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Aim Location Time periods Major taxa studied Methods Results Main conclusions Controlled experiments are increasingly important for investigating how and to what degree plant phenology responds to global climate change. Current experiments underline that chilling and forcing temperatures are two major environmental cues shaping the budburst date of temperate species, but whether experiments could reflect the observed responses to chilling has rarely been examined.Europe and North America.1951–2021.Temperate trees and shrubs.Using an experimental database of budburst dates for 50 species derived from previous literature and observational data of the same species at 12,579 stations in Europe and 1469 stations in the USA, we compared the response of forcing requirement (FR) of the budburst date to chilling accumulation (CA) between observations and experiments using a common measure of FR and CA.The median, variance and probability distribution of CA‐FR curves differed significantly between experiments and observations in most cases. The distinction in chilling effects between experiments and observations could be attributed to the difference in thermal space, heat stress, genetic variation among provenances, different forcing treatments adopted and plant materials used in the experiments.Our results suggest that the uncertainty of phenological models based solely on the experimental data needs to be re‐evaluated when predicting future spring phenological responses across broad spatial scales. [ABSTRACT FROM AUTHOR]

A comparative assessment of bud and wood phenology could aid a better understanding of tree growth dynamics. However, the reason for asynchronism or synchronism in leaf and cambial phenology remains unclear. To test the assumption that the temporal relationship between the budburst date and the onset date of wood formation is due to their common or different responses to environmental factors, we constructed a wood phenology dataset from previous literature, and compared it with an existing bud phenology dataset in Europe. We selected three common conifers (Larix decidua Mill. Picea abies (L.) H. Karst. and Pinus sylvestris L.) in both datasets and analyzed 909 records of the onset of wood formation at 47 sites and 238,720 records of budburst date at 3051 sites. We quantified chilling accumulation (CA) and forcing requirement (FR) of budburst and onset of wood formation based on common measures of CA and FR. We then constructed negative exponential CA–FR curves for bud and wood phenology separately. The results showed that the median, variance and probability distribution of CA–FR curves varied significantly between bud and wood phenology for three conifers. The different FR under the same chilling condition caused asynchronous bud and wood phenology. Furthermore, the CA–FR curves manifested that wood phenology was more sensitive to chilling than bud phenology. Thus, the FR of the onset of wood formation increases more than that of budburst under the same warming scenarios, explaining the stronger earlier trends in the budburst date than the onset date of woody formation simulated by the process-based model. Our work not only provides a possible explanation for asynchronous bud and wood phenology from the perspective of organ-specific responses to chilling and forcing, but also develops a phenological model for predicting both bud and wood phenology with acceptable uncertainties. [ABSTRACT FROM AUTHOR]

Plant phenology refers to cyclic plant growth events, and is one of the most important indicators of climate change. Integration of plant phenology information is crucial for understanding the ecosystem response to global change and modeling the material and energy balance of terrestrial ecosystems. Utilizing 24 552 in situ phenological observations of 24 representative woody plant species from the Chinese Phenology Observation Network (CPON), we have developed maps delineating species phenology (SP) and ground phenology (GP) of forests over China from 1951 to 2020. These maps offer a detailed spatial resolution of 0.1 ∘ and a temporal resolution of 1 d. Our method involves a model-based approach to upscale in situ phenological observations to SP maps, followed by the application of weighted average and quantile methods to derive GP maps from the SP data. The resulting SP maps for the 24 woody plants exhibit a high degree of concordance with in situ observations, manifesting an average deviation of 6.9 d for spring and 10.8 d for autumn phenological events. Moreover, the GP maps demonstrate robust alignment with extant land surface phenology (LSP) products sourced from remote sensing data, particularly within deciduous forests, where the average discrepancy is 8.8 d in spring and 15.1 d in autumn. This dataset provides an independent and reliable phenology data source for China on a long-time scale of 70 years, and contributes to more comprehensive research on plant phenology and climate change at both regional and national scales. The dataset can be accessed at 10.57760/sciencedb.07995 (Zhu and Dai, 2023). [ABSTRACT FROM AUTHOR]

