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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Plant Sci.</journal-id>
<journal-title>Frontiers in Plant Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Plant Sci.</abbrev-journal-title>
<issn pub-type="epub">1664-462X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpls.2025.1640530</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Plant Science</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Advances in light manipulation in greenhouse horticulture: the innovative smart covers</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Zamani</surname>
<given-names>Farzaneh</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
<role content-type="https://credit.niso.org/contributor-roles/formal-analysis/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Duri</surname>
<given-names>Luigi Giuseppe</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1391377/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mori</surname>
<given-names>Mauro</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
<role content-type="https://credit.niso.org/contributor-roles/funding-acquisition/"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Paradiso</surname>
<given-names>Roberta</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/123533/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/funding-acquisition/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
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</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Department of Agricultural Sciences, University of Naples Federico II</institution>, <addr-line>Naples</addr-line>,&#xa0;<country>Italy</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Department of Agriculture, Food, Natural Resources and Engineering (DAFNE), University of Foggia</institution>, <addr-line>Foggia</addr-line>,&#xa0;<country>Italy</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/27334/overview">Leo Marcelis</ext-link>, Wageningen University and Research, Netherlands</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/989002/overview">Laura Cammarisano</ext-link>, University of California, Davis, United States</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1800184/overview">Kami Baghalian</ext-link>, Writtle University College, United Kingdom</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Roberta Paradiso, <email xlink:href="mailto:rparadis@unina.it">rparadis@unina.it</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>07</day>
<month>10</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>16</volume>
<elocation-id>1640530</elocation-id>
<history>
<date date-type="received">
<day>03</day>
<month>06</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>04</day>
<month>09</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Zamani, Duri, Mori and Paradiso.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Zamani, Duri, Mori and Paradiso</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>
<p>Greenhouses play a key role in modern agriculture by creating controlled environments to fulfil specific plant climatic requirements, allowing the extension of the growing season and improving the crop productivity and product quality. Light, in terms of quantity (intensity), quality (spectral composition), and duration (photoperiod), is a crucial factor in driving plant performance in protected cultivation. Solar radiation is significantly affected by the greenhouse framework and cover material. The use of smart materials, including diffusive, photoselective, luminescent, and switchable covers, can positively modify the light intensity, spectrum, and distribution, improving the greenhouse light environment, hence the plant growth, morphology, and metabolism. This review summarizes the state of art of research on innovative covers suitable for modern greenhouse horticulture and their effects on plant performance in vegetable and ornamental crops.</p>
</abstract>
<kwd-group>
<kwd>diffusive covers</kwd>
<kwd>photoselective covers</kwd>
<kwd>luminescent covers</kwd>
<kwd>switchable covers</kwd>
<kwd>photosynthesis</kwd>
<kwd>temperature regulation</kwd>
<kwd>energy efficiency</kwd>
</kwd-group>
<counts>
<fig-count count="3"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="93"/>
<page-count count="18"/>
<word-count count="9665"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Crop and Product Physiology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<label>1</label>
<title>Introduction</title>
<p>
<bold>Light</bold> is essential in agriculture, driving both the plant photosynthesis and photomorphogenesis. Indeed, while photosynthesis enables plants to convert light into chemical energy, supporting growth and productivity, photomorphogenesis encompasses crucial developmental, morphological and metabolic changes in response to light stimuli, such as leaf expansion, stem elongation, flowering, and biosynthesis of antioxidant compounds (<xref ref-type="bibr" rid="B74">Paradiso and Proietti, 2022</xref>). These processes are interconnected, allowing plants to optimize the light energy utilization and the adaptation to the growth environment, and can be strategically harnessed in controlled horticulture.</p>
<p>Among the three main parameters of light, namely the intensity, spectral composition and photoperiod, light spectrum has been gaining increasing attention in the last years, as the knowledge of plant response to the different wavebands strongly increased, also thank to the use of light emitting diodes (LEDs) in plant research.</p>
<p>Plants perceive the light spectral composition through 5 distinct classes of specific photoreceptors, with a high sensitivity for the different wavebands even at very low light intensity (<xref ref-type="bibr" rid="B74">Paradiso and Proietti, 2022</xref>). In the visible range of light radiation, these wavebands correspond to different colors: blue (B, 445&#x2013;500 nm), green (G, 500&#x2013;580 nm), yellow (Y, 580&#x2013;600 nm), orange (O, 600&#x2013;620 nm), red (R, 620&#x2013;700 nm), and far red (FR, 700&#x2013;775 nm). Photoreceptors of the phytochrome family absorb R wavelengths; three different photoreceptors, cryptochromes, phototropins, and the ZTL/FKF1/LKP2 complex, perceive B and UV-A wavelengths; the UVR8 photoreceptor is sensitive to ultraviolet (UV) radiation, particularly UV-A (315&#x2013;380 nm) and UV-B (280&#x2013;315 nm). The light sensing machinery is very sophisticated, often involves the plant hormonal signaling pathways, and concerns numerous processes driven by light colors, in the complex phenomenon of photomorphogenesis (<xref ref-type="bibr" rid="B74">Paradiso and Proietti, 2022</xref>).</p>
<p>It is now known that R and B are the most efficient wavelengths in sustaining photosynthesis, driving the electron transport and rubisco activity (<xref ref-type="bibr" rid="B51">Liu and Van Iersel, 2021</xref>). The R light promotes plant growth, flowering and fruit production (<xref ref-type="bibr" rid="B92">Zhang et&#xa0;al., 2020</xref>), while B influences the leaf expansion and stem elongation and regulates stomatal opening. Together with R, FR can induce reproduction and trigger morphological changes to optimize the light capture in shade conditions, through shade avoidance mechanisms activated by low R-FR ratios. Additionally, B and UV stimulate the biosynthesis of antioxidants, to enhance the plant tolerance to stress conditions, eventually improving the produce quality (<xref ref-type="bibr" rid="B76">Rai, 2020</xref>; <xref ref-type="bibr" rid="B44">Jaiswal et&#xa0;al., 2021</xref>). The G light, alongside R and B, plays a key role in the assimilation process, penetrating deeper into the plant canopy and leaf tissues, hence supporting photosynthesis in the inner plant and leaf layers, where R and B are less effective. Moreover, G modulates some physiological processes, such as the stomatal opening, and morphological responses, like shade avoidance, complementing the R and B action (<xref ref-type="bibr" rid="B71">Paradiso et&#xa0;al., 2025</xref>).</p>
<p>The global adoption of <bold>protected cultivation</bold> has grown substantially and, according to recent estimates, vegetable greenhouse production covers more than 500,000 hectares, with a significant portion (90%) adopting plastic covers (<xref ref-type="bibr" rid="B24">Chavan et&#xa0;al., 2022</xref>). Glasshouses make up approximately 20% of the total surface area and are mainly located in regions, such as Europe (<xref ref-type="bibr" rid="B12">Baeza and L&#xf3;pez, 2012</xref>), where diverse climates present different challenges. For instance, Northern regions face low light intensity and temperature, and short photoperiod in winter, while Southern areas, particularly in Mediterranean basin, experience high radiation and heat (<xref ref-type="bibr" rid="B86">Von Elsner et&#xa0;al., 2000</xref>). Most other greenhouse structures are covered with plastic materials, often complemented by shading nets. These are more common in regions like Asia and North America, where cost-effective solutions are favored, and offer flexibility and efficiency, balancing light transmission with insulation (<xref ref-type="bibr" rid="B55">Maraveas, 2019</xref>).</p>
<p>Managing <bold>light in protected cultivation</bold> is critical for optimizing the production schedule and the crop yield. Innovative technologies such as diffusive or photoselective materials have been shown to increase crop productivity by enhancing light spectrum and distribution, also reducing heat stress and optimizing photosynthesis. Light-diffusing materials, for example, can increase crop productivity by 3% to 30% depending on the crop and growing conditions (<xref ref-type="bibr" rid="B89">Zhang et&#xa0;al., 2024a</xref>). With advancements in smart covers and light manipulation technologies, the efficiency of greenhouse farming continues to rise, reducing the energy consumption while improving the produce yield and quality (<xref ref-type="bibr" rid="B81">Shi et&#xa0;al., 2024</xref>).</p>
<p>Within the wavelength interval of photosynthetically active radiation (PAR), the <bold>intensity</bold> of light directly affects the biomass accumulation, hence covers that control the fraction of radiation entering in the greenhouse through reflection or diffusion can regulate the amount received by the crop (<xref ref-type="bibr" rid="B78">Romero et&#xa0;al., 2018</xref>). Low light intensity, like that occurring in winter cultivations, can reduce biomass production and yield (<xref ref-type="bibr" rid="B89">Zhang et&#xa0;al., 2024a</xref>). In this respect, light-diffusing covers, enhancing the light distribution in greenhouse at the canopy level, have been shown to improve the plant photosynthetic efficiency and the crop productivity. Diffusive plastic films increase the light transmittance and scatter light more evenly across the canopy, reducing photoinhibition in the upper canopy while increasing the amount of light energy reaching lower leaves (<xref ref-type="bibr" rid="B63">Moreno-Teruel et&#xa0;al., 2021</xref>). Plants grown under diffusive covers exhibit more uniform growth, higher yield, and better produce quality, with a limited energy input thank to the reduced supplementary lighting (<xref ref-type="bibr" rid="B33">Gattuso and Mazzola, 2023</xref>). Studies have also shown that altering <bold>spectral composition</bold> of solar radiation in greenhouses using photoselective materials, for example modifying the R-FR ratio (<xref ref-type="bibr" rid="B79">Schettini and Vox, 2010</xref>), can improve plant health and increase the crop productive performance (<xref ref-type="bibr" rid="B47">Lamnatou and Chemisana, 2013</xref>).</p>
<p>As climate change continues to alter global weather patterns, managing temperature and light in greenhouse becomes increasingly important for ensuring stable crop yields and product quality (<xref ref-type="bibr" rid="B38">Gruda et&#xa0;al., 2019</xref>). In this respect, photoselective covers can filter specific light wavelengths, helping to mitigate the temperature fluctuations, hence enhancing the plant photosynthesis and water-use efficiency, while improving the plant metabolism by boosting the biosynthesis of functional compounds (<xref ref-type="bibr" rid="B64">Mormile et&#xa0;al., 2019</xref>). Greenhouse covers that incorporate heat-controlling agents, such as those with near-infrared (NIR) reflective properties, can help mitigate high temperatures by reducing both the external heat entering the greenhouse and the internal heat generated by the absorption and re-radiation of infrared (IR) radiation from the soil. For example, in arid regions (e.g., Ishikawa in Japan), reflective films have been shown to reduce internal temperatures up to 9 &#xb0;C, allowing plants to maintain a healthy growth during extreme heat events (<xref ref-type="bibr" rid="B66">Murakami et&#xa0;al., 2017</xref>).</p>
