M. Riches, M. P. Vermeuel, H. D. Alwe, D. B. Millet, D. K. Farmer
Temperature and air humidity are critical environmental factors regulating photosynthesis and biogenic volatile organic compound (BVOC) emissions from plants, which influence air quality and climate change. While previous research has demonstrated the impacts of temperature on photosynthesis and BVOCs, the effects of humidity and the combined effects of temperature and humidity remain understudied. Here we discuss the discrete and synergistic impacts of temperature and humidity on ponderosa pine trees. We used a portable photosynthesis system coupled to a proton-transfer-reaction mass spectrometer to quantify leaf-level changes in photosynthesis, stomatal conductance, and emissions as a function of both temperature and humidity. Results demonstrate that all BVOC emissions investigated increased with temperature, regardless of humidity, in agreement with literature. To our knowledge, we present the first direct observation of temperature-dependent methyl vinyl ketone and methacrolein emissions from ponderosa pines. We find that elevated humidity enhances the baseline emissions of many BVOCs. Increasing relative humidity from 30% to 50% resulted in basal emission rates increasing between 1.7-fold for sesquiterpenes and 2.9-fold for 2-methyl-3-buten-2-ol. Our results may help explain field observations where BVOC emissions are decoupled from temperature under some conditions, and we clearly illustrate the need for further investigations on BVOC humidity sensitivity over larger (e.g., ecosystem) scales and on other plant species to improve chemical transport model predictions.
{"title":"Combined Effects of Air Humidity and Temperature on Biogenic Volatile Organic Compound Emissions and Photosynthesis","authors":"M. Riches, M. P. Vermeuel, H. D. Alwe, D. B. Millet, D. K. Farmer","doi":"10.1029/2025JD044827","DOIUrl":"10.1029/2025JD044827","url":null,"abstract":"<p>Temperature and air humidity are critical environmental factors regulating photosynthesis and biogenic volatile organic compound (BVOC) emissions from plants, which influence air quality and climate change. While previous research has demonstrated the impacts of temperature on photosynthesis and BVOCs, the effects of humidity and the combined effects of temperature and humidity remain understudied. Here we discuss the discrete and synergistic impacts of temperature and humidity on ponderosa pine trees. We used a portable photosynthesis system coupled to a proton-transfer-reaction mass spectrometer to quantify leaf-level changes in photosynthesis, stomatal conductance, and emissions as a function of both temperature and humidity. Results demonstrate that all BVOC emissions investigated increased with temperature, regardless of humidity, in agreement with literature. To our knowledge, we present the first direct observation of temperature-dependent methyl vinyl ketone and methacrolein emissions from ponderosa pines. We find that elevated humidity enhances the baseline emissions of many BVOCs. Increasing relative humidity from 30% to 50% resulted in basal emission rates increasing between 1.7-fold for sesquiterpenes and 2.9-fold for 2-methyl-3-buten-2-ol. Our results may help explain field observations where BVOC emissions are decoupled from temperature under some conditions, and we clearly illustrate the need for further investigations on BVOC humidity sensitivity over larger (e.g., ecosystem) scales and on other plant species to improve chemical transport model predictions.</p>","PeriodicalId":15986,"journal":{"name":"Journal of Geophysical Research: Atmospheres","volume":"131 3","pages":""},"PeriodicalIF":3.4,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://agupubs.onlinelibrary.wiley.com/doi/epdf/10.1029/2025JD044827","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146136843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Xihao Pan, Yuxuan Zhang, Chaoyang Xue, Uwe Kuhn, Isabella Hrabe de Angelis, Christopher Pöhlker, Jeannine Ditas, Lena Heins, Hedy M. Aardema, Hans A. Slagter, Maria Ll. Calleja, Antonis Dragoneas, David Walter, Björn Nillius, Qiaoqiao Wang, Nan Ma, Hang Su, Ulrich Pöschl, Gerald H. Haug, Ralf Schiebel, Yafang Cheng
Black carbon (BC) from maritime emissions plays a critical role by influencing radiation, cloud processes, and atmospheric dynamics in the marine atmosphere. These impacts depend on BC concentration and mixing state with other aerosol components. However, in situ observations of BC over oceans remain scarce, and the influence of the marine environment on the evolution of BC mixing state is not well understood. Here, we present shipborne measurements aboard the research sailing yacht S/Y Eugen Seibold during 10 Atlantic Ocean cruises. The data set spans 1,120 of measurement hours from near-coastal regions to remote ocean areas. In oceanic regions extending from tens to thousands of kilometers offshore, 1-min averaged BC concentrations were typically around 100 ng m−3, suggesting a well-mixed marine background. Despite the relatively small variability in BC mass concentrations, the mixing state of BC exhibits substantial differences between nearshore and remote oceanic regions. High number fractions (>50%) of BC particles without core-shell morphologies, characterized by BC externally attached to non-BC materials, were observed in near-coastal regions and decreased to ∼20% in remote oceanic regions. In ship-impacted regions, small freshly emitted BC particles tend to coagulate with other aerosol particles and forming non-core-shell attached structures, while high relative humidity (RH > 85%) tends to promote the formation of thick coatings. Our results provide new insights into climate-relevant properties and underscore the importance of coagulation and hygroscopic processing for the mixing state of BC in the marine atmosphere.
