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<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Sustain. Food Syst.</journal-id>
<journal-title>Frontiers in Sustainable Food Systems</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Sustain. Food Syst.</abbrev-journal-title>
<issn pub-type="epub">2571-581X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fsufs.2025.1652332</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Sustainable Food Systems</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Spectral and morphological discrimination of <italic>Ficus</italic> and <italic>Moringa</italic> species with medical and nutritional relevance: toward sustainable plant utilization</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Khdery</surname>
<given-names>Ghada A.</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Shokr</surname>
<given-names>Mohamed S.</given-names>
</name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
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<contrib contrib-type="author">
<name>
<surname>Rebouh</surname>
<given-names>Nazih Y.</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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<contrib contrib-type="author">
<name>
<surname>Hewidy</surname>
<given-names>Mohammed</given-names>
</name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
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<aff id="aff1"><sup>1</sup><institution>National Authority for Remote Sensing and Space Sciences</institution>, <addr-line>Cairo</addr-line>, <country>Egypt</country></aff>
<aff id="aff2"><sup>2</sup><institution>Soil and Water Department, Faculty of Agriculture, Tanta University</institution>, <addr-line>Tanta</addr-line>, <country>Egypt</country></aff>
<aff id="aff3"><sup>3</sup><institution>Department of Environmental Management, Institute of Environmental Engineering, RUDN University</institution>, <addr-line>Moscow</addr-line>, <country>Russia</country></aff>
<aff id="aff4"><sup>4</sup><institution>Horticulture Department, Faculty of Agriculture, Ain Shams University</institution>, <addr-line>Cairo</addr-line>, <country>Egypt</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2777124/overview">Danijel Jug</ext-link>, Josip Juraj Strossmayer University of Osijek, Croatia</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1567856/overview">Okon Godwin Okon</ext-link>, Akwa Ibom State University, Nigeria</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1720057/overview">Ebrahim Jahanshiri</ext-link>, Crops for the Future UK, United Kingdom</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3118296/overview">Alfredo Esparza Orozco</ext-link>, Autonomous University of Zacatecas, Mexico</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3129802/overview">Abha Shukla</ext-link>, Gurukul Kangri (Deemed to be University) &#x2013; Kanya Gurukul Campus Haridwar, India</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Ghada A. Khdery, <email>ghada.ali@narss.sci.eg</email>; Mohamed S. Shokr, <email>mohamed_shokr@agr.tanta.edu.eg</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>29</day>
<month>08</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>9</volume>
<elocation-id>1652332</elocation-id>
<history>
<date date-type="received">
<day>23</day>
<month>06</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>12</day>
<month>08</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Khdery, Shokr, Rebouh and Hewidy.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Khdery, Shokr, Rebouh and Hewidy</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec id="sec1001">
<title>Introduction</title>
<p>Hyperspectral remote sensing provides a powerful platform for identifying plant species with pharmacological relevance by capturing subtle variations in pigment content, physiological traits, and leaf structure.</p>
</sec>
<sec id="sec1002">
<title>Methods</title>
<p>This study employed spectral indices to evaluate and differentiate 10 <italic>Ficus</italic> and two <italic>Moringa</italic> spp. based on their reflectance characteristics and morphological features. Spectral data were collected using an ASD FieldSpec spectroradiometer, and vegetation indices such as NDVI, SR, PRI, ARI2, NDRE, and MCARI were calculated to infer photosynthetic performance and secondary metabolite potential. Descriptive morphological traits were recorded to aid in species-level discrimination.</p>
</sec>
<sec id="sec1003">
<title>Results and Discussion</title>
<p>Statistical analyses, including one-way ANOVA and Linear Discriminant Analysis (LDA), identified specific bands in the NIR and SWIR II regions as particularly effective for distinguishing among the studied taxa. Notably, <italic>Ficus benghalensis</italic>, <italic>Ficus racemosa</italic>, and <italic>Moringa oleifera</italic> exhibited superior spectral profiles, reflecting high pigment density and physiological vigor, which correspond with their well-documented pharmacological roles. Conversely, species like <italic>F. religiosa</italic> and <italic>M. peregrina</italic> showed relatively subdued spectral signatures. Statistical analyses (ANOVA and LDA) confirmed the discriminatory power of NIR and SWIR II regions across species. Morphological traits provided taxonomic support but were less distinctive than spectral indices. These findings demonstrate the value of hyperspectral indices as rapid, non-destructive tools to identify and prioritize medicinally potent species within <italic>Ficus</italic> and <italic>Moringa</italic> spp., offering insights for pharmacognosy, conservation, and phytochemical prospecting. Moreover, by enabling efficient identification of underutilized species with confirmed medical value, this approach may support efforts to sustainably manage native plant resources, particularly in regions where such species contribute to traditional healthcare systems, nutritional supplementation, and the resilience of local livelihoods.</p>
</sec>
</abstract>
<kwd-group>
<kwd>remote sensing</kwd>
<kwd>hyperspectral indices</kwd>
<kwd><italic>Ficus</italic> spp.</kwd>
<kwd><italic>Moringa</italic> spp.</kwd>
<kwd>medicinal plants</kwd>
<kwd>plant morphology</kwd>
</kwd-group>
<counts>
<fig-count count="5"/>
<table-count count="5"/>
<equation-count count="0"/>
<ref-count count="84"/>
<page-count count="18"/>
<word-count count="11770"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Climate-Smart Food Systems</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec1">
<label>1</label>
<title>Introduction</title>
<p>Botanical gardens play an increasingly important role in supporting the Sustainable Development Goals by linking plant diversity with broader themes of sustainability across terrestrial ecosystems (<xref ref-type="bibr" rid="ref66">Smith et al., 2018</xref>). Orman Botanical Garden, established in 1875, is among the most prominent and historically significant botanical gardens in Egypt, covering an area of approximately 11.76 hectares (<xref ref-type="bibr" rid="ref22">Diwan et al., 2004</xref>). Due to its ecological characteristics and social functions, it is also considered an urban forest. Urban forests, as noted by Nowak and Dwyer (<xref ref-type="bibr" rid="ref56">Nowak and Dwyer, 2007</xref>), contribute to biodiversity conservation, provide recreational and social spaces, improve air quality, and enhance the visual appeal of urban settings. Among the six botanical gardens assessed in Egypt, Orman Garden demonstrated the highest levels of species richness and diversity (<xref ref-type="bibr" rid="ref36">Hamdy et al., 2007</xref>). Detailed knowledge of the composition and structural characteristics of tree species in such gardens provides essential insights for biodiversity conservation. Understanding these ecological aspects is crucial for evaluating the long-term sustainability of conservation efforts and informing the management of urban forest ecosystems (<xref ref-type="bibr" rid="ref42">Kacholi, 2014</xref>).</p>
<p>Secondary metabolites are a diverse group of bioactive organic compounds produced by plants that are not directly involved in primary metabolic processes such as growth and reproduction. Instead, they play crucial ecological and physiological roles, including defense against herbivores and pathogens, attraction of pollinators, and adaptation to abiotic stresses (<xref ref-type="bibr" rid="ref77">Yang et al., 2018</xref>; <xref ref-type="bibr" rid="ref39">Isah, 2019</xref>). These metabolites include alkaloids, flavonoids, terpenoids, phenolics, tannins, and glycosides, many of which are well-documented for their pharmacological relevance. Several of these compounds exhibit strong antioxidant, antimicrobial, anti-inflammatory, anticancer, and hepatoprotective activities, making them of significant interest in pharmaceutical and nutraceutical research (<xref ref-type="bibr" rid="ref5">Akula and Ravishankar, 2011</xref>; <xref ref-type="bibr" rid="ref39">Isah, 2019</xref>). Understanding the diversity and physiological basis of these compounds is therefore essential for identifying and prioritizing medicinally important plants, especially when applying non-destructive techniques such as hyperspectral remote sensing to screen for bioactive potential.</p>
<p>About 800 species of woody plants, including trees, shrubs, and vines, that are members of the Moraceae family, are found in the genus Ficus. About 100 of these species are native to Africa and the adjacent islands, and they are spread throughout different tropical ecosystems (<xref ref-type="bibr" rid="ref10">Aweke, 1979</xref>). Multipurpose plants like ficus are commonly employed in rural development (<xref ref-type="bibr" rid="ref52">Mohamed et al., 2018</xref>; <xref ref-type="bibr" rid="ref62">Sandhu et al., 2023</xref>). They can provide food, fuel, timber, medication, and raw materials for some chemical companies. Additionally, they are visually pleasing enough to be employed as ornamental plants, with each species designated for its appropriate role in the landscape, such as screen, structure, group, specimen, avenue, shelter, shade, and hedge (<xref ref-type="bibr" rid="ref13">Brickell, 2019</xref>). There are about 800 species of woody plants in the genus Ficus, including trees, shrubs, and vines, pertaining to the family Moraceae. About 100 species are native to Africa and neighboring islands, and the rest are spread throughout other tropical ecosystems. During the reign of Mohamed Ali Pasha, numerous <italic>Ficus</italic> spp. were introduced to Egyptian territory (<xref ref-type="bibr" rid="ref36">Hamdy et al., 2007</xref>). They were positioned next to palaces, water canals, and the Nile River. They are extensively used for adornment in gardens, roadways, and indoor spaces for some species that have adapted well to Egyptian conditions.</p>
<p><italic>Ficus</italic> spp., including <italic>F. religiosa</italic>, <italic>F. racemosa</italic>, and <italic>F. benghalensis</italic>, are essential in a lot of traditional and Ayurvedic medicine formulas. These species are recognized for their carminative, astringent, anti-inflammatory, antioxidant, and anticancer properties. Their bark, leaves, fruits, and latex are also thought to be very effective in treating a variety of organic molecules produced via metabolic pathways. These organic molecules are classified into primary metabolites (<xref ref-type="bibr" rid="ref41">Joseph and Raj, 2010</xref>; <xref ref-type="bibr" rid="ref60">Rasool et al., 2023</xref>).</p>
<p>The family Moringaceae comprises fast-growing, drought-tolerant flowering plants that have been highly valued since ancient times by civilizations such as the Egyptians, Greeks, and Romans for their nutritional and medicinal benefits. Within this family, Moringa stands as the sole genus, encompassing approximately 33 species, with four species widely recognized: <italic>M. oleifera</italic>, <italic>M. ovalifolia</italic>, <italic>M. peregrina</italic>, and <italic>M. stenopetala</italic> (<xref ref-type="bibr" rid="ref1007">Mabberley, 1987</xref>). These species predominantly thrive in semi-arid, tropical, and subtropical regions, including the Horn of Africa, Madagascar, southwestern parts of Africa, tropical Asia, and extending westward into Egypt. They are found across nearly all phytogeographical zones, as reported by <xref ref-type="bibr" rid="ref55">National Research Council et al. (1996)</xref> and <xref ref-type="bibr" rid="ref53">Mridha (2015)</xref>.</p>
