Porous GaN on Si(1 1 1) and its application to hydrogen gas sensor

The growth of heterostructure of n-type GaN/AlN/Si(1 1 1) is carried out using the molecular beam epitaxy (MBE) Veeco model Gen II system. The surface morphology of the as-grown GaN sample showed pits on the GaN surface in a ratio small than those found by other research groups. Porous GaN samples were synthesized by an electrochemical etching technique combined with increasing the current density to 75 mA/cm². The formation of pore structures are of different sizes, the etched surface became hexagonal, and pore structures are confined to a smaller size. The PL results showed greater blue shift luminescence in comparison to results found by other research groups. The reduction in crystallite size is confirmed by an increase in the broadening of XRD spectra. Raman spectra also displayed a strong band at 522 cm⁻¹ from the Si(1 1 1) substrate, and a small band at 301 cm⁻¹. These are due to the acoustic phonons of Si. Two Raman active optical phonons are assigned to h-GaN at 139 cm⁻¹ and 568 cm⁻¹, due to E2 (low) and E2 (high) respectively. The sensitivity of the gas sensor is increased as a function of the hydrogen flow rate and they became much higher compared to the as-grown sample.     

An assessment of the black ocean pixel assumption for MODIS SWIR bands

Recent studies show that an atmospheric correction algorithm using shortwave infrared (SWIR) bands improves satellite-derived ocean color products in turbid coastal waters. In this paper, the black pixel assumption (i.e., zero water-leaving radiance contribution) over the ocean for the Moderate Resolution Imaging Spectroradiometer (MODIS) SWIR bands at 1240, 1640, and 2130 nm is assessed for various coastal ocean regions. The black pixel assumption is found to be generally valid with the MODIS SWIR bands at 1640 and 2130 nm even for extremely turbid waters. For the MODIS 1240 nm band, however, ocean radiance contribution is generally negligible in mildly turbid waters such as regions along the U.S. east coast, while some slight radiance contributions are observed in extremely turbid waters, e.g., some regions along the China east coast, the estuary of the La Plata River. Particularly, in the Hangzhou Bay, the ocean radiance contribution at the SWIR band 1240 nm results in an overcorrection of atmospheric and surface effects, leading to errors of MODIS-derived normalized water-leaving radiance at the blue reaching ~ 0.5 mW cm^− 2 μm^− 1 sr^− 1. In addition, we found that, for non-extremely turbid waters, i.e., the ocean contribution at the near-infrared (NIR) band < ~ 1.0 mW cm^− 2 μm^− 1 sr^− 1, there exists a good relationship in the regional normalized water-leaving radiances between the red and the NIR bands. Thus, for non-extremely turbid waters, such a red-NIR radiance relationship derived regionally can possibly be used for making corrections for the regional NIR ocean contributions without using the SWIR bands, e.g., for atmospheric correction of ocean color products derived from the Sea-viewing Wide Field-of-view Sensor (SeaWiFS).     

Screen-printed carbon electrode for choline based on MnO2 nanoparticles and choline oxidase/polyelectrolyte layers

This paper presents the amperometric biosensor that determines choline and cholinesterase activity using a screen printed graphite electrode. In order to detect H₂O₂ we have blanket modified the electrode material with manganese dioxide nanoparticles layer. Using layer-by-layer technique on the developed hydrogen peroxide sensitive electrode surface choline oxidase was incorporated into the interpolyelectrolyte nanofilm. Its ability to serve as a detector of choline in bulk analysis and cholinesterase assay was investigated. We examined the interferences from red-ox species and heavy metals in the blood and in the environmental sample matrixes. The sensor exhibited a linear increase of the amperometric signal at the concentration of choline ranging from 1.3 × 10⁻⁷ to 1.0 × 10⁻⁴ M, with a detection limit (evaluated as 3σ) of 130 nM and a sensitivity of 103 mA M⁻¹ cm⁻² under optimized potential applied (480 mV vs. Ag/AgCl). The biosensor retained its activity for more than 10 consecutive measurements and kept 75% of initial activity for three weeks of storage at 4 °C. The R.S.D. was determined as 1.9% for a choline concentration of 10⁻⁴ M (n = 10) with a typical response time of about 10 s. The developed choline biosensor was applied for butyrylcholinesterase assay showing a detection limit of 5 pM (3σ). We used the biosensor to develop the cholinesterase inhibitor assay. Detection limit for chlorpyrifos was estimated as 50 pM.     

