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At least 37 records · Page 2

Validation of a New NIRS Method for Measuring Muscle Oxygenation During Rhythmic Handgrip Exercise

Near infrared spectroscopy (NIRS) is commonly used to measure muscle oxygenation during exercise and recovery. Current NIRS algorithms do not account for variation in water content and optical pathlength during exercise. The current effort attempts to validate a newly developed NIRS algorithm during rhythmic handgrip exercise and recovery. Six female subjects, aver age 28 +/- 6 yrs, participated in the study. A venous catheter was placed in the retrograde direction in the antecubital space. A NIRS sensor with 30 mm source-detector separation was placed on the flexor digitorum profundus. Subjects performed two 5-min bouts of rhythmic handgrip exercise (2 s contraction/1 s relaxation) at 15% and 30% of maximal voluntary contraction. Venous blood was sampled before each bout, during the last minute of exercise, and after 5 minutes of recovery. Venous oxygen saturation (SvO2) was measured with a I-stat CG-4+ cartridge. Spectra were collected between 700-900 nm. A modified Beer's Law formula was used to calculate the absolute concentration of oxyhemoglobin (HbO2), deoxyhemoglobin (Hb) and water, as well as effective pathlength for each spectrum. Muscle oxygen saturation (SmO2) was calculated from the HbO2 and Hb results. The correlation between SvO2 and SmO2 was determined. Optical pathlength and water varied significantly during each exercise bout, with pathlength increasing approximately 20% and water increasing about 2%. R2 between blood and muscle SO2 was found to be 0.74, the figure shows the relationship over SvO2 values between 22% and 82%. The NIRS measurement was, on average, 6% lower than the blood measurement. It was concluded that pathlength changes during exercise because muscle contraction causes variation in optical scattering. Water concentration also changes, but only slightly. A new NIRS algorithm which accounts for exercise-induced variation in water and pathlength provided an accurate assessment of muscle oxygen saturation before, during and after exercise.

Hagan, R. Donald↗

NIR fluorescence lifetime macroscopic imaging with a time-gated SPAD camera

The performance of SwissSPAD2 (SS2), a large scale, widefield time-gated CMOS SPAD imager developed for fluorescence lifetime imaging, has recently been described in the context of visible range and fluorescence lifetime imaging microscopy (FLIM) of dyes with lifetimes in the 2.5 – 4 ns range. Here, we explore its capabilities in the NIR regime relevant for small animal imaging, where its sensitivity is lower and typical NIR fluorescent dye lifetimes are much shorter (1 ns or less). We carry out this study in a simple macroscopic imaging setup based on a compact NIR picosecond pulsed laser, an engineered diffuser-based illumination optics, and NIR optimized imaging lens suitable for well-plate or small animal imaging. Because laser repetition rates can vary between models, but the synchronization signal frequency accepted by SS2 is fixed to 20 MHz, we first checked that a simple frequency-division scheme enables data recording for different laser repetition rates. Next, we acquired data using different time gate widths, including gates with duration longer than the laser period, and analyzed the resulting data using both standard nonlinear least-square fit (NLSF) and phasor analysis. We show that the fixed synchronization rate and large gate widths characterizing SS2 (10 ns and over) are not an obstacle to accurately extracting lifetime in the 1 ns range and to distinguishing between close lifetimes. As a result, SS2 and similar very large gated SPAD imagers appear as a versatile alternative to other widefield time-resolved detectors for NIR fluorescence lifetime imaging, including preclinical molecular applications.

FLIM↗

Applying NIR and MIR spectroscopy for C and soil property prediction in northern cold-region ecosystems. Which approach works better?