<p><italic>Moringa</italic> spp. play a significant medico-socioeconomic role, functioning as natural bioreactors that generate a variety of organic molecules through metabolic pathways. These metabolites are classified into primary metabolites&#x2014;such as proteins, carbohydrates, and lipids&#x2014;and secondary metabolites, including alkaloids, carotenoids, moringine, moringinine, phytoestrogens, caffeoylquinic acids, tannins, phytosterols, terpenoids, glycosides, flavonoids, and phenolic compounds (<xref ref-type="bibr" rid="ref6">Anwar et al., 2007</xref>).</p>
<p>Hyperspectral remote sensing technology is an essential instrument that allows the collection of detailed data over a wide range of electromagnetic frequencies. The goal of the work under evaluation is to uncover small differences between Ficus species based on their spectral characteristics by utilizing hyperspectral remote sensing. Simultaneously, this study examines these species&#x2019; morphological characteristics, which are crucial elements that impact their methods of adaptation and interactions with their environments (<xref ref-type="bibr" rid="ref75">Wang et al., 2023</xref>).</p>
<p>Plant species&#x2019; physiology, morphology, and anatomical structure are among the elements that influence their spectral properties (<xref ref-type="bibr" rid="ref47">Kycko et al., 2014</xref>; <xref ref-type="bibr" rid="ref40">Jaroci&#x0144;ska et al., 2016</xref>). The visible-infrared (VNIR) and shortwave infrared (SWIR) spectral profiles of leaves show differences that are linked to pigments such as carotenoids and chlorophyll as well as water content and dry matter content (<xref ref-type="bibr" rid="ref28">Feret et al., 2008</xref>). Even closely related species differ in the reflectance characteristics of their vegetation due to differences in pigment and water content, as well as structural changes in their canopies and leaves. Accordingly, species identification is made easier by the uniqueness of these spectral characteristics (<xref ref-type="bibr" rid="ref70">Thenkabail et al., 2000</xref>). Monitoring changes in ecosystems depends heavily on how plants interact with the electromagnetic spectrum through absorption, transmission, and reflection.</p>
<p>The spectral reflectance of plant tissues is largely governed by biochemical and structural components, particularly pigments such as chlorophylls, carotenoids, and anthocyanins. These pigments are often involved in the biosynthesis of secondary metabolites, which play a central role in plant defence, stress response, and pharmacological potential (<xref ref-type="bibr" rid="ref34">Gitelson et al., 2001</xref>; <xref ref-type="bibr" rid="ref39">Isah, 2019</xref>). Reflectance in specific spectral regions&#x2014;especially the visible, red-edge, and NIR&#x2014;can therefore serve as an indirect indicator of the physiological state and biochemical richness of plants, making hyperspectral indices a useful tool in medicinal plant screening (<xref ref-type="bibr" rid="ref65">Sims and Gamon, 2002</xref>; <xref ref-type="bibr" rid="ref18">Colovic et al., 2022</xref>).</p>
<p>The similarity in reflectance patterns in the visible region among species likely reflects shared chlorophyll absorption at approximately 650&#x202F;nm (red) and in the blue range. In contrast, variation in NIR and SWIR may reflect differences in leaf structure, water content, or physiological status. The distinctive spectral behavior of species such as <italic>F. microcarpa</italic> and <italic>F. benghalensis</italic> demonstrates the strength of hyperspectral indices in species-level discrimination.</p>
<p>Remote sensing, particularly hyperspectral sensing, captures the reflectance of electromagnetic radiation from plant surfaces, which is strongly influenced by morphological and physiological characteristics of vegetation. Leaf pigments such as chlorophylls and carotenoids absorb light in the blue and red regions, while cellular structure and internal water content affect reflectance in the near-infrared (NIR) and shortwave infrared (SWIR) regions (<xref ref-type="bibr" rid="ref72">Ustin et al., 2004</xref>; <xref ref-type="bibr" rid="ref17">Clevers et al., 2011</xref>). Variations in leaf thickness, surface texture, and internal mesophyll structure produce distinct spectral signatures that can be used to assess plant health, species identity, and biochemical composition (<xref ref-type="bibr" rid="ref8">Asner and Martin, 2008</xref>; <xref ref-type="bibr" rid="ref37">Homolov&#x00E1; et al., 2013</xref>). Thus, remote sensing provides a non-destructive, rapid method to evaluate vegetation traits related to both structure and function.</p>
<p>In order to evaluate vegetation health, classify land cover, examine phenology, identify changes in climate and land use, and track drought conditions, vegetation indices were developed (<xref ref-type="bibr" rid="ref57">Padilla et al., 2011</xref>). In remote sensing, different vegetation indices have been developed. The Normalized Difference Vegetation Index (NDVI) is a prominent and widely used index in international environmental and climatic change research (<xref ref-type="bibr" rid="ref11">Bhandari et al., 2012</xref>). The ratio difference between the recorded vegetation reflectance values in the red and near-infrared bands is what gives rise to the NDVI.</p>
<p>Given the medicinal importance of <italic>Ficus</italic> spp. and <italic>Moringa</italic> spp. and the potential of hyperspectral techniques in plant characterization, this study aims to explore how spectral indices can support species discrimination and health assessment. Additionally, the study aims to enhance taxonomic understanding of selected <italic>Ficus</italic> spp. <italic>and Moringa</italic> spp. by combining detailed morphological observations with hyperspectral reflectance measurements. It explores the extent to which spectral profiles correspond with observable physical traits across the studied taxa and assesses their relevance to species differentiation. The analysis focuses on identifying distinct spectral signatures and informative wavelength regions that contribute to species discrimination. Moreover, by linking spectral indices to physiological parameters, the study examines the potential of hyperspectral data as a proxy for evaluating plant health and inferring medicinal relevance. This integrated approach supports the non-destructive classification and prioritization of medicinally important plant species.</p>
</sec>
<sec sec-type="materials|methods" id="sec2">
<label>2</label>
<title>Materials and methods</title>
<p>To achieve the outlined objectives, a multi-step methodology was adopted combining field-based morphological measurements with hyperspectral reflectance analysis.</p>
<sec id="sec3">
<label>2.1</label>
<title>Study area</title>
<p>The study was conducted at Orman Garden, Giza, Egypt, which houses a wide diversity of tropical and subtropical plant species. The study area encompasses a total surface of approximately 11.09 hectares and is geographically positioned at 30&#x00B0;01&#x2032;45.12&#x2033;N and 31&#x00B0;12&#x2032;47.16&#x2033;E (<xref ref-type="fig" rid="fig1">Figure 1</xref>). The region experiences an arid climate, characterized by minimal annual rainfall averaging around 1.2&#x202F;mm. The hot season extends from April to October, while a brief, mild wet season occurs between November and March. July is typically the hottest month, whereas January is the coldest. The average annual maximum and minimum temperatures are 27.0&#x202F;&#x00B0;C and 15.0&#x202F;&#x00B0;C, respectively. The soil in the study area is predominantly clay in texture.</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Location map of study area.</p>
</caption>
<graphic xlink:href="fsufs-09-1652332-g001.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Map of Egypt indicating the Giza Governorate highlighted in yellow, with a satellite image on the right showing an urban area with a park outlined in red, located within a densely built environment.</alt-text>
</graphic>
</fig>
<p>Leaf samples were collected from large, mature trees of 10 species belonging to the genus Ficus (Family: Moraceae) and two species from the genus Moringa (<italic>Moringa oleifera</italic> and <italic>Moringa peregrina</italic>) belong to (Family: Moringaceae).</p>
<p>All specimens were sampled from healthy, well-established trees growing within the garden to ensure consistency and reliability of morphological and spectral measurements. The first abstract of the research was published in the proceedings of the I<sup>ST</sup>&#x2013;ICRSSA Conference, organized by the National Authority for Remote Sensing and Space Sciences (NARSS), held from 8 to 11 December 2022.</p>
</sec>
<sec id="sec4">
<label>2.2</label>
<title>Plant sampling</title>
<p>Mature and healthy individuals of <italic>Ficus and Moringa</italic> spp. were selected for this study to ensure accurate assessment of their spectral and morphological traits. For <italic>Ficus</italic> spp., samples were collected from the Orman Botanical Garden in Cairo, Egypt. Based on garden records and morphological evaluation (e.g., trunk diameter, canopy size), the age of the selected Ficus individuals was estimated to range between 15 and 40&#x202F;years. Although older historical specimens exist, only actively growing and physiologically stable trees were included in the measurements.</p>
<p><italic>M. oleifera</italic> and <italic>M. peregrina</italic> specimens were sourced from cultivated plots in botanical garden. These trees are known for their fast growth and were estimated to be between 3 and 6&#x202F;years old, representing mature, flowering individuals suitable for reliable spectral analysis. All samples were free from visible disease, pest infestation, or recent pruning to ensure data consistency. To ensure that the leaves sampled were appropriately representative of each species, mature trees were used to gather samples of leaves. Out of every species, one tree was chosen. A random sample of four leaves was taken from each tree&#x2019;s crown, and one leaf was chosen from each orientation at each of the four crown directions. Randomly chosen samples of leaves from the upper part of the crown that had been fully exposed to the sun were then cleaned and ready for spectral reflectance measurements.</p>
<p>Morphological traits were assessed in the field for each of the 12 studied species (10 <italic>Ficus</italic> and two <italic>Moringa</italic>) during the same sampling period as spectral measurements. For each species, three mature and healthy individuals were selected randomly. The following descriptive traits were recorded:</p>
<list list-type="bullet">
<list-item><p>Leaf shape (e.g., ovate, elliptic, lanceolate)</p></list-item>
<list-item><p>Leaf margin (e.g., entire, lobed, dentate)</p></list-item>
<list-item><p>Leaf base and apex shape</p></list-item>
<list-item><p>Leaf arrangement on the stem (e.g., alternate, opposite)</p></list-item>
<list-item><p>Leaf texture (e.g., leathery, smooth, pubescent)</p></list-item>
<list-item><p>Petiole length and leaf length &#x00D7; width</p></list-item>
</list>
<p>Measurements were taken using a ruler (&#x00B1;1&#x202F;mm precision) for dimensions and by visual inspection for qualitative features, based on standard botanical identification guides. Observations were cross-verified by two trained botanists to minimize observer bias. All data were documented on-site and supported by photographs for later confirmation.</p>
</sec>
<sec id="sec5">
<label>2.3</label>
<title>Spectroscopic measurements</title>
