Distinguishing Cophylogenetic Signal from Phylogenetic Congruence Clarifies the Interplay Between Evolutionary History and Species Interactions

Abstract Interspecific interactions, including host–symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host and symbiont clades and knowledge of which host species interact with which symbiont, two questions are often asked: “Do closely re...

Full description

Saved in:
Bibliographic Details
Published inSystematic biology Vol. 73; no. 3; pp. 613 - 622
Main Authors Perez-Lamarque, Benoît, Morlon, Hélène
Format Journal Article
LanguageEnglish
Published US Oxford University Press 05.09.2024
Oxford University Press (OUP)
Subjects
Online AccessGet full text
ISSN1063-5157
1076-836X
1076-836X
DOI10.1093/sysbio/syae013

Cover

Loading…
Abstract Abstract Interspecific interactions, including host–symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host and symbiont clades and knowledge of which host species interact with which symbiont, two questions are often asked: “Do closely related hosts interact with closely related symbionts?” and “Do host and symbiont phylogenies mirror one another?.” These questions are intertwined and can even collapse under specific situations, such that they are often confused one with the other. However, in most situations, a positive answer to the first question, hereafter referred to as “cophylogenetic signal,” does not imply a close match between the host and symbiont phylogenies. It suggests only that past evolutionary history has contributed to shaping present-day interactions, which can arise, for example, through present-day trait matching, or from a single ancient vicariance event that increases the probability that closely related species overlap geographically. A positive answer to the second, referred to as “phylogenetic congruence,” is more restrictive as it suggests a close match between the two phylogenies, which may happen, for example, if symbiont diversification tracks host diversification or if the diversifications of the two clades were subject to the same succession of vicariance events. Here we apply a set of methods (ParaFit, PACo, and eMPRess), whose significance is often interpreted as evidence for phylogenetic congruence, to simulations under 3 biologically realistic scenarios of trait matching, a single ancient vicariance event, and phylogenetic tracking with frequent cospeciation events. The latter is the only scenario that generates phylogenetic congruence, whereas the first 2 generate a cophylogenetic signal in the absence of phylogenetic congruence. We find that tests of global-fit methods (ParaFit and PACo) are significant under the 3 scenarios, whereas tests of event-based methods (eMPRess) are only significant under the scenario of phylogenetic tracking. Therefore, significant results from global-fit methods should be interpreted in terms of cophylogenetic signal and not phylogenetic congruence; such significant results can arise under scenarios when hosts and symbionts had independent evolutionary histories. Conversely, significant results from event-based methods suggest a strong form of dependency between hosts and symbionts evolutionary histories. Clarifying the patterns detected by different cophylogenetic methods is key to understanding how interspecific interactions shape and are shaped by evolution.
AbstractList Interspecific interactions, including host–symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host and symbiont clades and knowledge of which host species interact with which symbiont, two questions are often asked: “Do closely related hosts interact with closely related symbionts?” and “Do host and symbiont phylogenies mirror one another?.” These questions are intertwined and can even collapse under specific situations, such that they are often confused one with the other. However, in most situations, a positive answer to the first question, hereafter referred to as “cophylogenetic signal,” does not imply a close match between the host and symbiont phylogenies. It suggests only that past evolutionary history has contributed to shaping present-day interactions, which can arise, for example, through present-day trait matching, or from a single ancient vicariance event that increases the probability that closely related species overlap geographically. A positive answer to the second, referred to as “phylogenetic congruence,” is more restrictive as it suggests a close match between the two phylogenies, which may happen, for example, if symbiont diversification tracks host diversification or if the diversifications of the two clades were subject to the same succession of vicariance events. Here we apply a set of methods (ParaFit, PACo, and eMPRess), whose significance is often interpreted as evidence for phylogenetic congruence, to simulations under 3 biologically realistic scenarios of trait matching, a single ancient vicariance event, and phylogenetic tracking with frequent cospeciation events. The latter is the only scenario that generates phylogenetic congruence, whereas the first 2 generate a cophylogenetic signal in the absence of phylogenetic congruence. We find that tests of global-fit methods (ParaFit and PACo) are significant under the 3 scenarios, whereas tests of event-based methods (eMPRess) are only significant under the scenario of phylogenetic tracking. Therefore, significant results from global-fit methods should be interpreted in terms of cophylogenetic signal and not phylogenetic congruence; such significant results can arise under scenarios when hosts and symbionts had independent evolutionary histories. Conversely, significant results from event-based methods suggest a strong form of dependency between hosts and symbionts evolutionary histories. Clarifying the patterns detected by different cophylogenetic methods is key to understanding how interspecific interactions shape and are shaped by evolution.