来自海洋排放的黑碳(BC)通过影响海洋大气中的辐射、云过程和大气动力学而发挥关键作用。这些影响取决于BC浓度和与其他气溶胶组分的混合状态。然而,海洋上BC的现场观测仍然很少,海洋环境对BC混合状态演变的影响还不清楚。在这里,我们展示了研究帆船S/Y Eugen Seibold在10次大西洋巡航期间的船载测量结果。该数据集涵盖了从近岸地区到远海地区的1120个测量小时。在离岸数万至数千公里的海洋区域,1分钟平均BC浓度通常在100 ng m - 3左右,表明海洋背景混合良好。尽管BC质量浓度的变化相对较小,但BC的混合状态在近岸和偏远海洋地区表现出实质性的差异。在近海岸地区观察到大量无核壳形态的BC颗粒(>50%),其特征是BC外部附着在非BC材料上,而在偏远的海洋地区则减少到约20%。在船舶撞击区域,新发射的小BC颗粒容易与其他气溶胶颗粒凝结形成非核壳附着结构,而较高的相对湿度(RH > 85%)容易促进厚涂层的形成。我们的研究结果为气候相关特性提供了新的见解,并强调了BC在海洋大气中混合状态的凝聚和吸湿处理的重要性。
{"title":"Black Carbon in the Marine Atmosphere: Concentration and Mixing State From Coastal to Remote Atlantic Regions","authors":"Xihao Pan, Yuxuan Zhang, Chaoyang Xue, Uwe Kuhn, Isabella Hrabe de Angelis, Christopher Pöhlker, Jeannine Ditas, Lena Heins, Hedy M. Aardema, Hans A. Slagter, Maria Ll. Calleja, Antonis Dragoneas, David Walter, Björn Nillius, Qiaoqiao Wang, Nan Ma, Hang Su, Ulrich Pöschl, Gerald H. Haug, Ralf Schiebel, Yafang Cheng","doi":"10.1029/2025JD045346","DOIUrl":"10.1029/2025JD045346","url":null,"abstract":"<p>Black carbon (BC) from maritime emissions plays a critical role by influencing radiation, cloud processes, and atmospheric dynamics in the marine atmosphere. These impacts depend on BC concentration and mixing state with other aerosol components. However, in situ observations of BC over oceans remain scarce, and the influence of the marine environment on the evolution of BC mixing state is not well understood. Here, we present shipborne measurements aboard the research sailing yacht S/Y <i>Eugen Seibold</i> during 10 Atlantic Ocean cruises. The data set spans 1,120 of measurement hours from near-coastal regions to remote ocean areas. In oceanic regions extending from tens to thousands of kilometers offshore, 1-min averaged BC concentrations were typically around 100 ng m<sup>−3</sup>, suggesting a well-mixed marine background. Despite the relatively small variability in BC mass concentrations, the mixing state of BC exhibits substantial differences between nearshore and remote oceanic regions. High number fractions (>50%) of BC particles without core-shell morphologies, characterized by BC externally attached to non-BC materials, were observed in near-coastal regions and decreased to ∼20% in remote oceanic regions. In ship-impacted regions, small freshly emitted BC particles tend to coagulate with other aerosol particles and forming non-core-shell attached structures, while high relative humidity (RH > 85%) tends to promote the formation of thick coatings. Our results provide new insights into climate-relevant properties and underscore the importance of coagulation and hygroscopic processing for the mixing state of BC in the marine atmosphere.</p>","PeriodicalId":15986,"journal":{"name":"Journal of Geophysical Research: Atmospheres","volume":"131 3","pages":""},"PeriodicalIF":3.4,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146136844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Air pollution in India is complex due to the multitude of sources and varying topography, rendering the interplay between meteorology and emission sources significant. To address this challenge, this work presents an integrated methodology for PM2.5 source apportionment in Bhopal, central India, combining dispersion-normalized positive matrix factorization (DN-PMF) with a machine-learning interpretability approach using Random Forest and SHAP (RF-SHAP). DN-PMF improves conventional source identification by incorporating air dilution effects, yielding refined source contributions for nine factors in Bhopal. Seasonal factor contributions peaked during periods with a lower boundary layer height, such as secondary sulfate during the winter season (21.3 μg m−3, 31.7%). The COVID-19 lockdowns, a quasi-natural emissions reduction experiment, led to a decrease in aerosol contributions from industrial, residential and traffic-related sources. However, during this period, crop residue burning was exposed as a major anthropogenic contributor, which together with unfavorable meteorology resulted in increased mean PM2.5 (50.6 ± 24.3 μg m−3) during the lockdowns compared to the reference period (36.7 ± 9.7 μg m−3). Using RF-SHAP the influence of meteorology and emission sources in driving secondary inorganic aerosol formation was examined. Secondary nitrate and residential fuel were identified as key contributors to exceedances of the Indian National Ambient Air Quality Standards (60 μg m−3, 24-hr average) at the study site. Integrating DN-PMF with RF-SHAP (driver analysis) enhanced source attribution by linking source contributions with their driving factors, establishing a framework for assessing pollution dynamics. This framework can help strengthen improved air quality initiatives in India, including the national Smart Cities Mission.
