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Speleology in Kazakhstan

Shakalov on 04 Jul, 2018
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. ...

New publications on hypogene speleogenesis

Klimchouk on 26 Mar, 2012
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,

The deepest terrestrial animal

Klimchouk on 23 Feb, 2012
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. ...

Caves - landscapes without light

akop on 05 Feb, 2012
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 sump is 1. in caves a sump is a section of flooded passage. this may be a perched sump, probably quite short, within a vadose cave and created by a local reverse passage gradient. alternatively it may be a major feature, where a cave passage descends below the regional water table into the phreas, as is common at the lower end of many cave systems. some short sumps can be dived without the use of breathing apparatus, but most are restricted to exploration by cave divers. logistics are a barrier to endless sump penetrations, but some have now been explored for many kilometers in length, notable in cocklebiddy cave, australia, the nohoch nah chich and other great flooded systems in mexico's yucatan, and behind keld head in yorkshire [9]. 2. a pool of underground water or point on an underground stream that has a submerged extension, the nature of which has not been determined [10]. 3. a place where the ceiling of a passage drops to and below water level in a cave, leaving no air space with the cave passage continuing underwater [13]. 4. a water trap.?

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KarstBase a bibliography database in karst and cave science.

Featured articles from Cave & Karst Science Journals
Chemistry and Karst, White, William B.
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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;
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Your search for palaeoenvironments. (Keyword) returned 2 results for the whole karstbase:
Palaeoenvironments in semi-arid northeastern Brazil inferred from high precision mass spectrometric speleothem and travertine ages and the dynamics of South American rainforests, 2004, Auler A. S. , Wang X. , Edwards R. L. , Cheng H. , Cristalli P. S. , Smart P. L. , Richards D. A.

Understanding past environmental changes in tropical rainforests is extremely important in order to assess the response of such environments to present and future climatic changes and understand causes and the present patterns of biodiversity.
Earlier hypothesis on the origin of biodiversity have stressed the role of past climatic changes in promoting speciation. According to the “refuge hypothesis” (Haffer, 1982), dry periods could have led to forest fragmentation, isolating more humid forested zones (called refuges) within an environment largely dominated by savannas. The refuge hypothesis does not assign timescales for rainforest fragmentation, although recent studies have suggested that speciation could have occurred over timescales of millions of years (Knapp and Mallet, 2003). Although the focus of heavy criticism (Colinvaux, et a., 2000), the refuge hypothesis has generated a large amount of research. In general, pollen studies (Colinvaux, et a., 1996, Haberle and Maslin, 1999) tend to support a continuous forest cover throughout late Quaternary climatic shifts, although large variations in rainfall have also been demonstrated by other pollen and isotopic studies (van der Hammen and Absy, 1994; Maslin and Burns, 2000).
Amazon and Atlantic rainforests are the two major forested zones in South America. Amazon rainforest, the largest rainforest in the world, comprise a total original area of 4.1 million km2 and is renowned for hosting the large biodiversity in the world (30% of all the world’s known plant and animal species). Atlantic rainforest, also a biodiversity hotspot, occurs along the coast and has been subjected to heavy deforestation since European arrival. Nowadays only c. 7% of its original forested area of 1.3 million km2 remains. These two rainforests are separated by drought-prone semi-arid northeastern (NE) Brazil. Our study does not address the refuge hypothesis directly although it sheds new light on the dynamics of forest expansion in the past as well as indicates alternative ways of promoting speciation. It has long been hypothesized, due to botanical (Mori, 1989; Andrade-Lima, 1982) and faunistic (Costa, 2003) similarities, that the Amazon and Atlantic rainforests were once linked in the past. Although numerous connecting routes have been postulated (Bigarella, et al, 1975; Por, 1992; De Oliveira, et al, 1999), the timing of forest expansion and their possible recurrence have remained elusive.
The study area lies in the driest portion of NE Brazil “dry corridor”, close to the village of Laje dos Negros, northern state of Bahia. Mean annual precipitation is around 480 mm and potential evapotranspiration is in excess of 1,400 mm/year (Fig.1). Present vegetation comprises a low arbustive scrubland known locally as caatinga. The area contains a well-developed underground karst (Auler and Smart, 2003) with abundant secondary calcite precipitates, both underground (speleothems) and on the surface (travertines).

New palaeontological assemblage, sedimentological and chronological data from the Pleistocene Ma U'Oi cave (northern Vietnam), 2006, Bacon Am, Demeter F, Rousse S, Long Vt, Duringer P, Antoine Po, Thuy Nk, Mai Bt, Huong Ntm, Dodo Y,
This paper describes recent material gathered during the second fieldwork at Ma U'Oi in November 2002 by a Vietnamese-French-Japanese team. The Ma U'Oi cave, located in the province of Hoa Binh (60 km SW from Hanoi), northern Vietnam, belongs to a karstic network developed in Triassic dark-grey limestones.The cave is filled with coarse-grained breccias containing numerous fossil remains, partially preserved at several loci inside the cave (wall, vault and ground). We describe new teeth which confirm the occurrence of mammal taxa already mentioned at Ma U'Oi (Bacon et al., 2004)[Bacon, A-M., Demeter, F., Schuster, M., Long, V.T., Thuy, N.K., Antoine, P-O., Sen, S., Nga, H.H., Huong, N.T.M., 2004. The Pleistocene Ma U'Oi cave, northern Vietnam: palaeontology, sedimentology and palaeoenvironments. Geobios 37, 305-314], while others, mainly microvertebrates, emphasize the occurrence of new species for the Pleistocene of Vietnam. We report here, for the first time, the occurrence of these microvertebrates of different groups (primates, rodents, insectivores, small reptiles and amphibians) in the faunal assemblage. Among mammal taxa, the presence of one more hominid affiliated to archaic Homo is also attested by our findings. U/Th dating carried out on 2 samples extracted from breccia speleothems confirms the biochronological estimate, with fossiliferous fillings ranging from late Middle Pleistocene to Late Pleistocene

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