Journal of Ecology and Environment

pISSN 2287-8327 eISSN 2288-1220

Article

Home Article View

Review

Published online March 6, 2025
https://doi.org/10.5141/jee.24.118

Journal of Ecology and Environment (2025) 49:05

A review of remote sensing applications in flower phenology detection

Ehsan Rahimi and Chuleui Jung*

Agricultural Science and Technology Institute, Andong National University, Andong 36729, Republic of Korea

Correspondence to:Chuleui Jung
E-mail cjung@andong.ac.kr

Received: December 27, 2024; Revised: February 13, 2025; Accepted: February 13, 2025

This article is licensed under a Creative Commons Attribution (CC BY) 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ The publisher of this article is The Ecological Society of Korea in collaboration with The Korean Society of Limnology

The shift in flowering phenology with plants blooming earlier due to climate change, disrupts the synchronization between plants and pollinators by creating temporal and spatial mismatches. Monitoring these shifts is essential, and remote sensing has become an invaluable tool for detecting flowering periods over vast areas. Despite the technological advancements, there remains a significant gap in comprehensive reviews that explore the use of remote sensing in flowering phenology and its impact on pollination ecology. Therefore, this study aims to review and summarize research on the remote sensing of flowers, with a particular focus on key techniques used to analyze flowering phenology. We categorized the application of remote sensing in the field of flowering phenology into four groups based on the type of data used: optical, Synthetic Aperture Radar (SAR), Unmanned Aerial Vehicle (UAV), and PhenoCam-based applications. In each section, we have reviewed and provided a summary of the studies conducted in this field, with a particular focus on those that primarily examine canola crop flowering. In conclusion, our findings reveal that Optical remote sensing, proves effective in capturing detailed imagery of flowering events, while SAR technology offers robust, all-weather monitoring capabilities. UAV-based remote sensing provides high-resolution, site-specific data, although it is constrained by operational limitations. PhenoCams offer valuable long-term monitoring but lack the spatial resolution for detailed analysis. Each remote sensing approach has distinct advantages and limitations, underscoring the need for integrated methods to improve flowering phenology assessments and enhance agricultural monitoring.

Keywords: climate change, optical, PhenoCams, plants, pollination, Synthetic Aperture Radar, Unmanned Aerial Vehicle

Agricultural practices occupy about one-third of the Earth’s land surface (Foley et al. 2005; Pye-Smith et al. 2022) and are a significant contributor to the degradation and fragmentation of natural habitats globally (Foley et al. 2005; Keenan et al. 2015; Rahimi and Dong 2022; Rands et al. 2010). To satisfy the demands of the projected global population by 2050, agricultural output must double (Bruinsma 2009; Tilman et al. 2011). In 2018, Africa faced significant food insecurity (Food and Agriculture Organization 2019), while India alone accounted for a quarter of the global food-insecure population (Mughal and Fontan Sers 2020). Concurrently, there is an increasing trend toward urbanization, with 56% of the world’s population currently residing in urban areas (Department of Economic and Social Affairs 2018; Seto and Ramankutty 2016). It is estimated that by 2030, urban land will expand by an additional 1.2 million square kilometers, potentially encroaching on fertile agricultural lands near urban centers (Hou et al. 2021; Seto et al. 2012).

In 2015, the global community, represented by all United Nations Member States, adopted ‘The 2030 Agenda for Sustainable Development.’ This initiative was designed to foster peace, prosperity, and sustainability for people and the planet. Central to this agenda are 17 sustainable development goals, including a key goal to eradicate hunger, ensure food security, enhance nutrition, and promote sustainable agriculture (General Assembly 2016). However, a report from the Food and Agriculture Organization in July 2021 indicated that the world is not on course to meet this goal by 2030, with projections suggesting that the number of people suffering from hunger could exceed 840 million (www.un.org). The world must transform the food and agriculture systems to adequately feed the current 690 million hungry people and an anticipated additional 2 billion by 2050 (www.un.org). The 2021 report on global food security and nutrition highlighted that even before the COVID-19 pandemic, progress toward eliminating hunger and malnutrition by 2030 was off track (UNICEF 2021).

The Millennium Ecosystem Assessment of 2005 (Millennium Ecosystem Assessment 2005) revealed a global decline in ecosystem services, with an almost 60% reduction in those evaluated and up to 70% specifically in regulating services like pollination. Presently, agriculture’s dependence on pollinators has intensified, leading to an increased need for more cultivated land, especially in developing countries. This indicates that as reliance on pollination services grows, there is a corresponding demand for expanding agricultural areas, particularly in less economically developed regions (Aizen et al. 2008; Bentrup et al. 2019; Potts et al. 2016). However, climate change is projected to increase by 1.5 to 5.8 degrees Celsius by the end of the 21st century (Pachauri et al. 2014). This temperature rise is known to impact pollination by disrupting plant-pollinator interactions (Chakraborty et al. 2021). These disruptions can occur through temporal (phenological) and spatial (distributional) mismatches, potentially altering the availability of mutualistic partners (Gérard et al. 2020; Hegland et al. 2009; Jordano 2016; Rafferty 2017; Schweiger et al. 2010).

Such mismatches can lead to the formation of new mutualistic networks between plants and pollinators (Biella et al. 2017). Spatial mismatches can be predicted using species distribution models for interacting species pairs (Devoto et al. 2007; Filazzola et al. 2021; Rahimi et al. 2022; Rahimi and Jung 2024c, 2024d; Schleuning et al. 2016). Temporal mismatches occur when the flowering period of plants and the activity periods of their pollinators are no longer synchronized (Rahimi and Jung 2024e; Straka and Starzomski 2014). This misalignment can reduce pollination efficiency, leading to lower crop yields and diminished food supply (Smith et al. 2015). Such mismatches are particularly critical for pollinator-dependent crops that form the backbone of global agricultural systems (Rahimi and Jung 2024b). However, not all plants respond uniformly to climate change (Brooker 2006; Inouye 2022; Kelly and Goulden 2008). While many studies report earlier flowering due to rising spring temperatures, some early-spring flowering angiosperms have been observed to bloom later. This delayed flowering could result from complex interactions between temperature, photoperiod, and other environmental factors, highlighting the need for nuanced phenological monitoring to understand species-specific responses (Gusain et al. 2024).

Since the 1960s, spring activities such as vegetation growth and flowering have consistently begun earlier (Craufurd and Wheeler 2009; Defila and Clot 2001; Hamunyela et al. 2013; Menzel 2000; Piao et al. 2019; Roetzer et al. 2000; Studer et al. 2005; Studer et al. 2007; Walther et al. 2002). This trend underscores the importance of timely and accurate tracking of flowering periods across various spatial scales. Peak flowering times are crucial for assessing crop growth and predicting yields (d’Andrimont et al. 2020; Panetta et al. 2018; Sulik and Long 2016; Zhang et al. 2023). It’s essential to measure the degree of temporal synchrony between pollinators and pollinator-dependent crops to identify areas at risk of pollinator shortages (Aizen et al. 2019; Carrasco et al. 2021; Giannini et al. 2017; Giannini et al. 2020; Marshall et al. 2023; Polce et al. 2014). Phenological monitoring is conducted through field observations and remote sensing (Rahimi and Jung 2024a, 2024f). Field observations record the timing of significant events like bud burst, leaf unfolding, flowering, and leaf color change (Schwartz 2003). In contrast, remote sensing offers improved spatial and temporal continuity and is more cost-effective, making it a preferred method for regional to global studies (John et al. 2020; Shen et al. 2014).

To assess the temporal mismatch between pollinators and flowering plants, particularly in pollinator-dependent crops, we need detailed information on the flowering phenology of plants, including the start, peak, and end of flowering. For pollinators, it’s essential to have data on their physiology, lifespan, and the timing of their first emergence, peak activity, and final day of activity (Kudo and Ida 2013; Petanidou et al. 2014). With this information, we can evaluate the degree of temporal alignment between flowers and pollinators. Recently, there has been a significant focus on estimating the flowering phenology of crops, forest trees, and wildflowers. Some studies have concentrated on identifying the start and end of crop flowering, while others have focused on detecting flowers in grasslands or flowering trees in forests, developing new methods and vegetation indices to distinguish flowering plants and analyze their phenology. However, a review summarizing these studies is lacking, and it appears that many researchers are unaware of the relevance of such work in the field of pollination ecology. This study aims to firstly provide concise and valuable information on flowering plants, pollinator-dependent crops, and the role of insect pollinators in food security, and secondly review and summarize studies on remote sensing of flowers, focusing on key remote sensing techniques, for analyzing flowering phenology.

We conducted a literature search using the ISI Web of Science, focusing on studies published between 2000 and 2024. Our search employed the following string: (Remote sensing* OR Satellite images* OR Multispectral* OR Synthetic Aperture Radar (SAR)* OR Hyperspectral* OR Phenocam* OR Unmanned Aerial Vehicle (UAV)*) AND (Flower phenology*). This yielded nearly 194 articles, which were narrowed down to 126 unique articles after removing duplicates. We specifically targeted studies that aimed to detect the flowering time of plants or crops, or that identified any phenological phases of flowers. After reviewing the titles and abstracts, we identified 48 articles that were aligned with our research objectives and recorded their key findings. To systematically analyze the methods and their effectiveness in assessing flowering phenology, we categorized the results into four general sections: optical, SAR, UAV, and PhenoCam-based approaches.

