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기사 소개

  • 요약
  • 초록
  • 서문
  • 프로토콜
  • 결과
  • 토론
  • 공개
  • 감사의 말
  • 자료
  • 참고문헌
  • 재인쇄 및 허가

요약

We present a protocol for performing three-point bending tests on sub-millimeter scale fibers using a custom-built mechanical testing device. The device can measure forces ranging from 20 µN up to 10 N and can therefore accommodate a variety of fiber sizes.

초록

Many load bearing biological structures (LBBSs)—such as feather rachises and spicules—are small (<1 mm) but not microscopic. Measuring the flexural behavior of these LBBSs is important for understanding the origins of their remarkable mechanical functions.

We describe a protocol for performing three-point bending tests using a custom-built mechanical testing device that can measure forces ranging from 10-5 to 101 N and displacements ranging from 10-7 to 10-2 m. The primary advantage of this mechanical testing device is that the force and displacement capacities can be easily adjusted for different LBBSs. The device's operating principle is similar to that of an atomic force microscope. Namely, force is applied to the LBBS by a load point that is attached to the end of a cantilever. The load point displacement is measured by a fiber optic displacement sensor and converted into a force using the measured cantilever stiffness. The device's force range can be adjusted by using cantilevers of different stiffnesses.

The device's capabilities are demonstrated by performing three-point bending tests on the skeletal elements of the marine sponge Euplectella aspergillum. The skeletal elements—known as spicules—are silica fibers that are approximately 50 µm in diameter. We describe the procedures for calibrating the mechanical testing device, mounting the spicules on a three-point bending fixture with a ≈1.3 mm span, and performing a bending test. The force applied to the spicule and its deflection at the location of the applied force are measured.

서문

By studying the architectures of load bearing biological structures (LBBSs), such as shell and bone, engineers have developed new composite materials that are both strong and tough 1. It has been shown that the remarkable mechanical properties of LBBSs and their bio-inspired counterparts are related to their intricate internal architectures 2. However, the relationships between LBBS architectures and mechanical properties are not fully understood. Measuring a LBBS's mechanical response is the first step toward understanding how its architecture enhances its mechanical properties.

However, it is important that the type of test used to measure a LBBS's mechanical response is consistent with its mechanical function. For example, since feathers must support aerodynamic loads, the primary function of a feather rachis is to provide flexural stiffness 3. Therefore, a bending test is preferred to a uniaxial tension test for measuring its mechanical response. In fact, many LBBSs—such as feather rachises 3, grass stems 4, and spicules 5,6,7,8—primarily deform by bending. This is because these LBBSs are slender—i.e., their length is much greater than their width or depth. However, performing bending tests on these LBBSs is challenging because the forces and displacements that they can withstand before failing range from 10-2 to 102 N and 10-4 to 10-3 m, respectively 3,4,5,7,8. Consequently, the device used to perform these mechanical tests should have force and displacement resolutions of ≈10-5 N and ≈10-7 m (i.e., 0.1% of the sensor's maximum measureable force and displacement), respectively.

Commercially available, large scale, mechanical testing systems typically cannot measure forces and displacements with this resolution. While atomic force microscope-based 9,10 or microelectromechanical systems-based 11 testing devices have adequate resolution, the maximum force (respective displacement) they can measure is smaller than the maximum force (respective displacement) that the LBBS can withstand. Therefore, to perform bending tests on these LBBSs, engineers and scientists must rely on custom-built mechanical testing devices 5,7,12,13. The primary advantage of these custom-built devices is that they can accommodate large ranges of forces and displacements. However, the construction and operation of these devices is not well documented in the literature.

A protocol is described for performing three-point bending tests using a custom-built mechanical testing device that can measure forces ranging from 10-5 to 101 N and displacements ranging from 10-7 to 10-2 m. Technical drawings, including all dimensions, of the components of the mechanical testing device are provided in the Supplementary Material. The primary advantage of this mechanical testing device is that the force and displacement ranges can be easily adjusted to suit different LBBSs. The device's operating principle is similar to that of an atomic force microscope 9. In this device, a specimen is placed across a trench cut in a stainless steel plate (see Figure 1A-C). The span of the trench is measured from optical micrographs to be 1278 ± 3 µm (mean ± standard deviation; n = 10). The trench edges support the specimen during a bending test (see Figure 1C, and D). This sample stage is attached to a three-axis translation stage and positioned beneath an aluminum wedge so that the wedge is located midway across the trench's span (see Figure 1C). By moving the stage in the figure-introduction-4562 direction (see Figure 1A, and C), the specimen is pushed into the wedge causing the specimen to bend.

