Quality Control of DAS VSP Data in Desert Environment Using Simulations and Matching Filters.

The unconsolidated near surface and large, daily temperature variations in the desert environment degrade the vertical seismic profiling (VSP) data, posing the need for rigorous quality control. Distributed acoustic sensing (DAS) VSP data are often benchmarked using geophone surveys as a gold standard. This study showcases a new simulation-based way to assess the quality of DAS VSP acquired in the desert without geophone data. The depth uncertainty of the DAS channels in the wellbore is assessed by calibrating against formation depth based on the concept of conservation of the energy flux. Using the 1D velocity model derived from checkshot data, we simulate both DAS and geophone VSP data via an elastic pseudo-spectral finite difference method, and estimate the source and receiver signatures using matching filters. These field geophone data show high amplitude variations between channels that cannot be replicated in the simulation. In contrast, the DAS simulation shows a high visual similarity with the field DAS first arrival waveforms. The simulated source and receiver signatures are visually indistinguishable from the field DAS data in this study. Since under perfect conditions, the receiver signatures should be invariant with depth, we propose a new DAS data quality control metric based on local variations of the receiver signatures which does not require geophone measurements.

Anion Effects on Spin Crossover Systems: From Supramolecular Chemistry to Magnetism.

The field of anion supramolecular chemistry has received more and more attention in recent years. Anions with diverse types and geometries have been widely used for the synthesis of ionic spin crossover (SCO) complexes. This review is devoted to anion effects on the molecular, supramolecular structures and magnetic properties of discrete SCO compounds. Firstly, typical anions used in the synthesis of these compounds are briefly summarized according to their various geometries. This is followed by a collection of representative examples of anion-based SCO compounds, whose SCO properties are analyzed in terms of supramolecular interactions, geometry and charge of anions. In the third part, anion effects on SCO complexes of different kinds of metal centers and ligands are outlined and finally remarks on the synthesis new type of ionic SCO complexes in the future are described.

Two-Dimensional Lanthanide Metal-Organic Frameworks as a Platform for Sensing Pollutant and Nitrophenols Reduction.

The discharge of harmful and toxic pollutants in water is destroying the ecosystem balance and human being health at an alarming rate. Therefore, the detection and removal of water pollutants by using stable and efficient materials are significant but challenging. Herein, three novel lanthanide metal-organic frameworks (Ln-MOFs), [La(L)(DMF)2(H2O)2]·H2O (LCUH-104), [Nd(L)(DMF)2(H2O)2]·H2O (LCUH-105), and [Pr(L)(DMF)2(H2O)2]·H2O (LCUH-106) [H3L = 5-(4-(tetrazol-5-yl)phenyl)isophthalic acid (H3TZI)] were solvothermally constructed and structurally characterized. In the three Ln-MOFs, dinuclear metallic clusters {Ln2} were connected by deprotonated tetrazol-containing dicarboxylate TZI3- to obtain a 2D layered framework with a point symbol of {42·84}·{46}. Their excellent chemical and thermal stabilities were beneficial to carry out fluorescence sensing and achieve the catalytic nitrophenols (NPs) reduction. Especially, the incorporation of the nitrogen-rich tetrazole ring into their 2D layered frameworks enables the fabrication of Pd nanocatalysts (Pd NPs@LCUH-104/105/106) and have dramatically enhanced catalytic activity by using the unique metal-support interactions between three Ln-MOFs and the encapsulating palladium nanoparticles (Pd NPs). Specifically, the reduction of NPs (2-NP, 3-NP, and 4-NP) in aqueous solution by Pd NPs@LCUH-104 exhibits exceptional conversion efficiency, remarkable rate constants (k), and outstanding cycling stability. The catalytic rate of Pd NPs@LCUH-104 for 4-NP is nearly 8.5 times more than that of Pd/C (wt 5%) and its turnover frequency value is 0.051 s-1, which indicate its excellent catalytic activity. Meanwhile, LCUH-105, as a multifunctional fluorescence sensor, exhibited excellent fluorescence detection of norfloxacin (NFX) (turn on) and Cr2O72- (turn off) with high selectivity and sensitivity at a low concentration, and the corresponding fluorescence enhancement/quenching mechanism has also been systematically investigated through various detection means and theoretical calculations.

