From ebcf6881010335a55f507e9c3efe795bc9383a3c Mon Sep 17 00:00:00 2001 From: turtle89431 Date: Mon, 4 May 2026 20:14:20 -0700 Subject: [PATCH] Scrape wikipedia-science: 655 new, 15 updated, 692 total (kb-cron) --- _index.db | Bin 4698112 -> 4718592 bytes data/en.wikipedia.org/wiki/Metascience-0.md | 34 ++ data/en.wikipedia.org/wiki/Metascience-1.md | 44 ++ data/en.wikipedia.org/wiki/Metascience-2.md | 51 +++ data/en.wikipedia.org/wiki/Metascience-3.md | 34 ++ data/en.wikipedia.org/wiki/Metascience-4.md | 41 ++ data/en.wikipedia.org/wiki/Metascience-5.md | 48 ++ data/en.wikipedia.org/wiki/Metascience-6.md | 52 +++ ...minescence_for_Organics_and_Chemicals-0.md | 51 +++ .../wiki/Scintillating_bolometer-0.md | 25 + ...sitive_high-resolution_ion_microprobe-0.md | 68 +++ .../wiki/Sira_(notified_body)-0.md | 55 +++ data/en.wikipedia.org/wiki/Spectronic_20-0.md | 30 ++ data/en.wikipedia.org/wiki/Spectronic_20-1.md | 30 ++ .../Total_Ozone_Mapping_Spectrometer-0.md | 37 ++ 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Narryer in Western Australia and then later at the nearby Jack Hills. These results and the SHRIMP analytical method itself were initially questioned but subsequent conventional analysis were partially confirmed. SHRIMP-I also pioneered ion microprobe studies of titanium, hafnium and sulfur isotopic systems. +Growing interest from commercial companies and other academic research groups, notably Prof. John de Laeter of Curtin University (Perth, Western Australia), led to the project in 1989 to build a commercial version of the instrument, the SHRIMP-II, in association with ANUTECH, the Australian National University's commercial arm. Refined ion optic designs in the mid-1990s prompted development and construction of the SHRIMP-RG (Reverse Geometry) with improved mass resolution. Further advances in design have also led to multiple ion collection systems (already introduced in the market by a French company years before), negative-ion stable isotope measurements and on-going work in developing a dedicated instrument for light stable isotopes. +Fifteen SHRIMP instruments have now been installed around the world and SHRIMP results have been reported in more than 2000 peer reviewed scientific papers. SHRIMP is an important tool for understanding early Earth history having analysed some of the oldest terrestrial material including the Acasta Gneiss and further extending the age of zircons from the Jack Hills and the oldest impact crater on the planet. Other significant milestones include the first U/Pb ages for lunar zircon and Martian apatite dating. More recent uses include the determination of Ordovician sea surface temperature, the timing of snowball Earth events and development of stable isotope techniques. + + +== Design and operation == + + +=== Primary column === +In a typical U–Pb geochronology analytical mode, a beam of (O2)1− primary ions are produced from a high-purity oxygen gas discharge in the hollow Ni cathode of a duoplasmatron. The ions are extracted from the plasma and accelerated at 10 kV. The primary column uses Köhler illumination to produce a uniform ion density across the target spot. The spot diameter can vary from ~5 μm to over 30 μm as required. Typical ion beam density on the sample is ~10 pA/μm2 and an analysis of 15–20 minutes creates an ablation pit of less than 1 μm. + + +=== Sample chamber === +The primary beam is 45° incident to the plane of the sample surface with secondary ions extracted at 90° and accelerated at 10 kV. Three quadrupole lenses focus the secondary ions onto a source slit and the design aims to maximise transmission of ions rather than preserving an ion image unlike other ion probe designs. A Schwarzschild objective lens provides reflected-light direct microscopic viewing of the sample during analysis. + + +=== Electrostatic analyzer === +The secondary ions are filtered and focussed according to their kinetic energy by a 1272 mm radius 90° electrostatic sector. A mechanically-operated slit provides fine-tuning of the energy spectrum transmitted into the magnetic sector and an electrostatic quadrupole lens is used to reduce aberrations in transmitting the ions to the magnetic sector. + + +=== Magnetic sector === +The electromagnet has a 1000 mm radius through 72.5° to focus the secondary ions according to their mass/charge ratio according to the principles of the Lorentz force. Essentially, the path of a less massive ion will have a greater curvature through the magnetic field than the path of a more massive ion. Thus, altering the current in the electromagnet focuses a particular mass species at the detector. + + +=== Detectors === +The ions pass through a collector slit in the focal plane of the magnetic sector and the collector assembly can be moved along an axis to optimise the focus of a given isotopic species. In typical U-Pb zircon analysis, a single secondary electron multiplier is used for ion counting. + + +=== Vacuum system === +Turbomolecular pumps evacuate the entire beam path of the SHRIMP to maximise transmission and reduce contamination. The sample chamber also employs a cryopump to trap contaminants, especially water. Typical pressures inside the SHRIMP are between ~7 × 10−9 mbar in the detector and ~1 × 10−6 mbar in the primary column (with oxygen duoplasmatron source). + + +=== Mass resolution and sensitivity === +In normal operations, the SHRIMP achieves mass resolution of 5000 with sensitivity >20 counts/sec/ppm/nA for lead from zircon. + + +== Applications == + + +=== Isotope dating === +For U-Th-Pb geochronology a beam of primary ions (O2)1− are accelerated and collimated towards the target where it sputters "secondary" ions from the sample. These secondary ions are accelerated along the instrument where the various isotopes of uranium, lead and thorium are measured successively, along with reference peaks for Zr2O+, ThO+ and UO+. Since the sputtering yield differs between ion species and relative sputtering yield increases or decreases with time depending on the ion species (due to increasing crater depth, charging effects and other factors), the measured relative isotopic abundances do not relate to the real relative isotopic abundances in the target. Corrections are determined by analysing unknowns and reference material (matrix-matched material of known isotopic composition), and determining an analytical-session specific calibration factor. + + +== SHRIMP instruments around the world == + + +== References == + + +== External links == +Founding SHRIMP Lab at Australian National University +Australian Scientific Instruments \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/Sira_(notified_body)-0.md b/data/en.wikipedia.org/wiki/Sira_(notified_body)-0.md new file mode 100644 index 000000000..a30a3c27c --- /dev/null +++ b/data/en.wikipedia.org/wiki/Sira_(notified_body)-0.md @@ -0,0 +1,55 @@ +--- +title: "Sira (notified body)" +chunk: 1/1 +source: "https://en.wikipedia.org/wiki/Sira_(notified_body)" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:12.660143+00:00" +instance: "kb-cron" +--- + +Sira is a UK-based notified body, specialising in ATEX, IECEX and North American product approvals. + + +== Foundation == +Sira began life as the British Scientific Instrument Research Association (BSIRA). It was founded in 1918 by a Committee of the Privy Council for the promotion of scientific and industrial research and supported by the DSIR. The first members of the association were representatives of the optical industry, but these were joined in the same year by the electrical scientific instrument, electromedical, and X-ray industries. Its first director of research was Sir Herbert Jackson (1863–1936). +BSIRA's London headquarters were destroyed in the Second World War and, in 1947, the association moved to a site in South Hill, Chislehurst, a Grade II Listed former private house called 'Sitka' By the 1960s, the association had become better-known as 'Sira'. It evolved into a group of British engineering companies, based in south London, that designed test equipment and provided calibration services. + + +== Fate == +In 2006, Sira Test and Certification Ltd, Sira Defence and Security, and Sira Environmental were owned by Volveré plc. In July 2009, Volvere sold Sira Test and Certification Ltd, Sira Certification Service and Sira Environmental Ltd to CSA International. + + +== Similar organizations == +Baseefa — a similar organization in the UK +Canadian Standards Association a similar organization in Canada; also serves as a competitive alternative for USA products +ETL SEMKO — a competing testing laboratory, part of Intertek; based in London, UK +IAPMO R&T — certification body based in Ontario, California, USA +MET Laboratories, Inc. — testing laboratory based in Baltimore, Maryland, USA +NTA Inc — certification agency based in Nappanee, Indiana, USA +NCC — a similar Brazilian approvals organisation +TÜV — a similar German approvals organisation +Underwriters Laboratories — testing organization, based in Northbrook, Illinois, USA +TRaC Global — a test laboratory and certification body based in the UK + + +== See also == +ANSI +Consumers Union +Good Housekeeping Seal +NEMKO +Product certification +Quality control +RoHS +Safety engineering + + +== References == + + +== External links == +Sira Certification +Sira Consulting Ltd +Sira Defence and Security +Sira Defence and Security +CSA International \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/Spectronic_20-0.md b/data/en.wikipedia.org/wiki/Spectronic_20-0.md new file mode 100644 index 000000000..94e56a42d --- /dev/null +++ b/data/en.wikipedia.org/wiki/Spectronic_20-0.md @@ -0,0 +1,30 @@ +--- +title: "Spectronic 20" +chunk: 1/2 +source: "https://en.wikipedia.org/wiki/Spectronic_20" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:13.785145+00:00" +instance: "kb-cron" +--- + +The Spectronic 20 is a brand of single-beam