Biogeochemical controls on metal behaviour in freshwater environments

2001 ◽  
Vol 54 (4) ◽  
pp. 261-320 ◽  
Author(s):  
Lesley A. Warren ◽  
Elizabeth A. Haack
1989 ◽  
Vol 4 ◽  
pp. 244-248 ◽  
Author(s):  
Donald L. Wolberg

The minerals pyrite and marcasite (broadly termed pyritic minerals) are iron sulfides that are common if not ubiquitous in sedimentary rocks, especially in association with organic materials (Berner, 1970). In most marine sedimentary associations, pyrite and marcasite are associated with organic sediments rich in dissolved sulfate and iron minerals. Because of the rapid consumption of sulfate in freshwater environments, however, pyrite formation is more restricted in nonmarine sediments (Berner, 1983). The origin of the sulfur in nonmarine environments must lie within pre-existing rocks or volcanic detritus; a relatively small, but significant contribution may derive from plant and animal decomposition products.


2021 ◽  
Vol 232 (5) ◽  
Author(s):  
Runrun Ding ◽  
Ling Tong ◽  
Weicheng Zhang

2020 ◽  
Vol 8 (3) ◽  
pp. 216 ◽  
Author(s):  
Cristiana Guerranti ◽  
Guido Perra ◽  
Tania Martellini ◽  
Luisa Giari ◽  
Alessandra Cincinelli

Plastic debris occurring in freshwater environments, which can either come from the surrounding terrestrial areas or transported from upstream, has been identified as one of the main sources and routes of plastic pollution in marine systems. The ocean is the final destination of land- based microplastic sources, but compared to marine environments, the occurrence and effects of microplastics in freshwater ecosystems remain largely unknown. A thorough examination of scientific literature on abundance, distribution patterns, and characteristics of microplastics in freshwater environments in Mediterranean tributary rivers has shown a substantial lack of information and the need to apply adequate and uniform measurement methods.


1997 ◽  
Vol 07 (03n04) ◽  
pp. 147-151 ◽  
Author(s):  
TARO OHTA ◽  
NOBUAKI ARAI ◽  
MASARU TANAKA ◽  
KOJI YOSHIDA

Japanese sea bass (Lateolabrax japonicus) is a typical euryhaline marine fish and frequently migrates from salt to freshwater environments during early life stages. We hypothesized that strontium concentrations in the otolith could be a useful index to examine freshwater entry because of its lower concentration in freshwater. Otoliths of Japanese sea bass juveniles collected in the Chikugo river and estuary were analyzed by Particle Induced X-ray Emission (PIXE) to see relationship between strontium concentration and ambient salinity. Strontium concentrations in otoliths of sea bass juveniles are significantly lower in the river samples than in brackish water samples.


2014 ◽  
Vol 10 (3) ◽  
pp. 491-504 ◽  
Author(s):  
Yu-Mei Chang ◽  
Ran Tang ◽  
Xin-Jie Dou ◽  
Ran Tao ◽  
Xiao-Wen Sun ◽  
...  

Transcriptome profiles of alkaline and freshwater environments ofLeuciscus waleckiiwere compared to explore the alkali-adapted mechanisms of a freshwater teleost.


Author(s):  
Xintong Li ◽  
Ruifeng Liang ◽  
Yong Li ◽  
Yaodan Zhang ◽  
Yuanming Wang ◽  
...  

2021 ◽  
Vol 4 (3) ◽  
Author(s):  
ANDRÉ NEL

Gaps in the fossil record are the major challenge for estimations of impacts of crises of biodiversity of the various clades. They can lead to important misinterpretations in the effects of the different events on the fauna and flora. It is especially the case for the end-Cretaceous, which is ‘near the midpoint of a 16-million-year gap in the insect fossil record’ (Schachat & Labandeira, 2021: 111). All the important Cretaceous insect Konzentrat Lagerstätten are before the Turonian. The analysis of Schachat et al. (2019) has reconstructed a massive loss of family-level diversity for the insects at the boundary Cretaceous-Cenozoic, a possible artefact due to this gap. An alternative scenario was that a turnover in the entomofauna occurred during the early Late Cretaceous in relation to the floristic changes of the Albian–Cenomanian (Nel et al., 2018). This turnover would have also affected the aquatic insects through important changes in the freshwater environments (Sinitshenkova & Zherikhin, 1996; Ivanov & Sukatsheva, 2002). The current knowledge on the odonatan fossil record suggests a pronounced turnover with the last records of several major clades during the Cenomanian-Turonian and first records of several modern ones during the same period (Nel et al., 2015). The widespread and very diverse Jurassic-Cretaceous family Aeschnidiidae is among the best examples of such extinctions supposed to have occurred after the Cenomanian, because of the absence of any fossil in younger strata.


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