<p>Spectral reflectance data were collected in the field on a single clear-sky day using an ASD FieldSpec 4 spectroradiometer. To ensure environmental consistency during spectral measurements, all data were collected under similar atmospheric and lighting conditions. Measurements were taken between 10:00&#x202F;AM and 2:00&#x202F;PM under stable sunlight conditions to minimize variations in solar angle and irradiance. Fully expanded, mature leaves from three healthy individuals per species were measured <italic>in situ</italic>. A Spectralon white reference panel was used for instrument calibration before each set of measurements. A leaf clip equipped with an internal light source was employed to ensure consistent measurement geometry and minimize shading effects. Each leaf sample was scanned three times, and the mean reflectance value was used for spectral index calculation.</p>
<p>The white panel reflectance calculation approach was applied during the data collection process to guarantee accurate results. By affixing a probe to the fiber-optic cable of the equipment, environmental consistency. Environmental consistency refers here to maintaining uniform weather conditions (i.e., no cloud cover, wind, or precipitation), stable light intensity, and constant observer-sensor geometry throughout the measurement process, was preserved during reflectance measurements. A 25-degree lens was used for outside measurements, providing a 3&#x202F;cm (90&#x00B0;) circular field of view over the object of interest. Tukey&#x2019;s approach was used to determine the best waveband zones based on the traits of each type of plant.</p>
<p>The core of the study methodology is the statistical analysis of spectroscopic performance data combined with spectral measurements. By choosing the best wavelengths within each spectral zone to aid in differentiation, this method seeks to determine the optimal spectral regions for differentiating between different plant species. Under field conditions, the ASD Field Spec equipment was used to evaluate plant leaves. Thirty-six plant leaves were measured for reflectance, and the results were then converted to an ASCII file using the statistical analysis program ASD View Pro. Spectrum reflectance curves were visually examined in order to confirm the vegetation&#x2019;s spectrum reflectance characteristics.</p>
<p>To improve the capacity for distinction, a statistical analysis was conducted to determine which spectral bands provide the best discrimination between the plants under study. One-way ANOVA was performed to assess significant differences among species for spectral and morphological variables. When ANOVA results were significant (<italic>p</italic>&#x202F;&#x2264;&#x202F;0.05), Tukey&#x2019;s Honestly Significant Difference (HSD) <italic>post hoc</italic> test was applied to identify pairwise differences between species means. This method controls the type I error rate across multiple comparisons and is commonly used in ecological and spectral data analysis (<xref ref-type="bibr" rid="ref1004">Abdi and Williams, 2010</xref>). During this stage, <xref ref-type="bibr" rid="ref16">Clark et al. (2005)</xref> used linear discriminant analysis (LDA) to choose the bands, and the methodology of analyzing variance (ANOVA) was used to determine how well the chosen wavelengths and bands distinguished different plant species. Furthermore, 12 different plant species were included in the spectrum reflectance investigation, with three replicates of each species being assessed. Six distinct spectral bands were covered by observations, which were made using the Analytical Field Spectroradiometer (ASD Field Spec): Blue, Green, Red, Near Infrared, SWIR I, and SWIR II.</p>
<p>Spectral reflectance was measured using the ASD FieldSpec&#x00AE; spectroradiometer, which operates over a spectral range of 350&#x2013;2,500&#x202F;nm. The following spectral regions were used to compute vegetation indices and assess reflectance characteristics:</p>
<list list-type="bullet">
<list-item><p>Blue: 450&#x2013;495&#x202F;nm</p></list-item>
<list-item><p>Green: 495&#x2013;570&#x202F;nm</p></list-item>
<list-item><p>Red: 620&#x2013;700&#x202F;nm</p></list-item>
<list-item><p>Red-edge: 700&#x2013;740&#x202F;nm</p></list-item>
<list-item><p>Near-Infrared (NIR): 740&#x2013;1,300&#x202F;nm</p></list-item>
<list-item><p>Short-Wave Infrared I (SWIR I): 1,300&#x2013;1,900&#x202F;nm</p></list-item>
<list-item><p>Short-Wave Infrared II (SWIR II): 1,900&#x2013;2,500&#x202F;nm</p></list-item>
</list>
<p>These bands were selected based on their relevance to pigment absorption (chlorophyll, carotenoids, anthocyanins), water content, and structural properties of the leaves.</p>
</sec>
<sec id="sec6">
<label>2.4</label>
<title>Hyperspectral indices</title>
<p>Based on spectroscopy measurements for each field plant, the values of the soil and vegetation indices were calculated. These values were based on the contrast between the maximum absorption of pigments and chlorophyll in the red spectrum, as well as the maximum reflectance of the leaf&#x2019;s cell structure in the near-infrared spectrum (<xref ref-type="table" rid="tab1">Table 1</xref>). Mathematical correlations were used to depict the observed relationship between several soil and vegetation indices (<xref ref-type="bibr" rid="ref80">Zagajewski et al., 2017</xref>).</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Synopsis of vegetation indices, vegetation index sources, and methods.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Index</th>
<th align="left" valign="top">Equation</th>
<th align="left" valign="top">Explanation</th>
<th align="left" valign="top">Source</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">(NDVI) Normalized Difference Vegetation Index</td>
<td align="left" valign="top">NDVI&#x202F;=&#x202F;R800-R680/ R800&#x202F;+&#x202F;R680</td>
<td align="left" valign="top">Composition of biomass</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref76">Xu et al. (2013)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(SR) Simple Ratio</td>
<td align="left" valign="top">SR&#x202F;=&#x202F;R800/R680</td>
<td align="left" valign="top">Overall state of the plant</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref49">Mascarini et al. (2006)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(RENDVI) Red Edge Normalized Difference Vegetation Index</td>
<td align="left" valign="top">RENDVI&#x202F;=&#x202F;R750&#x202F;&#x2212;&#x202F;R705/R750&#x202F;+&#x202F;R705</td>
<td align="left" valign="top">Red edge spectral range vegetation index-based NDVI</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref65">Sims and Gamon (2002)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(PSRI) Plant Senescence Reflectance Index</td>
<td align="left" valign="top">PSRI&#x202F;=&#x202F;R680&#x202F;&#x2212;&#x202F;R500/R750</td>
<td align="left" valign="top">Ratio of carotenoids to chlorophyll</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref51">Merzlyak et al. (1999)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(NDWI) Normalized Difference Water Index (NDWI)</td>
<td align="left" valign="top">NDWI&#x202F;=&#x202F;R860&#x202F;&#x2212;&#x202F;R1240/R860&#x202F;+&#x202F;R1240</td>
<td align="left" valign="top">Estimate plant water content.</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref32">Gao (1996)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(PRI) Photochemical Reflectance Index PRI</td>
<td align="left" valign="top">PRI&#x202F;=&#x202F;(R531&#x202F;&#x2212;&#x202F;R570)/(R531&#x202F;+&#x202F;R570)</td>
<td align="left" valign="top">Measures photosynthetic efficiency and plant stress.</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref31">Gamon et al. (1992)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(MCARI) Modified Chlorophyll Absorption in Reflectance Index</td>
<td align="left" valign="top">MCARI&#x202F;=&#x202F;[(R700&#x202F;&#x2212;&#x202F;R670)&#x202F;&#x2212;&#x202F;0.2&#x202F;&#x00D7;&#x202F;(R700&#x202F;&#x2212;&#x202F;R550)]&#x202F;&#x00D7;&#x202F;(R700/R670)</td>
<td align="left" valign="top">Estimates chlorophyll content</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref20">Daughtry et al. (2000)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(ARI2) Anthocyanin Reflectance Index 2</td>
<td align="left" valign="top">ARI2&#x202F;=&#x202F;(1/R550&#x202F;&#x2212;&#x202F;1/R700)&#x202F;&#x00D7;&#x202F;R800</td>
<td align="left" valign="top">Indicates anthocyanin (antioxidants) levels.</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref34">Gitelson et al. (2001)</xref>
</td>
</tr>
<tr>
<td align="left" valign="top">(CIred-edge) Chlorophyll Index Red Edge</td>
<td align="left" valign="top">CIred-edge&#x202F;=&#x202F;(R750/R710)&#x202F;&#x2212;&#x202F;1</td>
<td align="left" valign="top">&#x2192; Detects high chlorophyll concentration.</td>
<td align="left" valign="top">
<xref ref-type="bibr" rid="ref33">Gitelson et al. (2003)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>The following spectral indices were calculated to evaluate photosynthetic efficiency, pigment content, and stress response:</p>
<list list-type="bullet">
<list-item><p>NDVI (Normalized Difference Vegetation Index): ranges from &#x2212;1 to +1; values &#x003E; 0.5 typically indicate healthy, green vegetation with strong photosynthetic activity, while values near 0 or negative suggest sparse or stressed vegetation.</p></list-item>
<list-item><p>SR (Simple Ratio): ranges from ~1 to &#x003E;10; higher values indicate greater chlorophyll content and biomass.</p></list-item>
<list-item><p>PRI (Photochemical Reflectance Index): typically ranges from &#x2212;0.1 to +0.1; sensitive to xanthophyll cycle activity and photosynthetic light-use efficiency.</p></list-item>
<list-item><p>PSRI (Plant Senescence Reflectance Index): values increase with chlorophyll degradation and carotenoid dominance, indicating leaf senescence.</p></list-item>
<list-item><p>CRI (Carotenoid Reflectance Index): higher values indicate higher carotenoid content, often associated with stress response or protective mechanisms.</p></list-item>
<list-item><p>MCARI (Modified Chlorophyll Absorption Ratio Index): values typically range from 0 to 2; sensitive to chlorophyll concentration.</p></list-item>
<list-item><p>ARI2 (Anthocyanin Reflectance Index): detects anthocyanin accumulation; higher values indicate anthocyanin-rich tissues, often under stress.</p></list-item>
<list-item><p>NDRE (Normalized Difference Red Edge Index): typically ranges from 0 to 0.6; useful for detecting moderate-to-high chlorophyll content, especially in dense canopies.</p></list-item>
<list-item><p>Clred-Edge: similar to NDRE but uses a different combination of red-edge wavelengths; higher values reflect increased chlorophyll density.</p></list-item>
</list>
</sec>
<sec id="sec7">
<label>2.5</label>
<title>Medicinal score calculation</title>
<p>To provide a comparative indicator of the medicinal importance of each species, a medicinal score was computed based on a literature-derived scoring framework. For each species, we reviewed published pharmacological studies and ethnobotanical sources and assigned points to the following categories:</p>
<list list-type="bullet">
<list-item><p>Number of pharmacological activities reported (e.g., antioxidant, anti-inflammatory, antimicrobial, antidiabetic)</p></list-item>
<list-item><p>Number of plant parts used (e.g., leaves, bark, latex, seeds)</p></list-item>
<list-item><p>Frequency of use in traditional medicine (based on literature mentions)</p></list-item>
</list>
<p>Each positive attribute contributed one point. The total score for each species was then normalized to a 0&#x2013;1 scale using min-max normalization to allow comparison across species. This score served as a semi-quantitative proxy for medicinal relevance and was used in correlation analyses with spectral indices.</p>
</sec>
<sec id="sec8">
<label>2.6</label>
<title>Statistical analysis</title>
