Unpicking the signal thread of the sector web spider Zygiella x-notata
Identifieur interne : 000228 ( Pmc/Checkpoint ); précédent : 000227; suivant : 000229Unpicking the signal thread of the sector web spider Zygiella x-notata
Auteurs : Beth Mortimer [Royaume-Uni] ; Chris Holland [Royaume-Uni] ; James F. C. Windmill [Royaume-Uni] ; Fritz Vollrath [Royaume-Uni]Source :
- Journal of the Royal Society Interface [ 1742-5689 ] ; 2015.
Abstract
Remote sensing allows an animal to extend its morphology with appropriate conductive materials and sensors providing environmental feedback from spatially removed locations. For example, the sector web spider
Url:
DOI: 10.1098/rsif.2015.0633
PubMed: 26674191
PubMed Central: 4707845
Affiliations:
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PMC:4707845Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Unpicking the signal thread of the sector web spider <italic>Zygiella x-notata</italic>
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<front><div type="abstract" xml:lang="en"><p>Remote sensing allows an animal to extend its morphology with appropriate conductive materials and sensors providing environmental feedback from spatially removed locations. For example, the sector web spider <italic>Zygiella x-notata</italic>
uses a specialized thread as both a structural bridge and signal transmitter to monitor web vibrations from its retreat at the web perimeter. To unravel this model multifunctional system, we investigated <italic>Zygiella</italic>
's signal thread structure with a range of techniques, including tensile testing, laser vibrometry, electron microscopy and behavioural analysis. We found that signal threads varied significantly in the number of filaments; a result of the spider adding a lifeline each time it runs along the bridge. Our mechanical property analysis suggests that while the structure varies, its normalized load does not. We propose that the signal thread represents a complex and fully integrated multifunctional structure where filaments can be added, thus increasing absolute load-bearing capacity while maintaining signal fidelity. We conclude that such structures may serve as inspiration for remote sensing design strategies.</p>
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<journal-id journal-id-type="iso-abbrev">J R Soc Interface</journal-id>
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<issn pub-type="epub">1742-5662</issn>
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<article-meta><article-id pub-id-type="pmid">26674191</article-id>
<article-id pub-id-type="pmc">4707845</article-id>
<article-id pub-id-type="doi">10.1098/rsif.2015.0633</article-id>
<article-id pub-id-type="publisher-id">rsif20150633</article-id>
<article-categories><subj-group subj-group-type="hwp-journal-coll"><subject>1004</subject>
<subject>25</subject>
<subject>23</subject>
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<subj-group subj-group-type="heading"><subject>Research Articles</subject>
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<title-group><article-title>Unpicking the signal thread of the sector web spider <italic>Zygiella x-notata</italic>
</article-title>
<alt-title alt-title-type="short">Unpicking the signal thread of the sector web spider <italic>Zygiella x-notata</italic>
</alt-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Mortimer</surname>
<given-names>Beth</given-names>
</name>
<xref ref-type="aff" rid="af1">1</xref>
<xref ref-type="corresp" rid="cor1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Holland</surname>
<given-names>Chris</given-names>
</name>
<xref ref-type="aff" rid="af2">2</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Windmill</surname>
<given-names>James F. C.</given-names>
</name>
<xref ref-type="aff" rid="af3">3</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Vollrath</surname>
<given-names>Fritz</given-names>
</name>
<xref ref-type="aff" rid="af1">1</xref>
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<aff id="af1"><label>1</label>
<addr-line>Department of Zoology</addr-line>
,<institution>University of Oxford</institution>
,<addr-line>Oxford OX1 3PS</addr-line>
,<country>UK</country>
</aff>
<aff id="af2"><label>2</label>
<addr-line>Department of Materials Science and Engineering</addr-line>
,<institution>University of Sheffield</institution>
,<addr-line>Sheffield S1 3JD</addr-line>
,<country>UK</country>
</aff>
<aff id="af3"><label>3</label>
<addr-line>Department of Electronic and Electrical Engineering</addr-line>
,<institution>University of Strathclyde</institution>
,<addr-line>Glasgow G1 1XW</addr-line>
,<country>UK</country>
</aff>
<author-notes><corresp id="cor1">e-mail: <email>beth.mortimer@zoo.ox.ac.uk</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub"><day>6</day>
<month>12</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>6</day>
<month>12</month>
<year>2015</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the
. </pmc-comment>
<volume>12</volume>
<issue>113</issue>
<elocation-id>20150633</elocation-id>
<history><date date-type="received"><day>14</day>
<month>7</month>
<year>2015</year>
</date>
<date date-type="accepted"><day>23</day>
<month>11</month>
<year>2015</year>
</date>
</history>
<permissions><copyright-statement>© 2015 The Authors.</copyright-statement>
<copyright-year>2015</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>Published by the Royal Society under the terms of the Creative Commons Attribution License <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
, which permits unrestricted use, provided the original author and source are credited.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="rsif20150633.pdf"></self-uri>
<abstract><p>Remote sensing allows an animal to extend its morphology with appropriate conductive materials and sensors providing environmental feedback from spatially removed locations. For example, the sector web spider <italic>Zygiella x-notata</italic>
uses a specialized thread as both a structural bridge and signal transmitter to monitor web vibrations from its retreat at the web perimeter. To unravel this model multifunctional system, we investigated <italic>Zygiella</italic>
