Heat stress affects tassel development and reduces the kernel number of summer maize

Maize grain yield is drastically reduced by heat stress (HTS) during anthesis and early grain filling. However, the mechanism of HTS in reproductive organs and kernel numbers remains poorly understood. From 2018 to 2020, two maize varieties (ND372, heat tolerant; and XY335, heat sensitive) and two temperature regimens (HTS, heat stress; and CK, natural control) were evaluated, resulting in four treatments (372CK, 372HTS, 335CK, and 335HTS). HTS was applied from the nine-leaf stage (V9) to the anthesis stage. Various morphological traits and physiological activities of the tassels, anthers, and pollen from the two varieties were evaluated to determine their correlation with kernel count. The results showed that HTS reduced the number of florets, tassel volume, and tassel length, but increased the number of tassel branches. HTS accelerates tassel degradation and reduces pollen weight, quantity, and viability. Deformation and reduction in length and volume due to HTS were observed in both the Nongda 372 (ND372) and Xianyu 335 (XY335) varieties, with the average reductions being 22.9% and 35.2%, respectively. The morphology of the anthers changed more conspicuously in XY335 maize. The number of kernels per spike was reduced in the HTS group compared with the CK group, with the ND372 and XY335 varieties showing reductions of 47.3% and 59.3%, respectively. The main factors underlying the decrease in yield caused by HTS were reductions in pollen quantity and weight, tassel rachis, and branch length. HTS had a greater effect on the anther shape, pollen viability, and phenotype of XY335 than on those of ND372. HTS had a greater impact on anther morphology, pollen viability, and the phenotype of XY335 but had no influence on the appearance or dissemination of pollen from tassel.

[1]  Shenghui Zhou,et al.  Maize yield reduction and economic losses caused by ground-level ozone pollution with exposure- and flux-response relationships in the North China Plain. , 2022, Journal of environmental management.

[2]  A. Dinar,et al.  American Agriculture, Water Resources, and Climate Change , 2022, SSRN Electronic Journal.

[3]  Yingjun Zhang,et al.  Heat stress on maize with contrasting genetic background: Differences in flowering and yield formation , 2022, Agricultural and Forest Meteorology.

[4]  S. Jia,et al.  The effect of elevating temperature on the growth and development of reproductive organs and yield of summer maize , 2021, Journal of Integrative Agriculture.

[5]  Li Shujun,et al.  Responses of maize with different growth periods to heat stress around flowering and early grain filling , 2021 .

[6]  Pu Wang,et al.  Maximum lethal temperature for flowering and seed set in maize with contrasting male and female flower sensitivities , 2021 .

[7]  Z. Pan,et al.  Effects of optimized subsoiling tillage on field water conservation and summer maize (Zea mays L.) yield in the North China Plain , 2021 .

[8]  Z. Hao,et al.  Quantifying likelihoods of extreme occurrences causing maize yield reduction at the global scale. , 2019, The Science of the total environment.

[9]  W. Weckwerth,et al.  Male Sterility in Maize after Transient Heat Stress during the Tetrad Stage of Pollen Development1[OPEN] , 2019, Plant Physiology.

[10]  Pu Wang,et al.  Flowering dynamics, pollen, and pistil contribution to grain yield in response to high temperature during maize flowering , 2019, Environmental and Experimental Botany.

[11]  T. Rose,et al.  Australian rice varieties vary in grain yield response to heat stress during reproductive and grain filling stages , 2018, Journal of Agronomy and Crop Science.

[12]  Qingfeng Meng,et al.  Mitigating heat and chilling stress by adjusting the sowing date of maize in the North China Plain , 2018, Journal of Agronomy and Crop Science.

[13]  R. Perumal,et al.  Sensitivity of sorghum pollen and pistil to high-temperature stress. , 2018, Plant, cell & environment.

[14]  J. Farooq,et al.  Genetic behavior for kernal yield and its physio-agronomic attributes in maize at normal and high temperature regimes , 2018 .