A Multifunctional Co-Based Metal-Organic Framework as a Platform for Proton Conduction and Ni trophenols Reduction.

The design and development of proton conduction materials for clean energy-related applications is obviously important and highly desired but challenging. An ultrastable cobalt-based metal-organic framework Co-MOF, formulated as [Co2(btzip)2(µ2-OH2)] (namely, LCUH-103, H2btzip = 4, 6-bis(triazol-1-yl)-isophthalic acid) had been successfully synthesized via the hydrothermal method. LCUH-103 exhibits a three-dimensional framework and a one-dimensional microporous channel structure with scu topology based on the binuclear metallic cluster {Co2}. LCUH-103 indicated excellent chemical and thermal stability; peculiarly, it can retain its entire framework in acid and alkali solutions with different pH values for 24 h. The excellent stability is a prerequisite for studying its proton conductivity, and its proton conductivity σ can reach up to 1.25 × 10-3 S·cm-1 at 80 °C and 100% relative humidity (RH). In order to enhance its proton conductivity, the proton-conducting material Im@LCUH-103 had been prepared by encapsulating imidazole molecules into the channels of LCUH-103. Im@LCUH-103 indicated an excellent proton conductivity of 3.18 × 10-2 S·cm-1 at 80 °C and 100% RH, which is 1 order of magnitude higher than that of original LCUH-103. The proton conduction mechanism was systematically studied by various detection means and theoretical calculations. Meanwhile, LCUH-103 is also an excellent carrier for palladium nanoparticles (Pd NPs) via a wetness impregnation strategy, and the nitrophenols (4/3/2-NP) reduction in aqueous solution by Pd@LCUH-103 indicated an outstanding conversion efficiency, high rate constant (k), and exceptional cycling stability. Specifically, the k value of 4-NP reduction by Pd@LCUH-103 is superior to many other reported catalysts, and its k value is as high as 1.34 min-1 and the cycling stability can reach up to 6 cycles. Notably, its turnover frequency (TOF) value is nearly 196.88 times more than that of Pd/C (wt 5%) in the reaction, indicating its excellent stability and catalytic activity.

Series of Dual Functional Two-Dimensional RE-OFs for Nitrophenol Reduction and Dye Separation.

The rational design and preparation of stable and multifunctional metal-organic frameworks (MOFs) with excellent catalysis and adsorption properties are desirable but are great challenges. The nitrophenol (NP) reduction to aminophenols (APs) by using the catalyst Pd@MOFs is an effective strategy, which has attracted extensive attention in recent years. Here, we report four stable isostructural two-dimensional (2D) rare earth metal-organic frameworks [RE4(AAPA)6(DMA)2 (H2O)4][DMA]3[H2O]8 (namely LCUH-101, RE = Eu, Gd, Tb, Y; AAPA2- = 5-[(anthracen-9-yl-methyl)-amino]-1,3-isophthalate), which feature a 2D layer structure with sql topology of point symbol {44·62} and exhibit excellent chemical stability and thermostability. The as-synthesized Pd@LCUH-101 was utilized for the catalytic reduction of 2/3/4-nitrophenol, which indicates high catalytic activity and recyclability attributed to the synergistic effect between Pd nanoparticles and the 2D layered structure. Of note, the turnover frequency (TOF), the reaction rate constant (k), and the activation energy (Ea) of Pd@LCUH-101 (Eu) in the reduction of 4-NP, respectively, are 1.09 s-1, 2.17 min-1, and 50.2 kJ·mol-1, which show that it has superior catalytic activity. Remarkably, LCUH-101 (Eu, Gd, Tb, and Y) are multifunctional MOFs that can effectively absorb and separate mixed dyes. The appropriate interlayer spacing enables them to efficiently adsorb methylene blue (MB) and rhodamine B (RhB) in aqueous solution, with adsorption capacities of 0.97 and 0.41 g·g-1, respectively, which is one of the highest values among those of the reported MOF-based adsorbers. Meanwhile, LCUH-101 (Eu) can be used for the separation of the dye mixture MB/MO and RhB/MO, and the excellent reusability enables LCUH-101 (Eu) to be used as chromatographic column filters to quickly separate and recover dyes. Therefore, this work provides a new strategy for the exploitation of stable and efficient catalysts for NP reduction and adsorbents for dyes.

