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Mexcala Fizi
''Mexcala fizi'' is a species of jumping spider in the genus ''Mexcala'' that lives in Democratic Republic of the Congo and Tanzania. The spider was first defined in 2009 by Wanda Wesołowska, one of over 500 that the arachnologist described during her career. It mimics ants and ant-like wasps, living alongside and preying upon them. The spider is medium-sized, with a dark browncarapace between long and a brown abdomen between long. The female has not been described. Taxonomy ''Mexcala fizi'' is a jumping spider that was first described by the Polish arachnologist Wanda Wesołowska in 2009, one of over 500 species she identified during her career. She allocated the species to the genus ''Mexcala'', first raised by George and Elizabeth Peckham in 1902 as part of a thorough revision of the genus. The genus was a member of the tribe Heliophaninae alongside '' Pseudicius'' and '' Cosmophasis'', which was absorbed into Chrysillini by Wayne Maddison in 2015. The tribe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Mexcala Quadrimaculata
''Mexcala'' is a genus of jumping spiders that was first described by George and Elizabeth Peckham in 1902. The name is probably derived from the Nahuatl '' mezcal''. Species it contains twenty-one species, found only in Africa, Yemen, and Iran: *'' Mexcala agilis'' Lawrence, 1928 – Congo, Kenya, Malawi, Tanzania, Namibia *'' Mexcala angolensis'' Wesolowska, 2009 – Angola *'' Mexcala caerulea'' ( Simon, 1901) – West Africa *'' Mexcala elegans'' Peckham & Peckham, 1903 – Ivory Coast, Malawi, Namibia, Botswana, Zimbabwe, South Africa *'' Mexcala farsensis'' Logunov, 2001 – Iran *'' Mexcala fizi'' Wesolowska, 2009 – Congo, Tanzania *'' Mexcala formosa'' Wesolowska & Tomasiewicz, 2008 – Ethiopia *'' Mexcala kabondo'' Wesolowska, 2009 – Congo, Malawi, Tanzania *'' Mexcala macilenta'' Wesolowska & Russell-Smith, 2000 – Ethiopia, Tanzania *'' Mexcala meridiana'' Wesolowska, 2009 – South Africa *'' Mexcala monstrata'' Wesolowska & van Harten, 1994 – Egypt, Yemen *' ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Wayne Maddison
Wayne Paul Maddison , is a professor and Canada Research Chair at the departments of zoology and botany at the University of British Columbia, and the Director of the Spencer Entomological Collection at the Beaty Biodiversity Museum. His research concerns the phylogeny, biodiversity, and evolution of jumping spiders (Salticidae), of which he has discovered new species and genera. He has also done research in phylogenetic theory, developing and perfecting various methods used in comparative biology, such as character state inference in internal nodes through Maximum parsimony (phylogenetics), maximum parsimony, squared-change parsimony, or character correlation through the concentrated changes test or pairwise comparisons. In collaboration with David R. Maddison, he worked on thMesquiteopen-source phylogeny software, thMacCladeprogram, and the Tree of Life Web Project. His research has led him to discover new species of jumping spiders in Sarawak and Papua New Guinea. Selected pu ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Embolus (spider Anatomy)
The two palpal bulbs – also known as palpal organs and genital bulbs – are the copulatory organs of a male spider. They are borne on the last segment of the pedipalps (the front "limbs" of a spider), giving the spider an appearance often described as like wearing boxing gloves. The palpal bulb does not actually produce sperm, being used only to transfer it to the female. Palpal bulbs are only fully developed in adult male spiders and are not completely visible until after the final moult. In the majority of species of spider, the bulbs have complex shapes and are important in identification. Structure The palpal bulb of a mature male spider is borne on the last segment of the pedipalp. This segment usually has touch-sensitive hairs (setae) with nerves leading to them. The bulb itself is entirely without nerves, and hence without sensory organs and muscles, since these depend on nerves for their functioning, although some spiders have one or two muscles external to the bulb and ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Palpal Bulb