A CO2 sensor based upon a continuous-wave thermoelectrically-cooled quantum cascade laser

A CO₂ sensor based upon a continuous-wave thermoelectrically-cooled distributed feedback quantum cascade laser operating between 2305 and 2310 cm⁻¹ and a 54.2 cm long optical cell has been developed. Two approaches for direct absorption spectroscopy have been evaluated and applied for monitoring of the CO₂ concentration in gas lines and ambient laboratory air. In the first approach optical transmittance was derived from the single channel laser intensity, whilst in the second approach a ratio of signal and reference laser intensities (balanced detection) was used. The optimum residual absorption standard deviation was estimated to be 1.9 × 10⁻⁴ for 100 averages of 1 ms duration and 0.1 cm⁻¹ scans over the P(46) CO₂ absorption line of the ν₃ vibrational band at 2306.926 cm⁻¹. A CO₂ detection limit (1 standard deviation) of 36 ppb was estimated for 0.1 s average and balanced detection.     

Red tide detection and tracing using MODIS fluorescence data: A regional example in SW Florida coastal waters

Near real-time data from the MODIS satellite sensor was used to detect and trace a harmful algal bloom (HAB), or red tide, in SW Florida coastal waters from October to December 2004. MODIS fluorescence line height (FLH in W m^− 2 μm^− 1 sr^− 1) data showed the highest correlation with near-concurrent in situ chlorophyll-a concentration (Chl in mg m^− 3). For Chl ranging between 0.4 to 4 mg m^− 3 the ratio between MODIS FLH and in situ Chl is about 0.1 W m^− 2 μm^− 1 sr^− 1 per mg m^− 3 chlorophyll (Chl = 1.255 (FLH × 10)^0.86, r = 0.92, n = 77). In contrast, the band-ratio chlorophyll product of either MODIS or SeaWiFS in this complex coastal environment provided false information. Errors in the satellite Chl data can be both negative and positive (3-15 times higher than in situ Chl) and these data are often inconsistent either spatially or temporally, due to interferences of other water constituents. The red tide that formed from November to December 2004 off SW Florida was revealed by MODIS FLH imagery, and was confirmed by field sampling to contain medium (10⁴ to 10⁵ cells L^− 1) to high (> 10⁵ cells L^− 1) concentrations of the toxic dinoflagellate Karenia brevis. The FLH imagery also showed that the bloom started in mid-October south of Charlotte Harbor, and that it developed and moved to the south and southwest in the subsequent weeks. Despite some artifacts in the data and uncertainty caused by factors such as unknown fluorescence efficiency, our results show that the MODIS FLH data provide an unprecedented tool for research and managers to study and monitor algal blooms in coastal environments.     

Analyte selective response in solution-deposited tetrabenzoporphyrin thin-film field-effect transistor sensors

Organic thin film transistor (OTFT) chemical sensors rely on the specific electronic structure of the organic semiconductor (OSC) film for determining sensor stability and response to analytes. The delocalized electronic structure is influenced not only by the OSC molecular structure, but also the solid state packing and film morphology. Phthalocyanine (H₂Pc) and tetrabenzoporphyrin (H₂TBP) have similar molecular structures but different film microstructures when H₂Pc is vacuum deposited and H₂TBP is solution deposited. The difference in electronic structures is evidenced by the different mobilities of H₂TBP and H₂Pc OTFTs. H₂Pc has a maximum mobility of 8.6 × 10⁻⁴ cm² V⁻¹ s⁻¹ when the substrate is held at 250 °C during deposition and a mobility of 4.8 × 10⁻⁵ cm² V⁻¹ s⁻¹ when the substrate is held at 25 °C during deposition. Solution deposited H₂TBP films have a mobility of 5.3 × 10⁻³ cm² V⁻¹ s⁻¹, which is consistent with better long-range order and intermolecular coupling within the H₂TBP films compared to the H₂Pc films. Solution deposited H₂TBP also exhibits a textured film morphology with large grains and an RMS roughness 3-5 times larger than H₂Pc films with similar thicknesses. Despite these differences, OTFT sensors fabricated from H₂TBP and H₂Pc exhibit nearly identical analyte sensitivity and analyte response kinetics. The results suggest that while the interactions between molecules in the solid state determine conductivity, localized interactions between the analyte and the molecular binding site dominate analyte binding and determine sensor response.     