{"title":"Hybrid Model Resolved Impacts of COVID-19 Lockdowns on PM2.5 Sources in Bhopal, India: Role of Meteorology, Secondary Inorganic Aerosols, and Crop Residue Burning","authors":"Delwin Pullokaran, Ramya Sunder Raman, Ankur Bhardwaj, Diksha Haswani, Deeksha Shukla","doi":"10.1029/2025JD045361","DOIUrl":"https://doi.org/10.1029/2025JD045361","url":null,"abstract":"<p>Air pollution in India is complex due to the multitude of sources and varying topography, rendering the interplay between meteorology and emission sources significant. To address this challenge, this work presents an integrated methodology for PM<sub>2.5</sub> source apportionment in Bhopal, central India, combining dispersion-normalized positive matrix factorization (DN-PMF) with a machine-learning interpretability approach using Random Forest and SHAP (RF-SHAP). DN-PMF improves conventional source identification by incorporating air dilution effects, yielding refined source contributions for nine factors in Bhopal. Seasonal factor contributions peaked during periods with a lower boundary layer height, such as secondary sulfate during the winter season (21.3 μg m<sup>−3</sup>, 31.7%). The COVID-19 lockdowns, a quasi-natural emissions reduction experiment, led to a decrease in aerosol contributions from industrial, residential and traffic-related sources. However, during this period, crop residue burning was exposed as a major anthropogenic contributor, which together with unfavorable meteorology resulted in increased mean PM<sub>2.5</sub> (50.6 ± 24.3 μg m<sup>−3</sup>) during the lockdowns compared to the reference period (36.7 ± 9.7 μg m<sup>−3</sup>). Using RF-SHAP the influence of meteorology and emission sources in driving secondary inorganic aerosol formation was examined. Secondary nitrate and residential fuel were identified as key contributors to exceedances of the Indian National Ambient Air Quality Standards (60 μg m<sup>−3</sup>, 24-hr average) at the study site. Integrating DN-PMF with RF-SHAP (driver analysis) enhanced source attribution by linking source contributions with their driving factors, establishing a framework for assessing pollution dynamics. This framework can help strengthen improved air quality initiatives in India, including the national Smart Cities Mission.</p>","PeriodicalId":15986,"journal":{"name":"Journal of Geophysical Research: Atmospheres","volume":"131 2","pages":""},"PeriodicalIF":3.4,"publicationDate":"2026-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146096616","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yuting Lu, Mengmeng Li, Yiting Zhou, Hui Zhang, Wei Wang, Xin Huang, Tijian Wang, Bingliang Zhuang, Shu Li
Abnormally elevated ozone (O3) is observed during compound heatwave and drought (CHWD), posing severe environmental and socioeconomic threats. Response of O3 to CHWD is complicated by the vegetation-atmosphere feedbacks through influencing biogenic emissions and stomatal deposition. Here, we employed a regional meteorology-chemistry-vegetation coupled model, integrated with optimized drought emission algorithm and interactive dry deposition scheme, to investigate the vegetation-atmosphere feedbacks and their effects on O3 pollution during CHWD. Analysis shows that CHWD have intensified in the northern hemisphere, with more frequent occurrence, stronger intensity and longer duration compared to the average climatology. Unusually elevated O3 levels and exceedance frequency by more than 20% compared to normal conditions were observed during CHWD in the United States, western Europe and China. Model results indicate that heatwaves and droughts jointly lead to 10%–24% increase of summertime biogenic volatile organic compound emissions in vegetated regions, except in the severely drought-affected areas. Furthermore, extremely hot and dry conditions induce stomatal closure and suppress plant growth, inhibiting O3 stomatal removal by water-stressed vegetation. It is estimated that such intricate vegetation-atmosphere feedbacks substantially exacerbate O3 pollution during CHWD, with equal importance to that of increased photochemical rates. Our findings offer a novel perspective on the interactions between climate, vegetation, and chemistry regarding compound extreme weather events.