An amorphous MgF2 anti-reflective thin film for enhanced performance of inverted organic-inorganic perovskite solar cells.

The effective control of light plays an important role in optoelectronic devices. However, the effect of anti-reflection thin film (ARTF) in inverted perovskite solar cells (PSCs) (p-i-n) has so far remained elusive. Herein, MgF2 ARTF with different thicknesses (approximately 100, 330, and 560 nm) were deposited on the glass side of FTO conductive glass substrates by vacuum thermal evaporation. The results of reflectance and transmittance spectroscopy show that approximately 330 nm MgF2 ARTF can reduce reflectivity and increase transmittance on FTO conductive glass substrates. The results of SEM, XRD, and AFM show that the surface of amorphous MgF2 ARTF possesses a lot of nanoscale pits. The effect of the MgF2 ARTF on the performance of inverted perovskite solar cells (PSCs) (p-i-n) was investigated. The power conversion efficiencies (PCE) of inverted PSCs without and with MgF2 ARTF are 18.20 and 21.28%, respectively. The significant improvement in PCE of the devices with MgF2 ARTF is caused by the improvement in short-circuit current density. The stability results of the devices show that the PCE remains above 70% of the initial PCE after 300 h illumination.

Optimizing alginate dressings with allantoin and chemical modifiers to promote wound healing.

Wound healing requires diverse functionalities in dressings, and conventional materials often fall short in water absorption and moisture regulation. Natural sodium alginate is popular in wound dressings due to its excellent film-forming ability, biocompatibility, ionic crosslinking, and pH responsiveness. However, it has limitations in physical stability and solubility in aqueous environments. This study enhanced alginate dressings by incorporating allantoin and treating with calcium chloride and citric acid to improve physicochemical properties and mechanical performance. Treatments for S2 to S5 prevented dissociation and maintained integrity, with suitable water absorption (363 %-442 %) and water vapor transmission rates (612.53-715.39 g × m2 × day-1). The treatments also improved tensile strength (44.90-55.19 MPa). S2 had the highest migration ratio (52.71 %) of L929 cells and wound healing rates for mice skin (86.6 %), indicating that calcium chloride treatment is beneficial. All dressings (S1 to S5) exhibited low cytotoxicity against L929 cells and low hemolysis ratios, indicating good biocompatibility. Higher allantoin content improved wound healing efficacy. This study provides valuable insights for the design and development of alginate dressings in wound repair, expanding allantoin's application in wound healing.

Growth, structural, optical and electronic transport properties of tetragonal CH3NH3SnBr3 perovskite single crystals.

The structural and electronic transport properties of tetragonal CH3NH3SnBr3 single crystals (T-MASnBr3 SCs) are rarely reported. In this study, we synthesized T-MASnBr3 single crystals by volatilizing DMF solvent at room temperature. The crystal system and space group of the T-MASnBr3 SC are tetragonal and P4/mmm, respectively. In addition, the nitrogen atom in the methylamine group exhibits position disorder. The band gap of the T-MASnBr3 SC was determined to be 2.07 eV using the Tauc plot. Six fluorescence peaks and a lifetime up to 10 microseconds were observed in the steady-state fluorescence spectra and time-resolved fluorescence spectra of the T-MASnBr3 SC, respectively. The carrier mobility (electron) of T-MASnBr3 was 321 cm2 V-1 s-1. The curve of ln(square resistance) against T-1 was a straight line. The value of the activation energy (Ea) was 5421 J mol-1. The stability of the T-MASnBr3 SC was good before 473 K. The results indicate that T-MASnBr3 SCs have promising applications in the field of temperature sensors.

Photoluminescence and Electrical Properties of n-Ce-Doped ZnO Nanoleaf/p-Diamond Heterojunction.

The n-type Ce:ZnO (NL) grown using a hydrothermal method was deposited on a p-type boron-doped nanoleaf diamond (BDD) film to fabricate an n-Ce:ZnO NL/p-BDD heterojunction. It shows a significant enhancement in photoluminescence (PL) intensity and a more pronounced blue shift of the UV emission peak (from 385 nm to 365 nm) compared with the undoped heterojunction (n-ZnO/p-BDD). The prepared heterojunction devices demonstrate good thermal stability and excellent rectification characteristics at different temperatures. As the temperature increases, the turn-on voltage and ideal factor (n) of the device gradually decrease. The electronic transport behaviors depending on temperature of the heterojunction at different bias voltages are discussed using an equilibrium band diagram and semiconductor theoretical model.