Abstract Interspecific interactions, including host–symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host and symbiont clades and knowledge of which host species interact with which symbiont, two questions are often asked: “Do closely related hosts interact with closely related symbionts?” and “Do host and symbiont phylogenies mirror one another?.” These questions are intertwined and can even collapse under specific situations, such that they are often confused one with the other. However, in most situations, a positive answer to the first question, hereafter referred to as “cophylogenetic signal,” does not imply a close match between the host and symbiont phylogenies. It suggests only that past evolutionary history has contributed to shaping present-day interactions, which can arise, for example, through present-day trait matching, or from a single ancient vicariance event that increases the probability that closely related species overlap geographically. A positive answer to the second, referred to as “phylogenetic congruence,” is more restrictive as it suggests a close match between the two phylogenies, which may happen, for example, if symbiont diversification tracks host diversification or if the diversifications of the two clades were subject to the same succession of vicariance events. Here we apply a set of methods (ParaFit, PACo, and eMPRess), whose significance is often interpreted as evidence for phylogenetic congruence, to simulations under 3 biologically realistic scenarios of trait matching, a single ancient vicariance event, and phylogenetic tracking with frequent cospeciation events. The latter is the only scenario that generates phylogenetic congruence, whereas the first 2 generate a cophylogenetic signal in the absence of phylogenetic congruence. We find that tests of global-fit methods (ParaFit and PACo) are significant under the 3 scenarios, whereas tests of event-based methods (eMPRess) are only significant under the scenario of phylogenetic tracking. Therefore, significant results from global-fit methods should be interpreted in terms of cophylogenetic signal and not phylogenetic congruence; such significant results can arise under scenarios when hosts and symbionts had independent evolutionary histories. Conversely, significant results from event-based methods suggest a strong form of dependency between hosts and symbionts evolutionary histories. Clarifying the patterns detected by different cophylogenetic methods is key to understanding how interspecific interactions shape and are shaped by evolution.
Interspecific interactions, including host-symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host and symbiont clades and knowledge of which host species interact with which symbiont, two questions are often asked: “Do closely related hosts interact with closely related symbionts?” and “Do host and symbiont phylogenies mirror one another?”. These questions are intertwined and can even collapse under specific situations, such that they are often confused one with the other. However, in most situations, a positive answer to the first question, hereafter referred to as “cophylogenetic signal”, does not imply a close match between the host and symbiont phylogenies. It suggests only that past evolutionary history has contributed to shaping present-day interactions, which can arise, for example, through present-day trait matching, or from a single ancient vicariance event that increases the probability that closely related species overlap geographically. A positive answer to the second, referred to as “phylogenetic congruence”, is more restrictive as it suggests a close match between the two phylogenies, which may happen, for example, if symbiont diversification tracks host diversification or if the diversifications of the two clades were subject to the same succession of vicariance events. Here we apply a set of methods (ParaFit, PACo, and eMPRess), which significance is often interpreted as evidence for phylogenetic congruence, to simulations under three biologically realistic scenarios of trait matching, a single ancient vicariance event, and phylogenetic tracking with frequent cospeciation events. The latter is the only scenario that generates phylogenetic congruence, whereas the first two generate a cophylogenetic signal in the absence of phylogenetic congruence. We find that tests of global-fit methods (ParaFit and PACo) are significant under the three scenarios, whereas tests of event-based methods (eMPRess) are only significant under the scenario of phylogenetic tracking. Therefore, significant results from global-fit methods should be interpreted in terms of cophylogenetic signal and not phylogenetic congruence; such significant results can arise under scenarios when hosts and symbionts had independent evolutionary histories. Conversely, significant results from event-based methods suggest a strong form of dependency between hosts and symbionts evolutionary histories. Clarifying the patterns detected by different cophylogenetic methods is key to understanding how interspecific interactions shape and are shaped by evolution.
Interspecific interactions, including host-symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host and symbiont clades and knowledge of which host species interact with which symbiont, two questions are often asked: "Do closely related hosts interact with closely related symbionts?" and "Do host and symbiont phylogenies mirror one another?." These questions are intertwined and can even collapse under specific situations, such that they are often confused one with the other. However, in most situations, a positive answer to the first question, hereafter referred to as "cophylogenetic signal," does not imply a close match between the host and symbiont phylogenies. It suggests only that past evolutionary history has contributed to shaping present-day interactions, which can arise, for example, through present-day trait matching, or from a single ancient vicariance event that increases the probability that closely related species overlap geographically. A positive answer to the second, referred to as "phylogenetic congruence," is more restrictive as it suggests a close