spectrophotometer, designed to operate in the visible spectrum across a wavelength range of 340 nm to 950 nm, with a spectral bandpass of 20 nm. It is designed for quantitative absorption measurement at single wavelengths. Because it measures the transmittance or absorption of visible light through a solution, it is sometimes referred to as a colorimeter. The name of the instrument is a trademark of the manufacturer. +Developed by Bausch & Lomb and launched in 1953, the Spectronic 20 was the first low-cost spectrophotometer. It rapidly became an industry standard due to its low cost, durability and ease of use, and has been referred to as an "iconic lab spectrophotometer". Approximately 600,000 units were sold over its nearly 60 year production run. It has been the most widely used spectrophotometer worldwide. Production was discontinued in 2011 when it was replaced by the Spectronic 200, but the Spectronic 20 is still in common use. It is sometimes referred to as the "Spec 20". + +== Design == + +The Bausch & Lomb Spectronic 20 colorimeter uses a diffraction grating monochromator combined with a system for the detection, amplification, and measurement of light wavelengths in the 340 nm to 950 nm range. + +As shown in the schematic optical diagram (see left), polychromatic light from a source in the system passes through lenses which are reflected and dispersed by the diffraction grating to restrict the range of light wavelengths. This restricted range of wavelengths is then passed through the sample to be measured. The intensity of the transmitted light is determined by a phototube detector. Mechanical movement of the diffraction grating by means of the cam attached to the wavelength control enables the user to select for various wavelengths. This is the "λ knob", wherein λ refers to wavelength of light used for the measurement. + +== Quantitative measurements == + +Many substances absorb light in the ultraviolet - visible light range. Absorption at any particular wavelength in the ultraviolet visible range is proportional to the concentration of the substances in the solution or other medium, in accord with the Beer–Lambert relationship. In a practical sense, the Beer–Lambert relationship can be stated as: + + A = ε x l x c + +in which A is the absorbance measured by the instrument, ε is the molar absorption coefficient of the sample, l is the pathlength of the light beam through the sample, and c is the concentration of the substance in the solution or medium. The Spectronic 20 is thereby commonly used for quantitative determination of the concentration of a substance of interest. The Spectronic 20 measures the absorbance of light at a pre-determined concentration, and the concentration is calculated from the Beer–Lambert relationship. +The absorbance of the light is the base 10 logarithm of the ratio of the Transmittance of the pure solvent to the transmittance of the sample, and so the two absorbance and transmittance can be interconverted. Either transmittance or absorbance can therefore be plotted versus concentration using measurements from the Spectronic 20. Plotting a curve using percent transmittance of light yields an exponential curve. However, absorbance is linearly related to concentration, and so absorbance is often preferred for plotting a standard curve. This type of standard curve relates the concentration of the solution (on the x-axis) to measures of its absorbance (y-axis). +To obtain such a curve, a series of dilutions of known concentration of a solution are prepared and readings are obtained for each of the dilutions (see plot at left). In this plot, the slope of the line is the product ε x l. By measuring a series of standards and creating the standard curve, it is possible to quantify the amount or concentration of a substance within a sample by determining the absorbance on the Spec 20 and finding the corresponding concentration on the calibration curve. Alternatively, the logarithm of percent transmittance can be plotted versus concentration to create a standard curve using the same procedure. +The absorbance measured by the Spectronic 20 is the sum of the absorbance of each of the constituents of the solution. Therefore, the Spectronic 20 can be used to analyze more complex solutions. For example, if a sample solution has two light-absorbing compounds in it, then the user performs measurements at two different wavelengths and constructs standard curves for each compound. Then the concentration of each compound can be calculated algebraically. +The Spectronic 20 can be used for turbidimetric measurements. In microbiological work, the turbidity of a liquid culture of bacterial cells relates to the cell count, and OD600 measurements can be conducted for this purpose using the Spectronic 20. Likewise the turbidity of water suspensions of clays and other particles of size suitable for light scattering can be quantitatively determined by means of a Spectronic 20. In the past, the