An Electrospun Porous CuBi2O4 Nanofiber Photocathode for Efficient Solar Water Splitting.

While the CuBi2O4-based photocathode has emerged as an ideal candidate for photoelectrochemical water splitting, it is still far from its theoretical values due to poor charge carrier transport, poor electron-hole separation, and instability caused by self-photoelectric-corrosion with electrolytes. Establishing synthesis methods to produce a CuBi2O4 photocathode with sufficient cocatalyst sites would be highly beneficial for water splitting. Here, the platinum-enriched porous CuBi2O4 nanofiber (CuBi2O4/Pt) with uniform coverage and high surface area was prepared as a photocathode through an electrospinning and electrodeposition process for water splitting. The prepared photocathode material was composed of a CuBi2O4 nanofiber array, which has a freestanding porous structure, and the Pt nanoparticle is firmly embedded on the rough surface. The highly porous nanofiber structures allow the cocatalyst (Pt) better alignment on the surface of CuBi2O4, which can effectively suppress the electron-hole recombination at the electrolyte interface. The as-fabricated CuBi2O4 nanofiber has a tetragonal crystal structure, and its band gap was determined to be 1.8 eV. The self-supporting porous structure and electrocatalytic activity of Pt can effectively promote the separation of electron-hole pairs, thus obtaining high photocurrent density (0.21 mA/cm2 at 0.6 V vs. RHE) and incident photon-to-current conversion efficiency (IPCE, 4% at 380 nm). This work shows a new view for integrating an amount of Pt nanoparticles with CuBi2O4 nanofibers and demonstrates the synergistic effect of cocatalysts for future solar water splitting.

Synthesis, structure, mobility and memristor properties of tetragonal CH3NH3PbBr3 perovskite single crystals.

The structure, mobility and memristor properties of tetragonal CH3NH3PbBr3 single crystals (T-MAPbBr3 SC) are rarely reported. In this study, we synthesized T-MAPbBr3 SC with the P4/mmm (123) space group by the growing, dropping and growing (GDG) crystal seed method. A CH3NH3+ cation is a disordered state in T-MAPbBr3 SC. The mobility values of T-MAPbBr3 SC under light and dark conditions are 464.28 and -1685.3 cm2 V-1 s-1, respectively. The carrier types under light and dark conditions are holes and electrons, respectively. The memristor based on T-MAPbBr3 SC has a wide and low operating voltage window (0-0.9 V). The high and low resistances of the memristor based on T-MAPbBr3 SC achieve values of 41 and 0.35 GΩ, respectively. The values of high and low resistances are relatively stable for 100 cycles. Thus, the memristor device based on T-MAPbBr3 SC has good applications in the field of memristors.

Surface self-reconstructed amorphous/crystalline hybrid iron disulfide for high-efficiency water oxidation electrocatalysis.

Hybrid electrocatalysts derived from surface self-reconstruction during reaction processes can facilitate charge transfer between different phases and nanostructures by their unique interfaces. Herein, amorphous/crystalline hybrid iron disulfide obtained by self-reconstruction is developed for the first time for the oxygen evolution reaction (OER). The amorphous/crystalline hybrid FeS2 catalyst exhibited a high OER activity with an overpotential of only 189.5 mV (IR-corrected) to deliver 10 mA cm-2 in 1.0 M KOH, which was superior to that of the commercial RuO2. Notably, in the two-electrode system with the amorphous/crystalline hybrid FeS2 as the anode electrocatalyst and Pt/C as the cathode, the catalytic activity towards the overall water splitting was enhanced with a voltage of only 1.43 V at 10 mA cm-2. The phase, composition and surface structure were changed greatly before and after the reaction. All these surface reconstructions after the OER reaction may play significant roles in the high electronic catalytic efficiency. Therefore, the study of the surface reconstruction of catalysts during the reaction process is very important for the structure-performance relationship and the design of efficient hybrid electrocatalysts.

Free-Standing Electrospun W-Doped BiVO4 Porous Nanotubes for the Efficient Photoelectrochemical Water Oxidation.