<p>Given the increasing importance of optimizing lighting strategies to improve crop performance and greenhouse sustainability, this study aimed at critically reviewing how the light environment can be passively manipulated through innovative smart covers. Specifically, we examined how these materials influence light intensity, spectral composition, and uniformity of distribution, driving plant growth and productivity and produce quality, in controlled environment agriculture.</p>
</sec>
<sec id="s2">
<label>2</label>
<title>Method applied for the literature review</title>
<p>A comprehensive review of scientific literature was conducted using the Scopus and Google Scholar databases (last update December 2024), by using the following keywords: smart greenhouse covers, innovative greenhouse covers, diffusive covers, photoselective covers, switchable covers, shading nets. A total of 96 papers were analyzed, comprising 42 review articles and 54 research articles. Among the 54 research articles, some addressed multiple types of greenhouses covers. Specifically, 26 focused on diffusive and/or reflective covers, 34 on photo-selective covers, 10 on luminescent covers, and 7 on switchable covers, with overlaps among the different categories.</p>
<p>These studies were predominantly related to greenhouse experiments and encompassed a wide range of crops. Specifically, 10 articles focused on leafy vegetables, 34 on fruit vegetables, 5 on fruit and small trees, and 2 on ornamental and flower species, 2 on grains and 1 on <italic>Arabidopsis</italic>. Among these, tomato is the most studied crop, followed by cucumber, and lettuce. Other crops, including eggplant, melon, wild rocket, and cabbage, were less represented.</p>
<p>The 54 research articles were further categorized into major thematic groups based on their content and focus: Microclimate regulation (49 papers), Crop yield and product quality (39 papers), Plant stress response (5 papers), Light manipulation effects on plant physiology (10 papers), Plant health (6 papers). A Venn diagram illustrating this classification is shown in <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref>. The number within each section indicate the sum of studies in each category, along with their corresponding percentage on the total. The diagram was generated using Venny 2.1.0 software (Oliveros J.C., 2007-2015; <ext-link ext-link-type="uri" xlink:href="https://bioinfogp.cnb.csic.es/tools/venny/index.html">https://bioinfogp.cnb.csic.es/tools/venny/index.html</ext-link>). Four key themes - Microclimate Regulation, Plant Productivity, Product Quality, and Disease Control - are represented by distinct colors. Studies addressing multiple topics are in the overlapping sections, where the colors merge to indicate their shared focus.</p>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>Venn diagram representing the classification of the 54 research articles collected through the literature review based on the main topics. The distribution in each group is reported as both percentage of the total and number of papers. The diagram was created using the Venny 2.1.0 software (Oliveros J.C., 2007-2015; <ext-link ext-link-type="uri" xlink:href="https://bioinfogp.cnb.csic.es/tools/venny/index.html">https://bioinfogp.cnb.csic.es/tools/venny/index.html</ext-link>). Four different colors were assigned to the 4 main categories, and papers were grouped depending on their belonging to a single category or multiple categories, creating subsets derived from the overlap of the main categories.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpls-16-1640530-g001.tif">
<alt-text content-type="machine-generated">A four-set Venn diagram displays overlapping areas representing different categories: Plant productivity (yellow), Product quality (green), Microclimate regulation (purple), and Disease control (red). Numbered sections with percentages indicate the distribution of elements across these categories. For example, 37% in the purple-yellow overlap, and 14.8% represents the overlap of 3 categories. The result of all categories overlapping is 0%.</alt-text>
</graphic>
</fig>
</sec>
<sec id="s3">
<label>3</label>
<title>Traditional greenhouse covers</title>
<p>Greenhouse covers are traditionally made in glass, fiberglass and plastics, such as polyethylene (PE), polyvinyl chloride (PVC), polycarbonate (PC), and polyhydroxyalkanoates (PHA) (<xref ref-type="bibr" rid="B55">Maraveas, 2019</xref>). These plastic materials are widely used due to their cost-effectiveness, ease of installation, and ability to transmit light (<xref ref-type="bibr" rid="B57">Maraveas et&#xa0;al., 2023b</xref>). However, while traditional materials are effective for basic greenhouse operations, they show several limitations, including thermal insulation issues, UV-induced degradation, IR blocking, condensation buildup, dust accumulation, mechanical fragility, and environmental impact (<xref ref-type="bibr" rid="B57">Maraveas et&#xa0;al., 2023b</xref>).</p>
<p>The main properties of conventional covers are summarized in <xref ref-type="fig" rid="f2">
<bold>Figures&#xa0;2</bold>
</xref> and <xref ref-type="fig" rid="f3">
<bold>3</bold>
</xref>. Due to its strong PAR transmission (up to 90%) and NIR reflectance, which lowers the greenhouse&#x2019;s energy balance, <bold>glass</bold> is recommended as a cladding material. In contrast, plastic polymers have a generally higher NIR transmission (<xref ref-type="bibr" rid="B34">Ghani et&#xa0;al., 2019</xref>). Consequently, glass structures are required to house IR- (and temperature-) sensitive plants. However, glass covers, known for their durability, are nonetheless fragile, heavy, and costly to install. They block certain UV wavebands, essential for pigment formation, impacting plant development negatively (<xref ref-type="bibr" rid="B60">McCartney, 2017</xref>). <xref ref-type="bibr" rid="B88">Zhang et&#xa0;al. (2024b)</xref> highlighted the potential benefits of glass covers, which, when oriented East-West (E-W), can enhance thermal efficiency and photosynthesis, improving yield. However, the study also noted that glass covers can increase sensitivity to diseases, as they make plants more susceptible to <italic>Botrytis</italic> spp (<xref ref-type="bibr" rid="B30">Dueck et&#xa0;al., 2012</xref>). <bold>Fiberglass</bold> has a lower optical transparency and light transmission despite the better mechanical properties (<xref ref-type="bibr" rid="B34">Ghani et&#xa0;al., 2019</xref>). The <bold>PE</bold> is less expensive but has a limited lifespan, usually degrading within a few years due to UV exposure, which deteriorates its structure, worsening mechanical properties and reducing light transmittance, with a consequent negative impact on the crop growth (<xref ref-type="bibr" rid="B22">Castilla, 2013</xref>). The <bold>PC</bold> is more durable and UV-resistant compared to other plastics, but it still suffers from discoloration and gradual degradation over time, with an approximate lifespan of 8 to 10 years under greenhouse conditions (<xref ref-type="bibr" rid="B61">Montero et&#xa0;al., 2011</xref>).</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>Schematic representation of light behavior across the different greenhouse cover types. Conventional covers allow the partial transmission of NIR and FR while reflect UV radiation. Diffusive covers (DCs) scatter the incoming solar radiation more uniformly across the canopy, with no effect on light spectrum. Photoselective covers (PhCs) selectively filter the different wavebands, transmitting or reflecting specific wavelengths (e.g., UV, NIR, FR) or switch them to obtain specific spectral changes (e.g., enrichment in B or R). Switchable covers (SCs) dynamically modulate light and heat transmission in response to seasonal climatic changes, providing photothermal cooling in summer and photothermal heating in winter. Solid arrows represent the full light intensity; thin arrows represent the portion of reflected light; dashed arrows indicate the portion of transmitted light; red wavy arrows represent re-radiated or reflected energy.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpls-16-1640530-g002.tif">
<alt-text content-type="machine-generated">Illustration of four greenhouse models: Conventional covers do not allow UV rays to pass through. Diffusive Covers (DCs) spread sunlight evenly. Photoselective Covers (PhCs) filter specific wavelengths (B, R). Switchable Covers (SCs) provide summer cooling and winter heating through photothermal effects.</alt-text>
</graphic>
</fig>
<p>Another limitation of traditional covers is thermal insulation. A single layer of PE or glass offers poor insulation, raising the heating costs during cold seasons. Though double-layer PE improves thermal insulation, it reduces light transmission (by approximately 10-15%) compared to single-layer films, because of the higher absorption and scattering. This reduction affects the PAR spectrum uniformly, potentially limiting plant growth under low-light conditions (<xref ref-type="bibr" rid="B19">Boulard et&#xa0;al., 1996</xref>). Besides, the increase of the PE quantity used in double layer covers has a negative environmental impact. By an economical point of view, the frequent replacement of PE can increase the long-term expenses despite the lower initial cost, while higher-cost materials like glass and PC, more efficient in insulation, can reduce heating and cooling expenses over time (<xref ref-type="bibr" rid="B53">L&#xf3;pez-Marin et&#xa0;al., 2019</xref>). In harsh climates, the maintenance and replacement of greenhouse covers imply significant costs, prompting some operators to opt for cheaper, lower quality materials, which may reduce crop yields and increase expenditures in the long term, while worsening the greenhouse related pollution (<xref ref-type="bibr" rid="B84">Tanny, 2013</xref>).</p>
</sec>
<sec id="s4">
<label>4</label>
<title>Innovative smart covers</title>
<p>Unlike traditional covers, which primarily focus on physical durability and light transmission, smart covers incorporate technologies to control the greenhouse microclimate actively. These covers adjust parameters like light intensity, direction and spectrum, as well as thermal insulation, according to the specific crop needs, promoting the plant performance and optimizing the resource use efficiency.</p>
<sec id="s4_1">
<label>4.1</label>
<title>Diffusive covers (DCs)</title>
<p>The main properties of diffusive covers are summarized in <xref ref-type="fig" rid="f2">
<bold>Figures&#xa0;2</bold>
</xref> and <xref ref-type="fig" rid="f3">
<bold>3</bold>
</xref>. Diffusive covers scatter the incoming sunlight, spreading it more evenly across the greenhouse space compared to traditional clear covers. Light diffusion is achieved through the cover material itself or a specific coating, that alters the angle of incident rays, reducing the direct light intensity while minimizing the shadow areas (<xref ref-type="bibr" rid="B43">Hemming et&#xa0;al., 2016</xref>). This mechanism ensures that light penetrates deeper into the crop canopy, reaching lower and inner leaves, which otherwise would be shaded from the direct exposure (<xref ref-type="bibr" rid="B81">Shi et&#xa0;al., 2024</xref>). The DCs can increase the light uniformity index up to 20% compared to traditional covers, supporting a more uniform assimilation in the canopy profile and leading to a more balanced growth and higher yield (<xref ref-type="bibr" rid="B65">Moulton et&#xa0;al., 2020</xref>). Besides, diffusive light reduces stress conditions due to excessive radiation and photoinhibition, hence the plant need for photoprotective responses, allowing plants to better adapt to variable sunlight intensity (<xref ref-type="bibr" rid="B73">Paradiso et&#xa0;al., 2024</xref>).</p>