Here, developing reliable predictions of soil attributes is necessary to understand northern cold-region climate-soil feedback. Calibration models using near-infrared (NIR) and mid-infrared (MIR) spectroscopy were developed to predict eight commonly measured soil properties for 119 soil samples representing a range of vegetation types, parent materials, and soil types spanning >23° of latitude from southeast Alaska to the Canadian high Arctic. In order to obtain a more accurate prediction, this study compared the performance of linear and non-linear calibration techniques, including lasso regression (Lasso), support vector machine (SVM), random forest (RF) and classic partial least squares (PLS) to predict different soil properties of these soils. Comparing the four models, we noticed that their performance was quite similar for MIR overall, while NIR achieved better results with a PLS model for our dataset. PLS coupled with MIR showed a better performance for soil parameters, such as total organic carbon (TOC), total nitrogen (TN), cation exchange capacity (CEC) and clay (R-squared of 0.9, 0.81, 0.80, and 0.84) when compared with NIR (R-squared of 0.85, 0.72, 0.81 and 0.68). However, using either MIR or NIR spectroscopy, PLS predictions for bulk density (BD) and sand content were not accurate. The variable importance analysis based on the PLS model successfully estimated the relative contribution of wavelengths influencing soil property predictions most. Overall, TOC, TN, CEC and clay mineral predictions are closely related to the occurrence of specific spectral bands in the MIR region. For example, wavelengths at 2978 and 1761 cm -1 for TOC and TN, as well as at 3064 cm -1 for CEC, were selected as the most influential predictor variables. We demonstrated that MIR spectroscopy is a powerful tool for more extensive monitoring in soils of the northern cold climate region; however, NIR could be utilized for rapid estimates when the highest accuracy is not essential.

54 ENVIRONMENTAL SCIENCES↗

Optical properties of La{sub 2}CuO{sub 4} and La{sub 2-x}Ca{sub x}CuO{sub 4} crystallites in UV-vis-NIR region synthesized by sol-gel process

La{sub 2}CuO{sub 4} and La{sub 2-x}Ca{sub x}CuO{sub 4} crystallites were prepared via a simple sol-gel process. The as-prepared La{sub 2}CuO{sub 4} and La{sub 2} {sub -x}Ca{sub x}CuO{sub 4} crystallites were characterized by X-ray diffraction, transmission electron microscope and UV-vis-NIR spectra. Results show that the grain size of La{sub 2}CuO{sub 4} crystallites increases with the increase of heat treatment temperature from 600 Degree-Sign C to 800 Degree-Sign C. Optical properties show that La{sub 2}CuO{sub 4} crystallites have broad absorption both in the UV-vis region and in the NIR region. The band gap of the as-prepared crystallites decreases from 1.367 eV to 1.284 eV with the increase of calcination temperature from 600 Degree-Sign C to 800 Degree-Sign C. In the series of La{sub 2-x}Ca{sub x}CuO{sub 4} compounds (x = 0.05, 0.08, 0.10, 0.12, 0.15 and 0.20), all of the samples exhibit an orthogonal crystal structure and the solubility limit of Ca{sup 2+} in La{sub 2}CuO{sub 4} is within the range of x = 0.12-0.15. In the whole UV-vis-NIR region, La{sub 2-x}Ca{sub x}CuO{sub 4} crystallites exhibit a broad absorption and the corresponding band gap first increases and then decreases with increasing of Ca{sup 2+} content. - Highlights: Black-Right-Pointing-Pointer The optical band gap can be tuned by adjusting the grain size and Ca{sup 2+} content. Black-Right-Pointing-Pointer La{sub 2}CuO{sub 4} crystallites exhibit a broad absorption band both in the UV-vis region and in the NIR region. Black-Right-Pointing-Pointer The band gap increases from 1.284 eV to 1.319 eV with the decrease of heat treatment temperature. Black-Right-Pointing-Pointer In the whole UV-vis-NIR region, the La{sub 2-x}Ca{sub x}CuO{sub 4} crystallites displayed a broad absorption. Black-Right-Pointing-Pointer The band gap of La{sub 2-x}Ca{sub x}CuO{sub 4} increases linearly with doping level when 0 {<=} x {<=} 0.12.

