427 research outputs found
Aluminum application to restore water quality in eutrophic lakes: maximizing binding efficiency between aluminum and phosphorus
No full textHuser BJ. 2017. Aluminum application to restore water quality in eutrophic lakes: maximizing binding efficiency between aluminum and phosphorus. Lake Reserv Manage. 33:143-151.Aluminum (Al), typically added to lakes to reduce internal cycling of legacy phosphorus (P) in sediment, was added to the littoral zone of Lake Harriet (Minnesota) to inhibit the uptake of sediment P by buoyancy regulating species of plankton. Analytical results from sediment collected over an 11-year period showed that the added Al (32 g/m(2)) started to move outside the treatment zone almost immediately after treatment, with <5% remaining within the treatment area after 6 months. Although the original treatment design failed, the application method was, unexpectedly, a success with respect to binding efficiency between Al and P in the sediment. As the Al drifted to deeper areas of the lake, internal P release in non-treated, deeper areas of the lake declined and the binding ratio between Al and Al-bound P decreased, reaching 2.1 (molar) in profundal sediments 10years after treatment. The increased contact with available (mobile) sediment P increased binding efficiency, resulting in a 163-581% increase of P bound per unit Al compared to previous whole-lake aluminum treatments. The binding efficiency exceeded expectations showing that, in addition to the amount of Al added, treatment location and subsequent translocation of the Al floc can substantially affect binding efficiency and treatment effectiveness
Paracelsus, sein leben und denken.
No full text3 pages of manuscript notes inserted at end."Verzeichniss der schriften des Paracelsus nach deren ausgabe von Johann Huser bei Zetzner in Strassburg. 1616-1618": p. [243]-246.Mode of access: Internet
Towards a fuller understanding of selected molecular compounds
No full textThis work is separated into two distinct sections. The first section deals with the analysis by variable temperature single crystal X-ray diffraction of crystalline molecular materials with novel physical properties. The second section details the electron density analysis of selected crystalline compounds using high resolution, low temperature single crystal X-ray diffraction. Chapter 1 provides introduction to X-ray diffraction outlining the theory this work is based on. Chapter 2 introduces the molecular material studies based on materials containing the bis(ethylenedithio)-tetrathiaftilvalene molecule. The aim of these studies was to achieve a greater understanding of the materials and the changes they undergo when exposed to variations in temperature whilst in the crystalline state. These structural changes observed are very minor but have dramatic effects on the electrical properties of the materials studied. It became apparent that the only way to form a full understanding of these materials was to be able to 'see' the electronic configuration of the materials, not just their gross structure. The field of electron density analysis by X- ray diffraction is now a well documented area. Chapter 4 provides an introduction to the field of electron density analysis. Diffraction experiments were conducted on systems of different complexity to investigate this field and these results are reported in Chapter 5. No electron density analyses have been conducted on the molecular materials studied in Chapter 3 as yet, due to the lack of crystals of suitable quality. It was also noted that to fully categorise the nature of the physical changes occurring in these structures that a diffractometer capable of analysing these samples throughout the temperature range of their physical phenomena was needed. An outline for the development of such a diffractometer is detailed in Chapter 6, 'future works'
High sensitivity cameras can lower spatial resolution in high-resolution optical microscopy
No full textOrtkraß H, Müller M, Engdahl AK, Holst G, Huser T. High sensitivity cameras can lower spatial resolution in high-resolution optical microscopy. Nature Communications . 2024;15(1): 8886.High-resolution optical fluorescence microscopies and, in particular, super-resolution fluorescence microscopy, are rapidly adopting highly sensitive cameras as their preferred photodetectors. Camera-based parallel detection facilitates high-speed live cell imaging with the highest spatial resolution. Here, we show that the drive to use ever more sensitive, photon-counting image sensors in cameras can, however, have detrimental effects on the spatial resolution of the resulting images. This is particularly noticeable in applications that demand a high space-bandwidth product, where the image magnification is close to the Nyquist sampling limit of the sensor. Most scientists will often select image sensors based on parameters such as pixel size, quantum efficiency, signal-to-noise performance, dynamic range, and frame rate of the sensor. A parameter that is, however, typically overlooked is the sensor's modulation transfer function (MTF). We have determined the wavelength-specific MTF of front- and back-illuminated image sensors and evaluated how it affects the spatial resolution that can be achieved in high-resolution fluorescence microscopy modalities. We find significant differences in image sensor performance that cause the resulting spatial resolution to vary by up to 28%. This result shows that the choice of image sensor has a significant impact on the imaging performance of all camera-based optical microscopy modalities. © 2024. The Author(s)