's signal thread structure with a range of techniques, including tensile testing, laser vibrometry, electron microscopy and behavioural analysis. We found that signal threads varied significantly in the number of filaments; a result of the spider adding a lifeline each time it runs along the bridge. Our mechanical property analysis suggests that while the structure varies, its normalized load does not. We propose that the signal thread represents a complex and fully integrated multifunctional structure where filaments can be added, thus increasing absolute load-bearing capacity while maintaining signal fidelity. We conclude that such structures may serve as inspiration for remote sensing design strategies.</p>
</abstract>
<kwd-group><kwd>vibration</kwd>
<kwd>spider</kwd>
<kwd>remote sensing</kwd>
<kwd>silk</kwd>
</kwd-group>
<funding-group specific-use="FundRef"><award-group><funding-source><institution-wrap><institution>Magdalen College, Oxford</institution>
</institution-wrap>
</funding-source>
</award-group>
</funding-group>
<funding-group specific-use="FundRef"><award-group><funding-source><institution-wrap><institution>Leverhulme Trust</institution>
<institution-id>http://dx.doi.org/10.13039/501100000275</institution-id>
</institution-wrap>
</funding-source>
<award-id>F/08705/D</award-id>
</award-group>
</funding-group>
<funding-group specific-use="FundRef"><award-group><funding-source><institution-wrap><institution>European Research Council</institution>
<institution-id>http://dx.doi.org/10.13039/501100000781</institution-id>
</institution-wrap>
</funding-source>
<award-id>SP2-GA-2008-233409</award-id>
</award-group>
</funding-group>
<funding-group specific-use="FundRef"><award-group><funding-source><institution-wrap><institution>Engineering and Physical Sciences Research Council</institution>
<institution-id>http://dx.doi.org/10.13039/501100000266</institution-id>
</institution-wrap>
</funding-source>
<award-id>EP/K005693/1</award-id>
</award-group>
</funding-group>
<funding-group specific-use="FundRef"><award-group><funding-source><institution-wrap><institution>Biotechnology and Biological Sciences Research Council</institution>
<institution-id>http://dx.doi.org/10.13039/501100000268</institution-id>
</institution-wrap>
</funding-source>
<award-id>BB/H004637/1</award-id>
</award-group>
</funding-group>
<funding-group specific-use="FundRef"><award-group><funding-source><institution-wrap><institution>Air Force Office of Scientific Research</institution>
<institution-id>http://dx.doi.org/10.13039/100000181</institution-id>
</institution-wrap>
</funding-source>
<award-id>FA9550-12-1-0294</award-id>
</award-group>
</funding-group>
<funding-group specific-use="FundRef"><award-group><funding-source><institution-wrap><institution>Jesus College, Oxford</institution>
</institution-wrap>
</funding-source>
</award-group>
</funding-group>
<custom-meta-group><custom-meta><meta-name>cover-date</meta-name>
<meta-value>December 6, 2015</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body><sec id="s1"><label>1.</label>
<title>Introduction</title>
<p>Substrate-borne vibrations are a common source of information for a wide range of animals and plants [<xref rid="RSIF20150633C1" ref-type="bibr">1</xref>
–<xref rid="RSIF20150633C3" ref-type="bibr">3</xref>
]. Given their universality, monitoring these vibrations is important for both communication and predator–prey interactions [<xref rid="RSIF20150633C1" ref-type="bibr">1</xref>
]. A model system to study the importance of vibration sensing is the spiders, as they are typically highly haptic animals, possess sensitive vibration detectors on their legs and are well known to respond to vibrations [<xref rid="RSIF20150633C4" ref-type="bibr">4</xref>
–<xref rid="RSIF20150633C6" ref-type="bibr">6</xref>
]. Web-building spiders employ their web structure as a vibration transmission platform in addition to its function as a snare [<xref rid="RSIF20150633C7" ref-type="bibr">7</xref>
–<xref rid="RSIF20150633C10" ref-type="bibr">10</xref>
]. Most spiders sit on the web itself in order to best monitor vibrations emanating from potential mates, competing conspecifics, prey or predators [<xref rid="RSIF20150633C11" ref-type="bibr">11</xref>
–<xref rid="RSIF20150633C14" ref-type="bibr">14</xref>
]. However, some spiders adopt a remote sensing technique by using a silk signal thread, which allows them to hide in a retreat safe from predators and parasitoids [<xref rid="RSIF20150633C12" ref-type="bibr">12</xref>
,<xref rid="RSIF20150633C15" ref-type="bibr">15</xref>
], with the associated cost of extra time required to sense, monitor and locate web vibrations [<xref rid="RSIF20150633C16" ref-type="bibr">16</xref>
].</p>
<p><italic>Zygiella x-notata,</italic>
the sector web spider, builds a modified orb web with a mesh-free sector and a radius thread that acts as a signalling thread (<xref ref-type="fig" rid="RSIF20150633F1">figure 1</xref>
). This signal thread is built last during web construction and connects the central hub with the retreat [<xref rid="RSIF20150633C17" ref-type="bibr">17</xref>
], where the spider sits with one or two front legs monitoring the vibration of the signal thread (<xref ref-type="fig" rid="RSIF20150633F1">figure 1</xref>
inset) [<xref rid="RSIF20150633C16" ref-type="bibr">16</xref>
]. The spider will run to the hub along the signal thread when prey hits its web or in response to web vibration, indicating the signal thread's use to transmit vibrational sensory information to the spider [<xref rid="RSIF20150633C16" ref-type="bibr">16</xref>
,<xref rid="RSIF20150633C18" ref-type="bibr">18</xref>
]. As it moves along, the animal drags behind its dragline/lifeline, thus adding that to the signal thread [<xref rid="RSIF20150633C16" ref-type="bibr">16</xref>
] with possible implications for signal transduction and information transmission. While previous studies have examined <italic>Zygiella</italic>
web-building behaviour [<xref rid="RSIF20150633C17" ref-type="bibr">17</xref>
,<xref rid="RSIF20150633C19" ref-type="bibr">19</xref>
–<xref rid="RSIF20150633C21" ref-type="bibr">21</xref>
], none have focused on the structure and properties of the signal thread itself, which is the goal of this investigation.