Development of a dehydrogenase-based glucose anode using a molecular assembly composed of nile blue and functionalized SWCNTs and its applications to a glucose sensor and glucose/O2 biofuel cell

A simple and new way to immobilize glucose dehydrogenase (GDH) enzyme onto nile blue (NB) covalently assembled on the surface of functionalized single-walled carbon nanotubes (f-SWCNTs) modified glassy carbon (GC) electrode (GDH/NB/f-SWCNTs/GC electrode) was described. The GDH/NB/f-SWCNTs/GC electrode possesses promising characteristics as glucose sensor; a wide linear dynamic range of 100-1700 μM, low detection limit of 0.3 μM, fast response time (1-2 s), high sensitivity (14 μA cm⁻² mM⁻¹), anti-interference ability and anti-fouling. Moreover, the performance of the GDH/NB/f-SWCNTs/GC bioanode was successfully tested in a glucose/O₂ biofuel cell. The maximum power density delivered by the assembled glucose/O₂ biofuel cell could reach 32.0 μW cm⁻² at a cell voltage of 0.35 V with 40 mM glucose. The present procedure can be applied for preparing a potential platform to immobilize different enzymes for various bioelectrochemical applications.     

An electrochemical biosensor for determination of hydrogen peroxide using nanocomposite of poly(methylene blue) and FAD hybrid film

An electrochemical biosensor for determination of hydrogen peroxide (H₂O₂) has been developed by the hybrid film of poly(methylene blue) and FAD (PMB/FAD). The PMB/FAD hybrid film was performed in PBS (pH 7) containing methylene blue and FAD by cyclic voltammetry. Repeatedly scanning potential range of −0.6-1.1 V, FAD was immobilized on the electrode surface by electrostatic interaction while methylene blue was electropolymerized on electrode surface. This modified electrode was found surface confined and pH dependence. It showed good electrocatalytic reduction for H₂O₂, KBrO₃, KIO₃, and NaClO as well as electrocatalytic oxidation for NADH. At an applied potential of −0.45 V vs. Ag/AgCl, the sensor showed a rapid and linear response to H₂O₂ over the range from 0.1 μM to 960 μM, with a detection limit of 0.1 μM and a significant sensitivity of 1109 μA mM⁻¹ cm⁻² (S/N = 3). It presented excellent stability at room temperature, with a variation of response current less than 5% over 30 days.     

Poly(brilliant cresyl blue) electrogenerated on single-walled carbon nanotubes modified electrode and its application in mediated biosensing system

Single-walled carbon nanotubes (SWCNTs) functionalized with carboxylic acid groups were cast to glassy carbon electrode (GCE) to construct a three-dimensional nano-micro structured scaffold. Brilliant cresyl blue (BCB) was electropolymerized on the above-mentioned SWCNTs/GCE using continuous cycling between −0.7 and 0.9 V vs. SCE. PolyBCB yielded on SWCNTs/GCE exhibited the enhanced electrochemical redox behavior compared with that electrogenerated on bare GCE. The apparent surface coverage of PolyBCB obtained by SWCNTs/GCE was at least 10 times higher than that obtained by bare GCE, namely 4.8 × 10⁻⁹ and 3.6 × 10⁻¹⁰ mol cm⁻². The cyclic voltammograms recorded by PolyBCB/SWCNTs/GCE exhibited well-defined two peaks located at −0.25 V and −0.06 V, respectively, with a surface-controlled mechanism. In addition, morphologies of PolyBCB electrogenerated on GCE and SWCNTS/GCE were characterized by atomic force microscopy. Finally, this proposed PolyBCB/SWCNTs/GCE was used in the construction of the second-generation biosensors to hydrogen peroxide and glucose, with the enhanced analytical performance.     

