---
_id: '14850'
abstract:
- lang: eng
  text: Elaborate sexual signals are thought to have evolved and be maintained to
    serve as honest indicators of signaller quality. One measure of quality is health,
    which can be affected by parasite infection. Cnemaspis mysoriensis is a diurnal
    gecko that is often infested with ectoparasites in the wild, and males of this
    species express visual (coloured gular patches) and chemical (femoral gland secretions)
    traits that receivers could assess during social interactions. In this paper,
    we tested whether ectoparasites affect individual health, and whether signal quality
    is an indicator of ectoparasite levels. In wild lizards, we found that ectoparasite
    level was negatively correlated with body condition in both sexes. Moreover, some
    characteristics of both visual and chemical traits in males were strongly associated
    with ectoparasite levels. Specifically, males with higher ectoparasite levels
    had yellow gular patches with lower brightness and chroma, and chemical secretions
    with a lower proportion of aromatic compounds. We then determined whether ectoparasite
    levels in males influence female behaviour. Using sequential choice trials, wherein
    females were provided with either the visual or the chemical signals of wild-caught
    males that varied in ectoparasite level, we found that only chemical secretions
    evoked an elevated female response towards less parasitised males. Simultaneous
    choice trials in which females were exposed to the chemical secretions from males
    that varied in parasite level further confirmed a preference for males with lower
    parasites loads. Overall, we find that although health (body condition) or ectoparasite
    load can be honestly advertised through multiple modalities, the parasite-mediated
    female response is exclusively driven by chemical signals.</jats:p>
acknowledgement: "We thank Anuradha Batabyal and Shakilur Kabir for scientific discussions,
  and help with sampling and colour analyses. We thank Muralidhar and the central
  LCMS facility of the IISc for their technical support with the GCMS.\r\nResearch
  funding was provided by the Department of Science and Technology Fund for Improvement
  of S&T Infrastructure (DST-FIST), the Department of Biotechnology-Indian Institute
  of Science (DBT-IISc) partnership program and a Science and Engineering Research
  Board (SERB) grant to M.T. (EMR/2017/002228). Open Access funding provided by Indian
  Institute of Science. Deposited in PMC for immediate release."
article_number: jeb246217
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Arka
  full_name: Pal, Arka
  id: 6AAB2240-CA9A-11E9-9C1A-D9D1E5697425
  last_name: Pal
  orcid: 0000-0002-4530-8469
- first_name: Mihir
  full_name: Joshi, Mihir
  last_name: Joshi
- first_name: Maria
  full_name: Thaker, Maria
  last_name: Thaker
citation:
  ama: Pal A, Joshi M, Thaker M. Too much information? Males convey parasite levels
    using more signal modalities than females utilise. <i>Journal of Experimental
    Biology</i>. 2024;227(1). doi:<a href="https://doi.org/10.1242/jeb.246217">10.1242/jeb.246217</a>
  apa: Pal, A., Joshi, M., &#38; Thaker, M. (2024). Too much information? Males convey
    parasite levels using more signal modalities than females utilise. <i>Journal
    of Experimental Biology</i>. The Company of Biologists. <a href="https://doi.org/10.1242/jeb.246217">https://doi.org/10.1242/jeb.246217</a>
  chicago: Pal, Arka, Mihir Joshi, and Maria Thaker. “Too Much Information? Males
    Convey Parasite Levels Using More Signal Modalities than Females Utilise.” <i>Journal
    of Experimental Biology</i>. The Company of Biologists, 2024. <a href="https://doi.org/10.1242/jeb.246217">https://doi.org/10.1242/jeb.246217</a>.
  ieee: A. Pal, M. Joshi, and M. Thaker, “Too much information? Males convey parasite
    levels using more signal modalities than females utilise,” <i>Journal of Experimental
    Biology</i>, vol. 227, no. 1. The Company of Biologists, 2024.
  ista: Pal A, Joshi M, Thaker M. 2024. Too much information? Males convey parasite
    levels using more signal modalities than females utilise. Journal of Experimental
    Biology. 227(1), jeb246217.
  mla: Pal, Arka, et al. “Too Much Information? Males Convey Parasite Levels Using
    More Signal Modalities than Females Utilise.” <i>Journal of Experimental Biology</i>,
    vol. 227, no. 1, jeb246217, The Company of Biologists, 2024, doi:<a href="https://doi.org/10.1242/jeb.246217">10.1242/jeb.246217</a>.
  short: A. Pal, M. Joshi, M. Thaker, Journal of Experimental Biology 227 (2024).
corr_author: '1'
date_created: 2024-01-22T08:14:49Z
date_published: 2024-01-10T00:00:00Z
date_updated: 2025-09-04T11:50:21Z
day: '10'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1242/jeb.246217
external_id:
  isi:
  - '001214515700016'
  pmid:
  - '38054353'
file:
- access_level: open_access
  checksum: 136325372f6f45abaa62a71e2d23bfb6
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-23T12:08:24Z
  date_updated: 2024-01-23T12:08:24Z
  file_id: '14877'
  file_name: 2024_JourExperimBiology_Pal.pdf
  file_size: 594128
  relation: main_file
  success: 1
file_date_updated: 2024-01-23T12:08:24Z
has_accepted_license: '1'
intvolume: '       227'
isi: 1
issue: '1'
keyword:
- Insect Science
- Molecular Biology
- Animal Science and Zoology
- Aquatic Science
- Physiology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: Journal of Experimental Biology
publication_identifier:
  eissn:
  - 0022-0949
  issn:
  - 1477-9145
publication_status: published
publisher: The Company of Biologists
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://github.com/arka-pal/Cnemaspis-SexualSignaling
scopus_import: '1'
status: public
title: Too much information? Males convey parasite levels using more signal modalities
  than females utilise
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 227
year: '2024'
...
---
OA_type: free access
_id: '12166'
abstract:
- lang: eng
  text: Kerstin Johannesson is a marine ecologist and evolutionary biologist based
    at the Tjärnö Marine Laboratory of the University of Gothenburg, which is situated
    in the beautiful Kosterhavet National Park on the Swedish west coast. Her work,
    using marine periwinkles (especially Littorina saxatilis and L. fabalis) as main
    model systems, has made a remarkable contribution to marine evolutionary biology
    and our understanding of local adaptation and its genetic underpinnings.
article_processing_charge: No
article_type: editorial
author:
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: Roger
  full_name: Butlin, Roger
  last_name: Butlin
citation:
  ama: Westram AM, Butlin R. Professor Kerstin Johannesson–winner of the 2022 Molecular
    Ecology Prize. <i>Molecular Ecology</i>. 2023;32(1):26-29. doi:<a href="https://doi.org/10.1111/mec.16779">10.1111/mec.16779</a>
  apa: Westram, A. M., &#38; Butlin, R. (2023). Professor Kerstin Johannesson–winner
    of the 2022 Molecular Ecology Prize. <i>Molecular Ecology</i>. Wiley. <a href="https://doi.org/10.1111/mec.16779">https://doi.org/10.1111/mec.16779</a>
  chicago: Westram, Anja M, and Roger Butlin. “Professor Kerstin Johannesson–Winner
    of the 2022 Molecular Ecology Prize.” <i>Molecular Ecology</i>. Wiley, 2023. <a
    href="https://doi.org/10.1111/mec.16779">https://doi.org/10.1111/mec.16779</a>.
  ieee: A. M. Westram and R. Butlin, “Professor Kerstin Johannesson–winner of the
    2022 Molecular Ecology Prize,” <i>Molecular Ecology</i>, vol. 32, no. 1. Wiley,
    pp. 26–29, 2023.
  ista: Westram AM, Butlin R. 2023. Professor Kerstin Johannesson–winner of the 2022
    Molecular Ecology Prize. Molecular Ecology. 32(1), 26–29.
  mla: Westram, Anja M., and Roger Butlin. “Professor Kerstin Johannesson–Winner of
    the 2022 Molecular Ecology Prize.” <i>Molecular Ecology</i>, vol. 32, no. 1, Wiley,
    2023, pp. 26–29, doi:<a href="https://doi.org/10.1111/mec.16779">10.1111/mec.16779</a>.
  short: A.M. Westram, R. Butlin, Molecular Ecology 32 (2023) 26–29.
corr_author: '1'
date_created: 2023-01-12T12:10:28Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2025-04-23T08:44:33Z
day: '01'
department:
- _id: NiBa
doi: 10.1111/mec.16779
external_id:
  isi:
  - '000892168800001'
  pmid:
  - '36443277'
intvolume: '        32'
isi: 1
issue: '1'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1111/mec.16779
month: '01'
oa: 1
oa_version: Published Version
page: 26-29
pmid: 1
publication: Molecular Ecology
publication_identifier:
  eissn:
  - 1365-294X
  issn:
  - 0962-1083
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Professor Kerstin Johannesson–winner of the 2022 Molecular Ecology Prize
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2023'
...
---
_id: '14785'
abstract:
- lang: eng
  text: Small cryptic plasmids have no clear effect on the host fitness and their
    functional repertoire remains obscure. The naturally competent cyanobacterium
    Synechocystis sp. PCC 6803 harbours several small cryptic plasmids; whether their
    evolution with this species is supported by horizontal transfer remains understudied.
    Here, we show that the small cryptic plasmid DNA is transferred in the population
    exclusively by natural transformation, where the transfer frequency of plasmid‐encoded
    genes is similar to that of chromosome‐encoded genes. Establishing a system to
    follow gene transfer, we compared the transfer frequency of genes encoded in cryptic
    plasmids pCA2.4 (2378 bp) and pCB2.4 (2345 bp) within and between populations
    of two <jats:italic>Synechocystis</jats:italic> sp. PCC 6803 labtypes (termed
    Kiel and Sevilla). Our results reveal that plasmid gene transfer frequency depends
    on the recipient labtype. Furthermore, gene transfer via whole plasmid uptake
    in the Sevilla labtype ranged among the lowest detected transfer rates in our
    experiments. Our study indicates that horizontal DNA transfer via natural transformation
    is frequent in the evolution of small cryptic plasmids that reside in naturally
    competent organisms. Furthermore, we suggest that the contribution of natural
    transformation to cryptic plasmid persistence in Synechocystis is limited.
acknowledgement: "We thank the lab of Francisco Javier Florencio Bel-lido, Sevilla,
  Spain for supplying theSynechocystislabtype Sevilla used in this work and the lab
  of MartinHagemann, Rostock, Germany for supplying the pIGAplasmidusedinthiswork.WethankNilsHülterforfruitful
  discussions. We thank Fenna Stücker forgraphical illustrations and Katrin Schumann,
  FennaStücker,  and  Lidusha  Manivannan  for  technicalsupport.\r\nChilean National
  Agency for Research andDevelopment (ANID), Grant/Award Number:21191763; DeutscheForschungsgemeinschaft,
  Grant/AwardNumbers: 456882089, RTG2501; EuropeanResearch Council (ERC), Grant/AwardNumber:
  101043835"
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Fabian
  full_name: Nies, Fabian
  last_name: Nies
- first_name: Tanita
  full_name: Wein, Tanita
  last_name: Wein
- first_name: Dustin M.
  full_name: Hanke, Dustin M.
  last_name: Hanke
- first_name: Benjamin L
  full_name: Springstein, Benjamin L
  id: b4eb62ef-ac72-11ed-9503-ed3b4d66c083
  last_name: Springstein
  orcid: 0000-0002-3461-5391
- first_name: Jaime
  full_name: Alcorta, Jaime
  last_name: Alcorta
- first_name: Claudia
  full_name: Taubenheim, Claudia
  last_name: Taubenheim
- first_name: Tal
  full_name: Dagan, Tal
  last_name: Dagan
citation:
  ama: Nies F, Wein T, Hanke DM, et al. Role of natural transformation in the evolution
    of small cryptic plasmids in Synechocystis sp. PCC 6803. <i>Environmental Microbiology
    Reports</i>. 2023;15(6):656-668. doi:<a href="https://doi.org/10.1111/1758-2229.13203">10.1111/1758-2229.13203</a>
  apa: Nies, F., Wein, T., Hanke, D. M., Springstein, B. L., Alcorta, J., Taubenheim,
    C., &#38; Dagan, T. (2023). Role of natural transformation in the evolution of
    small cryptic plasmids in Synechocystis sp. PCC 6803. <i>Environmental Microbiology
    Reports</i>. Wiley. <a href="https://doi.org/10.1111/1758-2229.13203">https://doi.org/10.1111/1758-2229.13203</a>
  chicago: Nies, Fabian, Tanita Wein, Dustin M. Hanke, Benjamin L Springstein, Jaime
    Alcorta, Claudia Taubenheim, and Tal Dagan. “Role of Natural Transformation in
    the Evolution of Small Cryptic Plasmids in Synechocystis Sp. PCC 6803.” <i>Environmental
    Microbiology Reports</i>. Wiley, 2023. <a href="https://doi.org/10.1111/1758-2229.13203">https://doi.org/10.1111/1758-2229.13203</a>.
  ieee: F. Nies <i>et al.</i>, “Role of natural transformation in the evolution of
    small cryptic plasmids in Synechocystis sp. PCC 6803,” <i>Environmental Microbiology
    Reports</i>, vol. 15, no. 6. Wiley, pp. 656–668, 2023.
  ista: Nies F, Wein T, Hanke DM, Springstein BL, Alcorta J, Taubenheim C, Dagan T.
