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      <title>Soil temperature fluctuations modulated millet agriculture evolution in Neolithic East Asia</title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 20, May 2026. &lt;br/&gt;SignificanceAgriculture was the critical intermediary through which climate change influenced the trajectory of ancient civilizations, yet the mechanisms linking environmental shifts and early farming practices remain poorly delineated. In Neolithic East ...</description>
      <dc:title>Soil temperature fluctuations modulated millet agriculture evolution in Neolithic East Asia</dc:title>
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      <title>Subsurface soil inorganic carbon gains offset half of surface losses in China’s upland croplands over the last four decades</title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 19, May 2026. &lt;br/&gt;SignificanceThe prevailing assumption of millennial-scale stability has led to the widespread neglect of soil inorganic carbon (SIC) dynamics, especially in deep soil layers. Using a large-scale, depth-resolved resampling of China’s upland croplands, we ...</description>
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      <dc:creator>Andong CaiTianfu HanZhenghu ZhouKailou LiuXinpeng XuPete SmithQingzhu GaoYue LiMinggang XuaInstitute of Environment and Sustainable Development in Agriculture, Chinese Academy of Agricultural Sciences, Beijing 100081, Chinabhttps://ror.org/04ypx8c21School of Agriculture and Biomanufacturing, Zhengzhou University, Zhengzhou 450001, ChinacCenter for Ecological Research, Northeast Asia Biodiversity Research Center, NortheastForestry University, Harbin 150040, Chinadhttps://ror.org/04vrkaw11Jiangxi Institute of Red Soil and Germplasm Resources/Jiangxi Province Key Laboratory of Arable Land Improvement and Quality Enhancementl/National Engineering and Technology Research Center for Red Soil Improvement, Nanchang 331717, Jiangxi, Chinaehttps://ror.org/0313jb750State Key Laboratory of Efficient Utilization of Arable Land in China/Key Laboratory of Plant Nutrition and Fertilizer, Ministry of Agriculture and Rural Affairs/Institute of Agricultural Resources and Regional Planning, Chinese Academy of Agricultural Sciences, Beijing 100081, ChinafInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen AB24 3UU, Scotlandghttps://ror.org/05e9f5362Institute of Eco-environment and Industrial Technology, Shanxi Agricultural University, Taiyuan 030031, China</dc:creator>
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      <title>Targeted knockout of a host peroxisomal peptidase confers field resistance to maize lethal necrosis</title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 18, May 2026. &lt;br/&gt;SignificanceMaize lethal necrosis (MLN) is a serious viral disease threatening food security in East Africa. We found a previously unknown mechanism by which the virus exploits a specific maize peroxisomal peptidase to form replication compartments. This ...</description>
      <dc:title>Targeted knockout of a host peroxisomal peptidase confers field resistance to maize lethal necrosis</dc:title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 17, April 2026. &lt;br/&gt;SignificanceMagnesium (Mg) is an essential element for both plants and humans. As a staple food, rice represents a major dietary source of Mg, yet the mechanism underlying Mg loading into grain remains unclear. In this study, we identified a Mg ...</description>
      <dc:title>A magnesium efflux transporter required for seed development and eating quality in rice</dc:title>
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      <dc:creator>Sheng HuangKiyosumi HoriNaoki YamajiYuma YoshiokaMin NingYu NagayaTakaaki MiyajiNamiki Mitani-UenoShin-ichiro InoueJune-Sik KimMiho KashinoJian Feng MaaCollege of Agronomy, Hunan Agricultural University, Changsha 410128, ChinabInstitute of Plant Science and Resources, Okayama University, Kurashiki 710-0046, JapancNational Institute of Crop Science, National Agriculture Research Organization, Tsukuba, Ibaraki 305-8518, JapandGraduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Kita, Okayama 700-8530, JapaneDepartment of Genomics and Proteomics, Advanced Science Research Center, Okayama University, Kita, Okayama 700-8530, JapanfDepartment of Regulatory Biology, Saitama University, Saitama 338-8570, JapangRIKEN Center for Sustainable Resource Science, Tsurumi-ku, Yokohama 230-0045, Japan</dc:creator>