match between the two phylogenies, which may happen, for example, if symbiont diversification tracks host diversification or if the diversifications of the two clades were subject to the same succession of vicariance events. Here we apply a set of methods (ParaFit, PACo, and eMPRess), whose significance is often interpreted as evidence for phylogenetic congruence, to simulations under 3 biologically realistic scenarios of trait matching, a single ancient vicariance event, and phylogenetic tracking with frequent cospeciation events. The latter is the only scenario that generates phylogenetic congruence, whereas the first 2 generate a cophylogenetic signal in the absence of phylogenetic congruence. We find that tests of global-fit methods (ParaFit and PACo) are significant under the 3 scenarios, whereas tests of event-based methods (eMPRess) are only significant under the scenario of phylogenetic tracking. Therefore, significant results from global-fit methods should be interpreted in terms of cophylogenetic signal and not phylogenetic congruence; such significant results can arise under scenarios when hosts and symbionts had independent evolutionary histories. Conversely, significant results from event-based methods suggest a strong form of dependency between hosts and symbionts evolutionary histories. Clarifying the patterns detected by different cophylogenetic methods is key to understanding how interspecific interactions shape and are shaped by evolution.Interspecific interactions, including host-symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host and symbiont clades and knowledge of which host species interact with which symbiont, two questions are often asked: "Do closely related hosts interact with closely related symbionts?" and "Do host and symbiont phylogenies mirror one another?." These questions are intertwined and can even collapse under specific situations, such that they are often confused one with the other. However, in most situations, a positive answer to the first question, hereafter referred to as "cophylogenetic signal," does not imply a close match between the host and symbiont phylogenies. It suggests only that past evolutionary history has contributed to shaping present-day interactions, which can arise, for example, through present-day trait matching, or from a single ancient vicariance event that increases the probability that closely related species overlap geographically. A positive answer to the second, referred to as "phylogenetic congruence," is more restrictive as it suggests a close match between the two phylogenies, which may happen, for example, if symbiont diversification tracks host diversification or if the diversifications of the two clades were subject to the same succession of vicariance events. Here we apply a set of methods (ParaFit, PACo, and eMPRess), whose significance is often interpreted as evidence for phylogenetic congruence, to simulations under 3 biologically realistic scenarios of trait matching, a single ancient vicariance event, and phylogenetic tracking with frequent cospeciation events. The latter is the only scenario that generates phylogenetic congruence, whereas the first 2 generate a cophylogenetic signal in the absence of phylogenetic congruence. We find that tests of global-fit methods (ParaFit and PACo) are significant under the 3 scenarios, whereas tests of event-based methods (eMPRess) are only significant under the scenario of phylogenetic tracking. Therefore, significant results from global-fit methods should be interpreted in terms of cophylogenetic signal and not phylogenetic congruence; such significant results can arise under scenarios when hosts and symbionts had independent evolutionary histories. Conversely, significant results from event-based methods suggest a strong form of dependency between hosts and symbionts evolutionary histories. Clarifying the patterns detected by different cophylogenetic methods is key to understanding how interspecific interactions shape and are shaped by evolution.
Author Perez-Lamarque, Benoît
Morlon, Hélène
Author_xml – sequence: 1
  givenname: Benoît
  orcidid: 0000-0001-7112-7197
  surname: Perez-Lamarque
  fullname: Perez-Lamarque, Benoît
  email: benoit.perez@ens.psl.eu
– sequence: 2
  givenname: Hélène
  orcidid: 0000-0002-3195-7521
  surname: Morlon
  fullname: Morlon, Hélène
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38477631$$D View this record in MEDLINE/PubMed
https://hal.sorbonne-universite.fr/hal-04507008$$DView record in HAL
BookMark eNqFkU9v1DAQxS1URP_AlSOyxIUeUux14sTHNhS20kogFSRuluNMdl157WA7Rfsp-Mp12C1ClRCnZ9m_NzOed4qOnHeA0GtKLigR7H3cxc74LAoIZc_QCSU1LxrGvx_NZ86Kilb1MTqN8Y4QSnlFX6Bj1pR1zRk9Qb8-mJiMW08mbrLg1o-bnfVrcJCMxrdm7ZTFQ_Bb_OXvh9a7dZjAacCtVcEMBiJOG8A3LkEYrdrhK0g_ARy-vvd2SsY7FXZ4mdv5rMr1-HYEPdt-W5SekfgSPR-UjfDqoGfo28frr-2yWH3-dNNergpdMpqKgTEiGk2o6ruyb6jgnEHPh7KmCy1I3y8GIZqhyv8cKiWIUKpThKhO86pR0LEzdL6vu1FWjsFs83DSKyOXlys535GyIjUhzT3N7Ls9Owb_Y4KY5NZEDdYqB36KciEqzhtGuMjo2yfonZ9CXmGUbFGWlC8IrTL15kBN3Rb6P_0fY8lAuQd08DEGGKQ2Sc0LSkEZKymRc_pyn748pJ9tF09sj5X_aThswU_j_9gHUYLGNQ
CitedBy_id crossref_primary_10_7554_eLife_91745
crossref_primary_10_7554_eLife_91745_3
crossref_primary_10_1002_ajb2_70010
Cites_doi 10.1111/evo.13809
10.1111/j.1096-0031.1995.tb00005.x
10.1093/bioinformatics/btaa978
10.1038/s42003-022-03223-0
10.1128/msystems.01104-21
10.1111/jeb.13477
10.1126/science.abm7759
10.1016/j.tree.2013.11.003
10.1111/mec.16681
10.7554/eLife.91745
10.1038/nrmicro2262
10.1038/ncomms14319
10.1017/CBO9781139794749
10.2307/2992354
10.1146/annurev-ecolsys-102320-112823
10.1093/oso/9780198835851.001.0001
10.1111/j.1463-6409.1997.tb00421.x
10.1093/bioinformatics/btg412
10.1111/2041-210X.12736
10.1371/journal.pone.0061048
10.1016/j.tree.2021.06.006
10.24072/pcjournal.179
10.1111/ele.13918
10.1093/sysbio/syt054
10.1146/annurev-ecolsys-011720-121505
10.1111/nph.12150
10.1080/10635150490423430
10.1186/1748-7188-5-16
10.1111/ele.13757
10.1080/10635150252899734
ContentType Journal Article
Copyright The Author(s) 2024. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. 2024
The Author(s) 2024. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For permissions, please email: journals.permissions@oup.com.