    2023. Role of natural transformation in the evolution of small cryptic plasmids
    in Synechocystis sp. PCC 6803. Environmental Microbiology Reports. 15(6), 656–668.
  mla: Nies, Fabian, et al. “Role of Natural Transformation in the Evolution of Small
    Cryptic Plasmids in Synechocystis Sp. PCC 6803.” <i>Environmental Microbiology
    Reports</i>, vol. 15, no. 6, Wiley, 2023, pp. 656–68, doi:<a href="https://doi.org/10.1111/1758-2229.13203">10.1111/1758-2229.13203</a>.
  short: F. Nies, T. Wein, D.M. Hanke, B.L. Springstein, J. Alcorta, C. Taubenheim,
    T. Dagan, Environmental Microbiology Reports 15 (2023) 656–668.
date_created: 2024-01-10T10:41:07Z
date_published: 2023-12-01T00:00:00Z
date_updated: 2024-01-16T09:46:12Z
day: '01'
ddc:
- '570'
department:
- _id: MaLo
doi: 10.1111/1758-2229.13203
external_id:
  isi:
  - '001080203100001'
  pmid:
  - '37794696'
file:
- access_level: open_access
  checksum: d09ebb68fee61f4e2e09ec286c9cf1d3
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-16T09:42:10Z
  date_updated: 2024-01-16T09:42:10Z
  file_id: '14810'
  file_name: 2023_EnvirMicroBiolReports_Nies.pdf
  file_size: 1518350
  relation: main_file
  success: 1
file_date_updated: 2024-01-16T09:42:10Z
has_accepted_license: '1'
intvolume: '        15'
isi: 1
issue: '6'
keyword:
- Agricultural and Biological Sciences (miscellaneous)
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 656-668
pmid: 1
publication: Environmental Microbiology Reports
publication_identifier:
  eissn:
  - 1758-2229
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Role of natural transformation in the evolution of small cryptic plasmids in
  Synechocystis sp. PCC 6803
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2023'
...
---
_id: '14787'
abstract:
- lang: eng
  text: Understanding the phenotypic and genetic architecture of reproductive isolation
    is a long‐standing goal of speciation research. In several systems, large‐effect
    loci contributing to barrier phenotypes have been characterized, but such causal
    connections are rarely known for more complex genetic architectures. In this study,
    we combine “top‐down” and “bottom‐up” approaches with demographic modelling toward
    an integrated understanding of speciation across a monkeyflower hybrid zone. Previous
    work suggests that pollinator visitation acts as a primary barrier to gene flow
    between two divergent red‐ and yellow‐flowered ecotypes of<jats:italic>Mimulus
    aurantiacus</jats:italic>. Several candidate isolating traits and anonymous single
    nucleotide polymorphism loci under divergent selection have been identified, but
    their genomic positions remain unknown. Here, we report findings from demographic
    analyses that indicate this hybrid zone formed by secondary contact, but that
    subsequent gene flow was restricted by widespread barrier loci across the genome.
    Using a novel, geographic cline‐based genome scan, we demonstrate that candidate
    barrier loci are broadly distributed across the genome, rather than mapping to
    one or a few “islands of speciation.” Quantitative trait locus (QTL) mapping reveals
    that most floral traits are highly polygenic, with little evidence that QTL colocalize,
    indicating that most traits are genetically independent. Finally, we find little
    evidence that QTL and candidate barrier loci overlap, suggesting that some loci
    contribute to other forms of reproductive isolation. Our findings highlight the
    challenges of understanding the genetic architecture of reproductive isolation
    and reveal that barriers to gene flow other than pollinator isolation may play
    an important role in this system.
acknowledgement: We thank Julian Catchen for making modifications to Stacks to aid
  this project. Peter L. Ralph, Thomas Nelson, Roger K. Butlin, Anja M. Westram and
  Nicholas H. Barton provided advice, stimulating discussion and critical feedback.
  The project was supported by National Science Foundation grant DEB-1258199.
article_processing_charge: No
article_type: original
author:
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
- first_name: Madeline A.
  full_name: Chase, Madeline A.
  last_name: Chase
- first_name: Hanna
  full_name: McIntosh, Hanna
  last_name: McIntosh
- first_name: Matthew A.
  full_name: Streisfeld, Matthew A.
  last_name: Streisfeld
citation:
  ama: Stankowski S, Chase MA, McIntosh H, Streisfeld MA. Integrating top‐down and
    bottom‐up approaches to understand the genetic architecture of speciation across
    a monkeyflower hybrid zone. <i>Molecular Ecology</i>. 2023;32(8):2041-2054. doi:<a
    href="https://doi.org/10.1111/mec.16849">10.1111/mec.16849</a>
  apa: Stankowski, S., Chase, M. A., McIntosh, H., &#38; Streisfeld, M. A. (2023).
    Integrating top‐down and bottom‐up approaches to understand the genetic architecture
    of speciation across a monkeyflower hybrid zone. <i>Molecular Ecology</i>. Wiley.
    <a href="https://doi.org/10.1111/mec.16849">https://doi.org/10.1111/mec.16849</a>
  chicago: Stankowski, Sean, Madeline A. Chase, Hanna McIntosh, and Matthew A. Streisfeld.
    “Integrating Top‐down and Bottom‐up Approaches to Understand the Genetic Architecture
    of Speciation across a Monkeyflower Hybrid Zone.” <i>Molecular Ecology</i>. Wiley,
    2023. <a href="https://doi.org/10.1111/mec.16849">https://doi.org/10.1111/mec.16849</a>.
  ieee: S. Stankowski, M. A. Chase, H. McIntosh, and M. A. Streisfeld, “Integrating
    top‐down and bottom‐up approaches to understand the genetic architecture of speciation
    across a monkeyflower hybrid zone,” <i>Molecular Ecology</i>, vol. 32, no. 8.
    Wiley, pp. 2041–2054, 2023.
  ista: Stankowski S, Chase MA, McIntosh H, Streisfeld MA. 2023. Integrating top‐down
    and bottom‐up approaches to understand the genetic architecture of speciation
    across a monkeyflower hybrid zone. Molecular Ecology. 32(8), 2041–2054.
  mla: Stankowski, Sean, et al. “Integrating Top‐down and Bottom‐up Approaches to
    Understand the Genetic Architecture of Speciation across a Monkeyflower Hybrid
    Zone.” <i>Molecular Ecology</i>, vol. 32, no. 8, Wiley, 2023, pp. 2041–54, doi:<a
    href="https://doi.org/10.1111/mec.16849">10.1111/mec.16849</a>.
  short: S. Stankowski, M.A. Chase, H. McIntosh, M.A. Streisfeld, Molecular Ecology
    32 (2023) 2041–2054.
date_created: 2024-01-10T10:44:45Z
date_published: 2023-04-01T00:00:00Z
date_updated: 2024-01-16T10:10:00Z
day: '01'
department:
- _id: NiBa
doi: 10.1111/mec.16849
external_id:
  isi:
  - '000919244600001'
  pmid:
  - '36651268'
intvolume: '        32'
isi: 1
issue: '8'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/2022.01.28.478139
month: '04'
oa: 1
oa_version: Preprint
page: 2041-2054
pmid: 1
publication: Molecular Ecology
publication_identifier:
  eissn:
  - 1365-294X
  issn:
  - 0962-1083
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Integrating top‐down and bottom‐up approaches to understand the genetic architecture
  of speciation across a monkeyflower hybrid zone
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2023'
...
---
_id: '12159'
abstract:
- lang: eng
  text: The term “haplotype block” is commonly used in the developing field of haplotype-based
    inference methods. We argue that the term should be defined based on the structure
    of the Ancestral Recombination Graph (ARG), which contains complete information
    on the ancestry of a sample. We use simulated examples to demonstrate key features
    of the relationship between haplotype blocks and ancestral structure, emphasizing
    the stochasticity of the processes that generate them. Even the simplest cases
    of neutrality or of a “hard” selective sweep produce a rich structure, often missed
    by commonly used statistics. We highlight a number of novel methods for inferring
    haplotype structure, based on the full ARG, or on a sequence of trees, and illustrate
    how they can be used to define haplotype blocks using an empirical data set. While
    the advent of new, computationally efficient methods makes it possible to apply
    these concepts broadly, they (and additional new methods) could benefit from adding
    features to explore haplotype blocks, as we define them. Understanding and applying
    the concept of the haplotype block will be essential to fully exploit long and
    linked-read sequencing technologies.
acknowledgement: 'We thank the Barton group for useful discussion and feedback during
  the writing of this article. Comments from Roger Butlin, Molly Schumer''s Group,
  the tskit development team, editors and three reviewers greatly improved the manuscript.
  Funding was provided by SCAS (Natural Sciences Programme, Knut and Alice Wallenberg
  Foundation), an FWF Wittgenstein grant (PT1001Z211), an FWF standalone grant (grant
  P 32166), and an ERC Advanced Grant. YFC was supported by the Max Planck Society
  and an ERC Proof of Concept Grant #101069216 (HAPLOTAGGING).'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Daria
  full_name: Shipilina, Daria
  id: 428A94B0-F248-11E8-B48F-1D18A9856A87
  last_name: Shipilina
  orcid: 0000-0002-1145-9226
- first_name: Arka
  full_name: Pal, Arka
  id: 6AAB2240-CA9A-11E9-9C1A-D9D1E5697425
  last_name: Pal
  orcid: 0000-0002-4530-8469
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
- first_name: Yingguang Frank
  full_name: Chan, Yingguang Frank
  last_name: Chan
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: Shipilina D, Pal A, Stankowski S, Chan YF, Barton NH. On the origin and structure
    of haplotype blocks. <i>Molecular Ecology</i>. 2023;32(6):1441-1457. doi:<a href="https://doi.org/10.1111/mec.16793">10.1111/mec.16793</a>
  apa: Shipilina, D., Pal, A., Stankowski, S., Chan, Y. F., &#38; Barton, N. H. (2023).
    On the origin and structure of haplotype blocks. <i>Molecular Ecology</i>. Wiley.
    <a href="https://doi.org/10.1111/mec.16793">https://doi.org/10.1111/mec.16793</a>
  chicago: Shipilina, Daria, Arka Pal, Sean Stankowski, Yingguang Frank Chan, and
    Nicholas H Barton. “On the Origin and Structure of Haplotype Blocks.” <i>Molecular
    Ecology</i>. Wiley, 2023. <a href="https://doi.org/10.1111/mec.16793">https://doi.org/10.1111/mec.16793</a>.
  ieee: D. Shipilina, A. Pal, S. Stankowski, Y. F. Chan, and N. H. Barton, “On the
    origin and structure of haplotype blocks,” <i>Molecular Ecology</i>, vol. 32,
    no. 6. Wiley, pp. 1441–1457, 2023.
  ista: Shipilina D, Pal A, Stankowski S, Chan YF, Barton NH. 2023. On the origin
    and structure of haplotype blocks. Molecular Ecology. 32(6), 1441–1457.
  mla: Shipilina, Daria, et al. “On the Origin and Structure of Haplotype Blocks.”
    <i>Molecular Ecology</i>, vol. 32, no. 6, Wiley, 2023, pp. 1441–57, doi:<a href="https://doi.org/10.1111/mec.16793">10.1111/mec.16793</a>.
  short: D. Shipilina, A. Pal, S. Stankowski, Y.F. Chan, N.H. Barton, Molecular Ecology
    32 (2023) 1441–1457.
corr_author: '1'
date_created: 2023-01-12T12:09:17Z
date_published: 2023-03-01T00:00:00Z
date_updated: 2026-04-26T22:30:13Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/mec.16793
external_id:
  isi:
  - '000900762000001'
  pmid:
  - '36433653'
file:
- access_level: open_access
  checksum: b10e0f8fa3dc4d72aaf77a557200978a
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T08:15:41Z
  date_updated: 2023-08-16T08:15:41Z
  file_id: '14062'
  file_name: 2023_MolecularEcology_Shipilina.pdf
  file_size: 7144607
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T08:15:41Z
has_accepted_license: '1'
intvolume: '        32'
isi: 1
issue: '6'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 1441-1457
pmid: 1
project:
- _id: 05959E1C-7A3F-11EA-A408-12923DDC885E
  grant_number: P32166
  name: Snapdragon Speciation
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
- _id: bd6958e0-d553-11ed-ba76-86eba6a76c00
  grant_number: '101055327'
  name: Understanding the evolution of continuous genomes
publication: Molecular Ecology
publication_identifier:
  eissn:
  - 1365-294X
  issn:
  - 0962-1083
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '20694'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: On the origin and structure of haplotype blocks
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2023'
...
---
_id: '12521'
abstract:
- lang: eng
  text: Differentiated X chromosomes are expected to have higher rates of adaptive
    divergence than autosomes, if new beneficial mutations are recessive (the “faster-X
    effect”), largely because these mutations are immediately exposed to selection
    in males. The evolution of X chromosomes after they stop recombining in males,
    but before they become hemizygous, has not been well explored theoretically. We
    use the diffusion approximation to infer substitution rates of beneficial and
    deleterious mutations under such a scenario. Our results show that selection is
    less efficient on diploid X loci than on autosomal and hemizygous X loci under
    a wide range of parameters. This “slower-X” effect is stronger for genes affecting
    primarily (or only) male fitness, and for sexually antagonistic genes. These unusual
    dynamics suggest that some of the peculiar features of X chromosomes, such as
    the differential accumulation of genes with sex-specific functions, may start
    arising earlier than previously appreciated.
acknowledgement: We thank the Vicoso and Barton groups and ISTA Scientific Computing
  Unit. We also thank two anonymous reviewers for their valuable comments. This work
  was supported by the European Research Council under the European Union’s Horizon
  2020 research and innovation program (grant agreements no. 715257 and no. 716117).
article_number: qrac004
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Andrea
  full_name: Mrnjavac, Andrea
  id: 353FAC84-AE61-11E9-8BFC-00D3E5697425
  last_name: Mrnjavac
- first_name: Kseniia
  full_name: Khudiakova, Kseniia
  id: 4E6DC800-AE37-11E9-AC72-31CAE5697425
  last_name: Khudiakova
  orcid: 0000-0002-6246-1465
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
- first_name: Beatriz
  full_name: Vicoso, Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
  orcid: 0000-0002-4579-8306
citation:
  ama: 'Mrnjavac A, Khudiakova K, Barton NH, Vicoso B. Slower-X: Reduced efficiency
    of selection in the early stages of X chromosome evolution. <i>Evolution Letters</i>.
    2023;7(1). doi:<a href="https://doi.org/10.1093/evlett/qrac004">10.1093/evlett/qrac004</a>'
  apa: 'Mrnjavac, A., Khudiakova, K., Barton, N. H., &#38; Vicoso, B. (2023). Slower-X:
    Reduced efficiency of selection in the early stages of X chromosome evolution.