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      <title>Soil organic nitrogen rather than fertilizer drives dinitrogen losses in flooded rice systems</title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 17, April 2026. &lt;br/&gt;SignificanceFlooded rice fields lose large amounts of nitrogen as dinitrogen (N2), yet the sources of this loss remain unclear. Using a cutting-edge in situ isotopic technique, we show that most N2emissions arise not from fertilizer, as widely assumed, ...</description>
      <dc:title>Soil organic nitrogen rather than fertilizer drives dinitrogen losses in flooded rice systems</dc:title>
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      <dc:creator>Yuanyuan LeiZhijun WeiKaiye YeKees Jan van GroenigenYu LiuHongna CuiKlaus Butterbach-BahlPete SmithDeli ChenShu Kee LamWilliam R. HorwathWulf AmelungChaopu TiWei ZhouJingrui YangHongbo HeXudong ZhangSheng ZhouXiaoyuan YanLonglong XiaaState Key Laboratory of Soil and Sustainable Agriculture, Changshu National Agro-Ecosystem Observation and Research Station, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 211135, ChinabUniversity of Chinese Academy of Sciences, Nanjing 211135, ChinacDepartment of Geography, Faculty of Environment, Science and Economy, University of Exeter, Exeter EX4 4RJ, United KingdomdPioneer Center for Landscape Research in Sustainable Agricultural Futures, Department of Agroecology, Aarhus University, Aarhus 8000, DenmarkeInstitute for Meteorology and Climate Research, Karlsruhe Institute of Technology, Garmisch-Partenkirchen 82497, GermanyfInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen AB24 3UU, United KingdomgSchool of Agriculture, Food and Ecosystem Sciences, Faculty of Science, The University of Melbourne, Parkville, VIC 3010, AustraliahDepartment of Land, Air, and Water Resources, University of California, Davis, CA 95616iInstitute of Crop Science and Resource Conservation, Soil Science and Soil Ecology, University of Bonn, Bonn 53115, GermanyjInstitute of Bio- and Geosciences, Agrosphere Institute, Forschungszentrum Jülich, Jülich 52428, GermanykInstitute of Applied Ecology, Chinese Academy of Sciences, Shenyang 110016, ChinalEco-environmental Protection Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai 201403, China</dc:creator>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 16, April 2026. &lt;br/&gt;SignificancePathogen-driven manipulation of vector physiology represents a fundamental yet understudied survival strategy for optimizing transmission efficiency. This study reveals a sophisticated mechanism whereby the pinewood nematode utilizes exosome-...</description>
      <dc:title>Plant pathogenic nematode exosomes remodel vector tracheae to enhance pathogen transmission</dc:title>
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      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
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      <title>Combining process-based models with machine learning ensemble improves soil nitrous oxide estimates</title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 16, April 2026. &lt;br/&gt;</description>
      <dc:title>Combining process-based models with machine learning ensemble improves soil nitrous oxide estimates</dc:title>
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      <dc:creator>Stephen Del GrossoStephen OgleaNatural Resource Ecology Laboratory, Colorado State University, Fort Collins, CO 80523</dc:creator>
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      <title>Reversible and causal epigenetic information loss in liver aging and disease</title>
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      <description>PNAS Nexus, Volume 5, Issue 4, April 2026. &lt;br/&gt;The loss of epigenetic information has been proposed as a driver of aging and diseases, but the reversibility and causality of this process remain underexplored. Here, we analyze liver-unique methylation sites—genomic loci that show distinct methylation ...</description>
      <dc:title>Reversible and causal epigenetic information loss in liver aging and disease</dc:title>
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      <title>Gustatory sensing by ovipositor drives maternal avoidance of hesperidin to benefit the offspring in a major agricultural fly pest</title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 12, March 2026. &lt;br/&gt;SignificanceFemales of many insects choose egg-laying sites that balance their own preferences with the needs of their offspring. Oriental fruit fly females paradoxically prefer unripe mangoes, which are less nutritious than ripe fruits, and the basis of ...</description>