The Author(s) 2024. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.
Attribution
Copyright_xml – notice: The Author(s) 2024. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. 2024
– notice: The Author(s) 2024. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For permissions, please email: journals.permissions@oup.com.
– notice: The Author(s) 2024. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.
– notice: Attribution
DBID AAYXX
CITATION
NPM
K9.
7X8
1XC
VOOES
DOI 10.1093/sysbio/syae013
DatabaseName CrossRef
PubMed
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
Hyper Article en Ligne (HAL)
Hyper Article en Ligne (HAL) (Open Access)
DatabaseTitle CrossRef
PubMed
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitleList ProQuest Health & Medical Complete (Alumni)


MEDLINE - Academic
PubMed
CrossRef
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Zoology
Biology
Ecology
Environmental Sciences
EISSN 1076-836X
EndPage 622
ExternalDocumentID oai_HAL_hal_04507008v1
38477631
10_1093_sysbio_syae013
10.1093/sysbio/syae013
Genre Journal Article
GroupedDBID ---
-~X
.-4
.2P
.I3
0R~
123
18M
1TH
29Q
2FS
36B
4.4
48X
53G
5VS
5WD
70D
7X7
88E
88I
8AF
8AO
8CJ
8FE
8FH
8FI
8FJ
8G5
AAHBH
AAHKG
AAIMJ
AAISJ
AAJKP
AAJQQ
AAKGQ
AAMDB
AAMVS
AAOGV
AAPQZ
AAPXW
AARHZ
AAUAY
AAUQX
AAVAP
AAVLN
AAWDT
ABBHK
ABDBF
ABDFA
ABEJV
ABEUO
ABGNP
ABIME
ABIXL
ABJNI
ABMNT
ABNGD
ABNKS
ABPIB
ABPLY
ABPPZ
ABPQP
ABPTD
ABQLI
ABSMQ
ABSQW
ABTAH
ABTLG
ABUWG
ABVGC
ABWST
ABXSQ
ABXVV
ABXZS
ABZBJ
ABZEO
ACCCW
ACFRR
ACGEJ
ACGFO
ACGFS
ACGOD
ACHIC
ACIPB
ACNCT
ACPQN
ACPRK
ACSTJ
ACUFI
ACUHS
ACUKT
ACUTJ
ACVCV
ACZBC
ADBBV
ADEYI
ADFTL
ADGKP
ADGZP
ADHKW
ADHZD
ADIPN
ADNBA
ADOCK
ADQBN
ADRTK
ADULT
ADVEK
ADXPE
ADYVW
ADZTZ
ADZXQ
AEGPL
AEGXH
AEJOX
AEKPW
AEKSI
AELWJ
AEMDU
AENEX
AENZO
AEPUE
AETBJ
AEUPB
AEUYN
AEWNT
AFAZZ
AFFZL
AFGWE
AFIYH
AFKRA
AFKVX
AFOFC
AFSHK
AFYAG
AGINJ
AGKEF
AGKRT
AGMDO
AGQXC
AGSYK
AGUYK
AHMBA
AHXOZ
AHXPO
AIAGR
AIJHB
AILXY
AJDVS
AJEEA
AJNCP
AJWEG
AKHUL
AKWXX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALUQC
ALXQX
ANFBD
APIBT
APJGH
APWMN
AQDSO
AQVQM
ARIXL
ASAOO
ASPBG
ATDFG
ATGXG
ATTQO
AVWKF
AXUDD
AYOIW
AZFZN
AZQEC
BAYMD
BBNVY
BCRHZ
BENPR
BES
BEYMZ
BHONS
BHPHI
BKSAR
BPHCQ
BQDIO
BSWAC
BVXVI
C45
CAG
CBGCD
CCPQU
CDBKE
COF
CS3
CUYZI
CXTWN
CZ4
D1J
DAKXR
DEVKO
DFGAJ
DILTD
DU5
DWQXO
D~K
EAD
EAP
EAS
EBC
EBD
EBS
EE~
EHN
EJD
ELUNK
EMB
EMK
EMOBN
EPL
EPT
EST
ESX
F5P
F9B
FEDTE
FHSFR
FLUFQ
FOEOM
FQBLK
FYUFA
GAUVT
GJXCC
GNUQQ
GTFYD
GUQSH
H13
H5~
HAR
HCIFZ
HF~
HGD
HMCUK
HQ2
HTVGU
HVGLF
HW0
HZ~
I-F
IOX
IPSME
J21
JAAYA
JBMMH
JBS
JEB
JEFFH
JENOY
JHFFW
JKQEH
JLS
JLXEF
JPM
JST
JXSIZ
KAQDR
KBUDW
KOP
KSI
KSN
LK8
M-Z
M1P
M2O
M2P
M2Q
M49
M7P
MBTAY
MVM
N9A
NEJ
NGC
NLBLG
NOMLY
NU-
NVLIB
O0~
O9-
OAWHX
OBOKY
ODMLO
OJQWA
OJZSN
OVD
OWPYF
O~Y
P2P
PADUT
PAFKI
PB-
PCBAR
PEELM
PHGZT
PQQKQ
PROAC
PSQYO
Q1.