<p>By reducing direct sunlight, DCs also enhance the greenhouse microclimate by lowering temperature and increasing air relative humidity (RH). Applications in arid climate (e.g., Saudi Arabia) demonstrated that DCs can gain 77% diffuse radiation in the greenhouse in the warmest hours of sunny days, while slightly reducing the air temperature and maintaining a more constant RH level (<xref ref-type="bibr" rid="B5">Al-Helal et&#xa0;al., 2020</xref>). These covers increase the light use efficiency at the whole crop level up to 30%, leading to higher production with lower energy input (<xref ref-type="bibr" rid="B62">Moreno-Teruel et&#xa0;al., 2022</xref>). Specifically, reflective-diffusive films (RDCs), which also reflect a portion of NIR radiation while diffusing the visible portion of solar radiation, increase diffuse light by 85% compared to the corresponding traditional covers (with the same PE), reaching a diffusion percentage of 33% of the transmitted radiation. In the tested experimental conditions, they performed similarly to diffusive film (DF) in terms of temperature reduction and RH fluctuation (<xref ref-type="bibr" rid="B5">Al-Helal et&#xa0;al., 2020</xref>).</p>
<p>Evidence about the impact of diffusive covers on various horticultural crops are shown in <xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref> and summarized hereinafter, based on data available in literature concerning leaf, sprout and fruit vegetables, as well as some ornamental crops.</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>Effects of diffusive covers (DCs) on plant growth, photosynthesis and secondary metabolites content in vegetable and ornamental crops.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" rowspan="2" align="left">Species</th>
<th valign="middle" rowspan="2" align="left">Cultivar</th>
<th valign="middle" rowspan="2" align="left">Material</th>
<th valign="middle" rowspan="2" align="left">Cover characteristic</th>
<th valign="middle" colspan="2" align="left">Effects on plant growth, photosynthesis, secondary metabolites</th>
<th valign="middle" rowspan="2" align="left">References</th>
</tr>
<tr>
<th valign="middle" align="left">Increase</th>
<th valign="middle" align="left">Decrease</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="left">
<italic>Asparagus officinalis</italic> L.</td>
<td valign="middle" align="left">Tainan</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">12 % PAR diffusion, NIR-reflective, reducing heat</td>
<td valign="middle" align="left">Photosynthesis, transpiration rate, nutrient uptake, yield (+31.4%), mineral content (e.g., Ca and Mg)</td>
<td valign="middle" align="left">Crude fiber</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B26">Chen and Shen (2022)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Capsicum annuum</italic> L.</td>
<td valign="middle" align="left">Bell Boy</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">74.7% PAR transmission, natural ventilation, cooling through misting systems</td>
<td valign="middle" align="left">Photosynthesis, RH</td>
<td valign="middle" align="left">Transpiration rate</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B60">McCartney (2017)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Bemol RZ F1</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">55-60% diffusion, 85-90% PAR transmission</td>
<td valign="middle" align="left">Yield (+3.1%), higher weight and fruit size</td>
<td valign="middle" align="left">Infection of powdery mildew</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B10">&#xc1;valos-S&#xe1;nchez et&#xa0;al. (2023)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Cucumis sativus</italic> L.</td>
<td valign="middle" align="left">Sovana F1</td>
<td valign="middle" align="left">PE, EVA</td>
<td valign="middle" align="left">40% diffusion, 78-80% PAR transmission, NIR-reflective</td>
<td valign="middle" align="left">Yield (+24%), stem length, leaf area</td>
<td valign="middle" align="left">Water and energy consumption</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B7">Alsadon et&#xa0;al. (2016)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Sovana F1</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">40-60% diffusion,75-88% PAR transmission, NIR-reflective</td>
<td valign="middle" align="left">Yield (+20-22%), number of fruits (per m<sup>2</sup>), fruit fresh and dry weight</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B6">Al-Madani et&#xa0;al. (2024)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Diplotaxis tenuifolia</italic> L.</td>
<td valign="middle" align="left">Reset</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">58% diffusion, 90% PAR transmission, 30% UV-B transmission</td>
<td valign="middle" align="left">Yield (+36.5), K, Ca, Mg, Na, chlorophyll, carotenoids, phenolics, antioxidant activity (HAA, ABTS)</td>
<td valign="middle" align="left">S, ascorbic acid</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B72">Paradiso et&#xa0;al. (2023)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Nature</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">Shading nets: 50% and 79% light extinction,<break/>PE: light transmission and insulation properties</td>
<td valign="middle" align="left">Yield (50% shading), hydrophilic antioxidant activity, ascorbic acid, minerals (e.g., K, P, Ca, Mg)</td>
<td valign="middle" align="left">Yield as both leaf number and dry weight (79% shading)</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B21">Caruso et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Lactuca sativa</italic> L.</td>
<td valign="middle" align="left">Longifolia Lam. Crimor-INTA</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">93% light transmission</td>
<td valign="middle" align="left">Dry weight, stomatal conductance, Ca distribution</td>
<td valign="middle" align="left">Tipburn symptoms</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B15">B&#xe1;rcena et&#xa0;al. (2019)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Princess</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">Uniform light distribution and reduced shading</td>
<td valign="middle" align="left">Yield (+22%), chlorophylls, carotenoids, ascorbic acid, antioxidant activity (LAA, HAA)</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B28">Cozzolino et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="9" align="left">
<italic>Solanum lycopersicum</italic> L.</td>
<td valign="middle" align="left">Black Cherry, Brandy Sweet Plum, Cuban Yellow, Esterina Hybrid F1, Favorito F1</td>
<td valign="middle" align="left">PE, PC</td>
<td valign="middle" align="left">PE: 28% direct transmission and 62% diffusion.<break/>PC: 100% diffusion</td>
<td valign="middle" align="left">Plant growth, fruit yield, phenolics, lycopene, lutein</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B3">Ahmadi et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Cherry</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">80% transmission</td>
<td valign="middle" align="left">WUE</td>
<td valign="middle" align="left">Air temperature and heat stress</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B40">Hassanien et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">HMC44698 F1</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">55-60% diffusion, 85-90% transmission</td>
<td valign="middle" align="left">Yield (+3.2%), photosynthesis, gas exchange, WUE, fruit weight</td>
<td valign="middle" align="left">Leaf temperature, heat stress</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B63">Moreno-Teruel et&#xa0;al. (2021)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Ramyle RZ F1</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">55-60% diffusion, 85&#x2013;90 PAR transmission</td>
<td valign="middle" align="left">Yield (+4.2%), fruit weight, firmness, soluble solid</td>
<td valign="middle" align="left">Infection of powdery mildew and blight</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B10">&#xc1;valos-S&#xe1;nchez et&#xa0;al. (2023)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Sakura</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">58% light scattering, 90% transmission, 30% UV-B transmission</td>
<td valign="middle" align="left">Yield (from 20% to 48% depending on the nitrogen rate), lycopene, carotenoids, phenolics, ascorbic acid, antioxidant activity, nitrogen use efficiency</td>
<td valign="middle" align="left">Nitrogen, direct sunlight stress</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B73">Paradiso et&#xa0;al. (2024)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Shennong</td>
<td valign="middle" align="left">Glass</td>
<td valign="middle" align="left">E-W orientation rather than N-S, light interception enhancement and thermal efficiency</td>
<td valign="middle" align="left">Photosynthetic efficiency, yield</td>
<td valign="middle" align="left">Shading effects</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B88">Zhang et&#xa0;al. (2024b)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Zayda</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">25-30% solar radiation reduction</td>
<td valign="middle" align="left">Plant height, WUE</td>
<td valign="middle" align="left">Heat stress, <italic>Tuta absoluta</italic> infestation</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B31">Ezzaeria et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Komeet</td>
<td valign="middle" align="left">Glass</td>
<td valign="middle" align="left">50% diffusion, 78-79% transmission</td>
<td valign="middle" align="left">Yield (+7-11%), photosynthesis, dry matter</td>
<td valign="middle" align="left">Sensitivity to <italic>Botrytis</italic> spp.</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B30">Dueck et&#xa0;al. (2012)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Marenza</td>
<td valign="middle" align="left">PC</td>
<td valign="middle" align="left">50% PAR diffusion, 85% light transmission, 8% FR transmission</td>
<td valign="middle" align="left">Yield (+8%), photosynthesis</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B62">Moreno-Teruel et&#xa0;al. (2022)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Solanum melongena</italic> L.</td>
<td valign="middle" align="left">Valentine F1</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">IR absorption, UV stabilized</td>
<td valign="middle" align="left">Plant height, stem diameter, NAR, LAR, SLA</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B23">Cemek et&#xa0;al. (2005)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Valerianella locusta</italic> L.</td>
<td valign="middle" align="left">Princess</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">High light diffusion and transmission</td>
<td valign="middle" align="left">Yield (+22.4%), SPAD index, total ascorbic acid, nitrate</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B28">Cozzolino et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Chrysanthemum &#xd7; morifolium</italic> L.</td>
<td valign="middle" align="left">Midnight Time</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">Light diffusion, higher FR light transmission</td>
<td valign="middle" align="left">Plant growth, leaf area, shoot dry weight, number of lateral shoots, photosynthetic efficiency</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B59">Markvart et&#xa0;al. (2010)</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>The increasing or decreasing effects and the related percentage refer to results obtained in DCs compared to the corresponding clear covers.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>In <bold>asparagus</bold> (<italic>Asparagus officinalis</italic> L.), the comparison between a NIR-reflective diffusive coating and a traditional PE film revealed that both covers increased the heat accumulation compared to outside but, additionally, the NIR-reflective diffusive cover provided a more uniform light distribution, improving photosynthetic efficiency in the lower canopy. This led to higher spears yield and quality, with increased calcium and magnesium content. The NIR-reflective diffusive coating also promoted a more vigorous shoot emergence after mother stalk removal, suggesting its potential in enhancing long-term stem vegetables productivity in greenhouse (<xref ref-type="bibr" rid="B26">Chen and Shen, 2022</xref>).</p>
