomez-mestre and Miguel Tejedo
2005
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• Introduction
• Materials and methods
• Results
• Discussion
• Conclution
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• Introduction• Materials and methods
• Results
• Discussion
• Conclution
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Adaptation
Differences in phenotype among populations if have a genetic basis.
Confer fitness advantage in environment.
(Endler 1986; Sinervo and Basolo 1996).
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Exaptation
As a trait evolved for other usages, and later co-opted for its current function.
feather
Gould & Vrba(1982)
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Trait
Some traits may share a developmental history in spite of metamorphosis
Postmetamorphic traits may be affected by the environment experienced during premetamorphic stages
(Goater, 1994; Tejedo et al., 2000;Relyea, 2001; Relyea & Hoverman, 2003)
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• A trait under certain environmental in one life stage could be affected by selection acting on an associated trait from another life stage experiencing a different environment.
(Deban & Marks, 2002)
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Local adaptation of salinity tolerance
• linked to fitness
• genetic basis underlying the trait
(Gomez-Mestre & Tejedo 2003)
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Adaptation or Exaptation?
Salinity tolerance may have – direct action of selection– a correlated response to selection acting on s
ome other trait
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• Spain populations (even freshwater populations)have shown higher embryonic salinity tolerance than any of the UK populations
• steep South-to-North decreasing gradient in genetic diversity
(Beebee,1985)
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North-to-South in western Europe
• decreasing rainfall
• increasing evapotranspiration
• increasing summer drought
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• freshwater is the standard larval environment
• drought is a more common selective pressure than salinity
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Exaptation
salinity tolerance during embryonic and larval phases
drought tolerance during the terrestrial phases
• The salinity tolerance traits could have evolved as an exaptation.
(Arnold, 1994)
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Hypothesis
• relies on association between – salinity tolerance in the aquatic stages,– drought tolerance of the terrestrial juvenile an
d adult stages.
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• Introduction
• Materials and methods• Results
• Discussion
• Conclution
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Bufo calamita
http://www.herpetofauna.at/amphibien/bufo_calamita.php
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Three populations
• freshwater environments– Donana– Pedroso
• brackish environments– Jarales
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• Exposed juveniles to either humid or dry conditions for 5 weeks– survival– growth – behaviour: burying and prey capture
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Two hydric potentials
• Humid (12 replicates per population)
-150 kPa
• Dry (15 replicates per population)
-1150 kPa.
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vermiculite
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Burying and prey capture
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• Introduction
• Materials and methods
• Results• Discussion
• Conclution
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Survival
• Weight at metamorphosis significantly affected survival
• Neither population of origin nor humidity significantly affected survival
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Growth
• Growth was not the same across treatments.
• The dry environment significantly reduced growth rate.
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• However, neither population of origin nor its interaction with humidity affected growth rate.
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Burying
• Humidity had a very significant effect on proportion of time spent buried.
• Toadlets under dry conditions spent more time buried.
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Morphological changes
• Body length relative to body mass did not vary significantly between humidity treatments
• Population of origin did not affect relative changes in morphology.
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Prey capture success
Toadlets from the humid treatment – more attempts at prey capture– higher efficiency
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• Introduction
• Materials and methods
• Results
• Discussion• Conclution
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Decreased growth rates
• physiological adjustments,
• shifts in behaviour
• osmotic stress interfere with the control of tongue
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Decreased growth rates
• smaller size
• reduced ability to capture prey
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Lack of association between drought and salinity tolerance
• the reaction of the three populations across environments were remarkably paralle
• high similarity in drought tolerance among populations
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Explain why
• First– the level of drought used in the experiment m
ay not have been stressful enough
– may be expressed only at the hardest conditions
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• Secondly– populations are not isolated
– substantial variation in salinity tolerance within freshwater populations
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(Gomez-Mestre & Tejedo, 2003)
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• Third– different pathways for osmoregulatory physiol
ogy may simply
– however,dismiss the coupling hypothesis
• the information available on tadpole osmoregulation is scarce
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• aquatic and terrestrial stages may have different physiological responses to osmotic stress
• each evolving independently of the other.
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• Introduction
• Materials and methods
• Results
• Discussion
• Conclution
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Conclution
• Salinity tolerance in the aquatic phase of
B. calamita is more likely to have evolved in these populations as an adaptation, rather than an exaptation from drought tolerance.
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• Thanks for your attention
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• Environmental heterogeneity tends to increase the phenotypic plasticity of traits (when populations exchange migrants)
• However, when migration is restricted, selection under extreme conditions tends to favor local adaptation over plasticity
(Pigliucci 2001)
(Rawson and Hilbish 1991; Sultan and Spencer 2002)
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common garden experiments