<fig id="RSIF20150633F1" orientation="portrait" position="float"><label>Figure 1.</label>
<caption><p>Typical web from <italic>Zygiella x-notata</italic>
. The web is a modified orb web; a sector is kept free in a top corner, where the signal thread (purple) runs from the hub to a retreat. Inset is a spider at the retreat in resting position, with front leg on the signal thread. White bars denote 20 mm. (Online version in colour.)</p>
</caption>
<graphic xlink:href="rsif20150633-g1"></graphic>
</fig>
</p>
<p>The signal thread is made of the same material as the radial threads, i.e. dragline silk [<xref rid="RSIF20150633C22" ref-type="bibr">22</xref>
,<xref rid="RSIF20150633C23" ref-type="bibr">23</xref>
], commonly thought to contain mostly major ampullate silk, with some evidence (occasionally) of additional minor ampullate filaments [<xref rid="RSIF20150633C24" ref-type="bibr">24</xref>
–<xref rid="RSIF20150633C26" ref-type="bibr">26</xref>
]. Multiple filaments affect the vibrational properties of silks [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
], but they also affect the mechanical response of the thread. With implications for both vibrational and mechanical responses, the tension of the signal thread is higher than that of other radials [<xref rid="RSIF20150633C22" ref-type="bibr">22</xref>
]. Specifically, tensioning of the signal thread will directly affect transverse vibrational responses, as well as indirectly affecting longitudinal wave properties through changes in storage modulus [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
]. Tension is also important for the signal thread's primary function, which is the transmission of vibrations from the hub with minimal loss of information and energy [<xref rid="RSIF20150633C27" ref-type="bibr">27</xref>
].</p>
<p>This paper outlines the structure of the signal thread by firstly examining the properties of its constituents, i.e. dragline silk bundles. A combination of tensile testing, microscopy, behavioural measurement and laser vibrometry allows us to assess the constraints on the structure of the signal thread and the implications for vibration transmission.</p>
</sec>
<sec sec-type="methods" id="s2"><label>2.</label>
<title>Methods</title>
<sec id="s2a"><label>2.1.</label>
<title>Sample preparation</title>
<p>Spider silks from <italic>Z. x-notata</italic>
were either collected by forced reeling immobilized spiders [<xref rid="RSIF20150633C28" ref-type="bibr">28</xref>
,<xref rid="RSIF20150633C29" ref-type="bibr">29</xref>
] or taken from naturally spun web silks [<xref rid="RSIF20150633C26" ref-type="bibr">26</xref>
]. The spiders were collected in Oxford city and housed in 30 × 30 × 5 cm Perspex frames, kept in laboratory conditions (<italic>ca</italic>
20°C, 40% RH and a 16 L : 8 D cycle). Spiders were fed (<italic>Drosophila</italic>
) on their web after which it was collapsed for the spider to re-ingest and re-build. Signal threads were taken from webs that followed an initial set-up phase of at least three webs [<xref rid="RSIF20150633C30" ref-type="bibr">30</xref>
]. Webs were photographed before removing the signal thread. Dividers fixed onto a micromanipulator were used to remove the signal thread from these established webs. In all cases, two 12.5 mm thread specimens kept under natural web tension were transferred onto cardboard frames.</p>
<p>After signal threads were taken from newly built webs, the spiders’ thread repair behaviour was filmed with a Panasonic HDC-TM700 HD at 50 fps. In particular, the number of times the spider moves between the hub and retreat was recorded, termed ‘number of runs'.</p>
<p>For forced reeling, a large <italic>Zygiella</italic>
(0.0312 g) was selected and anaesthetized in carbon dioxide for 3 min, then caged dorsal-side-down using pins. The number of filaments and the type of silk (major and/or minor ampullate silk) were determined by observing spider spinnerets under a dissection microscope (Olympus SZ40, Tokyo, Japan), while the spider was reeled at a constant reeling speed of 20 mm s<sup>−1</sup>
, similar to the average natural spinning speed [<xref rid="RSIF20150633C29" ref-type="bibr">29</xref>
]. For all spiders, photographs were taken (for size), and weight was recorded.</p>
</sec>
<sec id="s2b"><label>2.2.</label>
<title>Signal thread characterization</title>
<p><italic>Zygiella</italic>
forced reeled (one spider, <italic>n</italic>