36 MATERIALS SCIENCE↗

Recyclable magnetic Fe3O4@SiO2/β-NaYF4:Yb3+,Tm3+/TiO2 composites with NIR enhanced photocatalytic activity

Highlights: • Fe{sub 3}O{sub 4}@SiO{sub 2}/β-NaYF{sub 4}:Yb{sup 3+},Tm{sup 3+}/TiO{sub 2} composites have been successfully fabricated. • The upconversion of energy transfer from β-NaYF{sub 4}:Yb{sup 3+},Tm{sup 3+} to TiO{sub 2} was confirmed. • Fe{sub 3}O{sub 4}@SiO{sub 2}/β-NaYF{sub 4}:Yb{sup 3+},Tm{sup 3+}/TiO{sub 2} composites exhibit photocatalytic activity in NIR. • The composites can be easily magnetic separated from water after application. • The composites show good stability indicated from four recycled tests. - Abstract: To extend the activities of TiO{sub 2} to the near infrared (NIR) region and to separate and recycle photocatalysts easily is vital for the high harvest of solar energy for sustainable society. The magnetic NIR activated Fe{sub 3}O{sub 4}@SiO{sub 2}/β-NaYF{sub 4}:Yb{sup 3+},Tm{sup 3+}/TiO{sub 2} (FS/UC/T) composites have been synthesized by using the solvothermal method by adding Fe{sub 3}O{sub 4}@SiO{sub 2} and Degussa P25 into the mixed solution of NaOH, ethanol, oleic acid, Re(NO{sub 3}){sub 3} and NH{sub 4}F. Moreover, the obtained composites were explored for photocatalytic applications. It was found that FS/UC/T emit UV–vis light under irradiation of 980 nm laser and efficient energy transfer from β-NaYF{sub 4}:Yb{sup 3+},Tm{sup 3+} to TiO{sub 2} was verified. The photodegradation experiments for treating methylene blue (MB), rhodamine B (RhB), methyl orange (MO) and colorless phenol were carried out to evaluate the photocatalytic activities of the samples. The photodegradation rates reach 76.62%, 68.48%, 30.05% and 27.16% for MB, RhB, MO and phenol under irradiation of 980 nm laser, respectively, which suggested magnetic FS/UC/T composite is an advanced NIR-driven photocatalyst. Moreover, the magnetic photocatalyst showed easy separation and good stability in the recycled tests. It suggested a promising system to utilize the NIR energy for photocatalysis based on TiO{sub 2} and to utilize the magnetic for separation of photocatalysts, which will contribute to practical environmental remediation in the future.

36 MATERIALS SCIENCE↗

Can Dust Injected by SNe Explain the NIR–MIR Excess in Young Massive Stellar Clusters?

We present a physically motivated model involving the different processes affecting supernova dust grains as they are incorporated into the thermalized medium within young massive star clusters. The model is used to explain the near- to mid-infrared (NIR–MIR) excess found in such clusters and usually modeled as a blackbody with temperature ∼(400--1000) K. In our approach, dust grains are efficiently produced in the clumpy ejecta of core-collapse supernovae, shattered into small pieces (≲0.05 μm) as they are incorporated into the hot and dense ISM, heated via frequent collisions with electrons and the absorption of energetic photons. Grains with small sizes can more easily acquire the high temperatures (∼1000 K) required to produce an NIR–MIR excess with respect to the emission of foreground PAHs and starlight. However, the extreme conditions inside young massive clusters make it difficult for these small grains to have a persistent manifestation at NIR–MIR wavelengths as they are destroyed by efficient thermal sputtering. Nevertheless, the chances for a persistent manifestation are increased by taking into account that small grains become increasingly transparent to their impinging ions as their sizes decrease. For an individual SN event, we find that the NIR–MIR excess lasts longer if the time required to incorporate all the grains into the thermalized medium is also longer, and, in some cases, comparable to the characteristic interval between supernova explosions. Our models can successfully explain the near-infrared excesses found in the star clusters observed in M33 assuming a low heating efficiency and mass loading. In this scenario, the presence of the NIR–MIR excess is an indication of efficient dust production in SNe and its subsequent destruction.

