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Gierlinger, N.

Publications and source records attributed to Gierlinger, N..

4 recordsLinked to original sources

Humidity-driven shape morphing enhances fog harvesting in porous cactus spines

Cacti develop spines instead of conventional leaves, which often serve as mechanical defence against herbivores and protection from excess sunlight. However, some cactus species grow porous and flexible spines, suggesting fundamentally different functions. Here we demonstrate that the porous spines of Turbinicarpus alonsoi, a cactus native to central Mexico, function as hygro-morphing fog harvesters. We discovered that the spines are highly hygroscopic and straighten when exposed to fog, leading to increased fog water collection rates. Experiments and numerical simulations confirm that straightening is driven by swelling-induced pressure in the cell walls of the spine tissue. Swelling results from capillary imbibition of fog water and predominantly generates expansion in the transverse plane, which causes the pre-curved spines to straighten. Despite their porosity and hygroscopicity, the spines prevent direct absorption of fog water into the living cortex due to the presence of a suberin-rich tissue layer at the spine base that instead promotes surface runoff towards the roots. Our work suggests that hygro-morphing emerges from distinct structural, biochemical and geometric adaptations of cactus spines, and enables a fine modulation of the flow dynamics on the surface of spines. The increasing plant water supply from fog by shape morphing provides a potential advantage for survival in a hot, semi-arid region with frequent fog formation. Significance statementIn many arid regions of the world, fog is a critical source of fresh water. Plants display striking ways to harvest this fog water. For cacti with porous spines, it has long been assumed that they collect fog water directly by capillary imbibition. However, we demonstrate that, in Turbinicarpus alonsoi, water-impermeable tissue at the spine base prevents direct transport of water into the living cortex. Instead, a dual process increases fog water collection: the curved spines initially imbibe fog water, which causes them to swell and straighten, and a thin liquid film then forms on the spine and runs off along the plant surface down to the roots. Hygro-morphing spines therefore enhance the capacity of cacti to collect fog water.

plant biology↗

3D (x-y-t) Raman imaging of tomato fruit cuticle: microchemistry during development

The cuticle of tomato fruits was studied in-situ using Confocal Raman Microscopy. Microsections from cuticles isolated at different developmental stages were scanned to reveal the distribution of cuticle components with a spatial resolution of 342 nm by univariate and multivariate data analysis. From the three main components, cutin, polysaccharides and aromatics, the latter one exhibit the strongest Raman scattering intensity. Therefore, Raman imaging opened the view on phenolic acids and flavonoids within the cuticle and resulted in three schematic cuticle models depicting development. At the earliest stage of development, which corresponded to the procuticle layer, phenolic acids were found across the entire cuticle. Based on a mixture analysis with reference component spectra, the phenolic acids were identified as mainly esterified p-coumaric acid together with free p-hydroxybenzoic acid. Later in development, during the cell expansion period of growth, phenolic acids accumulated in an outermost layer of the cuticle and in the middle region of the pegs. In these stages of development cellulose and pectin were appeared towards the epidermal layer, where later during ripening the flavonoid impregnation started. In the first ripening stage chalconaringenin was observed, while methoxylated chalcones were chosen by the algorithm to fit the mature cuticle spectra. The co-location with carbohydrates and esterified p-coumaric acid and methoxylated chalconaringenin suggest that they link polysaccharide and cutin domains. Within the cutin matrix, aromatics confer mechanical and thermal functions, while the outermost phenolic acid layer displays UV-B protection of the plant tissue. One-sentence summaryNew insights into the distribution of cutin, carbohydrates and phenolics along cross sections of green and mature tomato fruit cuticles by Raman mapping and multivariate data analysis.

biophysics↗

Mapping lignification dynamics with a combination of chemistry, data segmentation and ratiometric analysis

This article describes a new methodology for detailed mapping of the lignification capacity of plant cell walls that we have called "REPRISAL" for REPorter Ratiometrics Integrating Segmentation for Analyzing Lignification. REPRISAL consists of the combination of three separate approaches. In the first approach, H*, G* and S* monolignol chemical reporters, corresponding to p-coumaryl alcohol, coniferyl alcohol and sinapyl alcohol, are used to label the growing lignin polymer in a fluorescent triple labelling strategy based on the sequential use of 3 main bioorthogonal chemical reactions. In the second step, an automatic parametric and/or artificial intelligence (AI) segmentation algorithm is developed that assigns fluorescent image pixels to 3 distinct cell wall zones corresponding to cell corners (CC), compound middle lamella (CML) and secondary cell walls (SCW). The last step corresponds to the exploitation of a ratiometric approach enabling statistical analyses of differences in monolignol reporter distribution (ratiometric method 1) and proportions (ratiometric method 2) within the different cell wall zones. In order to demonstrate the potential of REPRISAL for investigating lignin formation we firstly describe its use to map developmentally-related changes in the lignification capacity of WT Arabidopsis interfascicular fiber cells. We then show how it can be used to reveal subtle phenotypical differences in lignification by analyzing the Arabidopsis prx64 peroxidase mutant and provide further evidence for the implication of the AtPRX64 protein in floral stem lignification. Finally, we demonstrate the general applicability of REPRISAL by using it to map lignification capacity in poplar, flax and maize.

plant biology↗

Cellulosic wall thickenings restrict cell expansion to shape the 3D puzzle sclereids of the walnut shell

Walnut (Juglans regia) kernels are protected by a tough shell consisting of polylobate sclereids that interlock into a 3D puzzle. The shape transformations from isodiametric to lobed cells is well documented for 2D pavement cells, but not for 3D puzzle sclereids. Here, we tackle the morphogenesis of these cells by using a combination of different imaging techniques. Serial face-microtomy enabled us to reconstruct tissue growth of whole walnut fruits in 3D and serial block face-scanning electron microscopy exposed cell shapes and their transformation in 3D during shell tissue development. In combination with Raman and fluorescence microscopy we revealed multiple loops of cellulosic thickenings in cell walls, acting as stiff restrictions during cell expansion and leading to the lobed cell shape. Our findings contribute to a better understanding of the 3D shape transformation of polylobate sclereids and the role of pectin and cellulose within this process.

plant biology↗