Improvements to a MODIS global terrestrial evapotranspiration algorithm

MODIS global evapotranspiration (ET) products by Mu et al. [Mu, Q., Heinsch, F. A., Zhao, M., Running, S. W. (2007). Development of a global evapotranspiration algorithm based on MODIS and global meteorology data. Remote Sensing of Environment, 111, 519-536. doi: 10.1016/j.rse.2007.04.015] are the first regular 1-km² land surface ET dataset for the 109.03 Million km² global vegetated land areas at an 8-day interval. In this study, we have further improved the ET algorithm in Mu et al. (2007a, hereafter called old algorithm) by 1) simplifying the calculation of vegetation cover fraction; 2) calculating ET as the sum of daytime and nighttime components; 3) adding soil heat flux calculation; 4) improving estimates of stomatal conductance, aerodynamic resistance and boundary layer resistance; 5) separating dry canopy surface from the wet; and 6) dividing soil surface into saturated wet surface and moist surface. We compared the improved algorithm with the old one both globally and locally at 46 eddy flux towers. The global annual total ET over the vegetated land surface is 62.8 × 10³ km³, agrees very well with other reported estimates of 65.5 × 10³ km³ over the terrestrial land surface, which is much higher than 45.8 × 10³ km³ estimated with the old algorithm. For ET evaluation at eddy flux towers, the improved algorithm reduces mean absolute bias (MAE) of daily ET from 0.39 mm day⁻¹ to 0.33 mm day⁻¹ driven by tower meteorological data, and from 0.40 mm day⁻¹ to 0.31 mm day⁻¹ driven by GMAO data, a global meteorological reanalysis dataset. MAE values by the improved ET algorithm are 24.6% and 24.1% of the ET measured from towers, within the range (10-30%) of the reported uncertainties in ET measurements, implying an enhanced accuracy of the improved algorithm. Compared to the old algorithm, the improved algorithm increases the skill score with tower-driven ET estimates from 0.50 to 0.55, and from 0.46 to 0.53 with GMAO-driven ET. Based on these results, the improved ET algorithm has a better performance in generating global ET data products, providing critical information on global terrestrial water and energy cycles and environmental changes.     

Effect of surface defects on biosensing properties of TiO2 nanotube arrays

In this paper, highly ordered titania nanotube (TNT) arrays fabricated by anodization were annealed at different temperatures in CO to create different concentrations of surface defects. The samples were characterized by SEM, XRD and XPS. The results showed different concentrations of Ti³⁺ defects were doped in TNT arrays successfully. Furthermore, after co-immobilized with horseradish peroxidase (HRP) and thionine chloride (Th), TNT arrays was employed as a biosensor to detect hydrogen peroxide (H₂O₂) using an amperometric method. Cyclic voltammetry results and UV-Vis absorption spectra presented that with an increase of Ti³⁺ defects concentration, the electron transfer rate and enzyme adsorption amount of TNT arrays were improved largely, which could be ascribed to the creation of hydroxyl groups on TNT surface due to dissociative adsorption of water by Ti³⁺ defects. Annealing in CO at 500 °C appeared to be the most favorable condition to achieve desirable nanotube array structure and surface defects density (0.27%), thus the TNT arrays showed the largest adsorption amount of enzyme (9.16 μg/cm²), faster electron transfer rate (1.34 × 10⁻³ cm/s) and the best response sensitivity (88.5 μA/mM l⁻¹).     

Detection of 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) by displacement of antibodies