79 ASTRONOMY AND ASTROPHYSICS↗

Cancer cell membrane-coated rare earth doped nanoparticles for tumor surgery navigation in NIR-II imaging window

With the attractive characteristics of low toxicity, narrow emission spectra, long fluorescence lifetime, and no photobleaching, rare-earth doped nanoparticles (RENPs) have become promising imaging nanoplatforms in the second near-infrared window (NIR-II, 1000–1700 nm). Many studies have been devoted to different surface modification strategies of RENPs to achieve good NIR-II tumor imaging property. However, the tumor imaging efficiency of these approaches remains disappointing. Herein, two methods were pursued to modify RENPs with either polyethylene glycol (PEG) or cancer-cell-membrane to generate PEGylated-RENPs and cancer-cell-membrane camouflaged RENPs (CC-RENPs), respectively. Furthermore, this study demonstrated that cancer-cell-membrane coating of RENPs greatly improved tumor imaging performance in NIR-II window than PEG coating. Besides, CC-RENPs uptakes in liver and spleen significantly decreased. Importantly, CC-RENPs was found to be capable to aid us to pursue precise resection of the tumor. In conclusion, CC-RENPs are capable of targeting tumors and show high tumor NIR-II imaging quality. They are highly promising nanomaterials for future medical applications.

62 RADIOLOGY AND NUCLEAR MEDICINE↗

A Performance Comparison of Low-Cost Near-Infrared (NIR) Spectrometers to a Conventional Laboratory Spectrometer for Rapid Biomass Compositional Analysis

The performance of a conventional laboratory near-infrared (NIR) spectrometer and two NIR spectrometer prototypes (a Texas Instruments NIRSCAN Nano evaluation model (EVM) and an InnoSpectra NIR-M-R2 spectrometer) are compared by collecting reflectance spectra of 270 well-characterized herbaceous biomass samples, building calibration models using the partial least squares (PLS-2) algorithm to predict five constituents of the samples from the reflectance spectra, and comparing the resulting model statistics. The prediction models developed using spectra from the Foss XDS spectrometer were slightly better than the prediction models developed using spectra from either the TI NIRSCAN Nano EVM and the InnoSpectra NIR-M-R2 as measured by the root mean square error (RMSECV) and the correlation coefficient (R 2 _cv) for “leave-one-out” cross-validation (CV). The models built from the two prototype units were not statistically significantly different from each other (p = 0.05). The Foss spectrometer has a larger wavelength range (400–2500 nm) compared with the two prototypes (900–1700 nm). When the spectra from the Foss XDS spectrometer were truncated so their wavelength range matched the wavelength range of the two prototype units, the resulting model was not statistically significantly different from the models from either prototype.

47 OTHER INSTRUMENTATION↗

Enhanced performance of dye-sensitized solar cells based on TiO{sub 2} with NIR-absorption and visible upconversion luminescence

TiO{sub 2} with NIR-absorption and visible upconversion luminescence (UC-TiO{sub 2}) is prepared by a sol-gel method and calcined at 700 Degree-Sign C for 6 h. The material broadens the response region of dye sensitized solar cells (DSSCs) from an ultraviolet-visible region to the whole region of the solar spectrum. It shifts NIR sunlight to visible light which matches the strong absorbing region of the dye (N719). DSSCs based on UC-TiO{sub 2} achieved higher conversion efficiency than that on raw TiO{sub 2}. UC-TiO{sub 2} was mixed with commercial raw TiO{sub 2} as additive, and the short-circuit current density, open-circuit voltage and conversion efficiency of the DSSC reached to the optimum values 13.38 mA/cm{sup 2}, 0.78 V and 6.63% (AM1.5 global), comparing with the blank values: 7.99 mA/cm{sup 2}, 0.75 V and 4.07%, respectively. Also the mechanisms of upconversion by multiphoton absorption and energy transfer processes are interpreted in this paper. - Graphical abstract: By introducing TiO{sub 2} with NIR-absorption and visible up-conversion luminescence into DSSC, a signal reflection was explored from ultra-violet region to visible region, and to near-IR region. Highlights: Black-Right-Pointing-Pointer TiO{sub 2} with NIR-absorption and visible up-conversion luminescence (UC-TiO{sub 2}) was prepared by a sol-gel method. Black-Right-Pointing-Pointer A systematic characterization and analysis was carried out to discuss the mechanism. Black-Right-Pointing-Pointer A significantly enhanced performance of DSSC was explored by using UC-TiO{sub 2} as an additive.