      <dc:title>Gustatory sensing by ovipositor drives maternal avoidance of hesperidin to benefit the offspring in a major agricultural fly pest</dc:title>
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      <title>Endocrine gland growth as the developmental switch for insect diapause</title>
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      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 12, March 2026. &lt;br/&gt;SignificanceHormonal signals control developmental plasticity by adjusting physiological states, allowing animals to adapt to environmental change. This requires the endocrine system to modulate hormone synthesis in response to external cues, but the ...</description>
      <dc:title>Endocrine gland growth as the developmental switch for insect diapause</dc:title>
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      <dc:creator>Kou WangZhong TianKirst King-JonesFen ZhuXiao-Ping WangWen LiuaHubei Key Laboratory of Resources Utilization and Sustainable Pest Management, Department of Plant Protection, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan 430070, ChinabDepartment of Biological Sciences, University of Alberta, Edmonton, Alberta T6G 2E9, Canada</dc:creator>
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   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2601427123?af=R">
      <title>A nematode-built conduit for cross kingdom biotrophic interaction</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2601427123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 12, March 2026. &lt;br/&gt;</description>
      <dc:title>A nematode-built conduit for cross kingdom biotrophic interaction</dc:title>
      <dc:identifier>doi:10.1073/pnas.2601427123</dc:identifier>
      <dc:source/>
      <dc:date>2026-03-18T07:00:00Z</dc:date>
      <dc:creator>Valerie M. WilliamsonShahid SiddiqueaDepartment of Plant Pathology, University of California, Davis, CA 95616bDepartment of Entomology and Nematology, University of California, Davis, CA 95616</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>12</prism:number>
      <prism:coverDate>2026-03-24T07:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-03-24T07:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2601427123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2601427123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2607080123?af=R">
      <title>Boosting crops’ natural capabilities could help feed a warming world</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2607080123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 12, March 2026. &lt;br/&gt;</description>
      <dc:title>Boosting crops’ natural capabilities could help feed a warming world</dc:title>
      <dc:identifier>doi:10.1073/pnas.2607080123</dc:identifier>
      <dc:source/>
      <dc:date>2026-03-18T07:00:00Z</dc:date>
      <dc:creator>Saima Sidik</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>12</prism:number>
      <prism:coverDate>2026-03-24T07:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-03-24T07:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2607080123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2607080123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2600783123?af=R">
      <title>Directed differentiation of bovine trophoblast stem cells: A useful in vitro model for placenta development</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2600783123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 11, March 2026. &lt;br/&gt;SignificanceThe placenta is essential for successful reproduction in mammalian species. Although the bovine placenta has been studied histologically, the cellular and molecular pathways governing trophoblast differentiation remain unclear. This study ...</description>
      <dc:title>Directed differentiation of bovine trophoblast stem cells: A useful in vitro model for placenta development</dc:title>
      <dc:identifier>doi:10.1073/pnas.2600783123</dc:identifier>
      <dc:source/>
      <dc:date>2026-03-11T07:00:00Z</dc:date>
      <dc:creator>Abdallah W. AbdelhadySarayut WinuthayanonM. Sofia OrtegaAndrew M. KelleherThomas E. SpenceraDivision of Animal Sciences, University of Missouri, Columbia, MO 65211bDepartment of Animal Sciences, University of Wisconsin-Madison, Madison, WI 53706cDivision of Obstetrics, Gynecology, and Women’s Health, University of Missouri, Columbia, MO 65211</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>11</prism:number>