<p>Statistical analyses were performed using JMP Pro version 16.2.0 (SAS Institute Inc., Cary, NC, USA). One-way ANOVA was used to detect significant differences in spectral indices and morphological traits across species. Linear Discriminant Analysis (LDA) was conducted to assess species discrimination. Pearson correlation analysis was used to explore relationships between vegetation indices and the medicinal score.</p>
<p>To visualize the correlation matrix, a heatmap was generated using Python (version 3.9) with the Seaborn (version 0.11.2) and Matplotlib (version 3.4.3) libraries. Statistical significance was annotated as follows: &#x002A;<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05, &#x002A;&#x002A;<italic>p</italic>&#x202F;&#x003C;&#x202F;0.01, &#x002A;&#x002A;&#x002A;<italic>p</italic>&#x202F;&#x003C;&#x202F;0.001. An alpha level of 0.05 was used as the threshold for statistical significance in all analyses, including ANOVA, LDA, and Pearson correlation.</p>
<p>To evaluate the relationships between hyperspectral vegetation indices and the medicinal score, a Pearson correlation matrix was computed using Python (pandas and seaborn packages). This method quantifies linear associations between variables, yielding correlation coefficients (r-values) ranging from &#x2212;1 to +1. Values closer to &#x00B1;1 indicate strong correlations. No regression models or variance partitioning were performed at this stage.</p>
</sec>
</sec>
<sec sec-type="results" id="sec9">
<label>3</label>
<title>Results</title>
<p>The following section presents the variation in spectral indices and morphological features across the examined taxa, highlighting statistically significant patterns related to their physiological and medicinal characteristics.</p>
<sec id="sec10">
<label>3.1</label>
<title>Morphological description</title>
<p>Morphological characteristics (e.g., leaf shape, margin, venation patterns) supported the spectral findings, with clear differences observed among the selected species. A combined analysis improved discrimination accuracy. The morphological traits of the taxa under investigation are shown in <xref ref-type="table" rid="tab2">Table 2</xref> to make it easier to determine which diagnostic features are most crucial.</p>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Morphological characteristics and color of <italic>Ficus</italic> and <italic>Moringa</italic> spp., leaves and bark.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Species</th>
<th align="left" valign="top">Leaf color</th>
<th align="left" valign="top">Leaf shape</th>
<th align="left" valign="top">Leaf margin</th>
<th align="left" valign="top">Leaf apex</th>
<th align="left" valign="top">Bark color</th>
<th align="left" valign="top">Abbreviation</th>
<th align="left" valign="top">Growth habits</th>
<th align="center" valign="top">Tree average height (m)</th>
<th align="center" valign="top">Single Leaf area (cm<sup>2</sup>)</th>
<th align="center" valign="top">Leaf dimension (cm)</th>
<th align="left" valign="top">Medical uses</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top"><italic>Ficus asperrima</italic></td>
<td align="left" valign="top">Pale green</td>
<td align="left" valign="top">Ovate-elliptic</td>
<td align="left" valign="top">Dentata</td>
<td align="left" valign="top">Mucronate</td>
<td align="left" valign="top">Gray to whitish, smooth</td>
<td align="left" valign="top">Asp</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">25</td>
<td align="center" valign="top">105</td>
<td align="center" valign="top">10&#x2013;14&#x202F;&#x00D7;&#x202F;7.5&#x2013;10</td>
<td align="left" valign="top">Antioxidant properties<break/>Anti-inflammatory effects<break/>Antimicrobial activity, Antidiabetic potential (<xref ref-type="bibr" rid="ref58">Patel et al., 2023</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. auriculata</italic></td>
<td align="left" valign="top">Dark green</td>
<td align="left" valign="top">Round ovate</td>
<td align="left" valign="top">Regularly or slowly dentate</td>
<td align="left" valign="top">Acuminate</td>
<td align="left" valign="top">Grayish brown, rough</td>
<td align="left" valign="top">Aur</td>
<td align="left" valign="top">Shrub</td>
<td align="center" valign="top">4</td>
<td align="center" valign="top">460.5</td>
<td align="center" valign="top">15&#x2013;30&#x202F;&#x00D7;&#x202F;15&#x2013;27</td>
<td align="left" valign="top">Antioxidant activity (<xref ref-type="bibr" rid="ref29">Gaire et al., 2011</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. benghalensis</italic></td>
<td align="left" valign="top">Rich green</td>
<td align="left" valign="top">Ovate</td>
<td align="left" valign="top">Finely and irregularly toothed</td>
<td align="left" valign="top">Mucronate</td>
<td align="left" valign="top">Grayish white</td>
<td align="left" valign="top">Beng</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">30</td>
<td align="center" valign="top">159</td>
<td align="center" valign="top">18&#x2013;20&#x202F;&#x00D7;&#x202F;8&#x2013;15</td>
<td align="left" valign="top">Antidiabetic, anti-inflammatory, wound healing (<xref ref-type="bibr" rid="ref48">Logesh et al., 2023</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. benjamina</italic></td>
<td align="left" valign="top">Shining dark green</td>
<td align="left" valign="top">Ovate or ovate-elliptic or rhomboid</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Acuminate</td>
<td align="left" valign="top">Gray to grayish white, smooth</td>
<td align="left" valign="top">Benj</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">50</td>
<td align="center" valign="top">35</td>
<td align="center" valign="top">4&#x2013;12&#x202F;&#x00D7;&#x202F;2&#x2013;6</td>
<td align="left" valign="top">Antioxidant compounds and antimicrobial agents (<xref ref-type="bibr" rid="ref38">Imran et al., 2014</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. elastica decora</italic></td>
<td align="left" valign="top">Rich Glossy Green upper surface and purplish for the lower surface</td>
<td align="left" valign="top">Elliptic</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Acute</td>
<td align="left" valign="top">Pale gray</td>
<td align="left" valign="top">Deco</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">35</td>
<td align="center" valign="top">210</td>
<td align="center" valign="top">8&#x2013;30&#x202F;&#x00D7;&#x202F;7&#x2013;10</td>
<td align="left" valign="top">Anti-inflammatory, analgesic and mild anti-diabetic activity (<xref ref-type="bibr" rid="ref25">EI-Domiaty et al., 2002</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. hispida</italic></td>
<td align="left" valign="top">Dark green</td>
<td align="left" valign="top">Elliptic</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Acuminate</td>
<td align="left" valign="top">Dark gray</td>
<td align="left" valign="top">Hisp</td>
<td align="left" valign="top">Shrub</td>
<td align="center" valign="top">3.5</td>
<td align="center" valign="top">132</td>
<td align="center" valign="top">10&#x2013;25&#x202F;&#x00D7;&#x202F;5&#x2013;10</td>
<td align="left" valign="top">Anti-inflammatory, antinociceptive, sedative, antidiarrheal, antiulcer, antimicrobial, antioxidant, hepatoprotective, antineoplastic, and antidiabetic activities (<xref ref-type="bibr" rid="ref15">Cheng et al., 2020</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. lutea</italic></td>
<td align="left" valign="top">Glossy green</td>
<td align="left" valign="top">Ovate to oblong-lanceolate</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Acute to acuminate</td>
<td align="left" valign="top">Gray, smooth</td>
<td align="left" valign="top">Lute</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">17.5</td>
<td align="center" valign="top">215</td>
<td align="center" valign="top">20&#x2013;43&#x202F;&#x00D7;&#x202F;5&#x2013;13</td>
<td align="left" valign="top">Antibacterial activity and antidiabetic activity (<xref ref-type="bibr" rid="ref74">van Staden and Lall, 2020</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. microcarpa</italic></td>
<td align="left" valign="top">Dark green</td>
<td align="left" valign="top">Ovate</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Acuminate</td>
<td align="left" valign="top">Grayish white</td>
<td align="left" valign="top">Carp</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">25</td>
<td align="center" valign="top">35</td>
<td align="center" valign="top">4&#x2013;12&#x202F;&#x00D7;&#x202F;2&#x2013;6</td>
<td align="left" valign="top">Anti-diabetes (<xref ref-type="bibr" rid="ref4">Akhtar et al., 2018</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. racemosa</italic></td>
<td align="left" valign="top">Pale green</td>
<td align="left" valign="top">Ovate</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Acuminate</td>
<td align="left" valign="top">Grayish brown</td>
<td align="left" valign="top">Race</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">30</td>
<td align="center" valign="top">48.5</td>
<td align="center" valign="top">10&#x2013;14&#x202F;&#x00D7;&#x202F;5&#x2013;4.</td>
<td align="left" valign="top">Skeleton diseases, diabetes, inflammatory, hyperlipidemia, hemorrhoids, respiratory, liver dysfunction, antitussive, hepatoprotective, antimicrobial (<xref ref-type="bibr" rid="ref64">Sharma et al., 2023</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. religiosa</italic></td>
<td align="left" valign="top">New leaves are purplish but later changing to mid-green</td>
<td align="left" valign="top">Ovate</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Acute</td>
<td align="left" valign="top">Gray</td>
<td align="left" valign="top">Reli</td>
<td align="left" valign="top">Tree</td>
<td align="center" valign="top">40</td>
<td align="center" valign="top">156</td>
<td align="center" valign="top">10&#x2013;18&#x202F;&#x00D7;&#x202F;8&#x2013;10</td>
<td align="left" valign="top">Antiulcer, antibacterial, antidiabetic (<xref ref-type="bibr" rid="ref14">Chandrasekar et al., 2010</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>Moringa peregrina</italic></td>
<td align="left" valign="top">Gray or waxy green</td>
<td align="left" valign="top">Bipinnate (2-pinnate); leaflets are obovate, oblanceolate, or spatulate</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Rounded to slightly acute</td>
<td align="left" valign="top">Gray, purple-gray, or bright brown</td>
<td align="left" valign="top"><italic>M. peregrina</italic></td>
<td align="left" valign="top">Deciduous small tree with tuberous rootstock; branches slender and crown ovoid</td>
<td align="center" valign="top">10</td>
<td align="center" valign="top">0.86</td>
<td align="center" valign="top">0.3&#x2013;2&#x202F;cm long &#x00D7; 0.2&#x2013;1.3&#x202F;cm wide</td>
<td align="left" valign="top">Anticancer activity, antihyperglycemic effect, antimicrobial properties (<xref ref-type="bibr" rid="ref26">Elbatran et al., 2005</xref>; <xref ref-type="bibr" rid="ref1">Abd Rani et al., 2018</xref>)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>M. peregrina</italic></td>
<td align="left" valign="top">Dark green on the upper surface, pale green on the lower surface</td>
<td align="left" valign="top">Tripinnately compound with ovate to elliptic leaflets</td>
<td align="left" valign="top">Entire</td>
<td align="left" valign="top">Rounded to obtuse</td>
<td align="left" valign="top">Whitish-gray with a thick, corky texture</td>
<td align="left" valign="top"><italic>M. oleifera</italic></td>
<td align="left" valign="top">Fast-growing, deciduous tree with a straight trunk and a spreading, open crown of drooping, fragile branches</td>
<td align="center" valign="top">11</td>
<td align="center" valign="top">3.4</td>
<td align="center" valign="top">2.0&#x2013;2.8, 0.9&#x2013;1.8</td>
<td align="left" valign="top">Antioxidant and anti, inflammatory, antidiabetic, hepatoprotective, antimicrobial<break/>(<xref ref-type="bibr" rid="ref27">Fahey, 2005</xref>; <xref ref-type="bibr" rid="ref36">Hamdy et al., 2007</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Descriptive statistics for tree height and single leaf area across the 12 studied species are presented in <xref ref-type="table" rid="tab2">Table 2</xref>. The average tree height was 23.42&#x202F;&#x00B1;&#x202F;14.62&#x202F;m, while the average single leaf area was 130.02&#x202F;&#x00B1;&#x202F;128.77&#x202F;cm<sup>2</sup>, reflecting substantial interspecific variation.</p>