We performed a network analysis using the igraph package (Csardi and Nepusz 2006) in R to visualize the relationships between frequently occurring keywords in the titles (> 2 times) of the selected papers. The network was constructed by treating keywords as nodes and their co-occurrences within paper titles as edges, forming connections. To group the keywords, we applied a community detection algorithm based on the Louvain method (Blondel et al. 2008), which identifies clusters of closely connected nodes within the network. This method ensures that keywords with stronger co-occurrence patterns are grouped into distinct communities, reflecting thematic areas within the reviewed studies. The groups were color-coded to enhance interpretability and represent specific research focuses, such as remote sensing techniques, phenology monitoring, and crop-specific studies.

Optical-based applications

Optical or multispectral remote sensing captures reflected or emitted electromagnetic radiation across the visible, near-infrared (NIR), and short-wave infrared (SWIR) wavelengths. Unlike active sensors, such as SAR, optical sensors are passive and rely on sunlight as the illumination source, making them sensitive to atmospheric conditions and diurnal variations (Zhu et al. 2018). These sensors provide valuable spectral information, enabling the identification and monitoring of vegetation and flowering phenology over large spatial extents. While this study does not focus on the technical aspects of optical remote sensing, previous research has extensively examined its capabilities, including the temporal and spatial resolutions of optical satellites such as Sentinel-2, Landsat, and MODIS (Chen et al. 2019; Dixon et al. 2021; Gim et al. 2020; John et al. 2020; Shin et al. 2023; Soubry et al. 2021; Zhang et al. 2022b). Table 1 summarizes key applications of optical remote sensing in studying flowering phenology.

Table 1 . The summary of optical-based applications in flower phenology.

StudyPlantLocationDataGoalKey results
Bogawski
et al. 2019
Betula pendula RothPolandLandsat, MODISSpatial pattern of flowering onsetBirch trees in urban areas began flowering significantly earlier than those in rural areas
Chen et al. 2019AlmondUSAPlanetScope, Sentinel-2, LandstatDeveloping an Enhanced Bloom Index (EBI), based on the multispectral remotely sensed dataEBI enhanced the signals of flowers and reduced the background noise from soil and green vegetation
Forsström
et al. 2019
Lingonberry, blueberryFinlandFieldSpec Pro FRMapping of the spatial distribution of understory speciesLingonberry and blueberry can be identified by their spectral signatures if ground reference data are available over the entire growing season
Chávez
et al. 2019
WildflowersChileAVHRRIdentifying blooming desertsThey detected the looming deserts as positive NDVI anomalies
Paz-Kagan
et al. 2019
Acacia salicina, Acacia
saligna
IsraelAirborne sensors, WorldView-2Identification and mappingAcacia can be monitored based on unique phenological signals
d’Andrimont et al. 2020RapeseedGermanySentinel-2Developing a method to automatically calculate peak floweringA novel methodology was proposed to map oil seed rape flowering phenology
Han et al. 2021RapeseedGermanySentinel-2, Landsat 8Introducing a new spectral indexThe Normalized Rapeseed Flowering Index (NRFI) for identifying the flowering
Dixon et al. 2021Corymbia calophyllaAustraliaDrone, PlanetScopeCreating extensive maps of flowering patternsThe new method predicts the proportion of flowering at the pixel level throughout the entire flowering period
Torgbor
et al. 2022
MangoGhanaSentinel-2Identification phenological stagesFlowering peaks in June/July
Ashourloo
et al. 2022
RapeseedIran, USASentinel-2Introducing an automatic method for rapeseed mappingThe proposed index for differentiating canola from other crops
Rahman
et al. 2022
AvocadoAustraliaSentinel-2Identification phenological stagesThe lowest EVI values were recorded during the flowering stage
Yi et al.
2022
SunflowerChinaSentinel-2Early-season identification and mappingThe sunflower crops were identified early, during the flowering stage in late July
Domingo
et al. 2023
Acacia dealbataSpainSentinel-2Distinguishing and mapping the spatial extentA flowering period was identified in March that was effective for A. dealbata discrimination
Dixon et al. 2023Corymbia calophyllaAustraliaPlanetScopeAssessing the impact of fire on the flowering patternsFire events decreased the proportion of flowering trees
Xiong et al. 2023ChestnutChinaSentinel-2Distribution mappingRandom forest ranked highest accuracy for mapping
Zang et al. 2023RapeseedChinaSentinel-2Introducing an automatic method for rapeseed mappingWith the proposed method, China rapeseed was mapped during 2017–2021
Tao et al. 2023RapeseedChinaSentinel-2Introducing a new index for mapping winter rapeseedThe phenology-Based Winter Rapeseed Index (PWRI) effectively distinguished between winter rapeseed and winter wheat
Shao et al. 2023RapeseedChina, GermanySentinel-2Introducing a Yellowness Index for rapeseed mappingThe proposed NYI exhibited the potential to capture yellow-flowering
Sun et al. 2024RapeseedChinaSentinel-2Exploring the effectiveness of a deep learning-based algorithm for detecting the early flowering stageThe PSPNet model, equipped with a ResNet-50 backbone, successfully fulfilled the requirements for precise classification
Fernando
et al. 2024
RapeseedCanadaPlanetScopeForecasting rapeseed yieldThe final model exhibited the potential of medium-resolution satellite imagery for yield prediction


SAR-based applications

SAR is an active remote sensing technology that emits microwave signals and measures their backscatter to capture detailed surface information. Unlike passive optical methods that depend on sunlight, SAR operates independently of weather and lighting conditions, making it effective for all-weather, day-or-night monitoring (Bhogapurapu et al. 2021; Wang et al. 2015). Its ability to penetrate cloud cover, vegetation, and soil to varying depths (depending on the wavelength) makes SAR particularly valuable in regions with frequent cloud cover or for applications requiring structural and moisture-related data. This unique capability has positioned SAR as a critical tool for monitoring phenology under challenging conditions (Liu et al. 2019; Lopez-Sanchez et al. 2012). Table 2 summarizes key SAR-based applications in studying flowering phenology.

Table 2 . The summary of Synthetic Aperture Radar (SAR)-based applications in flower phenology.

StudyPlantLocationDataGoalKey results
Cable et al. 2014Rapeseed, SoybeanCanadaRADARSAT-2Investigating the impact of acquisition time and incidence angle on various SAR polarimetricEach crop exhibited a characteristic rise and fall in backscatter response
Wiseman
et al. 2014
Rapeseed, SoybeanCanadaRADARSAT-2Investigating the relationship between RADARSAT-2 polarimetric SAR responses and the dry biomass of rapeseed and soybeanPolarimetric SAR responds to the accumulation of dry biomass
McNairn
et al. 2018
RapeseedCanadaRADARSAT-2, TerraSAR-XEstimating canola growth stagesThe new crop growth stage indicator and identified SAR polarimetric parameters were sensitive to phenological changes
Bhogapurapu et al. 2021RapeseedCanadaSentinel-1Introducing three polarimetric descriptors as pseudo-scattering-type parameter (θc), pseudo scattering entropy parameter (Hc), and co-pol purity parameter (mc)During the transition from the leaf development stage to the flowering stage, the θc parameter shifted by approximately 17°
Löw et al. 2021RapeseedGermanySentinel-1Identification of the phenological phases of rapeseedBy combining, polarimetric Alpha and Entropy, and backscatter (VV/VH) measurements, they detected phenological stages
Liu and Zhang 2023RapeseedChinaSentinel-1Developing a comprehensive approach for rapeseed mappingThe first publicly available 10-meter resolution product for rapeseed distribution in China
Zhao et al. 2023RapeseedChinaSentinel-1Exploring rapeseed characteristics by analyzing backscattering profilesBackscattering features during the flowering to maturity stages were particularly influential, leading to higher classification accuracy
Qadir et al. 2023SunflowerUkraineSentinel-1Monitor sunflower phenology by analyzing a time series of backscattering coefficientsTwo key phases were identified: the beginning of flowering (BoF) and the end of flowering (EoF)


UAV-based applications

UAV remote sensing employs UAVs equipped with sensors and cameras to acquire high-resolution imagery of the Earth’s surface. Its exceptional spatial resolution allows for detailed and site-specific monitoring, often exceeding the capabilities of satellite or airborne platforms (Osco et al. 2021). UAVs can be equipped with various sensors, including hyperspectral imagers, which offer narrow, contiguous wavelength bands (~10 nm) compared to the broader bands of multispectral sensors (~100 nm), enabling precise detection of subtle spectral variations (Chen et al. 2017). This versatility makes UAVs invaluable for fine-scale phenological studies. Table 3 summarizes key UAV-based applications in monitoring flowering phenology.

Table 3 . The summary Unmanned Aerial Vehicle (UAV)-based applications in flower phenology.