A molecular layer with low non-specific binding enabling determination of low concentrations of 3,4-methylenedioxymethamphetamine (MDMA) by the displacement of antibodies has been developed. Antibody Fab′-fragments at various concentrations have been site-directly immobilised on gold and intercalated with a hydrophilic non-ionic polymer that reduces non-specific binding. Bovine serum albumin conjugated with MDMA and various concentrations of anti-MDMA antibodies were bound to the layer. The amount of conjugates and antibodies bound was dependent on the amount of Fab′-fragments in the layer. Antibodies were also bound to the conjugates physisorbed directly onto the gold surface and in mixtures with the polymer or with a lipoamide. A high displacement of antibodies was observed by surface plasmon resonance (SPR) on interaction of MDMA with the different layers in buffer solution. No displacement could, however, be observed in saliva with the pure conjugate layer because of a high non-specific binding of proteins. When the conjugates were coupled to the surface through the antibody Fab-fragment/polymer layer, MDMA concentrations as low as 0.02 ng mL⁻¹ (0.14 nM) could easily be detected in buffer. In diluted saliva the lowest limit of detection was 0.4 ng mL⁻¹ enabling determination of drugs from saliva with a cut-off concentration of 2 ng mL⁻¹. The molecular layer of antibody Fab′-fragments and polymer thus shows great potential for binding conjugates and antibodies that can be displaced on the interaction with very low concentrations of small-sized molecules. A low non-specific binding is guaranteed by the presence of the hydrophilic polymer.     

Enhancing a leaf radiative transfer model to estimate concentrations and in vivo specific absorption coefficients of total carotenoids and chlorophylls a and b from single-needle reflectance and transmittance

The relative concentrations of different pigments within a leaf have significant physiological and spectral consequences. Photosynthesis, light use efficiency, mass and energy exchange, and stress response are dependent on relationships among an ensemble of pigments. This ensemble also determines the visible characteristics of a leaf, which can be measured remotely and used to quantify leaf biochemistry and structure. But current remote sensing approaches are limited in their ability to resolve individual pigments. This paper focuses on the incorporation of three pigments—chlorophyll a, chlorophyll b, and total carotenoids—into the LIBERTY leaf radiative transfer model to better understand relationships between leaf biochemical, biophysical, and spectral properties.Pinus ponderosa and Pinus jeffreyi needles were collected from three sites in the California Sierra Nevada. Hemispheric single-leaf visible reflectance and transmittance and concentrations of chlorophylls a and b and total carotenoids of fresh needles were measured. These data were input to the enhanced LIBERTY model to estimate optical and biochemical properties of pine needles. The enhanced model successfully estimated reflectance (RMSE = 0.0255, BIAS = 0.00477, RMS%E = 16.7%), had variable success estimating transmittance (RMSE = 0.0442, BIAS = 0.0294, RMS%E = 181%), and generated very good estimates of carotenoid concentrations (RMSE = 2.48 µg/cm², BIAS = 0.143 µg/cm², RMS%E = 20.4%), good estimates of chlorophyll a concentrations (RMSE = 10.7 µg/cm², BIAS = − 0.992 µg/cm², RMS%E = 21.1%), and fair estimates of chlorophyll b concentrations (RMSE = 7.49 µg/cm², BIAS = − 2.12 µg/cm², RMS%E = 43.7%). Overall root mean squared errors of reflectance, transmittance, and pigment concentration estimates were lower for the three-pigment model than for the single-pigment model. The algorithm to estimate three in vivo specific absorption coefficients is robust, although estimated values are distorted by inconsistencies in model biophysics. The capacity to invert the model from single-leaf reflectance and transmittance was added to the model so it could be coupled with vegetation canopy models to estimate canopy biochemistry from remotely sensed data.     

Targeting of multiple metabolites in neural cells monitored by using protein-based carbon nanotubes

Microdevices dedicated to monitor metabolite levels have recently enabled many applications in the field of cell analysis, to monitor cell growth and development of numerous cell lines. By combining the traditional technology used for electrochemical biosensors with nanoscale materials, it is possible to develop miniaturized metabolite biosensors with unique properties of sensitivity and detection limit. In particular, enzymes tend to adsorb onto carbon nanotubes and their optical or electrical activity can perturb the electronic properties. In the present work we propose multi-walled carbon nanotube-based biosensors to monitor a cell line highly sensitive to metabolic alterations, in order to evaluate lactate production and glucose uptake during different cell states. We achieve sensors for both lactate and glucose, with sensitivities of 40.1 μA mM⁻¹ cm⁻² and 27.7 μA mM⁻¹ cm⁻², and detection limits of 28 μM and 73 μM, respectively. This nano-biosensing technology is used to provide new information on cell line metabolism during proliferation and differentiation, which are unprecedented in cell biology.     