36 MATERIALS SCIENCE↗

A simple method to fabricate an NIR detector by PbTe nanowires in a large scale

Highlights: • PbTe nanowires were grown by tellurization of the Pb sheets for the first time. • It was observed a band gap value for the PbTe nanostructures in the NIR region. • NIR detector was fabricated in a large scale using a simple method. • Effect of Te concentration on morphology of PbTe nanostructures was investigated. - Abstract: A simple method was used to fabricate a near-infrared (NIR) detector using PbTe nanostructures. Samples were synthesized by tellurization of lead sheets in a tube furnace. PbTe nanostructures with wires and flakes shapes were grown on the lead sheets that were placed at 300 and 330 °C, respectively, while, PbTe nanoporous were grown at 360 and 390 °C. X-ray diffraction patterns and X-ray photoelectron spectra results indicated that, the PbTe phase was formed in all samples. UV–vis diffuse reflectance spectra measurements showed a band gap for the PbTe nanostructures in the near-infrared region of the electromagnetic spectrum. Actually, the results indicated that, the band gap values of the PbTe nanowires and nanoporous were 1.54 eV and 1.61 eV, respectively. Finally, the PbTe nanostructures were used as a simple photoresponse device under a red light source. The photoresponse results revealed, PbTe nanowires are promising for photoelectrical applications in the NIR region.

36 MATERIALS SCIENCE↗

Strong NIR II Chiroptical Response and Magnetic Anisotropy via Modular Installation of Chiral Capping Ligands on a Light-Emitting Diradicaloid Scaffold

Low-energy molecular lumiphores have seen increased interest due to potential imaging and communications applications. Specifically, molecules that emit in the near-infrared (NIR, 700–1700 nm) or telecom (∼1260–1625 nm) regions, where attenuation is minimized in biological tissue and optical fibers, respectively, can drastically improve image resolution and depth penetration; however, bright low-energy emission is rare due to exponentially decreasing quantum yields in this region. Chiral molecules exhibiting strong NIR or telecom absorption/emission would be of particular interest due to advanced security and spintronics applications, but these compounds remain scarce and are currently restricted to lanthanide or nanoparticle-based systems. Here, we report the synthesis of a chiral organic-based NIR emitter, enabled by simple peripheral installation of chiral capping ligands. These ligands twist the achiral NIR-emissive core, breaking inversion symmetry. Furthermore, this twisting enables strong chiroptical responses observed via static and transient circular dichroism and increased magnetic anisotropy through electron paramagnetic resonance (EPR) measurements, establishing this strategy as a promising method for the development of new chiral emitters and sensors.

Electron paramagnetic resonance spectroscopy↗

Performance enhancement of fullerene based solar cells upon NIR laser irradiation

Photovoltaic performance enhancement of fullerene based solar cells was achieved upon exposure to near-infrared (NIR) laser pulses. In this work, the solar cells were fabricated with poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl C 61 -butyric acid methyl ester (PCBM) under ambient conditions. The cells were then post-treated with NIR femto-second laser pulses at 800 nm for different intervals of time. An enhancement of 50% in the power conversion efficiency was achieved for the devices with 15 minutes of NIR laser irradiation compared to that of the control device. The enhancement in the power conversion efficiency is attributed to the formation of a covalent linkage between P3HT and PCBM as suggested by Matrix-assisted laser desorption/ionization time of flight mass spectroscopic analysis on a blend of a thiophene oligomer and PCBM before and after NIR laser exposure.

