Impacts of faulty grey infrastructures on the bathymetry and salinity of Vembanad Lake, a tropical estuary along the south west coast of India.

Environ Monit Assess

Centre for Aquatic Resource Management and Conservation, Kerala University of Fisheries and Ocean Studies, Panangad, Kochi, 682506, Kerala, India.

Published: February 2025

The fast degradation in bathymetry, floodwater retention capacity, and changes in salinity regimes of Vembanad-the largest wetland system in South India-and its impacts on the ecosystem services are assessed using high-resolution data sets on bathymetry and hydrography. Strengthening the outer banks of Kuttanad polders to promote paddy cultivation led to a sharp decline in its sediment (suspended) filtration potential, promoting heavy siltation and depth shrinkage of Vembanad Lake. With an area of 315 sq.km and an average depth of 8.5 m (south sector)/7.87 m (central sector), the lake had a retention capacity of 2617.5 MCM floodwaters in 1930 which was reduced to 384.7 MCM by 2020 (85.3% loss in retention capacity) due to area (162.5 sq.km) and depth (average 1.8 m in the south sector and 2.87 m in the central sector) shrinkages. This resulted in the prolonged inundation of low-lying areas and increased incidences of flash floods. Both sectors of the lake maintain limnetic and well-mixed conditions during the monsoon whereas during non-monsoon season, the central sector turns to polyhaline/mesohaline and oligohaline conditions with stratified, partially mixed, and well-mixed salinity stratifications unlike the south sector which perennially remain limnetic and well mixed. The observed shift in salinity regimes appears to promote hypertrophic conditions, biodiversity loss, and a sharp reduction in the black clam abundance of the south sector, which before the commissioning of Thannermukkom Barrage (TMB) was a major clam ground.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10661-025-13773-5DOI Listing

Publication Analysis

Top Keywords

retention capacity
12
south sector
12
vembanad lake
8
salinity regimes
8
central sector
8
south
6
sector
5
impacts faulty
4
faulty grey
4
grey infrastructures
4

Similar Publications

In this study, quercetin-incorporated squalene nanostructured lipid carriers (QS-NLCs) were developed to mitigate the pathological conditions of dry eye disease (DED). The melt emulsification method was used to prepare QS-NLCs. The resulting NLCs have 93.

View Article and Find Full Text PDF

Intermolecular interactions influenced the gelation and texture improvement of sturgeon surimi gels by walnut protein isolates.

Food Chem

March 2025

College of Food Science and Technology, Yunnan Agricultural University, 425 Fengyuan Road, Kunming 650201, Yunnan, China. Electronic address:

Intermolecular interaction is a key factor in the fortification of surimi gels by plant protein addition. Here, the effects of different intermolecular interactions, such as ionic, covalent and non-covalent interactions, on gel structure, gelation strength and water-holding properties were investigated, using sturgeon surimi fortified by three walnut isolates, including walnut meal (WM), protein isolate (WPI) and peptide (WP), as representatives. Quantitative creep-recovery analysis and soluble protein assay demonstrated that secondary bonds, mainly hydrophobic interaction and hydrogen bond, possibly played a dominant role in walnut protein-fortified surimi gels.

View Article and Find Full Text PDF

High internal phase Pickering emulsions (HIPPEs) hold broad application prospects in the modern food industry. This study developed a novel strategy for extracting starch from a non-conventional source (millet) followed by chemical modification to construct a ternary octenyl succinate millet starch/chitosan hydrochloride-epigallocatechin gallate (OMS/CHC-EGCG) complex to stabilize HIPPEs. The OMS/CHC-EGCG complex was assembled through electrostatic, hydrophobic, and hydrogen bonding interactions among OMS, CHC, and EGCG.

View Article and Find Full Text PDF

High performance of 5 V LiNiMnO cathode materials synthesized from recycled LiCO for sustainable Lithium-Ion batteries.

J Colloid Interface Sci

March 2025

Battery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC; Department of Chemical Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan, ROC; Department of Chemical and Materials Engineering & Center for Sustainability and Energy Technologies, Chang Gung University, Taoyuan City 333, Taiwan, ROC. Electronic address:

Lithium has become a critical element in the modern era due to the emergence of lithium-ion battery (LIB) technologies as a mean to lessen the environmental burden created by the energy usage from conventional sources. In this study, LiCO was obtained from spent LIBs using a hydrometallurgical method and sintered with Taylor Flow Reactor (TFR) synthesized NiMn(OH) precursor to synthesize high-voltage LiNiMnO (R-LNMO) cathode material for the first time and conducted a series of tests and inspections for structure, morphology, electrochemical lithium cycling behaviour and its controlling factors, electronic conductivity, lithium ion diffusion characteristics and self-discharge behaviour. The results are benchmarked with C-LNMO synthesized through a similar processing but using LiCO obtained from a commercial source.

View Article and Find Full Text PDF

Phosphorus is considered an ideal anode material for lithium ion storage by virtue of its high theoretical capacity and moderate lithiation potential. However, issues such as large volume expansion of phosphorus leading to an electrical loss of contact and instability of the solid electrolyte interface hinder its practical performance. Improvement strategies that can effectively suppress volume expansion and provide stable electrical contacts are urgently needed.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!