Phenotypic plasticity in the holoparasitic mistletoe Tristerix aphyllus (Loranthaceae): consequences of trait variation for successful establishment
Author
dc.contributor.author
Gonzáles, Wilfredo L.
Author
dc.contributor.author
Suárez, Lorena H.
Author
dc.contributor.author
Guiñez, Ricardo
Author
dc.contributor.author
Medel Contreras, Rodrigo
Admission date
dc.date.accessioned
2018-12-20T14:11:41Z
Available date
dc.date.available
2018-12-20T14:11:41Z
Publication date
dc.date.issued
2007
Cita de ítem
dc.identifier.citation
Evol Ecol (2007) 21:431–444
Identifier
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02697653
Identifier
dc.identifier.other
10.1007/s10682-006-9111-2
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/154590
Abstract
dc.description.abstract
The ability of a genotype to respond to changes in the environment through modifications in the phenotype is adaptive when the plastic genotypes attain a higher fitness than non-plastic genotypes. In this study we examine whether parasite traits involved in host infection exhibit adaptive phenotypic plasticity to the heterogeneous host microenvironment. We focused on a host-parasite relationship characterized by the holoparasitic mistletoe Tristerix aphyllus and the cactus host Echinopsis chilensis. Unlike most mistletoes, whose seeds are deposited on the host branches, seeds of T. aphyllus are often deposited on the spines of the cactus. The extremely long radicles of T. aphyllus have been suggested to represent a parasite adaptation to overcome the barriers to infection imposed by the spines of cacti. However, plastic rather than canalized phenotypes may represent a better strategy in changing environments. We evaluated whether T. aphyllus exhibits adaptive plasticity in radicle length through a sire half-sib genetic design under field conditions in two contrasting microenvironments (seeds deposited on spines 4 and 28 mm from the host surface). We used phenotypic and genotypic selection analyses to evaluate the relationship between radicle
length and seed establishment. Our results revealed significant phenotypic plasticity for radicle length and family level variation among maternal but not paternal families