While bismuth vanadate (BiVO4) has emerged as a promising photoanode in solar water splitting, it still suffers from poor electron-hole separation and electron transport properties. Therefore, the development of BiVO4 nanomaterials that enable performing high charge transfer rate at the interface and lowering charge recombination is urgent needed. Herein, cobalt borate (Co-B) nanoparticle arrays anchored on electrospun W-doped BiVO4 porous nanotubes (BiV0.97W0.03O4) was prepared for photoelectrochemical (PEC) water oxidation. One-dimensional, free-standing and porousBiV0.97W0.03O4/Co-B nanotubes was synthesized through electrospun and electrodeposition process. BiV0.97W0.03O4/Co-B arrays exhibit a unique self-supporting core-shell structure with rough porous surface, providing abundant conductive cofactor (W) and electrochemically active sites (Co) exposed to the electrolyte. When applied to PEC water oxidation. BiV0.97W0.03O4/Co-B modified FTO electrode displays high incident photon-to-current conversion efficiency (IPCE) of 33% at 405 nm (at 1.23 V vs. RHE) and its photocurrent density is about 4 times to the pristine nanotube. The higher PEC water oxidation properties of BiV0.97W0.03O4/Co-B porous nanotubes may be attributed to the effectively suppress the electron-hole recombination at electrolyte interface due to its self-supporting core-shell structure, the high electrocatalytic activity of Co and the good electrical conductivity of BiV0.97W0.03O4 arrays. This work offers a simple preparation strategy for the integrated Co-B nanoparticle with BiV0.97W0.03O4 nanotube, demonstrating the synergistic effect of co-catalysts for PEC water oxidation.

Synthesis, crystal structure and photoresponse of tetragonal phase single crystal CH3NH3PbCl3.

The performance of lead halogen perovskite is often closely related to its crystal structure. However, the chemical and optoelectronic properties of tetragonal phase single crystal MAPbCl3 (SC T-MAPbCl3) are rarely reported. In this study, we synthesized SC T-MAPbCl3 with the P4/mcc (124) space group by a modified inverse temperature crystallization (M-ITC) method. The twist angle of the Cl anion on the equatorial plane of the PbCl64- octahedron around the c-axis is 8.4°. The resistance (62 MΩ) of SC T-MAPbCl3 obviously decreased to 3 MΩ under 395 and 404 nm ultraviolet light. The photodetector based on SC T-MAPbCl3 under 3 V bias voltage exhibits high sensitivity (2.60 µA cm-2 under 1 W m-2 light intensity). The high selectivity of the device is in the ultraviolet region, rather than the visible region.

FeS2 crystal lattice promotes the nanostructure and enhances the electrocatalytic performance of WS2 nanosheets for the oxygen evolution reaction.

The control of surface elements and nanostructures is one of the effective ways to design and synthesize high performance catalysts. Herein, we, for the first time, prepare FeS2 crystal lattices on WS2 nanosheets (FeS2 CL@WS2 NS) by solvothermal methods for the oxygen evolution reaction (OER). The FeS2 CLs effectively prevent the oxidation and aggregation of WS2 nanosheets and increase the electrochemically active surface area. The abundant surface defect in the FeS2 CL@WS2 NS electrocatalyst reduces the stress between the crystal lattices of FeS2 and that of WS2. The overpotential (260 mV) of the FeS2 CL@WS2 NS electrocatalyst for the OER at a current density of 10 mA cm-2 is superior to those of WS2 NS/Ni foam (310 mV) and IrO2/Ni foam (300 mV) in 1.0 M KOH solution. An electrochemical-kinetic study shows that the Tafel slope of 54 mV per decade for the FeS2 CL@WS2 NS electrocatalyst is lower than those of WS2 NS (102 mV per decade) and IrO2/Ni foam (77 mV per decade). In addition, the charge transport resistor (2.3 Ω) of the FeS2 CL@WS2 NS electrocatalyst for the OER is smaller than that of WS2 NS. These faster kinetic properties, in turn, explain the high catalytic activity of the FeS2 CL@WS2 NS electrocatalyst for the OER. The XPS and HRTEM results of the post stability sample confirm that Fe2+ and W4+ are oxidized after durability measurement. Thus, we think that the FeS2 CL@WS2 NS electrocatalyst is a promising candidate for efficient, low-cost, and stable non-noble-metal-based OER electrocatalysts.

