The Land–Water Interface: Science for a Sustainable Biosphere1

2000 ◽  
Vol 10 (4) ◽  
pp. 939-940 ◽  
Author(s):  
Catherine M. Pringle ◽  
Mary Barber
Food Webs ◽  
2019 ◽  
Vol 18 ◽  
pp. e00107 ◽  
Author(s):  
Peter E. Schlichting ◽  
Cara N. Love ◽  
Sarah C. Webster ◽  
James C. Beasley

1999 ◽  
Vol 3 (3) ◽  
pp. 260-262 ◽  
Author(s):  
Eduardo Marvez ◽  
Debra Houry ◽  
Steven Weiss ◽  
Juliette Saussy ◽  
Dawne Orgeron
Keyword(s):  

2010 ◽  
pp. 97-129 ◽  
Author(s):  
Drew M. Talley ◽  
Gary R. Huxel ◽  
Marcel Holyoak
Keyword(s):  

2015 ◽  
Author(s):  
Kristy Deiner ◽  
Emanuel A. Fronhofer ◽  
Elvira Meächler ◽  
Jean-Claude Walser ◽  
Florian Altermatt

AbstractDNA sampled from the environment (eDNA) is becoming a game changer for uncovering biodiversity patterns. By combining a conceptual model and empirical data, we test whether eDNA transported in river networks can be used as an integrative way to assess eukaryotic biodiversity for broad spatial scales and across the land-water interface. Using an eDNA metabarcode approach we detected 296 families of eukaryotes, spanning 19 phyla across the catchment of a river. We show for a subset of these families that eDNA samples overcome spatial autocorrelation biases associated with classical community assessments by integrating biodiversity information over space. Additionally, we demonstrate that many terrestrial species can be detected; thus revealing that eDNA in river-water also incorporates biodiversity information across terrestrial and aquatic biomes. Environmental DNA transported in river networks offers a novel and spatially integrated way to assess total biodiversity for whole landscapes and will transform biodiversity data acquisition in ecology.“Eventually, all things merge into one, 32 and a river runs through it.” — Norman Maclean


2018 ◽  
Vol 32 (3) ◽  
pp. 351-357 ◽  
Author(s):  
Deepa Jaiswal ◽  
Ekabal Siddiqui ◽  
Kavita Verma ◽  
Jitendra Pandey

2020 ◽  
Author(s):  
Kimberly A. Carter-Fenk ◽  
Kevin Carter-Fenk ◽  
Michelle E Fiamingo ◽  
Heather Allen ◽  
John M. Herbert

<p>Surface-sensitive vibrational spectroscopy is a common tool for measuring molecular organization and intermolecular interactions at interfaces. Peak intensity ratios are typically used to extract molecular information from one-dimensional spectra but vibrational coupling between surfactant molecules can manifest as signal depletion in one-dimensional spectra. Through a combination of experiment and theory, we demonstrate the emergence of vibrational excitons in infrared reflection-absorption spectra of soluble and insoluble surfactants at the air/water interface. Vibrational coupling yields a signicant decrease in peak intensities corresponding to C-F vibrational modes of perfluorooctanoic acid molecules. Vibrational excitons also form between arachidic acid surfactants within a compressed monolayer, manifesting as signal reduction of C-H stretching modes. The aqueous phase ionic composition impacts surfactant intermolecular distances, thereby modulating vibrational coupling strength between surfactants. Our results serve as a cautionary tale against employing alkyl and fluoroalkyl vibrational peak intensities in analyses that are ubiquitous in interface science.</p>


2020 ◽  
Author(s):  
Kimberly A. Carter-Fenk ◽  
Kevin Carter-Fenk ◽  
Michelle E Fiamingo ◽  
Heather Allen ◽  
John M. Herbert

<p>Surface-sensitive vibrational spectroscopy is a common tool for measuring molecular organization and intermolecular interactions at interfaces. Peak intensity ratios are typically used to extract molecular information from one-dimensional spectra but vibrational coupling between surfactant molecules can manifest as signal depletion in one-dimensional spectra. Through a combination of experiment and theory, we demonstrate the emergence of vibrational excitons in infrared reflection-absorption spectra of soluble and insoluble surfactants at the air/water interface. Vibrational coupling yields a signicant decrease in peak intensities corresponding to C-F vibrational modes of perfluorooctanoic acid molecules. Vibrational excitons also form between arachidic acid surfactants within a compressed monolayer, manifesting as signal reduction of C-H stretching modes. The aqueous phase ionic composition impacts surfactant intermolecular distances, thereby modulating vibrational coupling strength between surfactants. Our results serve as a cautionary tale against employing alkyl and fluoroalkyl vibrational peak intensities in analyses that are ubiquitous in interface science.</p>


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