Spectronic 20 was used for clinical diagnostic purposes. \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/Spectronic_20-1.md b/data/en.wikipedia.org/wiki/Spectronic_20-1.md new file mode 100644 index 000000000..3ca34fa1f --- /dev/null +++ b/data/en.wikipedia.org/wiki/Spectronic_20-1.md @@ -0,0 +1,30 @@ +--- +title: "Spectronic 20" +chunk: 2/2 +source: "https://en.wikipedia.org/wiki/Spectronic_20" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:13.785145+00:00" +instance: "kb-cron" +--- + +== Use == +Before testing a sample, the Spectronic 20 is calibrated using a blank solution, which is the pure solvent that is used in the experimental sample. It is typically water or an organic solvent. In this calibration, the transmittance is set at 100% using the calibration knob of the instrument (the amplifier control knob in the figure at right). The instrument can also optionally be calibrated with a stock solution of a sample at a concentration known to have an absorbance of 2 or else vendor supplied standards, using the light absorption knob in the diagram shown at right. After calibration, the user places a 1/2 inch test tube or cuvette containing the sample solution to be measured into the sample compartment. Calibration is repeated each time the wavelength is changed. It or a standard reference sample is generally used to periodically check for drift. To measure wavelengths above 650 nm, the bottom of the instrument is opened, and a red filter and a red-sensitive photocell is installed. +The original design of the Spectronic 20 utilized an analog dial for readout of transmission from 100%T to 1%T (top scale), 0A - 2A (lower scale). Using the original instrument requires manual setting of the wavelength and making readings from a moving-needle analog display. + +== Replacement == +The Spectronic 20D (launched in 1985) and later the 20D+ replaced the analog dial with a red digital LED readout, offering greater precision in the readout, if not greater accuracy in the actual reading. A side-by-side comparison of the features of the 20+ and 20D+ is available in the 2001 operating manual. +The Spectronic 20 was replaced by the Spectronic 200 in the Thermo Scientific spectrophotometer product line in 2011. The Spectronic 200 utilizes an array detector and digital control of the measured wavelength, while retaining the characteristic λ knob of the Spec 20 for setting the wavelength. In addition to replicating the user modes of the Spec 20D+ (which it can emulate on a color LCD screen) the Spec 200 accommodates both test-tubes and square cuvettes without needing to install an adapter. Software modes described in the Spectronic 200's specifications include scanning, four wavelength simultaneous measurement, and quantitative analysis with up to four standards, in contrast to the SPEC 20D+ which offered only single point calibration. + +== Product line history == +Originally introduced by Bausch & Lomb in 1953, the product line was sold to Milton Roy in 1985. Milton Roy sold its instrument group to Life Sciences International, renamed Spectronic Instruments, Inc. in 1995. Spectronics Instruments was purchased by Thermo Optek in 1997, renamed Spectronic-Unicam in 2001 and Thermo-Spectronic in 2002. In 2003 the product line was moved to Madison, WI and the brand renamed to Thermo Electron. +With the merger of Thermo Electron and Fisher Scientific in 2006 the brand changed to Thermo Scientific, and remained such until the end of the production run. Spectronic 20 instruments found in labs today may bear any of the Bausch and Lomb, Milton Roy, Spectronic, Thermo Electron or Thermo Scientific brand names. + +== Popular culture == +The Spectronic 20 is apparently one of the few lab instruments to remain intact after the destruction of the laboratory in the movie Back to the Future. + +== References == + +== External links == +Spectronic 20, ChemLab Images and instructions (from Dartmouth College) +Manufacturer's SPEC 200 webpage (from current manufacturer) \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/Total_Ozone_Mapping_Spectrometer-0.md b/data/en.wikipedia.org/wiki/Total_Ozone_Mapping_Spectrometer-0.md new file mode 100644 index 000000000..b77c24909 --- /dev/null +++ b/data/en.wikipedia.org/wiki/Total_Ozone_Mapping_Spectrometer-0.md @@ -0,0 +1,37 @@ +--- +title: "Total Ozone Mapping Spectrometer" +chunk: 1/1 +source: "https://en.wikipedia.org/wiki/Total_Ozone_Mapping_Spectrometer" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:14.947524+00:00" +instance: "kb-cron" +--- + +The Total Ozone Mapping Spectrometer (TOMS) was a NASA satellite instrument, specifically a spectrometer, for measuring the ozone layer. Of the five TOMS instruments which were built, four entered successful orbit. The satellites carrying TOMS instruments were: + +Nimbus 7; launched October 24, 1978. Operated until 1 August 1994. Carried TOMS instrument number 1. +Meteor-3-5; launched 15 August 1991. Operated