Search PubMedSearch

SEARCH · Search PubMed

Results for “Arachnida”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 19 recordsLinked to original sources

Cytophysiological aspects of digestion and storage in the liver of a scorpion, Androctonus australis (Arachnida).

The liver of a scorpion, Androctonus australis (Arachnida), was examined electron-microscopically and cytochemically, emphasizing correlations between structure, cytochemistry and physiology. The liver consists of digestive diverticula and interstitial tissue. Digestive diverticula are composed of basophilic cells and digestive cells. Basophilic cells produce exoenzymes. Digestive cells ensure intracellular digestion of nutrients absorbed by pinocytosis and store glycogen, lipids and mineral salts; the wastes of the digestive process (guanine, uric acid, mineral elements, pigments) are concentrated in "brown body vacuoles" which are ejected into the lumen of the diverticula. The interstitial tissue stores glycogen and lipids; it contains many lysosome-like organelles rich in iron. Fasting induces a decrease of the ratio of the volume of the diverticula to that of the interstitial tissue, a slow disappearance of the reserves in both diverticula and interstitial tissue, an increase of synthesis in the basophilic cells, and a decrease of the number of vacuoles in the digestive cells. The digestive mode of the scorpions associates a primitive intracellular process with an advanced extracellular process. The interstitial tissue can be considered as homologous to the adipose tissue of insects and myriapods, although it is devoid of urate cells. The excretion of guanine and uric acid has a peculiar meaning, because these purine wastes do not come from endogenous catabolism.

Animals

Fine structure of tarsal sensory organs in the whip spider Admetus pumilio (Amblypygi, Arachnida).

The sensory organs on the tarsi of the antenniform first legs of the whip spider Admetus pumilio C. L. Koch (Amblypygi, Arachnida) were examined with the scanning and transmission electron microscope. At least four different types of hair sensilla were found: (1) thick-walled bristles, which have the characteristics of contact chemoreceptors (several chemoreceptive dendrites in the lumen plus two mechanoreceptors at the base); (2) short club sensilla, innervated by 4-6 neurons which terminate in a pore on the tip; they are possibly humidity receptors; (3) porous sensilla, which are either innervated by 20-25 neurons and have typical pore tubules, or they have 40-45 neurons but no pore tubules; both types are considered to be olfactory; (4) rod sensilla occur in clusters near segmental borders; they are innervated by only one large dendrite which branches inside the lumen. Other tarsal receptors are the claws, which correspond to contact chemoreceptors, and the pit organ which resembles the tarsal organ of spiders. Compared to other arthropod sensilla, the contact chemoreceptors are very similar to those of spiders, while the porous sensilla correspond structurally to olfactory receptors in insects; the club and rod sensilla seem to be typical for amblypygids.

Animals

Ultrastructural analysis of the X1X2X3O sex chromosome system during the spermatogenesis of Tegenaria domestica (Arachnida).

An ultrastructural study was performed on the sex chromosomes (male X1X2X3O) during the spermatogenesis of Tegenaria domestica (Arachnida, Agelenidae). This study was carried out using random and serially cut sections. During pachytene and diplotene the three X chromosomes are longitudinally paired. Each of these consists of a central core of condensed chromatin, surrounded by a field of dense chromatin projections through which the chromosomes are in contact with one another. These projections may be responsible for the recognition and pairing of the sex chromosomes and in some way participate in their non-disjunction during anaphase I. A study of the structure and behaviour of the sex chromosomes during spermatogenesis is also presented. The available information on non-synaptonemal complex-mediated chromosome pairing and a systematization of sex chromosome structure in spiders are discussed.

Animals

Distribution of acetylcholinesterase in the central nervous system of harvestmen (Arachnida: Opilionida).

Enzyme histochemical technique (Gomori and Koelle methods, reaction product development according to Lewis) was applied on 10 microm frozen sections of formalin-fixed material to demonstrate the distribution of acetylcholinesterase in the central nervous system (CNS) of harvestmen (Opilionida: Phalangiidae). Distinctly positive reactions were confined to the neuropil, showing strong staining especially in protocerebral brain centres (optic lobes, cerebral ganglia), the cheliceral ganglia (stomodeal bridge, afferent tracts), and the connective ring systems of the subesophageal nerve mass. The results obtained are discussed with regard to central coordinative functions of the respective brain parts.

Acetylcholinesterase

Characterization and synthesis of volatile compounds from the defensive secretions of some "daddy longlets" (Arachnida: Opiliones: Leiobunum spp.).

Analyses of the chief volatile constituents of the defensive secretions of three oplionids were carried out. Leiobunum nigripalpi produces three closely related C7 compounds: E-4-methyl-4-hexen-3-one(I), 4-methylhexan-3-one(II), and 4-methylhexan-3-ol(III), along with E-4-methyl-4-hepten-3-one(IV), E,E-2,4-dimethylhexa-2,4-dienal(IX), and a minor, unidentified component. L. leiopenis secretion contains E-4-methyl-4-hepten-3-one(IV), 4-methylheptan-3-one(V), E,E-2,4-dimethylhexa-2,4-dien-1-ol(VII), and E,E-2,4-dimethylhepta-2,4-dien-1-ol(VIII). L. calcar yields chiefly E-4,6-dimethyl-6-octen-3-one(VI) and E,E-2,4-dimethylhexa-2,4-dien-1-ol(VII). Six of these compounds are new natural products. The structures of these compounds, which can be regarded either as polyketide-derived or as modified isoprenoids, raise interesting biosynthetic questions.

Alcohols

Electrophoretic protein patterns of body extracts and species identification in some pseudoscorpions (Neobisiidae: Pseudoscorpiones: Arachnida).

The technique of the universal film agarose electrophoresis has been used to detect biochemical characteristics of the body extract proteins in 3 different species and 2 genera of the pseudoscorpion family Neobisiidae. The migration rate of these proteins as well as their relative abundance for Neobisium carpaticum Beier, Neobisium macrodactylum (Daday) and Roncus pannonius Curcić, Dimitrijević & Karamata, from Yugoslavia, were compared. Electrophoretic identifications of these species showed both species-specific and (probably) intergeneric differences. It is assumed that body protein electrophoresis can be also used: (a) to differentiate species in any stage of their life cycle, (b) to reveal the presence of sibling species, and to differentiate the taxonomic and evolutionary interrelations both in congeneric as well as in other, more distant taxa.

Animals

The distribution of acetylcholinesterase in the central nervous system of jumping spiders and wolf spiders (Arachnida, Araneida: Salticidae et Lycosidae).

The distribution and activity pattern of acetylcholinesterase in the central nervous system of salticid and lycosid spiders has been studied. Enzyme activity was limited to the neuropile mass. The salticid and lycosid species investigated showed different intensities of enzyme reactions in the protocerebrum. The differences observed may be related to the somewhat contrasting habits of these spider families. Reactions were strong especially in the optic ganglia (lamina glomerularis, corpora pedunculata) and in the cerebral ganglion, while the central body showed only weak to moderate activity. In the cheliceral ganglia, as in the pedipalpal and the leg ganglia, including the fibre tracts of the ventral cord the demonstration of acetylcholinesterase was of moderate to strong intensity.

Acetylcholinesterase