Q5Y
QBD
Q~Q
RD5
ROX
ROZ
RUSNO
RW1
RWL
RXO
RXW
S0X
SA0
SV3
TAE
TCN
TEORI
TLC
TN5
TUS
UBC
UKHRP
WH7
WHG
X7H
XOL
XSW
YAYTL
YKOAZ
YXANX
YXE
ZCG
ZY4
~02
~91
AAYXX
AGORE
AHGBF
AJBYB
CITATION
NPM
K9.
7X8
1XC
VOOES
ID FETCH-LOGICAL-c431t-f33098c01adb4d819663ed6f4712c90dd2f998f5847f5a909aaba00abc658aeb3
ISSN 1063-5157
1076-836X
IngestDate Wed Aug 13 07:44:08 EDT 2025
Wed Jul 30 11:17:50 EDT 2025
Thu Aug 28 04:58:06 EDT 2025
Mon Jul 21 05:46:49 EDT 2025
Thu Apr 24 22:56:59 EDT 2025
Tue Jul 01 01:54:23 EDT 2025
Wed Apr 02 07:03:59 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 3
Keywords parasitism
phylogenetic methods
Codiversification
cophylogeny
coevolution
symbiosis
codiversification
Language English
License This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/pages/standard-publication-reuse-rights)
https://academic.oup.com/pages/standard-publication-reuse-rights
The Author(s) 2024. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For permissions, please email: journals.permissions@oup.com.
Attribution: http://creativecommons.org/licenses/by
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c431t-f33098c01adb4d819663ed6f4712c90dd2f998f5847f5a909aaba00abc658aeb3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0001-7112-7197
0000-0002-3195-7521
OpenAccessLink https://hal.sorbonne-universite.fr/hal-04507008
PMID 38477631
PQID 3244162015
PQPubID 37498
PageCount 10
ParticipantIDs hal_primary_oai_HAL_hal_04507008v1
proquest_miscellaneous_2956683069
proquest_journals_3244162015
pubmed_primary_38477631
crossref_citationtrail_10_1093_sysbio_syae013
crossref_primary_10_1093_sysbio_syae013
oup_primary_10_1093_sysbio_syae013
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20240905
PublicationDateYYYYMMDD 2024-09-05
PublicationDate_xml – month: 09
  year: 2024
  text: 20240905
  day: 05
PublicationDecade 2020
PublicationPlace US
PublicationPlace_xml – name: US
– name: England
– name: Oxford
PublicationTitle Systematic biology
PublicationTitleAlternate Syst Biol
PublicationYear 2024
Publisher Oxford University Press
Oxford University Press (OUP)
Publisher_xml – name: Oxford University Press
– name: Oxford University Press (OUP)
References Balbuena (2024092310014230000_CIT0002) 2013; 8
Page (2024092310014230000_CIT0023) 1994; 10
Suzuki (2024092310014230000_CIT0041) 2022; 377
Legendre (2024092310014230000_CIT0017) 2002; 51
Hembry (2024092310014230000_CIT0014) 2020; 51
Groussin (2024092310014230000_CIT0011) 2017; 8
Ronquist (2024092310014230000_CIT0035) 1990; 39
Su (2024092310014230000_CIT0040) 2022; 5
Bright (2024092310014230000_CIT0005) 2010; 8
Santichaivekin (2024092310014230000_CIT0038) 2021; 37
Paradis (2024092310014230000_CIT0025) 2004; 20
Sanmartín (2024092310014230000_CIT0036) 2002; 25
Hayward (2024092310014230000_CIT0013) 2021; 24
Ronquist (2024092310014230000_CIT0033) 2003; 1
Perez-Lamarque (2024092310014230000_CIT0026) 2022; 7
Jousselin (2024092310014230000_CIT0016) 2009; 276
Blasco-Costa (2024092310014230000_CIT0004) 2021; 36
Dismukes (2024092310014230000_CIT0008) 2022; 53
Mittelbach (2024092310014230000_CIT0019) 2019
Bascompte (2024092310014230000_CIT0003) 2013
Maestri (2024092310014230000_CIT0018) 2024; 13
Satler (2024092310014230000_CIT0039) 2019; 73
Morand (2024092310014230000_CIT0020) 2015
Harmon (2024092310014230000_CIT0012) 2019; 32
Fuzessy (2024092310014230000_CIT0010) 2022; 25
Althoff (2024092310014230000_CIT0001) 2014; 29
de Vienne (2024092310014230000_CIT0007) 2013; 198
Perez-Lamarque (2024092310014230000_CIT0027) 2022; 2
Ronquist (2024092310014230000_CIT0032) 1998; 26