until December 1994. Was the first and last Soviet satellite to carry a USA made instrument. Carried TOMS instrument number 2. +ADEOS I; launched 17 August 1996. Operated until 30 June 1997. Mission was cut short by a spacecraft failure. +TOMS-Earth Probe; launched on July 2, 1996. Operated until 2 December 2006. Carried TOMS instrument number 3. +QuikTOMS; launched 21 September 2001. Suffered launch failure and did not enter orbit. +Nimbus 7 and Meteor-3-5 provided global measurements of total column ozone on a daily basis and together provided a complete data set of daily ozone from November 1978 to December 1994. After an eighteen-month period when the program had no on-orbit capability, TOMS-Earth Probe launched on 2 July 1996, followed by ADEOS I. ADEOS I was launched on August 17, 1996, and the TOMS-instrument onboard provided data until the satellite which housed it lost power on June 30, 1997. +TOMS-Earth Probe (Total Ozone Mapping Spectrometer - Earth Probe, TOMS-EP, originally just TOMS, COSPAR 1996-037A) was launched on July 2, 1996, from Vandenberg AFB by a Pegasus XL rocket. The satellite project was originally known as TOMS, back in 1989 when it was selected as a SMEX mission in the Explorer program. However, it found no funding as an Explorer mission and transferred to NASA's Earth Probe program, getting funding and becoming TOMS-EP. The small, 295 kg satellite was built for NASA by TRW; the single instrument was the TOMS 3 spectrometer. The satellite had a two-year planned life. TOMS-EP suffered a two-year delay to its launch due to launch failures of the first two Pegasus XL rockets. The launch delays led to alternations in the mission; the satellite was placed in a lower than originally planned orbit to achieve higher resolution and to enable more thorough study of UV-absorbing aerosols in the troposphere. The lower orbit was meant to complement measurements from ADEOS I enabling TOMS-EP to provide supplemental measurements. After ADEOS I failed in orbit, TOMS-EP was boosted to a higher orbit to replace ADEOS I. The transmitter for TOMS-Earth Probe failed on December 2, 2006. +The only total failure in the series was QuikTOMS, which was launched on September 21, 2001, on a Taurus rocket from Vandenberg AFB, but did not achieve orbit. +Since January 1, 2006, data from the Aura Ozone Monitoring Instrument (OMI) has replaced data from TOMS-Earth Probe. The Ozone Mapping and Profiler Suite on Suomi NPP and NOAA-20 have further continued the data record. + + +== Gallery == + + +== References == + + +== External links == + +TOMS home page +TOMS Volcanic Emissions Group + + +== Further reading == +Bhartia, Pawan Kumar; McPeters, Richard D. (2018). "The discovery of the Antarctic Ozone Hole". Comptes Rendus Geoscience. 350 (7). Elsevier BV: 335–340. Bibcode:2018CRGeo.350..335B. doi:10.1016/j.crte.2018.04.006. hdl:2060/20190002263. ISSN 1631-0713. \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/XyloTron-0.md b/data/en.wikipedia.org/wiki/XyloTron-0.md new file mode 100644 index 000000000..f20bc51bf --- /dev/null +++ b/data/en.wikipedia.org/wiki/XyloTron-0.md @@ -0,0 +1,45 @@ +--- +title: "XyloTron" +chunk: 1/1 +source: "https://en.wikipedia.org/wiki/XyloTron" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:16.064229+00:00" +instance: "kb-cron" +--- + +The XyloTron is an open-source, portable macroscopic wood identification system developed to support supply chain verification and the enforcement of laws against illegal logging. The device uses computer vision wood identification models to classify wood specimens based on their macroscopic anatomy and requires minimal operator training. Designed for use in laboratory and field settings, the system provides a non-destructive method to rapidly identify wood. The system's accuracy depends on the quality of the training data, the breadth and anatomical complexity of woods in the model, and the similarity of unknown samples to those included in the model. Use of the XyloTron is intended to help establish probable cause in cases of possible illegal logging, rather than for high-stakes legal enforcement or forensic confirmation. Microscopic analysis of wood specimens by a wood anatomist may still be required. + + +== Overview == +The XyloTron system was developed at the United States Department of Agriculture, Forest Service, Forest Products Laboratory in Madison, Wisconsin. Initial conceptual work began in late 2010. The XyloTron uses a laptop or desktop computer for computation and the XyloScope, which is specialized, custom-designed hardware that captures controlled imaging using a scientific-grade digital camera, lens, and lighting array. +Unlike traditional wood identification techniques that rely on microscopic analysis by trained experts, the XyloTron uses image-based classification. It captures standardized images of a wood surface using the XyloScope then compares the image of the unknown specimen against a model