ROSIS - An Advanced Imaging Spectrometer For The Monitoring Of Water Colour And Chlorophyll Fluorescence

Author(s):  
Roland Doerffer ◽  
Hartmut Grabl ◽  
Bernd Kunkel ◽  
Heinz van der Piepen
Author(s):  
Annalisa Di Cicco ◽  
Remika Gupana ◽  
Alexander Damm ◽  
Simone Colella ◽  
Federico Angelini ◽  
...  

The “FLEX 2018” cruise, organized by the CNR-ISMAR in frame of the ESA “FLEXSense Campaign 2018” and CMEMS project, provided a ground station for several bio-optical instruments that investigated the coastal waters of the Tyrrhenian Sea in June 2018. The field measurements were performed in time synergy with Sentinel 3A and Sentinel 3B satellites and HyPlant airborne imaging spectrometer. Active and passive fluorescence were investigated at different scales in coastal waters to support preparatory activities of the FLuorescence EXplorer (FLEX) satellite mission.


Sensors ◽  
2020 ◽  
Vol 20 (3) ◽  
pp. 815 ◽  
Author(s):  
Shanshan Du ◽  
Liangyun Liu ◽  
Xinjie Liu ◽  
Xinwei Zhang ◽  
Xianlian Gao ◽  
...  

The global monitoring of solar-induced chlorophyll fluorescence (SIF) using satellite-based observations provides a new way of monitoring the status of terrestrial vegetation photosynthesis on a global scale. Several global SIF products that make use of atmospheric satellite data have been successfully developed in recent decades. The Terrestrial Ecosystem Carbon Inventory Satellite (TECIS-1), the first Chinese terrestrial ecosystem carbon inventory satellite, which is due to be launched in 2021, will carry an imaging spectrometer specifically designed for SIF monitoring. Here, we use an extensive set of simulated data derived from the MODerate resolution atmospheric TRANsmission 5 (MODTRAN 5) and Soil Canopy Observation Photosynthesis and Energy (SCOPE) models to evaluate and optimize the specifications of the SIF Imaging Spectrometer (SIFIS) onboard TECIS for accurate SIF retrievals. The wide spectral range of 670−780 nm was recommended to obtain the SIF at both the red and far-red bands. The results illustrate that the combination of a spectral resolution (SR) of 0.1 nm and a signal-to-noise ratio (SNR) of 127 performs better than an SR of 0.3 nm and SNR of 322 or an SR of 0.5 nm and SNR of 472 nm. The resulting SIF retrievals have a root-mean-squared (RMS) diff* value of 0.15 mW m−2 sr−1 nm−1 at the far-red band and 0.43 mW m−2 sr−1 nm−1 at the red band. This compares with 0.20 and 0.26 mW m−2 sr−1 nm−1 at the far-red band and 0.62 and 1.30 mW m−2 sr−1 nm−1 at the red band for the other two configurations described above. Given an SR of 0.3 nm, the increase in the SNR can also improve the SIF retrieval at both bands. If the SNR is improved to 450, the RMS diff* will be 0.17 mW m−2 sr−1 nm−1 at the far-red band and 0.47 mW m−2 sr−1 nm−1 at the red band. Therefore, the SIFIS onboard TECIS-1 will provide another set of observations dedicated to monitoring SIF at the global scale, which will benefit investigations of terrestrial vegetation photosynthesis from space.


2018 ◽  
Vol 217 ◽  
pp. 523-536 ◽  
Author(s):  
Christian Frankenberg ◽  
Philipp Köhler ◽  
Troy S. Magney ◽  
Sven Geier ◽  
Peter Lawson ◽  
...  

2020 ◽  
Vol 84 ◽  
pp. 127-140
Author(s):  
BM Gaas ◽  
JW Ammerman

Leucine aminopeptidase (LAP) is one of the enzymes involved in the hydrolysis of peptides, and is sometimes used to indicate potential nitrogen limitation in microbes. Small-scale variability has the potential to confound interpretation of underlying patterns in LAP activity in time or space. An automated flow-injection analysis instrument was used to address the small-scale variability of LAP activity within contiguous regions of the Hudson River plume (New Jersey, USA). LAP activity had a coefficient of variation (CV) of ca. 0.5 with occasional values above 1.0. The mean CVs for other biological parameters—chlorophyll fluorescence and nitrate concentration—were similar, and were much lower for salinity. LAP activity changed by an average of 35 nmol l-1 h-1 at different salinities, and variations in LAP activity were higher crossing region boundaries than within a region. Differences in LAP activity were ±100 nmol l-1 h-1 between sequential samples spaced <10 m apart. Variogram analysis indicated an inherent spatial variability of 52 nmol l-1 h-1 throughout the study area. Large changes in LAP activity were often associated with small changes in salinity and chlorophyll fluorescence, and were sensitive to the sampling frequency. This study concludes that LAP measurements in a sample could realistically be expected to range from zero to twice the average, and changes between areas or times should be at least 2-fold to have some degree of confidence that apparent patterns (or lack thereof) in activity are real.


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