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  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2008
    In:  Journal of Comparative Physiology A Vol. 194, No. 1 ( 2008-1), p. 49-60
    In: Journal of Comparative Physiology A, Springer Science and Business Media LLC, Vol. 194, No. 1 ( 2008-1), p. 49-60
    Type of Medium: Online Resource
    ISSN: 0340-7594 , 1432-1351
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2008
    detail.hit.zdb_id: 1459295-2
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  • 2
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2009
    In:  Journal of Comparative Physiology A Vol. 195, No. 9 ( 2009-9), p. 805-814
    In: Journal of Comparative Physiology A, Springer Science and Business Media LLC, Vol. 195, No. 9 ( 2009-9), p. 805-814
    Type of Medium: Online Resource
    ISSN: 0340-7594 , 1432-1351
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2009
    detail.hit.zdb_id: 1459295-2
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2010
    In:  Journal of Comparative Physiology A Vol. 196, No. 7 ( 2010-7), p. 471-480
    In: Journal of Comparative Physiology A, Springer Science and Business Media LLC, Vol. 196, No. 7 ( 2010-7), p. 471-480
    Type of Medium: Online Resource
    ISSN: 0340-7594 , 1432-1351
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2010
    detail.hit.zdb_id: 1459295-2
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  • 4
    In: Journal of Insect Physiology, Elsevier BV, Vol. 56, No. 4 ( 2010-4), p. 398-404
    Type of Medium: Online Resource
    ISSN: 0022-1910
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2010
    detail.hit.zdb_id: 1482429-2
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    The Company of Biologists ; 2006
    In:  Journal of Experimental Biology Vol. 209, No. 14 ( 2006-07-15), p. 2611-2621
    In: Journal of Experimental Biology, The Company of Biologists, Vol. 209, No. 14 ( 2006-07-15), p. 2611-2621
    Abstract: Many arthropods and vertebrates possess tarsal adhesive pads densely covered with setae. The striking morphological convergence of `hairy' pads in lizards, spiders and several insect orders demonstrates the advantage of this design for substrate adhesion. Early functional explanations of hairy adhesive organs focused on the performance on rough substrates, where flexible setae can make more intimate contact. Recent theoretical and experimental work shows that the hairy design can also help to achieve self-cleaning properties,controllable detachment and increased adhesion. Several arguments have been proposed to explain why adhesive forces are maximised. First, the `Force scaling' hypothesis states that when adhesive forces scale linearly with the dimensions of the contact, adhesion is increased by dividing the contact zone into many microscopic subunits. Second, the `Fracture mechanics' argument implies that adhesion is maximised when the size of adhesive contacts is smaller than the critical crack length. Third, the `Work of adhesion' model suggests that adhesion increases due to the bending and stretching of setae and associated energy losses during detachment. Several morphological traits of hairy adhesive pads can be explained by the need to maximise the work of adhesion, while avoiding the sticking of setae to each other (self-matting). Firstly, if setae are oblique and convex toward the foot tip as typical of most hairy pads, arrays should achieve greater adhesion. Secondly, a branched seta morphology not only confers the advantage that setae can adapt to roughness at different length scales but also prevents self-matting and increases the work of adhesion. It is predicted from the `Work of adhesion' model that adhesion of pads with unbranched setae cannot be increased by subdividing the contact zone into ever finer subcontacts, because this would increasingly cause self-matting. However, contact splitting can increase adhesion if setae are branched. The greater density of setae in large animals has been interpreted by `Force scaling'. However, the existing data can be explained by the effect of seta branching and by a fundamental difference between `wet' and `dry' adhesive systems. As insects employ adhesive fluids, they can cope with small-scale surface roughness even with relatively blunt seta tips, whereas the dry systems of lizards and spiders require extremely fine endings.