Mountain ecosystems are sensitive to climate change, and vegetation phenology provides one of the best signals to exemplify ecosystem responses to climate change. Vegetation phenology of mountain ecosystems is usually characterized with an elevational pattern, with the growing season starts earlier and ends later in lower versus higher elevations. With climate change, this elevational gradient of vegetation phenology is likely to shift as well. However, both the patterns and the underlying driving forces for potential changes in this elevational gradient of vegetation phenology are still unclear. Here, we used 500‐m resolutioned normalized difference vegetation index (NDVI) data from Moderate Resolution Imaging Spectroradiometer (MODIS) for the period of 2001 to 2017 to investigate changes in the start of growing season (SOS) along the elevational gradient for six mountains in northern China dominated by broadleaf deciduous forests. We found that while SOS consistently advanced for most of the pixels, the elevational lapse rate of SOS (SE) showed various trends for different mountains. Specifically, SE showed a significant (p‐value <.05) decreasing trend for the two southernmost mountains, indicating an increasing elevational synchronization in SOS. However, such phenological synchronization was not found in other temperate mountains. As warming has caused relatively consistent increases in heat forcing across different elevations and among different mountains but has led to highly various changes in chilling hours between high and low elevations, we suggested that the distinctive pattern in elevational synchronicity of spring phenology between southern and northern mountains in temperate China was primarily due to their different recent changes in chilling hours. Our work provides a novel key hypothesis for explaining the divergent changes in elevational gradients of vegetation phenology that can be tested in other regions for mountain ecosystems. [ABSTRACT FROM AUTHOR]

Autumn phenology variation in temperate grassland is a direct indicator of land degradation, and a phenology‐based model has been used to simulate human‐induced land degradation. It is important to reveal how environmental factors influence autumn phenology of herbaceous plants. In this study, we examined the effects of temperature, photoperiod, and soil moisture on the leaf withering date (LWD) of four herbaceous species (Xanthium sibiricum, Plantago asiatica, Iris lactea, and Taraxacum mongolicum) at 15 sites in the Inner Mongolian steppe from 1981 to 2012. Then, we developed two process‐based models coupling the effects of the three factors based on an existing cold degree–days (CDD)‐based model for predicting the LWD of the four species. The new models showed better accuracy than CDD model during validation. The model structure and parameters suggested that soil moisture likely influenced LWD nonlinearly and presented a multiplicative interaction with temperature and photoperiod. In addition, photoperiod had divergent effects on the accumulation of cold temperature for different species and sites. For X. sibiricum, the photoperiod only determined the start of cold temperature accumulation. Considering the carryover effect of spring phenology did not improve model performance. Our study also showed that local adaptation of plants was commonly ignored when using same parameters in model calibration with observation data from multiple sites; however, model calibrations using site‐specific data were less stable, and the parameters could not be extrapolated across space. It will be necessary to establish a generalized regional model driven by both climatic and genotypic factors in future research. [ABSTRACT FROM AUTHOR]

Background and Aims: Spring phenological change of plants in response to global warming may affect many ecological processes and functions. Chilling temperature regulates budburst date by releasing dormancy. However, whether freezing temperature (<0°C) contributes to dormancy release is still debated. Our poor understanding of the role of chilling makes estimating shifts in budburst date difficult., Methods: A two-year chilling-forcing experiment was explicitly designed to test the effects of chilling temperatures on dormancy release of 9 temperate woody species in Beijing, China. A total of 1620 twigs were first exposed to a wide range of temperatures (-10 to 10 °C) with different durations and then moved to growth chambers. Based on budburst data in experimental conditions, we examined whether freezing temperatures are effective on dormancy release. We also developed a new framework for constructing chilling functions based on the curve between chilling duration and forcing requirement (FR) of budburst. The chilling function derived from this framework was not affected by experimental forcing conditions., Key Results: We demonstrated that freezing temperatures down to -10°C were effective in dormancy release. The rate of dormancy release, indicated by the rate of decay in chilling duration-FR curve, did not differ significantly between chilling temperatures in most cases, although it exhibited a maximum value at 0 or 5°C. The chilling function-associated phenological models could simulate budburst date from independent experimental and observational data with a mean RMSE of 7.07 days., Conclusions: The effective freezing temperatures found here are contrary to the well-known assumption of <0°C temperature generally not contributing to accumulated chilling in many previous chilling functions. A chilling function assuming that temperature below an upper-temperature threshold has the same effects on dormancy release could be adopted to calculate chilling accumulation when using experiments to develop spring phenological models based on the chilling-forcing relationship., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)