StudyPlantLocationDataGoalKey results
Ge et al. 2006Centaurea solstitialisUSASpec ProFRInvestigating the spectral reflectance of various flowering stagesSpectral differences between simulated flowering stages varied by spectral regions and phenological stages
Gai et al. 2011WildflowersCanadaASD FieldSpec-3Measuring the reflectance spectra of flowersThe linear unmixing model is an effective method for estimating the coverage of grassland flowers
Landmann et al. 2015WildflowersKenyaAISA/EagleCreating the first map of flowering and short-term floral cyclesOverall mapping accuracy was higher during the peak flowering period
Sulik and Long 2016RapeseedUSAASD FieldSpecProTMDetecting phenological stagesThey developed a Normalized Difference Yellowness Index (NDYI)
Ma et al. 2019RapeseedChinaASD FieldSpec 4Winter rapeseed biomass estimationResults indicated that rapeseed biomass could be reliably estimated by canopy hyperspectral data
Mahmud
et al. 2020
Solidago altissimaJapanASD Field Spec 4Mapping an invasiveDetection of S. altissima distribution was possible using a high-resolution satellite image
Neumann
et al. 2020
Calluna vulgarisGermanyDJI Phantom 4 Pro droneQuantifying spatial patterns of phenologyCalluna life-cycle phases can be spatially differentiated into pioneer, building, and mature phases in UAV imagery
Stanski et al. 2021Eriophorum vaginatumCanadaPhantom 4 Advanced Pro droneDeveloping a method for detecting tundra plant species’ flowersR-CNN architecture was capable of E. vaginatum flower species detection and counting
Zhang et al. 2022aRapeseedChinaRededge-MXEnhancing a shape-model method for extracting phenological stagesAmong vegetation indices, CIred-edge achieved the greatest accuracy in estimating the phenological stage dates
Gallmann
et al. 2022
WildflowersSwitzerlandDJI Matrice 600 PROFlower Mapping in GrasslandsSome flowers were detected poorly due to reasons such as lack of enough training data, and appearance changes due to phenology
Athira et al. 2023WildflowersIndiaOcean Optics USBQuantifying diverse floral colors across landscapesThe research introduced a novel approach that utilizes floral spectral reflectance data to study subtle changes in the landscape
Lee et al. 2023Tropical treesUSADJI Phantom Pro 4 droneDeveloping an advanced method integrating the Residual Networks 50 (ResNet50)The deep learning method achieved high accuracy in classifying flowers
Zhang et al. 2023AppleNetherlandsPhantom4 RTK,Introducing an innovative approach for quantifying flower intensity using single raw aerial imagesThe method was successful in the tree-level flower cluster estimation derived
Kopeć et al. 2023Echinocystis lobataPolandHySpex VNIRAssessing the impact of acquiring synchronized on-ground data and hyperspectral dataMapping an annual vine using remote sensing and machine learning is possible and highly effective
Thoday-Kennedy
et al. 2023
SafflowerAustraliaRedEdge-M multispectralIdentifying the onset of floweringEarly flowering genotypes often had lower peak NDVI values and a slower decay rate
Gupta et al. 2024Heterotheca subaxillarisIsraelDJI Phantom 4Developing a methodology to identify and mapRandom forest classification approach, achieving a remarkable 97.4% accuracy in identifying H. subaxillaris


PhenoCam-based applications

PhenoCam-based applications utilize automated digital cameras specifically designed for long-term monitoring of vegetation phenology. Unlike general digital repeat photography, which encompasses a wide range of camera types and technologies, PhenoCams are specialized systems that capture time-lapse images at regular intervals (Jose et al. 2023). Typically mounted on towers or other fixed structures, these cameras provide continuous observations of plant and ecosystem changes, making them invaluable for tracking phenological events over time (Crimmins and Crimmins 2008; Mann et al. 2022; Nijland et al. 2013). Their ability to capture temporal data complements other remote sensing methods by offering high temporal resolution, particularly for localized studies. Table 4 summarizes key PhenoCam-based applications in monitoring flowering phenology.

Table 4 . The summary PhenoCam-based applications in flower phenology.

StudyPlantLocationDataGoalKey results
Nijland et al. 2013Hedysarum alpinumCanadaPentax K100D digital SLRExploring whether time-lapse photography could be used to monitor the phenological development of a forest standRepeat photography and image analysis were effective in detecting all key phenological events
Mann et al. 2022Dryas octopetala, Dryas integrifoliaGreenlandTimelapseCam ProIntroducing a method for automated monitoring of flowering phenologyThe convolutional neural network was effective in collecting flower phenology data
Funada and Tsutsumida 2022CherryJapan-Developing a deep-learning model using ‘YOLOv4’ to detect cherry blossoms from street-level photographsThe object-detection model achieved an overall accuracy of 83%
Andreatta
et al. 2023
WildflowersGermanyTLC 100, BrinnoDeveloped a workflow for extracting flowering phenology in grassland species mixtures usingThe random forest classifiers demonstrated high accuracy in predicting the cover of wildflowers

The review of remote sensing methods for analyzing flowering phenology—optical, SAR, UAV, and PhenoCam—reveals a diverse array of capabilities and limitations, highlighting the strengths and challenges inherent to each technique. Optical methods, evaluated across 20 studies, stand out for their high spatial resolution and efficacy in mapping flowering periods and spatial distributions. SAR methods, covered in 8 studies, offer significant advantages in all-weather monitoring, capable of penetrating cloud cover and capturing data irrespective of lighting conditions (Table 5). UAV methods, discussed in 16 studies, provide high-resolution and site-specific data that is invaluable for detailed flower detection and phenological stage mapping. UAVs offer flexibility in application and high spatial resolution, which is beneficial for capturing nuanced plant health and phenology data. PhenoCam methods, explored in 4 studies, are notable for their long-term monitoring capabilities and effectiveness in capturing continuous temporal data on flowering events.

Table 5 . A summary comparison of reviewed methods.

MethodNumber of studiesKey focus areasExamples of key findings
Optical20Flowering onset, bloom indices, phenological stages, spatial distribution- Enhanced Bloom Index (EBI): Improved detection of flowering events by reducing background noise from vegetation and soil
- Effective Mapping: Successfully mapped flowering periods and spatial distribution across different environments
- Phenological Indicators: Various indices like NDVI and specific bloom indices were used to assess and monitor flowering stages
SAR8Growth stages, phenological phases, polarimetric response- Growth Stage Indicators: Identified distinct SAR parameters sensitive to phenological changes, such as the θc parameter shift during flowering
- Phenological Phases: Detailed mapping of growth stages and phenological phases using SAR’s ability to capture changes in vegetation structure
UAV16Reflectance spectra, flower coverage, phenological stages, high-resolution mapping- High-Resolution Mapping: UAVs provide detailed, high-resolution imagery for precise flower detection and mapping, though detection accuracy can vary
- Reflectance Spectra: Effective in assessing spectral differences between flowering stages and vegetation types
- Variable Detection: Challenges with variable detection due to changing phenological states and the need for extensive training data
PhenoCam4Phenological monitoring, automated detection, time-lapse photography- Long-Term Monitoring: Effective for monitoring flowering events over time with high temporal resolution
- Automated Detection: Convolutional neural networks and deep learning models achieved high accuracy in detecting and classifying flowering phenology
- Event Detection: Successful in capturing key phenological events using repeat photography and time-lapse techniques

SAR: Synthetic Aperture Radar; UAV: Unmanned Aerial Vehicle.



Geographically, North America has seen widespread adoption of all methods, reflecting a broad application of remote sensing techniques across various environments. Europe has focused predominantly on optical and PhenoCam methods, leveraging their strengths in spatial and temporal analysis. In contrast, Asia has shown a significant emphasis on UAV studies, highlighting the region’s interest in high-resolution, site-specific data. Each method’s challenges—ranging from atmospheric interference for optical methods, complex data processing for SAR, high costs for UAVs, to spatial resolution limitations for PhenoCam—underscore the need for continued research and development. Future directions include enhancing data integration across methods, improving algorithmic approaches, and expanding research to encompass a wider geographic scope to address these challenges comprehensively and advance the field of flowering phenology analysis.

Table 6 summarizes the spectral bands commonly used in remote sensing for flowering phenology detection, highlighting their characteristics, associated vegetation indices, and applications. The Visible (Red) band (620–750 nm) is sensitive to chlorophyll absorption and is effective in isolating flowering signals, with indices like the Enhanced Bloom Index (EBI) and NDVI reducing background noise from vegetation and soil. The NIR band (750–900 nm) reflects strongly in healthy vegetation, aiding in differentiating flowers from surrounding vegetation and supporting indices such as NDVI and the Normalized Rapeseed Flowering Index (NRFI) in agricultural applications. The SWIR band (1,300–2,500 nm) is sensitive to vegetation water content and physiological changes, with the Normalized Difference Water Index (NDWI) monitoring water stress and its impact on flowering behavior. Together, these spectral bands provide critical insights into flowering phenology across diverse environments and crops.

Table 6 . Summary of spectral band characteristics, vegetation indices, and flowering detection applications.

Spectral bandWavelength range (nm)CharacteristicsVegetation indicesRelevance to flowering detection
Visible (Red)620–750Sensitive to chlorophyll absorption; highlights flowering signals against green vegetationEnhanced Bloom Index (EBI), NDVIEffective in identifying flowering onset and reducing soil/vegetation background noise (Chen et al. 2019)
Near-Infrared (NIR)750–900Reflects strongly in healthy vegetation, differentiating it from flowers or soilNDVI, Normalized Rapeseed Flowering Index (NRFI)Aids in mapping flowering phenology, particularly in agricultural landscapes like rapeseed fields (Han et al. 2021; Zang et al. 2023)
Shortwave infrared (SWIR)1,300–2,500Sensitive to vegetation water content; highlights physiological changes during phenological stagesNormalized Difference Water Index (NDWI)Tracks water stress and phenological changes affecting flowering behavior (Chávez et al. 2019)


Network visualization

Figure 1 displays the network visualization of keywords that appear more than twice across 48 study titles. Keywords for component 1 are data, remote, sensing, invasive, phenological, stages, vegetation, spectral, winter, canola, assessment, growth, classification, different, and hyperspectral. The keywords suggest a focus on remote sensing techniques and their applications in studying vegetation and crop growth. Terms like “data,” “remote,” “sensing,” and “hyperspectral” indicate a reliance on advanced technologies for collecting and analyzing environmental data. The presence of “invasive,” “phenological,” and “stages” highlights a concern with various stages of vegetation growth and the impact of different factors on these stages. Keywords such as “winter,” “canola,” and “assessment” suggest seasonal and crop-specific studies, implying that this community deals with the classification and assessment of vegetation and crops through sophisticated sensing methods. This community likely represents research focused on improving the accuracy of environmental assessments and understanding the dynamics of plant growth through technological advancements.

Figure 1. Network visualization of frequent keywords (> 2 times) in the titles of 48 study titles.

