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Lignin is one of the most studied and analyzed materials due to its importance in cell structure and in lignocellulosic biomass. Because lignin exhibits autofluorescence, methods have been developed that allow it to be analyzed and characterized directly in plant tissue and in samples of lignocellulose fibers. Compared to destructive and costly analytical techniques, fluorescence microscopy presents suitable alternatives for the analysis of lignin autofluorescence. Therefore, this review article analyzes the different methods that exist and that have focused specifically on the study of lignin because with the revised methods, lignin is characterized efficiently and in a short time. The existing qualitative methods are Epifluorescence and Confocal Laser Scanning Microscopy; however, other semi-qualitative methods have been developed that allow fluorescence measurements and to quantify the differences in the structural composition of lignin. The methods are fluorescence lifetime spectroscopy, two-photon microscopy, Föster resonance energy transfer, fluorescence recovery after photobleaching, total internal reflection fluorescence, and stimulated emission depletion. With these methods, it is possible to analyze the transport and polymerization of lignin monomers, distribution of lignin of the syringyl or guaiacyl type in the tissues of various plant species, and changes in the degradation of wood by pulping and biopulping treatments as well as identify the purity of cellulose nanofibers though lignocellulosic biomass.

Cellulose is the main polymer that gives strength to the cell wall and is located in the primary and secondary cell walls of plants. In Cactaceae, there are no studies on the composition of cellulose. The objective of this work was to analyze the crystallinity composition and anatomical distribution of cellulose in Cactaceae vascular tissue. Twenty-five species of Cactaceae were collected, dried, and milled. Cellulose was purified and analyzed with Fourier transform infrared spectroscopy, the crystallinity indexes were calculated, and statistical analyzes were performed. Stem sections were fixed, cut, and stained with safranin O/fast green, for observation with epifluorescence microscopy. The crystalline cellulose ratios had statistical differences between Echinocereus pectinatus and Coryphantha pallida. All cacti species presented a higher proportion of crystalline cellulose. The fluorescence emission of the cellulose was red in color and distributed in the primary wall of non-fibrous species; while in the fibrous species, the distribution was in the pits. The high percentages of crystalline cellulose may be related to its distribution in the non-lignified parenchyma and primary walls of tracheary elements with helical or annular thickenings of non-fibrous species, possibly offering structural rigidity and forming part of the defense system against pathogens.

Vanilla planifolia is a species of commercial importance. However, vanilla presents gene erosion problems due to its clonal reproduction. In the Huasteca of Hidalgo, there is no information on vanilla populations. Therefore, the objectives of this study were to identify the current populations and the potential distribution of, and the morphological variation in, the labellum of V. planifolia in the Huasteca of Hidalgo. Twenty-two accessions were located and selected. Based on 21 environmental variables, the niche modeling of the potential distribution was carried out with the MaxEnt program; with the Jackknife test being used to identify the variables that contributed to the model. Flowers from 22 accessions were collected and the labellum of each flower was dissected. Subsequently, 64 morphological variables were obtained and various multivariate analyses were performed. The results showed three regions, defined by the highest to the lowest probability that V. planifolia was distributed. The precipitation of the driest month, altitude, and vegetation cover delimited the distribution. Five different morphotypes were distinguished, and the main differences were associated with the middle part of the labellum as well as the entrance of pollinators to the flower; therefore, the characterization of the labellum showed an infraspecific variation in V. planifolia in populations of the Huasteca of Hidalgo.

The xylem of Cactaceae is a complex system with different types of cells whose main function is to conduct and store water, mostly during the development of primary xylem, which has vessel elements and wide-band tracheids. The anatomy of primary xylem of Cactaceae has been widely studied, but little is known about its chemical composition. The aim of this study was to determine the structural chemical composition of the primary xylem of Cactaceae and to compare it with the anatomy in the group. Seeds from eight cacti species were used, representing the Pereskioideae, Opuntioideae, and Cactoideae subfamilies. Seeds were germinated and grown for 8 months. Subsequently, only the stem of the seedling was selected, dried, milled, and processed following the TAPPI T-222 om-02 norm; lignin was quantified using the Klason method and cellulose with the Kurshner-Höffer method. Using Fourier transform infrared spectroscopy, the percentage of syringyl and guaiacyl in lignin was calculated. Seedlings of each species were fixed, sectioned, and stained for their anatomical description and fluorescence microscopy analysis for the topochemistry of the primary xylem. The results showed that there were significant differences between species ( < 0.05), except in the hemicelluloses. Through a principal component analysis, it was found that the amount of extractive-free stem and hot water-soluble extractives were the variables that separated the species, followed by cellulose and hemicelluloses since the seedlings developed mainly parenchyma cells and the conductive tissue showed vessel elements and wide-band tracheids, both with annular and helical thickenings in secondary walls. The type of lignin with the highest percentage was guaiacyl-type, which is accumulated mainly in the vessels, providing rigidity. Whereas in the wide-band tracheids from metaxylem, syringyl lignin accumulated in the secondary walls S2 and S3, which permits an efficient flow of water and gives the plant the ability to endure difficult conditions during seedling development. Only one species can be considered to have paedomorphosis since the conductive elements had a similar chemistry in primary and secondary xylem.