      <prism:coverDate>2026-03-17T07:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-03-17T07:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2600783123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2600783123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2519395123?af=R">
      <title>D-amino acid aminotransferase1 regulates grain chalkiness in rice by modulating endoplasmic reticulum stress response</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2519395123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 10, March 2026. &lt;br/&gt;SignificanceImproving grain appearance is a priority for rice breeding, as chalkiness markedly reduces commercial value. Here, we identify a previously unrecognized metabolic pathway involving D-amino acids that regulates this trait. We show that theD-...</description>
      <dc:title>D-amino acid aminotransferase1 regulates grain chalkiness in rice by modulating endoplasmic reticulum stress response</dc:title>
      <dc:identifier>doi:10.1073/pnas.2519395123</dc:identifier>
      <dc:source/>
      <dc:date>2026-03-06T08:00:00Z</dc:date>
      <dc:creator>Hui DongJie LeiYunlu TianJuan LiuHang YangXiaokang JiangRushuang ZhangYu ZhangRongbo ChenYiqun BaoFeng LiuYulong RenYaping LuXi LiuShijia LiuXue YangErchao DuanXuan TengYunlong WangChuanwei GuYipeng ZhangXiaoli ChenYunpeng ZhangHongyi XuRui ShaXia XuRuomeng LiGongyu LiYihua WangJianmin WanaState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Zhongshan Biological Breeding Laboratory, Jiangsu Nanjing Rice Germplasm Resources National Field Observation and Research Station, Nanjing Agricultural University, Nanjing 210095, ChinabTianjin Key Laboratory of Biosensing and Molecular Recognition, Research Center for Analytical Science, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, Tianjin 300071, ChinacCollege of Life Sciences, Nanjing Agricultural University, Nanjing 210095, ChinadState Key Laboratory of Crop Gene Resources and Breeding, National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>10</prism:number>
      <prism:coverDate>2026-03-10T07:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-03-10T07:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2519395123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2519395123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2524808123?af=R">
      <title>Coupled machine learning–ecosystem ensemble models substantially improve predictions of nitrous oxide (N2O) fluxes from US croplands</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2524808123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 10, March 2026. &lt;br/&gt;SignificanceNitrous oxide (N2O) is a potent and increasingly important greenhouse gas currently responsible for ~7% of human-caused atmospheric warming. Agriculture is a major emitter of N2O globally, and agricultural soils are a major if still uncertain ...</description>
      <dc:title>Coupled machine learning–ecosystem ensemble models substantially improve predictions of nitrous oxide (N2O) fluxes from US croplands</dc:title>
      <dc:identifier>doi:10.1073/pnas.2524808123</dc:identifier>
      <dc:source/>
      <dc:date>2026-03-04T08:00:00Z</dc:date>
      <dc:creator>Prateek SharmaBruno BassoAditya ManurajMichael S. MurilloNeville MillarTommaso TadielloMukta SharmaMathieu DelandmeterG. Philip RobertsonaDepartment of Earth and Environmental Sciences, Michigan State University, East Lansing, MI 48824bW.K. Kellogg Biological Station, Michigan State University, Hickory Corners, MI 49060cU.S. Department of Energy, Great Lakes Bioenergy Research Center, Michigan State University, East Lansing, MI 48824dDepartment of Computational Mathematics, Science and Engineering, Michigan State University, East Lansing, MI 48824eGembloux Agro-Bio Tech, University of Liege, Gembloux B-5030, BelgiumfDepartment of Plant, Soil and Microbial Sciences, Michigan State University, East Lansing, MI 48824</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>10</prism:number>
      <prism:coverDate>2026-03-10T07:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-03-10T07:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2524808123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2524808123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2516099123?af=R">
      <title>Glycosylation of glyphosate drives residue reduction and herbicide tolerance in rice</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2516099123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 9, March 2026. &lt;br/&gt;SignificanceWeeds pose a major threat to rice yield losses, driving the urgent need for judicious glyphosate application and glyphosate-tolerant rice varieties in modern agriculture. Transgenic lines with glyphosate tolerance are available, but developing ...</description>