Keywords for component 2 are flowering, phenology, series, time, approach, based, species, forest, monitoring, deep, identification, learning, detection, flower, and imagery. Component 2 revolves around the study of plant phenology and species monitoring, with an emphasis on methodologies and technologies used for observing and identifying plant species. Keywords such as “flowering,” “phenology,” and “monitoring” suggest a primary focus on tracking plant development stages and changes over time. The inclusion of terms like “species,” “forest,” and “detection” points to a broader interest in understanding various plant species within forest ecosystems. The terms “deep,” “learning,” and “imagery” imply the use of advanced techniques, such as machine learning and remote imaging, for identifying and analyzing plant species. This community appears to be dedicated to enhancing methods for monitoring plant phenology and developing more accurate approaches for species identification and tracking using innovative technologies.

Keywords for component 3 are using, index, sentinel, method, new, rapeseed, mapping, time-series, crop, china, and polarimetric. Component 3 focuses on crop mapping and analysis, with particular attention to innovative methods and applications. Keywords such as “index,” “sentinel,” and “method” indicate the use of specific techniques and tools for crop analysis, possibly involving satellite data or remote sensing indices. The term “new” suggests ongoing advancements or novel approaches in this area. “Rapeseed,” “crop,” and “mapping” highlight the practical applications of these methods in agricultural contexts, specifically related to crop management and monitoring. The mention of “time-series” and “polarimetric” suggests a focus on analyzing temporal changes and using polarimetric data to enhance the accuracy of crop assessments. Additionally, the reference to “China” implies a geographical focus, potentially indicating that this community’s research is concentrated on crop management and analysis within China. This community seems dedicated to applying new methodologies for detailed and effective crop mapping and monitoring.

Optical-based applications

The optical-based studies have employed a wide range of optical data sources, from satellites like Sentinel-2 and Landsat to MODIS. This variety allows for different spatial and temporal resolutions, which is a strength as it shows the flexibility of optical methods in capturing flower phenology across different contexts. However, reliance on satellite imagery with medium to low resolution (e.g., MODIS, AVHRR) may limit the precision in detecting fine-scale phenological changes, particularly in heterogeneous environments.

Several studies (e.g., Ashourloo et al. 2022; Chen et al. 2019; d’Andrimont et al. 2020; Han et al. 2021; Shao et al. 2023; Tao et al. 2023; Zang et al. 2023) have introduced new methodologies for automatic crop mapping or spectral indices tailored for specific crops or conditions, such as the EBI and the NRFI. These indices are innovative and offer potential improvements in accuracy. However, the generalizability of these indices to other crops or environments remains uncertain and should be further validated.

These studies also highlight how flowering phenology can be effectively monitored across various climates and plant species, from birch trees in urban Poland to rapeseed in China. However, results vary depending on the region and plant species, suggesting that local environmental conditions significantly influence the success of these methods. For instance, the spatial resolution required to map rapeseed in dense agricultural landscapes might differ from that needed to detect flowering in sparsely distributed wildflowers in Chile (Chávez et al. 2019). There is also a consistent finding that optical methods can successfully identify and map flowering stages (e.g., Dixon et al. 2021; Domingo et al. 2023). However, the accuracy and precision of these detections often depend on the availability of ground truth data (Forsström et al. 2019). The need for extensive ground validation is a recurring theme, which could limit the scalability of these methods in regions where such data are not readily available.

These studies primarily focus on Europe, China, and the USA, with fewer studies in tropical or arid regions. Moreover, common crops like rapeseed are frequently studied, while other economically important or ecologically significant species receive less attention. This indicates a potential bias in research that could overlook critical phenological changes in underrepresented areas and species. Many studies use time-series data to capture phenological changes (e.g., Sentinel-2 data in multiple studies). However, the temporal resolution may not be sufficient to capture rapid phenological events, such as sudden flowering onset triggered by specific climatic conditions. The studies show significant potential for practical applications in agriculture and ecology, such as forecasting crop yields (Fernando et al. 2024) and assessing the impact of environmental factors like fire (Dixon et al. 2023). These applications highlight the value of optical methods in managing and adapting to environmental changes. However, the translation of these methods into operational tools for farmers or land managers is not thoroughly discussed in most studies, which could limit their real-world impact.

SAR-based applications

These studies primarily utilize SAR data from RADARSAT-2 and Sentinel-1, with some incorporating TerraSAR-X. SAR offers unique advantages, such as the ability to penetrate cloud cover and provide data under all weather conditions, which is particularly beneficial for monitoring phenology in areas with frequent cloud cover. However, SAR data are more complex to interpret compared to optical data, requiring advanced processing techniques. The reliance on different SAR sensors across studies is both a strength (diversity of data) and a potential limitation (differences in data consistency and resolution). Several studies (Cable et al. 2014; McNairn et al. 2018; Wiseman et al. 2014) have focused on polarimetric SAR, which analyzes different polarization states of the radar signal. This approach is effective for distinguishing between different crop types and detecting phenological changes. The introduction of novel polarimetric descriptors (Bhogapurapu et al. 2021) adds value by enhancing the sensitivity of SAR data to phenological stages. However, the complexity of polarimetric analysis may limit its accessibility for broader applications without specialized expertise.

The studies consistently show that SAR data are effective in identifying key phenological stages in crops like rapeseed and soybean. For example, McNairn et al. (2018) and Löw et al. (2021) successfully used SAR to detect stages of rapeseed growth. Zhao et al. (2023) further confirm the capability of SAR in distinguishing flowering to maturity stages with high classification accuracy. This consistency underscores SAR’s robustness in phenological monitoring. However, the results are highly dependent on the specific SAR parameters and polarimetric techniques used, suggesting a need for standardization.

While SAR-based methods have been widely tested in Canada and China, their application to different crops (e.g., sunflower in Ukraine) shows variability in effectiveness. For instance, while rapeseed phenology is well-documented, the identification of sunflower phenological stages in Ukraine highlights different backscattering responses, emphasizing the need to tailor SAR analysis to specific crop types and regional conditions. The studies focus predominantly on rapeseed, with only one study (Qadir et al. 2023) extending the application to sunflower. This narrow focus limits the generalizability of the findings to other crops with different phenological patterns. Expanding SAR-based research to a wider variety of crops could enhance our understanding of its applicability across diverse agricultural landscapes. Also, while Sentinel-1 offers frequent revisits and high spatial resolution, there are still limitations in capturing rapid phenological changes. The temporal resolution may be insufficient for crops with short flowering periods, leading to potential gaps in data. The reliance on SAR alone might also overlook the benefits of integrating with optical data to provide a more comprehensive phenological assessment.

UAV-based applications

These studies have utilized a wide range of UAV platforms and sensors, from simple RGB cameras (e.g., DJI Phantom series) to advanced hyperspectral sensors (e.g., HySpex VNIR). This diversity allows for a broad exploration of UAV applications in flower phenology, capturing different aspects of plant development. However, the variation in sensor types and resolutions complicates the comparison of results across studies, as different sensors have unique strengths and limitations. Several studies, such as those by Ge et al. (2006) and Sulik and Long (2016), focus on spectral reflectance data to identify phenological stages or develop indices like the Normalized Difference Yellowness Index (NDYI). While spectral analysis is powerful for detecting subtle phenological changes, it often requires high-quality, consistent data, which may not always be available, particularly in diverse and complex field conditions.

More recent studies (Gupta et al. 2024; Lee et al. 2023; Stanski et al. 2021) incorporate advanced machine learning models, such as R-CNN architecture and Random Forest classifiers, to enhance the accuracy of flower detection and classification. These approaches represent a significant advancement in UAV-based phenology, offering precise, automated analysis. However, they also require substantial computational resources and expertise, potentially limiting their accessibility for broader applications. The studies consistently demonstrate that UAVs are effective tools for identifying and mapping phenological stages. For example, Zhang et al. (2022a) found that the CIred-edge vegetation index was highly accurate in estimating phenological stage dates for rapeseed, while Neumann et al. (2020) successfully quantified spatial patterns of phenology in Calluna vulgaris using UAV imagery. These findings underline UAVs’ potential in fine-scale phenological monitoring, especially in heterogeneous landscapes.

Despite the overall success, some studies, such as Gallmann et al. (2022), report challenges in accurately detecting certain flower species. Issues like insufficient training data and changes in flower appearance due to phenology highlight the limitations of current UAV-based methods. This indicates a need for more robust, adaptable models that can account for such variability. While the studies cover a range of locations and plant species, there is a noticeable concentration on certain crops, such as rapeseed and wildflowers. This focus limits the generalizability of the results, as different crops and regions may exhibit different phenological patterns and responses to UAV-based monitoring. Expanding the research to include a wider variety of crops and ecosystems would enhance the understanding and applicability of UAV technology in phenology.

PhenoCam-based applications

These studies leverage PhenoCams and time-lapse photography as primary data collection tools for monitoring phenological changes in various plant species. These methods offer a cost-effective and accessible approach to capturing continuous phenological data over time, with particular strength in visualizing changes that occur gradually, such as flowering events. For instance, Nijland et al. (2013) successfully utilized time-lapse photography to monitor phenological events in Hedysarum alpinum, demonstrating the method’s effectiveness in detecting key phenological stages. More recent studies, such as Mann et al. (2022) and Funada and Tsutsumida (2022), incorporate machine learning models, like convolutional neural networks (CNNs) and YOLOv4, for automated phenology monitoring. These models enhance the efficiency and accuracy of data analysis by automating the identification and classification of phenological stages. However, the reliance on advanced algorithms also introduces complexity, requiring significant computational resources and expertise in machine learning.