[15]  I. Lorite,et al.  Impact of high temperatures in maize: Phenology and yield components , 2018 .

[16]  T. Dresselhaus,et al.  Tracking maize pollen development by the Leaf Collar Method , 2017, Plant Reproduction.

[17]  K. Tesfaye,et al.  Climate change impacts and potential benefits of heat-tolerant maize in South Asia , 2017, Theoretical and Applied Climatology.

[18]  Bo Shen,et al.  Genetic Male Sterility (Ms44) Increases Maize Grain Yield , 2017 .

[19]  C. Müller,et al.  Temperature increase reduces global yields of major crops in four independent estimates , 2017, Proceedings of the National Academy of Sciences.

[20]  P. H. Zaidi,et al.  Dissecting heat stress tolerance in tropical maize (Zea mays L.) , 2017 .

[21]  Xiaohong Yang,et al.  Complex genetic architecture underlies maize tassel domestication , 2017, The New phytologist.

[22]  Raziel A. Ordóñez,et al.  Modelling the impact of heat stress on maize yield formation , 2016 .

[23]  J. Prueger,et al.  Temperature extremes: Effect on plant growth and development , 2015 .

[24]  Zhiguo Cao,et al.  Fine-grained maize tassel trait characterization with multi-view representations , 2015, Comput. Electron. Agric..

[25]  D. B. Walden,et al.  Anther development of maize (Zea mays) and longstamen rice (Oryzalongistaminata) revealed by cryo-SEM, with foci on locular dehydration and pollen arrangement , 2015, Plant Reproduction.

[26]  Rachel Warren,et al.  Global crop yield response to extreme heat stress under multiple climate change futures , 2014 .

[27]  José Crossa,et al.  Identification of Drought, Heat, and Combined Drought and Heat Tolerant Donors in Maize , 2013 .

[28]  M. E. Otegui,et al.  Heat stress effects around flowering on kernel set of temperate and tropical maize hybrids , 2011 .

[29]  F. Vale,et al.  Vitamin A Metabolite, All-trans-retinoic Acid, Mediates Alternative Splicing of Protein Kinase C δVIII (PKCδVIII) Isoform via Splicing Factor SC35* , 2010, The Journal of Biological Chemistry.

[30]  R. Suwa,et al.  High temperature effects on photosynthate partitioning and sugar metabolism during ear expansion in maize (Zea mays L.) genotypes. , 2010, Plant physiology and biochemistry : PPB.

[31]  P. Stamp,et al.  Effect of heat stress on the photosynthetic apparatus in maize (Zea mays L.) grown at control or high temperature , 2004 .

[32]  M. Herrero Male and female synchrony and the regulation of mating in flowering plants. , 2003, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[33]  J. I. Lizaso,et al.  Quantitative Relationships between Pollen Shed Density and Grain Yield in Maize , 2003 .

[34]  M. Tollenaar,et al.  Kernel number response to plant density in tropical, temperate, and tropical × temperate maize hybrids , 2020 .

[35]  R. Mittler,et al.  Plant adaptations to the combination of drought and high temperatures. , 2018, Physiologia plantarum.

[36]  P.V.V. Prasad,et al.  Field Crops and the Fear of Heat Stress – Opportunities, Challenges and Future Directions☆ , 2015 .

[37]  P. H. Zaidi,et al.  Maize production in a changing climate: Impacts, adaptation, and mitigation strategies , 2012 .

[38]  M. Herrero,et al.  Global warming and sexual plant reproduction. , 2009, Trends in plant science.

[39]  Z. Ali,et al.  BREEDING POTENTIAL FOR HIGH TEMPERATURE TOLERANCE IN CORN (ZEA MAYS L.) , 2006 .

[40]  B. Vasilas,et al.  Pollen Viability, Pollen Shedding, and Combining Ability for Tassel Heat Tolerance in Maize 1 , 1987 .