    <i>Evolution Letters</i>. Oxford University Press. <a href="https://doi.org/10.1093/evlett/qrac004">https://doi.org/10.1093/evlett/qrac004</a>'
  chicago: 'Mrnjavac, Andrea, Kseniia Khudiakova, Nicholas H Barton, and Beatriz Vicoso.
    “Slower-X: Reduced Efficiency of Selection in the Early Stages of X Chromosome
    Evolution.” <i>Evolution Letters</i>. Oxford University Press, 2023. <a href="https://doi.org/10.1093/evlett/qrac004">https://doi.org/10.1093/evlett/qrac004</a>.'
  ieee: 'A. Mrnjavac, K. Khudiakova, N. H. Barton, and B. Vicoso, “Slower-X: Reduced
    efficiency of selection in the early stages of X chromosome evolution,” <i>Evolution
    Letters</i>, vol. 7, no. 1. Oxford University Press, 2023.'
  ista: 'Mrnjavac A, Khudiakova K, Barton NH, Vicoso B. 2023. Slower-X: Reduced efficiency
    of selection in the early stages of X chromosome evolution. Evolution Letters.
    7(1), qrac004.'
  mla: 'Mrnjavac, Andrea, et al. “Slower-X: Reduced Efficiency of Selection in the
    Early Stages of X Chromosome Evolution.” <i>Evolution Letters</i>, vol. 7, no.
    1, qrac004, Oxford University Press, 2023, doi:<a href="https://doi.org/10.1093/evlett/qrac004">10.1093/evlett/qrac004</a>.'
  short: A. Mrnjavac, K. Khudiakova, N.H. Barton, B. Vicoso, Evolution Letters 7 (2023).
corr_author: '1'
date_created: 2023-02-06T13:59:12Z
date_published: 2023-02-01T00:00:00Z
date_updated: 2026-04-26T22:30:23Z
day: '01'
ddc:
- '570'
department:
- _id: GradSch
- _id: BeVi
doi: 10.1093/evlett/qrac004
ec_funded: 1
external_id:
  isi:
  - '001021692200001'
  pmid:
  - '37065438'
file:
- access_level: open_access
  checksum: a240a041cb9b9b7c8ba93a4706674a3f
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T11:43:33Z
  date_updated: 2023-08-16T11:43:33Z
  file_id: '14068'
  file_name: 2023_EvLetters_Mrnjavac.pdf
  file_size: 2592189
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T11:43:33Z
has_accepted_license: '1'
intvolume: '         7'
isi: 1
issue: '1'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 256E75B8-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '716117'
  name: Optimal Transport and Stochastic Dynamics
- _id: 250BDE62-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715257'
  name: Prevalence and Influence of Sexual Antagonism on Genome Evolution
publication: Evolution Letters
publication_identifier:
  issn:
  - 2056-3744
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
related_material:
  record:
  - id: '18531'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 'Slower-X: Reduced efficiency of selection in the early stages of X chromosome
  evolution'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2023'
...
---
_id: '14613'
abstract:
- lang: eng
  text: 'Many insects carry an ancient X chromosome - the Drosophila Muller element
    F - that likely predates their origin. Interestingly, the X has undergone turnover
    in multiple fly species (Diptera) after being conserved for more than 450 MY.
    The long evolutionary distance between Diptera and other sequenced insect clades
    makes it difficult to infer what could have contributed to this sudden increase
    in rate of turnover. Here, we produce the first genome and transcriptome of a
    long overlooked sister-order to Diptera: Mecoptera. We compare the scorpionfly
    Panorpa cognata X-chromosome gene content, expression, and structure, to that
    of several dipteran species as well as more distantly-related insect orders (Orthoptera
    and Blattodea). We find high conservation of gene content between the mecopteran
    X and the dipteran Muller F element, as well as several shared biological features,
    such as the presence of dosage compensation and a low amount of genetic diversity,
    consistent with a low recombination rate. However, the two homologous X chromosomes
    differ strikingly in their size and number of genes they carry. Our results therefore
    support a common ancestry of the mecopteran and ancestral dipteran X chromosomes,
    and suggest that Muller element F shrank in size and gene content after the split
    of Diptera and Mecoptera, which may have contributed to its turnover in dipteran
    insects.'
acknowledged_ssus:
- _id: ScienComp
acknowledgement: "We thank the Vicoso lab for their assistance with specimen collection,
  and Tim Connallon for valuable comments and suggestions on earlier versions of the
  manuscript. Computational resources and support were provided by the Scientific
  Computing unit at the ISTA. This research was supported by grants from the Austrian
  Science Foundation to C.L.\r\n(FWF ESP 39), and to B.V. (FWF SFB F88-10)."
article_number: msad245
article_processing_charge: Yes
article_type: original
author:
- first_name: Clementine
  full_name: Lasne, Clementine
  id: 02225f57-50d2-11eb-9ed8-8c92b9a34237
  last_name: Lasne
  orcid: 0000-0002-1197-8616
- first_name: Marwan N
  full_name: Elkrewi, Marwan N
  id: 0B46FACA-A8E1-11E9-9BD3-79D1E5697425
  last_name: Elkrewi
  orcid: 0000-0002-5328-7231
- first_name: Melissa A
  full_name: Toups, Melissa A
  id: 4E099E4E-F248-11E8-B48F-1D18A9856A87
  last_name: Toups
  orcid: 0000-0002-9752-7380
- first_name: Lorena Alexandra
  full_name: Layana Franco, Lorena Alexandra
  id: 02814589-eb8f-11eb-b029-a70074f3f18f
  last_name: Layana Franco
  orcid: 0000-0002-1253-6297
- first_name: Ariana
  full_name: Macon, Ariana
  id: 2A0848E2-F248-11E8-B48F-1D18A9856A87
  last_name: Macon
- first_name: Beatriz
  full_name: Vicoso, Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
  orcid: 0000-0002-4579-8306
citation:
  ama: Lasne C, Elkrewi MN, Toups MA, Layana Franco LA, Macon A, Vicoso B. The scorpionfly
    (Panorpa cognata) genome highlights conserved and derived features of the peculiar
    dipteran X chromosome. <i>Molecular Biology and Evolution</i>. 2023;40(12). doi:<a
    href="https://doi.org/10.1093/molbev/msad245">10.1093/molbev/msad245</a>
  apa: Lasne, C., Elkrewi, M. N., Toups, M. A., Layana Franco, L. A., Macon, A., &#38;
    Vicoso, B. (2023). The scorpionfly (Panorpa cognata) genome highlights conserved
    and derived features of the peculiar dipteran X chromosome. <i>Molecular Biology
    and Evolution</i>. Oxford University Press. <a href="https://doi.org/10.1093/molbev/msad245">https://doi.org/10.1093/molbev/msad245</a>
  chicago: Lasne, Clementine, Marwan N Elkrewi, Melissa A Toups, Lorena Alexandra
    Layana Franco, Ariana Macon, and Beatriz Vicoso. “The Scorpionfly (Panorpa Cognata)
    Genome Highlights Conserved and Derived Features of the Peculiar Dipteran X Chromosome.”
    <i>Molecular Biology and Evolution</i>. Oxford University Press, 2023. <a href="https://doi.org/10.1093/molbev/msad245">https://doi.org/10.1093/molbev/msad245</a>.
  ieee: C. Lasne, M. N. Elkrewi, M. A. Toups, L. A. Layana Franco, A. Macon, and B.
    Vicoso, “The scorpionfly (Panorpa cognata) genome highlights conserved and derived
    features of the peculiar dipteran X chromosome,” <i>Molecular Biology and Evolution</i>,
    vol. 40, no. 12. Oxford University Press, 2023.
  ista: Lasne C, Elkrewi MN, Toups MA, Layana Franco LA, Macon A, Vicoso B. 2023.
    The scorpionfly (Panorpa cognata) genome highlights conserved and derived features
    of the peculiar dipteran X chromosome. Molecular Biology and Evolution. 40(12),
    msad245.
  mla: Lasne, Clementine, et al. “The Scorpionfly (Panorpa Cognata) Genome Highlights
    Conserved and Derived Features of the Peculiar Dipteran X Chromosome.” <i>Molecular
    Biology and Evolution</i>, vol. 40, no. 12, msad245, Oxford University Press,
    2023, doi:<a href="https://doi.org/10.1093/molbev/msad245">10.1093/molbev/msad245</a>.
  short: C. Lasne, M.N. Elkrewi, M.A. Toups, L.A. Layana Franco, A. Macon, B. Vicoso,
    Molecular Biology and Evolution 40 (2023).
corr_author: '1'
date_created: 2023-11-27T16:14:37Z
date_published: 2023-12-01T00:00:00Z
date_updated: 2026-04-26T22:31:06Z
day: '01'
ddc:
- '570'
department:
- _id: BeVi
doi: 10.1093/molbev/msad245
external_id:
  isi:
  - '001122489000003'
  pmid:
  - '37988296'
file:
- access_level: open_access
  checksum: 47c1c72fb499f26ea52d216b242208c8
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-02T11:39:38Z
  date_updated: 2024-01-02T11:39:38Z
  file_id: '14727'
  file_name: 2023_MolecularBioEvo_Lasne.pdf
  file_size: 8623505
  relation: main_file
  success: 1
file_date_updated: 2024-01-02T11:39:38Z
has_accepted_license: '1'
intvolume: '        40'
isi: 1
issue: '12'
keyword:
- Genetics
- Molecular Biology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 34ae1506-11ca-11ed-8bc3-c14f4c474396
  grant_number: F8810
  name: The highjacking of meiosis for asexual reproduction
- _id: ebb230e0-77a9-11ec-83b8-87a37e0241d3
  grant_number: ESP39 49461
  name: Mechanisms and Evolution of Reproductive Plasticity
publication: Molecular Biology and Evolution
publication_identifier:
  eissn:
  - 1537-1719
  issn:
  - 0737-4038
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
related_material:
  link:
  - description: News on ISTA webpage
    relation: press_release
    url: https://ista.ac.at/en/news/on-the-hunt/
  record:
  - id: '14614'
    relation: research_data
    status: public
  - id: '19386'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: The scorpionfly (Panorpa cognata) genome highlights conserved and derived features
  of the peculiar dipteran X chromosome
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 40
year: '2023'
...
---
_id: '12051'
abstract:
- lang: eng
  text: Transcription of the ribosomal RNA precursor by RNA polymerase (Pol) I is
    a major determinant of cellular growth, and dysregulation is observed in many
    cancer types. Here, we present the purification of human Pol I from cells carrying
    a genomic GFP fusion on the largest subunit allowing the structural and functional
    analysis of the enzyme across species. In contrast to yeast, human Pol I carries
    a single-subunit stalk, and in vitro transcription indicates a reduced proofreading
    activity. Determination of the human Pol I cryo-EM reconstruction in a close-to-native
    state rationalizes the effects of disease-associated mutations and uncovers an
    additional domain that is built into the sequence of Pol I subunit RPA1. This
    “dock II” domain resembles a truncated HMG box incapable of DNA binding which
    may serve as a downstream transcription factor–binding platform in metazoans.
    Biochemical analysis, in situ modelling, and ChIP data indicate that Topoisomerase
    2a can be recruited to Pol I via the domain and cooperates with the HMG box domain–containing
    factor UBF. These adaptations of the metazoan Pol I transcription system may allow
    efficient release of positive DNA supercoils accumulating downstream of the transcription
    bubble.
acknowledgement: "The authors especially thank Philip Gunkel for his contribution.
  We thank all\r\npast and present members of the Engel lab, Achim Griesenbeck, Colyn
  Crane-\r\nRobinson, Christophe Lotz, Marlene Vayssieres, Klaus Grasser, Herbert
  Tschochner, and Philipp Milkereit for help and discussion; Gerhard Lehmann and Nobert
  Eichner for IT support; Joost Zomerdijk for UBF-constructs, Volker Cordes for the
  Hela P2 cell line; Remco Sprangers for shared cell culture; Dina Grohmann and the
  Archaea Center for fermentation; and Thomas\r\nDresselhaus for access to fluorescence
  microscopes. This work was in part supported by the Emmy-Noether Programm (DFG grant
  no. EN 1204/1-1 to C Engel) of the German Research Council and Collaborative Research
  Center 960 (TP-A8 to C Engel)."
article_number: e202201568
article_processing_charge: No
article_type: original
author:
- first_name: Julia L
  full_name: Daiß, Julia L
  last_name: Daiß
- first_name: Michael
  full_name: Pilsl, Michael
  last_name: Pilsl
- first_name: Kristina
  full_name: Straub, Kristina
  last_name: Straub
- first_name: Andrea
  full_name: Bleckmann, Andrea
  last_name: Bleckmann
- first_name: Mona
  full_name: Höcherl, Mona
  last_name: Höcherl
- first_name: Florian B
  full_name: Heiss, Florian B
  last_name: Heiss
- first_name: Guillermo
  full_name: Abascal-Palacios, Guillermo
  last_name: Abascal-Palacios
- first_name: Ewan P
  full_name: Ramsay, Ewan P
  last_name: Ramsay
- first_name: Katarina
  full_name: Tluckova, Katarina
  id: 4AC7D980-F248-11E8-B48F-1D18A9856A87
  last_name: Tluckova
- first_name: Jean-Clement
  full_name: Mars, Jean-Clement
  last_name: Mars
- first_name: Torben
  full_name: Fürtges, Torben
  last_name: Fürtges
- first_name: Astrid
  full_name: Bruckmann, Astrid
  last_name: Bruckmann
- first_name: Till
  full_name: Rudack, Till
  last_name: Rudack
- first_name: Carrie A
  full_name: Bernecky, Carrie A
  id: 2CB9DFE2-F248-11E8-B48F-1D18A9856A87
  last_name: Bernecky
  orcid: 0000-0003-0893-7036
- first_name: Valérie
  full_name: Lamour, Valérie
  last_name: Lamour
- first_name: Konstantin
  full_name: Panov, Konstantin
  last_name: Panov
- first_name: Alessandro
  full_name: Vannini, Alessandro
  last_name: Vannini
- first_name: Tom
  full_name: Moss, Tom
  last_name: Moss
- first_name: Christoph
  full_name: Engel, Christoph
  last_name: Engel
citation:
  ama: Daiß JL, Pilsl M, Straub K, et al. The human RNA polymerase I structure reveals
    an HMG-like docking domain specific to metazoans. <i>Life Science Alliance</i>.