The studies employ a variety of camera systems, ranging from simple digital SLRs (e.g., Pentax K100D) to specialized time-lapse cameras (e.g., TimelapseCam Pro, Brinno). This diversity allows for flexibility in capturing phenological data across different environments and species. However, the variation in camera quality and setup may affect the consistency and comparability of results across different studies. The studies consistently demonstrate that PhenoCams are effective tools for capturing and analyzing phenological events. For example, Nijland et al. (2013) showed that repeat photography could effectively detect all key phenological events in a forest stand, while Mann et al. (2022) found that a CNN model could effectively collect flower phenology data for Dryas species in Greenland. These findings underscore the utility of PhenoCams for detailed phenological monitoring, particularly in remote or challenging environments.

The studies primarily focus on specific regions and plant species, such as Dryas in Greenland and cherry blossoms in Japan. While these studies provide valuable insights, the limited geographic and species coverage restricts the generalizability of the findings. Expanding research to include a broader range of ecosystems and plant species would provide a more comprehensive understanding of phenological patterns and responses to environmental changes. The effectiveness of PhenoCam-based phenology monitoring largely depends on the quality of the imagery captured. Variations in lighting conditions, camera angles, and image resolution can impact the accuracy of phenological observations. Finally, we summarized the strengths, limitations, challenges, and future directions of four remote sensing methods—Optical, SAR, UAV, and PhenoCam—while highlighting their suitability for specific applications in phenology studies (Table 7). Table 7 provides a comprehensive comparison to guide the selection of appropriate methods based on research goals and practical considerations.

Table 7 . Summary of strengths, limitations, challenges, and future directions for each method.

MethodStrengthsLimitationsChallengesFuture directionsSuitable for
OpticalHigh spatial resolution; effective for large-scale mapping and detecting flowering events.Sensitive to atmospheric conditions and vegetation cover; may require ground truthing.Atmospheric interference, need for extensive ground validation.Development of more robust indices and integration with complementary data types.Large-scale mapping, bloom indices, spatial distribution studies.
SARAll-weather capabilities; provide detailed growth stage indicators.Complex data processing; is less effective for detecting detailed flowering events.Complex processing and limited resolution for small-scale flowering detection.Improvement in spatial resolution and better integration with optical data.Biomass estimation, growth stage monitoring, phenological phase detection.
UAVVery high-resolution, site-specific data; flexible and adaptable.High operational costs; weather-dependent; challenges in consistent detection accuracy.Cost, weather dependence, and variability in detection due to changing phenological states.Reduction in costs, improvement in algorithms, and expansion of applications.Precise flower detection, detailed phenological stage mapping, and site-specific studies.
PhenoCamProvides long-term, high-frequency monitoring; effective for phenological events over time.Limited spatial coverage; less effective for mapping large areas.Limited resolution and applicability to broader spatial scales.Integration with high-resolution methods and expansion of study areas.Long-term phenological monitoring and automated detection of flowering events.

SAR: Synthetic Aperture Radar; UAV: Unmanned Aerial Vehicle.


This study provides a comprehensive review of various remote sensing methods—Optical, SAR, UAV, and PhenoCam—used in flower phenology research. Through a detailed analysis of existing literature, we have identified the key strengths, limitations, and applications of each method highlighting how they contribute to understanding and monitoring flowering events across different plant species and environments. We aimed to highlight the potential of these remote sensing technologies to capture the flowering times of flowers and pollinator-dependent crops, thereby addressing the temporal mismatches between plants and their pollinators. This review underscores the importance of utilizing remote sensing techniques to better understand and mitigate temporal mismatches between flowering plants and their pollinators, ultimately contributing to more effective conservation and management strategies for pollinator-dependent ecosystems.

CNNs: Convolutional neural networks

EBI: Enhanced Bloom Index

NDWI: Normalized Difference Water Index

NDYI: Normalized Difference Yellowness Index

NIR: Near-infrared

NRFI: Normalized Rapeseed Flowering Index

SAR: Synthetic Aperture Radar

SWIR: Short-wave infrared

UAV: Unmanned Aerial Vehicle

Conceptualization, ER and CJ; Validation, CJ; Formal Analysis; Investigation, ER; Resources, CJ; Data Curation, ER; Writing – Original Draft, ER; Preparation, ER; Writing – Review & Editing, CJ; Supervision, CJ; Project Administration, CJ; Funding Acquisition, CJ. All authors have read and agreed to the published version of the manuscript.

This research was funded by RDA Korea, grant number RS-2023-00232847, and the National Research Foundation of Korea (National Research Foundation of Korea (NRF-2018R1A6A1A03024862).

