A New Approach to Link Satellite Observations with Human Health by Aircraft Measurements

Author(s):  
Britta Mey ◽  
Manfred Wendisch ◽  
Heiko J. Jahn
2019 ◽  
Vol 19 (19) ◽  
pp. 12261-12293 ◽  
Author(s):  
Enrico Dammers ◽  
Chris A. McLinden ◽  
Debora Griffin ◽  
Mark W. Shephard ◽  
Shelley Van Der Graaf ◽  
...  

Abstract. Ammonia (NH3) is an essential reactive nitrogen species in the biosphere and through its use in agriculture in the form of fertilizer (important for sustaining humankind). The current emission levels, however, are up to 4 times higher than in the previous century and continue to grow with uncertain consequences to human health and the environment. While NH3 at its current levels is a hazard to environmental and human health, the atmospheric budget is still highly uncertain, which is a product of an overall lack of measurements. The capability to measure NH3 with satellites has opened up new ways to study the atmospheric NH3 budget. In this study, we present the first estimates of NH3 emissions, lifetimes and plume widths from large (>∼5 kt yr−1) agricultural and industrial point sources from Cross-track Infrared Sounder (CrIS) satellite observations across the globe with a consistent methodology. The same methodology is also applied to the Infrared Atmospheric Sounding Interferometer (IASI) (A and B) satellite observations, and we show that the satellites typically provide comparable results that are within the uncertainty of the estimates. The computed NH3 lifetime for large point sources is on average 2.35±1.16 h. For the 249 sources with emission levels detectable by the CrIS satellite, there are currently 55 locations missing (or underestimated by more than an order of magnitude) from the current Hemispheric Transport Atmospheric Pollution version 2 (HTAPv2) emission inventory and only 72 locations with emissions within a factor of 2 compared to the inventories. The CrIS emission estimates give a total of 5622 kt yr−1, for the sources analyzed in this study, which is around a factor of ∼2.5 higher than the emissions reported in HTAPv2. Furthermore, the study shows that it is possible to accurately detect short- and long-term changes in emissions, demonstrating the possibility of using satellite-observed NH3 to constrain emission inventories.


2019 ◽  
Vol 12 (11) ◽  
pp. 6125-6141 ◽  
Author(s):  
Minqiang Zhou ◽  
Bavo Langerock ◽  
Mahesh Kumar Sha ◽  
Nicolas Kumps ◽  
Christian Hermans ◽  
...  

Abstract. The Total Carbon Column Observing Network (TCCON) column-averaged dry air mole fraction of CH4 (XCH4) measurements have been widely used to validate satellite observations and to estimate model simulations. The GGG2014 code is the standard TCCON retrieval software used in performing a profile scaling retrieval. In order to obtain several vertical pieces of information in addition to the total column, in this study, the SFIT4 retrieval code is applied to retrieve the CH4 mole fraction vertical profile from the Fourier transform spectrometer (FTS) spectrum at six sites (Ny-Ålesund, Sodankylä, Bialystok, Bremen, Orléans and St Denis) during the time period of 2016–2017. The retrieval strategy of the CH4 profile retrieval from ground-based FTS near-infrared (NIR) spectra using the SFIT4 code (SFIT4NIR) is investigated. The degree of freedom for signal (DOFS) of the SFIT4NIR retrieval is about 2.4, with two distinct pieces of information in the troposphere and in the stratosphere. The averaging kernel and error budget of the SFIT4NIR retrieval are presented. The data accuracy and precision of the SFIT4NIR retrievals, including the total column and two partial columns (in the troposphere and stratosphere), are estimated by TCCON standard retrievals, ground-based in situ measurements, Atmospheric Chemistry Experiment – Fourier Transform Spectrometer (ACE-FTS) satellite observations, TCCON proxy data and AirCore and aircraft measurements. By comparison against TCCON standard retrievals, it is found that the retrieval uncertainty of SFIT4NIR XCH4 is similar to that of TCCON standard retrievals with systematic uncertainty within 0.35 % and random uncertainty of about 0.5 %. The tropospheric and stratospheric XCH4 from SFIT4NIR retrievals are assessed by comparison with AirCore and aircraft measurements, and there is a 1.0 ± 0.3 % overestimation in the SFIT4NIR tropospheric XCH4 and a 4.0 ± 2.0 % underestimation in the SFIT4NIR stratospheric XCH4, which are within the systematic uncertainties of SFIT4NIR-retrieved partial columns in the troposphere and stratosphere respectively.


2019 ◽  
Author(s):  
Enrico Dammers ◽  
Chris A. McLinden ◽  
Debora Griffin ◽  
Mark W. Shephard ◽  
Shelley Van Der Graaf ◽  
...  

