Ecophysiological Responses of Two Olive Tree Cultivars (Olea europaea L. CV Koroneiki and Chemlali) Under Three Water Treatments

In this paper, our objective is to assess and compare the effects of three levels of irrigation application on the ecophysiological behavior and plant dry matter accumulation of two young olive tree cultivars Koroneiki, a promising greek cultivar, and Chemlali, the best local cultivar. According to this assessment, we can determine the most efficient water treatment that could be suitable for Mediterranean environments subjected to water shortage conditions. Measurements were made in the green house of the Tunisian Olive tree Institute under normal day-light conditions from March, 16th to April, 21st 2015. Three water treatments were applied which are T100% (control treatment: Daily irrigation at 100% of Available Water Content (AWC)), T50% (Daily irrigation at 50% of AWC) and T0% (Without watering). The results showed that the two olive tree cultivars possess important mechanisms to overtake limited water resources. However, some striking variations existed between the two cultivars studied. Indeed, as water stress increased (T0%), Chemlali maintained longer a high midday leaf water potential compared (- 4.54 MPa) to Koroneiki (- 5.8 MPa). T50% treatment seems to be sufficient for both cultivars. Measurements of total Osmotic Adjustment (OA) showed that olive trees use this mechanism to create very negative leaf water potentials in order to be able to extract water from a dry root environment. The root/shoot ratio of Chemlali plants at T50% treatment was the highest (1.08) comparatively with the other two treatments (0.70 and 0.79 for T100% and T0% AWC water treatments, respectively). This result shows that Chemlali plants valorize low quantities of water (T50%) rather than high quantities (T100%) and Koroneiki plants behave better when it is irrigated at 100% AWC. To conclude, Chemlali plants irrigated at 50% AWC, compared to Koroneiki plants, are the most suitable to tolerate water restriction conditions

Synthesis, crystal structure, DFT calculations, Hirshfeld surface analysis, energy frameworks, molecular dynamics and docking studies of novel isoxazolequinoxaline derivative (IZQ) as anti-cancer drug

Quinoxaline derivatives with the molecular formula C8H6N2] also named benzopyrazines, which are a valuable class of heterocyclic compounds useful for their numerous industrial and pharmaceutical applications. The new isoxazolquinoxalin (IZQ) 3-pheny1-14(3-(p-toly1)-4,5-dihydroisoxazol-5yl)methyl)quinoxalin-2(1H)- one (5) has been synthesized with good yield by stirring the compounds of 1-allyl-3-phenylquinoxalin-2(1H)-one (3, 3.8mmol), and (E)-4 methylbenzaldehydeoxime (4, 1.3mmol) in 20 ml of chloroform. The aqueous solution of sodium hypochlorite (10 ml of water bleach 12 degrees) was added drop wise using bromine funnel. The mixture was stirring at 0 degrees C temperature for 6 hours. Then it dried to obtain a crude product which on recrystallization with ethanol afforded the title compound (5) as colourless rectangular block shape crystals, and then confirmed by H NMR, LC-MS spectra. The structure of the compound has been confirmed by single crystal X-ray diffraction technique. The compound crystallizes in the monoclinic crystal system with the space group P2(1)/c. The unit cell constants; a =15.9437(6) angstrom, b =16.3936(6) angstrom, c =7.4913(3) angstrom, and beta =94.178(2)degrees. DFT calculations were carried out and HOMO-LUMO energy levels have been determined. In the structure, both Intermolecular and intramolecular hydrogen bonds of the type C-H center dot center dot center dot O were observed along with C-H center dot center dot center dot cg interactions. Hirshfeld surface studies were performed to understand the different interaction contacts of the molecule and the molecular packing strength of the crystal. Energy frameworks were constructed through different intermolecular interaction energies to investigate the stability of the compound and to know type of the dominate energy. Docking studies predicted anti-cancer activity of the title molecule against homo sapiens protein (pdb code:6HVH) and exhibited prominent interactions at active site region. (C) 2021 Elsevier B.V. All rights reserved

Perspectives on Preparedness for Chemical, Biological, Radiological, and Nuclear Threats in the Middle East and North Africa Region: Application of Artificial Intelligence Techniques

Over the past 3 decades, the diversity of ethnic, religious, and political backgrounds worldwide, particularly in countries of the Middle East and North Africa (MENA), has led to an increase in the number of intercountry conflicts and terrorist attacks, sometimes involving chemical and biological agents. This warrants moving toward a collaborative approach to strengthening preparedness in the region. In disaster medicine, artificial intelligence techniques have been increasingly utilized to allow a thorough analysis by revealing unseen patterns. In this study, the authors used text mining and machine learning techniques to analyze open-ended feedback from multidisciplinary experts in disaster medicine regarding the MENA region's preparedness for chemical, biological, radiological, and nuclear (CBRN) risks. Open-ended feedback from 29 international experts in disaster medicine, selected based on their organizational roles and contributions to the academic field, was collected using a modified interview method between October and December 2022. Machine learning clustering algorithms, natural language processing, and sentiment analysis were used to analyze the data gathered using R language accessed through the RStudio environment. Findings revealed negative and fearful sentiments about a lack of accessibility to preparedness information, as well as positive sentiments toward CBRN preparedness concepts raised by the modified interview method. The artificial intelligence analysis techniques revealed a common consensus among experts about the importance of having accessible and effective plans and improved health sector preparedness in MENA, especially for potential chemical and biological incidents. Findings from this study can inform policymakers in the region to converge their efforts to build collaborative initiatives to strengthen CBRN preparedness capabilities in the healthcare sector

3,4,6-Trimethyl-1-phenyl-5-(thiophen-3-yl)-1H-pyrazolo[3,4-b]pyridine

In the title compound, C19H17N3S, the pyrazolo[3,4-b]pyridine unit is slightly bowed across the C—C bond common to the two rings. In the crystal, ribbons extending along the a-axis direction are formed by C—H...π(ring) interactions. The ribbons are packed into corrugated layers inclined to the ac plane by approximately 22°. The thiophenyl group is rotationally disordered over two sites 180° apart in a 0.606 (2)/0.394 (2) ratio

Ethyl 4-(3,4,6-trimethyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-yl)benzoate

In the title compound, C24H23N3O2, the dihedral angles between the pyrazolopyridine ring system (r.m.s. deviation = 0.001 Å) and the N-bound and C-bound benzene rings are 15.95 (2) and 83.71 (4)°, respectively. The conformation of the former is influenced by an intramolecular C—H...N hydrogen bond, which generates an S(6) ring. In the crystal, stepped layers are generated by three sets of C—H...π interactions

5-Nitro-1-(prop-2-yn-1-yl)-1H-indazole

The packing of the title molecule, C10H7N3O2, features the formation of weak dimers via pairwise C—H...O interactions across centers of symmetry. The prop-2-yn-1-yl moiety is twisted out of the plane of the indazole unit by 78.53 (17)°

2-[(Prop-2-yn-1-yl)amino]anilinium chloride

The title compound, C9H11N2+·Cl−, is an anilinium chloride salt, in which the Car—N—C—C (ar = aromatic) torsion angle is −84.95 (18)°. In the crystal, a bilayer of cation–anion sheets runs parallel to (100), primarily through an extensive range of N—H...Cl hydrogen bonds. Weak offset π-stacking interactions between the benzene rings stack molecules along c