We refer to the wedge as the load point tip (LPT) and the component of the device that contains the wedge as the load point (LP). The LP is attached to the end of a cantilever whose displacement is measured by a fiber optic displacement sensor (FODS). The FODS emits infrared light, which is reflected off of a mirror located on the top surface of the LP (see Figure 1B) and received by an optical fiber in the FODS. A ≈5 mm square piece of a polished silicon wafer is used as the LP mirror and is affixed to the LP using epoxy. The FODS measures displacements by comparing the intensities of the emitted and reflected light. The cantilever stiffness and displacement are used to compute the force, figure-introduction-5564, experienced by the wedge due to its interaction with the specimen. The cantilever displacement is also used to compute the displacement of the specimen's cross-section beneath the wedge, figure-introduction-5824. Cantilever-based force sensors have been used in a number of micro- and macro-scale mechanical testing studies 10,11,12,13,14. The specific design presented here is adapted from a mechanical testing device used for performing adhesive contact experiments 14. A similar design has also been used in a commercially available micro-tribometer 15,16.

figure-introduction-6548
Figure 1: Overview of the custom-built mechanical testing device. (A) A computer aided design rendering of the device. The stage components are highlighted in green. The force sensing subassembly (cantilever, load point (LP)) is highlighted in red. (B) A magnified view of (A). The LP mirror is shown in blue on the top surface of the LP beneath the FODS and is labeled LPM. (C) The coordinate system used to describe the motion of the translation stage. By leveling the stage in step 1.9 of the protocol, the figure-introduction-7237 direction is made to coincide with the vector normal to the surface of the LP mirror. (D) A schematic of the three-point bending configuration showing the deformation of the spicule and the measured displacements figure-introduction-7535, and figure-introduction-7610. Please click here to view a larger version of this figure.

The device's capabilities are demonstrated by performing three-point bending tests on the skeletal elements of the marine sponge Euplectella aspergillum6,7. This sponge's skeleton is an assembly of filaments, called spicules (see Figure 2A). The spicules are ≈50 µm thick and are composed primarily of silica 6. Biosilica-based spicules are found in sponges belonging to the classes Demospongiae, Homoscleromorpha, and Hexactinellida. Sponges, such as E. aspergillum, that belong to the class Hexactinellida are also known as "glass sponges." While the spicules of glass sponges are composed primarily of silica, it has been shown that the silica often contains an organic matrix composed of either collagen 17,18 or chitin 19,20,21. This organic matrix plays an important role in silica biomineralization 18,20. Furthermore, in some spicules the organic matrix also serves as a template for the biomineralization of calcium 22. In addition to being distributed within the silica, the organic matrix can also form distinct layers that partition the spicule's silica into concentric, cylindrical lamellae 6,23. It has been shown that this concentric, lamellar architecture can affect the spicules' deformation behavior 6,7,8,24,25,26. Consequently, the spicules' mechanical properties are determined by a combination of their chemistry (i.e., the chemical structure of the silica-protein composite) and their architecture 27. Both the chemical structure and architecture of glass sponge spicules are still under investigation 24,28,29.

Most of the spicules in E. aspergillum are cemented together to form a stiff skeletal cage. However, at the base of the skeleton there is a tuft of very long (≈10 cm) spicules known as the anchor spicules (see Figure 2A). We describe the protocol for performing three-point bending tests on small sections of the anchor spicules.

In step 1 of the protocol, the procedure for assembling and aligning the components of the custom-built mechanical testing device is described. Steps 2 and 4 of the protocol provide instructions for generating calibration data used to compute forces and displacements in the bending test. The steps taken to prepare a section of a spicule and mount it to the test fixture are described in step 3. The procedure for conducting the bending test on the spicule section is described in step 5. Finally, in the Representative Results section the calibration data obtained in steps 2 and 4 are used along with the bending test data obtained in step 5 to compute figure-introduction-11471 and figure-introduction-11543.

figure-introduction-11673
Figure 2: Procedure for sectioning and inspecting E. aspergillum spicules. (A) The skeleton of E. aspergillum. The tuft of free-standing anchor spicules is shown at the base of the skeleton. The scale bar is ~25 mm. (B) A single anchor spicule is held in place on a microscope slide using a #00000 red sable brush and sectioned using a razor blade. The scale bar is ~12 mm. (C) A section of an E. aspergillum spicule placed across the trench on the sample stage. The trench edges and trench ridge are highlighted in teal and orange, respectively. The spicule is pushed against the trench ridge to ensure that its axis is perpendicular to the trench edges. (D) A micrograph of a spicule that passes the inspection procedure described in step 3.4 of the protocol, which describes how to determine if a spicule section is damaged and should be discarded. (E) A micrograph of a spicule containing many cracks and missing large sections of silica layers that would fail the inspection procedure described in step 3.4 of the protocol. Scale bars =  250 µm (C), 100 µm (D), and 100 µm (E). Please click here to view a larger version of this figure.

