A Spider’s World: Senses and Behavior

By F. Barth, Ann Biederman-Thorson. 2001

349 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/7542cccc0b271ab01001862e5b7153068d13508f

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Citations in the corpus

Spider's attack versus cricket's escape: velocity modes determine success (2006, methodology): “00/0 2006 The Association for the S Few integrated approaches, with the notable exceptions of the batemoth model (Fullard 1987), the spiderefly model (Barth 2002) and the frogespider model (Suter 2003), have included a view of both partners.”
The Morphology And Phylogeny Of Dionychan Spiders (Araneae: Araneomorphae) (2014, background): “Upon examination under SEM, it is not clear that the depressions correspond to slit sensilla, which otherwise occur in relatively hard cuticle (Barth, 2002; those of the ALS are on softer cuticle, but have a different appearance).”
Sensory biology of Phalangida harvestmen (Arachnida, Opiliones): a review, with new morphological data on 18 species (2009, methodology): “The world of Phalangida appears to be a near-range one, quite different from a spider’s world, because the latter can detect prey walking 50 cm from them and conspecifics signalling acoustically from more than 3 m (Barth 2002a).”
Complex courtship displays facilitate male reproductive success and plasticity in signaling across variable environments (2011, background): “Spectral sensitivity data on wolf spiders, as well as the wandering spider, Cupiennius salei, provide no indication that these spiders can detect the IR wavelengths emitted by the illuminator (~ 850 nm; Devoe et al., 1969; Devoe, 1972; Barth, 2002).”
Grade Changes in Brain–Body Allometry: Morphological and Behavioural Correlates of Brain Size in Miniature Spiders, Insects and Other Invertebrates (2011, background): “In insects and spiders, much of the processing of inputs occurs at relatively peripheral neural levels, including both the sensory and the motor processes (Barth, 2002; Chapman, 1982), which offers further opportunities to economize on brain tissue (economies of this sort also occur in vertebrates—e”
Morphological phylogeny of cobweb spiders and their relatives (Araneae, Araneoidea, Theridiidae) (2004, unknown): “Barth FG. 2001.”
Seismic communication and mate choice in wolf spiders: components of male seismic signals and mating success (2008, background): “…in agonistic encounters (Rovner 1968; Aspey 1977a, b), species recognition (Stratton & Uetz 1981, 1983, 1986), female stimulation and/or pacification (Maklakov et al. 2003), courtship (Uetz 2000; Barth 2002; Rypstra et al. 2003) and mate choice (Parri et al. 1997, 2002; Rivero et al. 2000).”