A coral-like macroporous gold-platinum hybrid 3D electrode for enzyme-free glucose detection

We are introducing a macroporous Au-Pt hybrid 3D electrode to be used for enzyme-free glucose detection. The proposed hybrid electrode was fabricated with a three dimensional structure by electroplating platinum nanoparticles onto the surface of the coral-like macroporous Au. It was then physically analyzed by using field emission scanning electron microscopy (FESEM). The porosity and window pore size of the macroporous Au electrode were 50% and 100-300 nm, respectively. The diameters of the Pt nanoparticles ranged from 10 to 15 nm. Through cyclic voltammograms in a 1 M sulfuric acid solution, we confirmed that the hybrid electrode exhibited a much larger surface activation area with a roughness factor (RF) of 2024.7 than the macroporous Au electrode with a roughness of 46.07. The highly improved surface activation area was caused by the electroplated Pt nanoparticles. The hybrid electrode exhibited a much stronger electrocatalytic activity due to glucose oxidation than the macroporous Au electrode. At 0.4 V, it responded linearly to the glucose up to 20 mM in a neutral media with a detection limit of 0.025 mM and detection sensitivity of 39.53 μA mM⁻¹ cm⁻² without being affected by interfering species. It also showed a stable recovery response to the step changes of the glucose concentration.     

Continental-scale net radiation and evapotranspiration estimated using MODIS satellite observations

Evapotranspiration (ET) is a major pathway for water loss from many ecosystems, and its seasonal variation affects soil moisture and net ecosystem CO₂ exchange. We developed an algorithm to estimate ET using a semi-empirical Priestley-Taylor (PT) approach, which can be applied at a range of spatial scales. We estimated regional net radiation (R_net) at monthly time scales using MODerate resolution Imaging Spectroradiometer (MODIS) albedo and land surface temperature. Good agreement was found between satellite-based estimates of monthly R_net and field-measured R_net, with a RMSE of less than 30 W m^− 2. An adjustable PT coefficient was parameterized as a function of leaf area index and soil moisture based on observations from 27 AmeriFlux eddy covariance sites. The biome specific optimization using tower-based observations performed well, with a RMSE of 17 W m^− 2 and a correlation of 0.90 for predicted monthly latent heat. We implemented the approach within the hydrology module of the CASA biogeochemical model, and used it to estimate ET at a 1 km spatial resolution for the conterminous United States (CONUS). The RMSE of modeled ET was reduced to 21.1 mm mon^− 1, compared to 27.1 mm mon^− 1 in the original CASA model. The monthly ET rates averaged over the Mississippi River basin were similar to those derived using GRACE satellite measurements and river discharge data. ET varied substantially over the CONUS, with annual mean values of 110 ± 76 mm yr^− 1 in deserts, 391 ± 176 mm yr^− 1 in savannas and grasslands, and 840 ± 234 mm yr^− 1 in broadleaf forests. The PT coefficient was the main driver for the spatial variation of ET in arid areas, whereas R_net controlled ET when mean annual precipitation was higher than approximately 400 mm yr^− 1.     

Improved hydrogen-sensing performance of a Pd/GaN Schottky diode with a surface plasma treatment approach

The improved hydrogen-sensing performance of a Pd/GaN Schottky diode with a simple surface treatment is demonstrated. The studied device with an inductively coupled-plasma (ICP)-treatment shows both the good sensitivity and fast response. A high hydrogen detection sensing response of 2.05 × 10⁵, under exposing to a 10,000 ppm H₂/air gas at room temperature, is obtained. It is found that, due to the increased surface roughness, more hydrogen atoms are adsorbed on the active layer which leads to the substantial increase of current change. In addition, the studied device shows a stable and widespread reverse voltage operating regime (−0.3 to −3 V) and a fast response about of 2.9 s. Therefore, this simple surface treatment approach gives the promise for hydrogen sensing applications.     