    Type of Medium: Online Resource
    ISSN: 1477-9145 , 0022-0949
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2006
    detail.hit.zdb_id: 1482461-9
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  • 6
    Online Resource
    Online Resource
    The Company of Biologists ; 2008
    In:  Journal of Experimental Biology Vol. 211, No. 20 ( 2008-10-15), p. 3333-3343
    In: Journal of Experimental Biology, The Company of Biologists, Vol. 211, No. 20 ( 2008-10-15), p. 3333-3343
    Abstract: Adhesive pads on the legs of animals can be classified as either `smooth'or `hairy' (fibrillar). It has been proposed that the hairy design conveys superior and controllable adhesion. However, no study has yet compared the basic performance of both systems. As such, we measured single-pad friction and adhesion forces in sample hairy (Gastrophysa viridula) and smooth(Carausius morosus) pads and simultaneously recorded contact area. Adhesion and friction forces per unit pad area were very similar in smooth and hairy systems. Insect pads of both types adhere via a thin film of liquid secretion. As found previously for the smooth system, forces in the fibrillar system strongly decreased with larger amounts of fluid secretion present, suggesting that the fluid mainly serves to maximize contact on rough substrates. One essential prerequisite for the control of surface attachment during locomotion is the direction-dependence of adhesive pads. We compared the mechanisms of direction-dependence in smooth and hairy systems by performing proximal and distal slides. Both types of pad exhibited a large drop in friction when moved away from the body, although this effect was more extreme for the hairy system. Direction-dependence is explained in both smooth and fibrillar systems by the instability of the tarsal chain, causing the whole pad to peel off. In the fibrillar pads, anisotropy additionally arises from the direction-dependence of individual setae.
    Type of Medium: Online Resource
    ISSN: 1477-9145 , 0022-0949
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2008
    detail.hit.zdb_id: 1482461-9
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  • 7
    Online Resource
    Online Resource
    The Company of Biologists ; 2015
    In:  Journal of Experimental Biology ( 2015-01-01)
    In: Journal of Experimental Biology, The Company of Biologists, ( 2015-01-01)
    Abstract: The flexibility of insect adhesive pads is crucial for their ability to attach on rough surfaces. Here we use transparent substrates with micropillars to test in adult cockroaches (Nauphoeta cinerea) whether and how the stiffness of smooth adhesive pads changes when shear forces are applied, and whether the insect's age has any influence. We found that during pulls towards the body, the pad's ability to conform to the surface microstructures was improved in comparison to a contact without shear, suggesting that shear forces make the pad more compliant. The mechanism underlying this shear-dependent increase in compliance is still unclear. The effect was not explained by viscoelastic creep, changes in normal pressure, or shear-induced pad rolling, which brings new areas of cuticle into surface contact. Adhesive pads were significantly stiffer in older cockroaches. Stiffness increased most rapidly in cockroaches aged between 2.5 and 4 months. The increase in stiffness is likely based on wear and repair of the delicate adhesive cuticle. Recent wear (visualised by methylene blue staining) was not age-dependent, whereas permanent damage (visible as brown scars) accumulated with age, reducing the pads' flexibility.
    Type of Medium: Online Resource
    ISSN: 1477-9145 , 0022-0949
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2015
    detail.hit.zdb_id: 1482461-9
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  • 8
    In: Journal of Experimental Biology, The Company of Biologists
    Abstract: Terrestrial arthropods achieve waterproofing by a layer of cuticular hydrocarbons (CHCs). At the same time, CHCs also serve as communication signals. To maintain waterproofing under different climate conditions, insects adjust the chemical composition of their CHC layer, but this may affect the communication via CHC. The detailed acclimatory changes of CHCs and how these influence their physical properties are still unknown. Here, we studied acclimation in two closely related ant species with distinct CHC profiles, Myrmica rubra and Myrmica ruginodis, in response to constant or fluctuating temperature and humidity regimes. We measured how acclimation affected CHC composition and viscosity, and the ants’ drought survival. In both species, CHC composition showed strong, predictable responses to temperature regimes. Warm-acclimated individuals had higher proportions of linear alkanes, and less methyl-branched or unsaturated CHCs. These changes coincided with higher solid content and viscosity of CHCs in warm-acclimated ants. Temperature fluctuation caused effects similar to constant-cool conditions in M. rubra, but led to entirely different profiles in M. ruginodis, suggesting that fluctuating and constant conditions pose very different challenges. Acclimation to dry conditions led to higher absolute amounts of CHCs, which increased the ants’ drought survival, whereas temperature acclimation did not. Hence, the temperature-induced CHC changes cannot be explained by the need for waterproofing alone. While these changes could be non-adaptive, we propose that they serve to maintain a constant CHC viscosity, which may be essential for communication and other functions.