<p>Diffusive covers enhanced the plant growth and fruit production of <bold>pepper</bold> (<italic>Capsicum annuum</italic> L.) in a Natural Ventilation Augmented Cooling (NVAC) greenhouse in Quebec (Canada) (<xref ref-type="bibr" rid="B60">McCartney, 2017</xref>). In this experiment, the improved light diffusion and moderated temperature led to a 28% increase in photosynthetic rate and a 31% reduction in transpiration, ultimately benefiting plant growth. Similarly, diffusive PE increased the leaf area, hence the photosynthetically active surface and assimilation capacity, which contributed to improved growth and productivity of pepper in a Mediterranean greenhouse in Southern Europe, leading to a higher marketable fruits yield (+3.1% compared to commercial PE) (<xref ref-type="bibr" rid="B10">&#xc1;valos-S&#xe1;nchez et&#xa0;al., 2023</xref>).</p>
<p>The use of diffusive PE films increased the leaf area and shoot elongation in greenhouse <bold>cucumber</bold> (<italic>Cucumis sativus</italic> L.) grown under arid conditions in middle east and north Africa, leading to higher biomass accumulation and fruit yield (+22% compared to conventional PE). Particularly, the enhanced light penetration into the canopy and the reduced heat stress resulted in a significant increase in fruit number and size (<xref ref-type="bibr" rid="B6">Al-Madani et&#xa0;al., 2024</xref>).</p>
<p>Despite the short stature, also some leafy vegetables, like <bold>lettuce</bold> (<italic>Lactuca sativa</italic> L.) and <bold>spinach</bold> (<italic>Spinacia oleracea</italic> L.), benefit from diffusive light due to their dense canopy. Indeed, in these crops light scattering enhanced photosynthetic activity and biomass accumulation, increasing yield by 8-10% (<xref ref-type="bibr" rid="B43">Hemming et&#xa0;al., 2016</xref>). In contrast, some evidence highlighted a counterproductive effect of a PE diffusive cover on lettuce as it reduced PAR by 27% compared to control, without lowering air temperature but increasing the occurrence of tipburn (<xref ref-type="bibr" rid="B15">B&#xe1;rcena et&#xa0;al., 2019</xref>). However, the increment in leaf number, avoided any negative effect on fresh and dry weight. Besides, a shade cover (lowering PAR by 76%) used as additional treatment prevented tipburn symptoms. Still in lettuce, the use of diffusive PE film showed to boost the chlorophyll synthesis, to promote a more uniform growth and to improve the health status, with a significant increase in the yield (+22% compared to conventional PE) and leaf content of total ascorbic acid (+9.4%) (<xref ref-type="bibr" rid="B28">Cozzolino et&#xa0;al., 2020</xref>).</p>
<p>
<bold>Tomato</bold> (<italic>Solanum lycopersicum</italic> L.) is the most studied fruit vegetable under DCs and, in general, it shows a considerable improvement in photosynthetic efficiency and fruit yield when grown under a even light distribution. Indeed, this is particularly beneficial for those crops with erect habit in which the lower canopy usually faces light limitations while the upper one is exposed to light intensities above the saturation level. In these crops, diffusive covers alleviate shading of lower leaf layers and reduces photoinhibition in top leaves, while minimizing heat stress and photodamage, especially under strong sunlight conditions (<xref ref-type="bibr" rid="B42">Hemming et&#xa0;al., 2008</xref>). A PE cover with moderate diffusion properties enhanced photosynthetic activity (+21.5%) and increased tomato yield (3.2%) in Mediterranean climate, Almer&#xed;a, Spain (<xref ref-type="bibr" rid="B63">Moreno-Teruel et&#xa0;al., 2021</xref>). Studies conducted in the South of Italy also show that DCs boosted both early and total marketable yields of cherry tomato, with different increases depending on the rate of nitrogen fertilization (<xref ref-type="bibr" rid="B73">Paradiso et&#xa0;al., 2024</xref>). Additionally, combining DCs with a protein hydrolyzed biostimulant enhanced nutrient uptake and secondary metabolite production (i.e., phenols), improving the nutritional profile in cherry tomato (<xref ref-type="bibr" rid="B73">Paradiso et&#xa0;al., 2024</xref>). In tomato grown under a diffusive polyethylene (D-PE) film, a 15% increase in light intensity in the low canopy compared to conventional PE lead to a significantly higher photosynthetic efficiency (<xref ref-type="bibr" rid="B62">Moreno-Teruel et&#xa0;al., 2022</xref>). In tomato, highly diffusive covers can also enhanced the fruit quality and nutritional profiles, increasing lycopene, lutein, and phenolics content (+10.5%, +1.03%, and +14.5% respectively) (<xref ref-type="bibr" rid="B3">Ahmadi et&#xa0;al., 2018</xref>). Polycarbonate covers also resulted in an 8% increase in yield and improved photosynthetic efficiency in tomato (<xref ref-type="bibr" rid="B62">Moreno-Teruel et&#xa0;al., 2022</xref>).</p>
<p>Based on data from literature reported in <xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>, the highest number of crops investigated under DCs belongs to the botanical family of Solanaceae, with 19 papers in total, with 9 studies focusing on <bold>tomato</bold>, 2 on <bold>pepper</bold> and 1 on <bold>eggplant</bold> (<italic>Solanum melongena</italic> L.; <xref ref-type="bibr" rid="B23">Cemek et&#xa0;al., 2005</xref>). In these crops, the use of DCs revealed a positive impact on plant growth and yield by improving light conditions and moderating temperature fluctuations. On fruit vegetables, covers like stabilized PE-UV and PE-IR enhance photosynthesis, and increase plant growth and fruit size and yield. These effects are presumably related to the plant protection from excessive UV radiation, reducing stress conditions, and the more stable microclimate.</p>
<p>The findings suggest that diffusive covers, such as D-PC and D-PE, have a broad impact also on plant nutritional and metabolic responses, particularly in terms of secondary metabolite production which enhances the overall product quality. For instance, an increase in the biosynthesis of carotenoids (i.e., lycopene and lutein) was found in <bold>tomato</bold>, <bold>lettuce,</bold> and <bold>melons</bold>, leading to healthier plants and a better product nutraceutical profile (<xref ref-type="bibr" rid="B3">Ahmadi et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B17">Baxevanou et&#xa0;al., 2018</xref>).</p>
<p>Referring to the mechanisms underlying the plant response to diffuse light, it has been hypothesized that it enhances the growth hormone efficiency, potentially influencing hormone-driven growth responses (<xref ref-type="bibr" rid="B41">He et&#xa0;al., 2021</xref>). These effects may include improved auxin distribution, supporting shoot elongation and balanced biomass allocation.</p>
<p>The effect of diffuse light has been also tested in floriculture. Specifically, <bold>
<italic>Chrysanthemums</italic>
</bold> (<italic>Chrysanthemum &#xd7; morifolium</italic> L.) showed to benefit from scattered light, increasing CO<sub>2</sub> assimilation rate per leaf area unit (+5%), dry matter accumulation (+9.5%), number of lateral stems (+11%), and leaf area (+8%) compared with the control (<xref ref-type="bibr" rid="B59">Markvart et&#xa0;al., 2010</xref>). However, it is worth noting that the larger plant size observed under diffuse light led to a counterproductive increase in internal canopy shading compared to the direct light control.</p>
</sec>
<sec id="s4_2">
<label>4.2</label>
<title>Photoselective covers (PhCs)</title>
<p>The main properties of photoselective covers are summarized in <xref ref-type="fig" rid="f2">
<bold>Figures&#xa0;2</bold>
</xref> and <xref ref-type="fig" rid="f3">
<bold>3</bold>
</xref>. Photoselective covers, available as colored or clear polymers, reduce the radiation reaching the crop by selectively blocking some wavelengths, altering light quality for desired physiological, phenological and morphological responses (<xref ref-type="bibr" rid="B70">Pandey et&#xa0;al., 2023</xref>). Some PhCs are designed to allow the passage of specific wavelengths, such as R to modulate the R-B-FR ratio to regulate the plant growth rate and architecture, and UV-B to stimulate the secondary metabolite production (<xref ref-type="bibr" rid="B83">Tafoya et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B87">Wong et&#xa0;al., 2020</xref>). <xref ref-type="bibr" rid="B76">Rai, 2020</xref> showed that the increased exposure to UV (both A and B) radiation strongly induced gene expression changes in <italic>Arabidopsis</italic> and, in addition to promoting the plant growth, it modifies the response and interaction of various photoreceptors and alter RNA transcription. However, photoselective films experience a 2-4% reduction in light transmittance in their life span, due to weathering, and condensation can lower transmittance by an additional 5% (<xref ref-type="bibr" rid="B2">Abdel-Galil, 2014</xref>). Photo-induced pigment degradation within plastic matrixes can impair the cover performance, though recent materials are more durable, with some lasting up to 15 years (<xref ref-type="bibr" rid="B18">Blanke, 2008</xref>).</p>
<p>The modified light spectrum provided by photoselective films influences growth hormone regulation, promoting stem elongation and biomass accumulation (<xref ref-type="bibr" rid="B41">He et&#xa0;al., 2021</xref>). <xref ref-type="table" rid="T2">
<bold>Table&#xa0;2</bold>
</xref> shows data about the effects of PhCs on various horticultural crops and how targeted growth responses, including flowering and increase of fruit size, can be attained.</p>
<table-wrap id="T2" position="float">
<label>Table&#xa0;2</label>
<caption>
<p>Effects of photoselective covers (PhCs) on plant growth, photosynthesis and secondary metabolites content in fruit, vegetable and ornamental crops.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" rowspan="2" align="center">Species</th>
<th valign="middle" rowspan="2" align="center">Cultivar</th>
<th valign="middle" rowspan="2" align="center">Material composition</th>
<th valign="middle" rowspan="2" align="center">Cover characteristic</th>
<th valign="middle" colspan="2" align="center">Effects on plant growth, photosynthesis, secondary metabolites</th>
<th valign="middle" rowspan="2" align="center">References</th>
</tr>
<tr>
<th valign="middle" align="center">Increase</th>
<th valign="middle" align="center">Decrease</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="left">
<italic>Actinidia deliciosa</italic> L.</td>
<td valign="middle" align="left">Hayward</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">PAR transmission: W (79.6%), G (72.7%), R (73.1%), B (77.2%)</td>
<td valign="middle" align="left">W: Dry weight, soluble solids content<break/>R: vegetative vigor and carbon partitioning</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B16">Basile et&#xa0;al. (2012)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Arabidopsis thaliana</italic> L.</td>
<td valign="middle" align="left">Wild type and mutants: uvr8-2, cry1cry2, cry1cry2uvr8-2</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">Wavebands transmission (UV-B: 290&#x2013;315 nm, UV-Asw: 315&#x2013;350 nm, UV-Alw: 350&#x2013;400 nm, B: 400&#x2013;500 nm)</td>
<td valign="middle" align="left">Epidermal UV screening, CHALCONE SYNTHASE transcript abundance, acclimation to drought stress</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B76">Rai (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Brassica oleracea</italic> L.</td>
<td valign="middle" align="left">
<italic>Capitata</italic> F1</td>
<td valign="middle" align="left">PP, PLA</td>
<td valign="middle" align="left">R enhancement by 26%, reduction B and Y-G light</td>
<td valign="middle" align="left">Biomass, WUE, photosynthesis, stress tolerance</td>
<td valign="middle" align="left">Stomatal conductance, transpiration rate</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B45">Khramov et&#xa0;al. (2022)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Capsicum annuum</italic> L.</td>
<td valign="middle" align="left">Ghia</td>
<td valign="middle" align="left">Glass</td>
<td valign="middle" align="left">Blocks most of the UV, R and FR, reducing B light transmission</td>
<td valign="middle" align="left">Upregulation of ABA-related signaling genes (e. g., PHOT1, PHYA),<break/>ion flux in guard cells</td>
<td valign="middle" align="left">Water use, stomatal pore size</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B93">Zhao et&#xa0;al. (2021)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Citrullus lanatus</italic> L.</td>
<td valign="middle" align="left">Bengala</td>
<td valign="middle" align="left">EVA</td>
<td valign="middle" align="left">B (400&#x2013;500 nm) and R light (600&#x2013;700 nm) enhancement</td>