36 MATERIALS SCIENCE↗

Rigid cationic ligands enable high-efficiency NIR-II photoluminescence in copper( i ) iodide hybrid semiconductors

Near-infrared (NIR) luminescent materials are pivotal for advanced optoelectronic and biomedical applications, yet attaining efficient emission in the NIR-II region (950-1400 nm) remains challenging. Here, we introduce a ligand cationization strategy for designing copper(i) iodide-organic hybrid materials that emit in the NIR-II region (920-1120 nm) with PLQYs up to 8.58%. By incorporating rigid cationic ligands with CuI modules, we synergistically achieve bandgap narrowing (to 1.51 eV) and structural rigidification via ionic-dative bonding, effectively suppressing non-radiative decay while extending emission beyond 1100 nm. Coupled with solution processability-enabled by the successful synthesis of nanometer-sized nanoparticles in various shapes-and excellent thermal stability (≥210 °C), this work establishes ligand cationization as a universal approach for designing efficient NIR-II emitters.

Chen, Jingwen↗

Invited Article: Radon and thoron intercomparison experiments for integrated monitors at NIRS, Japan

Inhalation of radon ({sup 222}Rn) and its short-lived decay products and of products of the thoron ({sup 220}Rn) series accounts for more than half of the effective dose from natural radiation sources. At this time, many countries have begun large-scale radon and thoron surveys and many different measurement methods and instruments are used in these studies. Consequently, it is necessary to improve and standardize technical methods of measurements and to verify quality assurance by intercomparisons between laboratories. Four international intercomparisons for passive integrating radon and thoron monitors were conducted at the NIRS (National Institute of Radiological Sciences, Japan). Radon exercises were carried out in the 24.4 m{sup 3} inner volume walk-in radon chamber that has systems to control radon concentration, temperature, and humidity. Moreover, the NIRS thoron chamber with a 150 dm{sup 3} inner volume was utilized to provide three thoron intercomparisons. At present, the NIRS is the only laboratory world-wide that has carried out periodic thoron intercomparison of passive monitors. Fifty laboratories from 26 countries participated in the radon intercomparison, using six types of detectors (charcoal, CR-39, LR 115, polycarbonate film, electret plate, and silicon photodiode). Eighteen laboratories from 12 countries participated in the thoron intercomparisons, using two etch-track types (CR-39 and polycarbonate) detectors. The tests were made under one to three different exposures to radon and thoron. The data presented in this paper indicated that the performance quality of laboratories for radon measurement has been gradually increasing. Results of thoron exercises showed that the quality for thoron measurements still needs further development and additional studies are needed to improve its measuring methods. The present paper provides a summary of all radon and thoron international intercomparisons done at NIRS from 2007 to date and it describes the present status on radon and thoron passive, one-time cycle monitors.

61 RADIATION PROTECTION AND DOSIMETRY↗

Multiwavelength optical and NIR variability analysis of the Blazar PKS 0027-426

ABSTRACT We present multiwavelength spectral and temporal variability analysis of PKS 0027-426 using optical griz observations from Dark Energy Survey between 2013 and 2018 and VEILS Optical Light curves of Extragalactic TransienT Events (VOILETTE) between 2018 and 2019 and near-infrared (NIR) JKs observations from Visible and Infrared Survey Telescope for Astronomy Extragalactic Infrared Legacy Survey (VEILS) between 2017 and 2019. Multiple methods of cross-correlation of each combination of light curve provides measurements of possible lags between optical–optical, optical–NIR, and NIR–NIR emission, for each observation season and for the entire observational period. Inter-band time lag measurements consistently suggest either simultaneous emission or delays between emission regions on time-scales smaller than the cadences of observations. The colour–magnitude relation between each combination of filters was also studied to determine the spectral behaviour of PKS 0027-426. Our results demonstrate complex colour behaviour that changes between bluer when brighter, stable when brighter, and redder when brighter trends over different time-scales and using different combinations of optical filters. Additional analysis of the optical spectra is performed to provide further understanding of this complex spectral behaviour.