    Type of Medium: Online Resource
    ISSN: 1477-9145 , 0022-0949
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2018
    detail.hit.zdb_id: 1482461-9
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  • 9
    Online Resource
    Online Resource
    The Company of Biologists ; 2004
    In:  Journal of Experimental Biology Vol. 207, No. 1 ( 2004-01-01), p. 67-74
    In: Journal of Experimental Biology, The Company of Biologists, Vol. 207, No. 1 ( 2004-01-01), p. 67-74
    Abstract: Tarsal adhesive pads enable insects to hold on to smooth plant surfaces. Using a centrifuge technique, we tested whether a 'wet adhesion' model of a thin film of liquid secreted between the pad and the surface can explain adhesive and frictional forces in Asian Weaver ants (Oecophylla smaragdina). When forces are acting parallel to the surface, pads in contact with the surface can slide smoothly. Force per unit pad contact area was strongly dependent on sliding velocity and temperature. Seemingly consistent with the effect of a thin liquid film in the contact zone, (1) frictional force linearly increased with sliding velocity, (2) the increment was greater at lower temperatures and (3) no temperature dependence was detected for low-rate perpendicular detachment forces. However, we observed a strong,temperature-independent static friction that was inconsistent with a fully lubricated contact. Static friction was too large to be explained by the contribution of other (sclerotized) body parts. Moreover, the rate-specific increase of shear stress strongly exceeded predictions derived from estimates of the adhesive liquid film's thickness and viscosity. Both lines of evidence indicate that the adhesive secretion alone is insufficient to explain the observed forces and that direct interaction of the soft pad cuticle with the surface ('rubber friction') is involved.
    Type of Medium: Online Resource
    ISSN: 1477-9145 , 0022-0949
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2004
    detail.hit.zdb_id: 1482461-9
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    The Royal Society ; 2015
    In:  Royal Society Open Science Vol. 2, No. 7 ( 2015-07), p. 150129-
    In: Royal Society Open Science, The Royal Society, Vol. 2, No. 7 ( 2015-07), p. 150129-
    Abstract: Contamination of body surfaces can negatively affect many physiological functions. Insects have evolved different adaptations for removing contamination, including surfaces that allow passive self-cleaning and structures for active cleaning. Here, we study the function of the antenna cleaner in Camponotus rufifemur ants, a clamp-like structure consisting of a notch on the basitarsus facing a spur on the tibia, both bearing cuticular ‘combs’ and ‘brushes’. The ants clamp one antenna tightly between notch and spur, pull it through, and subsequently clean the antenna cleaner itself with the mouthparts. We simulated cleaning strokes by moving notch or spur over antennae contaminated with fluorescent particles. The notch removed particles more efficiently than the spur, but both components eliminated more than 60% of the particles with the first stroke. Ablation of bristles, brush and comb strongly reduced the efficiency, indicating that they are essential for cleaning. To study how comb and brush remove particles of different sizes, we contaminated antennae of living ants, and anaesthetized them immediately after they had performed the first cleaning stroke. Different-sized beads were trapped in distinct zones of the notch, consistent with the gap widths between cuticular outgrowths. This suggests that the antenna cleaner operates like a series of sieves that remove the largest objects first, followed by smaller ones, down to the smallest particles that get caught by adhesion.
    Type of Medium: Online Resource
    ISSN: 2054-5703
    Language: English
    Publisher: The Royal Society
    Publication Date: 2015
    detail.hit.zdb_id: 2787755-3
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