<td valign="middle" align="left">Yield (+10%), weight, number of female flowers</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B48">Lemari&#xe9; et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Citrus jambhiri Lush.</italic> L.</td>
<td valign="middle" align="left">Kinnow Mandarin</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">R and G nets: enhanced spectra for growth,<break/>W and S nets: light distribution, UV reduction.<break/>Stainless steel screen: heat reflection, light transmission</td>
<td valign="middle" align="left">R and W net: plant height, budding success, N, P, Zn and Fe content</td>
<td valign="middle" align="left">Stem diameter</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B20">Brar et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Citrus sinensis &#xd7; Poncirus trifoliata</italic> L.</td>
<td valign="middle" align="left">Daisy</td>
<td valign="middle" align="left">Red, Green, White, Silver, and Stainless-Steel Screen Nets</td>
<td valign="middle" align="left">R and G nets: enhanced spectra for growth,<break/>W and S nets: light distribution; UV reduction<break/>Stainless steel screen: heat reflection; light transmission</td>
<td valign="middle" align="left">R and W: diameter, internodal sprout length, leaf area, budding success, N, P, Zn</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B20">Brar et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Cucumis melo</italic> L.</td>
<td valign="middle" align="left">Charentais</td>
<td valign="middle" align="left">EVA</td>
<td valign="middle" align="left">B (400&#x2013;500 nm) and R (600&#x2013;700 nm) enhancement</td>
<td valign="middle" align="left">Yield (+52%), size, weight, sugars</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B48">Lemari&#xe9; et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Earl&#x2019;s Knight Natsukei</td>
<td valign="middle" align="left">PE, PP</td>
<td valign="middle" align="left">60-70% PAR transmission, 45-50% NIR absorption</td>
<td valign="middle" align="left">Soluble solid content, brix, fructose and sucrose</td>
<td valign="middle" align="left">Heat stress</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B66">Murakami et&#xa0;al. (2017)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Cucumis sativus</italic> L.</td>
<td valign="middle" align="left">Aseel Hy, Safa 62</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">UVT: UV diffusion and visible light,<break/>UVO: UV blocking</td>
<td valign="middle" align="left">Yield (+21-25%), chlorophyll, phosphorus content</td>
<td valign="middle" align="left">
<italic>Aphis gossypii</italic> infestations, total phenolics, stress symptoms</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B1">Abd El-Aal et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Modan</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">10-40% light transmission</td>
<td valign="middle" align="left">Yield (+48%), leaf area, dry weight,<break/>transpiration, stomatal conductance, CO<sub>2</sub> assimilation</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B83">Tafoya et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="3" align="left">
<italic>Diplotaxis tenuifolia</italic> L.</td>
<td valign="middle" align="left">Nature</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">50-79 % light extinction, 64.6%-76.8% PAR reduction</td>
<td valign="middle" align="left">Se, antioxidant activity (e. g., ascorbic acid and lipophilic, phenolic compounds)</td>
<td valign="middle" align="left">5.93-15.01% temperature</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B21">Caruso et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Reset</td>
<td valign="middle" align="left">PMMA</td>
<td valign="middle" align="left">Converts UV radiation into R and B, enhancing spectral quality</td>
<td valign="middle" align="left">yield (+30%), photosynthetic efficiency, chlorophyll content, antioxidant activity, leaf greenness</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B72">Paradiso et&#xa0;al. (2023)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Ramat</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">R/FR, B/R, or B/FR ratios alternation</td>
<td valign="middle" align="left">Yield, flowers and fruits quality</td>
<td valign="middle" align="left">Height</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B49">Li et&#xa0;al. (2000)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Eruca vesicaria</italic> L.</td>
<td valign="middle" align="left">Rocket</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">27% UV-B transmission</td>
<td valign="middle" align="left">Secondary metabolite (e. g., phenolic acids and flavonoids, luteolin and quercetin)</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B64">Mormile et&#xa0;al. (2019)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Fragaria &#xd7; ananassa</italic> L.</td>
<td valign="middle" align="left">Elsanta</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">68-88% PAR transmission, of R/FR, B/R, or B/FR ratios alternation</td>
<td valign="middle" align="left">Yield (+51%), flowers and fruits quality (more compact)</td>
<td valign="middle" align="left">Petiole length</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B32">Fletcher et&#xa0;al. (2002)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Lactuca sativa</italic> L.</td>
<td valign="middle" align="left">Kucheryavets Odesskiy</td>
<td valign="middle" align="left">PP, PLA</td>
<td valign="middle" align="left">R enhancement by 26%, B and Y-G light reduction</td>
<td valign="middle" align="left">Biomass<break/>photosynthesis rates<break/>leaf area, carbon assimilation, WUE</td>
<td valign="middle" align="left">Stomatal conductance, transpiration</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B45">Khramov et&#xa0;al. (2022)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Mimosa Roxa Salad Bowel</td>
<td valign="middle" align="left">PSF</td>
<td valign="middle" align="left">Temperature reduction up to 1.9&#xa0;&#xb0;C,</td>
<td valign="middle" align="left">Fresh and dry weight, leaf area, stem elongation, highest SPAD chlorophyll, flavonoid and anthocyanin</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B8">Amaro de Sales et&#xa0;al. (2021)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Malus domestica</italic> L.</td>
<td valign="middle" align="left">Pinova, Fuji Kiku 8</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">7-18% UV transmission</td>
<td valign="middle" align="left">Fruit color intensity</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B18">Blanke (2008)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Medicago truncatula</italic> L.</td>
<td valign="middle" align="left">Jemalong A17, F83005-5</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">Wavebands transmission UV-B: 290&#x2013;315 nm, UV-Asw: 315&#x2013;350 nm, UV-Alw: 350&#x2013;400 nm, B: 400&#x2013;500 nm</td>
<td valign="middle" align="left">Epidermal UV screening, Chalcone synthase, transcript abundance, acclimation to drought stress</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B76">Rai (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Prunus avium</italic> L.</td>
<td valign="middle" align="left">Lapins</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">R/FR reduction, R, B, and R-B absorb UV and re-emit it as R, B, or both</td>
<td valign="middle" align="left">Apical shoot growth, more vegetative activity</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B79">Schettini and Vox (2010)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Prunus persica</italic> L.</td>
<td valign="middle" align="left">Messapia</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">R/FR reduction, R, B, and R-B absorb UV and re-emit it as R, B, or both</td>
<td valign="middle" align="left">Annual shoot growth and shoot length</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B79">Schettini and Vox (2010)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Rubus idaeus</italic> L.</td>
<td valign="middle" align="left">San Rafael</td>
<td valign="middle" align="left">EVA</td>
<td valign="middle" align="left">Enhances B (400&#x2013;500 nm) and R light (600&#x2013;700 nm)</td>
<td valign="middle" align="left">Yield (+15%), flower production, sugar content</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B48">Lemari&#xe9; et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="3" align="left">
<italic>Solanum lycopersicum</italic> L.</td>
<td valign="middle" align="left">Brenda</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">90-100% UVA transmission, Anti NIR, heat reduction, LDe for cooler environments</td>
<td valign="middle" align="left">Highest yield, quality and market distribution</td>
<td valign="middle" align="left">Anti NIR and LDe provided the lowest yields due to reduced PAR and higher temperatures</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B53">Lopez Marin et&#xa0;al. (2019)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Oasis and Genio</td>
<td valign="middle" align="left">Glass</td>
<td valign="middle" align="left">20% light transmission, dye-sensitized solar cell filters UV to enhance R and FR</td>
<td valign="middle" align="left">Lycopene, &#x3b2;-carotene, antioxidant capacity</td>
<td valign="middle" align="left">Yield, chlorophyll content, transpiration rate, stomatal conductance, photosynthetic rate</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B68">Ntinas et&#xa0;al. (2019)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Glass, PE</td>
<td valign="middle" align="left">NIR filters: heat reduction, and FIR filters heat retention</td>
<td valign="middle" align="left">Yield (+3-10%)</td>
<td valign="middle" align="left">Water use</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B78">Romero et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="2" align="left">
<italic>Solanum melongena</italic> L.</td>
<td valign="middle" align="left">Tracey</td>
<td valign="middle" align="left">Glass with DSSC</td>
<td valign="middle" align="left">Filters sunlight to reduce R and B transmission while reducing overall light intensity</td>
<td valign="middle" align="left">Flower abortion rates, total sugars</td>
<td valign="middle" align="left">Xanthophyll pigments (e. g., antheraxanthin, zeaxanthin, violaxanthin), yield</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B25">Chavan et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Ecavi</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">3-5% UV transmission</td>
<td valign="middle" align="left">Yield (+20%), height, leaf production, fruit quantity</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B46">Kittas et&#xa0;al. (2006)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Solanum tuberosum</italic> L.</td>
<td valign="middle" align="left">Sirtema</td>
<td valign="middle" align="left">EVA</td>
<td valign="middle" align="left">B (400&#x2013;500 nm) and R light (600&#x2013;700 nm) enhancement</td>
<td valign="middle" align="left">Yield (+11-13%) harvest time advanced by 8 days, small-sized tubers.</td>
<td valign="middle" align="left"/>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B48">Lemari&#xe9; et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Triticum durum</italic> L.</td>
<td valign="middle" align="left">Cappelli</td>
<td valign="middle" align="left">PE</td>
<td valign="middle" align="left">Reduction R/FR R, B, and R- B absorb UV radiation and retransmit it in specific wavelengths (R, B, or both)</td>
<td valign="middle" align="left">Stem height, dry weight, lateral tiller production (with differences in tiller survival between R and B)</td>
<td valign="middle" align="left">Stomatal conductance, lateral tillers, leaf area</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B29">De Salvador et&#xa0;al. (2008)</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>The increasing or decreasing effects and the related percentage refer to results obtained in DCs compared to the corresponding clear covers.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>Leafy vegetables, such as <bold>lettuce</bold>, show strong adaptability to spectral modifications, that enhance photosynthesis and biomass accumulation while improving water use efficiency and secondary metabolite production, hence they are suitable as advanced light manipulation technologies. In lettuce, polypropylene covers increasing R and reducing B and Y-G light significantly improved the assimilation rate and reduced stomatal conductance and transpiration, leading to a higher water use efficiency and biomass compared to non-modified cover (<xref ref-type="bibr" rid="B45">Khramov et&#xa0;al., 2022</xref>). Additionally, photoselective films enhanced both stress tolerance and produce quality in red lettuce by decreasing temperature (up to 1.9 &#xb0;C), boosting leaf area, chlorophyll content, fresh and dry weight, as well as secondary metabolites, including flavonoids and anthocyanins (<xref ref-type="bibr" rid="B8">Amaro de Sales et&#xa0;al., 2021</xref>).</p>