    2022;5(11). doi:<a href="https://doi.org/10.26508/lsa.202201568">10.26508/lsa.202201568</a>
  apa: Daiß, J. L., Pilsl, M., Straub, K., Bleckmann, A., Höcherl, M., Heiss, F. B.,
    … Engel, C. (2022). The human RNA polymerase I structure reveals an HMG-like docking
    domain specific to metazoans. <i>Life Science Alliance</i>. Life Science Alliance.
    <a href="https://doi.org/10.26508/lsa.202201568">https://doi.org/10.26508/lsa.202201568</a>
  chicago: Daiß, Julia L, Michael Pilsl, Kristina Straub, Andrea Bleckmann, Mona Höcherl,
    Florian B Heiss, Guillermo Abascal-Palacios, et al. “The Human RNA Polymerase
    I Structure Reveals an HMG-like Docking Domain Specific to Metazoans.” <i>Life
    Science Alliance</i>. Life Science Alliance, 2022. <a href="https://doi.org/10.26508/lsa.202201568">https://doi.org/10.26508/lsa.202201568</a>.
  ieee: J. L. Daiß <i>et al.</i>, “The human RNA polymerase I structure reveals an
    HMG-like docking domain specific to metazoans,” <i>Life Science Alliance</i>,
    vol. 5, no. 11. Life Science Alliance, 2022.
  ista: Daiß JL, Pilsl M, Straub K, Bleckmann A, Höcherl M, Heiss FB, Abascal-Palacios
    G, Ramsay EP, Tluckova K, Mars J-C, Fürtges T, Bruckmann A, Rudack T, Bernecky
    C, Lamour V, Panov K, Vannini A, Moss T, Engel C. 2022. The human RNA polymerase
    I structure reveals an HMG-like docking domain specific to metazoans. Life Science
    Alliance. 5(11), e202201568.
  mla: Daiß, Julia L., et al. “The Human RNA Polymerase I Structure Reveals an HMG-like
    Docking Domain Specific to Metazoans.” <i>Life Science Alliance</i>, vol. 5, no.
    11, e202201568, Life Science Alliance, 2022, doi:<a href="https://doi.org/10.26508/lsa.202201568">10.26508/lsa.202201568</a>.
  short: J.L. Daiß, M. Pilsl, K. Straub, A. Bleckmann, M. Höcherl, F.B. Heiss, G.
    Abascal-Palacios, E.P. Ramsay, K. Tluckova, J.-C. Mars, T. Fürtges, A. Bruckmann,
    T. Rudack, C. Bernecky, V. Lamour, K. Panov, A. Vannini, T. Moss, C. Engel, Life
    Science Alliance 5 (2022).
date_created: 2022-09-06T18:45:23Z
date_published: 2022-09-01T00:00:00Z
date_updated: 2024-10-21T06:01:48Z
day: '01'
ddc:
- '570'
department:
- _id: CaBe
doi: 10.26508/lsa.202201568
external_id:
  isi:
  - '000972702600001'
file:
- access_level: open_access
  checksum: 4201d876a3e5e8b65e319d03300014ad
  content_type: application/pdf
  creator: dernst
  date_created: 2022-09-08T06:41:14Z
  date_updated: 2022-09-08T06:41:14Z
  file_id: '12062'
  file_name: 2022_LifeScienceAlliance_Daiss.pdf
  file_size: 3183129
  relation: main_file
  success: 1
file_date_updated: 2022-09-08T06:41:14Z
has_accepted_license: '1'
intvolume: '         5'
isi: 1
issue: '11'
keyword:
- Health
- Toxicology and Mutagenesis
- Plant Science
- Biochemistry
- Genetics and Molecular Biology (miscellaneous)
- Ecology
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
publication: Life Science Alliance
publication_identifier:
  issn:
  - 2575-1077
publication_status: published
publisher: Life Science Alliance
quality_controlled: '1'
scopus_import: '1'
status: public
title: The human RNA polymerase I structure reveals an HMG-like docking domain specific
  to metazoans
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 5
year: '2022'
...
---
_id: '12152'
abstract:
- lang: eng
  text: ESCRT-III filaments are composite cytoskeletal polymers that can constrict
    and cut cell membranes from the inside of the membrane neck. Membrane-bound ESCRT-III
    filaments undergo a series of dramatic composition and geometry changes in the
    presence of an ATP-consuming Vps4 enzyme, which causes stepwise changes in the
    membrane morphology. We set out to understand the physical mechanisms involved
    in translating the changes in ESCRT-III polymer composition into membrane deformation.
    We have built a coarse-grained model in which ESCRT-III polymers of different
    geometries and mechanical properties are allowed to copolymerise and bind to a
    deformable membrane. By modelling ATP-driven stepwise depolymerisation of specific
    polymers, we identify mechanical regimes in which changes in filament composition
    trigger the associated membrane transition from a flat to a buckled state, and
    then to a tubule state that eventually undergoes scission to release a small cargo-loaded
    vesicle. We then characterise how the location and kinetics of polymer loss affects
    the extent of membrane deformation and the efficiency of membrane neck scission.
    Our results identify the near-minimal mechanical conditions for the operation
    of shape-shifting composite polymers that sever membrane necks.
acknowledgement: "A.S . received an award from European Research Council (https://erc.europa.eu,
  “NEPA\"\r\n802960), and an award from the Royal Society (https://royalsociety.org,
  UF160266). L. H.-K.\r\nreceived an award from the Biotechnology and Biological Sciences
  Research Council (https://\r\nwww.ukri.org/councils/bbsrc/). E. L. received an award
  from the University College London (https://www.ucl.ac.uk/biophysics/news/2022/feb/applications-biop-brian-duff-and-ipls-summerundergraduate-studentships-now-open,
  Brian Duff Undergraduate Summer Research Studentship). B.B. and A.S. received an
  award from Volkswagen Foundation https://www.volkswagenstiftung.de/en/foundation,
  Az 96727), and an award from Medical Research Council (https://www.ukri.org/councils/mrc,
  MC_CF1226). A. R. received an\r\naward from the Swiss National Fund for Research
  (https://www.snf.ch/en, 31003A_130520,\r\n31003A_149975, and 31003A_173087) and
  an award from the European Research Council\r\nConsolidator (https://erc.europa.eu,
  311536). The funders had no role in study design, data collection and analysis,
  decision to publish, or preparation of the manuscript."
article_number: e1010586
article_processing_charge: No
article_type: original
author:
- first_name: Xiuyun
  full_name: Jiang, Xiuyun
  last_name: Jiang
- first_name: Lena
  full_name: Harker-Kirschneck, Lena
  last_name: Harker-Kirschneck
- first_name: Christian Eduardo
  full_name: Vanhille-Campos, Christian Eduardo
  id: 3adeca52-9313-11ed-b1ac-c170b2505714
  last_name: Vanhille-Campos
- first_name: Anna-Katharina
  full_name: Pfitzner, Anna-Katharina
  last_name: Pfitzner
- first_name: Elene
  full_name: Lominadze, Elene
  last_name: Lominadze
- first_name: Aurélien
  full_name: Roux, Aurélien
  last_name: Roux
- first_name: Buzz
  full_name: Baum, Buzz
  last_name: Baum
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
citation:
  ama: Jiang X, Harker-Kirschneck L, Vanhille-Campos CE, et al. Modelling membrane
    reshaping by staged polymerization of ESCRT-III filaments. <i>PLOS Computational
    Biology</i>. 2022;18(10). doi:<a href="https://doi.org/10.1371/journal.pcbi.1010586">10.1371/journal.pcbi.1010586</a>
  apa: Jiang, X., Harker-Kirschneck, L., Vanhille-Campos, C. E., Pfitzner, A.-K.,
    Lominadze, E., Roux, A., … Šarić, A. (2022). Modelling membrane reshaping by staged
    polymerization of ESCRT-III filaments. <i>PLOS Computational Biology</i>. Public
    Library of Science. <a href="https://doi.org/10.1371/journal.pcbi.1010586">https://doi.org/10.1371/journal.pcbi.1010586</a>
  chicago: Jiang, Xiuyun, Lena Harker-Kirschneck, Christian Eduardo Vanhille-Campos,
    Anna-Katharina Pfitzner, Elene Lominadze, Aurélien Roux, Buzz Baum, and Anđela
    Šarić. “Modelling Membrane Reshaping by Staged Polymerization of ESCRT-III Filaments.”
    <i>PLOS Computational Biology</i>. Public Library of Science, 2022. <a href="https://doi.org/10.1371/journal.pcbi.1010586">https://doi.org/10.1371/journal.pcbi.1010586</a>.
  ieee: X. Jiang <i>et al.</i>, “Modelling membrane reshaping by staged polymerization
    of ESCRT-III filaments,” <i>PLOS Computational Biology</i>, vol. 18, no. 10. Public
    Library of Science, 2022.
  ista: Jiang X, Harker-Kirschneck L, Vanhille-Campos CE, Pfitzner A-K, Lominadze
    E, Roux A, Baum B, Šarić A. 2022. Modelling membrane reshaping by staged polymerization
    of ESCRT-III filaments. PLOS Computational Biology. 18(10), e1010586.
  mla: Jiang, Xiuyun, et al. “Modelling Membrane Reshaping by Staged Polymerization
    of ESCRT-III Filaments.” <i>PLOS Computational Biology</i>, vol. 18, no. 10, e1010586,
    Public Library of Science, 2022, doi:<a href="https://doi.org/10.1371/journal.pcbi.1010586">10.1371/journal.pcbi.1010586</a>.
  short: X. Jiang, L. Harker-Kirschneck, C.E. Vanhille-Campos, A.-K. Pfitzner, E.
    Lominadze, A. Roux, B. Baum, A. Šarić, PLOS Computational Biology 18 (2022).
corr_author: '1'
date_created: 2023-01-12T12:08:10Z
date_published: 2022-10-17T00:00:00Z
date_updated: 2025-06-12T06:19:28Z
day: '17'
ddc:
- '570'
department:
- _id: AnSa
doi: 10.1371/journal.pcbi.1010586
ec_funded: 1
external_id:
  isi:
  - '000924885500005'
  pmid:
  - '36251703'
file:
- access_level: open_access
  checksum: bada6a7865e470cf42bbdfa67dd471d2
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-24T10:45:01Z
  date_updated: 2023-01-24T10:45:01Z
  file_id: '12359'
  file_name: 2022_PLoSCompBio_Jiang.pdf
  file_size: 2641067
  relation: main_file
  success: 1
file_date_updated: 2023-01-24T10:45:01Z
has_accepted_license: '1'
intvolume: '        18'
isi: 1
issue: '10'
keyword:
- Computational Theory and Mathematics
- Cellular and Molecular Neuroscience
- Genetics
- Molecular Biology
- Ecology
- Modeling and Simulation
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: eba2549b-77a9-11ec-83b8-a81e493eae4e
  call_identifier: H2020
  grant_number: '802960'
  name: 'Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines'
- _id: eba0f67c-77a9-11ec-83b8-cc8501b3e222
  grant_number: '96752'
  name: 'The evolution of trafficking: from archaea to eukaryotes'
publication: PLOS Computational Biology
publication_identifier:
  issn:
  - 1553-7358
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://github.com/sharonJXY/3-filament-model
scopus_import: '1'
status: public
title: Modelling membrane reshaping by staged polymerization of ESCRT-III filaments
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 18
year: '2022'
...
---
_id: '12234'
abstract:
- lang: eng
  text: Hybrid speciation—the origin of new species resulting from the hybridization
    of genetically divergent lineages—was once considered rare, but genomic data suggest
    that it may occur more often than once thought. In this study, Noguerales and
    Ortego found genomic evidence supporting the hybrid origin of a grasshopper that
    is able to exploit a broader range of host plants than either of its putative
    parents.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
citation:
  ama: 'Stankowski S. Digest: On the origin of a possible hybrid species. <i>Evolution</i>.
    2022;76(11):2784-2785. doi:<a href="https://doi.org/10.1111/evo.14632">10.1111/evo.14632</a>'
  apa: 'Stankowski, S. (2022). Digest: On the origin of a possible hybrid species.
    <i>Evolution</i>. Wiley. <a href="https://doi.org/10.1111/evo.14632">https://doi.org/10.1111/evo.14632</a>'
  chicago: 'Stankowski, Sean. “Digest: On the Origin of a Possible Hybrid Species.”
    <i>Evolution</i>. Wiley, 2022. <a href="https://doi.org/10.1111/evo.14632">https://doi.org/10.1111/evo.14632</a>.'
  ieee: 'S. Stankowski, “Digest: On the origin of a possible hybrid species,” <i>Evolution</i>,
    vol. 76, no. 11. Wiley, pp. 2784–2785, 2022.'
  ista: 'Stankowski S. 2022. Digest: On the origin of a possible hybrid species. Evolution.
    76(11), 2784–2785.'
  mla: 'Stankowski, Sean. “Digest: On the Origin of a Possible Hybrid Species.” <i>Evolution</i>,
    vol. 76, no. 11, Wiley, 2022, pp. 2784–85, doi:<a href="https://doi.org/10.1111/evo.14632">10.1111/evo.14632</a>.'
  short: S. Stankowski, Evolution 76 (2022) 2784–2785.
corr_author: '1'
date_created: 2023-01-16T09:50:48Z
date_published: 2022-11-01T00:00:00Z
date_updated: 2025-06-11T13:40:40Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/evo.14632
external_id:
  isi:
  - '000855751600001'
  pmid:
  - '36112597'
file:
- access_level: open_access
  checksum: 4c0f05083b414ac0323a1b9ee1abc275
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-27T11:28:38Z
  date_updated: 2023-01-27T11:28:38Z
  file_id: '12425'
  file_name: 2022_Evolution_Stankowski.pdf
  file_size: 287282
  relation: main_file
  success: 1
file_date_updated: 2023-01-27T11:28:38Z
has_accepted_license: '1'
intvolume: '        76'
isi: 1
issue: '11'
keyword:
- General Agricultural and Biological Sciences
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '11'
oa: 1
oa_version: Published Version
page: 2784-2785
pmid: 1
publication: Evolution
publication_identifier:
  eissn:
  - 1558-5646
  issn:
  - 0014-3820
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Digest: On the origin of a possible hybrid species'
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 76
year: '2022'
...