Optical deformation of red blood cells trapped on a narrow waveguide
No full textReduced blood deformability is clinically linked to several diseases. It is important to develop sensitive tools to measure the loss of blood deformability. The evanescent field of an optical waveguide can trap and propel red blood cells along the waveguide. Here we propose to use the evanescent field from a narrow optical waveguide to trap and deform red blood cells. We demonstrate that the intensity gradient of the evanescent field at the edge of narrow waveguides (1-3 ?m) can be used to squeeze a blood cell. The RBCs are squeezed to a size comparable to the waveguide width. When the laser is switched on the cell is attracted towards the waveguide and is held in place. Subsequently, the part of the cell not on the waveguide is pulled in across the waveguide. The result is a cell (7-8 ?m in diameter) squeezed down to a significantly smaller width (typically 3 ?m). The cell regains its original shape when laser is switched-off
Time-gated single photon counting enables separation of CARS microscopy data from multiphoton-excited tissue autofluorescence
No full textLy S, McNerney G, Fore S, Chan J, Huser T. Time-gated single photon counting enables separation of CARS microscopy data from multiphoton-excited tissue autofluorescence. Optics Express. 2007;15(25):16839-16851.We demonstrate time-gated confocal imaging as a means to separate coherent anti-Stokes Raman scattering (CARS) microscopy data from multi-photon excited endogenous fluorescence in tissue. CARS is a quasi-instantaneous process and its signal decay time is only limited by the system's instrument response function (IRF). Signals due to two-photon-excited (TPE) tissue autofluorescence with excited state lifetimes on the nanosecond scale can be identified and separated from the CARS signal by employing time-gating techniques. We demonstrate this improved contrast on the example of CARS microscopy of intact roots of plant seedlings as well as on rat arterial tissue. (c) 2007 Optical Society of America
Pulse length variation causing spectral distortions in OPO-based hyperspectral coherent Raman scattering microscopy
No full textPilger C, Hachmeister H, Greife P, Weiss A, Wiebusch G, Huser T. Pulse length variation causing spectral distortions in OPO-based hyperspectral coherent Raman scattering microscopy. Optics Express. 2018;26(22):28312-28322.Picosecond optical parametric oscillators (OPOs) with broad wavelength tunability are frequently used as light sources in hyperspectral coherent Raman scattering (CRS) microscopy. We investigate how changes in the pulse length during OPO wavelength tuning of the pump beam affect hyperspectral CRS imaging. We find that significant distortions of the resulting CRS spectra occur if the OPO is operated without monitoring pulse length variations. By utilizing a custom-written MATLAB based control program to counteract changes in pulse length, normalized and reproducible data sets can be acquired. We demonstrate this by comparing hyperspectral data obtained from pure substances, as well as relevant biological specimens
Temporal and spatial trends for trace metals in streams and rivers across Sweden (1996-2009)
No full textLong term data series (1996 through 2009) for trace metals were analyzed from a large number of streams and rivers across Sweden varying in tributary watershed size from 0.05 to 48 193 km(2). The final data set included 139 stream sites with data for arsenic (As), cobalt (Co), copper (Cu), chromium (Cr), nickel (Ni), lead (Pb), zinc (Zn), and vanadium (V). Between 7% and 46% of the sites analyzed showed significant trends according to the seasonal Kendall test. However, in contrast to previous studies and depositional patterns, a substantial portion of the trends were positive, especially for V (100%), As (95%), and Pb (68%). Other metals (Zn and Cr) generally decreased, were mixed (Ni and Zn), or had very few trends (Co) over the study period. Trends by region were also analyzed and some showed significant variation between the north and south of Sweden. Regional trends for both Cu and Pb were positive (60% and 93%, respectively) in the southern region but strongly negative (93% and 75 %, respectively) in the northern region. Kendall's tau coefficients were used to determine dependence between metals and potential in-stream drivers including total organic carbon (TOC), iron (Fe), pH, and sulphate (SO(4)(2-)). TOC and Fe correlated positively and strongly with As, V, Pb, and Co while pH and SO(4)(2) generally correlated weakly, or not at all with the metals studied
A role for amphiphysin in AP-1/clathrin coat formation
No full textTransport of cargo within the endocytic and secretory pathway is generally mediated by coated vesicles. Clathrin, in combination with different adaptor proteins, is the major coat protein for vesicle formation at the plasma membrane, endosomes, and the trans-Golgi network (TGN). Best characterized is the formation of clathrin coats for endocytosis at the plasma membrane involving the adaptor protein complex AP-2. Clathrin and AP-2 were shown to be at the centre of a complex interactome of proteins accessory to vesicle formation. Considerably less is known about the formation of clathrin coated carriers at the TGN and endosomes, where the adaptor protein complex AP-1 plays a major role.
