Change of mechanical characteristics in spider silk capture threads after contact with prey
Source abstract
Abstract
Most spiders rely on specialized capture threads to subdue prey. Cribellate spiders use capture threads, whose adhesion is based on thousands of nanofibers instead of specialized glue. The nanofibers adhere due to van der Waals and hygroscopic forces, but the adhesion is strengthened by an interaction with the cuticular hydrocarbons (CHCs) covering almost all insects. The interaction between CHCs and cribellate threads becomes visible through migration of the CHCs into the thread even far beyond the point of contact. In this study, we were able to show that the migrated CHCs not only influence adhesion but also change the mechanical characteristics of the thread. While adhesion, extensibility and total energy decreased in threads treated with CHCs from different insects, we observed an increasing force required to break threads. Such mechanical changes could be beneficial for the spider: Upon the first impact of the insect in the web, it is important to absorb all the energy without breaking. Afterwards, a reduction in extensibility could cause the insect to stay closer to the web and thus become additionally entangled in neighboring threads. An increased tensile force would additionally ensure that for insects already in the web, it is even harder to free themselves. Taken together, all these changes make it unlikely that cribellate spiders reuse their capture threads, if not reacting rapidly and removing the prey insect before the CHCs can spread across the thread. STATEMENT OF SIGNIFICANCE: Cribellate spiders use capture threads that, unlike other spiders, consist of nanofibers and do not rely glue. Instead, prey adheres mainly because their surface compounds, so-called cuticular hydrocarbons (CHCs), interact with the thread, this way generating strong adhesion forces. Previous studies on biomechanics and adhesion of cribellate threads only dealt with artificial surfaces, neglecting any interaction with surface compounds. This study examines the dramatical mechanical changes of a cribellate thread after interaction with prey CHCs, showing modifications of the thread's extensibility, tensile force and total energy. Our results highlight the importance of studying mechanical properties of silk not only in an artificial context, but also in real life.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Silk-based biomaterials and applications · Spider Taxonomy and Behavior Studies · Adhesion, Friction, and Surface Interactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (62)
Show source-provided references
1. Evidence from multiple species that spider silk glue component ASG2 is a spidroin10.1038/srep21589 ↗
2. Direct solvation of glycoproteins by salts in spider silk glues enhances adhesion and helps to explain the evolution of modern spider orb webs10.1021/bm401800y ↗
3. The contribution of atmospheric water vapour to the formation and efficiency of a spider's capture web10.1098/rspb.1992.0055 ↗
4. Systematics and evolution of spiders (Araneae)10.1146/annurev.es.22.110191.003025 ↗
5. Towards a phylogeny of entelegyne spiders (Araneae, Araneomorphae, Entelegynae)
6. Evolution of adhesive mechanisms in cribellar spider prey capture thread: evidence for van der Waals and hygroscopic forces10.1046/j.1095-8312.2002.00099.x ↗
7. Adhesion enhancement of cribellate capture threads by epicuticular waxes of the insect prey sheds new light on spider web evolution
8. Cribellate thread production in spiders: complex processing of nano-fibres into a functional capture thread10.1016/j.asd.2015.07.003 ↗
9. Small behavioral adaptations enable more effective prey capture by producing 3D-structured spider threads10.1038/s41598-019-53764-4 ↗
10. Morphological adaptation of the calamistrum to the cribellate spinning process in Deinopoidae (Uloboridae, Deinopidae)10.1098/rsos.150617 ↗
11. Spider diversification through space and time10.1146/annurev-ento-061520-083414 ↗
12. Compounds in the droplets of the orb spider's viscid spiral10.1038/345526a0 ↗
13. Glycoprotein glue beneath a spider web's aqueous coat10.1007/BF01134447 ↗
14. Adhesive recruitment by the viscous capture threads of araneoid orb-weaving spiders10.1242/jeb.02682 ↗
15. Waals and hygroscopic forces of adhesion generated by spider capture threads10.1242/jeb.00618 ↗
16. The ability of spider cribellar prey capture thread to hold insects with different surface features10.2307/2389897 ↗
17. Sex attractant pheromone of the house fly: isolation, identification and synthesis10.1126/science.174.4004.76 ↗
18. Cuticular hydrocarbons in ants (Hymenoptera: Formicidae) and other insects: how and why they differ among individuals, colonies, and species