  1. Aizen MA, Aguiar S, Biesmeijer JC, Garibaldi LA, Inouye DW, Jung C, et al. Global agricultural productivity is threatened by increasing pollinator dependence without a parallel increase in crop diversification. Glob Change Biol. 2019;25(10):3516-27. https://doi.org/10.1111/gcb.14736.
    Pubmed KoreaMed CrossRef
  2. Aizen MA, Garibaldi LA, Cunningham SA, Klein AM. Long-term global trends in crop yield and production reveal no current pollination shortage but increasing pollinator dependency. Curr Biol 2008;18(20):1572-5. https://doi.org/10.1016/j.cub.2008.08.066.
    Pubmed CrossRef
  3. Andreatta D, Bachofen C, Dalponte M, Klaus VH, Buchmann N. Extracting flowering phenology from grassland species mixtures using time-lapse cameras. Remote Sens Environ. 2023;298:113835. https://doi.org/10.1016/j.rse.2023.113835.
    CrossRef
  4. Ashourloo D, Nematollahi H, Huete A, Aghighi H, Azadbakht M, Shahrabi HS, et al. A new phenology-based method for mapping wheat and barley using time-series of Sentinel-2 images. Remote Sens Environ. 2022;280:113206. https://doi.org/10.1016/j.rse.2022.113206.
    CrossRef
  5. Athira K, Jaishanker RN, Rajan SC, Dadhwal VK. Remote sensing of flowers. Ecol Inform. 2023;78:102369. https://doi.org/10.1016/j.ecoinf.2023.102369.
    CrossRef
  6. Bentrup G, Hopwood J, Adamson NL, Vaughan M. Temperate agroforestry systems and insect pollinators: a review. Forests. 2019;10(11):981. https://doi.org/10.3390/f10110981.
    CrossRef
  7. Bhogapurapu N, Dey S, Bhattacharya A, Mandal D, Lopez-Sanchez JM, McNairn H, et al. Dual-polarimetric descriptors from Sentinel-1 GRD SAR data for crop growth assessment. ISPRS J Photogramm Remote Sens. 2021;178:20-35. https://doi.org/10.1016/j.isprsjprs.2021.05.013.
    CrossRef
  8. Biella P, Ollerton J, Barcella M, Assini S. Network analysis of phenological units to detect important species in plant-pollinator assemblages: can it inform conservation strategies? Comm Ecol. 2017;18:1-10. https://doi.org/10.1556/168.2017.18.1.1.
    CrossRef
  9. Blondel VD, Guillaume JL, Lambiotte R, Lefebvre E. Fast unfolding of communities in large networks. J Stat Mech: Theory Exp. 2008;10:P10008.
    CrossRef
  10. Bogawski P, Grewling Ł, Jackowiak B. Predicting the onset of Betula pendula flowering in Poznań (Poland) using remote sensing thermal data. Sci Total Environ. 2019;658:1485-99. https://doi.org/10.1016/j.scitotenv.2018.12.295.
    Pubmed CrossRef
  11. Brooker RW. Plant-plant interactions and environmental change. New Phytol. 2006;171(2):271-84. https://doi.org/10.1111/j.1469-8137.2006.01752.x.
    Pubmed CrossRef
  12. Cable JW, Kovacs JM, Jiao X, Shang J. Agricultural monitoring in northeastern Ontario, Canada, using multi-temporal polarimetric RADARSAT-2 data. Remote Sens. 2014;6(3):2343-71. https://doi.org/10.3390/rs6032343.
    CrossRef
  13. Carrasco L, Papeş M, Lochner EN, Ruiz BC, Williams AG, Wiggins GJ. Potential regional declines in species richness of tomato pollinators in North America under climate change. Ecol Appl. 2021;31(3):e02259. https://doi.org/10.1002/eap.2259.
    Pubmed CrossRef
  14. Chakraborty P, Chatterjee S, Smith BM, Basu P. Seasonal dynamics of plant pollinator networks in agricultural landscapes: how important is connector species identity in the network? Oecologia. 2021;196:825-37. https://doi.org/10.1007/s00442-021-04975-y.
    Pubmed CrossRef
  15. Chávez RO, Moreira-Muñoz A, Galleguillos M, Olea M, Aguayo J, Latín A, et al. GIMMS NDVI time series reveal the extent, duration, and intensity of "blooming desert" events in the hyper-arid Atacama Desert, Northern Chile. Int J Appl Earth Obs Geoinf. 2019;76:193-203. https://doi.org/10.1016/j.jag.2018.11.013.
    CrossRef
  16. Chen B, Huang B, Xu B. Multi-source remotely sensed data fusion for improving land cover classification. ISPRS J Photogramm Remote Sens. 2017;124:27-39. https://doi.org/10.1016/j.isprsjprs.2016.12.008.
    CrossRef
  17. Chen B, Jin Y, Brown P. An enhanced bloom index for quantifying floral phenology using multi-scale remote sensing observations. ISPRS J Photogramm Remote Sens. 2019;156:108-20. https://doi.org/10.1016/j.isprsjprs.2019.08.006.
    CrossRef
  18. Craufurd PQ, Wheeler TR. Climate change and the flowering time of annual crops. J Exp Bot. 2009;60(9):2529-39. https://doi.org/10.1093/jxb/erp196.
    Pubmed CrossRef
  19. Crimmins MA, Crimmins TM. Monitoring plant phenology using digital repeat photography. Environ Manage. 2008;41(6):949-58. https://doi.org/10.1007/s00267-008-9086-6.
    Pubmed CrossRef
  20. Csardi G, Nepusz T. The igraph software package for complex network research. InterJournal Complex Systems. 2006;1695:1-9.
  21. d'Andrimont R, Taymans M, Lemoine G, Ceglar A, Yordanov M, van der Velde M. Detecting flowering phenology in oil seed rape parcels with Sentinel-1 and -2 time series. Remote Sens Environ. 2020;239:111660. https://doi.org/10.1016/j.rse.2020.111660.
    Pubmed KoreaMed CrossRef
  22. Defila C, Clot B. Phytophenological trends in Switzerland. Int J Biometeorol. 2001;45(4):203-7. https://doi.org/10.1007/s004840100101.
    Pubmed CrossRef
  23. Department of Economic and Social Affairs. 2018. https://www.un.org/en/desa/2018-revision-world-urbanization-prospects. Accessed 1 Jul 2024.
  24. Devoto M, Zimmermann M, Medan D. Robustness of plant-flower visitor webs to simulated climate change. Ecol Austral. 2007;17(1):37-50.
  25. Dixon DJ, Callow JN, Duncan JMA, Setterfield SA, Pauli N. Satellite prediction of forest flowering phenology. Remote Sens Environ. 2021;255:112197. https://doi.org/10.1016/j.rse.2020.112197.
    CrossRef
  26. Dixon DJ, Duncan JMA, Callow JN, Setterfield SA, Pauli N. Fire reduces eucalypt forest flowering phenology at the landscape-scale. Sci Total Environ. 2023;894:164828. https://doi.org/10.1016/j.scitotenv.2023.164828.
    Pubmed CrossRef
  27. Domingo D, Pérez-Rodríguez F, Gómez-García E, Rodríguez-Puerta F. Assessing the efficacy of phenological spectral differences to detect invasive alien Acacia dealbata using Sentinel-2 data in Southern Europe. Remote Sens. 2023;15(3):722. https://doi.org/10.3390/rs15030722.
    CrossRef
  28. Fernando H, Ha T, Nketia KA, Attanayake A, Shirtliffe S. Machine learning approach for satellite-based subfield canola yield prediction using floral phenology metrics and soil parameters. Precision Agric. 2024;25:1386-403. https://doi.org/10.1007/s11119-024-10116-1.
    CrossRef
  29. Filazzola A, Matter SF, MacIvor JS. The direct and indirect effects of extreme climate events on insects. Sci Total Environ. 2021;769:145161. https://doi.org/10.1016/j.scitotenv.2021.145161.
    Pubmed CrossRef
  30. Foley JA, Defries R, Asner GP, Barford C, Bonan G, Carpenter SR, et al. Global consequences of land use. Science. 2005;309(5734):570-4. https://doi.org/10.1126/science.1111772.
    Pubmed CrossRef
  31. Food and Agriculture Organization. 2019. https://openknowledge.fao.org/items/f73edb75-4017-497b-8ca3-e66ea2109560. Accessed 1 Jul 2024.
  32. Forsström P, Peltoniemi J, Rautiainen M. Seasonal dynamics of lingonberry and blueberry spectra. Silva Fennica. 2019;53(2):10150. https://doi.org/10.14214/sf.10150.
    CrossRef
  33. Funada S, Tsutsumida N. IGARSS 2022-2022 IEEE International Geoscience and Remote Sensing Symposium; 2022 July 17-22; Kuala Lumpur, Malaysia; 2022. p. 5645-7.
    CrossRef
  34. Gai Y, Fan W, Xu X, Zhang Y. 2011 IEEE International Geoscience and Remote Sensing Symposium; 2011 July 24-29; Vancouver, BC, Canada. 2011; 2011. p. 1243-6.
    CrossRef
  35. Gallmann J, Schüpbach B, Jacot K, Albrecht M, Winizki J, Kirchgessner N, et al. Flower mapping in grasslands with drones and deep learning. Front Plant Sci. 2022;12:774965. https://doi.org/10.3389/fpls.2021.774965.
    Pubmed KoreaMed CrossRef
  36. Ge S, Everitt J, Carruthers R, Gong P, Anderson G. Hyperspectral characteristics of canopy components and structure for phenological assessment of an invasive weed. Environ Monit Assess. 2006;120(1-3):109-26. https://doi.org/10.1007/s10661-005-9052-1.
    Pubmed CrossRef
  37. Gérard M, Vanderplanck M, Wood T, Michez D. Global warming and plant-pollinator mismatches. Emerg Top Life Sci. 2020;4(1):77-86. https://doi.org/10.1042/ETLS20190139.
    Pubmed KoreaMed CrossRef
  38. Giannini TC, Costa WF, Borges RC, Miranda L, da Costa CPW, Saraiva AM, et al. Climate change in the Eastern Amazon: crop-pollinator and occurrence-restricted bees are potentially more affected. Reg Environ Change. 2020;20:9. https://doi.org/10.1007/s10113-020-01611-y.
    CrossRef
  39. Giannini TC, Costa WF, Cordeiro GD, Imperatriz-Fonseca VL, Saraiva AM, Biesmeijer J, et al. Projected climate change threatens pollinators and crop production in Brazil. PLoS One. 2017;12(8):e0182274. https://doi.org/10.1371/journal.pone.0182274.
    Pubmed KoreaMed CrossRef
  40. Gim HJ, Ho CH, Jeong S, Kim J, Feng S, Hayes MJ. Improved mapping and change detection of the start of the crop growing season in the US Corn Belt from long-term AVHRR NDVI. Agric For Meteorol. 2020;294:108143. https://doi.org/10.1016/j.agrformet.2020.108143.
    CrossRef
  41. Gupta SK, Ben-Dor E, Sternberg M. Unveiling the invasion: advancing ecological mapping of Heterotheca subaxillaris through integrated remote sensing techniques with drones and satellites. IEEE J Sel Top Appl Earth Obs Remote Sens. 2024;17:7193-211. https://doi.org/10.1109/JSTARS.2024.3374232.
    CrossRef
  42. Gusain K, Chauhan V, Singh H, Singh M. In: Singh H, editor. Urban forests, climate change and environmental pollution. Cham: Springer; 2024. p. 331-50.
    CrossRef