A biomineral is a crystalline or amorphous mineral product of the biochemical activity of an organism and the local accumulation of elements available in the environment. The cactus family has been characterized by accumulating calcium oxalates, although other biominerals have been detected. Five species of Cacteae were studied to find biominerals. For this, anatomical sections and Fourier transform infrared, field emission scanning electron microscopy and energy dispersive x-ray spectrometry analyses were used. In the studied regions of the five species, they presented prismatic or spherulite dihydrate calcium oxalate crystals, as the predominant biomineral. Anatomical sections of Astrophytum asterias showed prismatic crystals and Echinocactus texensis amorphous silica bodies in the hypodermis. New findings were for Ariocarpus retusus subsp. trigonus peaks assigned to calcium carbonate and for Mammillaria sphaerica peaks belonging to silicates.

During the last decades, the possibility of using species resistant to droughts and extreme temperatures has been analyzed for use in the production of lignocellulosic materials and biofuels. Succulent species are considered to identify their potential use; however, little is known about Asparagaceae species. Therefore, this work aimed to characterize chemically-anatomically the stems of Asparagaceae species. Stems of 10 representative species of Asparagaceae were collected, and samples were divided into two. One part was processed to analyze the chemical composition, and the second to perform anatomical observations. The percentage of extractives and lignocellulose were quantified, and crystalline cellulose and syringyl/guaiacyl lignin were quantified by Fourier transform infrared spectroscopy. Anatomy was observed with epifluorescence microscopy. The results show that there were significant differences between the various species (p < 0.05) in the percentages of extractives and lignocellulosic compounds. In addition, there were anatomical differences in fluorescence emission that correlated with the composition of the vascular tissue. Finally, through the characterization of cellulose fibers together with the proportion of syringyl and guaiacyl, it was obtained that various species of the Asparagaceae family have the potential for use in the production of lignocellulosic materials and the production of biofuels.

The shape of the flower can vary based on the type of pollinator or the environment in which the plant develops. In Vanilla insignis , there are no studies that analyse the shape of the labellum of the flower as has been done in V. planifolia . Therefore, the study aimed to determine the variation in the shape of the labellum of V. insignis through a morphometric analysis in different environmental conditions in the state of Quintana Roo, Mexico. The results showed that there were significant differences in the variables analysed. Principal component analysis and dendrogram analysis reveal that four V. insignis morphotypes were possibly associated with soil water availability conditions because there were significant differences between the variables that define the apical region. In addition, the distribution of the morphotypes corresponded with the presence of humidity regardless of geographical distances such as in the populations of Tenampulco, Puebla and Caobas, Quintana Roo. The presence of these morphotypes allows the development of conservation programmes and genetic improvement of the species of V. insignis and related commercial species.

Vanilla planifolia is a species of commercial importance. However, vanilla presents gene erosion problems due to its clonal reproduction. In the Huasteca of Hidalgo, there is no information on vanilla populations. Therefore, the objectives of this study were to identify the current populations and the potential distribution of, and the morphological variation in, the labellum of V. planifolia in the Huasteca of Hidalgo. Twenty-two accessions were located and selected. Based on 21 environmental variables, the niche modeling of the potential distribution was carried out with the MaxEnt program; with the Jackknife test being used to identify the variables that contributed to the model. Flowers from 22 accessions were collected and the labellum of each flower was dissected. Subsequently, 64 morphological variables were obtained and various multivariate analyses were performed. The results showed three regions, defined by the highest to the lowest probability that V. planifolia was distributed. The precipitation of the driest month, altitude, and vegetation cover delimited the distribution. Five different morphotypes were distinguished, and the main differences were associated with the middle part of the labellum as well as the entrance of pollinators to the flower; therefore, the characterization of the labellum showed an infraspecific variation in V. planifolia in populations of the Huasteca of Hidalgo.