= 10) and signal thread silks (nine spiders, <italic>n</italic>
= 63) were mechanically deformed in a Zwick tensile tester (5 N load cell, Z0.5, Zwick GMBH, Germany) at a rate of 40% min<sup>−1</sup>
. For specific specimens (<italic>n</italic>
= 5 spiders, <italic>n</italic>
= 16 threads), the pre-tension was measured by closing the clamps to find zero load. Slack on the sample was removed from the raw data to allow alignment of the load–strain curves. As the cross-sectional area is difficult to measure (although it can be estimated), load data were analysed instead of stress data.</p>
<p>For diameter measurements, threads were imaged under frame-tension in a scanning electron microscope (SEM; Neoscope 2000, Nikon Instruments, UK) at 10 kV high vacuum following sputter coating for 150 s at 18 mA with gold/palladium (Quorum Technologies SC7620), giving a coating of 12.5 nm. Broken ends from stress–strain experiments were also imaged to measure the approximate number of filaments (with two repeats per signal thread), examples shown in electronic supplementary material, figure S1. Average thread diameter measurement from broken ends will be an underestimate as threads will have been pulled apart.</p>
<p>Selected signal threads were characterized for their vibrational properties using a laser Doppler vibrometer system (PSV 300, Polytec), fitted with a close-up unit (OFV 056), as described in detail elsewhere [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
]. <italic>Zygiella</italic>
specimens were kept under tension in a Deben microtest tensile stage (2 N load cell, Deben, UK), and the first reading was taken straight after the frame was cut, under ‘natural tension’. For strain control, further tension was then added by extending the specimen using the tensile tester. Pre-load was calculated by using the post-break tension at zero load. Signal threads were measured for their transverse sonic properties in the middle of the silk thread, which was vibrated using amplified sound transmitted from a loud speaker over frequencies of 1–30 kHz. A ∼55 dB sound pressure level was used, measured using a reference microphone (Brüel & Kjaer 4138). Data from the laser vibrometer were fast-Fourier transform filtered (lowpass mode, using an ideal filter, cut-off 0.004 s) and the baseline (defined as average magnitude 25–30 kHz) was calculated. The magnitude versus frequency data were plotted by deducting the magnitude of threads at higher tension from the magnitude data of the same threads at lower tension (<xref ref-type="fig" rid="RSIF20150633F5">figure 5</xref>
). Published wavespeed data on silks [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
] allowed us to use the peaks at expected frequencies to estimate the fundamental mode. The peak-finding algorithm used a 40% height increase over 20 points, where adjoining peaks were interpreted as one peak. The frequency of the highest section of a fundamental mode peak was used to calculate the wavespeed.</p>
</sec>
<sec id="s2c"><label>2.3.</label>
<title>Statistics</title>
<p>The number of runs and other parameters were correlated using Microsoft E<sc>xcel</sc>
, which calculates an <italic>R</italic>
<sup>2</sup>
-value, where 1 is a perfect linear relationship and 0 is a random relationship. Spearman's rank coefficient (<italic>ρ</italic>
) was also calculated to quantify the correlation between the two terms, as the assumptions of the more powerful Pearson's correlation were not met. Significance, here defined as <italic>p</italic>
< 0.05, was determined by reference to a critical values table [<xref rid="RSIF20150633C31" ref-type="bibr">31</xref>
].</p>
</sec>
</sec>
<sec id="s3"><label>3.</label>
<title>Results and discussion</title>
<sec id="s3a"><label>3.1.</label>
<title>Forced reeled silk bundle structure and properties</title>
<p>Our SEM observations showed that signal threads always contain multiple silk filaments (<xref ref-type="fig" rid="RSIF20150633F2">figure 2</xref>
). To help determine the exact number of filaments, we used forced reeled <italic>Zygiella</italic>
silk as reference. Forced reeled silks are of a known type, the number of filaments can be controlled, and it is made from the same silks as the signal thread. As our observations (from both dissection and SEM) showed, forced reeled silk bundles are two major and two minor ampullate silk filaments (<xref ref-type="fig" rid="RSIF20150633F2">figure 2</xref>
<italic>a</italic>
).
