Chitin in Strawberry Cultivation: Foliar Growth and Defense Response Promotion, but Reduced Fruit Yield and Disease Resistance by Nutrient Imbalances.

Strawberry cultivation is associated with high mineral fertilizer doses and extensive use of chemical plant protection products. Based on previous research, we expected that chitin application to peat substrate would increase the nutrient availability and activate the plant systemic defense response, resulting in higher strawberry yields and fewer disease symptoms. We set up two experiments in which the temporal variability and differences in initial nutrient concentrations of the growing media were taken into account. Chitin treatment resulted in the attraction of plant growth-promoting fungi toward the plant root, such as species from genera Mortierella and Umbelopsis. In addition, by the end of the experiments 87 mg of mineral nitrogen (N) per liter of substrate was mineralized, which can be related to the observed increase in plant shoot biomass. This, however, led to nutrient imbalances in plant shoots and fruit; N concentration in the leaves increased over 30%, exceeding the optimal range, while phosphorous (P) and potassium (K) deficiencies occurred, with concentrations lower than 50% of the optimal range. This may explain the decreased fruit yield and disease resistance of the fruit toward Botrytis cinerea. In contrast, chitin caused a clear defense priming effect in the strawberry leaves, with a strong induction of the jasmonic acid response, resulting in fewer foliar disease symptoms. Chitin causes positive effects on shoot growth and foliar disease resistance, but caution needs to be taken for nutrient imbalances leading to negative influences on root growth, fruit production, and disease susceptibility toward B. cinerea.[Formula: see text] Copyright © 2021 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.

Ontogenesis of opercular deformities in gilthead sea bream Sparus aurata: a histological description.

The aim of this study was to characterize histological changes during opercular osteogenesis in farmed gilthead sea bream Sparus aurata larvae from 7 to 69 days post hatching (dph) and compare normal osteogenesis with that of deformed opercles. Mild opercular deformities were first detected in 19 dph larvae by folding of the opercle's distal edge into the gill chamber. Here, the variation in the phenotype and the irregular bone structure at the curled part of the opercles is described and compared with the histology of normal opercles. Results indicated that deformed opercles still undergo bone growth with the addition of new matrix by osteoblasts at the opercular surface, especially at its edges. No significant difference was found in bone thickness between deformed and normal opercles. In addition to differences in bone architecture, differences in collagen fibre thickness between normal and deformed opercles were also found.

Medium characterization from interface-wave impedance and ellipticity using simultaneous displacement and pressure measurements.

The interface-wave impedance and ellipticity are wave attributes that interrelate the full waveforms as observed in different components. For each of the fluid/elastic-solid interface waves, i.e., the pseudo-Rayleigh (pR) and Stoneley (St) waves, the impedance and ellipticity are found to have different functional dependencies on Young's modulus and Poisson's ratio. By combining the attributes in a cost function, unique and stable estimates of these parameters can be obtained, particularly when using the St wave. In a validation experiment, the impedance of the laser-excited pR wave is successfully extracted from simultaneous measurements of the normal particle displacement and the fluid pressure at a water/aluminum interface. The displacement is measured using a laser Doppler vibrometer (LDV) and the pressure with a needle hydrophone. Any LDV measurement is perturbed by refractive-index changes along the LDV beam once acoustic waves interfere with the beam. Using a model that accounts for these perturbations, an impedance decrease of 28% with respect to the plane wave impedance of the pR wave is predicted for the water/aluminum configuration. Although this deviation is different for the experimentally extracted impedance, there is excellent agreement between the observed and predicted pR waveforms in both the particle displacement and fluid pressure.

Determination of thermoelastic material properties by differential heterodyne detection of impulsive stimulated thermal scattering.

The underlying working principle of detecting impulsive stimulated scattering signals in a differential configuration of heterodyne diffraction detection is unraveled by involving optical scattering theory. The feasibility of the method for the thermoelastic characterization of coating-substrate systems is demonstrated on the basis of simulated data containing typical levels of noise. Besides the classical analysis of the photoacoustic part of the signals, which involves fitting surface acoustic wave dispersion curves, the photothermal part of the signals is analyzed by introducing thermal wave dispersion curves to represent and interpret their grating wavelength dependence. The intrinsic possibilities and limitations of both inverse problems are quantified by making use of least and most squares analysis.

N-cadherin is required for cytodifferentiation during zebrafish odontogenesis.

N-cadherin is a well-studied classic cadherin involved in multiple developmental processes and is also known to have a signaling function. Using the zebrafish (Danio rerio) as a model, we tested the hypothesis that tooth morphogenesis is accompanied by dynamic changes in N-cadherin distribution and that absence of N-cadherin disturbs tooth development. N-cadherin, encoded by the gene cdh2, is absent during the initiation and morphogenesis stages of both primary (first-generation) and replacement teeth, as demonstrated by immunohistochemistry. However, N-cadherin is up-regulated at the onset of differentiation of cells of the inner dental epithelium and the dental papilla, i.e., the ameloblasts and odontoblasts, respectively. In the inner dental epithelium, N-cadherin is co-expressed with E-cadherin, excluding the occurrence of cadherin switching such as observed during human tooth development. While early lethality of N-cadherin knockout mice prevents any functional study of N-cadherin in mouse odontogenesis, zebrafish parachute (pac) mutants, deficient for N-cadherin, survive beyond the age when primary teeth normally start to form. In these mutants, the first tooth forms, but its development stops at the early cytodifferentiation stage. N-cadherin deficiency also completely inhibits the development of the other first-generation teeth, possibly due to the absence of N-cadherin signaling once the first tooth has differentiated.