프로토콜

1. Assembly and Alignment

  1. Choose a cantilever whose stiffness is appropriate for the intended experiment. Attach the LP to the cantilever using #4-40 socket head cap screws (SHCSs) (see Figure 3A). Take care to not plastically deform the cantilever arms while attaching the LP.

figure-protocol-430
Figure 3: Procedure for assembling the cantilever force sensor and measuring its stiffness. (A) The load point (LP) is attached to the cantilever (C), with the load point tip (LPT) pointed upward. (B) The cantilever and LP subassembly is attached to the cantilever plate, denoted as CP. The recessed pocket of the cantilever plate is shown beneath the cantilever arms. (C) The cantilever plate is attached to the underside of the frame so that the side of the plate shown in (B) is facing the figure-protocol-1097 direction. The FODS micrometer is denoted as FM. (D) The wire hook and calibration weights used in step 2 of the protocol are shown hanging from the hole in the LPT. Please click here to view a larger version of this figure.

  1. Apply a few drops of 2-propanol to a lint free cotton swab and wipe the surface of the LP mirror. Inspect the mirror for scratches and replace the mirror if it is damaged.
  2. Loosely attach the cantilever to the cantilever plate using #6-32 SHCSs on the side of the plate containing the recessed pocket with the LPT pointing away from the plate (see Figure 3B). Insert the 1/8" alignment pins through the cantilever and plate, tighten the screws, and then remove the alignment pins.
  3. Retract the FODS as much as possible by turning the FODS micrometer counter-clockwise (see Figure 3C). Loosely attach the cantilever plate to the frame using #6-32 SHCSs with the LPT pointing in the figure-protocol-2339 direction (see Figure 1A). Insert the 1/8" alignment pins through the frame and cantilever plate, tighten the screws, and then remove the alignment pins (see Figure 3C).
  4. Turn on the power supply and set the voltage to 12.00 V in constant voltage mode using the adjustment knob. Then turn on the voltage output and confirm that the current draw displayed on the power supply's LCD screen is roughly 60-70 mA. Wait at least one hour for the current draw to reach steady state to reduce voltage measurement uncertainty.
  5. Open and run the the Basic_Data program (see Supplementary Code files). Turn the FODS micrometer (see Figure 3C and Figure 4A) clockwise to move the FODS toward the LP mirror until the output voltage displayed on the user interface graph reaches a maximum value.
    1. Adjust the gain of the FODS by turning the set screws on the side of the FODS housing so that the voltage output is 5.0 V. Turn the FODS micrometer counter-clockwise to retract the FODS.
  6. Turn on the microscope illuminator and adjust the microscope position and focus using the two manual translation stages so that the LPT is centered in the field of view. Stop the Basic_Data program by clicking the 'Stop' button.
  7. Open the motor controller user interface software. Use the potentiometer slider on the figure-protocol-3978-axis motor controller to move the stage to the maximum allowable travel in the figure-protocol-4142 direction and set the home position by clicking the 'Home' button in the user interface.
    1. Use the potentiometer slider on the figure-protocol-4372-axis motor controller to move the stage to the maximum allowable travel in the figure-protocol-4519 direction and set the home position. Close the user interface software.
  8. Seat the stage on the stage base plate (see Figure 4A) so that the tips of the micrometer heads on the leveling plate rest in the stage base plate divots. Place a bubble level on the isolation table and adjust the pressure in each of the table's legs by turning the valve arm thumb screws so that the surface is level.
    1. Move the bubble level to the top of the stage leveling plate and adjust the micrometers so that it is also level. Note the micrometer positions and remove the stage from the stage base plate. Note: The protocol can be paused here.

figure-protocol-5378
Figure 4: The mechanical testing device as assembled in steps 1.9 and 3.7 of the protocol. (A) The sample stage (SS), is attached to the translation stage (TS), and is leveled using the micrometers on the stage leveling plate (SLP), which are seated on the stage base plate (SBP). The stage base plate is attached to the optical breadboard of the isolation table. The cantilever (C); cantilever plate (CP); and fiber optic displacement sensor (FODS) compose the force sensing system. (B) The load point (LP) is attached to the cantilever and the load point tip (LPT) is positioned over the spicule on the sample stage. During a bending test, the displacement of the LP is measured using the FODS. The initial distance between the FODS and the LP mirror is controlled by the FODS micrometer (FM) shown in (A). (C) A micrograph of the spicule laying across the trench in the sample stage, positioned beneath the LPT. Scale bar = 250 µm (C). Please click here to view a larger version of this figure.