<p>
<bold>Wild rocket</bold> (cultivar &#x2018;Reset&#x2019;) showed a 30% improvement in chlorophyll content and consequently a higher photosynthetic efficiency and leaf growth and yield due to UV-to-R/B spectrum conversion (<xref ref-type="bibr" rid="B72">Paradiso et&#xa0;al., 2023</xref>). By converting harmful UV radiation, these films can improve crop resilience to sunlight-induced stress playing a pivotal role in mitigating abiotic stress, as reported by <xref ref-type="bibr" rid="B70">Pandey et&#xa0;al. (2023)</xref>.</p>
<p>Members of Cucurbitaceae family exhibit notable responses to light manipulation strategies. <bold>Melon</bold> (<italic>Cucumis melo</italic> L.) showed a strong benefit from spectral changes in terms of productivity. Precisely, ethylene-vinyl acetate (EVA) films enhancing B and R transmission boosted yield by 52% (through both fruit size and weight) and sugar content, compared to standard film (<xref ref-type="bibr" rid="B48">Lemari&#xe9; et&#xa0;al., 2018</xref>). Furthermore, NIR-absorbing PE films alleviate heat stress in melon, maintaining photosynthesis and enhancing soluble solids (<xref ref-type="bibr" rid="B66">Murakami et&#xa0;al., 2017</xref>).</p>
<p>These findings highlight the potential of targeted light management for optimizing fruit quality and yield. <bold>Cucumber</bold> plants showed a better growth under UV-transmitting covers, which increased yield by 21-25%, and enhanced leaf chlorophyll and phosphorus content. Furthermore, visible light diffusion through these covers mitigated environmental stress symptoms, leading to better plant health and reducing <italic>Aphis gossypii</italic> infestations (<xref ref-type="bibr" rid="B1">Abd El-Aal et&#xa0;al., 2018</xref>).</p>
<p>Members of the Solanaceae family, such as tomato, eggplant, and potato, show varying responses to PhCs materials and light manipulation strategies. <bold>Tomato</bold> grown under PE films with high UVA transmission (90-100%) and anti-NIR properties achieved higher yields and better fruit quality compared to the corresponding conventional cover. However, in some environments, anti-NIR films reduced PAR and raised temperatures, which negatively impacted yields. The PE covers with 3-5% UV transmission boosted <bold>eggplant</bold> yield by 20%, along with improvements in height, leaf production, and fruit quantity (<xref ref-type="bibr" rid="B46">Kittas et&#xa0;al., 2006</xref>). <bold>Potato</bold> (<italic>Solanum tuberosum</italic> L.) under EVA covers enhancing B and R transmission showed a yield increase of 11-13% (through more numerous smaller tubers) and enabled an earlier harvest (-8 days) compared to the standard EVA film without photoselective additives (<xref ref-type="bibr" rid="B48">Lemari&#xe9; et&#xa0;al., 2018</xref>).</p>
<p>EVA copolymer-enhanced covers applied to <bold>watermelon</bold> (<italic>Citrullus lanatus</italic> L.) and <bold>potato</bold> improved fruit size and weight, sugar content, and yield (+10-12%), while anticipating the harvest (<xref ref-type="bibr" rid="B48">Lemari&#xe9; et&#xa0;al., 2018</xref>). In <bold>tomato</bold>, plants under 90-100% UV-A transmission films achieved superior fruit yield and quality compared to other light-modifying technologies such as LDe (light diffusing energy) and anti-NIR covers (<xref ref-type="bibr" rid="B53">Lopez Marin et&#xa0;al., 2019</xref>). These covers can enhance secondary metabolite production, enriching the nutritional value of crops. For example, UV-B blocking films increased the phenolic acids and quercetin content in <bold>rocket</bold> (<italic>Eruca vesicaria</italic>), bolstering the plant stress resilience (<xref ref-type="bibr" rid="B64">Mormile et&#xa0;al., 2019</xref>), and high R/FR ratios enhanced the antioxidant activity in <bold>strawberries</bold> (<italic>Fragaria &#xd7; ananassa</italic> L.) (<xref ref-type="bibr" rid="B32">Fletcher et&#xa0;al., 2002</xref>).</p>
<p>Beside the plant growth and metabolism, specific spectrum manipulation can alleviate biotic stress by controlling pathogen development and improving the plant reaction. For instance, a negative impact on fungi can be due to the higher UV-A transmission, such as in certain diffusive PEs, that may create unfavorable conditions for fungal growth and reproduction, inhibiting spore germination and mycelium development. Besides, a positive influence on the plant can depend on the enhanced light availability, improving photosynthetic efficiency, leading to stronger plant vigor, and strengthening the natural defense mechanisms and tolerance to pathogen infections. Consistently, UV-blocking films helped reducing biotic stresses, significantly lowering the occurrence of fungal diseases such as powdery mildew and early blight in <bold>tomato</bold> and <bold>pepper</bold> (<xref ref-type="bibr" rid="B10">Avalos-S&#xe1;nchez et&#xa0;al., 2023</xref>).</p>
<p>In a trial for a new NIR-reflective film, <xref ref-type="bibr" rid="B7">Alsadon et&#xa0;al. (2016)</xref> measured a lowering of the average temperature by 9 &#xb0;C compared to outside the greenhouse. The experiment also compared other commercial covers (no details on the types), which also showed a temperature decrease but of smaller magnitude (7 and 6 &#xb0;C). Gas exchange parameters (photosynthetic and transpiration rate, and stomatal conductance) were associated with temperature variations, showing an inverse correlation with temperatures. The improvement in photosynthetic response resulted in a higher yield in <bold>cucumber</bold> (<italic>Cucumis sativus</italic> L.).</p>
<p>Red light enriched spectra stimulated tiller production and shoot growth in <bold>wheat</bold> (<italic>Triticum aestivum</italic> L.) (<xref ref-type="bibr" rid="B29">De Salvador et&#xa0;al., 2008</xref>).</p>
<p>Various hail nets (red, blue, grey, and white) with photoselective properties were tested on <bold>kiwifruit</bold> (<italic>Actinidia chinensis</italic> var. <italic>deliciosa</italic> A. Chev.), with a shading effect ranging from 20.4% to 27.3% of PAR (<xref ref-type="bibr" rid="B16">Basile et&#xa0;al., 2012</xref>). All net treatments determined an increment in light scattering and changes in light spectrum and influenced productive traits: red and blue nets increased fruit weight and dry matter content, while grey and white nets improved fruit firmness and reduced fruit drop, indicating that net color can be used to modulate both fruit yield and quality. However, different response to shading and spectral changes were observed in the two years of observation, highlighting the occurrence of the interaction of treatments with climate conditions.</p>
<p>On plants of the genus <bold>
<italic>Prunus</italic>
</bold> (<italic>P. avium</italic> L. and <italic>P. persica</italic> L.) grown in pots, various plastic photoselective and photoluminescent films were tested, revealing that altering the spectrum (mainly R and FR) affected the vegetative activity and photomorphogenesis of cherry and peach shoot, and highlighting how the use of B photoselective films is useful in containing the plant size while R and G covers to increase it (<xref ref-type="bibr" rid="B79">Schettini and Vox, 2010</xref>).</p>
<p>In <bold>lemon</bold> (<italic>Citrus jambhiri</italic> L.), red nets help mitigate thermal stress by diffusing solar radiation, which reduces excessive heat buildup and enhances nutrient content and growth (<xref ref-type="bibr" rid="B20">Brar et&#xa0;al., 2020</xref>).</p>
<p>In the ornamental plant <bold>
<italic>Anthurium andraeanum</italic>
</bold>, PE, NIR filters increase the flower stem yields by 3-10% (<xref ref-type="bibr" rid="B78">Romero et&#xa0;al., 2018</xref>). In <bold>chrysanthemum</bold> (<italic>Dendranthema grandiflorum</italic> L.), R-FR spectrum enhanced plant height and flower quality (<xref ref-type="bibr" rid="B49">Li et&#xa0;al., 2000</xref>).</p>
<sec id="s4_2_1">
<label>4.2.1</label>
<title>Luminescent photoselective covers (LPhCs)</title>
<p>The luminescent photoselective covers include the three primary classes of materials used in luminescent covers: organic dye molecules, quantum dots, and rare earth ions.</p>
<p>Organic-Based Dyes in Luminescent Covers (ODLC), especially polycyclic aromatic hydrocarbons (PAHs), offer significant potential for LPhCs due to their high fluorescence quantum yields and affordability. These dyes absorb light at specific wavelengths (efficiently shifting photons with energies above their bandgap) and convert it into usable energy, while light at other wavelengths either passes through the material or is dissipated as heat. PAHs, such as perylene derivatives, excel in absorbing G light, which is less efficient for photosynthesis than B or R, making them advantageous for the agricultural use (<xref ref-type="bibr" rid="B14">Banal et&#xa0;al., 2017</xref>).</p>
<p>Quantum Dots (QDs) in LPhCs exhibit fluorescence in colors that vary with the particle size, with smaller crystals emitting shorter wavelengths. This size-dependent tunability enables the precise control over the light spectrum emission (<xref ref-type="bibr" rid="B77">Resch-Genger et&#xa0;al., 2008</xref>). In greenhouse applications, QDs embedded in films transform UV and B into R radiation that better support photosynthesis (<xref ref-type="bibr" rid="B54">Makarov et&#xa0;al., 2019</xref>). Compared to organic dyes such as PAHs, QDs offer a greater separation between absorbance and emission spectra, minimizing reabsorption and improving light efficiency (<xref ref-type="bibr" rid="B54">Makarov et&#xa0;al., 2019</xref>). Nonetheless, practical challenges persist in modulating QDs emission to match the plant requirement and optimize growth, as environmental variables like sunlight intensity and geographical location can influence their effectiveness (<xref ref-type="bibr" rid="B80">Shen and Yin, 2022</xref>).</p>
<p>These innovative LPhCs enhance photosynthetic efficiency, significantly benefiting leafy greens in growing conditions with limited PAR, by improving plant physiological traits and enhancing pigment concentrations and overall leaf health. In <bold>wild rocket</bold> (<italic>Diplotaxis tenuifolia</italic> L.), photoluminescent films promoted photosynthetic pigment concentrations (<xref ref-type="bibr" rid="B72">Paradiso et&#xa0;al., 2023</xref>).</p>
<p>Dye-Sensitized Solar Cell (DSSC) integrated glass reduced light intensity, mitigating flower abortion while boosting xanthophyll pigments such as zeaxanthin and violaxanthin in <bold>eggplant</bold> (<xref ref-type="bibr" rid="B25">Chavan et&#xa0;al., 2020</xref>). Advanced glass covers with DSSC filters (UV- and FR- blocking) improved chlorophyll content and photosynthetic rates, and enhanced lycopene, &#x3b2;-carotene, total carotenoids and antioxidant capacities in <bold>tomato</bold> cultivars (<xref ref-type="bibr" rid="B68">Ntinas et&#xa0;al., 2019</xref>). In contrast, the use of these covers on <bold>pepper</bold> (<italic>Capsicum annuum</italic> L.) reduced the stomata size and abscisic acid production, resulting in a faster stomatal response to light changes, and compromising water use efficiency (<xref ref-type="bibr" rid="B93">Zhao et&#xa0;al., 2021</xref>). Similarly, <bold>cabbage</bold> (<italic>Brassica oleracea</italic> L.) showed higher photosynthetic rate under increased R and reduced B and Y-G wavelengths (<xref ref-type="bibr" rid="B45">Khramov et&#xa0;al., 2022</xref>).</p>
<p>High quantum efficiency and durability of materials are priority features in designing luminescent solar concentrators (LSCs) (<xref ref-type="bibr" rid="B37">Griffini et&#xa0;al., 2013</xref>). Integrating photovoltaic (PV) technologies into greenhouse settings has frequently led to yield reductions (<xref ref-type="bibr" rid="B27">Cossu et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B52">Loik et&#xa0;al., 2017</xref>), although spectral-shifting covers using perylene and QDs were proven to improve the productive crop potential. However, cost-efficiency often outweighs high-performance requisites in horticulture. This balance between cost and crop productivity continues to drive innovation in greenhouse technologies.</p>