---
_id: '12247'
abstract:
- lang: eng
  text: Chromosomal inversions have been shown to play a major role in a local adaptation
    by suppressing recombination between alternative arrangements and maintaining
    beneficial allele combinations. However, so far, their importance relative to
    the remaining genome remains largely unknown. Understanding the genetic architecture
    of adaptation requires better estimates of how loci of different effect sizes
    contribute to phenotypic variation. Here, we used three Swedish islands where
    the marine snail Littorina saxatilis has repeatedly evolved into two distinct
    ecotypes along a habitat transition. We estimated the contribution of inversion
    polymorphisms to phenotypic divergence while controlling for polygenic effects
    in the remaining genome using a quantitative genetics framework. We confirmed
    the importance of inversions but showed that contributions of loci outside inversions
    are of similar magnitude, with variable proportions dependent on the trait and
    the population. Some inversions showed consistent effects across all sites, whereas
    others exhibited site-specific effects, indicating that the genomic basis for
    replicated phenotypic divergence is only partly shared. The contributions of sexual
    dimorphism as well as environmental factors to phenotypic variation were significant
    but minor compared to inversions and polygenic background. Overall, this integrated
    approach provides insight into the multiple mechanisms contributing to parallel
    phenotypic divergence.
acknowledgement: We thank everyone who helped with fieldwork, snail processing, and
  DNA extractions, particularly Laura Brettell, Mårten Duvetorp, Juan Galindo, Anne-Lise
  Liabot, Irena Senčić, and Zuzanna Zagrodzka. We also thank Rui Faria and Jenny Larsson
  for their contributions, with inversions and shell shape respectively. KJ was funded
  by the Swedish research council Vetenskapsrådet, grant number 2017-03798. R.K.B.
  and E.K. were funded by the European Research Council (ERC-2015-AdG-693030-BARRIERS).
  R.K.B. was also funded by the Natural Environment Research Council and the Swedish
  Research Council Vetenskapsrådet.
article_processing_charge: No
article_type: original
author:
- first_name: Eva L.
  full_name: Koch, Eva L.
  last_name: Koch
- first_name: Mark
  full_name: Ravinet, Mark
  last_name: Ravinet
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: Kerstin
  full_name: Johannesson, Kerstin
  last_name: Johannesson
- first_name: Roger K.
  full_name: Butlin, Roger K.
  last_name: Butlin
citation:
  ama: Koch EL, Ravinet M, Westram AM, Johannesson K, Butlin RK. Genetic architecture
    of repeated phenotypic divergence in Littorina saxatilis evolution. <i>Evolution</i>.
    2022;76(10):2332-2346. doi:<a href="https://doi.org/10.1111/evo.14602">10.1111/evo.14602</a>
  apa: Koch, E. L., Ravinet, M., Westram, A. M., Johannesson, K., &#38; Butlin, R.
    K. (2022). Genetic architecture of repeated phenotypic divergence in Littorina
    saxatilis evolution. <i>Evolution</i>. Wiley. <a href="https://doi.org/10.1111/evo.14602">https://doi.org/10.1111/evo.14602</a>
  chicago: Koch, Eva L., Mark Ravinet, Anja M Westram, Kerstin Johannesson, and Roger
    K. Butlin. “Genetic Architecture of Repeated Phenotypic Divergence in Littorina
    Saxatilis Evolution.” <i>Evolution</i>. Wiley, 2022. <a href="https://doi.org/10.1111/evo.14602">https://doi.org/10.1111/evo.14602</a>.
  ieee: E. L. Koch, M. Ravinet, A. M. Westram, K. Johannesson, and R. K. Butlin, “Genetic
    architecture of repeated phenotypic divergence in Littorina saxatilis evolution,”
    <i>Evolution</i>, vol. 76, no. 10. Wiley, pp. 2332–2346, 2022.
  ista: Koch EL, Ravinet M, Westram AM, Johannesson K, Butlin RK. 2022. Genetic architecture
    of repeated phenotypic divergence in Littorina saxatilis evolution. Evolution.
    76(10), 2332–2346.
  mla: Koch, Eva L., et al. “Genetic Architecture of Repeated Phenotypic Divergence
    in Littorina Saxatilis Evolution.” <i>Evolution</i>, vol. 76, no. 10, Wiley, 2022,
    pp. 2332–46, doi:<a href="https://doi.org/10.1111/evo.14602">10.1111/evo.14602</a>.
  short: E.L. Koch, M. Ravinet, A.M. Westram, K. Johannesson, R.K. Butlin, Evolution
    76 (2022) 2332–2346.
date_created: 2023-01-16T09:54:15Z
date_published: 2022-10-01T00:00:00Z
date_updated: 2023-08-04T09:42:11Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/evo.14602
external_id:
  isi:
  - '000848449100001'
  pmid:
  - '35994296'
file:
- access_level: open_access
  checksum: defd8a4bea61cf00a3c88d4a30e2728c
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-30T08:45:35Z
  date_updated: 2023-01-30T08:45:35Z
  file_id: '12439'
  file_name: 2022_Evolution_Koch.pdf
  file_size: 2990581
  relation: main_file
  success: 1
file_date_updated: 2023-01-30T08:45:35Z
has_accepted_license: '1'
intvolume: '        76'
isi: 1
issue: '10'
keyword:
- General Agricultural and Biological Sciences
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 2332-2346
pmid: 1
publication: Evolution
publication_identifier:
  eissn:
  - 1558-5646
  issn:
  - 0014-3820
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '13066'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Genetic architecture of repeated phenotypic divergence in Littorina saxatilis
  evolution
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 76
year: '2022'
...
---
_id: '12264'
abstract:
- lang: eng
  text: Reproductive isolation (RI) is a core concept in evolutionary biology. It
    has been the central focus of speciation research since the modern synthesis and
    is the basis by which biological species are defined. Despite this, the term is
    used in seemingly different ways, and attempts to quantify RI have used very different
    approaches. After showing that the field lacks a clear definition of the term,
    we attempt to clarify key issues, including what RI is, how it can be quantified
    in principle, and how it can be measured in practice. Following other definitions
    with a genetic focus, we propose that RI is a quantitative measure of the effect
    that genetic differences between populations have on gene flow. Specifically,
    RI compares the flow of neutral alleles in the presence of these genetic differences
    to the flow without any such differences. RI is thus greater than zero when genetic
    differences between populations reduce the flow of neutral alleles between populations.
    We show how RI can be quantified in a range of scenarios. A key conclusion is
    that RI depends strongly on circumstances—including the spatial, temporal and
    genomic context—making it difficult to compare across systems. After reviewing
    methods for estimating RI from data, we conclude that it is difficult to measure
    in practice. We discuss our findings in light of the goals of speciation research
    and encourage the use of methods for estimating RI that integrate organismal and
    genetic approaches.
acknowledgement: 'We are grateful to the participants of the ESEB satellite symposium
  ‘Understanding reproductive isolation: bridging conceptual barriers in  speciation  research’  in  2021  for  the  interesting  discussions  that  helped  us  clarify  the  thoughts  presented  in  this  article.  We  thank  Roger
  Butlin, Michael Turelli and two anonymous reviewers for their thoughtful comments
  on this manuscript. We are also very grateful to Roger Butlin and the Barton Group
  for the continued conversa-tions about RI. In addition, we thank all participants
  of the speciation survey. Part of this work was funded by the Austrian Science Fund
  FWF (grant P 32166)'
article_processing_charge: Yes (via OA deal)
article_type: review
author:
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
- first_name: Parvathy
  full_name: Surendranadh, Parvathy
  id: 455235B8-F248-11E8-B48F-1D18A9856A87
  last_name: Surendranadh
  orcid: 0000-0001-6395-386X
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: Westram AM, Stankowski S, Surendranadh P, Barton NH. What is reproductive isolation?
    <i>Journal of Evolutionary Biology</i>. 2022;35(9):1143-1164. doi:<a href="https://doi.org/10.1111/jeb.14005">10.1111/jeb.14005</a>
  apa: Westram, A. M., Stankowski, S., Surendranadh, P., &#38; Barton, N. H. (2022).
    What is reproductive isolation? <i>Journal of Evolutionary Biology</i>. Wiley.
    <a href="https://doi.org/10.1111/jeb.14005">https://doi.org/10.1111/jeb.14005</a>
  chicago: Westram, Anja M, Sean Stankowski, Parvathy Surendranadh, and Nicholas H
    Barton. “What Is Reproductive Isolation?” <i>Journal of Evolutionary Biology</i>.
    Wiley, 2022. <a href="https://doi.org/10.1111/jeb.14005">https://doi.org/10.1111/jeb.14005</a>.
  ieee: A. M. Westram, S. Stankowski, P. Surendranadh, and N. H. Barton, “What is
    reproductive isolation?,” <i>Journal of Evolutionary Biology</i>, vol. 35, no.
    9. Wiley, pp. 1143–1164, 2022.
  ista: Westram AM, Stankowski S, Surendranadh P, Barton NH. 2022. What is reproductive
    isolation? Journal of Evolutionary Biology. 35(9), 1143–1164.
  mla: Westram, Anja M., et al. “What Is Reproductive Isolation?” <i>Journal of Evolutionary
    Biology</i>, vol. 35, no. 9, Wiley, 2022, pp. 1143–64, doi:<a href="https://doi.org/10.1111/jeb.14005">10.1111/jeb.14005</a>.
  short: A.M. Westram, S. Stankowski, P. Surendranadh, N.H. Barton, Journal of Evolutionary
    Biology 35 (2022) 1143–1164.
corr_author: '1'
date_created: 2023-01-16T09:59:24Z
date_published: 2022-09-01T00:00:00Z
date_updated: 2025-04-15T08:20:40Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/jeb.14005
external_id:
  isi:
  - '000849851100002'
  pmid:
  - '36063156'
file:
- access_level: open_access
  checksum: f08de57112330a7ee88d2e1b20576a1e
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-30T10:05:31Z
  date_updated: 2023-01-30T10:05:31Z
  file_id: '12448'
  file_name: 2022_JourEvoBiology_Westram.pdf
  file_size: 3146793
  relation: main_file
  success: 1
file_date_updated: 2023-01-30T10:05:31Z
has_accepted_license: '1'
intvolume: '        35'
isi: 1
issue: '9'
keyword:
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 1143-1164
pmid: 1
project:
- _id: 05959E1C-7A3F-11EA-A408-12923DDC885E
  grant_number: P32166
  name: Snapdragon Speciation
publication: Journal of Evolutionary Biology
publication_identifier:
  eissn:
  - 1420-9101
  issn:
  - 1010-061X
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '12265'
    relation: other
    status: public
scopus_import: '1'
status: public
title: What is reproductive isolation?
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 35
year: '2022'
...
---
_id: '12265'
acknowledgement: We  are  very  grateful  to  the  authors  of  the  commentaries  for  the  interesting
  discussion and to Luke Holman for handling this set of manuscripts. Part of this
  work was funded by the Austrian Science Fund FWF (grant P 32166).
article_processing_charge: Yes (via OA deal)
article_type: letter_note
author:
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
- first_name: Parvathy
  full_name: Surendranadh, Parvathy
  id: 455235B8-F248-11E8-B48F-1D18A9856A87
  last_name: Surendranadh
  orcid: 0000-0001-6395-386X
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: 'Westram AM, Stankowski S, Surendranadh P, Barton NH. Reproductive isolation,
    speciation, and the value of disagreement: A reply to the commentaries on ‘What
    is reproductive isolation?’ <i>Journal of Evolutionary Biology</i>. 2022;35(9):1200-1205.
    doi:<a href="https://doi.org/10.1111/jeb.14082">10.1111/jeb.14082</a>'
  apa: 'Westram, A. M., Stankowski, S., Surendranadh, P., &#38; Barton, N. H. (2022).
    Reproductive isolation, speciation, and the value of disagreement: A reply to
    the commentaries on ‘What is reproductive isolation?’ <i>Journal of Evolutionary
    Biology</i>. Wiley. <a href="https://doi.org/10.1111/jeb.14082">https://doi.org/10.1111/jeb.14082</a>'
  chicago: 'Westram, Anja M, Sean Stankowski, Parvathy Surendranadh, and Nicholas
    H Barton. “Reproductive Isolation, Speciation, and the Value of Disagreement:
    A Reply to the Commentaries on ‘What Is Reproductive Isolation?’” <i>Journal of
    Evolutionary Biology</i>. Wiley, 2022. <a href="https://doi.org/10.1111/jeb.14082">https://doi.org/10.1111/jeb.14082</a>.'
  ieee: 'A. M. Westram, S. Stankowski, P. Surendranadh, and N. H. Barton, “Reproductive
    isolation, speciation, and the value of disagreement: A reply to the commentaries
    on ‘What is reproductive isolation?,’” <i>Journal of Evolutionary Biology</i>,
    vol. 35, no. 9. Wiley, pp. 1200–1205, 2022.'
  ista: 'Westram AM, Stankowski S, Surendranadh P, Barton NH. 2022. Reproductive isolation,
    speciation, and the value of disagreement: A reply to the commentaries on ‘What
    is reproductive isolation?’ Journal of Evolutionary Biology. 35(9), 1200–1205.'
  mla: 'Westram, Anja M., et al. “Reproductive Isolation, Speciation, and the Value
    of Disagreement: A Reply to the Commentaries on ‘What Is Reproductive Isolation?’”