<fig id="RSIF20150633F2" orientation="portrait" position="float"><label>Figure 2.</label>
<caption><p>SEM image of <italic>Zygiella</italic>
silks: (<italic>a</italic>
) false colour SEM of forced reeled silks, where a double of larger silk (yellow; assumed major ampullate silk) and a double of smaller silk (green; assumed minor ampullate silk) are coextruded, and (<italic>b</italic>
) naturally spun signal thread taken from a new web and kept under tension, where multiple silks are used. White bar denotes 10 µm. The fine particles are ‘dust’, presumably attracted to the silks owing to electrostatic charging [<xref rid="RSIF20150633C32" ref-type="bibr">32</xref>
]. (Online version in colour.)</p>
</caption>
<graphic xlink:href="rsif20150633-g2"></graphic>
</fig>
</p>
<p>Forced reeled silk has a known number of fibres and thus their load–extension curves can be used to calibrate the number of filaments in load–extension curves of silk bundles of unknown composition, assuming load correlates with the number of filaments. The load–strain and stress–strain responses of forced reeled <italic>Zygiella</italic>
silks are shown in <xref ref-type="fig" rid="RSIF20150633F3">figure 3</xref>
. Some filaments showed double the load modulus (and breaking load) of others. Area allocation of the whole (two major and two minor) or half the area aligned the stress–strain curves (<xref ref-type="fig" rid="RSIF20150633F3">figure 3</xref>
<italic>b</italic>
), implying that load data (modulus and maximum load) can be used as a proxy for the number of filaments present. This variation in load was probably owing to breaking of filaments during sample mounting. There is evidence of slightly different stress–strain contours for double (black) versus single (pink) fibres after alignment (<xref ref-type="fig" rid="RSIF20150633F3">figure 3</xref>
<italic>b</italic>
), which will be due to mechanical interaction between two fibres that would increase stiffness [<xref rid="RSIF20150633C33" ref-type="bibr">33</xref>
]. Interestingly, the number of breaking points in <xref ref-type="fig" rid="RSIF20150633F3">figure 3</xref>
(defined by a sharp reduction in load) varied from one to three, hence the signal thread did not always break as a whole, nor did filaments break individually.
<fig id="RSIF20150633F3" orientation="portrait" position="float"><label>Figure 3.</label>
<caption><p>Tensile responses of 10 bundles of ampullate silks forced reeled from <italic>Zygiella</italic>
: (<italic>a</italic>
) load and (<italic>b</italic>
) stress, where pink curves (where the load modulus is half) use half the total area, and black curves use the whole area. (Online version in colour.)</p>
</caption>
<graphic xlink:href="rsif20150633-g3"></graphic>
</fig>
</p>
<p>This provides important insights into the composition of <italic>Zygiella</italic>
signal threads. In terms of mechanical response, the stress–strain contours of major ampullate silks are similar to other species [<xref rid="RSIF20150633C34" ref-type="bibr">34</xref>
]. However, for <italic>Zygiella</italic>
, the minor ampullate silk contours are also similar to major ampullate silk, which is quite unlike other species [<xref rid="RSIF20150633C35" ref-type="bibr">35</xref>
]. For example, in <italic>Nephila,</italic>
the minor ampullate silks have higher extensions notable during tensile testing of major/minor dragline bundles; furthermore, in this species, consistent stresses are taken by major and minor silk filaments as they break independently (electronic supplementary material, figure S2). In contrast, <italic>Zygiella</italic>
major or minor filaments break around 15% strain, with variation in the load taken by different filaments following the initial break, indicating more variability in filament strength of both silk types. Therefore, bundling of major and minor ampullate silks leads to thread ‘ropes' composed of filaments with different diameters, thus giving varied responses to tension. Also of importance in this context is the supercontraction ability of major ampullate silk, which is lacking in minor ampullate [<xref rid="RSIF20150633C36" ref-type="bibr">36</xref>
,<xref rid="RSIF20150633C37" ref-type="bibr">37</xref>
], where the major ampullate silk will contract up to 30% when exposed to high humidity [<xref rid="RSIF20150633C36" ref-type="bibr">36</xref>
]. This supercontraction provides major ampullate silk with a wide range of stiffnesses, directly influencing longitudinal waves, and providing the spider with a mechanism to closely control tension through pulling supercontracted fibres, directly influencing transverse waves [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
]. In combination with minor ampullate silk, which does not contract, this sets up a system which could be stable or tunable, depending on the ratio of major to minor ampullate silk filaments.</p>
</sec>
<sec id="s3b"><label>3.2.</label>
<title>Comparison with signal thread structure and properties</title>
<p>Compared with the forced reeled control threads, the signal threads taken from <italic>Zygiella</italic>
webs had many more silk filaments. Signal threads also had fibres of varying diameters, which supports our hypothesis that major and minor ampullate silks are bundled during signal thread construction (<xref ref-type="fig" rid="RSIF20150633F2">figure 2</xref>
<italic>b</italic>
). For naturally spun signal threads (i.e. not repair), the number of silk filaments varied from 8 to 16 filaments, as shown in the SEM images of broken ends after tensile testing (see electronic supplementary material, figure S1). Repaired signal threads showed a broader range of silk filaments present, varying from 4 to 14. Although the diameter of a single silk filament had only a weak (and non-significant) correlation with spider weight (<italic>R</italic>
<sup>2</sup>
= 0.80, <italic>ρ</italic>
<sub>7</sub>
= 0.70, <italic>p</italic>
> 0.05), the <italic>total</italic>
diameter of the signal thread did not correlate with spider size (neither weight nor carapace width, <italic>R</italic>
<sup>2</sup>
= 0). These data suggest that signal thread size is not constrained by spider size and both signal thread building and repair are flexible behaviours not rigidly controlled between spiders or within an individual.</p>
<p>Expanding the methodology used in <xref ref-type="fig" rid="RSIF20150633F3">figure 3</xref>
to infer the number of filaments present from the tensile load data, <xref ref-type="fig" rid="RSIF20150633F4">figure 4</xref>
compares the load–extension curves of dragline silk bundles to signal threads taken from the same spider (<xref ref-type="fig" rid="RSIF20150633F4">figure 4</xref>
<italic>a</italic>
), and the effect of the number of runs on the load–extension curves taken from the same spider (<xref ref-type="fig" rid="RSIF20150633F4">figure 4</xref>
<italic>b</italic>
).