79 ASTRONOMY AND ASTROPHYSICS↗

A Near-Infrared (NIR) Global Multispectral Map of the Moon from Clementine

In May and June of 1994, the NASA/DoD Clementine Mission acquired global, 11- band, multispectral observations of the lunar surface using the ultraviolet-visible (UVVIS) and near-infrared (NIR) camera systems. The global 5-band UVVIS Digital Image Model (DIM) of the Moon at 100 m/pixel was released to the Planetary Data System (PDS) in 2000. The corresponding NIR DIM has been compiled by the U.S. Geological Survey for distribution to the lunar science community. The recently released NIR DIM has six spectral bands (1100, 1250, 1500, 2000, 2600, and 2780 nm) and is delivered in 996 quads at 100 m/pixel (303 pixels/degree). The NIR data were radiometrically corrected, geometrically controlled, and photometrically normalized to form seamless, uniformly illuminated mosaics of the lunar surface.

Eliason, E. M.↗

A quantitative comparison of simultaneous BOLD fMRI and NIRS recordings during functional brain activation

Near-infrared spectroscopy (NIRS) has been used to noninvasively monitor adult human brain function in a wide variety of tasks. While rough spatial correspondences with maps generated from functional magnetic resonance imaging (fMRI) have been found in such experiments, the amplitude correspondences between the two recording modalities have not been fully characterized. To do so, we simultaneously acquired NIRS and blood-oxygenation level-dependent (BOLD) fMRI data and compared Delta(1/BOLD) (approximately R(2)(*)) to changes in oxyhemoglobin, deoxyhemoglobin, and total hemoglobin concentrations derived from the NIRS data from subjects performing a simple motor task. We expected the correlation with deoxyhemoglobin to be strongest, due to the causal relation between changes in deoxyhemoglobin concentrations and BOLD signal. Instead we found highly variable correlations, suggesting the need to account for individual subject differences in our NIRS calculations. We argue that the variability resulted from systematic errors associated with each of the signals, including: (1) partial volume errors due to focal concentration changes, (2) wavelength dependence of this partial volume effect, (3) tissue model errors, and (4) possible spatial incongruence between oxy- and deoxyhemoglobin concentration changes. After such effects were accounted for, strong correlations were found between fMRI changes and all optical measures, with oxyhemoglobin providing the strongest correlation. Importantly, this finding held even when including scalp, skull, and inactive brain tissue in the average BOLD signal. This may reflect, at least in part, the superior contrast-to-noise ratio for oxyhemoglobin relative to deoxyhemoglobin (from optical measurements), rather than physiology related to BOLD signal interpretation.

Non-NASA Center↗

Application of Principal Component Analysis to NIR Spectra of Phyllosilicates: A Technique for Identifying Phyllosilicates on Mars

Orbital near-infrared (NIR) reflectance spectra of the martian surface from the OMEGA and CRISM instruments have identified a variety of phyllosilicates in Noachian terrains. The types of phyllosilicates present on Mars have important implications for the aqueous environments in which they formed, and, thus, for recognizing locales that may have been habitable. Current identifications of phyllosilicates from martian NIR data are based on the positions of spectral absorptions relative to laboratory data of well-characterized samples and from spectral ratios; however, some phyllosilicates can be difficult to distinguish from one another with these methods (i.e. illite vs. muscovite). Here we employ a multivariate statistical technique, principal component analysis (PCA), to differentiate between spectrally similar phyllosilicate minerals. PCA is commonly used in a variety of industries (pharmaceutical, agricultural, viticultural) to discriminate between samples. Previous work using PCA to analyze raw NIR reflectance data from mineral mixtures has shown that this is a viable technique for identifying mineral types, abundances, and particle sizes. Here, we evaluate PCA of second-derivative NIR reflectance data as a method for classifying phyllosilicates and test whether this method can be used to identify phyllosilicates on Mars.

Rampe, E. B.↗