The two palpal bulbs – also known as palpal organs and genital bulbs – are the copulatory organs of a male spider. They are borne on the last segment of the pedipalps (the front "limbs" of a spider), giving the spider an appearance often described as like wearing boxing gloves. The palpal bulb does not actually produce sperm, being used only to transfer it to the female. Palpal bulbs are only fully developed in adult male spiders and are not completely visible until after the final moult. In the majority of species of spider, the bulbs have complex shapes and are important in identification. Structure The palpal bulb of a mature male spider is borne on the last segment of the pedipalp. This segment usually has touch-sensitive hairs (setae) with nerves leading to them. The bulb itself is entirely without nerves, and hence without sensory organs and muscles, since these depend on nerves for their functioning, although some spiders have one or two muscles external to the bulb and ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pedipalp
Pedipalps (commonly shortened to palps or palpi) are the second pair of appendages of chelicerates – a group of arthropods including spiders, scorpions, horseshoe crabs, and sea spiders. The pedipalps are lateral to the chelicerae ("jaws") and anterior to the first pair of walking legs. Overview Pedipalps are composed of six segments or articles: the coxa, the trochanter, the femur, the short patella, the tibia, and the tarsus. In spiders, the coxae frequently have extensions called maxillae or gnathobases, which function as mouth parts with or without some contribution from the coxae of the anterior legs. The limbs themselves may be simple tactile organs outwardly resembling the legs, as in spiders, or chelate weapons ( pincers) of great size, as in scorpions. The pedipalps of Solifugae are covered in setae, but have not been studied in detail. Comparative studies of pedipalpal morphology may suggest that leg-like pedipalps are primitive in arachnids. At present, the only ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Arthropod Leg
The arthropod leg is a form of jointed appendage of arthropods, usually used for walking. Many of the terms used for arthropod leg segments (called podomeres) are of Latin origin, and may be confused with terms for bones: ''coxa'' (meaning hip, plural ''coxae''), ''trochanter'', ''femur'' (plural ''femora''), ''tibia'' (plural ''tibiae''), ''tarsus'' (plural ''tarsi''), ''ischium'' (plural ''ischia''), ''metatarsus'', ''carpus'', ''dactylus'' (meaning finger), ''patella'' (plural ''patellae''). Homologies of leg segments between groups are difficult to prove and are the source of much argument. Some authors posit up to eleven segments per leg for the most recent common ancestor of extant arthropods but modern arthropods have eight or fewer. It has been argued that the ancestral leg need not have been so complex, and that other events, such as successive loss of function of a ''Hox''-gene, could result in parallel gains of leg segments. In arthropods, each of the leg segments ar ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Sternum (arthropod Anatomy)
The sternum (pl. "sterna") is the ventral portion of a segment of an arthropod thorax or abdomen. In insects, the sterna are usually single, large sclerites, and external. However, they can sometimes be divided in two or more, in which case the subunits are called sternites, and may also be modified on the terminal abdominal segments so as to form part of the functional genitalia, in which case they are frequently reduced in size and development, and may become internalized and/or membranous. For a detailed explanation of the terminology, see Kinorhynchs have tergal and sternal plates too, though seemingly not homologous with those of arthropods.Sørensen, M. V. et al. Phylogeny of Kinorhyncha based on morphology and two molecular loci. PLoS One 10, 1–33 (2015). Ventrites are externally visible sternites. Usually the first sternite is covered up, so that vertrite numbers do not correspond to sternid numbers. The term is also used in other arthropod groups such as crustaceans ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Maxilla (spider)
The anatomy of spiders includes many characteristics shared with other arachnids. These characteristics include bodies divided into two tagmata (sections or segments), eight jointed legs, no wings or antennae, the presence of chelicerae and pedipalps, simple eyes, and an exoskeleton, which is periodically shed. Spiders also have several adaptations that distinguish them from other arachnids. All spiders are capable of producing silk of various types, which many species use to build webs to ensnare prey. Most spiders possess venom, which is injected into prey (or defensively, when the spider feels threatened) through the fangs of the chelicerae. Male spiders have specialized pedipalps that are used to transfer sperm to the female during mating. Many species of spiders exhibit a great deal of sexual dimorphism. External anatomy Spiders, unlike insects, have only two main body parts ( tagmata) instead of three: a fused head and thorax (called a cephalothorax or proso ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Labium (arthropod Mouthpart)