19. Release from prey preservation behavior via prey switch allowed diversification of cuticular hydrocarbon profiles in digger wasps10.1111/evo.13322 ↗
20. Physical properties of insect cuticular hydrocarbons: the effects of chain length, methyl-branching and unsaturation10.1016/0305-0491(95)00081-X ↗
21. How do cuticular hydrocarbons evolve? Physiological constraints and climatic and biotic selection pressures act on a complex functional trait
22. Adaptive dynamics of cuticular hydrocarbons in Drosophila10.1111/jeb.12988 ↗
23. Regionalization of surface lipids in insects10.1098/rspb.2015.2994 ↗
24. Cuticular hydrocarbon profiles differ between ant body parts: implications for communication and our understanding of CHC diffusion10.1093/cz/zoab012 ↗
25. Communication versus waterproofing: the physics of insect cuticular hydrocarbons
26. Structure and analysis of insect hydrocarbons10.1017/CBO9780511711909.003 ↗
27. Water-proofing properties of cuticular lipids10.1093/icb/38.3.471 ↗
28. Insect cuticular hydrocarbon composition influences their interaction with spider capture threads10.1242/jeb.242514 ↗
29. Factors affecting numbers and kinds of prey caught in artificial spider webs, with considerations of how orb webs trap prey
30. Molecular nanosprings in spider capture-silk threads10.1038/nmat858 ↗
31. Capture thread extensibility of orb-weaving spiders: testing punctuated and associative explanations of character evolution10.1111/j.1095-8312.2000.tb00203.x ↗
32. Uncoiling springs promote mechanical functionality of spider cribellate silk
33. Temperature mediates the effect of humidity on the viscoelasticity of glycoprotein glue within the droplets of an orb-weaving spider's prey capture threads
34. Wet webs work better: humidity, supercontraction and the performance of spider orb webs
35. Humidity-mediated changes in an orb spider's glycoprotein adhesive impact prey retention time10.1242/jeb.148080 ↗
36. Adhesion of spider cribellate silk enhanced in high humidity by mechanical plasticization of the underlying fiber10.1016/j.jmbbm.2020.104200 ↗
37. Sahni · 2014 · 203
38. The effect of solvents on the contraction and mechanical properties of spider silk10.1016/S0032-3861(98)00266-3 ↗
39. Biomimetic combs as antiadhesive tools to manipulate nanofibers10.1021/acsanm.0c00130 ↗
40. Unraveling the mechanical properties of composite silk threads spun by cribellate orb-weaving spiders10.1242/jeb.02327 ↗
41. Are you what you eat? A highly transient and prey-influenced gut microbiome in the grey house spider Badumna longinqua10.1111/mec.15370 ↗
42. Prey acceptance and conditional foraging behavior in the cribellate-web spider Titanoeca quadriguttata (Araneae: Titanoecidae)10.1636/JoA-S-18-083 ↗
43. Comparison of the unsaturated cuticular hydrocarbons of male and female house crickets, acheta domesticus (L.)(Orthoptera: Gryllidae)10.1016/0020-1790(80)90015-3 ↗
44. Cuticular hydrocarbons of adults of the cowpea weevil, callosobruchus maculatus10.1007/BF00988645 ↗
45. Coping with the climate: cuticular hydrocarbon acclimation of ants under constant and fluctuating conditions
46. PoweR: a reproducible research tool to ease Monte Carlo power simulation studies for goodness-of-fit tests in R10.18637/jss.v069.i03 ↗
47. Fox · 2018
48. Bayes factor approaches for testing interval null hypotheses10.1037/a0024377 ↗
49. R.D. Morey, J.N. Rouder, BayesFactorPCL: an R package for computing, Bayes factor for a variety of psychological research designs (available on the comprehensive r archive network), Comprehensive R Archive Network, Web-based, 2010, https://research.rug.nl/en/publications/bayesfactorpcl-an-r-package-for-computing-bayes-factor-for-a-vari.
50. Bayesian estimation supersedes the t test10.1037/a0029146 ↗
51. Wickham · 2016
52. Variation in the material properties of spider dragline silk across species10.1007/s00339-005-3427-6 ↗
53. Spider capture silk: performance implications of variation in an exceptional biomaterial10.1002/jez.420 ↗
54. Thread biomechanics in the two orb-weaving spiders Araneus diadematus (Araneae, Araneidae) and Uloborus walckenaerius (Araneae, Uloboridae)10.1002/jez.1402710102 ↗
55. Comparative study of orb web hygroscopicity and adhesive spiral composition in three araneid spiders10.1002/jez.1402590203 ↗
56. Silken toolkits: biomechanics of silk fibers spun by the orb web spider Argiope argentata (Fabricius 1775)10.1242/jeb.02275 ↗
57. Supercontraction on cribellate spider spiral silk with wet-rebuilt micro-structure10.1016/j.msec.2010.08.002 ↗
58. Punctuated evolution of viscid silk in spider orb webs supported by mechanical behavior of wet cribellate silk10.1007/s00114-017-1489-x ↗
59. Why do only certain insects escape from a spider's web?10.1007/BF00389023 ↗
60. Jeffreys · 1961
61. Lee · 2014
62. Multiple structures interactively influence prey capture efficiency in spider orb webs10.1016/j.anbehav.2010.09.011 ↗