<fig id="RSIF20150633F4" orientation="portrait" position="float"><label>Figure 4.</label>
<caption><p>Load–strain curves of <italic>Zygiella</italic>
silks: (<italic>a</italic>
) forced reeled and signal threads from the same spider, where pink shows the curve where 1 MA (major ampullate silk) is taking the load, blues are 2 MA (cyan forced reeled, dark blue signal thread) and black is 6 MA (minor ampullate silk is assumed to be coextruded with MA). (<italic>b</italic>
) Load–strain curves of signal threads from one spider, where the number of runs was recorded. Cyan is two runs, orange is four runs, green eight runs, purple 10 runs and black 14 runs, which correlate with initial modulus and maximum load (in N). Inset is a scatter graph showing maximum load versus number of runs from signal threads from multiple spiders. (Online version in colour.)</p>
</caption>
<graphic xlink:href="rsif20150633-g4"></graphic>
</fig>
</p>
<p>Signal threads displayed higher breaking loads and higher load moduli than their forced reeled counterpart control owing to the use of multiple filaments (<xref ref-type="fig" rid="RSIF20150633F4">figure 4</xref>
<italic>a</italic>
). Post-yield hardening was also a factor—an effect that can be caused by the interaction of strands together, whether mechanically or electrostatically [<xref rid="RSIF20150633C32" ref-type="bibr">32</xref>
,<xref rid="RSIF20150633C38" ref-type="bibr">38</xref>
]. Furthermore, the number of spider runs along the signal thread correlates closely with the load modulus (<italic>R</italic>
<sup>2</sup>
= 0.70, <italic>ρ</italic>
<sub>24</sub>
= 0.84, <italic>p</italic>
< 0.01) and maximum load (inset <xref ref-type="fig" rid="RSIF20150633F4">figure 4</xref>
<italic>b</italic>
; <italic>R</italic>
<sup>2</sup>
= 0.77, <italic>ρ</italic>
<sub>24</sub>
= 0.87, <italic>p</italic>
< 0.01). Therefore, as the animal moves on the signal thread, more dragline silk bundles are integrated into the signal thread. Although statistically significant, the variation seen in the relationship between number of runs and mechanical properties suggests that differing numbers of filaments may be added per run, most probably owing to the additional use of minor ampullate silk filaments.</p>
<p>In support of the load data, the number of runs also correlated with the number of broken ends seen in the SEM (<italic>R</italic>
<sup>2</sup>
= 0.64, <italic>ρ</italic>
<sub>23</sub>
= 0.87, <italic>p</italic>
< 0.01), whereas the number of breaks seen in the stress–strain response had no relationship (<italic>R</italic>
<sup>2</sup>
= 0.03, <italic>ρ</italic>
<sub>24</sub>
= −0.19, <italic>p</italic>
> 0.05). Variability in the number of breaks provides insights into functional aspects of the system. Concurrent breaking of multiple filaments points to interactions within the signal thread structure, allowing the sharing of load and cracks to propagate between filaments. Conversely, breaking in separate units shows that filaments can become separated from each other and that some filaments can take more load than others during tensile testing.</p>
<p>In combination, our data allow us to infer the structure of the <italic>Zygiella</italic>
signal thread whereby multiple silk strands of bundled (i.e. co-spun) major and minor ampullate silks vary in filament number between webs, even between webs of the same individual. Further studies are needed to confirm the presence of major and minor ampullate silk in the signal thread and how they are co-spun. The signal thread structure is therefore remarkably unconstrained, with movement of the spider to and from the retreat during prey capture leading to thicker signal thread ropes as more silk filaments are recruited. This suggests that the signal thread's structure in terms of number and size of constituent filaments may well be relatively unimportant for its signalling function.</p>
</sec>
<sec id="s3c"><label>3.3.</label>
<title>Implications of signal thread structure</title>
<p>The number and size of various filaments in a signal thread will have implications for the thread's signalling function as it affects the thread's static stress, i.e. its load normalized by its cross-sectional area. Static stress has a direct effect on transverse wave properties, it also has an indirect effect on longitudinal wave properties and it will also affect damping of vibrations [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
]. The observed variability in signal thread structure, therefore, raises two questions: first, on how static stress differs between signal threads of different sizes and second, whether different filaments within an individual signal thread contribute evenly to static stress.</p>
<p>Regarding static stress, thread pre-tension (absolute load) correlated with the load modulus (<italic>R</italic>
<sup>2</sup>
= 0.77, <italic>ρ</italic>
<sub>14</sub>
= 0.65, 0.05 < <italic>p</italic>
< 0.01), which (as we have shown) also correlated with the number of runs (<xref ref-type="fig" rid="RSIF20150633F4">figure 4</xref>
). A difference also occurred between repaired and new signal threads in terms of their pre-tension, with new signal threads (the natural condition) having higher pre-tensions. It seems that the spider tensioned additional silk filaments as they were added, thus increasing the total absolute load as the signal thread increased in size.</p>
<p>Importantly, this lead to similar static stresses (normalized loads) between signal threads of different sizes, regardless of the size, type or number of filaments added. Such a constancy of static stress would mean that sonic properties related to time (such as propagation speed and resonant frequency) will be consistent; for example, transverse wavespeed of the signal thread will be equal to the square root of stress divided by density [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