<p>The morphological characteristics of <italic>M. peregrina</italic> and <italic>M. oleifera</italic>, particularly leaf shape, margin, and apex, reveal distinct differences that support their taxonomic classification and assist in spectral discrimination. For instance, <italic>Moringa peregrina</italic> exhibits bipinnate leaves with obovate to spatulate leaflets, whereas <italic>M. oleifera</italic> has tripinnate leaves with ovate to elliptic leaflets. These variations in leaf structure, along with differences in leaf size (ranging from 0.3 to 2&#x202F;cm for <italic>M. peregrina</italic> and 2.0&#x2013;2.8&#x202F;cm for <italic>M. oleifera</italic>), highlight the species&#x2019; morphological distinctiveness.</p>
<p>Additionally, the bark color and texture further distinguish the two species. <italic>M. peregrina</italic> has a gray or waxy green color with a corky, whitish-gray texture, while <italic>M. oleifera</italic> has a pale green underside and a whitish-gray bark.</p>
</sec>
<sec id="sec11">
<label>3.2</label>
<title>Spectral analyses</title>
<sec id="sec12">
<label>3.2.1</label>
<title>Ficus species</title>
<p>All taxa exhibited a similar spectral trend across the 400&#x2013;2,500&#x202F;nm range, with a characteristic dip in the red region and a peak in the near-infrared region, as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>.</p>
<fig position="float" id="fig2">
<label>Figure 2</label>
<caption>
<p>Spectral characteristics pattern for <italic>Ficus</italic> spp.</p>
</caption>
<graphic xlink:href="fsufs-09-1652332-g002.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Line graph titled "Data Reflectance" showing reflectance against wavelength for various Ficus species. The x-axis represents wavelength in nanometers from 350 to 2350, and the y-axis represents reflectance in units from 0.0 to 1.2. Various species like Ficus benghalensis and Ficus asperrima are color-coded in the legend.</alt-text>
</graphic>
</fig>
<p><italic>F. lutea</italic> showed lower reflectance values in the SWIR I region, while <italic>F. religiosa</italic> had reduced reflectance in the NIR zone (<xref ref-type="fig" rid="fig2">Figure 2</xref>). Among all species, <italic>F. benghalensis</italic> showed higher spectral reflectance across most regions, with the exception of SWIR II.</p>
<p>The ANOVA and <italic>post hoc</italic> Tukey tests (<xref ref-type="fig" rid="fig3">Figure 3</xref>) identified statistically significant differences in spectral reflectance across species. Reflectance values in the blue region showed limited variance between species, while greater variation was observed in the SWIR II region.</p>
<fig position="float" id="fig3">
<label>Figure 3</label>
<caption>
<p>ANOVA and Tukey&#x2019;s analyses to differentiation among <italic>Ficus</italic> spp. within the Blue, Green, and NIR Red, SWIRI, and SWIR II Zones.</p>
</caption>
<graphic xlink:href="fsufs-09-1652332-g003.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Boxplots display spectral reflectance of various Ficus and Moringa species across six bands: Blue, Green, Red, NIR, SWIR I, and SWIR II. Each plot compares species reflectance with a threshold of 0.05, using one-way ANOVA and Tukey-Kramer HSD test for assessing inter-species differences.</alt-text>
</graphic>
</fig>
<p>Linear Discriminant Analysis (LDA) conducted on the spectral data of <italic>Ficus</italic> spp. revealed that the first discriminant function (DF1) explained 84.7% of the total variance, and the second function (DF2) accounted for an additional 10.5%. The spectral regions that contributed most significantly to class separation were found in the near-infrared (700&#x2013;1,300&#x202F;nm) and SWIR1 (1,500&#x2013;1,750&#x202F;nm) regions. The model achieved a cross-validated classification accuracy of 91.3%. Statistical testing using Wilks&#x2019; Lambda confirmed the significance of the model (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.001), indicating robust discriminatory capability among <italic>Ficus</italic> species.</p>
<p>Spectral reflectance analysis showed that most species exhibited similar responses in the visible spectrum. However, interspecific differences were observed in the near-infrared (NIR) and shortwave infrared (SWIR) regions.</p>
<p><italic>F. benghalensis</italic> exhibited high reflectance across most regions except SWIR II, while <italic>F. religiosa</italic> showed reduced reflectance in the NIR range. <italic>Ficus lutea</italic> had lower reflectance in SWIR I, and <italic>F. microcarpa</italic> was differentiated by its reflectance in the visible band.</p>
<p>The ANOVA and Tukey&#x2019;s <italic>post hoc</italic> tests identified green, red, NIR, and SWIR II as the spectral regions with the greatest ability to discriminate among species, whereas the blue band showed minimal variance across taxa.</p>
<p>As shown in <xref ref-type="table" rid="tab3">Table 3</xref>, the results indicate that Linear Discriminate Analysis (LDA) was successful in determining ideal wavelengths and wavebands for a range of plants under investigation. This analytical method successfully identified the unique wavelength connected to every wild plant.</p>
<table-wrap position="float" id="tab3">
<label>Table 3</label>
<caption>
<p>The optimal wavelength for discerning between the various plant species under investigation.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Plant name</th>
<th align="center" valign="top">Optimal wavelength (nm)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top"><italic>Ficus asperrima</italic></td>
<td align="center" valign="top">426&#x2013;613 to 625&#x2013;873 to 887</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. auriculata</italic></td>
<td align="center" valign="top">428&#x2013;613 to 623&#x2013;875 to 887</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. benghalensis</italic></td>
<td align="center" valign="top">425&#x2013;623 to 631&#x2013;859 to 870</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. benghalensis</italic></td>
<td align="center" valign="top">425&#x2013;426&#x2013;614 to 632&#x2013;861 to 883</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. benjamina</italic></td>
<td align="center" valign="top">425&#x2013;426&#x2013;614 to 632&#x2013;861 to 883</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. decora</italic></td>
<td align="center" valign="top">427 to 430&#x2013;595 to 629&#x2013;853 to 893</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. hispida</italic></td>
<td align="center" valign="top">350 to 431&#x2013;589 to 914</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. lutea</italic></td>
<td align="center" valign="top">427&#x2013;629 to 645&#x2013;851 to 866</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. microcarpa</italic></td>
<td align="center" valign="top">426&#x2013;427&#x2013;610 to 625&#x2013;866 to 883</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. racemosa</italic></td>
<td align="center" valign="top">425&#x2013;612 to 620&#x2013;865 to 876</td>
</tr>
<tr>
<td align="left" valign="top"><italic>F. religiosa</italic></td>
<td align="center" valign="top">426 to 629&#x2013;865 to 1,012</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec13">
<label>3.2.2</label>
<title>Moringa species</title>
<p>The reflectance spectra for <italic>M. peregrina</italic> and <italic>M. oleifera</italic> were measured across the 350&#x2013;2,500&#x202F;nm wavelength range (<xref ref-type="fig" rid="fig4">Figure 4</xref>). The data reveal that both species exhibit similar overall spectral patterns, with noticeable differences in reflectance values across certain wavelength regions. <italic>M. oleifera</italic> consistently showed higher reflectance values than Moringa peregrina, particularly in the near-infrared region (700&#x2013;1,350&#x202F;nm).</p>
<fig position="float" id="fig4">
<label>Figure 4</label>
<caption>
<p>Spectral characteristics pattern for <italic>Moringa</italic> spp.</p>
</caption>
<graphic xlink:href="fsufs-09-1652332-g004.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Graph showing reflectance data of Moringa peregrina and Moringa oleifera across wavelengths from 350 to 2450 nanometers. Reflectance is on the y-axis, and wavelength is on the x-axis. Moringa peregrina is represented by a blue line and Moringa oleifera by a red line, with fluctuations in reflectance values.</alt-text>
</graphic>
</fig>
<p>For the <italic>Moringa</italic> spp., LDA results showed that DF1 and DF2 explained 89.2 and 7.1% of the variance, respectively. The key wavelengths contributing to species separation were also located in the NIR and SWIR 1 regions. The classification accuracy reached 93.2%, highlighting the effectiveness of hyperspectral features in differentiating <italic>Moringa oleifera</italic> and <italic>Moringa peregrina</italic>. The model was statistically significant (Wilks&#x2019; Lambda, <italic>p</italic>&#x202F;&#x003C;&#x202F;0.001), confirming its robustness for spectral classification.</p>
</sec>
</sec>
<sec id="sec14">
<label>3.3</label>
<title>Vegetation indices</title>
<sec id="sec15">
<label>3.3.1</label>
<title><italic>Ficus</italic> spp.</title>
<p>The analysis of hyperspectral vegetation indices across 10 <italic>Ficus</italic> spp. revealed significant interspecific variations that reflect their physiological status. These variations, when interpreted alongside known phytochemical profiles from the literature, may provide preliminary insights into potential medicinal relevance. <xref ref-type="table" rid="tab4">Table 4</xref> summarizes the computed values for 10 spectral indices, including NDVI, SR, PSRI, CRI, RENDVI, PRI, MCARI, ARI2, NDRE, and CIred-edge.</p>
<table-wrap position="float" id="tab4">
<label>Table 4</label>
<caption>
<p>Mean vegetation index values across 10 <italic>Ficus</italic> spp.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Plant name</th>
<th align="center" valign="top">NDVI</th>
<th align="center" valign="top">SR</th>
<th align="center" valign="top">PSRI</th>
<th align="center" valign="top">CRI</th>
<th align="center" valign="top">RENDVI</th>
<th align="center" valign="top">PRI</th>
<th align="center" valign="top">MCARI</th>
<th align="center" valign="top">ARI2</th>
<th align="center" valign="top">NDRE</th>
<th align="center" valign="top">Clred-Edge</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle"><italic>Ficus benghalensis</italic></td>
<td align="center" valign="middle">0.945</td>
<td align="center" valign="middle">39.339</td>
<td align="center" valign="middle">0.518</td>
<td align="center" valign="middle">18.56</td>
<td align="center" valign="middle">0.876</td>
<td align="center" valign="bottom">0.1297</td>
<td align="center" valign="bottom">0.51200</td>
<td align="center" valign="bottom">0.3034</td>
<td align="center" valign="bottom">0.6139</td>
<td align="center" valign="bottom">0.62014</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. asperrima</italic></td>
<td align="center" valign="middle">0.517</td>
<td align="center" valign="middle">12.219</td>
<td align="center" valign="middle">0.467</td>
<td align="center" valign="middle">18.565</td>
<td align="center" valign="middle">0.387</td>
<td align="center" valign="bottom">0.0787</td>
<td align="center" valign="bottom">0.22609</td>
<td align="center" valign="bottom">&#x2212;0.0704</td>
<td align="center" valign="bottom">0.49160</td>
<td align="center" valign="bottom">0.43323</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. racemosa</italic></td>
<td align="center" valign="middle">0.732</td>
<td align="center" valign="middle">12.219</td>
<td align="center" valign="middle">0.414</td>
<td align="center" valign="middle">9.252</td>
<td align="center" valign="middle">0.291</td>
<td align="center" valign="bottom">0.1002</td>
<td align="center" valign="bottom">0.71162</td>
<td align="center" valign="bottom">0.74063</td>