Hutchinson (2024092310014230000_CIT0015) 2017; 8
Pichon (2024092310014230000_CIT0029) 2023; 01
Page (2024092310014230000_CIT0024) 1995
Szöllősi (2024092310014230000_CIT0042) 2013; 62
Sanmartín (2024092310014230000_CIT0037) 2004; 53
Ronquist (2024092310014230000_CIT0034) 2003
Poisot (2024092310014230000_CIT0030) 2015; 23
Fahrenholz (2024092310014230000_CIT0009) 1912; 41
Conow (2024092310014230000_CIT0006) 2010; 5
Muchhala (2024092310014230000_CIT0021) 2009; 276
Ronquist (2024092310014230000_CIT0031) 1995; 11
Perez-Lamarque (2024092310014230000_CIT0028) 2023; 32
Page (2024092310014230000_CIT0022) 1994; 43
References_xml – volume: 73
  start-page: 2295
  year: 2019
  ident: 2024092310014230000_CIT0039
  article-title: Inferring processes of coevolutionary diversification in a community of Panamanian strangler figs and associated pollinating wasps
  publication-title: Evolution Int. J. Org. Evol
  doi: 10.1111/evo.13809
– volume: 276
  start-page: 187
  year: 2009
  ident: 2024092310014230000_CIT0016
  article-title: Fine-scale cospeciation between Brachycaudus and Buchnera aphidicola: bacterial genome helps define species and evolutionary relationships in aphids
  publication-title: Proc. Biol. Sci
– volume: 41
  start-page: 371
  year: 1912
  ident: 2024092310014230000_CIT0009
  article-title: Ectoparasiten und abstammungslehre
  publication-title: Zool. Anz
– volume: 01
  start-page: 2023.04.04.535603
  year: 2023
  ident: 2024092310014230000_CIT0029
  article-title: Telling mutualistic and antagonistic ecological networks apart by learning their multiscale structure
  publication-title: bioRxiv
– volume: 11
  start-page: 73
  year: 1995
  ident: 2024092310014230000_CIT0031
  article-title: Reconstructing the history of host-parasite associations using generalised parsimony
  publication-title: Cladistics
  doi: 10.1111/j.1096-0031.1995.tb00005.x
– volume: 43
  start-page: 58
  year: 1994
  ident: 2024092310014230000_CIT0022
  article-title: Maps between trees and cladistic analysis of historical associations among genes, organisms, and areas
  publication-title: Syst. Biol
– volume: 25
  start-page: 75
  year: 2002
  ident: 2024092310014230000_CIT0036
  article-title: New solutions to old problems: widespread taxa, redundant distributions and missing areas in event-based biogeography
  publication-title: Anim. Biodivers. Conserv
– volume: 37
  start-page: 2481
  year: 2021
  ident: 2024092310014230000_CIT0038
  article-title: EMPRess: a systematic cophylogeny reconciliation tool
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btaa978
– volume: 5
  start-page: 284
  year: 2022
  ident: 2024092310014230000_CIT0040
  article-title: Pollinator sharing, copollination, and speciation by host shifting among six closely related dioecious fig species
  publication-title: Commun. Biol
  doi: 10.1038/s42003-022-03223-0
– volume: 7
  start-page: e0110421
  year: 2022
  ident: 2024092310014230000_CIT0026
  article-title: Limited evidence for microbial transmission in the phylosymbiosis between Hawaiian spiders and their microbiota
  publication-title: mSystems
  doi: 10.1128/msystems.01104-21
– volume: 32
  start-page: 769
  year: 2019
  ident: 2024092310014230000_CIT0012
  article-title: Detecting the macroevolutionary signal of species interactions
  publication-title: J. Evol. Biol
  doi: 10.1111/jeb.13477
– volume: 377
  start-page: 1328
  year: 2022
  ident: 2024092310014230000_CIT0041
  article-title: Codiversification of gut microbiota with humans
  publication-title: Science (80-.)