</sec>
</sec>
<sec id="s4_3">
<label>4.3</label>
<title>Switchable covers (SCs)</title>
<p>The main properties of switchable covers are summarized in <xref ref-type="fig" rid="f2">
<bold>Figures&#xa0;2</bold>
</xref> and <xref ref-type="fig" rid="f3">
<bold>3</bold>
</xref>. The optimal characteristics of a greenhouse cover vary according to the geographic location and crop type, as no single cover material is universally suited to all crop-climate combinations. Typically, greenhouse covers have fixed optical properties that regulate the amount of sunlight entering the structure. As a result, the intensity and quality of sunlight (including spectrum and balance between direct and diffused light) may not be ideal for the crop throughout its growth cycle, since light requirements change in the developmental stages (<xref ref-type="bibr" rid="B13">Baeza et&#xa0;al., 2019</xref>). To address these limitations, new materials with switchable optical properties are being developed, allowing nearly instant adjustments to light conditions inside the greenhouse or employing supplementary methods like temporary coatings, mobile/fixed screens, and heating/cooling systems (<xref ref-type="bibr" rid="B13">Baeza et&#xa0;al., 2019</xref>).</p>
<fig id="f3" position="float">
<label>Figure&#xa0;3</label>
<caption>
<p>Material properties and effects on greenhouse environment and plant behavior of the different innovative greenhouse covers.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fpls-16-1640530-g003.tif">
<alt-text content-type="machine-generated">Diagram illustrating three types of greenhouse covers: Diffusive, Photoselective, and Switchable. Diffusive covers enhance light diffusion and reduce temperature fluctuations, benefiting photosynthesis and plant growth. Photoselective covers modify light spectrum transmission to improve photosynthesis and flowering. Switchable covers adjust to seasonal changes, preventing stress and enhancing crop yield and quality. Each section includes a greenhouse illustration with the sun's rays.</alt-text>
</graphic>
</fig>
<p>Switchable covers (SCs) are dynamic materials that adjust their features in response to environmental changes, such as temperature or light intensity, offering greater flexibility in regulating light and thermal parameters during the different plant developmental stages. These covers dynamically filter PAR and NIR light, optimizing light quality to improve photosynthesis. For instance, electrochromic and thermochromic covers adjust transparency in response to environmental triggers, optimizing the growth conditions in greenhouse. This technology reduces the heat stress while enhancing photosynthetic efficiency, ensuring consistent growth even in extreme conditions (<xref ref-type="bibr" rid="B13">Baeza et&#xa0;al., 2019</xref>, <xref ref-type="bibr" rid="B11">2020</xref>). Many PhCs and SCs are engineered with UV stabilizers and weather-resistant polymers to extend lifespan up to 10&#x2013;15 years (e.g., <xref ref-type="bibr" rid="B18">Blanke, 2008</xref>; <xref ref-type="bibr" rid="B11">Baeza et&#xa0;al., 2020</xref>).</p>
<p>Effects of SCs on plant growth, photosynthesis and secondary metabolism in vegetables and ornamentals are shown in <xref ref-type="table" rid="T3">
<bold>Table&#xa0;3</bold>
</xref>.</p>
<table-wrap id="T3" position="float">
<label>Table&#xa0;3</label>
<caption>
<p>Effects of switchable covers (SCs) on plant growth, photosynthesis and secondary metabolites content in vegetable and ornamental crops.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" rowspan="2" align="center">Species</th>
<th valign="middle" rowspan="2" align="center">Cultivar</th>
<th valign="middle" rowspan="2" align="center">Material composition</th>
<th valign="middle" rowspan="2" align="center">Cover characteristic</th>
<th valign="middle" colspan="2" align="center">Effects on plant growth, photosynthesis, secondary metabolites</th>
<th valign="middle" rowspan="2" align="center">References</th>
</tr>
<tr>
<th valign="middle" align="center">Increase</th>
<th valign="middle" align="center">Decrease</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="middle" align="left">
<italic>Anthurium andraeanum</italic> L.</td>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Thermochromic glass</td>
<td valign="middle" align="left">Switchable FIR filter (65% reduction)</td>
<td valign="middle" align="left">Yield (+3-10%)<break/>Estimated data (Modelling study)</td>
<td valign="middle" align="left">NIR-selective filters: water use</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B78">Romero et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Cucumis melo</italic> L.</td>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Thermochromic PC</td>
<td valign="middle" align="left">Passive heating during cold season, cooling effect at high temperatures</td>
<td valign="middle" align="left">Early flowering, stable, sugar content</td>
<td valign="middle" align="left">Heat stress</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B70">Pandey et&#xa0;al. (2023)</xref>
</td>
</tr>
<tr>
<td valign="middle" rowspan="4" align="left">
<italic>Solanum lycopersicum</italic> L.</td>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Electrochromic glass</td>
<td valign="middle" align="left">NIR selective filters, TIR filters<break/>dynamic control of light transmission (NIR, PAR, TIR), change properties based on temperature (28&#xb0;-30&#xa0;&#xb0;C)</td>
<td valign="middle" align="left">Yield (+12-22%), fruit quality, microclimate control</td>
<td valign="middle" align="left">Energy and resource use, disease risk</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B13">Baeza et&#xa0;al. (2019)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Thermochromic polymer: VO<sub>2</sub>
<break/>Photochromic polymer: SPs, DAEs<break/>Electrochromic polymer: PANI, PEDOT</td>
<td valign="middle" align="left">PAR + NIR filters; dynamic adaptation to high solar radiation; automatic shading effect in response to temperature (26&#xb0;-32&#xa0;&#xb0;C)</td>
<td valign="middle" align="left">Yield (+15%)<break/>Estimated data (Modelling study)</td>
<td valign="middle" align="left">Water consumption, supra-optimal temperature exposure</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B11">Baeza et&#xa0;al. (2020)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Thermochromic PE</td>
<td valign="middle" align="left">Switchable NIR filter (10% PAR reduction), 28&#xb0;-30&#xa0;&#xb0;C</td>
<td valign="middle" align="left">Yield (+15-20%)</td>
<td valign="middle" align="left">Potential winter performance</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B78">Romero et&#xa0;al. (2018)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Thermochromic PE: (OPV)<break/>Review article</td>
<td valign="middle" align="left">Dynamically adjusts light transmission based on sunlight intensity</td>
<td valign="middle" align="left">Yield (+19%), earlier harvest, fruit quality, WUE</td>
<td valign="middle" align="left">Heat stress</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B82">Soussi et&#xa0;al. (2022)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Solanum tuberosum</italic> L.</td>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Thermochromic laminated PE</td>
<td valign="middle" align="left">Adaptive light control, extreme heat reduction</td>
<td valign="middle" align="left">Growth, earlier harvest</td>
<td valign="middle" align="left">Risk of temperature-related stress</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B70">Pandey et&#xa0;al. (2023)</xref>
</td>
</tr>
<tr>
<td valign="middle" align="left">
<italic>Rubus idaeus</italic> L.</td>
<td valign="middle" align="left">Unspecified</td>
<td valign="middle" align="left">Thermochromic glass with IR filtering</td>
<td valign="middle" align="left">Dynamic shading effect, temperature fluctuations reduction</td>
<td valign="middle" align="left">Fruit quality, better sugar accumulation</td>
<td valign="middle" align="left">Excessive shading effects</td>
<td valign="middle" align="left">
<xref ref-type="bibr" rid="B70">Pandey et&#xa0;al. (2023)</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>The increasing or decreasing effects and the related percentage refer to results obtained in DCs compared to the corresponding clear covers.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>In Mediterranean climates, these covers can significantly improve light and temperature conditions, especially in regions with fluctuating climate (<xref ref-type="bibr" rid="B78">Romero et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B82">Soussi et&#xa0;al., 2022</xref>). Indeed, SCs stabilize physiological processes by preventing excessive transpiration and reducing stress-induced metabolic changes. It is modelled that this regulation promotes crop health in high-value vegetables like <bold>tomato</bold> and ornamentals like <bold>
<italic>Anthurium andraeanum</italic>
</bold>, ensuring stable growth even under challenging environmental conditions (<xref ref-type="bibr" rid="B78">Romero et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B82">Soussi et&#xa0;al., 2022</xref>). It is estimated that under SCs <bold>tomato</bold> yield can increase up to 20% due to the improved environmental conditions (<xref ref-type="bibr" rid="B78">Romero et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B13">Baeza et&#xa0;al., 2019</xref>). Additionally, by stabilizing temperature and minimizing stress responses, SCs have an indirect positive influence on plant hormonal balance. This is particularly beneficial for sensitive crops like <bold>tomato</bold>, where hormonal disruptions can negatively impact plant productivity (<xref ref-type="bibr" rid="B78">Romero et&#xa0;al., 2018</xref>).</p>
<p>For fruit crops, in <bold>melons</bold>, SCs promoted early flowering and increased sugar content while mitigating heat stress during high temperature periods (<xref ref-type="bibr" rid="B70">Pandey et&#xa0;al., 2023</xref>). Dynamic shading improved fruit quality and sugar accumulation in <bold>raspberry</bold> (<italic>Rubus idaeus</italic>), though excessive shading remains a potential drawback (<xref ref-type="bibr" rid="B70">Pandey et&#xa0;al., 2023</xref>).</p>
<p>In tuber crops like <bold>potato</bold> (<italic>Solanum tuberosum</italic> L.), thermochromic covers help regulate temperature, reducing extreme heat exposure and promoting growth and earlier harvest (<xref ref-type="bibr" rid="B70">Pandey et&#xa0;al., 2023</xref>).</p>
<p>Overall, the efficiency of SCs varies across the crop types: to summarize, high-value ornamentals benefit from stabilized physiological processes, root and tuber crops experience enhanced early growth, and fruit vegetables show improvements in yield, fruit quality, and stress tolerance. However, SCs application is influenced by several other factors, such as initial and maintenance costs, crop productivity goals, local climate, and technological support (<xref ref-type="bibr" rid="B3">Ahmadi et&#xa0;al., 2018</xref>).</p>
</sec>
<sec id="s4_4">
<label>4.4</label>
<title>Control technologies and technological relevance</title>
<p>
<bold>Passive dynamic control technologies</bold> represent a significant advancement in greenhouse management, as they automatically adapt their properties in response to environmental changes, without requiring external energy input. These technologies allow materials to react to varying climate parameters such as temperature, sunlight, and humidity, thereby enhancing the energy efficiency while maintaining better growth conditions in greenhouse (<xref ref-type="bibr" rid="B82">Soussi et&#xa0;al., 2022</xref>; <xref ref-type="bibr" rid="B90">Zhang et&#xa0;al., 2022</xref>; <xref ref-type="bibr" rid="B35">Ghiasi et&#xa0;al., 2023</xref>). For instance, thermochromic materials alter their properties based on temperature fluctuations, effectively reducing heat gain and providing thermal comfort for the plants (<xref ref-type="bibr" rid="B69">Padilla et&#xa0;al., 2021</xref>). Similarly, photochromic materials adjust their transparency in response to light levels, minimizing the glare (<xref ref-type="bibr" rid="B67">Nikolaou et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B50">Lin et&#xa0;al., 2022</xref>). Additionally, photoelectric materials, including crystalline and inorganic thin-film glazing, not only provide shading to protect plants from excessive sunlight but also generate energy, further contributing to the sustainability of greenhouse operations (<xref ref-type="bibr" rid="B85">Timmermans et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B58">Maraveas et&#xa0;al., 2021</xref>, <xref ref-type="bibr" rid="B56">2023a</xref>).</p>
