The role of dung beetle species in nitrous oxide emission, ammonia volatilization, and nutrient cycling.

This study evaluated the role of dung beetle species alone or associated under different species on nitrous oxide (N2O) emission, ammonia volatilization, and the performance of pearl millet [Pennisetum glaucum (L.)]. There were seven treatments, including two controls (soil and soil + dung without beetles), single species of Onthophagus taurus [Shreber, 1759] (1), Digitonthophagus gazella [Fabricius, 1787] (2), or Phanaeus vindex [MacLeay, 1819] (3); and their assemblages (1 + 2 and 1 + 2 + 3). Nitrous oxide emission was estimated for 24 days, when pearl millet was planted in sequence to assess growth, nitrogen yield (NY), and dung beetle activity. Dung beetle species presented greater N2O flow of dung on the 6th day (80 g N2O-N ha-1 day-1) compared to soil and dung (2.6 g N2O-N ha-1 day-1). Ammonia emissions varied with the presence of dung beetles (P < 0.05), and D. gazella had less NH3-N on days 1, 6, and 12 with averages of 2061, 1526, and 1048 g ha-1 day-1, respectively. The soil N content increased with dung + beetle application. Dung application affected pearl millet herbage accumulation (HA) regardless of dung beetle presence, and averages ranged from 5 to 8 g DM bucket-1. A PCA analysis was applied to analyze variation and correlation to each variable, but it indicated a low principal component explanation (less than 80%), not enough to explain the variation in findings. Despite the greater dung removal, the largest species, P. vindex and their species combination, need to be more studied to get a better understanding about their contribution on greenhouse gases. The presence of dung beetles prior to planting improved pearl millet production by enhancing N cycling, although assemblages with the three beetle species enhanced N losses to the environment via denitrification.

A combined study using ligand-based design, synthesis, and pharmacological evaluation of analogues of the acetaminophen ortho-regioisomer with potent analgesic activity.

A ligand-based drug design study was performed to acetaminophen regioisomers as analgesic candidates employing quantum chemical calculations at the DFT/B3LYP level of theory and the 6-31G* basis set. To do so, many molecular descriptors were used such as highest occupied molecular orbital, ionization potential, H-O bond dissociation energies, and spin densities, which might be related to quench reactivity of the tyrosyl radical to give N-acetyl-p-benzosemiquinone-imine through an initial electron withdrawing or hydrogen atom abstraction. Based on this in silico work, the most promising molecule, orthobenzamol, was synthesized and tested. The results expected from the theoretical prediction were confirmed in vivo using mouse models of nociception such as writhing, paw licking, and hot plate tests. All biological results suggested an antinociceptive activity mediated by opioid receptors. Furthermore, at 90 and 120 min, this new compound had an effect that was comparable to morphine, the standard drug for this test. Finally, the pharmacophore model is discussed according to the electronic properties derived from quantum chemistry calculations.