{"title":"Vegetation-Atmosphere Feedbacks Exacerbate Ozone Pollution During Compound Heatwave and Drought in the Northern Hemisphere","authors":"Yuting Lu, Mengmeng Li, Yiting Zhou, Hui Zhang, Wei Wang, Xin Huang, Tijian Wang, Bingliang Zhuang, Shu Li","doi":"10.1029/2025JD044433","DOIUrl":"https://doi.org/10.1029/2025JD044433","url":null,"abstract":"<p>Abnormally elevated ozone (O<sub>3</sub>) is observed during compound heatwave and drought (CHWD), posing severe environmental and socioeconomic threats. Response of O<sub>3</sub> to CHWD is complicated by the vegetation-atmosphere feedbacks through influencing biogenic emissions and stomatal deposition. Here, we employed a regional meteorology-chemistry-vegetation coupled model, integrated with optimized drought emission algorithm and interactive dry deposition scheme, to investigate the vegetation-atmosphere feedbacks and their effects on O<sub>3</sub> pollution during CHWD. Analysis shows that CHWD have intensified in the northern hemisphere, with more frequent occurrence, stronger intensity and longer duration compared to the average climatology. Unusually elevated O<sub>3</sub> levels and exceedance frequency by more than 20% compared to normal conditions were observed during CHWD in the United States, western Europe and China. Model results indicate that heatwaves and droughts jointly lead to 10%–24% increase of summertime biogenic volatile organic compound emissions in vegetated regions, except in the severely drought-affected areas. Furthermore, extremely hot and dry conditions induce stomatal closure and suppress plant growth, inhibiting O<sub>3</sub> stomatal removal by water-stressed vegetation. It is estimated that such intricate vegetation-atmosphere feedbacks substantially exacerbate O<sub>3</sub> pollution during CHWD, with equal importance to that of increased photochemical rates. Our findings offer a novel perspective on the interactions between climate, vegetation, and chemistry regarding compound extreme weather events.</p>","PeriodicalId":15986,"journal":{"name":"Journal of Geophysical Research: Atmospheres","volume":"131 2","pages":""},"PeriodicalIF":3.4,"publicationDate":"2026-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146091506","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kira M. Holland, Alison S. Criscitiello, Joseph R. McConnell, Bradley R. Markle, Hanaa A. K. Yousif, Emma Skelton, Sophia M. Wensman, Britta J. L. Jensen, Dominic A. Winski, Seth W. Campbell, Nathan J. Chellman
Ice cores from Mt. Logan, the second highest peak in North America located in the St. Elias mountains in southwest Yukon, Canada, have provided conflicting accumulation records, thus the hydroclimate response to changing atmospheric conditions in the highest elevation regions is not well constrained. Here, we present the accumulation record from the new 325 m Mt. Logan ice core drilled at 5,334 m asl on the summit plateau in May 2022. Multi-parameter annual layer counting, confirmed with radionuclide and volcanic tephra measurements, extends to 1911 CE, associated with a depth of 257 m. The thinning-corrected annual accumulation record reveals an average rate of 3.0 m water equivalent per year (m weq a−1) from 1912 to 2020 CE, greater than six times higher than the previous estimate of ∼0.41 m weq a−1 from the 2002 Mt. Logan Prospector Russell Col core. Correlation analysis between the annual accumulation record and regional climate data sets (e.g., Japanese 55-year Reanalysis, weather stations) reveal a strong positive relationship with warm-season total precipitable water and temperature. Thus, we suggest interdecadal precipitation variability on Mt. Logan is at least partially driven by warm-season atmospheric water vapor loading, potentially related to atmospheric temperature responses associated with the warm-season Alaska Blocking Index. Further, the record reveals a statistically significant increase in accumulation of 0.13 m weq per decade since 1970. These results reveal a drastically different Mt. Logan ice core record and provide a new warm-season perspective on drivers of high-elevation accumulation variability in the North Pacific.
