Effect of timing and graded levels of nitrogen and potassium in SRI cultivation

A field experiment was carried out at Annamalai University Experimental farm, Annamalai nagar, during Kuruvai and Navarai in the year 2008-09. To study the timing and graded levels of nitrogen and potassium in rice crop under SRI (System of rice intensification) cultivation. The experiment was laid out on deep clay soil by adopting randomized block design with factorial technique (FRBD). The results of field experiment revealed that the maximum growth and yield attributes were recorded in the treatment which received P2O5 as fully basal dose and nitrogen as three split doses viz., 50% basal and 25% each at tillering and panicle initiation stages. Potassium was applied as 33.3% K2O each at 15, 30 and 45 DAT. This treatment significantly recorded higher grain yield of 6278.7 kg ha-1 in field experiment – I and 6577.9 kg ha-1 in field experiment – II; and the straw yield of 7010.3 and 7309.7 kg ha-1 in field experiment I and II respectively. The shoot and grain uptake of nutrients (N, P and K) were high during 15, 30 and 45 DAT and at harvest which received 33.3 % K2O each at 15, 30 and 45 DAT

Observations of the 6 Centimeter Lines of OH in Evolved (OH/IR) Stars

Recent observational and theoretical advances have called into question traditional OH maser pumping models in evolved (OH/IR) stars. The detection of excited-state OH lines would provide additional constraints to discriminate amongst these theoretical models. In this Letter, we report on VLA observations of the 4750 MHz and 4765 MHz lines of OH toward 45 sources, mostly evolved stars. We detect 4765 MHz emission in the star forming regions Mon R2 and LDN 1084, but we do not detect excited-state emission in any evolved stars. The flux density and velocity of the 4765 MHz detection in Mon R2 suggests that a new flaring event has begun.Comment: 4 pages, to appear in ApJ

Circumstellar masers in the Magellanic Clouds

We have searched for 22 GHz H2O and 43/86/129 GHz SiO masers in bright IRAS point sources in the SMC and LMC, to test whether the kinematics of the mass loss from these stars depends on metallicity. H2O masers were detected in the red supergiants IRAS04553-6825 and IRAS05280-6910, and tentatively in the luminous IR object IRAS05216-6753 and the AGB star IRAS05329-6708. SiO masers were detected in IRAS04553-6825. The outflow velocity increases between the H2O masing zone near the dust-formation region and the more distant OH masing zone from 18 to 26 km/s for IRAS04553-6825 and from 6 to 17 km/s for IRAS05280-6910. The total sample of LMC targets is analysed in comparison with circumstellar masers in the Galactic Centre. The photon fluxes of circumstellar masers in the LMC are very similar to those in the Galactic Centre. The expansion velocities in the LMC appear to be 20% lower than for similarly bright OH masers in the Galactic Centre, but the data are consistent with no difference in expansion velocity. OH/IR stars in the LMC appear to have slower accelerating envelopes than OH/IR stars in the Galactic Centre. Masers in the LMC have blue-asymmetric emission profiles. This may be due to the amplification of stellar and/or free-free radiation, rather than the amplification of dust emission, and may be more pronounced in low metallicity envelopes. SiO maser strength increases with the photometric amplitude at 2.2 micron but is independent of the photometric amplitude at 10 micron. This suggests a strong connection between shocks in the dust-free SiO masing zone and the dust formation process. Appendices describe H2O maser emission from R Dor in the Milky Way, optical echelle spectroscopy of IRAS04553-6825, and the properties of masers in the Galactic Centre (Abridged).Comment: 19 pages, 17 figures. Accepted for publication in Astronomy & Astrophysics Main Journa

Magnetic Particle-Scanning for Ultrasensitive Immunodetection On-Chip

We describe the concept of magnetic particle-scanning for on-chip detection of biomolecules: a magnetic particle, carrying a low number of antigens (Ag's) (down to a single molecule), is transported by hydrodynamic forces and is subjected to successive stochastic reorientations in an engineered magnetic energy landscape. The latter consists of a pattern of substrate-bound small magnetic particles that are functionalized with antibodies (Ab's). Subsequationuent counting of the captured Ag-carrying particles provides the detection signal. The magnetic particle-scanning principle is investigated in a custom-built magneto-microfluidic chip and theoretically described by a random walk-based model, in which the trajectory of the contact point between an Ag-carrying particle and the small magnetic particle pattern is described by stochastic moves over the surface of the mobile particle, until this point coincides with the position of an Ag, resulting in the binding of the particle. This model explains the particular behavior of previously reported experimental dose-response curves obtained for two different ligand-receptor systems (biotin/streptavidin and TNF-alpha) over a wide range of concentrations. Our model shows that magnetic particle-scanning results in a very high probability of irrununocomplex formation for very low Ag concentrations, leading to an extremely low limit of detection, down to the single molecule-per-particle level. When compared to other types of magnetic particle-based surface coverage assays, our strategy was found to offer a wider dynamic range (>8 orders of magnitude), as the system does not saturate for concentrations as high as 10(11) Ag molecules in a 5 mu L drop. Furthermore, by emphasizing the importance of maximizing the encounter probability between the Ag and the Ab to improve sensitivity, our model also contributes to explaining the behavior of other particle-based heterogeneous immunoassays

Intracellular protein determination using droplet-based immunoassays

This paper describes the implementation of a sensitive, on-chip immunoassay for the analysis of intracellular proteins, developed using microdroplet technology. The system offers a number of analytical functionalities, enabling the lysis of low cell numbers, as well as protein detection and quantification, integrated within a single process flow. Cells were introduced into the device in suspension and were electrically lysed in situ. The cell lysate was subsequently encapsulated together with antibody-functionalized beads into stable, water-in-oil droplets, which were stored on-chip. The binding of intracellular proteins to the beads was monitored fluorescently. By analyzing many individual droplets and quantifying the data obtained against standard additions, we measured the level of two intracellular proteins, namely, HRas-mCitrine, expressed within HEK-293 cells, and actin-EGFP, expressed within MCF-7 cells. We determined the concentrations of these proteins over 5 orders of magnitude, from 50 pM to 1 μM. The results from this semiautomated method were compared to those for determinations made using Western blots, and were found not only to be faster, but required a smaller number of cells

Microfluidics: reframing biological enquiry

The underlying physical properties of microfluidic tools have led to new biological insights through the development of microsystems that can manipulate, mimic and measure biology at a resolution that has not been possible with macroscale tools. Microsystems readily handle sub-microlitre volumes, precisely route predictable laminar fluid flows and match both perturbations and measurements to the length scales and timescales of biological systems. The advent of fabrication techniques that do not require highly specialized engineering facilities is fuelling the broad dissemination of microfluidic systems and their adaptation to specific biological questions. We describe how our understanding of molecular and cell biology is being and will continue to be advanced by precision microfluidic approaches and posit that microfluidic tools - in conjunction with advanced imaging, bioinformatics and molecular biology approaches - will transform biology into a precision science

26th Annual Computational Neuroscience Meeting (CNS*2017): Part 3 - Meeting Abstracts - Antwerp, Belgium. 15–20 July 2017

This work was produced as part of the activities of FAPESP Research,\ud Disseminations and Innovation Center for Neuromathematics (grant\ud 2013/07699-0, S. Paulo Research Foundation). NLK is supported by a\ud FAPESP postdoctoral fellowship (grant 2016/03855-5). ACR is partially\ud supported by a CNPq fellowship (grant 306251/2014-0)