    <i>Journal of Evolutionary Biology</i>, vol. 35, no. 9, Wiley, 2022, pp. 1200–05,
    doi:<a href="https://doi.org/10.1111/jeb.14082">10.1111/jeb.14082</a>.'
  short: A.M. Westram, S. Stankowski, P. Surendranadh, N.H. Barton, Journal of Evolutionary
    Biology 35 (2022) 1200–1205.
corr_author: '1'
date_created: 2023-01-16T09:59:37Z
date_published: 2022-09-01T00:00:00Z
date_updated: 2025-04-15T08:20:40Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/jeb.14082
external_id:
  isi:
  - '000849851100009'
file:
- access_level: open_access
  checksum: 27268009e5eec030bc10667a4ac5ed4c
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-30T10:14:09Z
  date_updated: 2023-01-30T10:14:09Z
  file_id: '12449'
  file_name: 2022_JourEvoBiology_Westram_Response.pdf
  file_size: 349603
  relation: main_file
  success: 1
file_date_updated: 2023-01-30T10:14:09Z
has_accepted_license: '1'
intvolume: '        35'
isi: 1
issue: '9'
keyword:
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 1200-1205
project:
- _id: 05959E1C-7A3F-11EA-A408-12923DDC885E
  grant_number: P32166
  name: Snapdragon Speciation
publication: Journal of Evolutionary Biology
publication_identifier:
  eissn:
  - 1420-9101
  issn:
  - 1010-061X
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '12264'
    relation: other
    status: public
scopus_import: '1'
status: public
title: 'Reproductive isolation, speciation, and the value of disagreement: A reply
  to the commentaries on ‘What is reproductive isolation?’'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 35
year: '2022'
...
---
_id: '12280'
abstract:
- lang: eng
  text: 'In repeated interactions, players can use strategies that respond to the
    outcome of previous rounds. Much of the existing literature on direct reciprocity
    assumes that all competing individuals use the same strategy space. Here, we study
    both learning and evolutionary dynamics of players that differ in the strategy
    space they explore. We focus on the infinitely repeated donation game and compare
    three natural strategy spaces: memory-1 strategies, which consider the last moves
    of both players, reactive strategies, which respond to the last move of the co-player,
    and unconditional strategies. These three strategy spaces differ in the memory
    capacity that is needed. We compute the long term average payoff that is achieved
    in a pairwise learning process. We find that smaller strategy spaces can dominate
    larger ones. For weak selection, unconditional players dominate both reactive
    and memory-1 players. For intermediate selection, reactive players dominate memory-1
    players. Only for strong selection and low cost-to-benefit ratio, memory-1 players
    dominate the others. We observe that the supergame between strategy spaces can
    be a social dilemma: maximum payoff is achieved if both players explore a larger
    strategy space, but smaller strategy spaces dominate.'
acknowledgement: "This work was supported by the European Research Council (https://erc.europa.eu/)\r\nCoG
  863818 (ForM-SMArt) (to K.C.), and the European Research Council Starting Grant
  850529: E-DIRECT (to C.H.). The funders had no role in study design, data collection
  and analysis, decision to publish, or preparation of the manuscript."
article_number: e1010149
article_processing_charge: No
article_type: original
author:
- first_name: Laura
  full_name: Schmid, Laura
  id: 38B437DE-F248-11E8-B48F-1D18A9856A87
  last_name: Schmid
  orcid: 0000-0002-6978-7329
- first_name: Christian
  full_name: Hilbe, Christian
  id: 2FDF8F3C-F248-11E8-B48F-1D18A9856A87
  last_name: Hilbe
  orcid: 0000-0001-5116-955X
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Martin
  full_name: Nowak, Martin
  last_name: Nowak
citation:
  ama: Schmid L, Hilbe C, Chatterjee K, Nowak M. Direct reciprocity between individuals
    that use different strategy spaces. <i>PLOS Computational Biology</i>. 2022;18(6).
    doi:<a href="https://doi.org/10.1371/journal.pcbi.1010149">10.1371/journal.pcbi.1010149</a>
  apa: Schmid, L., Hilbe, C., Chatterjee, K., &#38; Nowak, M. (2022). Direct reciprocity
    between individuals that use different strategy spaces. <i>PLOS Computational
    Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pcbi.1010149">https://doi.org/10.1371/journal.pcbi.1010149</a>
  chicago: Schmid, Laura, Christian Hilbe, Krishnendu Chatterjee, and Martin Nowak.
    “Direct Reciprocity between Individuals That Use Different Strategy Spaces.” <i>PLOS
    Computational Biology</i>. Public Library of Science, 2022. <a href="https://doi.org/10.1371/journal.pcbi.1010149">https://doi.org/10.1371/journal.pcbi.1010149</a>.
  ieee: L. Schmid, C. Hilbe, K. Chatterjee, and M. Nowak, “Direct reciprocity between
    individuals that use different strategy spaces,” <i>PLOS Computational Biology</i>,
    vol. 18, no. 6. Public Library of Science, 2022.
  ista: Schmid L, Hilbe C, Chatterjee K, Nowak M. 2022. Direct reciprocity between
    individuals that use different strategy spaces. PLOS Computational Biology. 18(6),
    e1010149.
  mla: Schmid, Laura, et al. “Direct Reciprocity between Individuals That Use Different
    Strategy Spaces.” <i>PLOS Computational Biology</i>, vol. 18, no. 6, e1010149,
    Public Library of Science, 2022, doi:<a href="https://doi.org/10.1371/journal.pcbi.1010149">10.1371/journal.pcbi.1010149</a>.
  short: L. Schmid, C. Hilbe, K. Chatterjee, M. Nowak, PLOS Computational Biology
    18 (2022).
corr_author: '1'
date_created: 2023-01-16T10:02:51Z
date_published: 2022-06-14T00:00:00Z
date_updated: 2025-04-14T07:52:47Z
day: '14'
ddc:
- '000'
- '570'
department:
- _id: KrCh
doi: 10.1371/journal.pcbi.1010149
ec_funded: 1
external_id:
  isi:
  - '000843626800031'
  pmid:
  - '35700167'
file:
- access_level: open_access
  checksum: 31b6b311b6731f1658277a9dfff6632c
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-30T11:28:13Z
  date_updated: 2023-01-30T11:28:13Z
  file_id: '12460'
  file_name: 2022_PlosCompBio_Schmid.pdf
  file_size: 3143222
  relation: main_file
  success: 1
file_date_updated: 2023-01-30T11:28:13Z
has_accepted_license: '1'
intvolume: '        18'
isi: 1
issue: '6'
keyword:
- Computational Theory and Mathematics
- Cellular and Molecular Neuroscience
- Genetics
- Molecular Biology
- Ecology
- Modeling and Simulation
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
publication: PLOS Computational Biology
publication_identifier:
  eissn:
  - 1553-7358
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Direct reciprocity between individuals that use different strategy spaces
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 18
year: '2022'
...
---
_id: '10604'
abstract:
- lang: eng
  text: Maternally inherited Wolbachia transinfections are being introduced into natural
    mosquito populations to reduce the transmission of dengue, Zika, and other arboviruses.
    Wolbachia-induced cytoplasmic incompatibility provides a frequency-dependent reproductive
    advantage to infected females that can spread transinfections within and among
    populations. However, because transinfections generally reduce host fitness, they
    tend to spread within populations only after their frequency exceeds a critical
    threshold. This produces bistability with stable equilibrium frequencies at both
    0 and 1, analogous to the bistability produced by underdominance between alleles
    or karyotypes and by population dynamics under Allee effects. Here, we analyze
    how stochastic frequency variation produced by finite population size can facilitate
    the local spread of variants with bistable dynamics into areas where invasion
    is unexpected from deterministic models. Our exemplar is the establishment of
    wMel Wolbachia in the Aedes aegypti population of Pyramid Estates (PE), a small
    community in far north Queensland, Australia. In 2011, wMel was stably introduced
    into Gordonvale, separated from PE by barriers to A. aegypti dispersal. After
    nearly 6 years during which wMel was observed only at low frequencies in PE, corresponding
    to an apparent equilibrium between immigration and selection, wMel rose to fixation
    by 2018. Using analytic approximations and statistical analyses, we demonstrate
    that the observed fixation of wMel at PE is consistent with both stochastic transition
    past an unstable threshold frequency and deterministic transformation produced
    by steady immigration at a rate just above the threshold required for deterministic
    invasion. The indeterminacy results from a delicate balance of parameters needed
    to produce the delayed transition observed. Our analyses suggest that once Wolbachia
    transinfections are established locally through systematic introductions, stochastic
    “threshold crossing” is likely to only minimally enhance spatial spread, providing
    a local ratchet that slightly—but systematically—aids area-wide transformation
    of disease-vector populations in heterogeneous landscapes.
acknowledgement: We thank S. O'Neill, C. Simmons, and the World Mosquito Project for
  providing access to unpublished data. S. Ritchie provided valuable insights into
  Aedes aegypti biology and the literature describing A. aegypti populations near
  Cairns. We thank B. Cooper for help with the figures and D. Shropshire, S. O'Neill,
  S. Ritchie, A. Hoffmann, B. Cooper, and members of the Cooper lab for comments on
  an earlier draft. Comments from three reviewers greatly improved our presentation.
article_processing_charge: No
article_type: original
author:
- first_name: Michael
  full_name: Turelli, Michael
  last_name: Turelli
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: Turelli M, Barton NH. Why did the Wolbachia transinfection cross the road?
    Drift, deterministic dynamics, and disease control. <i>Evolution Letters</i>.
    2022;6(1):92-105. doi:<a href="https://doi.org/10.1002/evl3.270">10.1002/evl3.270</a>
  apa: Turelli, M., &#38; Barton, N. H. (2022). Why did the Wolbachia transinfection
    cross the road? Drift, deterministic dynamics, and disease control. <i>Evolution
    Letters</i>. Wiley. <a href="https://doi.org/10.1002/evl3.270">https://doi.org/10.1002/evl3.270</a>
  chicago: Turelli, Michael, and Nicholas H Barton. “Why Did the Wolbachia Transinfection
    Cross the Road? Drift, Deterministic Dynamics, and Disease Control.” <i>Evolution
    Letters</i>. Wiley, 2022. <a href="https://doi.org/10.1002/evl3.270">https://doi.org/10.1002/evl3.270</a>.
  ieee: M. Turelli and N. H. Barton, “Why did the Wolbachia transinfection cross the
    road? Drift, deterministic dynamics, and disease control,” <i>Evolution Letters</i>,
    vol. 6, no. 1. Wiley, pp. 92–105, 2022.
  ista: Turelli M, Barton NH. 2022. Why did the Wolbachia transinfection cross the
    road? Drift, deterministic dynamics, and disease control. Evolution Letters. 6(1),
    92–105.
  mla: Turelli, Michael, and Nicholas H. Barton. “Why Did the Wolbachia Transinfection
    Cross the Road? Drift, Deterministic Dynamics, and Disease Control.” <i>Evolution
    Letters</i>, vol. 6, no. 1, Wiley, 2022, pp. 92–105, doi:<a href="https://doi.org/10.1002/evl3.270">10.1002/evl3.270</a>.
  short: M. Turelli, N.H. Barton, Evolution Letters 6 (2022) 92–105.
date_created: 2022-01-09T09:45:17Z
date_published: 2022-02-01T00:00:00Z
date_updated: 2025-06-11T13:45:56Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1002/evl3.270
external_id:
  isi:
  - '000754412600008'
  pmid:
  - '35127140'
file:
- access_level: open_access
  checksum: 7e9a37e3b65b480cd7014a6a4a7e460a
  content_type: application/pdf
  creator: dernst
  date_created: 2022-07-29T06:59:10Z
  date_updated: 2022-07-29T06:59:10Z
  file_id: '11689'
  file_name: 2022_EvolutionLetters_Turelli.pdf
  file_size: 2435185
  relation: main_file
  success: 1
file_date_updated: 2022-07-29T06:59:10Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
issue: '1'
keyword:
- genetics
- ecology
- evolution
- behavior and systematics
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 92-105
pmid: 1
publication: Evolution Letters
publication_identifier:
  eissn:
  - 2056-3744
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '11686'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Why did the Wolbachia transinfection cross the road? Drift, deterministic dynamics,
  and disease control
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6
year: '2022'
...
---
_id: '15272'
abstract:
- lang: eng
  text: The assembly of neuronal circuits involves the migrations of neurons from
    their place of birth to their final location in the nervous system, as well as
    the coordinated growth and patterning of axons and dendrites. In screens for genes
    required for patterning of the nervous system, we identified the <jats:italic>catp-8/P5A-ATPase</jats:italic>
    as an important regulator of neural patterning. P5A-ATPases are part of the P-type
    ATPases, a family of proteins known to serve a conserved function as transporters
    of ions, lipids and polyamines in unicellular eukaryotes, plants, and humans.