trained on verified reference specimens. The system’s hardware and software are open source. Models used by the XyloTron are trained using labeled image datasets of known wood species, typically derived from scientific-quality reference collections. Because it is designed to work offline, the XyloTron can be deployed in remote field locations without internet access. Field trials in South America, Southeast Asia, and Africa have demonstrated the system’s utility in identifying timber suspected to be harvested illegally with minimal field agent training. + +The initial design of the XyloScope was published in 2019 with engineering drawings and a bill of materials for the hardware, then was superseded by the 2020 publication of the XyloTron 2.0. The update added UV illumination and variable positioning of the lighting array, a mechanically superior design for focal stability, and freely available software for general imaging, reference imaging, and wood identification. Also included was a bill of materials, design files for the electronics, all 3D files, and an illustrated assembly manual. The XyloTron 2.0 supports imaging woods (or other materials) with UV fluorescence, as well as macroscopic imaging of charcoal for computer vision wood identification. +Research using the XyloTron focused first on collaborative work developing wood identification models for specific regions. or groups of endangered or related species. Subsequently, scientists explored how much “noise” these models could tolerate and how to build highly accurate, larger models, for example, to cover North American commercial hardwoods. Current work is focused primarily on extracting wood anatomical data from XyloTron image datasets. + + +== XyloPhone == + +The cost for a XyloTron unit is too high for many field deployment/inspection contexts. To address this cost concern, the Forest Products Laboratory developed a smartphone complement to the XyloTron, the XyloPhone. The XyloPhone unit is attached to a smartphone by a model-specific slide-on adapter that centers the XyloPhone unit over the phone’s built-in, high-resolution camera. By leveraging the comparative ubiquity of smartphones and by sourcing much lower-cost components (for example, the lens from a magnifying loupe rather than an expensive scientific lens) the price-point for a XyloPhone was less than one-twelfth that of a XyloTron. The XyloPhone design also incorporates white-light and UV illumination but lacks the ability to reposition the lighting array for charcoal identification. + + +== Other uses == + +The XyloTron and XyloPhone were primarily intended to facilitate rapid macroscopic identification of wood, but both systems are suited to capture images of any objects that show interesting macroscopic variation, from fungi to feathers to fabrics to fuzzy leaves – or anything else one cares to examine. + + +== See also == +Illegal logging +Wood anatomy +Forest governance +Timber mafia + + +== References == + + +== External links == +Video demonstration of the XyloTron +Global Timber Tracking Network +European Commission page on illegal logging, with links to FLEGT Regulation (adopted in 2005) and EU Timber Regulation (adopted in 2010) \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/Z-tube-0.md b/data/en.wikipedia.org/wiki/Z-tube-0.md new file mode 100644 index 000000000..1403a093a --- /dev/null +++ b/data/en.wikipedia.org/wiki/Z-tube-0.md @@ -0,0 +1,16 @@ +--- +title: "Z-tube" +chunk: 1/1 +source: "https://en.wikipedia.org/wiki/Z-tube" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:17.202821+00:00" +instance: "kb-cron" +--- + +The Z-tube is an experimental apparatus for measuring the tensile strength of a liquid. +It consists of a Z-shaped tube with open ends, filled with a liquid, and set on top of a spinning table. If the tube were straight, the liquid would immediately fly out one end or the other of the tube as it began to spin. By bending the ends of the tube back towards the center of rotation, a shift of the liquid away from center will result in the water level in one end of the tube rising and thus increasing the pressure in that end of the tube, and consequently returning the liquid to the center of the tube. By measuring the rotational speed and the distance from the center of rotation to the liquid level in the bent ends of the tube, the pressure reduction inside the tube can be calculated. +Negative pressures, (i.e. less than zero absolute pressure, or in other words, tension) have been reported using water processed to remove dissolved gases. Tensile strengths up to 280 atmospheres have been reported for water in glass. + + +== References == \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/Zeeman_slower-0.md b/data/en.wikipedia.org/wiki/Zeeman_slower-0.md new file mode 100644 index 000000000..f17c716d5 --- /dev/null +++ b/data/en.wikipedia.org/wiki/Zeeman_slower-0.md @@ -0,0 +1,433 @@ +--- +title: "Zeeman slower" +chunk: 1/2 +source: "https://en.wikipedia.org/wiki/Zeeman_slower" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:18.309776+00:00" +instance: "kb-cron" +--- + +In atomic physics, a Zeeman slower is a scientific instrument that is commonly used in atomic physics to slow and cool a beam of hot atoms to speeds of several meters per second and temperatures below a kelvin. The gas-phase atoms used in atomic physics are often generated in an oven by heating a solid or liquid atomic sample to temperatures where the vapor pressure is high enough that a substantial number of atoms are in the gas phase. These atoms effuse out of a hole in the oven with average speeds on the order of hundreds of m/s and large velocity distributions (due to their high temperature). The Zeeman slower is attached close to where the hot atoms exit the oven and are used to slow them to less than 10 m/s (slowing) with a very small velocity spread (cooling). +A Zeeman slower consists of a cylinder, through which an atomic beam travels, a pump laser that counterpropagates with respect to the beam's direction, and a magnetic field (commonly produced by a solenoid-like coil) that points along the cylinder's axis with a spatially varying magnitude. The pump laser, which is required to be near-resonant with atomic transition, Doppler-slows a certain velocity class within the velocity distribution of the beam. The spatially varying magnetic field is designed to Zeeman-shift the resonant frequency to match the decreasing Doppler shift as the atoms are slowed to lower velocities while they propagate through the Zeeman slower, allowing the pump laser to be continuously resonant and provide a slowing force. + +== History == +The Zeeman slower was first developed by Harold J. Metcalf and William D. Phillips (who was awarded 1/3 of the 1997 Nobel Prize in Physics in part work for his work on the Zeeman slower). The achievement of these low temperatures led the way for the experimental realization of Bose–Einstein condensation, and a Zeeman slower can be part of such an apparatus. + +== Principle == +According to the principles of Doppler cooling, an atom modelled as a two-level atom can be cooled using a laser. If it moves in a specific direction and encounters a counter-propagating laser beam resonant with its transition, it is very likely to absorb a photon. The absorption of this photon gives the atom a "kick" in the direction that is consistent with momentum conservation and brings the atom to its excited state. However, this state is unstable, and some time later the atom decays back to its ground state via spontaneous emission (after a time on the order of nanoseconds; for example, in rubidium-87, the excited state of the D2 transition has a lifetime of 26.2 ns). The photon will be reemitted (and the atom will again increase its speed), but its direction will be random. When averaging over a large number of these processes applied to one atom, one sees that the absorption process decreases the speed always in the same direction (as the absorbed photon comes from a monodirectional source), whereas the emission process does not lead to any change in the speed of the atom because the emission direction is random. Thus the atom is being effectively slowed down by the laser beam. +There is nevertheless a problem in this basic scheme because of the Doppler effect. The resonance of the atom is rather narrow (on the order of a few megahertz), and after having decreased its momentum by a few recoil momenta, it is no longer in resonance with the pump beam because in its frame, the frequency of the laser has shifted. The Zeeman slower uses the fact that a magnetic field can change the resonance frequency of an atom using the Zeeman effect to tackle this problem. +The average acceleration (due to many photon absorption events over time) of an atom with mass + + + + M + + + {\displaystyle M} + +, a cycling transition with frequency + + + + ω + = + c + k + + + δ + + + {\displaystyle \omega =ck+\delta } + +, and linewidth + + + + γ + + + {\displaystyle \gamma } + +, that is in the presence of a laser beam that has wavenumber + + + + k + + + {\displaystyle k} + +, and intensity + + + + I + = + + s + + 0 + + + + I + + s + + + + + {\displaystyle I=s_{0}I_{s}} + + (where + + + + + I + + s + + + = + ℏ + c + γ + + k + + 3 + + + + / + + ( + 12 + π + ) + + + {\displaystyle I_{s}=\hbar c\gamma k^{3}/(12\pi )} + + is the saturation intensity of the laser) is + + + + + + + + a + → + + + + = + + + + ℏ + + + + k + → + + + + γ + + + 2 + M + + + + + + + s + + 0 + + + + 1 + + + + s + + 0 + + + + + ( + 2 + + δ + ′ + + + / + + γ + + ) + + 2 + + + + + + . + + + {\displaystyle {\vec {a}}={\frac {\hbar {\vec {k}}\gamma }{2M}}{\frac {s_{0}}{1+s_{0}+(2\delta '/\gamma )^{2}}}.