  43. Hamunyela E, Verbesselt J, Roerink G, Herold M. Trends in spring phenology of western European deciduous forests. Remote Sens. 2013;5(12):6159-79. https://doi.org/10.3390/rs5126159.
    CrossRef
  44. Han J, Zhang Z, Cao J. Developing a new method to identify flowering dynamics of rapeseed using Landsat 8 and Sentinel-1/2. Remote Sens. 2021;13(1):105. https://doi.org/10.3390/rs13010105.
    CrossRef
  45. Hegland SJ, Nielsen A, Lázaro A, Bjerknes AL, Totland Ø. How does climate warming affect plant-pollinator interactions? Ecol Lett. 2009;12(2):184-95. https://doi.org/10.1111/j.1461-0248.2008.01269.x.
    Pubmed CrossRef
  46. Hou D, Meng F, Prishchepov AV. How is urbanization shaping agricultural land-use? Unraveling the nexus between farmland abandonment and urbanization in China. Landsc Urban Plan. 2021;214:104170. https://doi.org/10.1016/j.landurbplan.2021.104170.
    CrossRef
  47. Inouye DW. Climate change and phenology. WIREs Climate Change. 2022;13(3):e764. https://doi.org/10.1002/wcc.764.
    CrossRef
  48. John A, Ong J, Theobald EJ, Olden JD, Tan A, HilleRisLambers J. Detecting montane flowering phenology with CubeSat imagery. Remote Sens. 2020;12(18):2894. https://doi.org/10.3390/rs12182894.
    CrossRef
  49. Jordano P. Natural history matters: how biological constraints shape diversified interactions in pollination networks. J Anim Ecol. 2016;85(6):1423-6. https://doi.org/10.1111/1365-2656.12584.
    Pubmed CrossRef
  50. Jose K, Chaturvedi RK, Jeganathan C, Behera MD, Singh CP. Plugging the gaps in the global PhenoCam monitoring of forests-the need for a PhenoCam network across Indian forests. Remote Sens. 2023;15(24):5642. https://doi.org/10.3390/rs15245642.
    CrossRef
  51. Keenan RJ, Reams GA, Achard F, de Freitas JV, Grainger A, Lindquist E. Dynamics of global forest area: results from the FAO Global Forest Resources Assessment 2015. For Ecol Manag. 2015;352:9-20. https://doi.org/10.1016/j.foreco.2015.06.014.
    CrossRef
  52. Kelly AE, Goulden ML. Rapid shifts in plant distribution with recent climate change. Proc Natl Acad Sci U S A. 2008;105(33):11823-6. https://doi.org/10.1073/pnas.0802891105.
    Pubmed KoreaMed CrossRef
  53. Kopeć D, Zakrzewska A, Halladin-Dąbrowska A, Wylazłowska J, Sławik Ł. The essence of acquisition time of airborne hyperspectral and on-ground reference data for classification of highly invasive annual vine Echinocystis lobata (Michx.) Torr. & A. Gray. GISci Remote Sens. 2023;60(1):2204682. https://doi.org/10.1080/15481603.2023.2204682.
    CrossRef
  54. Kudo G, Ida TY. Early onset of spring increases the phenological mismatch between plants and pollinators. Ecology. 2013;94(10):2311-20. https://doi.org/10.1890/12-2003.1.
    Pubmed CrossRef
  55. Landmann T, Piiroinen R, Makori DM, Abdel-Rahman EM, Makau S, Pellikka P, et al. Application of hyperspectral remote sensing for flower mapping in African savannas. Remote Sens Environ. 2015;166:50-60. https://doi.org/10.1016/j.rse.2015.06.006.
    CrossRef
  56. Lee CKF, Song G, Muller-Landau HC, Wu S, Wright SJ, Cushman K, et al. Cost-effective and accurate monitoring of flowering across multiple tropical tree species over two years with a time series of high-resolution drone imagery and deep learning. ISPRS J Photogramm Remote Sens. 2023;201:92-103. https://doi.org/10.1016/j.isprsjprs.2023.05.022.
    CrossRef
  57. Liu CA, Chen ZX, Shao Y, Chen JS, Hasi T, Pan HZ. Research advances of SAR remote sensing for agriculture applications: a review. J Integr Agric. 2019;18(3):506-25. https://doi.org/10.1016/S2095-3119(18)62016-7.
    CrossRef
  58. Liu W, Zhang H. Mapping annual 10m rapeseed extent using multisource data in the Yangtze River Economic Belt of China (2017-2021) on Google Earth Engine. Int J Appl Earth Obs Geoinf. 2023;117:103198. https://doi.org/10.1016/j.jag.2023.103198.
    CrossRef
  59. Lopez-Sanchez JM, Cloude SR, Ballester-Berman JD. Rice phenology monitoring by means of SAR polarimetry at X-band. IEEE Trans Geosci Remote Sens. 2012;50(7):2695-709. https://doi.org/10.1109/TGRS.2011.2176740.
    CrossRef
  60. Löw J, Ullmann T, Conrad C. The impact of phenological developments on interferometric and polarimetric crop signatures derived from Sentinel-1: examples from the DEMMIN study site (Germany). Remote Sens. 2021;13(15):2951. https://doi.org/10.3390/rs13152951.
    CrossRef
  61. Ma Y, Fang S, Peng Y, Gong Y, Wang D. Remote estimation of biomass in winter oilseed rape (Brassica napus L.) using canopy hyperspectral data at different growth stages. Appl Sci. 2019;9(3):545. https://doi.org/10.3390/app9030545.
    CrossRef
  62. Mahmud MR, Numata S, Hosaka T. Mapping an invasive goldenrod of Solidago altissima in urban landscape of Japan using multi-scale remote sensing and knowledge-based classification. Ecol Indic. 2020;111:105975. https://doi.org/10.1016/j.ecolind.2019.105975.
    CrossRef
  63. Mann HMR, Iosifidis A, Jepsen JU, Welker JM, Loonen MJJE, Høye TT. Automatic flower detection and phenology monitoring using time-lapse cameras and deep learning. Remote Sens Ecol Conserv. 2022;8(6):765-77. https://doi.org/10.1002/rse2.275.
    CrossRef
  64. Marshall L, Leclercq N, Weekers T, El Abdouni I, Carvalheiro LG, Kuhlmann M, et al. Potential for climate change driven spatial mismatches between apple crops and their wild bee pollinators at a continental scale. Global Environ Change. 2023;83:102742. https://doi.org/10.1016/j.gloenvcha.2023.102742.
    CrossRef
  65. McNairn H, Jiao X, Pacheco A, Sinha A, Tan W, Li Y. Estimating canola phenology using synthetic aperture radar. Remote Sens Environ. 2018;219:196-205. https://doi.org/10.1016/j.rse.2018.10.012.
    CrossRef
  66. Menzel A. Trends in phenological phases in Europe between 1951 and 1996. Int J Biometeorol. 2000;44:76-81. https://doi.org/10.1007/s004840000054.
    Pubmed CrossRef
  67. Millennium Ecosystem Assessment. Ecosystems and human well-being: synthesis. Washington: Island Press; 2005.
  68. Mughal M, Fontan Sers C. Cereal production, undernourishment, and food insecurity in South Asia. Rev Dev Econ. 2020;24(2):524-45.
    CrossRef
  69. Neumann C, Behling R, Schindhelm A, Itzerott S, Weiss G, Wichmann M, et al. The colors of heath flowering-quantifying spatial patterns of phenology in Calluna life-cycle phases using high-resolution drone imagery. Remote Sens Ecol Conserv. 2020;6(1):35-51. https://doi.org/10.1002/rse2.121.
    CrossRef
  70. Nijland W, Coops NC, Coogan SCP, Bater CW, Wulder MA, Nielsen SE, et al. Vegetation phenology can be captured with digital repeat photography and linked to variability of root nutrition in Hedysarum alpinum. Appl Veg Sci. 2013;16(2):317-24. https://doi.org/10.1111/avsc.12000.
    CrossRef
  71. Osco LP, Junior JM, Ramos APM, de Castro Jorge LA, Fatholahi SN, de Andrade Silva J, et al. A review on deep learning in UAV remote sensing. Int J Appl Earth Obs Geoinf. 2021;102:102456. https://doi.org/10.1016/j.jag.2021.102456.
    CrossRef
  72. Pachauri RK, Allen MR, Barros VR, Broome J, Cramer W, Christ R, et al. Contribution of Working Groups I, II and III to the fifth assessment report of the intergovernmental panel on climate change. Geneva: IPCC; 2014.
  73. Panetta AM, Stanton ML, Harte J. Climate warming drives local extinction: evidence from observation and experimentation. Sci Adv. 2018;4(2):eaaq1819. https://doi.org/10.1126/sciadv.aaq1819.
    Pubmed KoreaMed CrossRef
  74. Paz-Kagan T, Silver M, Panov N, Karnieli A. Multispectral approach for identifying invasive plant species based on flowering phenology characteristics. Remote Sens. 2019;11(8):953. https://doi.org/10.3390/rs11080953.
    CrossRef
  75. Petanidou T, Kallimanis AS, Sgardelis SP, Mazaris AD, Pantis JD, Waser NM. Variable flowering phenology and pollinator use in a community suggest future phenological mismatch. Acta Oecol. 2014;59:104-11. https://doi.org/10.1016/j.actao.2014.06.001.
    CrossRef
  76. Piao S, Liu Q, Chen A, Janssens IA, Fu Y, Dai J, et al. Plant phenology and global climate change: current progresses and challenges. Glob Chang Biol. 2019;25(6):1922-40. https://doi.org/10.1111/gcb.14619.
    Pubmed CrossRef
  77. Polce C, Garratt MP, Termansen M, Ramirez-Villegas J, Challinor AJ, Lappage MG, et al. Climate-driven spatial mismatches between British orchards and their pollinators: increased risks of pollination deficits. Glob Chang Biol. 2014;20(9):2815-28. https://doi.org/10.1111/gcb.12577.
    Pubmed KoreaMed CrossRef
  78. Potts SG, Imperatriz-Fonseca V, Ngo HT, Aizen MA, Biesmeijer JC, Breeze TD, et al. Safeguarding pollinators and their values to human well-being. Nature. 2016;540(7632):220-9. https://doi.org/10.1038/nature20588.
    Pubmed CrossRef
  79. Pye-Smith C, Thornton P, Wollenberg E, Loboguerrero AM, Campbell BM. The future for urban agriculture: is it time to rewrite the rules of agriculture? Wageningen, the Netherlands: Clim-Eat; 2022. Wageningen, the Netherlands: Clim-Eat; 2022.
  80. Qadir A, Skakun S, Eun J, Prashnani M, Shumilo L. Sentinel-1 time series data for sunflower (Helianthus annuus) phenology monitoring. Remote Sens Environ. 2023;295:113689. https://doi.org/10.1016/j.rse.2023.113689.
    CrossRef
  81. Rafferty NE. Effects of global change on insect pollinators: multiple drivers lead to novel communities. Curr Opin Insect Sci. 2017;23:22-7. https://doi.org/10.1016/j.cois.2017.06.009.
    Pubmed CrossRef
  82. Rahimi E, Bak S, Jung C. Estimating Geographic range shifts of Vespa simillima after Vespa velutina (Hymenoptera: Vespidae) invasion in South Korea. J Apic. 2022;37(4):383-7.
    CrossRef