<td align="center" valign="bottom">0.26161</td>
<td align="center" valign="bottom">0.17255</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. religiosa</italic></td>
<td align="center" valign="middle">0.104</td>
<td align="center" valign="middle">11.764</td>
<td align="center" valign="middle">0.345</td>
<td align="center" valign="middle">8.954</td>
<td align="center" valign="middle">0.171</td>
<td align="center" valign="bottom">0.0586</td>
<td align="center" valign="bottom">0.54690</td>
<td align="center" valign="bottom">&#x2212;0.0188</td>
<td align="center" valign="bottom">0.33523</td>
<td align="center" valign="bottom">0.23038</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. auriculata</italic></td>
<td align="center" valign="middle">0. 215</td>
<td align="center" valign="middle">15.562</td>
<td align="center" valign="middle">0.449</td>
<td align="center" valign="middle">22.974</td>
<td align="center" valign="middle">0.334</td>
<td align="center" valign="bottom">0.0773</td>
<td align="center" valign="bottom">0.28150</td>
<td align="center" valign="bottom">0.18335</td>
<td align="center" valign="bottom">0.49667</td>
<td align="center" valign="bottom">0.43303</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. hispida</italic></td>
<td align="center" valign="middle">0. 466</td>
<td align="center" valign="middle">10.382</td>
<td align="center" valign="middle">0.224</td>
<td align="center" valign="middle">11.514</td>
<td align="center" valign="middle">0.315</td>
<td align="center" valign="bottom">0.0476</td>
<td align="center" valign="bottom">0.18423</td>
<td align="center" valign="bottom">&#x2212;0.2097</td>
<td align="center" valign="bottom">0.47478</td>
<td align="center" valign="bottom">0.43309</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. microcarpa</italic></td>
<td align="center" valign="middle">0.452</td>
<td align="center" valign="middle">3.8630</td>
<td align="center" valign="middle">0.300</td>
<td align="center" valign="middle">1.707</td>
<td align="center" valign="middle">0.307</td>
<td align="center" valign="bottom">0.0344</td>
<td align="center" valign="bottom">0.18476</td>
<td align="center" valign="bottom">0.12843</td>
<td align="center" valign="bottom">0.28059</td>
<td align="center" valign="bottom">0.20757</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. decora</italic></td>
<td align="center" valign="middle">0.395</td>
<td align="center" valign="middle">12.141</td>
<td align="center" valign="middle">0.352</td>
<td align="center" valign="middle">11.217</td>
<td align="center" valign="middle">0.237</td>
<td align="center" valign="bottom">0.0895</td>
<td align="center" valign="bottom">0.14210</td>
<td align="center" valign="bottom">0.47144</td>
<td align="center" valign="bottom">0.50402</td>
<td align="center" valign="bottom">0.44293</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. lutea</italic></td>
<td align="center" valign="middle">0.521</td>
<td align="center" valign="middle">18.201</td>
<td align="center" valign="middle">0.482</td>
<td align="center" valign="middle">12.304</td>
<td align="center" valign="middle">0.355</td>
<td align="center" valign="bottom">0.0635</td>
<td align="center" valign="bottom">0.61784</td>
<td align="center" valign="bottom">&#x2212;0.3608</td>
<td align="center" valign="bottom">0.42901</td>
<td align="center" valign="bottom">0.34197</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>F. benjamina</italic></td>
<td align="center" valign="middle">0.508</td>
<td align="center" valign="middle">25.477</td>
<td align="center" valign="middle">0.486</td>
<td align="center" valign="middle">24.917</td>
<td align="center" valign="middle">0.3721</td>
<td align="center" valign="bottom">0.107056</td>
<td align="center" valign="bottom">0.3227</td>
<td align="center" valign="bottom">&#x2212;0.33692</td>
<td align="center" valign="bottom">0.55099</td>
<td align="center" valign="bottom">0.49342</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>All values represent species-averaged reflectance-derived indices computed from leaf-level spectral data.</p>
</table-wrap-foot>
</table-wrap>
<p>Results for <italic>F. benghalensis</italic> demonstrated the highest NDVI (0.945), SR (39.3), and RENDVI (0.876) values, indicating high leaf-level chlorophyll content and strong physiological activity. It also showed high CRI (18.56), ARI2 (0.303), and MCARI (0.512), indicating rich carotenoid and anthocyanin content. PRI (0.129) and NDRE (0.614) were elevated, reflecting strong photosynthetic efficiency and nitrogen status. PSRI (0.518) and CIred-edge (0.620) also supported robust plant health as revealed by spectral analysis in this study. The known medicinal applications of <italic>F. benghalensis</italic>, including treatment of diabetes, inflammation, and microbial infections, have been previously documented (<xref ref-type="bibr" rid="ref54">Murugesu et al., 2021</xref>) although not based on spectral data.</p>
<p><italic>F. asperrima</italic> showed NDVI of 0.517 and SR of 12.2. CRI was relatively high (18.56), while ARI2 had a negative value (&#x2212;0.070). MCARI (0.226), PRI (0.078), RENDVI (0.387), NDRE (0.492), and CIred-edge (0.433) were moderate.</p>
<p><italic>F. racemosa</italic> exhibited high MCARI (0.711) and ARI2 (0.741). NDVI (0.732) and SR (12.2) were also relatively high. PRI (0.100), NDRE (0.262), and RENDVI (0.291) showed intermediate values. CRI (9.25) and PSRI (0.414) were within mid-range.</p>
<p><italic>F. religiosa</italic> recorded the lowest NDVI (0.104) and RENDVI (0.171). SR (11.76), CRI (8.95), and PSRI (0.345) were low to moderate. MCARI (0.547) was relatively high, while PRI (0.058), ARI2 (&#x2212;0.019), and NDRE (0.335) were comparatively low.</p>
<p><italic>F. auriculata</italic> showed high CRI (22.97), SR (15.56), and PSRI (0.449). NDVI (0.215) and MCARI (0.282) were moderate, while ARI2 (0.183), NDRE (0.497), PRI (0.077), RENDVI (0.334), and CIred-edge (0.433) were within intermediate ranges.</p>
<p><italic>F. hispida</italic> showed NDVI of 0.466, SR of 10.38, and CRI of 11.51. MCARI was 0.184, and ARI2 had a negative value (&#x2212;0.210).</p>
<p>PRI (0.048), RENDVI (0.315), and CIred-edge (0.433) were also relatively low. These values point to limited photosynthetic and pigment activity. The species is traditionally used for laxative and skin treatments, though its spectral profile suggests modest phytochemical output.</p>
<p><italic>F. microcarpa</italic> recorded the lowest SR (3.86), CRI (1.71), and PRI (0.034), suggesting low pigment activity and limited stress adaptation. NDVI (0.452) and PSRI (0.300) were moderate, while MCARI (0.185), ARI2 (0.128), and NDRE (0.281) reflected limited photosynthetic activity. CIred-edge (0.208) and RENDVI (0.307) values also confirmed weak chlorophyll performance.</p>
<p><italic>F. decora</italic> presented moderate NDVI (0.395), SR (12.14), and CRI (11.22). It showed high ARI2 (0.471), moderate MCARI (0.142), and NDRE (0.504). RENDVI (0.237) and PRI (0.089) indicated stable physiological status. The pigment reflectance and anthocyanin presence suggest a moderate medicinal potential, possibly linked to antioxidant properties.</p>
<p><italic>F. lutea</italic> showed a strong SR (18.20), PSRI (0.482), and CRI (12.30), indicating high carotenoid and senescence activity. NDVI (0.521), MCARI (0.618), and ARI2 (&#x2212;0.360) revealed photosynthetic capacity and pigment variation. Although NDRE (0.429) and CIred-edge (0.342) were moderate, the negative ARI2 suggests limited anthocyanin content. Overall, this species holds potential for moderate medicinal value.</p>
<p><italic>F. benjamina</italic> displayed high SR (25.48), CRI (24.91), and NDRE (0.551), along with moderate NDVI (0.508), PSRI (0.486), and MCARI (0.323). ARI2 (&#x2212;0.337) and PRI (0.107) reflected mixed pigment activity. RENDVI (0.372) and CIred-edge (0.493) supported its healthy physiological profile. These indices support its use in treating infections and inflammation, particularly related to its antioxidant potential.</p>
</sec>
<sec id="sec16">
<label>3.3.2</label>
<title><italic>Moringa</italic> spp.</title>
<p><xref ref-type="table" rid="tab5">Table 5</xref> presents the calculated vegetation indices for <italic>M. peregrina</italic> and <italic>M. oleifera</italic>.</p>
<table-wrap position="float" id="tab5">
<label>Table 5</label>
<caption>
<p>Mean vegetation index values for <italic>M. peregrina</italic> and <italic>M. oleifera</italic> species.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Index</th>
<th align="center" valign="top"><italic>Moringa peregrina</italic></th>
<th align="center" valign="top"><italic>Moringa oleifera</italic></th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">NDVI</td>
<td align="center" valign="middle">0.3553</td>
<td align="center" valign="middle">0.48703</td>
</tr>
<tr>
<td align="left" valign="middle">SR</td>
<td align="center" valign="middle">2.10263</td>
<td align="center" valign="middle">7.355033</td>
</tr>
<tr>
<td align="left" valign="top">PSRI</td>
<td align="center" valign="middle">&#x2212;0.0387</td>
<td align="center" valign="middle">&#x2212;0.0161</td>
</tr>
<tr>
<td align="left" valign="middle">RENDVI</td>
<td align="center" valign="middle">0.1157</td>
<td align="center" valign="middle">0.4982</td>
</tr>
<tr>
<td align="left" valign="top">NDWI</td>
<td align="center" valign="top">0.03150</td>
<td align="center" valign="top">0.02537</td>
</tr>
<tr>
<td align="left" valign="top">PRI</td>
<td align="center" valign="top">&#x2212;0.010022</td>
<td align="center" valign="top">0.041967</td>
</tr>
<tr>
<td align="left" valign="top">MCARI</td>
<td align="center" valign="top">0.161392794</td>
<td align="center" valign="top">0.096367</td>
</tr>
<tr>
<td align="left" valign="top">ARI2</td>
<td align="center" valign="top">&#x2212;0.02272</td>
<td align="center" valign="top">&#x2212;0.56906</td>
</tr>
<tr>
<td align="left" valign="top">NDRE</td>
<td align="center" valign="top">0.115628</td>
<td align="center" valign="top">0.498151</td>
</tr>
<tr>
<td align="left" valign="top">Clred-edge</td>
<td align="center" valign="top">0.080305</td>
<td align="center" valign="top">0.490331</td>
</tr>
</tbody>
</table>
</table-wrap>
<p><italic>M. oleifera</italic> exhibited the highest NDVI (0.487), SR (7.36). PSRI (&#x2212;0.016) and NDWI (0.025) were relatively low. PRI (0.042), MCARI (0.096), and ARI2 (&#x2212;0.569) showed variable values. NDRE (0.498), RENDVI (0.498), and CIred-edge (0.490) were among the highest recorded across species.</p>
<p><italic>M. peregrina</italic> presented lower NDVI (0.355), SR (2.10). PSRI (&#x2212;0.039) and NDWI (0.032) were also low. PRI (&#x2212;0.010), MCARI (0.161), ARI2 (&#x2212;0.023), NDRE (0.116), RENDVI (0.116), and CIred-edge (0.080) were consistently lower than those observed in <italic>M. oleifera.</italic></p>
</sec>
</sec>
<sec id="sec17">
<label>3.4</label>
<title>Correlation analysis between spectral indices and medicinal score</title>
<p>The correlation matrix (<xref ref-type="fig" rid="fig5">Figure 5</xref>) illustrates the relationships between selected hyperspectral vegetation indices and the computed medicinal score for various plant species. Among the indices analyzed, NDVI showed a moderately strong positive correlation (<italic>r</italic>&#x202F;=&#x202F;0.50) with medicinal score, indicating that vegetation vigor is associated with medicinal potential. Similarly, MCARI and RENDVI exhibited notable correlations with medicinal score (<italic>r</italic>&#x202F;=&#x202F;0.44 and 0.40, respectively).</p>
<fig position="float" id="fig5">
<label>Figure 5</label>
<caption>
<p>Correlation showing relationships between spectral indices and the calculated medicinal value across all plant species.</p>
</caption>
<graphic xlink:href="fsufs-09-1652332-g005.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Correlation heatmap depicting the relationship between plant indices and medical scores. Colors range from blue (negative correlation) to red (positive correlation). Significant levels are marked: &#x002A; for p &#x003C; 0.05, &#x002A;&#x002A; for p &#x003C; 0.01, &#x002A;&#x002A;&#x002A; for p &#x003C; 0.001. A legend indicates Pearson correlation coefficients on the side.</alt-text>
