@ARTICLE{TreeBASE2Ref18976,
author = {Jiri Hulcr and Anthony Cognato},
title = {Repeated evolution of theft in fungus farming ambrosia beetles.},
year = {2010},
keywords = {},
doi = {},
url = {http://},
pmid = {},
journal = {Evolution},
volume = {},
number = {},
pages = {},
abstract = {We report repeated evolution of fungal crop stealing, termed mycocleptism, among ambrosia beetles. Ambrosia beetles, dominant wood degraders in the tropics, create tunnels in dead trees and employ gardens of symbiotic fungi to extract nutrients from wood. The mycocleptic species seek brood galleries of other species, and exploit their established fungal gardens by tunneling through the ambient mycelium-laden wood. Instead of carrying their own fungal sybmbionts, mycocleptae depend on adopting the fungal assemblages of their host species, as shown by an analysis of fungal DNA from beetle galleries. The evidence for widespread horizontal exchange of fungi between beetles challenges the traditional concept of ambrosia fungi as species-specific symbionts. Fungus stealing appears to be an evolutionarily successful strategy. It evolved independently in several beetle clades, two of which have radiated, and at least one case was accompanied by a loss of the beetles' fungus-transpor! ting organs. We demonstrate this using the first robust phylogeny of one of the world's largest group of ambrosia beetles, Xyleborini.}
}
Citation for Study 10528
Citation title:
"Repeated evolution of theft in fungus farming ambrosia beetles.".
Study name:
"Repeated evolution of theft in fungus farming ambrosia beetles.".
This study is part of submission 10518
(Status: Published).
Citation
Hulcr J., & Cognato A. 2010. Repeated evolution of theft in fungus farming ambrosia beetles. Evolution, .
Authors
-
Hulcr J.
(submitter)
517-256-1894
-
Cognato A.
Abstract
We report repeated evolution of fungal crop stealing, termed mycocleptism, among ambrosia beetles. Ambrosia beetles, dominant wood degraders in the tropics, create tunnels in dead trees and employ gardens of symbiotic fungi to extract nutrients from wood. The mycocleptic species seek brood galleries of other species, and exploit their established fungal gardens by tunneling through the ambient mycelium-laden wood. Instead of carrying their own fungal sybmbionts, mycocleptae depend on adopting the fungal assemblages of their host species, as shown by an analysis of fungal DNA from beetle galleries. The evidence for widespread horizontal exchange of fungi between beetles challenges the traditional concept of ambrosia fungi as species-specific symbionts. Fungus stealing appears to be an evolutionarily successful strategy. It evolved independently in several beetle clades, two of which have radiated, and at least one case was accompanied by a loss of the beetles' fungus-transpor! ting organs. We demonstrate this using the first robust phylogeny of one of the world's largest group of ambrosia beetles, Xyleborini.
External links
About this resource
- Canonical resource URI:
http://purl.org/phylo/treebase/phylows/study/TB2:S10528
- Other versions:
Nexus
NeXML
- Show BibTeX reference
@ARTICLE{TreeBASE2Ref18976,
author = {Jiri Hulcr and Anthony Cognato},
title = {Repeated evolution of theft in fungus farming ambrosia beetles.},
year = {2010},
keywords = {},
doi = {},
url = {http://},
pmid = {},
journal = {Evolution},
volume = {},
number = {},
pages = {},
abstract = {We report repeated evolution of fungal crop stealing, termed mycocleptism, among ambrosia beetles. Ambrosia beetles, dominant wood degraders in the tropics, create tunnels in dead trees and employ gardens of symbiotic fungi to extract nutrients from wood. The mycocleptic species seek brood galleries of other species, and exploit their established fungal gardens by tunneling through the ambient mycelium-laden wood. Instead of carrying their own fungal sybmbionts, mycocleptae depend on adopting the fungal assemblages of their host species, as shown by an analysis of fungal DNA from beetle galleries. The evidence for widespread horizontal exchange of fungi between beetles challenges the traditional concept of ambrosia fungi as species-specific symbionts. Fungus stealing appears to be an evolutionarily successful strategy. It evolved independently in several beetle clades, two of which have radiated, and at least one case was accompanied by a loss of the beetles' fungus-transpor! ting organs. We demonstrate this using the first robust phylogeny of one of the world's largest group of ambrosia beetles, Xyleborini.}
}
- Show RIS reference
TY - JOUR
ID - 18976
AU - Hulcr,Jiri
AU - Cognato,Anthony
T1 - Repeated evolution of theft in fungus farming ambrosia beetles.
PY - 2010
KW -
UR - http://dx.doi.org/
N2 - We report repeated evolution of fungal crop stealing, termed mycocleptism, among ambrosia beetles. Ambrosia beetles, dominant wood degraders in the tropics, create tunnels in dead trees and employ gardens of symbiotic fungi to extract nutrients from wood. The mycocleptic species seek brood galleries of other species, and exploit their established fungal gardens by tunneling through the ambient mycelium-laden wood. Instead of carrying their own fungal sybmbionts, mycocleptae depend on adopting the fungal assemblages of their host species, as shown by an analysis of fungal DNA from beetle galleries. The evidence for widespread horizontal exchange of fungi between beetles challenges the traditional concept of ambrosia fungi as species-specific symbionts. Fungus stealing appears to be an evolutionarily successful strategy. It evolved independently in several beetle clades, two of which have radiated, and at least one case was accompanied by a loss of the beetles' fungus-transpor! ting organs. We demonstrate this using the first robust phylogeny of one of the world's largest group of ambrosia beetles, Xyleborini.
L3 -
JF - Evolution
VL -
IS -
ER -
Go to search
Citation
Taxa
Matrices
Trees
Analyses