Electrochemical performances of B doped and undoped diamond-like carbon (DLC) films deposited by femtosecond pulsed laser ablation for heavy metal detection using square wave anodic stripping voltammetric (SWASV) technique

Pure diamond-like carbon (DLC) thin films and boron-doped DLC thin films have been deposited on silicon substrates using femtosecond pulsed laser. The amorphous carbon materials (DLC), have been deposited at room temperature by ablating graphite targets with an amplified Ti:sapphire laser of 800 nm wavelength and a pulse duration of 150 fs in high vacuum conditions. Doping with boron has been performed by ablating alternatively graphite and boron targets.In this study, the DLC films were used as working electrodes for the electrochemical detection of trace heavy metals namely, Cd²⁺, Pb²⁺, Ni²⁺ and Hg²⁺, by using square wave anodic stripping voltammetry (SWASV) technique. Four metals were detected at −1.3 V deposition potential, and 90 s deposition time. The DLC films have been characterized by multiwavelength Raman spectrometry and high resolution scanning electron microscopy. The effect of the boron doping on the electrochemical behavior has been shown. The a-C:B 8%/Si₃N₄ electrode gives the more sensitive detection. The four metals are detected simultaneously with a detection limit of 1 μg/L or 2 μg/L and a dynamic range from 1 or 2 to 25 μg/L for every metal, as presented in third table of this article. The different sensitivities obtained are 6.2, 20.0, 1.2 and 6.6 μA/ppb or μA μg⁻¹ L for Cd²⁺, Pb²⁺, Ni²⁺ and Hg²⁺, respectively.     

A four-band semi-analytical model for estimating chlorophyll a in highly turbid lakes: The case of Taihu Lake, China

Accurate estimation of phytoplankton chlorophyll a (Chla) concentration from remotely sensed data is particularly challenging in turbid, productive waters. The objectives of this study are to validate the applicability of a semi-analytical three-band algorithm in estimating Chla concentration in the highly turbid, widely variable waters of Taihu Lake, China, and to improve the algorithm using a proposed four-band algorithm. The improved algorithm is expressed as [Rrs(λ₁)^− 1 − Rrs(λ₂)^− 1][Rrs(λ₄)^− 1 − Rrs(λ₃)^− 1]^− 1. The two semi-analytical algorithms are calibrated and evaluated against two independent datasets collected from 2007 and 2005 in Taihu Lake. Strong linear relationships were established between measured Chla concentration and that derived from the three-band algorithm of [Rrs^− 1(660) − Rrs^− 1(692)]Rrs(740) and the four-band algorithm of [Rrs^− 1(662) − Rrs^− 1(693)][Rrs^− 1(740) − Rrs^− 1(705)]^− 1. The first algorithm accounts for 87% and 80% variation in Chla concentration in the 2007 and 2005 datasets, respectively. The second algorithm accounts for 97% of variability in Chla concentration for the 2007 dataset and 87% of variation in the 2005 dataset. The three-band algorithm has a mean relative error (MRE) of 43.9% and 34.7% for the 2007 and 2005 datasets. The corresponding figures for the four-band algorithm are 26.7% and 28.4%. This study demonstrates the potential of the four-band model in estimating Chla even in highly turbid case 2 waters.     

Combining the triangle method with thermal inertia to estimate regional evapotranspiration — Applied to MSG-SEVIRI data in the Senegal River basin

Spatially distributed estimates of evaporative fraction and actual evapotranspiration are pursued using a simple remote sensing technique based on a remotely sensed vegetation index (NDVI) and diurnal changes in land surface temperature. The technique, known as the triangle method, is improved by utilizing the high temporal resolution of the geostationary MSG-SEVIRI sensor. With 15 min acquisition intervals, the MSG-SEVIRI data allow for a precise estimation of the morning rise in land surface temperature which is a strong proxy for total daytime sensible heat fluxes. Combining the diurnal change in surface temperature, dT_s with an interpretation of the triangular shaped dT_s − NDVI space allows for a direct estimation of evaporative fraction. The mean daytime energy available for evapotranspiration (R_n − G) is estimated using several remote sensors and limited ancillary data. Finally regional estimates of actual evapotranspiration are made by combining evaporative fraction and available energy estimates. The estimated evaporative fraction (EF) and actual evapotranspiration (ET) for the Senegal River basin have been validated against field observations for the rainy season 2005. The validation results showed low biases and RMSE and R² of 0.13 [−] and 0.63 for EF and RMSE of 41.45 W m^− 2 and R² of 0.66 for ET.