]. However, the effect of static stress on damping is a complicated matter that needs further study—interplay between filament diameter, wave type, tension and silk structure would affect vibration amplitude [<xref rid="RSIF20150633C27" ref-type="bibr">27</xref>
,<xref rid="RSIF20150633C39" ref-type="bibr">39</xref>
,<xref rid="RSIF20150633C40" ref-type="bibr">40</xref>
].</p>
<p>Our data so far suggest multiple filaments in the signal thread integrate and interact with one another. This is supported by post-strain hardening, tensile break points (<xref ref-type="fig" rid="RSIF20150633F3">figure 3</xref>
<italic>a,b</italic>
), and additionally SEM images of signal threads (<xref ref-type="fig" rid="RSIF20150633F2">figure 2</xref>
<italic>b</italic>
). To further investigate whether individual filaments contribute evenly to static stress within the signal thread, we measured signal thread transverse resonance over a range of pre-tensions (<xref ref-type="fig" rid="RSIF20150633F5">figure 5</xref>
). Using standing waves, the thread will vibrate at high amplitude at preferred frequencies (known as resonance), similar to a guitar string. At a fixed filament length, the wavespeed is proportional to the resonant frequency (transverse wavespeed is calculated in <xref ref-type="fig" rid="RSIF20150633F5">figure 5</xref>
<italic>b</italic>
). Therefore, resonance in the transverse direction (i.e. displacement perpendicular to fibre axis) provides a useful, non-destructive way to measure static stress in bundles of filaments [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
]. One resonant frequency peak indicates that the signal thread is vibrating as a whole, whereas several peaks indicate that different units of the thread are vibrating independently. The change in resonant properties over tension tells us whether the signal thread structure is altering.
<fig id="RSIF20150633F5" orientation="portrait" position="float"><label>Figure 5.</label>
<caption><p>The vibrational properties of a <italic>Zygiella</italic>
signal thread: (<italic>a</italic>
) difference in magnitude plot, where the magnitude of a signal thread at high tension is subtracted from the same signal thread at low tension. There is one resonant peak at 0.0024 N (blue) and three at 0.0041 N (pink). Light colours give the data determined to be a peak, which are labelled with numbers. (<italic>b</italic>
) Transverse wavespeed versus load, using the data points in panel (<italic>a</italic>
). The dashed curve gives a theoretical relationship, where transverse wavespeed is the square root of stress divided by density. The cross-sectional area used to calculate static stress is based on an estimation from SEM measurement. Data points below this line have a lower static stress than theory, and above have a higher static stress than theory. (Online version in colour.)</p>
</caption>
<graphic xlink:href="rsif20150633-g5"></graphic>
</fig>
</p>
<p>Thus, it appears signal threads can have multiple, separate resonant peaks not caused by harmonics (multiples of resonant frequencies), which has not been reported in previous research on spider silks [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
]. This means that the multiple filaments in the signal thread are able to have different static stresses, caused either by different cross-sectional areas, and/or tension being shared by the filaments unevenly. Specifically for this signal thread, more load correlates with a simultaneous increase and decrease in static stress (<xref ref-type="fig" rid="RSIF20150633F5">figure 5</xref>
<italic>b</italic>
). This leads us to propose that some filaments were separating and vibrating independently. However, resonant peak splitting was seen at static stresses beyond yield (after the kink in the dashed curve), which is likely to have also introduced the multiple break points seen during the tensile testing. Our data on pre-load and previous work [<xref rid="RSIF20150633C22" ref-type="bibr">22</xref>
] suggest that the signal threads are kept at loads below the yield point under natural conditions.</p>
<p>Our evidence, therefore, points towards an integrated filament structure at natural tensions, where thin filaments (0.3–1.2 µm in diameter) are attracted and attached to each other (most probably electrostatically [<xref rid="RSIF20150633C32" ref-type="bibr">32</xref>
]) and thus share tension to create a constant static stress. What does this mean for information flow along a signal thread? Signal threads should generally vibrate as a whole, and as more filaments are added, they are integrated into the signal thread structure with little to no change in static stress. From a biological perspective, signal thread structure is beneficial for propagation times along the signal thread—there will be no change in propagation speed as more filaments are added. It also means that usually a <italic>single</italic>
signal is received by the spider, regardless of signal thread size, which leads to simpler processing requirements for the spider's nervous system and more accurate, rapid responses to information transmitted through the web.</p>
<p>In terms of potential applications, the signal thread structure inspires remote sensing technologies. Regarding passive remote sensing, silks offer high fidelity signal transmission [<xref rid="RSIF20150633C9" ref-type="bibr">9</xref>