  83. Rahimi E, Dong P. What are the main human pressures affecting Iran's protected areas? J Environ Stud Sci. 2022;12:682-91. https://doi.org/10.1007/s13412-022-00785-7.
    CrossRef
  84. Rahimi E, Jung C. Comparative analysis of supervised and phenology-based approaches for crop mapping: a case study in South Korea. Korean J Remote Sens. 2024a;40(2):179-90.
  85. Rahimi E, Jung C. A global estimation of potential climate change effects on pollinator-dependent crops. Agric Res. 2024b. https://doi.org/10.1007/s40003-024-00802-x.
    CrossRef
  86. Rahimi E, Jung C. Global trends in climate suitability of bees: ups and downs in a warming world. Insects. 2024c;15(2):127. https://doi.org/10.3390/insects15020127.
    Pubmed KoreaMed CrossRef
  87. Rahimi E, Jung C. A new SDM-based approach for assessing climate change effects on plant-pollinator networks. Insects. 2024d;15(11):842. https://doi.org/10.3390/insects15110842.
    Pubmed KoreaMed CrossRef
  88. Rahimi E, Jung C. Spatial overlap between bees and pollinator-dependent crops in Europe and North America. J Sustain Agric Environ. 2024e;3(4):e270021. https://doi.org/10.1002/sae2.70021.
    CrossRef
  89. Rahimi E, Jung C. The efficiency of long short-term memory (LSTM) in phenology-based crop classification. Korean J Remote Sens. 2024f;40(1):57-69. https://doi.org/10.7780/kjrs.2024.40.1.6.
  90. Rahman MM, Robson A, Brinkhoff J. Potential of time-series Sentinel 2 data for monitoring avocado crop phenology. Remote Sens. 2022;14(23):5942. https://doi.org/10.3390/rs14235942.
    CrossRef
  91. Rands MR, Adams WM, Bennun L, Butchart SH, Clements A, Coomes D, et al. Biodiversity conservation: challenges beyond 2010. Science. 2010;329(5997):1298-303. https://doi.org/10.1126/science.1189138.
    Pubmed CrossRef
  92. Roetzer T, Wittenzeller M, Haeckel H, Nekovar J. Phenology in central Europe - differences and trends of spring phenophases in urban and rural areas. Int J Biometeorol. 2000;44:60-6. https://doi.org/10.1007/s004840000062.
    Pubmed CrossRef
  93. Schleuning M, Fründ J, Schweiger O, Welk E, Albrecht J, Albrecht M, et al. Ecological networks are more sensitive to plant than to animal extinction under climate change. Nat Commun. 2016;7:13965. https://doi.org/10.1038/ncomms13965.
    Pubmed KoreaMed CrossRef
  94. Schwartz MD. Phenology: an integrative environmental science. Dordrecht: Springer; 2003.
    Pubmed CrossRef
  95. Schweiger O, Biesmeijer JC, Bommarco R, Hickler T, Hulme PE, Klotz S, et al. Multiple stressors on biotic interactions: how climate change and alien species interact to affect pollination. Biol Rev. 2010;85(4):777-95. https://doi.org/10.1111/j.1469-185X.2010.00125.x.
    Pubmed CrossRef
  96. Seto KC, Ramankutty N. Hidden linkages between urbanization and food systems. Science. 2016;352(6288):943-5. https://doi.org/10.1126/science.aaf7439.
    Pubmed CrossRef
  97. Seto KC, Reenberg A, Boone CG, Fragkias M, Haase D, Langanke T, et al. Urban land teleconnections and sustainability. Proc Natl Acad Sci U S A. 2012;109(20):7687-92. https://doi.org/10.1073/pnas.1117622109.
    Pubmed KoreaMed CrossRef
  98. Shen M, Tang Y, Chen J, Yang X, Wang C, Cui X, et al. Earlier-season vegetation has greater temperature sensitivity of spring phenology in northern hemisphere. PLoS One. 2014;9(2):e88178. https://doi.org/10.1371/journal.pone.0088178.
    Pubmed KoreaMed CrossRef
  99. Shao C, Shuai Y, Wu H, Deng X, Zhang X, Xu A. Development of a spectral index for the detection of yellow-flowering vegetation. Remote Sens. 2023;15(7):1725. https://doi.org/10.3390/rs15071725.
    CrossRef
  100. Shin N, Saitoh TM, Takeuchi Y, Miura T, Aiba M, Kurokawa H, et al. Monitoring of land cover changes and plant phenology by remote-sensing in East Asia. Ecol Res. 2023;38(1):111-33. https://doi.org/10.1111/1440-1703.12371.
    CrossRef
  101. Smith MR, Singh GM, Mozaffarian D, Myers SS. Effects of decreases of animal pollinators on human nutrition and global health: a modelling analysis. Lancet. 2015;386(10007):1964-72. https://doi.org/10.1016/S0140-6736(15)61085-6.
    Pubmed CrossRef
  102. Soubry I, Manakos I, Kalaitzidis C. Recent advances in land surface phenology estimation with multispectral sensing. GISTAM. 2021:134-45.
    CrossRef
  103. Stanski K, Myers-Smith IH, Lucas CG. Flower detection using object analysis: new ways to quantify plant phenology in a warming tundra biome. IEEE J Sel Top Appl Earth Obs Remote Sens. 2021;14:9287-96. https://doi.org/10.1109/JSTARS.2021.3110365.
    CrossRef
  104. Straka JR, Starzomski BM. Humming along or buzzing off? The elusive consequences of plant-pollinator mismatches. J Pollinat Ecol. 2014;13:129-45. https://doi.org/10.26786/1920-7603(2014)18.
    CrossRef
  105. Studer S, Appenzeller C. Defila C Inter-annual variability and decadal trends in alpine spring phenology: a multivariate analysis approach. Clim Change. 2005;73:395-414. https://doi.org/10.1007/s10584-005-6886-z.
    CrossRef
  106. Studer S, Stöckli R, Appenzeller C, Vidale PL. A comparative study of satellite and ground-based phenology. Int J Biometeorol. 2007;51(5):405-14. https://doi.org/10.1007/s00484-006-0080-5.
    Pubmed CrossRef
  107. Sulik JJ, Long DS. Spectral considerations for modeling yield of canola. Remote Sens Environ. 2016;184:161-74. https://doi.org/10.1016/j.rse.2016.06.016.
    CrossRef
  108. Sun Y, Hao Z, Chang H, Yang J, Ding G, Guo Z, et al. Accurate mapping of rapeseed fields in the initial flowering stage using Sentinel-2 satellite images and convolutional neural networks. Ecol Indic. 2024;162:112027. https://doi.org/10.1016/j.ecolind.2024.112027.
    CrossRef
  109. Tao JB, Zhang XY, Wu QF, Yun W. Mapping winter rapeseed in South China using Sentinel-2 data based on a novel separability index. J Integr Agric. 2023;22(6):1645-57. https://doi.org/10.1016/j.jia.2022.10.008.
    CrossRef
  110. Thoday-Kennedy E, Banerjee B, Panozzo J, Maharjan P, Hudson D, Spangenberg G, et al. Dissecting physiological and agronomic diversity in safflower populations using proximal phenotyping. Agriculture. 2023;13(3):620. https://doi.org/10.3390/agriculture13030620.
    CrossRef
  111. Tilman D, Balzer C, Hill J, Befort BL. Global food demand and the sustainable intensification of agriculture. Proc Natl Acad Sci U S A. 2011;108(50):20260-4. https://doi.org/10.1073/pnas.1116437108.
    KoreaMed CrossRef
  112. Torgbor BA, Rahman MM, Robson A, Brinkhoff J, Khan A. Assessing the potential of Sentinel-2 derived vegetation indices to retrieve phenological stages of mango in Ghana. Horticulturae. 2022;8(1):11. https://doi.org/10.3390/horticulturae8010011.
    CrossRef
  113. UNICEF. 2021. https://data.unicef.org/resources/sofi-2021/. Accessed 1 Jul 2024.
  114. Walther GR, Post E, Convey P, Menzel A, Parmesan C, Beebee TJ, et al. Ecological responses to recent climate change. Nature. 2002;416(6879):389-95. https://doi.org/10.1038/416389a.
    CrossRef
  115. Wang D, Zhou Q, Su Y, Chen Z. 2015 Fourth International Conference on Agro- Geoinformatics (Agro-geoinformatics); 2015 July 20-24; Istanbul: Turkey, 2015; 2015. p. 312-7.
    CrossRef
  116. Wiseman G, McNairn H, Homayouni S, Shang J. RADARSAT-2 polarimetric SAR response to crop biomass for agricultural production monitoring. IEEE J Sel Top Appl Earth Obs Remote Sens. 2014;7(11):4461-71. https://doi.org/10.1109/JSTARS.2014.2322311.
    CrossRef
  117. Xiong N, Chen H, Li R, Su H, Dai S, Wang J. A method of chestnut forest identification based on time series and key phenology from Sentinel-2. Remote Sens. 2023;15(22):5374. https://doi.org/10.3390/rs15225374.
    CrossRef
  118. Yi Z, Jia L, Chen Q, Jiang M, Zhou D, Zeng Y. Early-season crop identification in the Shiyang River basin using a deep learning algorithm and time-series Sentinel-2 data. Remote Sens. 2022;14(21):5625. https://doi.org/10.3390/rs14215625.
    CrossRef
  119. Zang Y, Qiu Y, Chen X, Chen J, Yang W, Liu Y, et al. Mapping rapeseed in China during 2017-2021 using Sentinel data: an automated approach integrating rule-based sample generation and a one-class classifier (RSG-OC). GISci Remote Sens. 2023;60(1):2163576. https://doi.org/10.1080/15481603.2022.2163576.
    CrossRef
  120. Zhang C, Valente J, Wang W, Guo L, Comas AT, van Dalfsen P, et al. Feasibility assessment of tree-level flower intensity quantification from UAV RGB imagery: a triennial study in an apple orchard. ISPRS J Photogramm Remote Sens. 2023;197:256-73. https://doi.org/10.1016/j.isprsjprs.2023.02.003.
    CrossRef
  121. Zhang C, Xie Z, Shang J, Liu J, Dong T, Tang M, et al. Detecting winter canola (Brassica napus) phenological stages using an improved shape-model method based on time-series UAV spectral data. Crop J. 2022a;10(5):1353-62. https://doi.org/10.1016/j.cj.2022.03.001.
    CrossRef
  122. Zhang H, Liu W, Zhang L. Seamless and automated rapeseed mapping for large cloudy regions using time-series optical satellite imagery. ISPRS J Photogramm Remote Sens. 2022b;184:45-62. https://doi.org/10.1016/j.isprsjprs.2021.12.001.
    CrossRef
  123. Zhao L, Wang S, Xu Y, Sun W, Shi L, Yang J, et al. Evaluating the capability of Sentinel-1 data in the classification of canola and wheat at different growth stages and in different years. Remote Sens. 2023;15(11):2731. https://doi.org/10.3390/rs15112731.
    CrossRef
  124. Zhu L, Suomalainen J, Liu J, Hyyppä J, Kaartinen H, Haggren H. A review: remote sensing sensors. InTech. 2018. https://doi.org/10.5772/intechopen.71049.
    CrossRef

Share this article on

Related articles in JECOENV

Close ✕

Journal of Ecology and Environment

pISSN 2287-8327 eISSN 2288-1220