In vitro studies showed the minimal requirements for association of AP-1 to liposomal membranes to be activated ARF1, phosphoinositides, and either sorting signals or unknown cytosolic factors. We have used a liposome floatation assay to identify cytosolic proteins collaborating with AP-1 at the membrane. Separation of proteins from bovine brain cytosol with several chromatographic methods yielded an active fraction containing amphiphysin 1, amphiphysin 2, and endophilin A1. All three proteins are expressed in brain and known to be involved in AP-2/clathrin coat formation. They consist of an N-terminal N-BAR (Bin, amphiphysin, Rvs) domain for dimerization and membrane binding and a C-terminal SH3 (Src homology 3) domain for interaction with dynamin and synaptojanin. Amphiphysin 1 and 2 in addition contain a middle domain with binding sites for adaptors and clathrin. It was proposed that amphiphysins and endophilin are targeted to membranes with high curvature, such as the neck of a forming vesicle, where they recruit dynamin and synaptojanin in preparation for vesicle fission and uncoating.
In this thesis, I bacterially expressed and purified all three proteins and tested them in the floatation assay for AP-1 membrane binding activity. Only amphiphysin 2 showed activity, both as a homodimer and as a heterodimer with amphiphysin 1. Activity depended on a motif that was shown to bind to AP-1, AP-2, and clathrin in GST pull-down experiments.
Endogenous amphiphysins in primary neurons, as well as transiently expressed in neuronal or fibroblast cell lines, co-localized with AP-1 at the TGN. In addition, when expressed at high levels in neuronal cells, amphiphysins aggregated and interfered dominantly with the TGN localization of AP-1. Both phenomena depended on the presence of the clathrin and adaptor interaction sequence in the amphiphysins. Furthermore, both amphiphysins could be cross-linked to AP-1 in vivo.
Our results indicate that amphiphysin 1 and 2 function not only in clathrin coated vesicle formation for endocytosis at the plasma membrane, but are also part of the machinery forming AP-1/clathrin coats at the TGN and endosomes. This suggests that the machineries for CCV formation with AP-1 and AP-2 at different locations in the cell share more components than previously anticipated
Super-resolution upgrade for deep tissue imaging featuring simple implementation
No full textByers P, Kellerer T, Li M, Chen Z, Huser T, Hellerer T. Super-resolution upgrade for deep tissue imaging featuring simple implementation. Nature Communications . 2025;16(1): 5386.Deep tissue imaging with high contrast close to or even below the optical resolution limit is still challenging due to optical aberrations and scattering introduced by dense biological samples. This results in high complexity and cost of microscopes that can facilitate such challenges. Here, we demonstrate a cost-effective and simple to implement method to turn most two-photon laser-scanning microscopes into a super-resolution microscope for deep tissue imaging. We realize this by adding inexpensive optical devices, namely a cylindrical lens, a field rotator, and a sCMOS camera to these systems. By combining two-photon excitation with patterned line-scanning and subsequent image reconstruction, we achieve imaging of sub-cellular structures in Pinus radiata, mouse heart muscle and zebrafish. In addition, the penetration depth of super-resolved imaging in highly scattering tissue is considerably extended by using the camera's lightsheet shutter mode. The flexibility of our method allows the examination of a variety of thick samples with a variety of fluorescent markers and microscope objective lenses. Thus, with a cost-efficient modification of a multi-photon microscope, an up to twofold resolution enhancement is demonstrated down to at least 70mum deep in tissue. © 2025. The Author(s)
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