Organic-inorganic hybrid (CH3NH3)2FeCuI4Cl2 and (CH3NH3)2InCuI6 for ultraviolet light photodetectors.

Photodetectors play a key role in the military, aerospace, communications, bio-imaging, etc. In this study, we fabricate photodetector devices based on (CH3NH3)2FeCuI4Cl2 (MA2FeCuI4Cl2) and (CH3NH3)2InCuI6 (MA2InCuI6) for the first time. We find that the device based on MA2InCuI6 is highly selective for ultraviolet light (880 nA mW-1) and shows high anti-interference for visible-light (20-50 nA mW-1). The electrochemical impedance results indicate that the value (480 ± 10 Ω) of the resistance based on the MA2InCuI6 photodetector device is much smaller than that (1 ± 0.001 MΩ) based on the MA2FeCuI4Cl2 photodetector device, which in turn proves the difference in photoelectric response.

[The latest developments of the mercurial sphygmomanometers' substitute products].

Mercurial sphygmomanometer is widely applied to NIBP as the basic medical equipment in hospitals, but it is dangerous. With the world-wide limit of mercurial sphygmomanometers, it is inevitable that the mercurial sphygmomanometers would be eliminated. At the same time, according to the requirement of the medical staff and for the technical side of medical engineering, we should set up a claim for the mercurial sphygmomanometers' substitute products.

Semi-Transparent and Stable Solar Cells for Building Integrated Photovoltaics: The Confinement Effects of the Polymer Gel Electrolyte inside Mesoporous Films.

The semi-transparent solar cells are promising to be applied in building integrated photovoltaic (BIPV) and tandem solar cells. In this study, we fabricate semi-transparent and stable solar cells for BIPV by utilizing a poly (ethylene oxide) electrolyte and controlling the size of TiO2 nanoparticles and the thickness of the TiO2 film. The power conversion efficiency of the semi-transparent (over 50% transmittance at 620-750 nm) and quasi-solid solar cells is 5.78% under standard AM1.5G, 100 mW cm-2. The higher conductivity and smaller diffusion resistance of the quasi-solid electrolyte inside the mesoporous TiO2 film indicate the confinement effects of the polymer electrolyte inside a mesoporous TiO2 film. The unsealed semi-transparent and quasi-solid solar cell retains its initial efficiency during 1000 h irradiation in humid air.

Edge/Defect-Rich, Metallic, and Oxygen-Heteroatom-Doped WS2 Superstructure with Superior Electrocatalytic Performance for Green Solar Energy Conversion.

Two-dimensional tungsten sulfide is widely applied in electrocatalysis. However, WS2 possesses catalytic active sites located at the layer edge and an inert surface for catalysis. Therefore, increasing the exposure of active sites at the edge and effectively activating the inert sites on the surface is an important challenge. Here, an edge/defect-rich and oxygen-heteroatom-doped WS2 (ED-O-WS2 ) superstructure was synthesized. The power-conversion efficiency (PCE) of dye-sensitized solar cells (DSCs) based on an ED-O-WS2 counter electrode reached 10.36 % (under 1 sun, AM 1.5, 100 mW cm-2 ) and 11.19 % (under 40 mW cm-2 ). These values are, to our knowledge, the highest reported efficiency for DSCs based on Pt-free counter electrodes in I3 - /I- electrolytes. Analysis of the micro/nano structure and the electrocatalytic mechanism indicate that ED-O-WS2 exhibits metallic properties in the electrolyte, and that abundant edges and defects as well as oxygen doping in ED-O-WS2 play an important role in improving the catalytic activity of WS2 . Moreover, ED-O-WS2 displays better catalytic reversibility for I3 - /I- electrolytes than Pt.

Lack of the serotonin transporter does not prevent mineralocorticoid hypertension in rat and mouse.

We hypothesized that lack of a functional serotonin transporter (SERT) would increase basal blood pressure and enhance the development of deoxycorticosterone acetate (DOCA)-salt hypertension compared to wild type (WT) controls. Mean arterial blood pressure was measured in WT and SERT knockout (KO) mice and rat models through radiotelemetry. Basal blood pressures were not different between respective WT and KO. Moreover, blood pressure elevated similarly (~50 mm Hg) in all strains given DOCA and salt. Thus, the lack of functional SERT did not prevent development of DOCA-salt induced hypertension or modify basal blood pressure significantly.