} + + +In the rest frame of the atoms with velocity + + + + v + + + {\displaystyle v} + + in the atomic beam, the frequency of the laser beam is shifted by + + + + + k + + L + + + v + + + {\displaystyle k_{L}v} + +. In the presence of a magnetic field + + + + B + + + {\displaystyle B} + +, the atomic transition is Zeeman-shifted by an amount + + + + + μ + ′ + + B + + / + + ℏ + + + {\displaystyle \mu 'B/\hbar } + + (where + + + + + μ + ′ + + + + {\displaystyle \mu '} + + is the magnetic moment of the transition). Thus, the effective detuning of the laser from the zero-field resonant frequency of the atoms is + + + + + + δ + ′ + + = + δ + + + k + v + − + + + + + μ + ′ + + B + + ℏ + + + . + + + {\displaystyle \delta '=\delta +kv-{\frac {\mu 'B}{\hbar }}.} + + +The atoms for which + + + + + δ + ′ + + = + 0 + + + {\displaystyle \delta '=0} + + will experience the largest acceleration, namely + + + + + a + = + η + + a + + max + + + , + + + {\displaystyle a=\eta a_{\text{max}},} + + +where + + + + η + = + + s + + 0 + + + + / + + ( + 1 + + + + s + + 0 + + + ) + + + {\displaystyle \eta =s_{0}/(1+s_{0})} + +, and + + + + + a + + max + + + = + ℏ + k + γ + + / + + ( + 2 + M + ) + + + {\displaystyle a_{\text{max}}=\hbar k\gamma /(2M)} + +. +The most common approach is to require that we have a magnetic field profile that varies in the + + + + z + + + {\displaystyle z} + + direction such that the atoms experience a constant acceleration + + + + a + = + η + + a + + max + + + + + {\displaystyle a=\eta a_{\text{max}}} + + as they fly along the axis of the slower. It has been recently shown, however, that a different approach yields better results. +In the constant-deceleration approach we get + + + + + v + ( + z + ) + = + + + + v + + i + + + 2 + + + − + 2 + a + z + + + , + + + {\displaystyle v(z)={\sqrt {v_{i}^{2}-2az}},} + \ No newline at end of file diff --git a/data/en.wikipedia.org/wiki/Zeeman_slower-1.md b/data/en.wikipedia.org/wiki/Zeeman_slower-1.md new file mode 100644 index 000000000..4ec22cfe2 --- /dev/null +++ b/data/en.wikipedia.org/wiki/Zeeman_slower-1.md @@ -0,0 +1,227 @@ +--- +title: "Zeeman slower" +chunk: 2/2 +source: "https://en.wikipedia.org/wiki/Zeeman_slower" +category: "reference" +tags: "science, encyclopedia" +date_saved: "2026-05-05T03:14:18.309776+00:00" +instance: "kb-cron" +--- + + + + + B + ( + z + ) + = + + + + ℏ + k + + + μ + ′ + + + + v + + + + + + ℏ + δ + + + μ + ′ + + + + = + + + + ℏ + k + + v + + i + + + + + μ + ′ + + + + + + 1 + − + + + + 2 + a + + + v + + i + + + 2 + + + + + z + + + + + + + + ℏ + δ + + + μ + ′ + + + + , + + + {\displaystyle B(z)={\frac {\hbar k}{\mu '}}v+{\frac {\hbar \delta }{\mu '}}={\frac {\hbar kv_{i}}{\mu '}}{\sqrt {1-{\frac {2a}{v_{i}^{2}}}z}}+{\frac {\hbar \delta }{\mu '}},} + + +where + + + + + v + + i + + + + + {\displaystyle v_{i}} + + is the maximal velocity class that will be slowed; all the atoms in the velocity distribution that have velocities + + + + v + < + + v + + i + + + + + {\displaystyle v + + v + + i + + + + + {\displaystyle v>v_{i}} + + will not be slowed at all. The parameter + + + + η + + + {\displaystyle \eta } + + (which determines the required laser intensity) is normally chosen to be around 0.5. If a Zeeman slower were to be operated with + + + + η + ≈ + 1 + + + {\displaystyle \eta \approx 1} + +, then after absorbing a photon and moving to the excited state, the atom would preferentially re-emit a photon in the direction of the laser beam (due to stimulated emission), which would counteract the slowing process. + +== Realization == +The required form of the spatially inhomogeneous magnetic field as we showed above has the form + + + + + B + ( + z + ) + = + + B + + 0 + + + + + + B + + a + + + + + 1 + − + z + + / + + + z + + 0 + + + + + . + + + {\displaystyle B(z)=B_{0}+B_{a}{\sqrt {1-z/z_{0}}}.} + + +This field can be realized a few different ways. The most popular design requires wrapping a current-carrying wire with many layered windings where the field is strongest (around 20–50 windings) and few windings where the field is weak. Alternative designs include a single-layer coil that varies in the pitch of the winding and an array of permanent magnets in various configurations. + +== Outgoing atoms == +The Zeeman slower is usually used as a preliminary step to cool the atoms in order to trap them in a magneto-optical trap. Thus it aims at a final velocity of about 10 m/s (depending on the atom used), starting with a beam of atoms with a velocity of a few hundred meters per second. The final speed to be reached is a compromise between the technical difficulty of having a long Zeeman slower and the maximal speed allowed for an efficient loading into the trap. +A limitation of setup can be the transverse heating of the beam. It is linked to the fluctuations of the speed along the three axes around its mean values, since the final speed was said to be an average over a large number of processes. These fluctuations are linked to the atom having a Brownian motion due to the random reemission of the absorbed photon. They may cause difficulties when loading the atoms in the next trap. + +== References == \ No newline at end of file