brackish environment
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Author(s):  
G. William M. Harrison ◽  
Anna Lene Claussen ◽  
Christian Schulbert ◽  
Axel Munnecke

AbstractBryostromatolites are found in stressed environments from the Paleozoic to the Recent. They are formed by alternating layers of bryozoans and microbes. This study investigates recent bryostromatolites in brackish ponds in the Netherlands to better understand ancient analogues and the environments which hosted them. They formed a fringing reef at the site Ronde Weel and a barrier reef at Kaaskenswater. The ponds had low biodiversity with only one bivalve species, two gastropod species, one ostracod species, and three diatom species comprising most of the easily fossilizable taxa; one isopod species, one decapod species, and two polychaete species were also present. Observations of microbial layers and cementation practices indicate that an alternation of bryozoan-favouring conditions and microbe-favouring conditions is essential to forming bryostromatolites. The collected bryostromatolites only had tiny living bryozoan patches. Water tests confirmed a brackish environment but with enriched arsenic and titanium concentrations and periodic euxinia. The extreme environment explains the lack of biodiversity and may provide information about the environments in which past bryostromatolites formed.


The Holocene ◽  
2020 ◽  
Vol 31 (1) ◽  
pp. 108-120
Author(s):  
Angelica Ballesteros-Prada ◽  
Mariel Luengo ◽  
Isabel Vilanova ◽  
Enrique Fucks ◽  
Emiliana Bernasconi

In this investigation, we carried out a Mid-Holocene paleoenvironmental reconstruction based on fossilized benthic foraminifera, retrieved from sedimentary deposits located in Bahía Samborombón coastal plain. A total of 38 species, grouped into 19 genera, were identified. The assemblage, constituted mainly by Buccella peruviana (d’Orbigny), Cribroelphidium poeyanum (d’Orbigny), Ammonia parkinsoniana (d’Orbigny) and Ammonia tepida (Cushman), indicate predominantly abnormal marine conditions, characterized by low oxygen levels between ca. 6880–6640 and 5600–5430 yrs cal. BP. During this interval, a quantitative analysis carried out on the assemblages as well as indexes suggest found three different paleoenvironments. The first one, occurring ca. 6880–6640 yrs cal. BP, was a brackish environment with low oxygenation levels and low bottom energy. Then, ca. 6500–6250 yrs cal. BP, an environment with more marine influence, increased oxygen levels and higher energy prevailed. This higher oxygenation could be related to the flow of seawater into the area during the Mid-Holocene sea-level highstand. The third paleoenvironment developed ca. 5590–5430 yrs cal. BP, was under a gradual transition back to a brackish environment with low oxygen levels as well as low energy.


Webbia ◽  
2019 ◽  
Vol 74 (1) ◽  
pp. 167-177
Author(s):  
Kaire Torn ◽  
Anneliis Peterson ◽  
Kristjan Herkül ◽  
Ülo Suursaar

2018 ◽  
Vol 32 (26) ◽  
pp. 3954-3965
Author(s):  
Cécile Finco ◽  
Coralie Pontoreau ◽  
Cyril Schamper ◽  
Sylvain Massuel ◽  
Gaghik Hovhannissian ◽  
...  

2017 ◽  
Vol 15 (3) ◽  
Author(s):  
Esteban Avigliano ◽  
Jorge Pisonero ◽  
Alejandro Dománico ◽  
Sebastián Sánchez ◽  
Alejandra V. Volpedo

ABSTRACT The streaked prochilod, Prochilodus lineatus, represents the most important fishery in the La Plata Basin (South America). Our objective was to analyze brackish environment use by the streaked prochilod captured from Paraná and Uruguay rivers. To accomplish this, lapillus otolith sections were analyzed for Sr:Ca with laser ablation-inductively coupled plasma-mass spectrometry (LA ICP-MS) to infer habitat use of fish. To the interpretation of transects, a threshold that represents the transition between freshwater and brackish environments was calculated using the Sr:Ca ratio of the otolith edge of specimens captured in the first section of the La Plata Estuary (salinity ≥ 0.5 PSU). The percentage of fish using the estuary was higher in the Paraná (37%) than the Uruguay River (5%). Change-point analysis showed that fish entered the estuary between 1 and 3 times throughout life at a wide range of ages (0-15 years). These incursions had no obvious periodicity. This information should be integrated into future management actions, which should also be specific to each area since migration patterns differ between the major rivers of the basin.


2017 ◽  
Vol 91 (2) ◽  
pp. 695-703 ◽  
Author(s):  
I. Taal ◽  
M. Rohtla ◽  
L. Saks ◽  
R. Svirgsden ◽  
M. Kesler ◽  
...  

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