{"title":"Unexpectedly High Accumulation Rates in the 2022 Mt. Logan Ice Core Reveal Warm-Season Drivers of Precipitation Variability","authors":"Kira M. Holland, Alison S. Criscitiello, Joseph R. McConnell, Bradley R. Markle, Hanaa A. K. Yousif, Emma Skelton, Sophia M. Wensman, Britta J. L. Jensen, Dominic A. Winski, Seth W. Campbell, Nathan J. Chellman","doi":"10.1029/2025JD044951","DOIUrl":"https://doi.org/10.1029/2025JD044951","url":null,"abstract":"<p>Ice cores from Mt. Logan, the second highest peak in North America located in the St. Elias mountains in southwest Yukon, Canada, have provided conflicting accumulation records, thus the hydroclimate response to changing atmospheric conditions in the highest elevation regions is not well constrained. Here, we present the accumulation record from the new 325 m Mt. Logan ice core drilled at 5,334 m asl on the summit plateau in May 2022. Multi-parameter annual layer counting, confirmed with radionuclide and volcanic tephra measurements, extends to 1911 CE, associated with a depth of 257 m. The thinning-corrected annual accumulation record reveals an average rate of 3.0 m water equivalent per year (m weq a<sup>−1</sup>) from 1912 to 2020 CE, greater than six times higher than the previous estimate of ∼0.41 m weq a<sup>−1</sup> from the 2002 Mt. Logan Prospector Russell Col core. Correlation analysis between the annual accumulation record and regional climate data sets (e.g., Japanese 55-year Reanalysis, weather stations) reveal a strong positive relationship with warm-season total precipitable water and temperature. Thus, we suggest interdecadal precipitation variability on Mt. Logan is at least partially driven by warm-season atmospheric water vapor loading, potentially related to atmospheric temperature responses associated with the warm-season Alaska Blocking Index. Further, the record reveals a statistically significant increase in accumulation of 0.13 m weq per decade since 1970. These results reveal a drastically different Mt. Logan ice core record and provide a new warm-season perspective on drivers of high-elevation accumulation variability in the North Pacific.</p>","PeriodicalId":15986,"journal":{"name":"Journal of Geophysical Research: Atmospheres","volume":"131 2","pages":""},"PeriodicalIF":3.4,"publicationDate":"2026-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://agupubs.onlinelibrary.wiley.com/doi/epdf/10.1029/2025JD044951","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146099470","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marcus Lofverstrom, Adam Herrington, Andreas Born, Rebecca Beadling
Katabatic storms in southeastern Greenland are fierce, density-driven, downslope wind events with substantial implications for the local and downstream weather conditions and climate. This study presents a detailed assessment of their representation across three generations of global reanalysis products (ERA5, ERA-Interim, and ERA40) from the European Centre for Medium-Range Weather Forecasts, paired with a hierarchy of simulations at different grid resolutions with the Community Earth System Model version 2 (CESM2). Using the high-resolution (2.5-km resolution) Copernicus Arctic Regional Reanalysis (CARRA) as a benchmark, we find that the global reanalysis data sets systematically underestimate wind speeds (around 30% in ERA5 and 50% in ERA-Interim and ERA40) and fail to capture key structural features of these regional storms. Similar deficiencies are observed in CESM2 simulations when using standard latitude-longitude grids at 1–2