      <dc:title>Glycosylation of glyphosate drives residue reduction and herbicide tolerance in rice</dc:title>
      <dc:identifier>doi:10.1073/pnas.2516099123</dc:identifier>
      <dc:source/>
      <dc:date>2026-02-23T08:00:00Z</dc:date>
      <dc:creator>Fulai YangYuehua WangWentao ZhouChengfeng XueFengshou DongYongquan ZhengMeng ZhangLi ChenJun ZhangXinglu PanRuifeng YaoaState Key Laboratory of Chemo and Biosensing, Hunan Provincial Key Laboratory of Plant Functional Genomics and Developmental Regulation, College of Biology, Longping Agricultural College, Hunan University, Changsha 410082, ChinabYuelushan Laboratory, Changsha 410082, ChinacHunan Research Center of the Basic Discipline for Cell Signaling, College of Biology, Hunan University, Changsha 410082, ChinadState Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>9</prism:number>
      <prism:coverDate>2026-03-03T08:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-03-03T08:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2516099123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2516099123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2522267123?af=R">
      <title>Stripe rust fungus subverts wheat phase separation–mediated immunity to promote infection</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2522267123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 8, February 2026. &lt;br/&gt;SignificanceLiquid–liquid phase separation (LLPS) orchestrates efficient plant immune responses against pathogens, yet how pathogens disrupt host LLPS to facilitate invasion remains unclear. Here, we found thatPuccinia striiformiseffector Hasp170 ...</description>
      <dc:title>Stripe rust fungus subverts wheat phase separation–mediated immunity to promote infection</dc:title>
      <dc:identifier>doi:10.1073/pnas.2522267123</dc:identifier>
      <dc:source/>
      <dc:date>2026-02-17T08:00:00Z</dc:date>
      <dc:creator>Tong YanJinren ZhaoCan ChenJunda HuJiyuan ZhangJialiu WangSomying WanseeNing WangCong JiangXiaofeng FangZhensheng KangLijun YangChunlei TangXiaojie WangaState Key Laboratory for Crop Stress Resistance and High-Efficiency Production, College of Plant Protection, Northwest A&amp;F University, Yangling, Shaanxi 712100, ChinabKey Laboratory of Integrated Pest Management on Crops in Central China (Ministry of Agriculture and Rural Affairs), Hubei Key Laboratory of Crop Disease, Insect Pests and Weeds Control, Institute of Plant Protection and Soil Science, Hubei Academy of Agricultural Sciences, Wuhan 430064, ChinacCollege of International Education, Northwest A&amp;F University, Yangling, Shaanxi 712100, ChinadCenter for Plant Biology, School of Life Sciences, Tsinghua University, Beijing 100000, China</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>8</prism:number>
      <prism:coverDate>2026-02-24T08:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-02-24T08:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2522267123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2522267123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2527021123?af=R">
      <title>Foliar dewdroplet–induced redox cascades promote early flowering in Brassicaceae plants</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2527021123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 8, February 2026. &lt;br/&gt;SignificanceWater microdroplets are regarded as microreactors capable of generating various reactive species, including reactive oxygen species (ROS), at their interfaces. However, our understanding of the impact of microdroplet chemistry on the natural ...</description>
      <dc:title>Foliar dewdroplet–induced redox cascades promote early flowering in Brassicaceae plants</dc:title>
      <dc:identifier>doi:10.1073/pnas.2527021123</dc:identifier>
      <dc:source/>
      <dc:date>2026-02-17T08:00:00Z</dc:date>
      <dc:creator>Yu ZhengBolei ChenChun BaoYu XiaChangli ZengMaoyong SongJianbo ShiLigang HuYongguang YinXiaoyun CuiJuline AuverlotJean-Philippe ReichheldGuibin JiangYong LiangDaoxiu ZhouRichard N. ZareaHubei Key Laboratory of Environmental and Health Effects of Persistent Toxic Substances, School of Environment and Health, Jianghan University, Wuhan 430056, ChinabState Key Laboratory of Environmental Chemistry and Toxicology, Research Center for Eco-environmental Sciences, Chinese Academy of Sciences, Beijing 100085, ChinacInstitute of Plant Science Paris-Saclay, CNRS, INRA, Université Paris-Saclay, Orsay 91405, FrancedNational Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan 430070, ChinaeLaboratoire Génome et Développement des Plantes, CNRS, Université Perpignan, Perpignan 66860, FrancefDepartment of Chemistry, Stanford University, Stanford, CA 94305</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>8</prism:number>