The mouthparts of arthropods have evolution, evolved into a number of forms, each adaptation, adapted to a different style or mode of feeding. Most mouthparts represent modified, paired appendages, which in ancestral forms would have appeared more like legs than mouthparts. In general, arthropods have mouthparts for cutting, chewing, piercing, sucking, shredding, siphoning, and filtering. This article outlines the basic elements of four arthropod groups: insects, myriapods, crustaceans and chelicerates. Insects are used as the model, with the novel mouthparts of the other groups introduced in turn. Insects are not, however, the Arthropod#Classification of arthropods, ancestral form of the other arthropods discussed here. Insects Insect mouthparts exhibit a range of forms. The earliest insects had chewing mouthparts. Specialisation includes mouthparts modified for siphoning, piercing, sucking and sponging. These modifications have evolved a number of times. For example, m ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chelicerae
The chelicerae () are the mouthparts of the subphylum Chelicerata, an arthropod group that includes arachnids, horseshoe crabs, and sea spiders. Commonly referred to as "jaws", chelicerae may be shaped as either articulated fangs, or similarly to pincers. Some chelicerae, such as those found on nearly all spiders, are hollow and contain (or are connected to) venom glands, and are used to inject venom into prey or a perceived threat. In ''Pisaurina mira'', also known as the nursery web spider, the chelicerae are utilized to snatch the prey once it becomes within reach, facilitating the "sit-and-wait ambush predator" behavior. Both pseudoscorpions and harvestmen have structures on their chelicerae that are used for grooming (papillae in pseudoscorpions, cheliceral teeth in Opiliones). Types Chelicerae can be divided into three kinds: jackknife chelicerae, scissor chelicerae, and 3-segmented chelate chelicerae. Jackknife chelicerae The jackknife chelicera is subchelate (with ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Heliophanus
''Heliophanus'' is a genus of the spider family Salticidae (jumping spiders). Most of the almost 170 described species occur in Africa, with many others found in the Palearctic region from Europe to Japan. Species , the World Spider Catalog accepted the following species: * '' Heliophanus abditus'' Wesołowska, 1986 – Syria * '' Heliophanus aberdarensis'' Wesołowska, 1986 – Kenya * '' Heliophanus activus'' ( Blackwall, 1877) – Seychelles * '' Heliophanus acutissimus'' Wesołowska, 1986 – Algeria * '' Heliophanus aeneus'' ( Hahn, 1832) – Palearctic * '' Heliophanus aethiopicus'' Wesołowska, 2003 – Ethiopia * '' Heliophanus africanus'' Wesołowska, 1986 – South Africa * '' Heliophanus agricola'' Wesołowska, 1986 – Algeria, Spain * '' Heliophanus agricoloides'' Wunderlich, 1987 – Canary Islands * '' Heliophanus alienus'' Wesołowska, 1986 – Cameroon * '' Heliophanus anymphos'' Wesołowska, 2003 – Kenya * '' Heliophanus apiatus'' Simon, 1868 – Spain ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Jerzy Prószyński
Jerzy Prószyński (born 1935 in Warsaw) is a Polish arachnologist specializing in systematics of jumping spiders (family Salticidae). He is a graduate of the University of Warsaw, a long-term employee of the Siedlce University of Natural Sciences and Humanities and the Institute of Zoology of the Polish Academy of Sciences in Warsaw. Biography In 1957 he completed his biological studies at the University of Warsaw. During his studies he was employed at the Institute of Zoology of the Polish Academy of Sciences in Warsaw, where he conducted research on spiders in the Kampinos Forest. Between 1963 and 1967 he lectured on zoology at the University of Ghana. In 1966 he obtained his Ph.D. at the Adam Mickiewicz University in Poznań. A year later he was given the opportunity to pursue a postdoctoral fellowship at Harvard University, but he was refused a passport. In 1972 he was employed at the Higher School of Education in Siedlce (later the Siedlce University of Natural Scien ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