2. Cantilever Stiffness Measurement

  1. Run the Basic_Data program and turn the FODS micrometer clockwise until the output voltage is approximately 4 V. Stop the program by clicking the 'Stop' button.
  2. Measure the mass of the wire hook and calibration weights using an analytical balance.
  3. Open the Cantilever_Calibration program (see Supplementary Code files) and enter the desired file name for the force calibration output file in the text box in the user interface.
  4. Run the Cantilever_Calibration program and click 'OK' when prompted to enter the mass of the first calibration weight. Wait for the output voltage displayed in the user interface graph to stop oscillating and click the green 'Voltage Stabilized' button to take a voltage measurement.
  5. Use tweezers to hang the wire hook from the hole in the LPT so that the hook is facing away from the microscope objective (see Figure 3D). Use the tweezers to damp the vibration of the cantilever caused by the addition of the hook.
    1. Enter the mass of the hook in grams in the dialog box and click 'OK'. As in the previous step, wait for the output voltage to stop oscillating before clicking the 'Voltage Stabilized' button.
  6. Use tweezers to hang the first weight on the wire hook and repeat the process of taking a voltage measurement as described in the previous step. Repeat this step until either all of the calibration weights have been hung or the output voltage is less than 1.8 V. At this point, click 'Cancel' in the dialog box to exit the Cantilever_Calibration program.
  7. Turn the FODS micrometer counter-clockwise to retract the FODS. Carefully remove the hook and weights from the LPT.
    NOTE: The force calibration output file is a tab delimited list of the force applied by the calibration masses, the mean of 100 FODS output voltage readings and the standard deviation of those readings. The Representative Results section describes how this data file is processed to measure the cantilever stiffness.

3. Specimen Preparation

  1. Wear nitrile gloves when handling the E. aspergillum sponge skeletons and store the skeletons in sealed containers when they are not being handled.
    CAUTION: Since the spicules are composed primarily of silica, broken spicule fragments are sharp and can become embedded in skin, leading to irritation.
  2. Use a pair of tweezers to grasp one anchor spicule by its distal end and pull to remove it from the skeleton (see Figure 2A). Place the spicule on a clean microscope slide.
  3. Hold the spicule against the slide near the midpoint along its length using a #00000 red sable brush. Cut a ≈4 mm section of the spicule by pushing a razor blade against the spicule on either side of the brush perpendicular to the slide surface (see Figure 2B). Discard the large distal and proximal spicule sections and keep the ≈4 mm section.
  4. Inspect the 4-mm spicule section using a polarized light microscope at 10x magnification (see Figure 2C-E). Discard the spicule section and return to step 3.2 if it is missing large regions of silica layers (see Figure 2E). Handle inspected spicule sections exclusively using the #00000 red sable brush to avoid introducing any new damage to their silica layers.
  5. Clean any spicule fragments or other particles from the surface of the sample stage with a brush or compressed air. Then apply a few drops of 2-propanol to a lint free cotton swab and wipe the sample stage. Avoid contact with the areas of the stage coated with non-reflective paint.Note: The paint is used to reduce the number of specular reflections in the images taken during the bending test.
  6. Transfer the spicule section to the sample stage. Position the spicule section across the trench with the desired span for the bending test and gently push it in the figure-protocol-11039 direction against the trench ridge. Ensure that the spicule is perpendicular to the trench edges (see Figure 2C).
  7. Seat the stage on the stage base plate so that the tips of the micrometer spindles rest in the stage base plate divots. If needed, adjust the micrometers on the stage leveling plate to the values noted in step 1.9 of the protocol.