      <prism:coverDate>2026-02-24T08:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-02-24T08:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2527021123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2527021123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2524949123?af=R">
      <title>Parasitic castration by a viral protein tyrosine phosphatase targeting the host cell cycle checkpoint protein Rad9A</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2524949123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 7, February 2026. &lt;br/&gt;SignificanceParasitism often leads to the disruption of the host reproductive system, known as parasitic castration, yet the mechanisms underlying this remain elusive. Here, we report a strategy whereby parasitic wasps employ their domesticated ...</description>
      <dc:title>Parasitic castration by a viral protein tyrosine phosphatase targeting the host cell cycle checkpoint protein Rad9A</dc:title>
      <dc:identifier>doi:10.1073/pnas.2524949123</dc:identifier>
      <dc:source/>
      <dc:date>2026-02-09T08:00:00Z</dc:date>
      <dc:creator>Hongshuai GaoMujuan GuoXin YangRongmin HuKun WuLan PangXiqian YeJianhua HuangXuexin ChenZhizhi WangaZhejiang Engineering Research Center for Biological Control of Crop Pathogens and Insects, Zhejiang Key Laboratory of Biology and Ecological Regulation of Crop Pathogens and Insects, Ministry of Agriculture and Rural Affairs Key Lab of Molecular Biology of Crop Pathogens and Insect Pests, State Key Lab of Rice Biology and Breeding, Institute of Insect Sciences, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, ChinabHunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, College of Plant Protection, Hunan Agricultural University, Changsha 410128, China</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>7</prism:number>
      <prism:coverDate>2026-02-17T08:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-02-17T08:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2524949123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2524949123?af=R</prism:url>
      <prism:copyright/>
   </item>
   <item rdf:about="https://www.pnas.org/doi/abs/10.1073/pnas.2520476123?af=R">
      <title>Identification of a stylet-secreted effector protein family as a core component of root-knot nematode feeding tubes</title>
      <link>https://www.pnas.org/doi/abs/10.1073/pnas.2520476123?af=R</link>
      <description>Proceedings of the National Academy of Sciences, Volume 123, Issue 6, February 2026. &lt;br/&gt;SignificanceRoot-knot nematodes represent the most damaging group of plant-parasitic nematodes impacting global crop production. These obligate, sedentary endoparasites produce an essential structure, called a feeding tube, inside the giant feeding cells ...</description>
      <dc:title>Identification of a stylet-secreted effector protein family as a core component of root-knot nematode feeding tubes</dc:title>
      <dc:identifier>doi:10.1073/pnas.2520476123</dc:identifier>
      <dc:source/>
      <dc:date>2026-02-03T08:00:00Z</dc:date>
      <dc:creator>Richard S. HusseyMelissa G. MitchumRebekah L. PaulRaquel O. RochaJohn P. ShieldsLesa J. BeameraDepartment of Plant Pathology and Institute of Plant Breeding, Genetics, and Genomics, University of Georgia, Athens, GA 30602bDepartment of Plant Pathology and Ecology, The Connecticut Agricultural Experiment Station, New Hanover, CT 06511cDepartment of Cellular Biology, Georgia Electron Microscopy Core Facility, University of Georgia, Athens, GA 30602dDepartment of Biochemistry, University of Missouri, Columbia, MO 65211</dc:creator>
      <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
      <prism:volume>123</prism:volume>
      <prism:number>6</prism:number>
      <prism:coverDate>2026-02-10T08:00:00Z</prism:coverDate>
      <prism:coverDisplayDate>2026-02-10T08:00:00Z</prism:coverDisplayDate>
      <prism:doi>10.1073/pnas.2520476123</prism:doi>
      <prism:url>https://www.pnas.org/doi/abs/10.1073/pnas.2520476123?af=R</prism:url>
      <prism:copyright/>
   </item>
</rdf:RDF>