</graphic>
</fig>
<p>Other indices such as PRI (<italic>r</italic>&#x202F;=&#x202F;0.31), SR (<italic>r</italic>&#x202F;=&#x202F;0.29), and Clred-Edge (<italic>r</italic>&#x202F;=&#x202F;&#x2212;0.10) displayed lower correlations, while ARI2 and NDRE were weakly and negatively correlated (<italic>r</italic>&#x202F;=&#x202F;&#x2212;0.20 and &#x2212;0.15, respectively), suggesting limited diagnostic relevance in predicting medicinal potential. These results identify NDVI, MCARI, and RENDVI as the most reliable spectral indicators of medicinal importance among the tested indices.</p>
</sec>
</sec>
<sec sec-type="discussion" id="sec18">
<label>4</label>
<title>Discussion</title>
<p>While the previous section detailed the quantitative spectral differences among taxa, this section interprets those patterns in the context of plant structure and known medicinal attributes. Morphological characteristics, particularly leaf shape, margin, and apex, demonstrated marked differences among the species, supporting their taxonomic distinctiveness and aiding in spectral discrimination. For example, <italic>F. auriculata</italic> exhibited large, round-ovate leaves with a high single leaf area (460.5&#x202F;cm<sup>2</sup>), contrasting sharply with the smaller, ovate leaves of <italic>F. microcarpa</italic> (35&#x202F;cm<sup>2</sup>). These physical differences, alongside variations in bark color and growth form (tree vs. shrub), are important taxonomic tools.</p>
<p>Spectral reflectance of plant leaves is the absorption occurring at 650&#x202F;nm in the visible red range. This absorption is mostly caused by chlorophyll pigments found in the green-leaf chloroplasts, which are found in the Palisade leaf&#x2019;s outer layers. Furthermore, these spectra differ from white ones by having a similar degree of absorption in the blue band. As such, the majority of visible wavelength reflectance is found in the green area of the spectrum. According to <xref ref-type="bibr" rid="ref30">Gamal et al. (2020)</xref>, <xref ref-type="bibr" rid="ref45">Khdery et al. (2021)</xref>, <xref ref-type="bibr" rid="ref44">Khdery et al. (2023)</xref>, and <xref ref-type="bibr" rid="ref79">Yones et al. (2024)</xref>, given that all the samples are vegetative samples, the spectral reflectance pattern of the taxa under investigation, as depicted in <xref ref-type="fig" rid="fig2">Figure 2</xref>, revealed the same trend in spectrum reflectance.</p>
<p>The results show that every single plant species is highly compatible with the overall spectral signature, especially in different spectral regions like the visible and infrared light. Interestingly, it was found that, in comparison to the SWIR1 region, the SWIR II region had less reflectance (<xref ref-type="bibr" rid="ref3">Aboelghar and Khdery, 2017</xref>).</p>
<p>The findings suggest that SWIR II wavelengths are particularly effective in discriminating among Ficus species, aligning with previous studies (Aboelghar et al., 2017). The visible region, especially the blue band, offered limited discriminatory power. Notably, species such as <italic>F. hispida</italic> and <italic>F. benjamina</italic> demonstrated characteristic high reflectance in the NIR region, which may reflect structural or biochemical traits.</p>
<p>Both <italic>Moringa</italic> spp. exhibited typical spectral behavior associated with healthy green vegetation, including low reflectance in the visible region (400&#x2013;700&#x202F;nm), a pronounced red edge near 700&#x202F;nm, and strong reflectance in the NIR range.</p>
<p>Notably, distinct water absorption features were observed around 1,450&#x202F;nm, 1,950&#x202F;nm, and 2,500&#x202F;nm, consistent with known water-related absorption bands. These differences between <italic>M. oleifera</italic> and <italic>M. peregrina</italic> in the NIR and SWIR regions may reflect variations in internal leaf structure, water content, or pigment concentration.</p>
<p>The spectral characteristics of plant species are influenced by their physiological, morphological, and anatomical traits (<xref ref-type="bibr" rid="ref35">Gitelson et al., 2024</xref>). Species with large, thick, and dark leaves, such as <italic>F. benghalensis</italic>, exhibited higher NDVI and chlorophyll content, consistent with strong vegetative health and photosynthetic capacity. These findings align with previous work by <xref ref-type="bibr" rid="ref7">Apan et al. (2003)</xref> and <xref ref-type="bibr" rid="ref73">Uto and Kosugi (2012)</xref>, who demonstrated the significant role of structural and pigment properties in shaping vegetation spectra.</p>
<p>The moderate NDVI and SR values recorded for <italic>F. asperrima</italic> may reflect average chlorophyll content and light absorption efficiency at the leaf level, suggesting moderate physiological performance relative to other <italic>Ficus</italic> species examined. Low PRI and MCARI, may indicate limited photosynthetic performance and average vegetation density. The negative ARI2 value suggests minimal anthocyanin presence, which could correlate with its relatively lower traditional medicinal use, such as in wound healing.</p>
<p>In contrast, <italic>F. racemosa</italic> displayed high MCARI and ARI2 values, indicating strong pigment concentration and photosynthetic activity. The moderate PRI and NDRE values suggest a balanced nitrogen status and moderate physiological stress. These spectral traits are in line with its well-documented anti-inflammatory and astringent properties in ethno medicine (<xref ref-type="bibr" rid="ref68">Bhivasane et al., 2024</xref>). These spectral features are consistent with the species&#x2019; known pharmacological relevance; however, no direct link between these indices and specific medicinal functions is implied (<xref ref-type="bibr" rid="ref58">Patel et al., 2023</xref>).</p>
<p>Our findings revealed significant correlations between spectral indices such as NDVI, MCARI, and ARI2 and the estimated medicinal score. These indices are known to reflect chlorophyll content, anthocyanin levels, and overall metabolic activity, which are closely tied to the presence of bioactive secondary metabolites (<xref ref-type="bibr" rid="ref31">Gamon et al., 1992</xref>; <xref ref-type="bibr" rid="ref21">Delegido et al., 2013</xref>). This supports previous studies suggesting that hyperspectral features can be used as non-destructive proxies for estimating the pharmacological relevance of plant species.</p>
<p>Notably, <italic>F. benghalensis</italic> demonstrated exceptional NDVI (0.945) and SR (39.3), along with high ARI2 (0.30), MCARI (0.51), and NDRE (0.61), indicative of robust pigment accumulation&#x2014;including anthocyanins, chlorophyll, and nitrogen-associated pigments&#x2014;suggesting strong physiological performance (<xref ref-type="bibr" rid="ref49">Mascarini et al., 2006</xref>). These reflect its medicinal value in wound healing, antimicrobial, and antidiabetic applications.</p>
<p><italic>F. benjamina</italic> exhibited high SR (25.47), CRI (24.91), and NDRE (0.55), indicating elevated structural and pigment-related reflectance features. Conversely, <italic>F. religiosa</italic> presented lower NDVI (0.104) and PRI (0.058), possibly suggesting environmental stress or reduced chlorophyll content. This trend was mirrored in its spectral indices, including weaker PSRI and CRI, making it less potent from a spectral and medicinal perspective (<xref ref-type="bibr" rid="ref43">Khdery, 2020</xref>; <xref ref-type="bibr" rid="ref45">Khdery et al., 2021</xref>; <xref ref-type="bibr" rid="ref44">Khdery et al., 2023</xref>; <xref ref-type="bibr" rid="ref78">Yones et al., 2019</xref>). The low NDVI and RENDVI values observed in <italic>F. religiosa</italic> may reflect poor chlorophyll content and possible physiological stress. Despite this, the species continues to be valued in herbal medicine, potentially due to the presence of non-photosynthetic phytochemicals (<xref ref-type="bibr" rid="ref23">Dmitriev et al., 2023</xref>).</p>
<p>In <italic>F. auriculata</italic>, elevated CRI and PSRI values suggest strong carotenoid activity and potential onset of senescence. Moderate ARI2 and NDRE levels may indicate some antioxidant potential and nitrogen assimilation.</p>
<p>The low MCARI and negative ARI2 in <italic>F. hispida</italic> point to limited chlorophyll and anthocyanin content, possibly reflecting lower metabolic or photosynthetic activity in this species.</p>
<p>The red-edge indices (RENDVI and Clred-edge) further supported this differentiation, with healthier species showing higher values. This is in line with the red-edge&#x2019;s established sensitivity to chlorophyll concentration and stress levels (<xref ref-type="bibr" rid="ref50">Maxwell and Johnson, 2000</xref>; <xref ref-type="bibr" rid="ref81">Zarco-Tejada et al., 2003</xref>).</p>
<p>Linear Discriminant Analysis (LDA) identified unique wavelength ranges specific to several <italic>Ficus</italic> species&#x2014;especially <italic>F. hispida</italic>, <italic>F. racemosa</italic>, and <italic>F. religiosa</italic>&#x2014;reinforcing the potential for hyperspectral separation of species with both taxonomic and pharmacological importance. These findings confirm that hyperspectral indices, when integrated with morphological features, provide a powerful tool for assessing medicinal plant potential among <italic>Ficus</italic> species (<xref ref-type="bibr" rid="ref45">Khdery et al., 2021</xref>; <xref ref-type="bibr" rid="ref44">Khdery et al., 2023</xref>). The differences observed in the reflectance spectra between <italic>M. peregrina</italic> and <italic>M. oleifera</italic> can be attributed to variations in leaf structure, water content, and pigment concentration. The higher reflectance values of <italic>M. oleifera</italic> in the NIR region suggest a denser or more scattering internal leaf structure compared to <italic>M. peregrina</italic>. This is consistent with the known characteristics of <italic>M. oleifera</italic>, which generally has thicker leaves and a higher water retention capacity.</p>
<p>Distinct absorption features around 1,450&#x202F;nm, 1,950&#x202F;nm, and 2,500&#x202F;nm correspond to water absorption bands, and the depth of these features suggests slightly lower water content in <italic>M. peregrina</italic>. In the visible region, both species show low reflectance due to chlorophyll absorption, but <italic>M. oleifera</italic> reflects slightly more in the green (~550&#x202F;nm), indicating higher chlorophyll content, consistent with its antioxidant and anti-inflammatory properties (<xref ref-type="bibr" rid="ref2">AbdAlla et al., 2023</xref>; <xref ref-type="bibr" rid="ref71">Tshabalala et al., 2021</xref>; <xref ref-type="bibr" rid="ref61">R&#x00E9;bufa et al., 2017</xref>).</p>
<p>The spectral profile of <italic>M. oleifera</italic>, characterized by high NDVI, SR, reflects strong vegetative vigor and carotenoid presence. Moderate MCARI and high NDRE/RENDVI values may indicate robust chlorophyll expression and nitrogen content, supporting the species&#x2019; efficiency in photosynthesis and metabolism. These traits are consistent with its documented pharmacological applications in antioxidant defence and metabolic regulation.</p>
<p>In contrast, <italic>M. peregrina</italic> exhibited lower spectral index values across most parameters. Despite this, the negative PSRI and modest NDWI suggest healthy and hydrated foliage. Although the overall spectral intensity is lower than that of <italic>M. oleifera</italic>, <italic>M. peregrina</italic> still retains significance in specific traditional uses such as dermatological and anti-inflammatory treatments.</p>
<p>Morphologically, <italic>M. oleifera</italic> has darker, tripinnate leaves and a broader vegetation, contributing to stronger NIR reflectance, while <italic>M. peregrina</italic> has smaller, bipinnate, waxy leaves that may reduce internal scattering. This structure aligns with its adaptation to arid environments, as supported by the shallower water absorption features and higher NDWI (<xref ref-type="bibr" rid="ref69">Taha, 2016</xref>).</p>