Abstract. Ammonia (NH3) is an essential reactive nitrogen species in the biosphere and through its use in agriculture in the form of fertilizer important for sustaining human kind. The current emission levels however, are up to four times higher than in the previous century and continue to grow with uncertain consequences to human health and the environment. While NH3 at its current levels is a hazard to the environmental and human health the atmospheric budget is still highly uncertain, which is a product of an overall lack of measurements. The capability to measure NH3 with satellites has opened up new ways to study the atmospheric NH3 budget. In this study we present the first estimates of NH3 emissions, lifetimes, and plume widths from large (> ~ 5 kt/yr) agricultural and industrial point sources from CrIS satellite observations across the globe with a consistent methodology. The same methodology is also applied to the IASI (A and B) satellite observations and we show that the satellites typically provide comparable results that are within the uncertainty of the estimates. The computed NH3 lifetime for large point sources is on average 2.35 ± 1.16 hours. For the 249 sources with emission levels detectable by the CrIS satellite, there are currently 55 locations missing (or underestimated by more than an order of magnitude) from the current HTAPv2 emission inventory, and only 72 locations with emissions within a factor 2 compared to the inventories. We find a total of 5622 kt/yr, for the sources analyzed in this study, which is equivalent to a factor ~ 2.5 between the CrIS estimated and HTAPv2 emissions. Furthermore, the study shows that it is possible to accurately detect short and long-term changes in emissions, demonstrating the possibility of using satellite observed NH3 to constrain emission inventories.


2004 ◽  
Author(s):  
Lisheng Xu ◽  
Yongzhong Wang ◽  
Jilie Ding ◽  
Andrew Y. S. Cheng ◽  
Xiuwan Chen ◽  
...  

2021 ◽  
pp. jech-2021-216725
Author(s):  
Margarita Triguero-Mas ◽  
Isabelle Anguelovski ◽  
Helen V S Cole

The COVID-19 pandemic crisis has compromised the ‘healthy cities’ vision, as it has unveiled the need to give more prominence to caring tasks while addressing intersectional social inequities and environmental injustices. However, much-needed transdisciplinary approaches to study and address post-COVID-19 healthy cities challenges and agendas have been scarce so far. To address this gap, we propose a ‘just ecofeminist healthy cities’ research approach, which would be informed by the caring city, environmental justice, just ecofeminist sustainability and the healthy cities paradigms and research fields. Our proposed approach aims to achieve the highest standards of human health possible for the whole population—yet putting the health of socially underprivileged residents in the centre—through preserving and/or improving the existing physical, social and political environment. Importantly, the proposed approach recognises all spheres of daily life (productive, reproductive, personal and political) and their connections with inequities, justice and power dynamics. Last, the just ecofeminist healthy cities approach understands human health as interconnected with the health of non-human animals and the ecosystem. We illustrate the proposed new approach focusing on the implications for women’s health and public green spaces research and propose principles and practices for its operationalisation.


2021 ◽  
Vol 7 (3) ◽  
pp. 186-192
Author(s):  
Semyon V. Kuznetsov ◽  
Yuri A. Molin ◽  
Sergey Yu. Melikhov

The article describes one of the most urgent needs of the investigation the development of a fundamentally new approach to the forensic medical assessment of harm to human health caused by environmental crimes. Th e special signifi cance of new approaches to establishing a causal relationship between a committed environmental off ense and harm to life and (or) health, including for distinguishing from other possible anthropogenic impacts, is shown. A practical example of expert assistance to the investigation in establishing the circumstances to be proved during the investigation of an environmental crime is given.


2019 ◽  
Vol 2019 ◽  
pp. 187-190
Author(s):  
Emilia VISILEANU ◽  
Alexandra ENE ◽  
Alina Popescu ◽  
Razvan SCARLAT ◽  
Dana STEFANESCU ◽  
...  

The main goal of the study was to develop new innovative aspects such as a new approach to produce comfortable UV shielding fabrics with UPF > +50 by engineering innovative structured textiles surfaces, combining natural selected dyes and modified nanoclays leading to high UV rays reflection and increased use of renewable resources (natural dyes) and safe natural minerals (clays) with high impact on human health and environment (avoidance of the substances excluded by eco- labels and the REACH SVHC candidate list) were envisaged. The paper present the level of UPF obtained by using different textile materials treated with NanomerR I.31PS, Nanomer clay and NanomerR I.28 E, Nanomer clay.


2008 ◽  
Vol 8 (7) ◽  
pp. 1897-1910 ◽  
Author(s):  
S. Tilmes ◽  
R. Müller ◽  
R. J. Salawitch ◽  
U. Schmidt ◽  
C. R. Webster ◽  
...  

Abstract. Chemical ozone loss in winter 1991–1992 is recalculated based on observations of the HALOE satellite instrument, Version 19, ER-2 aircraft measurements and balloon data. HALOE satellite observations are shown to be reliable in the lower stratosphere below 400 K, at altitudes where the measurements are most likely disturbed by the enhanced sulfate aerosol loading, as a result of the Mt.~Pinatubo eruption in June 1991. Significant chemical ozone loss (13–17 DU) is observed below 380 K from Kiruna balloon observations and HALOE satellite data between December 1991 and March 1992. For the two winters after the Mt. Pinatubo eruption, HALOE satellite observations show a stronger extent of chemical ozone loss towards lower altitudes compared to other Arctic winters between 1991 and 2003. In spite of already occurring deactivation of chlorine in March 1992, MIPAS-B and LPMA balloon observations indicate that chlorine was still activated at lower altitudes, consistent with observed chemical ozone loss occurring between February and March and April. Large chemical ozone loss of more than 70 DU in the Arctic winter 1991–1992 as calculated in earlier studies is corroborated here.


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