Hello everyone!
I pleased to invite you to the official site of Central Asian Karstic-Speleological commission ("Kaspeko")
There, we regularly publish reports about our expeditions, articles and reports on speleotopics, lecture course for instructors, photos etc. ...
Dear Colleagues, This is to draw your attention to several recent publications added to KarstBase, relevant to hypogenic karst/speleogenesis: Corrosion of limestone tablets in sulfidic ground-water: measurements and speleogenetic implications Galdenzi,
A recent publication of Spanish researchers describes the biology of Krubera Cave, including the deepest terrestrial animal ever found:
Jordana, Rafael; Baquero, Enrique; Reboleira, Sofía and Sendra, Alberto. ...
Exhibition dedicated to caves is taking place in the Vienna Natural History Museum
The exhibition at the Natural History Museum presents the surprising variety of caves and cave formations such as stalactites and various crystals. ...
Did you know?
That naked karst, bare karst is karst topography developed beneath a temporary cover. some naked karsts develop beneath a temporary cover of snow (nival karst) or water [17]. synonyms: (french.) karst nu; (german.) oberflachlicher nackter karst; (greek.) gymnon karst; (italian.) carso nudo; (russian.) goly karst or otkryty karst; (spanish.) karst desnudo; (turkish.) ciplak karst; (yugoslavian.) goli krs. see also exposed karst.?
Three new hypogean species of the Iberian genus Roncocreagris Mahnert, 1974 are described from mainland Portugal: R. borgesi sp. nov. and R. gepesi sp. nov. from caves in the Sicó massif, and R. occidentalis sp. nov. from caves in the Montejunto and Cesaredas karst plateau. This brings to nine the number of known hypogean species of the mostly Iberian genus Roncocreagris: five from Portugal and four from Spain. Ecological comments and new localities for some of the previously known species are also included.
In Europe, Asellus cavaticus Leydig until 1963 was the only species known of a phyletic line that extended from Britain to Austria. Until the works of Racovitza in 1919 all the Asellus of the underground world were reported to this species, first known subterranean Asellus. The taxonomic criteria of Racovitza allowed to determine many subspecies. Later on Chappuis refuses to give names to the different encountered forms. Taking as type forms the individuals of the grotte de Sainte-Reine (Meurthe-et-Moselle), considered very similar to the original type forms, we think to be able to define a new subspecies puteanus for the Asellus of a well in Beaujolais. This form differs from cavaticus f. typ. for the form of the male copulation organ, the male pleopod and the number of spines on the dactlya and pereiopodes. A more detailed description of the subspecies valdensis Chappuis is given based on specimens from a cave of the Plateau of Crémieu (Isère).
The Mammoth Cave system includes more than 175 kilometers of explored passages in Mammoth Cave National Park, Kentucky. Although biologists have explored the caves intermittently since 1822, the inventory of living organisms in the system is still incomplete. The present study lists approximately 200 species of animals, 67 species of algae, 27 species of fungi, and 7 species of twilight-zone bryophytes. The fauna is composed of 22% troglobites, 36% troglophiles, 22% trogloxenes, and 20% accidentals, and includes protozoans, sponges, triclads, nematodes, nematomorphs, rotifers, oligochaetes, gastropods, cladocerans, copepods, ostracods, isopods, amphipods, decapods, pseudoscorpions, opilionids, spiders, mites and ticks, tardigrades, millipedes, centipedes, collembolans, diplurans, thysanurans, cave crickets, hemipterans, psocids, moths, flies, fleas, beetles, fishes, amphibians, birds, and mammals. The Mammoth Cave community has evolved throughout the Pleistocene concomitantly with development of the cave system. The troglobitic fauna is derived from 4 sources: (1) troglobite speciation in situ in the system itself; (2) dispersal along a north Pennyroyal plateau corridor; (3) dispersal along a south Pennyroyal plateau corridor; and (4) dispersal across the southwest slope of the Cumberland saddle merokarst.
The Mammoth Cave system includes more than 175 kilometers of explored passages in Mammoth Cave National Park, Kentucky. Although biologists have explored the caves intermittently since 1822, the inventory of living organisms in the system is still incomplete. The present study lists approximately 200 species of animals, 67 species of algae, 27 species of fungi, and 7 species of twilight-zone bryophytes. The fauna is composed of 22% troglobites, 36% troglophiles, 22% trogloxenes, and 20% accidentals, and includes protozoans, sponges, triclads, nematodes, nematomorphs, rotifers, oligochaetes, gastropods, cladocerans, copepods, ostracods, isopods, amphipods, decapods, pseudoscorpions, opilionids, spiders, mites and ticks, tardigrades, millipedes, centipedes, collembolans, diplurans, thysanurans, cave crickets, hemipterans, psocids, moths, flies, fleas, beetles, fishes, amphibians, birds, and mammals. The Mammoth Cave community has evolved throughout the Pleistocene concomitantly with development of the cave system. The troglobitic fauna is derived from 4 sources: (1) troglobite speciation in situ in the system itself; (2) dispersal along a north Pennyroyal plateau corridor; (3) dispersal along a south Pennyroyal plateau corridor; and (4) dispersal across the southwest slope of the Cumberland saddle merokarst.
The Nullarbor Plain is a low plateau of Tertiary limestone covering an area of 194,175 km2 in southern Australia. It has a semi-arid climate and supports a stunted vegetation. Ninety-five species of arthropods have been recorded from 47 Nullarbor caves, and many of these species are widely distributed across the Plain. Two possible explanations for their distribution are discussed. Subterranean migration may occur through the widespread zone of small interconnecting cavities in the Nullarbor Limestone, but this has not yet been confirmed. While cave arthropods are confined to the cool, moist cave environment during the day, they have been observed at night in cave entrances, in dolines and on the surface of the Plain. Cave "breathing", similarity in cave and epigean climate at night, strong winds, occasional heavy rain and numerous animal burrows all contribute towards favourable conditions for surface migration.
During 1971, members of the University of N.S.W. Speleological Society (UNSWSS) were working on a project to determine water table levels, as represented by sumps, in some of the Bungonia Caves. It was soon realised that the accuracy of heights determined from the available surface surveys, usually "forestry compass" traverses, was insufficient. The author was asked to provide more accurate surface levels and, consequently, two trips were organised on 24-25 July and 31 July 1971 with the aim of establishing a differential levelling net in the plateau area. Personnel on the first trip comprised E.G. Anderson and A.J. Watson (Senior Photogrammetrist, N.S.W. Lands Department), surveyors, and A.J. Pavey and M. Caplehorn, UNSWSS, assistants. On the second trip, M. Caplehorn was replaced by A. Culberg, UNSWSS.