  doi: 10.1126/science.abm7759
– volume: 23
  start-page: 420
  year: 2015
  ident: 2024092310014230000_CIT0030
  article-title: When is co-phylogeny evidence of coevolution? Parasite divers
  publication-title: Diversif. Evol. Ecol. Meets Phylogenetics
– volume: 29
  start-page: 82
  year: 2014
  ident: 2024092310014230000_CIT0001
  article-title: Testing for coevolutionary diversification: linking pattern with process
  publication-title: Trends Ecol. Evol
  doi: 10.1016/j.tree.2013.11.003
– volume-title: Mutualistic networks
  year: 2013
  ident: 2024092310014230000_CIT0003
– volume: 32
  start-page: 6671
  year: 2023
  ident: 2024092310014230000_CIT0028
  article-title: Comparing different computational approaches for detecting long-term vertical transmission in host-associated microbiota
  publication-title: Mol. Ecol
  doi: 10.1111/mec.16681
– volume: 13
  start-page: RP91745
  year: 2024
  ident: 2024092310014230000_CIT0018
  article-title: Recent evolutionary origin and localized diversity hotspots of mammalian coronaviruses
  publication-title: eLife
  doi: 10.7554/eLife.91745
– volume: 8
  start-page: 218
  year: 2010
  ident: 2024092310014230000_CIT0005
  article-title: A complex journey: transmission of microbial symbionts
  publication-title: Nat. Rev. Microbiol
  doi: 10.1038/nrmicro2262
– volume: 8
  start-page: 14319
  year: 2017
  ident: 2024092310014230000_CIT0011
  article-title: Unraveling the processes shaping mammalian gut microbiomes over evolutionary time
  publication-title: Nat. Commun
  doi: 10.1038/ncomms14319
– volume-title: Parasite diversity and diversification
  year: 2015
  ident: 2024092310014230000_CIT0020
  doi: 10.1017/CBO9781139794749
– volume: 39
  start-page: 323
  year: 1990
  ident: 2024092310014230000_CIT0035
  article-title: Process and pattern in the evolution of species associations
  publication-title: Syst. Zool
  doi: 10.2307/2992354
– volume: 53
  start-page: 275
  year: 2022
  ident: 2024092310014230000_CIT0008
  article-title: Cophylogenetic methods to untangle the evolutionary history of ecological interactions
  publication-title: Annu. Rev. Ecol. Evol. Syst
  doi: 10.1146/annurev-ecolsys-102320-112823
– volume-title: Community ecology
  year: 2019
  ident: 2024092310014230000_CIT0019
  doi: 10.1093/oso/9780198835851.001.0001
– volume: 26
  start-page: 313
  year: 1998
  ident: 2024092310014230000_CIT0032
  article-title: Phylogenetic approaches in coevolution and biogeography
  publication-title: Zool. Scr
  doi: 10.1111/j.1463-6409.1997.tb00421.x
– volume: 20
  start-page: 289
  year: 2004
  ident: 2024092310014230000_CIT0025
  article-title: APE: analyses of phylogenetics and evolution in R language
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btg412
– volume: 10
  start-page: 155
  year: 1994
  ident: 2024092310014230000_CIT0023
  article-title: Parallel phylogenies: reconstructing the history of host-parasite assemblages
  publication-title: Cladistics
– volume: 8
  start-page: 932
  year: 2017
  ident: 2024092310014230000_CIT0015
  article-title: paco: implementing Procrustean Approach to Cophylogeny in R
  publication-title: Methods Ecol. Evol
  doi: 10.1111/2041-210X.12736
– volume: 8
  start-page: e61048
  year: 2013
  ident: 2024092310014230000_CIT0002
  article-title: PACo: a novel procrustes application to cophylogenetic analysis
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0061048
– volume: 36
  start-page: 907
  year: 2021
  ident: 2024092310014230000_CIT0004
  article-title: Next-generation cophylogeny: unravelling eco-evolutionary processes
  publication-title: Trends Ecol. Evol
  doi: 10.1016/j.tree.2021.06.006
– volume: 1
  start-page: 22
  year: 2003
  ident: 2024092310014230000_CIT0033
  article-title: Parsimony analysis of coevolving species associations
  publication-title: Tangled trees: phylogeny, cospeciation and coevolution
– volume: 2
  start-page: e59
  year: 2022
  ident: 2024092310014230000_CIT0027
  article-title: Do closely related species interact with similar partners? Testing for phylogenetic signal in bipartite interaction networks
  publication-title: Peer Community J
  doi: 10.24072/pcjournal.179
– year: 2003
  ident: 2024092310014230000_CIT0034
– volume: 25
  start-page: 320
  year: 2022
  ident: 2024092310014230000_CIT0010
  article-title: Phylogenetic congruence between Neotropical primates and plants is driven by frugivory
  publication-title: Ecol. Lett
  doi: 10.1111/ele.13918
– volume: 62
  start-page: 901
  year: 2013
  ident: 2024092310014230000_CIT0042
  article-title: Efficient exploration of the space of reconciled gene trees
  publication-title: Syst. Biol
  doi: 10.1093/sysbio/syt054
– volume: 51
  start-page: 215
  year: 2020
  ident: 2024092310014230000_CIT0014
  article-title: Ecological interactions and macroevolution: a new field with old roots
  publication-title: Annu. Rev. Ecol. Evol. Syst
  doi: 10.1146/annurev-ecolsys-011720-121505
– volume: 276
  start-page: 2147
  year: 2009
  ident: 2024092310014230000_CIT0021
  article-title: Going to great lengths: selection for long corolla tubes in an extremely specialized bat-flower mutualism
  publication-title: Proc. Biol. Sci
– volume: 198
  start-page: 347
  year: 2013
  ident: 2024092310014230000_CIT0007
  article-title: Cospeciation vs host-shift speciation: methods for testing, evidence from natural associations and relation to coevolution
  publication-title: New Phytol
  doi: 10.1111/nph.12150
– volume: 53
  start-page: 216
  year: 2004
  ident: 2024092310014230000_CIT0037
  article-title: Southern hemisphere biogeography inferred by event-based models: plant versus animal patterns
  publication-title: Syst. Biol
  doi: 10.1080/10635150490423430
– volume: 5
  start-page: 1
  year: 2010
  ident: 2024092310014230000_CIT0006
  article-title: Jane: a new tool for the cophylogeny reconstruction problem
  publication-title: Algorithms Mol. Biol
  doi: 10.1186/1748-7188-5-16
– volume-title: TreeMap. Computer program distributed by the author
  year: 1995
  ident: 2024092310014230000_CIT0024
– volume: 24
  start-page: 1681
  year: 2021
  ident: 2024092310014230000_CIT0013
  article-title: A broadscale analysis of host-symbiont cophylogeny reveals the drivers of phylogenetic congruence
  publication-title: Ecol. Lett
  doi: 10.1111/ele.13757
– volume: 51
  start-page: 217
  year: 2002
  ident: 2024092310014230000_CIT0017
  article-title: A statistical test for host-parasite coevolution
  publication-title: Syst. Biol
  doi: 10.1080/10635150252899734
SSID ssj0011651
Score 2.484165
Snippet Abstract Interspecific interactions, including host–symbiont associations, can profoundly affect the evolution of the interacting species. Given the...
