KarstBase a bibliography database in karst and cave science.
Featured articles from Cave & Karst Science Journals
Characterization of minothems at Libiola (NW Italy): morphological, mineralogical, and geochemical study, Carbone Cristina; Dinelli Enrico; De Waele Jo
Chemistry and Karst, White, William B.
The karst paradigm: changes, trends and perspectives, Klimchouk, Alexander
Long-term erosion rate measurements in gypsum caves of Sorbas (SE Spain) by the Micro-Erosion Meter method, Sanna, Laura; De Waele, Jo; Calaforra, José Maria; Forti, Paolo
The use of damaged speleothems and in situ fault displacement monitoring to characterise active tectonic structures: an example from Zapadni Cave, Czech Republic , Briestensky, Milos; Stemberk, Josef; Rowberry, Matt D.;
Featured articles from other Geoscience Journals
Karst environment, Culver D.C.
Mushroom Speleothems: Stromatolites That Formed in the Absence of Phototrophs, Bontognali, Tomaso R.R.; D’Angeli Ilenia M.; Tisato, Nicola; Vasconcelos, Crisogono; Bernasconi, Stefano M.; Gonzales, Esteban R. G.; De Waele, Jo
Calculating flux to predict future cave radon concentrations, Rowberry, Matt; Marti, Xavi; Frontera, Carlos; Van De Wiel, Marco; Briestensky, Milos
Microbial mediation of complex subterranean mineral structures, Tirato, Nicola; Torriano, Stefano F.F;, Monteux, Sylvain; Sauro, Francesco; De Waele, Jo; Lavagna, Maria Luisa; D’Angeli, Ilenia Maria; Chailloux, Daniel; Renda, Michel; Eglinton, Timothy I.; Bontognali, Tomaso Renzo Rezio
Evidence of a plate-wide tectonic pressure pulse provided by extensometric monitoring in the Balkan Mountains (Bulgaria), Briestensky, Milos; Rowberry, Matt; Stemberk, Josef; Stefanov, Petar; Vozar, Jozef; Sebela, Stanka; Petro, Lubomir; Bella, Pavel; Gaal, Ludovit; Ormukov, Cholponbek;
ISS-UIS
International Journal of Speleology, 1974, Vol 6, Issue 1, p. 1-0
Ecological and Faunistic Data on the Stenasellidae (Crustacea Isopoda Asellota of Subterranean Waters).
Magniez Guy
Abstract:
Some important morphological features, which are discussed here, point out that the Stenasellids (Crustacea Isopoda Asellota) must be considered as a true family (Stenasellidae), independent from the Asellidae. A definition and a renewed diagnosis of the Stenasellidae Dudich, 1924, are given. Their relationships must be pursued, especially in the marine Parastenetroidea and in the psammic Microcerberidae. Until 1938, the group was known only from subterranean waters of southern Europe. Now, several genera and many thermophile species from north-tropical underground waters have been discovered in Africa (5 gen., 12 sp.), Asia (1 gen., 2 sp.) and Central America (1 gen., 4 sp.). The Stenasellids are very active burrowers. Such a behaviour explains how their phyletic lines had colonized the continental underground waters, by migrations from the littoral gravels to the underflow of rivers, phreatic alluvial waters and fìnally, to the karstic waters. The typical medium for the life of the group is represented by the phreatic zones of African shields arenas. In European phyletic lines, the speciation seems to be linked with tertiary subsidences (within the Tyrrhenian area, for the line of Stenasellus virei). The European species which have survived quaternary glaciations may have diversified themselves (rising of subspecies), recolonizing newly vacant biotopes in postglacial ages.
Some important morphological features, which are discussed here, point out that the Stenasellids (Crustacea Isopoda Asellota) must be considered as a true family (Stenasellidae), independent from the Asellidae. A definition and a renewed diagnosis of the Stenasellidae Dudich, 1924, are given. Their relationships must be pursued, especially in the marine Parastenetroidea and in the psammic Microcerberidae. Until 1938, the group was known only from subterranean waters of southern Europe. Now, several genera and many thermophile species from north-tropical underground waters have been discovered in Africa (5 gen., 12 sp.), Asia (1 gen., 2 sp.) and Central America (1 gen., 4 sp.). The Stenasellids are very active burrowers. Such a behaviour explains how their phyletic lines had colonized the continental underground waters, by migrations from the littoral gravels to the underflow of rivers, phreatic alluvial waters and fìnally, to the karstic waters. The typical medium for the life of the group is represented by the phreatic zones of African shields arenas. In European phyletic lines, the speciation seems to be linked with tertiary subsidences (within the Tyrrhenian area, for the line of Stenasellus virei). The European species which have survived quaternary glaciations may have diversified themselves (rising of subspecies), recolonizing newly vacant biotopes in postglacial ages.