    While the function of many P-type ATPases is relatively well understood, the function
    of P5A-ATPases in metazoans remained elusive. We show here, that the <jats:italic>Caenorhabditis
    elegans</jats:italic> ortholog <jats:italic>catp-8/P5A-ATPase</jats:italic> is
    required for defined aspects of nervous system development. Specifically, the
    <jats:italic>catp-8/P5A-ATPase</jats:italic> serves functions in shaping the elaborately
    sculpted dendritic trees of somatosensory PVD neurons. Moreover, <jats:italic>catp-8/P5A-ATPase</jats:italic>
    is required for axonal guidance and repulsion at the midline, as well as embryonic
    and postembryonic neuronal migrations. Interestingly, not all axons at the midline
    require <jats:italic>catp-8/P5A-ATPase</jats:italic>, although the axons run in
    the same fascicles and navigate the same space. Similarly, not all neuronal migrations
    require <jats:italic>catp-8/P5A-ATPase</jats:italic>. A CATP-8/P5A-ATPase reporter
    is localized to the ER in most, if not all, tissues and <jats:italic>catp-8/P5A-ATPase</jats:italic>
    can function both cell-autonomously and non-autonomously to regulate neuronal
    development. Genetic analyses establish that <jats:italic>catp-8/P5A-ATPase</jats:italic>
    can function in multiple pathways, including the Menorin pathway, previously shown
    to control dendritic patterning in PVD, and Wnt signaling, which functions to
    control neuronal migrations. Lastly, we show that <jats:italic>catp-8/P5A-ATPase</jats:italic>
    is required for localizing select transmembrane proteins necessary for dendrite
    morphogenesis. Collectively, our studies suggest that <jats:italic>catp-8/P5A-ATPase</jats:italic>
    serves diverse, yet specific, roles in different genetic pathways and may be involved
    in the regulation or localization of transmembrane and secreted proteins to specific
    subcellular compartments.
article_number: e1009475
article_processing_charge: No
article_type: original
author:
- first_name: Leo T. H.
  full_name: Tang, Leo T. H.
  last_name: Tang
- first_name: Meera
  full_name: Trivedi, Meera
  last_name: Trivedi
- first_name: Jenna
  full_name: Freund, Jenna
  last_name: Freund
- first_name: Christopher J.
  full_name: Salazar, Christopher J.
  last_name: Salazar
- first_name: Maisha
  full_name: Rahman, Maisha
  last_name: Rahman
- first_name: Nelson
  full_name: Ramirez, Nelson
  id: 39831956-E4FE-11E9-85DE-0DC7E5697425
  last_name: Ramirez
- first_name: Garrett
  full_name: Lee, Garrett
  last_name: Lee
- first_name: Yu
  full_name: Wang, Yu
  last_name: Wang
- first_name: Barth D.
  full_name: Grant, Barth D.
  last_name: Grant
- first_name: Hannes E.
  full_name: Bülow, Hannes E.
  last_name: Bülow
citation:
  ama: Tang LTH, Trivedi M, Freund J, et al. The CATP-8/P5A-type ATPase functions
    in multiple pathways during neuronal patterning. <i>PLOS Genetics</i>. 2021;17(7).
    doi:<a href="https://doi.org/10.1371/journal.pgen.1009475">10.1371/journal.pgen.1009475</a>
  apa: Tang, L. T. H., Trivedi, M., Freund, J., Salazar, C. J., Rahman, M., Ramirez,
    N., … Bülow, H. E. (2021). The CATP-8/P5A-type ATPase functions in multiple pathways
    during neuronal patterning. <i>PLOS Genetics</i>. Public Library of Science. <a
    href="https://doi.org/10.1371/journal.pgen.1009475">https://doi.org/10.1371/journal.pgen.1009475</a>
  chicago: Tang, Leo T. H., Meera Trivedi, Jenna Freund, Christopher J. Salazar, Maisha
    Rahman, Nelson Ramirez, Garrett Lee, Yu Wang, Barth D. Grant, and Hannes E. Bülow.
    “The CATP-8/P5A-Type ATPase Functions in Multiple Pathways during Neuronal Patterning.”
    <i>PLOS Genetics</i>. Public Library of Science, 2021. <a href="https://doi.org/10.1371/journal.pgen.1009475">https://doi.org/10.1371/journal.pgen.1009475</a>.
  ieee: L. T. H. Tang <i>et al.</i>, “The CATP-8/P5A-type ATPase functions in multiple
    pathways during neuronal patterning,” <i>PLOS Genetics</i>, vol. 17, no. 7. Public
    Library of Science, 2021.
  ista: Tang LTH, Trivedi M, Freund J, Salazar CJ, Rahman M, Ramirez N, Lee G, Wang
    Y, Grant BD, Bülow HE. 2021. The CATP-8/P5A-type ATPase functions in multiple
    pathways during neuronal patterning. PLOS Genetics. 17(7), e1009475.
  mla: Tang, Leo T. H., et al. “The CATP-8/P5A-Type ATPase Functions in Multiple Pathways
    during Neuronal Patterning.” <i>PLOS Genetics</i>, vol. 17, no. 7, e1009475, Public
    Library of Science, 2021, doi:<a href="https://doi.org/10.1371/journal.pgen.1009475">10.1371/journal.pgen.1009475</a>.
  short: L.T.H. Tang, M. Trivedi, J. Freund, C.J. Salazar, M. Rahman, N. Ramirez,
    G. Lee, Y. Wang, B.D. Grant, H.E. Bülow, PLOS Genetics 17 (2021).
date_created: 2024-04-03T07:57:12Z
date_published: 2021-07-01T00:00:00Z
date_updated: 2024-04-10T08:57:16Z
day: '01'
ddc:
- '570'
department:
- _id: MaDe
doi: 10.1371/journal.pgen.1009475
external_id:
  pmid:
  - '34197450'
file:
- access_level: open_access
  checksum: 7352b195e4db6d404f702fe6ad8b55ad
  content_type: application/pdf
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  date_created: 2024-04-10T08:53:43Z
  date_updated: 2024-04-10T08:53:43Z
  file_id: '15308'
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  relation: main_file
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file_date_updated: 2024-04-10T08:53:43Z
has_accepted_license: '1'
intvolume: '        17'
issue: '7'
keyword:
- Cancer Research
- Genetics (clinical)
- Genetics
- Molecular Biology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLOS Genetics
publication_identifier:
  issn:
  - 1553-7404
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
status: public
title: The CATP-8/P5A-type ATPase functions in multiple pathways during neuronal patterning
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 17
year: '2021'
...
---
_id: '10568'
abstract:
- lang: eng
  text: Genetic adaptation and phenotypic plasticity facilitate the migration into
    new habitats and enable organisms to cope with a rapidly changing environment.
    In contrast to genetic adaptation that spans multiple generations as an evolutionary
    process, phenotypic plasticity allows acclimation within the life-time of an organism.
    Genetic adaptation and phenotypic plasticity are usually studied in isolation,
    however, only by including their interactive impact, we can understand acclimation
    and adaptation in nature. We aimed to explore the contribution of adaptation and
    plasticity in coping with an abiotic (salinity) and a biotic (Vibrio bacteria)
    stressor using six different populations of the broad-nosed pipefish Syngnathus
    typhle that originated from either high [14–17 Practical Salinity Unit (PSU)]
    or low (7–11 PSU) saline environments along the German coastline of the Baltic
    Sea. We exposed wild caught animals, to either high (15 PSU) or low (7 PSU) salinity,
    representing native and novel salinity conditions and allowed animals to mate.
    After male pregnancy, offspring was split and each half was exposed to one of
    the two salinities and infected with Vibrio alginolyticus bacteria that were evolved
    at either of the two salinities in a fully reciprocal design. We investigated
    life-history traits of fathers and expression of 47 target genes in mothers and
    offspring. Pregnant males originating from high salinity exposed to low salinity
    were highly susceptible to opportunistic fungi infections resulting in decreased
    offspring size and number. In contrast, no signs of fungal infection were identified
    in fathers originating from low saline conditions suggesting that genetic adaptation
    has the potential to overcome the challenges encountered at low salinity. Offspring
    from parents with low saline origin survived better at low salinity suggesting
    genetic adaptation to low salinity. In addition, gene expression analyses of juveniles
    indicated patterns of local adaptation, trans-generational plasticity and developmental
    plasticity. In conclusion, our study suggests that pipefish are locally adapted
    to the low salinity in their environment, however, they are retaining phenotypic
    plasticity, which allows them to also cope with ancestral salinity levels and
    prevailing pathogens.
acknowledgement: We are grateful for the help of Kristina Dauven, Andreas Ebner, Janina
  Röckner, and Paulina Urban for fish collection in the field and fish maintenance.
  Furthermore, we thank Fabian Wendt for setting up the aquaria system and Tatjana
  Liese, Paulina Urban, Jakob Gismann, and Thorsten Reusch for support with DNA extraction
  and analysis of pipefish population structure. The authors acknowledge support of
  Isabel Tanger, Agnes Piecyk, Jonas Müller, Grace Walls, Sebastian Albrecht, Julia
  Böge, and Julia Stefanschitz for their support in preparing cDNA and running of
  Fluidigm chips. A special thank goes to Diana Gill for general lab support, ordering
  materials and just being the good spirit of our molecular lab, to Till Bayer for
  bioinformatics support and to Melanie Heckwolf for fruitful discussion and feedback
  on the manuscript. HG is very grateful for inspirational office space with ocean
  view provided by Lisa Hentschel and family. This manuscript has been released as
  a pre-print at BIORXIV.
article_number: '626442'
article_processing_charge: No
article_type: original
author:
- first_name: Henry
  full_name: Goehlich, Henry
  last_name: Goehlich
- first_name: Linda
  full_name: Sartoris, Linda
  id: 2B9284CA-F248-11E8-B48F-1D18A9856A87
  last_name: Sartoris
- first_name: Kim-Sara
  full_name: Wagner, Kim-Sara
  last_name: Wagner
- first_name: Carolin C.
  full_name: Wendling, Carolin C.
  last_name: Wendling
- first_name: Olivia
  full_name: Roth, Olivia
  last_name: Roth
citation:
  ama: Goehlich H, Sartoris L, Wagner K-S, Wendling CC, Roth O. Pipefish locally adapted
    to low salinity in the Baltic Sea retain phenotypic plasticity to cope with ancestral
    salinity levels. <i>Frontiers in Ecology and Evolution</i>. 2021;9. doi:<a href="https://doi.org/10.3389/fevo.2021.626442">10.3389/fevo.2021.626442</a>
  apa: Goehlich, H., Sartoris, L., Wagner, K.-S., Wendling, C. C., &#38; Roth, O.
    (2021). Pipefish locally adapted to low salinity in the Baltic Sea retain phenotypic
    plasticity to cope with ancestral salinity levels. <i>Frontiers in Ecology and
    Evolution</i>. Frontiers Media. <a href="https://doi.org/10.3389/fevo.2021.626442">https://doi.org/10.3389/fevo.2021.626442</a>
  chicago: Goehlich, Henry, Linda Sartoris, Kim-Sara Wagner, Carolin C. Wendling,
    and Olivia Roth. “Pipefish Locally Adapted to Low Salinity in the Baltic Sea Retain
    Phenotypic Plasticity to Cope with Ancestral Salinity Levels.” <i>Frontiers in
    Ecology and Evolution</i>. Frontiers Media, 2021. <a href="https://doi.org/10.3389/fevo.2021.626442">https://doi.org/10.3389/fevo.2021.626442</a>.
  ieee: H. Goehlich, L. Sartoris, K.-S. Wagner, C. C. Wendling, and O. Roth, “Pipefish
    locally adapted to low salinity in the Baltic Sea retain phenotypic plasticity
    to cope with ancestral salinity levels,” <i>Frontiers in Ecology and Evolution</i>,
    vol. 9. Frontiers Media, 2021.
  ista: Goehlich H, Sartoris L, Wagner K-S, Wendling CC, Roth O. 2021. Pipefish locally
    adapted to low salinity in the Baltic Sea retain phenotypic plasticity to cope
    with ancestral salinity levels. Frontiers in Ecology and Evolution. 9, 626442.
  mla: Goehlich, Henry, et al. “Pipefish Locally Adapted to Low Salinity in the Baltic
    Sea Retain Phenotypic Plasticity to Cope with Ancestral Salinity Levels.” <i>Frontiers
    in Ecology and Evolution</i>, vol. 9, 626442, Frontiers Media, 2021, doi:<a href="https://doi.org/10.3389/fevo.2021.626442">10.3389/fevo.2021.626442</a>.
  short: H. Goehlich, L. Sartoris, K.-S. Wagner, C.C. Wendling, O. Roth, Frontiers
    in Ecology and Evolution 9 (2021).
date_created: 2021-12-20T07:53:19Z
date_published: 2021-03-25T00:00:00Z
date_updated: 2023-08-17T06:27:22Z
day: '25'
ddc:
- '597'
department:
- _id: SyCr
doi: 10.3389/fevo.2021.626442
external_id:
  isi:
  - '000637736300001'
file:
- access_level: open_access
  checksum: 8d6e2b767bb0240a9b5a3a3555be51fd
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  creator: alisjak
  date_created: 2021-12-20T10:44:20Z
  date_updated: 2021-12-20T10:44:20Z
  file_id: '10572'
  file_name: 2021_Frontiers_Goehlich.pdf
  file_size: 3175085
  relation: main_file
  success: 1
file_date_updated: 2021-12-20T10:44:20Z
has_accepted_license: '1'
intvolume: '         9'
isi: 1
keyword:
- ecology
- evolution
- behavior and systematics
- trans-generational plasticity
- genetic adaptation
- local adaptation
- phenotypic plasticity
- Baltic Sea
- climate change
- salinity
- syngnathids
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
publication: Frontiers in Ecology and Evolution
publication_identifier:
  issn:
  - 2296-701X
publication_status: published
publisher: Frontiers Media
quality_controlled: '1'
scopus_import: '1'
status: public
title: Pipefish locally adapted to low salinity in the Baltic Sea retain phenotypic
  plasticity to cope with ancestral salinity levels
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 9
year: '2021'
...
---
_id: '10838'
abstract:
- lang: eng
  text: Combining hybrid zone analysis with genomic data is a promising approach to
    understanding the genomic basis of adaptive divergence. It allows for the identification
    of genomic regions underlying barriers to gene flow. It also provides insights
    into spatial patterns of allele frequency change, informing about the interplay
    between environmental factors, dispersal and selection. However, when only a single
    hybrid zone is analysed, it is difficult to separate patterns generated by selection
    from those resulting from chance. Therefore, it is beneficial to look for repeatable
    patterns across replicate hybrid zones in the same system. We applied this approach
    to the marine snail Littorina saxatilis, which contains two ecotypes, adapted
    to wave-exposed rocks vs. high-predation boulder fields. The existence of numerous
    hybrid zones between ecotypes offered the opportunity to test for the repeatability
    of genomic architectures and spatial patterns of divergence. We sampled and phenotyped
    snails from seven replicate hybrid zones on the Swedish west coast and genotyped
    them for thousands of single nucleotide polymorphisms. Shell shape and size showed
    parallel clines across all zones. Many genomic regions showing steep clines and/or
    high differentiation were shared among hybrid zones, consistent with a common
    evolutionary history and extensive gene flow between zones, and supporting the
    importance of these regions for divergence. In particular, we found that several
    large putative inversions contribute to divergence in all locations. Additionally,
    we found evidence for consistent displacement of clines from the boulder–rock
    transition. Our results demonstrate patterns of spatial variation that would not
    be accessible without continuous spatial sampling, a large genomic data set and
    replicate hybrid zones.
acknowledgement: "We thank everyone who helped with fieldwork, snail processing and
  DNA extractions, particularly Laura Brettell, Mårten Duvetorp, Juan Galindo, Anne-Lise
  Liabot, Mark Ravinet, Irena Senčić and Zuzanna Zagrodzka. We are also grateful to
  Edinburgh Genomics for library preparation and sequencing, to Stuart Baird and Mark
  Ravinet for helpful discussions, and to three anonymous reviewers for their constructive
  comments. This work was supported by the Natural Environment Research Council (NE/K014021/1),
  the European Research Council (AdG-693030-BARRIERS), Swedish Research Councils Formas
  and Vetenskapsrådet through a Linnaeus grant to the Centre for Marine Evolutionary
  Biology (217-2008-1719), the European Regional Development Fund (POCI-01-0145-FEDER-030628),
  and the Fundação para a iência e a Tecnologia,\r\nPortugal (PTDC/BIA-EVL/\r\n30628/2017).