Interspecific interactions, including host–symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host...
Interspecific interactions, including host-symbiont associations, can profoundly affect the evolution of the interacting species. Given the phylogenies of host...
SourceID hal
proquest
pubmed
crossref
oup
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 613
SubjectTerms Biodiversity
Biodiversity and Ecology
Environmental Sciences
Interspecific relationships
Life Sciences
Phylogenetics
Phylogeny
Symbionts
Systematics, Phylogenetics and taxonomy
Title Distinguishing Cophylogenetic Signal from Phylogenetic Congruence Clarifies the Interplay Between Evolutionary History and Species Interactions
URI https://www.ncbi.nlm.nih.gov/pubmed/38477631
https://www.proquest.com/docview/3244162015
https://www.proquest.com/docview/2956683069
https://hal.sorbonne-universite.fr/hal-04507008
Volume 73
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLbKJiReELdBYSCDkHhAZs61yWNHWxXopklbpYmXyHactVJJpl4mbX-Cd34tx5c6jVbE4CW1Yjdxcr4cf8c-5xih95zHHqdJSIQfMxJ28pykkYhIUBQe50WHRlRFIx8dx8Nx-PU8Om-1fm14La2W_JO42RpX8j9ShXMgVxUl-w-SdReFE1AG-cIRJAzHO8m4pz7Q8mJl55FEBe8MdBmoL5WGVblmqPBEFUDSqAAT-GKuHag_CjBsp8VU5XmYSJ07Yn45Y9fOfUte2QdQznUmN7FJ2KQiNKfamUuFMIt62s8S3dM6Q7TN81Qr4bm8ISP2g81hTNL4kmWlF-z7zgfnqJpbf4ChWcqf6Z_EOgHYaQo_1H5YUW3Ubg9_1DlVxyfrWQ-jg4E1EaBZZhyW9lwnJkmgNz28rfVtRqzrBTyQLjBJTYRrM8H2sHuanfQG2ejL8bdmrcu0PeyOsgkAAZguKEOaXIFlveuDCQJKf7d72DscuDUqL9abe7ruupSgwYHpyoHtSIPy3Jsoh9tGMOUtm0Zzm7NH6KE1SnDXIOwxasnyCbpvtim9hlJf2NJev46LhD_YgWEBTb5XuslT9LMJStwEJTagxAqUuFFRgxI7UGIAJXagxBaUeBOU2IISAyixBSXeBOUzNB70zz4Pid31gwggs0tSBAFNE0E9lvMwB8IKnFjmcQEsyhcpzXO_SNOkUMv7RcRSmjLGGaWMCyDTTPJgD-2UVSlfIKy4dRpJnlOfhyrvUR6locfjPGEwkHX8NiJrwWTCpsRXO7PMMuOaEWRGkJkVZBt9cO0vTTKYP7Z8p1C0brQdWdAIYPDXK-2vUZJZ1bPIwAoCQwq4e9RGb101DAxqtY-VslotMj8FSy0JaJy20XODLnerAF4eEAvv5V26-Qo9qD_ofbSzBDC8Bia-5G_sJ_Eb80nrAQ
linkProvider EBSCOhost
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Distinguishing+cophylogenetic+signal+from+phylogenetic+congruence+clarifies+the+interplay+between+evolutionary+history+and+species+interactions&rft.jtitle=Systematic+biology&rft.au=Perez-Lamarque%2C+Beno%C3%AEt&rft.au=Morlon%2C+H%C3%A9l%C3%A8ne&rft.date=2024-09-05&rft.pub=Oxford+University+Press+%28OUP%29&rft.issn=1063-5157&rft.eissn=1076-836X&rft_id=info:doi/10.1093%2Fsysbio%2Fsyae013&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=oai_HAL_hal_04507008v1
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1063-5157&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1063-5157&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1063-5157&client=summon