<p>Vegetation indices further confirm these differences: <italic>M. oleifera</italic> shows high NDVI, and NDRE values, consistent with superior pigment content and photosynthetic capacity, aligning with its broad therapeutic uses including hepatoprotection and metabolic regulation. <italic>M. peregrina</italic>, though lower in most indices, shows decent water retention and pigment signals, which support its application in dermatological and traditional remedies (<xref ref-type="bibr" rid="ref15">Cheng et al., 2020</xref>). Spectral analysis of <italic>M. oleifera</italic> and <italic>M. peregrina</italic> indicated marked physiological divergence. <italic>M. oleifera</italic> exhibited high NDVI (0.487), SR (7.36) and NDRE (0.498), which are known to correlate with increased chlorophyll, carotenoid, and nitrogen content, respectively (<xref ref-type="bibr" rid="ref59">Pe&#x00F1;uelas et al., 1993</xref>; <xref ref-type="bibr" rid="ref33">Gitelson et al., 2003</xref>; <xref ref-type="bibr" rid="ref81">Zarco-Tejada et al., 2003</xref>; <xref ref-type="bibr" rid="ref1005">Pe&#x00F1;uelas et al., 1995</xref>), as also outlined in <xref ref-type="table" rid="tab4">Table 4</xref>. These parameters are consistent with its well-documented roles in antioxidant, hepatoprotective, and antidiabetic therapies (<xref ref-type="bibr" rid="ref24">Dung et al., 2023</xref>).</p>
<p>These findings demonstrate that hyperspectral indices effectively distinguish <italic>Moringa</italic> spp. based on their physiological and structural features. While spectral traits showed potential associations with literature-based medicinal relevance, further targeted biochemical analyses are needed to establish direct pharmacological links. Overall, the vegetation indices corroborate the spectral reflectance results, highlighting that <italic>M. oleifera</italic> exhibits superior photosynthetic activity, pigment content, and structural health compared to <italic>Moringa peregrina</italic>, while <italic>M. peregrina</italic> may possess slight advantages in water retention under dry conditions.</p>
<p>The observed correlations between spectral indices and medicinal scores suggest preliminary associations between physiological activity and traditional medicinal relevance. While the correlation coefficients were moderate, they indicate that certain hyperspectral traits may reflect underlying biochemical or pharmacological properties, supporting their utility in exploratory screening applications. NDVI, which reflects chlorophyll density and biomass, showed a clear positive correlation with medicinal potential, supporting findings by <xref ref-type="bibr" rid="ref46">Kizilgeci et al. (2021)</xref> that associate high NDVI with metabolic activity and secondary metabolite synthesis. MCARI, which emphasizes chlorophyll absorption in the red region, also correlated well with medicinal score, reinforcing its usefulness for detecting physiologically active plants (<xref ref-type="bibr" rid="ref33">Gitelson et al., 2003</xref>). The strong association of RENDVI, which is sensitive to vegetation structure and red-edge changes, further validates its application in identifying medicinally significant species (<xref ref-type="bibr" rid="ref21">Delegido et al., 2013</xref>; <xref ref-type="bibr" rid="ref18">Colovic et al., 2022</xref>).</p>
<p>On the other hand, ARI2 and NDRE did not correlate strongly with medicinal value. These indices, although effective in assessing stress-related pigments and nitrogen status, may not reflect the specific biochemical profiles responsible for pharmacological effects. Similarly, PSRI&#x2019;s negative correlation may be due to its association with senescence, which often reduces the biosynthesis of active compounds. These findings highlight the importance of selecting spectral indices aligned with physiological markers of medicinal relevance. NDVI, MCARI, and RENDVI emerge as priority tools for remote sensing-based medicinal plant screening.</p>
<p>It is worth noting that the current sampling strategy prioritized interspecific variation under controlled conditions. Future work with broader replication per species will allow intra-species variability assessments.</p>
<p>Also, to further enhance the interpretation of spectral&#x2013;medicinal relationships, future work is encouraged to include direct phytochemical quantification and bioactivity assays. These analyses would complement the current literature-based scoring framework and provide stronger empirical validation for the use of hyperspectral indices in assessing medicinal potential.</p>
<p>Findings are reinforced by recent studies demonstrating the utility of hyperspectral remote sensing as a proxy for detecting plant biochemical traits relevant to medicinal potential. <xref ref-type="bibr" rid="ref12">Boonrat et al. (2025)</xref> applied hyperspectral imaging combined with machine learning to dynamically map total phenolic and flavonoid contents in sunflower microgreens, achieving <italic>R</italic><sup>2</sup> values up to 0.97 for flavonoids&#x2014;highlighting strong spectral correlations with secondary metabolite levels. <xref ref-type="bibr" rid="ref67">Song and Wang (2022)</xref> developed a hyperspectral index that effectively tracks seasonal changes in the chlorophyll-to-carotenoid ratio in deciduous forests, showing strong relationships with field-measured pigment ratios. This study contributes to the growing body of literature advocating for non-destructive, spectral-based approaches to screen and prioritize medicinal plants for conservation and pharmacological research.</p>
<p>Spectral variation among species may reflect ecological adaptations, such as differences in leaf structure, water use, or stress tolerance. High NIR and red-edge reflectance often indicate traits linked to resilience and productivity. Such traits can guide conservation priorities, especially for species adapted to harsh or shifting environments (<xref ref-type="bibr" rid="ref19">Corbin et al., 2025</xref>).</p>
<p>Also, Spectral variation among the studied species revealed insights into their ecological adaptations. For example, differences in NDWI and PRI values suggest varying water use strategies and photoprotective mechanisms, respectively. Such traits are particularly relevant in arid and semi-arid regions where physiological resilience is key to survival. These variations can serve as functional indicators for prioritizing species in conservation planning or selecting candidates for climate-resilient agriculture. Recent research confirms that hyperspectral data can effectively capture such traits and predict species responses to environmental stressors, thereby supporting their use in ecological monitoring and conservation strategies (<xref ref-type="bibr" rid="ref9">Asner et al., 2015</xref>; <xref ref-type="bibr" rid="ref63">Schneider et al., 2017</xref>).</p>
</sec>
<sec sec-type="conclusions" id="sec19">
<label>5</label>
<title>Conclusion</title>
<p>This study demonstrates the utility of hyperspectral indices for taxonomic discrimination of plant species. While spectral traits were analyzed in relation to literature-derived medicinal relevance scores, further pharmacological and biochemical assays are required to substantiate any medicinal claims. This study demonstrated the effectiveness of integrating hyperspectral remote sensing with morphological analysis as a non-invasive approach for identifying medicinally relevant <italic>Ficus</italic> spp. and <italic>Moringa</italic> spp. based on their physiological Vigor and phytochemical potential. The reflectance spectra across the 350&#x2013;2,500&#x202F;nm range revealed species-specific spectral patterns, with the Near-Infrared (NIR) and Short-Wave Infrared (SWIR) regions being the most informative for spectral discrimination.</p>
<p>Among the <italic>Ficus</italic> spp., <italic>F. benghalensis</italic> and <italic>F. racemosa</italic> exhibited high NDVI, SR, and ARI2 values, indicating strong photosynthetic activity and accumulation of key pigments such as chlorophylls, carotenoids, and anthocyanins. These pigment profiles are consistent with physiological vigor and may be indirectly associated with the species&#x2019; reported medicinal properties, such as antimicrobial, wound healing, and anti-diabetic applications. <italic>F. benjamina</italic> also showed high reflectance in chlorophyll-and nitrogen-sensitive indices, supporting its documented antioxidant and anti-inflammatory roles. In contrast, <italic>F. religiosa</italic> displayed the lowest NDVI and NIR reflectance, suggesting reduced physiological vitality and possible environmental stress, consistent with its relatively limited pigment-based medicinal value. For the <italic>Moringa</italic> spp., <italic>M. oleifera</italic> consistently demonstrated higher NIR reflectance, NDVI, SR, and NDRE values compared to <italic>M. peregrina</italic>, reflecting greater leaf density, chlorophyll and carotenoid content, and nitrogen assimilation. These spectral traits are related strongly with its well-established pharmacological functions including antioxidant, hepatoprotective, and metabolic regulation. Conversely, <italic>M. peregrina</italic>, although spectrally less vigorous, showed spectral signals consistent with its drought tolerance and niche medicinal uses in dermatological and anti-inflammatory treatments. Morphologically, species with broader, darker leaves&#x2014;such as <italic>F. benghalensis</italic> and <italic>M. oleifera</italic>&#x2014;exhibited stronger spectral signatures, while species with narrower or waxy leaves&#x2014;such as <italic>F. microcarpa</italic> and <italic>M. peregrina</italic>&#x2014;reflected weaker signals. Absorption features near 1,450&#x202F;nm, 1,950&#x202F;nm, and 2,500&#x202F;nm further revealed interspecific differences in leaf water content, particularly between the <italic>Moringa</italic> spp.</p>
<p>Vegetation indices such as NDVI, PSRI, MCARI, and RE-NDVI were significantly correlated with morphological traits like leaf area, apex shape, and pigmentation across all species. These findings reinforce the utility of hyperspectral imaging, combined with morphological observation, as a non-destructive and precise approach for identifying medicinally relevant plant species and prioritizing them for further pharmacological investigation.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="sec20">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec sec-type="author-contributions" id="sec21">
<title>Author contributions</title>
<p>GK: Conceptualization, Data curation, Formal analysis, Investigation, Supervision, Methodology, Project administration, Resources, Software, Validation, Visualization, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. MS: Conceptualization, Data curation, Writing &#x2013; original draft. NR: Conceptualization, Data curation, Methodology, Writing &#x2013; original draft. MH: Conceptualization, Data curation, Visualization, Writing &#x2013; original draft.</p>
</sec>
<sec sec-type="funding-information" id="sec22">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. This publication has been supported by the RUDN University Scientific Projects Grant System, project No. 202786-2-000.</p>
</sec>
<ack>
<p>The authors would like to acknowledge the National Authority of Remote Sensing and Space Science (NARSS) in Cairo, Egypt. The authors would thank RUDN University as this publication has been supported by the RUDN University Scientific Projects Grant System, project No. 202786-2-000.</p>
</ack>
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<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
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<title>Generative AI statement</title>
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<title>Publisher&#x2019;s note</title>
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</sec>
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