  A.M.W. and R.F. were\r\nfunded by the European Union’s Horizon 2020 research and
  innovation\r\nprogramme under Marie Skłodowska-Curie\r\ngrant agreements\r\nno.
  754411/797747 and no. 706376, respectively."
article_processing_charge: No
article_type: original
author:
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: Rui
  full_name: Faria, Rui
  last_name: Faria
- first_name: Kerstin
  full_name: Johannesson, Kerstin
  last_name: Johannesson
- first_name: Roger
  full_name: Butlin, Roger
  last_name: Butlin
citation:
  ama: Westram AM, Faria R, Johannesson K, Butlin R. Using replicate hybrid zones
    to understand the genomic basis of adaptive divergence. <i>Molecular Ecology</i>.
    2021;30(15):3797-3814. doi:<a href="https://doi.org/10.1111/mec.15861">10.1111/mec.15861</a>
  apa: Westram, A. M., Faria, R., Johannesson, K., &#38; Butlin, R. (2021). Using
    replicate hybrid zones to understand the genomic basis of adaptive divergence.
    <i>Molecular Ecology</i>. Wiley. <a href="https://doi.org/10.1111/mec.15861">https://doi.org/10.1111/mec.15861</a>
  chicago: Westram, Anja M, Rui Faria, Kerstin Johannesson, and Roger Butlin. “Using
    Replicate Hybrid Zones to Understand the Genomic Basis of Adaptive Divergence.”
    <i>Molecular Ecology</i>. Wiley, 2021. <a href="https://doi.org/10.1111/mec.15861">https://doi.org/10.1111/mec.15861</a>.
  ieee: A. M. Westram, R. Faria, K. Johannesson, and R. Butlin, “Using replicate hybrid
    zones to understand the genomic basis of adaptive divergence,” <i>Molecular Ecology</i>,
    vol. 30, no. 15. Wiley, pp. 3797–3814, 2021.
  ista: Westram AM, Faria R, Johannesson K, Butlin R. 2021. Using replicate hybrid
    zones to understand the genomic basis of adaptive divergence. Molecular Ecology.
    30(15), 3797–3814.
  mla: Westram, Anja M., et al. “Using Replicate Hybrid Zones to Understand the Genomic
    Basis of Adaptive Divergence.” <i>Molecular Ecology</i>, vol. 30, no. 15, Wiley,
    2021, pp. 3797–814, doi:<a href="https://doi.org/10.1111/mec.15861">10.1111/mec.15861</a>.
  short: A.M. Westram, R. Faria, K. Johannesson, R. Butlin, Molecular Ecology 30 (2021)
    3797–3814.
corr_author: '1'
date_created: 2022-03-08T11:28:32Z
date_published: 2021-08-01T00:00:00Z
date_updated: 2024-10-09T21:01:47Z
day: '01'
ddc:
- '570'
department:
- _id: BeVi
doi: 10.1111/mec.15861
external_id:
  isi:
  - '000669439700001'
  pmid:
  - '33638231'
file:
- access_level: open_access
  checksum: d5611f243ceb63a0e091d6662ebd9cda
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  creator: dernst
  date_created: 2022-03-08T11:31:30Z
  date_updated: 2022-03-08T11:31:30Z
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  file_size: 1726548
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  success: 1
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keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 3797-3814
pmid: 1
publication: Molecular Ecology
publication_identifier:
  eissn:
  - 1365-294X
  issn:
  - 0962-1083
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Using replicate hybrid zones to understand the genomic basis of adaptive divergence
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
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  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 30
year: '2021'
...
---
_id: '9252'
abstract:
- lang: eng
  text: 'This paper analyses the conditions for local adaptation in a metapopulation
    with infinitely many islands under a model of hard selection, where population
    size depends on local fitness. Each island belongs to one of two distinct ecological
    niches or habitats. Fitness is influenced by an additive trait which is under
    habitat‐dependent directional selection. Our analysis is based on the diffusion
    approximation and accounts for both genetic drift and demographic stochasticity.
    By neglecting linkage disequilibria, it yields the joint distribution of allele
    frequencies and population size on each island. We find that under hard selection,
    the conditions for local adaptation in a rare habitat are more restrictive for
    more polygenic traits: even moderate migration load per locus at very many loci
    is sufficient for population sizes to decline. This further reduces the efficacy
    of selection at individual loci due to increased drift and because smaller populations
    are more prone to swamping due to migration, causing a positive feedback between
    increasing maladaptation and declining population sizes. Our analysis also highlights
    the importance of demographic stochasticity, which exacerbates the decline in
    numbers of maladapted populations, leading to population collapse in the rare
    habitat at significantly lower migration than predicted by deterministic arguments.'
acknowledgement: We thank the reviewers for their helpful comments, and also our colleagues,
  for illuminating discussions over the long gestation of this paper.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Eniko
  full_name: Szep, Eniko
  id: 485BB5A4-F248-11E8-B48F-1D18A9856A87
  last_name: Szep
- first_name: Himani
  full_name: Sachdeva, Himani
  id: 42377A0A-F248-11E8-B48F-1D18A9856A87
  last_name: Sachdeva
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: 'Szep E, Sachdeva H, Barton NH. Polygenic local adaptation in metapopulations:
    A stochastic eco‐evolutionary model. <i>Evolution</i>. 2021;75(5):1030-1045. doi:<a
    href="https://doi.org/10.1111/evo.14210">10.1111/evo.14210</a>'
  apa: 'Szep, E., Sachdeva, H., &#38; Barton, N. H. (2021). Polygenic local adaptation
    in metapopulations: A stochastic eco‐evolutionary model. <i>Evolution</i>. Wiley.
    <a href="https://doi.org/10.1111/evo.14210">https://doi.org/10.1111/evo.14210</a>'
  chicago: 'Szep, Eniko, Himani Sachdeva, and Nicholas H Barton. “Polygenic Local
    Adaptation in Metapopulations: A Stochastic Eco‐evolutionary Model.” <i>Evolution</i>.
    Wiley, 2021. <a href="https://doi.org/10.1111/evo.14210">https://doi.org/10.1111/evo.14210</a>.'
  ieee: 'E. Szep, H. Sachdeva, and N. H. Barton, “Polygenic local adaptation in metapopulations:
    A stochastic eco‐evolutionary model,” <i>Evolution</i>, vol. 75, no. 5. Wiley,
    pp. 1030–1045, 2021.'
  ista: 'Szep E, Sachdeva H, Barton NH. 2021. Polygenic local adaptation in metapopulations:
    A stochastic eco‐evolutionary model. Evolution. 75(5), 1030–1045.'
  mla: 'Szep, Eniko, et al. “Polygenic Local Adaptation in Metapopulations: A Stochastic
    Eco‐evolutionary Model.” <i>Evolution</i>, vol. 75, no. 5, Wiley, 2021, pp. 1030–45,
    doi:<a href="https://doi.org/10.1111/evo.14210">10.1111/evo.14210</a>.'
  short: E. Szep, H. Sachdeva, N.H. Barton, Evolution 75 (2021) 1030–1045.
corr_author: '1'
date_created: 2021-03-20T08:22:10Z
date_published: 2021-05-01T00:00:00Z
date_updated: 2025-06-12T06:35:39Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/evo.14210
external_id:
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  - '000636966300001'
  pmid:
  - '33742441'
file:
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  file_size: 734102
  relation: main_file
  success: 1
file_date_updated: 2021-08-11T13:39:19Z
has_accepted_license: '1'
intvolume: '        75'
isi: 1
issue: '5'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
- General Agricultural and Biological Sciences
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 1030-1045
pmid: 1
publication: Evolution
publication_identifier:
  eissn:
  - 1558-5646
  issn:
  - 0014-3820
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
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    relation: research_data
    status: public
scopus_import: '1'
status: public
title: 'Polygenic local adaptation in metapopulations: A stochastic eco‐evolutionary
  model'
tmp:
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    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 75
year: '2021'
...
---
_id: '9374'
abstract:
- lang: eng
  text: If there are no constraints on the process of speciation, then the number
    of species might be expected to match the number of available niches and this
    number might be indefinitely large. One possible constraint is the opportunity
    for allopatric divergence. In 1981, Felsenstein used a simple and elegant model
    to ask if there might also be genetic constraints. He showed that progress towards
    speciation could be described by the build‐up of linkage disequilibrium among
    divergently selected loci and between these loci and those contributing to other
    forms of reproductive isolation. Therefore, speciation is opposed by recombination,
    because it tends to break down linkage disequilibria. Felsenstein then introduced
    a crucial distinction between “two‐allele” models, which are subject to this effect,
    and “one‐allele” models, which are free from the recombination constraint. These
    fundamentally important insights have been the foundation for both empirical and
    theoretical studies of speciation ever since.
acknowledgement: RKB was funded by the Natural Environment Research Council (NE/P012272/1
  & NE/P001610/1), the European Research Council (693030 BARRIERS), and the Swedish
  Research Council (VR) (2018‐03695). MRS was funded by the National Science Foundation
  (Grant No. DEB1939290).
article_processing_charge: No
article_type: original
author:
- first_name: Roger K.
  full_name: Butlin, Roger K.
  last_name: Butlin
- first_name: Maria R.
  full_name: Servedio, Maria R.
  last_name: Servedio
- first_name: Carole M.
  full_name: Smadja, Carole M.
  last_name: Smadja
- first_name: Claudia
  full_name: Bank, Claudia
  last_name: Bank
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
- first_name: Samuel M.
  full_name: Flaxman, Samuel M.
  last_name: Flaxman
- first_name: Tatiana
  full_name: Giraud, Tatiana
  last_name: Giraud
- first_name: Robin
  full_name: Hopkins, Robin
  last_name: Hopkins
- first_name: Erica L.
  full_name: Larson, Erica L.
  last_name: Larson
- first_name: Martine E.
  full_name: Maan, Martine E.
  last_name: Maan
- first_name: Joana
  full_name: Meier, Joana
  last_name: Meier
- first_name: Richard
  full_name: Merrill, Richard
  last_name: Merrill
- first_name: Mohamed A. F.
  full_name: Noor, Mohamed A. F.
  last_name: Noor
- first_name: Daniel
  full_name: Ortiz‐Barrientos, Daniel
  last_name: Ortiz‐Barrientos
- first_name: Anna
  full_name: Qvarnström, Anna
  last_name: Qvarnström
citation:
  ama: Butlin RK, Servedio MR, Smadja CM, et al. Homage to Felsenstein 1981, or why
    are there so few/many species? <i>Evolution</i>. 2021;75(5):978-988. doi:<a href="https://doi.org/10.1111/evo.14235">10.1111/evo.14235</a>
  apa: Butlin, R. K., Servedio, M. R., Smadja, C. M., Bank, C., Barton, N. H., Flaxman,
    S. M., … Qvarnström, A. (2021). Homage to Felsenstein 1981, or why are there so
    few/many species? <i>Evolution</i>. Wiley. <a href="https://doi.org/10.1111/evo.14235">https://doi.org/10.1111/evo.14235</a>
  chicago: Butlin, Roger K., Maria R. Servedio, Carole M. Smadja, Claudia Bank, Nicholas
    H Barton, Samuel M. Flaxman, Tatiana Giraud, et al. “Homage to Felsenstein 1981,
    or Why Are There so Few/Many Species?” <i>Evolution</i>. Wiley, 2021. <a href="https://doi.org/10.1111/evo.14235">https://doi.org/10.1111/evo.14235</a>.
  ieee: R. K. Butlin <i>et al.</i>, “Homage to Felsenstein 1981, or why are there
    so few/many species?,” <i>Evolution</i>, vol. 75, no. 5. Wiley, pp. 978–988, 2021.
  ista: Butlin RK, Servedio MR, Smadja CM, Bank C, Barton NH, Flaxman SM, Giraud T,
    Hopkins R, Larson EL, Maan ME, Meier J, Merrill R, Noor MAF, Ortiz‐Barrientos
    D, Qvarnström A. 2021. Homage to Felsenstein 1981, or why are there so few/many
    species? Evolution. 75(5), 978–988.
  mla: Butlin, Roger K., et al. “Homage to Felsenstein 1981, or Why Are There so Few/Many
    Species?” <i>Evolution</i>, vol. 75, no. 5, Wiley, 2021, pp. 978–88, doi:<a href="https://doi.org/10.1111/evo.14235">10.1111/evo.14235</a>.
  short: R.K. Butlin, M.R. Servedio, C.M. Smadja, C. Bank, N.H. Barton, S.M. Flaxman,
    T. Giraud, R. Hopkins, E.L. Larson, M.E. Maan, J. Meier, R. Merrill, M.A.F. Noor,
    D. Ortiz‐Barrientos, A. Qvarnström, Evolution 75 (2021) 978–988.
date_created: 2021-05-06T04:34:47Z
date_published: 2021-04-19T00:00:00Z
date_updated: 2024-10-21T06:02:11Z
day: '19'
department:
- _id: NiBa
doi: 10.1111/evo.14235
external_id:
  isi:
  - '000647224000001'
intvolume: '        75'
isi: 1
issue: '5'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
- General Agricultural and Biological Sciences
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://onlinelibrary.wiley.com/doi/10.1111/evo.14235
month: '04'
oa: 1
oa_version: Published Version
page: 978-988
publication: Evolution
publication_identifier:
  eissn:
  - 1558-5646
  issn:
  - 0014-3820
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Homage to Felsenstein 1981, or why are there so few/many species?
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 75
year: '2021'
...