], and this paper has shown that the signal thread structure itself also contributes towards stable signal transmission properties. Furthermore, the structure also could be applied in active remote sensing applications, for example through implementation in piezoelectric energy harvesting materials and structures, where deformation (for example from vibration) is transformed into electricity [<xref rid="RSIF20150633C41" ref-type="bibr">41</xref>
]. Inspired by the signal thread design, these piezoelectric fibre bundles could come in a variety of sizes for different contexts, from microelectromechanical systems (MEMS), to large cables for civil applications [<xref rid="RSIF20150633C42" ref-type="bibr">42</xref>
], where deformation response can be closely controlled through bundle tensioning. Use of coated silks (e.g. zinc oxide nanowires [<xref rid="RSIF20150633C41" ref-type="bibr">41</xref>
]) in composite energy harvesting systems could allow tuning of fibre moduli to be implemented for different contexts [<xref rid="RSIF20150633C43" ref-type="bibr">43</xref>
], and silk's high toughness could additionally be useful in vibration damping applications [<xref rid="RSIF20150633C44" ref-type="bibr">44</xref>
].</p>
</sec>
</sec>
<sec id="s4"><label>4.</label>
<title>Conclusion</title>
<p>A combination of tensile testing, electron microscopy and laser vibrometry has shown us that the signal thread of <italic>Z. x-notata</italic>
is flexible in composition with apparently weak selection pressures to conserve the number of filaments present. Signal thread function would be unaffected by thread dimensions, because propagation speeds remain constant, being a function of static stress. Our data support the hypothesis that the signal thread is a fully integrated structure, which vibrates as a whole under natural static stresses. This allows the spider to readily respond to signal thread vibration, regardless of its size, with no cost of time delay or extra signal processing required. This suggests that the signal thread represents a complex, multifunctional, sensory structure allowing for variation in structural or load-bearing performance, while maintaining signal fidelity. From an industrial perspective, it might serve as inspiration for future development of multifunctional remote sensing materials and structures.</p>
</sec>
<sec sec-type="supplementary-material"><title>Supplementary Material</title>
<supplementary-material content-type="local-data" id="SD1"><caption><title>Figure S1.</title>
</caption>
<media mimetype="application" mime-subtype="tif" xlink:href="rsif20150633supp1.tif" orientation="portrait" id="d36e902" position="anchor"></media>
</supplementary-material>
</sec>
<sec sec-type="supplementary-material"><title>Supplementary Material</title>
<supplementary-material content-type="local-data" id="SD2"><caption><title>Figure S2.</title>
</caption>
<media mimetype="application" mime-subtype="tif" xlink:href="rsif20150633supp2.tif" orientation="portrait" id="d36e910" position="anchor"></media>
</supplementary-material>
</sec>
</body>
<back><ack><title>Acknowledgements</title>
<p>The authors thank Shira Gordon for her help setting up vibrometry experiments. For help with spider husbandry, we thank India Stephenson and Sam Trigg. For help with tensile testing, we thank Nick Hawkins. For his comments on a version of the manuscript, we thank Clive Siviour.</p>
</ack>
<sec id="s5"><title>Ethics</title>
<p>Being invertebrates, all spiders were handled according to local laboratory risk assessments/institutional ethical guidelines and do not currently fall under regulation by the UK Home Office or EU legislation.</p>
</sec>
<sec id="s6"><title>Data accessibility</title>
<p>Some data supporting this article have been uploaded as part of the electronic supplementary material. Any further data can be requested from the corresponding author.</p>
</sec>
<sec id="s7"><title>Authors' contributions</title>
<p>B.M. and F.V. conceived the research. B.M. prepared all samples. B.M. and J.F.C.W. set up vibrometry experiments. B.M. analysed the data and C.H. assisted with data interpretation. B.M. wrote the manuscript, and all authors participated in manuscript preparation and editing.</p>
</sec>
<sec id="s8"><title>Competing interests</title>
<p>We have no competing interests.</p>
</sec>
<sec id="s9"><title>Funding</title>
<p>For funding, we thank The Leverhulme Trust (F/08705/D), the US Air Force Office of Scientific Research (FA9550-12-1-0294), the European Research Council (SP2-GA-2008-233409), EPSRC (EP/K005693/1), BBSRC (BB/H004637/1), Magdalen College, Oxford and Jesus College, Oxford.</p>
</sec>
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<tree><country name="Royaume-Uni"><noRegion><name sortKey="Mortimer, Beth" sort="Mortimer, Beth" uniqKey="Mortimer B" first="Beth" last="Mortimer">Beth Mortimer</name>
</noRegion>
<name sortKey="Holland, Chris" sort="Holland, Chris" uniqKey="Holland C" first="Chris" last="Holland">Chris Holland</name>
<name sortKey="Vollrath, Fritz" sort="Vollrath, Fritz" uniqKey="Vollrath F" first="Fritz" last="Vollrath">Fritz Vollrath</name>
<name sortKey="Windmill, James F C" sort="Windmill, James F C" uniqKey="Windmill J" first="James F. C." last="Windmill">James F. C. Windmill</name>
</country>
</tree>
</affiliations>
</record>
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EXPLOR_STEP=$WICRI_ROOT/Ticri/CIDE/explor/HapticV1/Data/Pmc/Checkpoint
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Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Ticri/CIDE |area= HapticV1 |flux= Pmc |étape= Checkpoint |type= RBID |clé= PMC:4707845 |texte= Unpicking the signal thread of the sector web spider Zygiella x-notata }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Checkpoint/RBID.i -Sk "pubmed:26674191" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Checkpoint/biblio.hfd \ | NlmPubMed2Wicri -a HapticV1
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