Journal Article•
Notes on Maratus Karsch 1878 and related jumping spiders from Australia, with five new species (Araneae: Salticidae: Euophryinae), version 2
About: This article is published in Peckhamia.The article was published on 2012-01-01 and is currently open access. It has received 23 citations till now. The article focuses on the topics: Euophryinae & Maratus.
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TL;DR: The proposed relationships indicate that a strongly ant- like body has evolved at least 12 times in salticids, and a strongly beetle-like body at least 8 times, according to both molecular and morphological information.
Abstract: The classification of jumping spiders (Salticidae) is revised to bring it into accord with recent phylogenetic work. Of the 610 recognized extant and fossil genera, 588 are placed at least to subfamily, most to tribe, based on both molecular and morphological information. The new subfamilies Onomastinae, Asemoneinae, and Eupoinae, and the new tribes Lapsiini, Tisanibini, Neonini, Mopsini, and Nannenini, are described. A new unranked clade, the Simonida, is recognized. Most other family-group taxa formerly ranked as subfamilies are given new status as tribes or subtribes. The large long-recognized clade recently called the Salticoida is ranked as a subfamily, the Salticinae, with the name Salticoida reassigned to its major subgroup (the sister group to the Amycoida). Heliophaninae Petrunkevitch and Pelleninae Petrunkevitch are considered junior synonyms of Chrysillini Simon and Harmochirina Simon respectively. Spartaeinae Wanless and Euophryini Simon are preserved despite older synonyms. The genus...
149 citations
Cites background from "Notes on Maratus Karsch 1878 and re..."
...…2005b, 2008a, b; Arnedo & Gillespie 2006; Andriamalala 2007; Ruiz et al. 2007; Su et al. 2007; Logunov & Azarkina 2008b; Azarkina 2009; Hill 2009, 2012; Otto & Hill 2011a, 2012a, b, 2013a, b, 2014a, b, c; Prószyński & Deeleman-Rheinhold 2012, 2013; Zhang & Maddison 2012a, b, c, d, 2013, 2015;…...
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...112, 117, 123, 125, 136; Otto & Hill 2012b)....
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...112), whose males have remarkably diverse, complex and colourful ornaments (Żabka 1987b; Otto & Hill 2011a, 2012a, b, 2013a, b, 2014a, b, c; Waldock 2013, 2014) and courtship behaviours (Hill 2009; Otto & Hill 2010, 2011a, b; Girard et al. 2011)....
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TL;DR: 3-dimensional nanostructures that produce the rainbow colours on the abdomen of miniature peacock spiders are shown, demonstrating that the design principle of the peacock spider’ scales could inspire novel, miniature light-dispersive components.
Abstract: Colour produced by wavelength-dependent light scattering is a key component of visual communication in nature and acts particularly strongly in visual signalling by structurally-coloured animals during courtship. Two miniature peacock spiders (Maratus robinsoni and M. chrysomelas) court females using tiny structured scales (~ 40 × 10 μm2) that reflect the full visual spectrum. Using TEM and optical modelling, we show that the spiders’ scales have 2D nanogratings on microscale 3D convex surfaces with at least twice the resolving power of a conventional 2D diffraction grating of the same period. Whereas the long optical path lengths required for light-dispersive components to resolve individual wavelengths constrain current spectrometers to bulky sizes, our nano-3D printed prototypes demonstrate that the design principle of the peacock spiders’ scales could inspire novel, miniature light-dispersive components.
59 citations
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TL;DR: In order to explore the effect of adding formal morphological data to previous molecular phylogenetic studies, and to find morphological synapomorphies, eighty-two morphological characters were scored for 203 euophryine species and seven outgroup species; however, the morphological dataset does not perform as well as the molecular dataset in resolving the phylogeny of EUophryinae.
Abstract: Morphological traits of euophryine jumping spiders were studied to clarify generic limits in the Euophryinae and to permit phylogenetic classification of genera lacking molecular data. One hundred and eight genera are recognized within the subfamily. Euophryine generic groups and the delimitation of some genera are reviewed in detail. In order to explore the effect of adding formal morphological data to previous molecular phylogenetic studies, and to find morphological synapomorphies, eighty-two morphological characters were scored for 203 euophryine species and seven outgroup species. The morphological dataset does not perform as well as the molecular dataset (genes 28S, Actin 5C; 16S-ND1, COI) in resolving the phylogeny of Euophryinae, probably because of frequent convergence and reversal. The formal morphological data were mapped on the phylogeny in order to seek synapomorphies, in hopes of extending the phylogeny to include taxa for which molecular data are not available. Because of homoplasy, few globally-applicable morphological synapomorphies for euophryine clades were found. However, synapomorphies that are unique locally in subclades still help to delimit euophryine generic groups and genera. The following synonyms of euophryine genera are proposed: Maeotella with Anasaitis; Dinattus with Corythalia; Paradecta with Compsodecta; Cobanus, Chloridusa and Wallaba with Sidusa; Tariona with Mopiopia; Nebridia with Amphidraus; Asaphobelis and Siloca with Coryphasia; Ocnotelus with Semnolius; Palpelius with Pristobaeus; Junxattus with Laufeia; Donoessus with Colyttus; Nicylla, Pselcis and Thianitara with Thiania. The new genus Saphrys is erected for misplaced species from southern South America.
36 citations
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TL;DR: It is proposed that this pre-existing, qualitative sensory experience—‘sensory bias’—is also found in spiders, leading to the convergent evolution of super black for mating displays in jumping spiders.
Abstract: Male peacock spiders ( Maratus, Salticidae) compete to attract female mates using elaborate, sexually selected displays. They evolved both brilliant colour and velvety black. Here, we use scanning electron microscopy, hyperspectral imaging and finite-difference time-domain optical modelling to investigate the deep black surfaces of peacock spiders. We found that super black regions reflect less than 0.5% of light (for a 30° collection angle) in Maratus speciosus (0.44%) and Maratus karrie (0.35%) owing to microscale structures. Both species evolved unusually high, tightly packed cuticular bumps (microlens arrays), and M. karrie has an additional dense covering of black brush-like scales atop the cuticle. Our optical models show that the radius and height of spider microlenses achieve a balance between (i) decreased surface reflectance and (ii) enhanced melanin absorption (through multiple scattering, diffraction out of the acceptance cone of female eyes and increased path length of light through absorbing melanin pigments). The birds of paradise (Paradiseidae), ecological analogues of peacock spiders, also evolved super black near bright colour patches. Super black locally eliminates white specular highlights, reference points used to calibrate colour perception, making nearby colours appear brighter, even luminous, to vertebrates. We propose that this pre-existing, qualitative sensory experience-'sensory bias'-is also found in spiders, leading to the convergent evolution of super black for mating displays in jumping spiders.
28 citations
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TL;DR: Optical modelling revealed that the filament array constitutes a novel structural coloration system, which subtly fine tunes the scale reflectance to the observed blue coloration.
Abstract: Jumping spiders are well known for their acute vision and often bright colours. The male peacock spider Maratus splendens is richly coloured by scales that cover the body. The colours of the white, cream and red scales, which have an elaborate shape with numerous spines, are pigmentary. Blue scales are unpigmented and have a structural colour, created by an intricate photonic system consisting of two chitinous layers with ridges, separated by an air gap, with on the inner sides of the chitin layers an array of filaments. We have characterized the optical properties of the scales by microspectrophotometry, imaging scatterometry and light and scanning electron microscopy. Optical modelling revealed that the filament array constitutes a novel structural coloration system, which subtly fine tunes the scale reflectance to the observed blue coloration.
23 citations