Cargando…
Functional trade-offs in cribellate silk mediated by spinning behavior
Web-building spiders are an extremely diverse predatory group due to their use of physiologically differentiated silk types in webs. Major shifts in silk functional properties are classically attributed to innovations in silk genes and protein expression. Here, we disentangle the effects of spinning...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591232/ https://www.ncbi.nlm.nih.gov/pubmed/31235797 http://dx.doi.org/10.1038/s41598-019-45552-x |
_version_ | 1783429686399860736 |
---|---|
author | Michalik, Peter Piorkowski, Dakota Blackledge, Todd A. Ramírez, Martín J. |
author_facet | Michalik, Peter Piorkowski, Dakota Blackledge, Todd A. Ramírez, Martín J. |
author_sort | Michalik, Peter |
collection | PubMed |
description | Web-building spiders are an extremely diverse predatory group due to their use of physiologically differentiated silk types in webs. Major shifts in silk functional properties are classically attributed to innovations in silk genes and protein expression. Here, we disentangle the effects of spinning behavior on silk performance of the earliest types of capture threads in spider webs for the first time. Progradungula otwayensis produces two variations of cribellate silk in webs: ladder lines are stereotypically combed with the calamistrum while supporting rail lines contain silk that is naturally uncombed, spun without the intervention of the legs. Combed cribellate silk is highly extensible and adhesive suggesting that the reserve warp and cribellate fibrils brings them into tension only near or after the underlying axial fibers are broken. In contrast, these three fiber components are largely aligned in the uncombed threads and deform as a single composite unit that is 5–10x stronger, but significantly less adhesive, allowing them to act as structural elements in the web. Our study reveals that cribellate silk can occupy a surprisingly diverse performance space, accessible through simple changes in spider behavior, which may have facilitated the impressive diversification of web architectures utilizing this ancient silk. |
format | Online Article Text |
id | pubmed-6591232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65912322019-07-02 Functional trade-offs in cribellate silk mediated by spinning behavior Michalik, Peter Piorkowski, Dakota Blackledge, Todd A. Ramírez, Martín J. Sci Rep Article Web-building spiders are an extremely diverse predatory group due to their use of physiologically differentiated silk types in webs. Major shifts in silk functional properties are classically attributed to innovations in silk genes and protein expression. Here, we disentangle the effects of spinning behavior on silk performance of the earliest types of capture threads in spider webs for the first time. Progradungula otwayensis produces two variations of cribellate silk in webs: ladder lines are stereotypically combed with the calamistrum while supporting rail lines contain silk that is naturally uncombed, spun without the intervention of the legs. Combed cribellate silk is highly extensible and adhesive suggesting that the reserve warp and cribellate fibrils brings them into tension only near or after the underlying axial fibers are broken. In contrast, these three fiber components are largely aligned in the uncombed threads and deform as a single composite unit that is 5–10x stronger, but significantly less adhesive, allowing them to act as structural elements in the web. Our study reveals that cribellate silk can occupy a surprisingly diverse performance space, accessible through simple changes in spider behavior, which may have facilitated the impressive diversification of web architectures utilizing this ancient silk. Nature Publishing Group UK 2019-06-24 /pmc/articles/PMC6591232/ /pubmed/31235797 http://dx.doi.org/10.1038/s41598-019-45552-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Michalik, Peter Piorkowski, Dakota Blackledge, Todd A. Ramírez, Martín J. Functional trade-offs in cribellate silk mediated by spinning behavior |
title | Functional trade-offs in cribellate silk mediated by spinning behavior |
title_full | Functional trade-offs in cribellate silk mediated by spinning behavior |
title_fullStr | Functional trade-offs in cribellate silk mediated by spinning behavior |
title_full_unstemmed | Functional trade-offs in cribellate silk mediated by spinning behavior |
title_short | Functional trade-offs in cribellate silk mediated by spinning behavior |
title_sort | functional trade-offs in cribellate silk mediated by spinning behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591232/ https://www.ncbi.nlm.nih.gov/pubmed/31235797 http://dx.doi.org/10.1038/s41598-019-45552-x |
work_keys_str_mv | AT michalikpeter functionaltradeoffsincribellatesilkmediatedbyspinningbehavior AT piorkowskidakota functionaltradeoffsincribellatesilkmediatedbyspinningbehavior AT blackledgetodda functionaltradeoffsincribellatesilkmediatedbyspinningbehavior AT ramirezmartinj functionaltradeoffsincribellatesilkmediatedbyspinningbehavior |