<p>to modify their properties, facilitating real- By integrating these innovative materials, greenhouse managers can optimize growing conditions while saving resources.</p>
<p>
<bold>Active dynamic control technologies</bold> require an external energy source time adjustments tailored to specific environmental conditions (<xref ref-type="bibr" rid="B11">Baeza et&#xa0;al., 2020</xref>). These systems provide a precise control over light transmission and diffusion, which can significantly enhance plant growth and energy efficiency. For instance, electrochromic materials can change their opacity or color in response to an applied electric current, allowing for meticulous control over both light and heat transmission (<xref ref-type="bibr" rid="B11">Baeza et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B56">Maraveas et&#xa0;al., 2023a</xref>). On the other hand, mechano-chromic materials adjust their properties through mechanical inputs, such as deformation, which further enhances their adaptation to varying environmental scenarios (<xref ref-type="bibr" rid="B39">Guo et&#xa0;al., 2024</xref>). Additionally, polarized particle devices, including Suspended Particle Devices (SPDs) and Polymer Dispersed Liquid Crystals (PDLCs), are controlled via electrical signals to effectively modulate light and heat in the greenhouse (<xref ref-type="bibr" rid="B36">Ghosh et&#xa0;al., 2024</xref>). By incorporating these advanced technologies, greenhouse operators can optimize growing conditions dynamically, to improve crop yield and resource management.</p>
<p>To improve plastic properties, like temperature resistance, heat dissipation, droplet formation and dust deposition prevention, some functional additives, fillers, air bubbles, reinforcements (e.g., glass or carbon fiber), and colorants are often incorporated <xref ref-type="bibr" rid="B22">Castilla (2013)</xref>. Examples are UV absorbers and stabilizers that help protect plants in greenhouse while blocking UV-B radiation over 40 kJ/m&#xb2;, controlling the UV transmission rate, typically 70-90% in common materials (<xref ref-type="bibr" rid="B91">Zhang et&#xa0;al., 2019</xref>). Anti-fog and IR-blocking additives further prevent fogging and restrict harmful IR radiation (<xref ref-type="bibr" rid="B46">Kittas et&#xa0;al., 2006</xref>).</p>
<p>To protect plastic films and panels from UV damage and photodegradation, stabilizers and additives like black carbon modify the optical properties of cladding materials (<xref ref-type="bibr" rid="B4">Aldaftari et&#xa0;al., 2019</xref>). The UV absorbers and additives also shield plants from harmful radiation and help limit the spread of pests and pathogens (<xref ref-type="bibr" rid="B9">Ant&#xf3;n et&#xa0;al., 2014</xref>).</p>
<p>Infrared light absorbers minimize heat loss and short-wave emission, typically having wavelengths between 700 and 2500 nm. Long-wave absorbers (2500-40,000 nm) reduce heat loss from plants in greenhouse by absorbing these wavelengths. Surfactants and antistatic agents lower surface tension to reduce the dust accumulation on plastic films (<xref ref-type="bibr" rid="B57">Maraveas et&#xa0;al., 2023b</xref>).</p>
<p>Red-emitting plastic greenhouse extensions provide stunning and vivid patterns and colors. As the pigment volume fraction increases, the efficiency of greenhouse gases rises. For optimal radiation control, HVAC (heating, ventilation, and air conditioning) systems are generally more effective than pigments, as titanium dioxide (TiO<sub>2</sub>) and diamond particles in pigments can selectively reflect near-IR (800&#x2013;2500 nm) while transmitting visible light at shorter wavelengths (<xref ref-type="bibr" rid="B4">Aldaftari et&#xa0;al., 2019</xref>).</p>
<p>Diamond-based pigments are advanced materials used in greenhouse cladding to optimize light management and thermal control. They effectively reduce heat buildup while allowing sufficient light for photosynthesis, offering a cost-efficient alternative to traditional cooling systems. Their unique optical properties enable them to reflect near-IR radiation while transmitting visible light, surpassing conventional pigments like TiO<sub>2</sub> in performance. Additionally, TiO<sub>2</sub> particles are less effective in reflecting IR radiation, and diamond particle-based pigments have been shown to reduce radiation (<xref ref-type="bibr" rid="B4">Aldaftari et&#xa0;al., 2019</xref>). Transparent Solar Distillers (TSD) combine TiO<sub>2</sub> nanoparticles in multi-purpose greenhouse coverings to use solar energy for water desalination (<xref ref-type="bibr" rid="B75">Rabhy et&#xa0;al., 2019</xref>). These TSD pigments also enhance greenhouse cladding by managing incoming and outgoing energy wavelengths. By filtering high-energy wavelengths during the day, greenhouse covers prevent overheating while ensuring sufficient light for photosynthesis. At night, they retain heat by limiting long-wavelength energy loss, supporting stable internal temperatures for crop growth and development.</p>
<p>One of the more recent innovations involves the use of antimony tin oxide (ATO) nanoparticles in plastic films, which help manage solar radiation while maintaining adequate light levels for photosynthesis. These nanoparticles reduce the amount of heat absorbed by the greenhouse while allowing enough PAR to pass through, ensuring both energy efficiency and healthy crop growth (<xref ref-type="bibr" rid="B89">Zhang et&#xa0;al., 2024a</xref>).</p>
</sec>
</sec>
<sec id="s5" sec-type="discussion">
<label>5</label>
<title>Discussion and conclusions</title>
<p>The reviewed studies highlight the importance of selecting the appropriate greenhouse cover based on the specific climatic conditions, crop type, and desired outcomes. Smart covers support sustainable greenhouse farming by regulating light and temperature, reducing the need for artificial lighting, heating and cooling, thereby lowering the overall energy use. Indeed, advanced materials are durable and weather-resistant, adjust transparency and minimize temperature and humidity fluctuations, enhancing plant performance, and maximizing the resource use efficiency. Besides, they filter UV rays, reducing pest diffusion and limiting chemical treatments.</p>
<p>It is worth noting that no cover type is universally superior and each one shows strengths and limitations and can fully express its potential in different crop-environment conditions.</p>
<p>
<bold>Diffusive covers</bold> improve light uniformity in the canopy profile, increasing plant photosynthesis and crop yield, especially in high-light environments. They are universally applicable across climates and crop types and are low-maintenance solutions. On the downside, they can reduce PAR, leading to disorders in light-sensitive plants.</p>
<p>
<bold>Photoselective covers</bold> determine changes in light spectrum, increasing plant growth and promoting modulation of target photomorphogenic responses (e.g., flowering, secondary metabolites biosynthesis), while reducing heat stress. Additionally, they can help alleviate pathogen pressure (via UV filtering) and microclimate adjustments (via NIR reflection). However, optimizing one wavelength can be disadvantageous to another and lead to spectrum imbalance and the increase in nutritional quality can lead to a decrease in yield. Besides, they do not allow spectrum manipulation through the crop phenological stages.</p>
<p>
<bold>Luminescent Photoselective Covers</bold> convert less useful UV radiation into photosynthetically active radiation, boosting pigment and antioxidant levels and enhancing photosynthetic performance under low-light conditions. In addition, they allow spectrum changes when weather conditions change. On the other hand, latitude impacts their reliability therefore careful system calibration is needed to avoid spectrum imbalance.</p>
<p>
<bold>Switchable covers</bold> dynamically adjust light transmission in PAR and NIR wavebands in response to environmental cues, enabling seasonal photothermal control, which improve crop performance. They offer flexibility and energy efficiency and are ideal for regions with fluctuating weather conditions. They overcome the limits of photoselective covers, allowing adjustment of light and thermal environment according to the plant requirement in the different phenological stages. Clearly this sensitivity, together with the need for frequent and efficient sensors calibration, turns out to be higher initial cost and maintenance.</p>
<p>To summarize, the simpler technologies (DC, PhC) offer benefits with lower technical requirements and cost, while more advanced technologies (LPhC, SC) allow specific and dynamic responses but need higher technical specialization of farmers and are more expensive. However, they are not mutually exclusive, hence future innovation in the greenhouse industry could rely on hybrid solutions, combining different technologies.</p>
<p>In conclusion, the adoption of innovative smart covers can provide an effective tool to enhance the produce yield and quality while reducing the greenhouse energy cost and environmental impact, but two remarks are needed. The first is that the improvement in biochemical traits (like vitamins and antioxidants) may not always translate into a greater economic gain for farmers; the second concerns the environmental impact of the cover disposal.</p>
<p>Future research should continue to optimize the spectral properties of greenhouse covers for specific crops and climates, to achieve the best possible balance between productivity and quality, and sustainability. Specifically, it should focus on the characterization of response of the different crops (particularly in high-value and specialty plants) and the fine-tuning of spectral and thermal properties of covers to meet the specific crop and climate requirements. Integrating smart technologies such as advanced sensors and automated control systems could allow for dynamic adjustments of the greenhouse environment to optimize growth conditions. Research should also prioritize the development of recyclable and biodegradable cost-effective materials to improve their environmental and economic sustainability. On these bases, collaboration between material experts, agronomists, and greenhouse engineers will be crucial in achieving breakthroughs that meet both economic and environmental needs.</p>
</sec>
</body>
<back>
<sec id="s6" sec-type="author-contributions">
<title>Author contributions</title>
<p>FZ: Data curation, Formal analysis, Writing &#x2013; original draft. LD: Data curation, Writing &#x2013; review &amp; editing. MM: Writing &#x2013; review &amp; editing, Funding acquisition. RP: Conceptualization, Funding acquisition, Writing &#x2013; review &amp; editing.</p>
</sec>
<sec id="s7" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research and/or publication of this article. The research was funded by Campania Region, through the project &#x201c;INnovare il comparto Agroalimentare moduLAndo la radiazione solaRE (INALARE)&#x201d;, Piani di sviluppo rurale (P.S.R.) 2023 - Misura 16.1.2 - Sostegno ai Gruppi Operativi del PEI (Partenariato Europeo dell&#x2019;Innovazione) per l&#x2019;attuazione di progetti di diffusione delle innovazioni nell&#x2019;ambito del rafforzamento dell&#x2019;AKIS campano, and by Ministero dell&#x2019;agricoltura, della sovranit&#xe0; alimentare e delle foreste (MASAF), through the project &#x201c;Innovazioni di processo e di prodotto in agricoltura biologica di specie officinali e loro valorizzazione (InBiOf)&#x201d;.</p>
</sec>
<ack>
<title>Acknowledgments</title>
<p>The authors gratefully acknowledge Alessandro Borrelli, Research Fellow at the University of Naples Federico II, for his support in preparing the figures.</p>
</ack>
<sec id="s8" sec-type="COI-statement">
<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>
</sec>
<sec id="s9" sec-type="ai-statement">
<title>Generative AI statement</title>
<p>The author(s) declare that no Generative AI was used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec id="s10" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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