4. Voltage-displacement Interpolation File

  1. Open the Bending_Test program (see Supplementary Code files). Set the 'step size' to 2 µm, 'maximum displacement' to 0.5 mm, 'low voltage stop' to 1.5 V, and 'high voltage stop' to 4.6 V using the text boxes shown in the user interface.
    1. Select the desired image and data directories and the output file name using the text boxes in the user interface. Set the 'save images' switch in the user interface to the down position and click the green rectangular button below the words 'Voltage Difference' so that it becomes illuminated.
  2. Run the Bending_Test program and wait for the motor controller and camera interfaces to initialize.
  3. Turn on the illuminator and adjust the brightness so that the LPT is visible. Turn the FODS micrometer clockwise until the output voltage displayed in the user interface graph is ~1.7 V.
    1. Use the potentiometer slider on the figure-protocol-12636-axis motor controller to move the stage in the figure-protocol-12751 direction until it is ~1 cm below the LPT and set the figure-protocol-12873-axis home position by clicking the "Home" button.
  4. Use the potentiometer sliders on the figure-protocol-13060- and figure-protocol-13133-axis motor controllers to position the LPT over the center of the thin steel strip located on the sample stage in the figure-protocol-13321 direction from the trench. Use the potentiometer slider on the figure-protocol-13454-axis motor controller to move the stage in the figure-protocol-13569 direction until the stage is within the microscope's field of view.
  5. Use the potentiometer slider on the figure-protocol-13755-axis motor controller to move the stage in the figure-protocol-13870 direction while watching the output voltage graph in the user interface. Determine the approximate position at which the LPT contacts the stage's surface by looking for a change in voltage with further movement of the stage. Retract the stage approximately 10 µm.
  6. Click the button labeled "Begin Test". When prompted, enter values of 0.003 V and 0.001 mm for 'touch sensitivity' and 'touch off step size', respectively. Wait for the test to complete.
    NOTE: After this point, do not remove the stage from the stage base plate until the bending test is complete in order to ensure accurate displacement measurements. The voltage-displacement interpolation output file is a tab delimited list of the mean of 100 FODS output voltage readings and the standard deviation of those readings along with the figure-protocol-14786-axis stage position at every stage displacement increment. The Representative Results section describes how this data file is used to convert measured FODS output voltages to LP displacements.

5. Bending Test

  1. Open and run the Basic_Data program and turn the FODS micrometer counter-clockwise until the output voltage displayed on the user interface graph is approximately 3 V. Use the potentiometer slider on the figure-protocol-15357-axis motor controller to position the LPT between the trench edges above the spicule (see Figure 4C).
    1. Use the potentiometer slider on the figure-protocol-15622-axis motor controller to move the stage in the figure-protocol-15737 direction until the LPT is below the top surface of the trench ridge (see Figure 5A). Finally, use the potentiometer slider on the figure-protocol-15983-axis motor controller to bring the front surface of the trench ridge into focus so that the complete width of the LP is between the edges of the trench ridge. Stop the Basic_Data program by clicking the 'Stop' button.
  2. Open and run the Center_LoadPoint program (see Supplementary Code file). Use the figure-protocol-16419-axis motor controller to move the stage until the LPT is nearly in contact with the right trench edge. Click the "Find Edge" button.
  3. When prompted, use the figure-protocol-16661-axis motor controller to move the stage until the LPT is nearly in contact with the left trench edge. Click the "Find Edge" button. Wait for the program to position the LPT mid-way across the trench span (see Figure 5B).
    NOTE: After this point it is important not to adjust the figure-protocol-17069-axis motor controller as this will result in a misalignment of the LPT.
  4. Open the Bending_Test program. Set the step size to 2 µm, maximum displacement to 0.5 mm, low voltage stop to 1.5 V, and high voltage stop to 4.5 V using the text boxes in the user interface.
    1. Select the desired image and data directories and the output file name using the text boxes in the user interface. Set the 'save images' switch in the user interface to the up position and click the green rectangular button below words 'Voltage Difference' so that it is not illuminated.
  5. Run the Bending_Test program and wait for the motor controller and camera interfaces to initialize.
  6. Move the stage in the figure-protocol-17940 direction using the potentiometer slider on the motor controller until the spicule is within the microscope's field of view. Use the potentiometer slider on the figure-protocol-18190-axis motor controller to move the stage until the spicule is under the LPT.
    1. Adjust the microscope focus knobs so that the spicule is in focus in the user interface (see Figure 4C). Turn the FODS micrometer counter-clockwise until the output voltage is approximately 1.8 V.
  7. Use the potentiometer slider on the z-axis motor controller to move the stage in the figure-protocol-18718 direction while watching the output voltage graph in the user interface. Determine the approximate position at which the LPT contacts the spicule by looking for a change in voltage with further movement of the stage. Retract the stage approximately 50 µm.
  8. Click "Begin Test" and wait until the bending test is completed and the stage returns to the figure-protocol-19158-axis home position.
    NOTE: The stage will move in 2 µm increments (as is prescribed in step 5.4 of the protocol) in the figure-protocol-19374 direction, bending the spicule (see Figure 5C) until one of several stopping conditions is met. The stopping conditions are: a) the maximum stage displacement of 0.5 mm is reached; b) the spicule breaks and the program detects a large drop in the FODS output voltage; or c) the high voltage limit of 4.5 V is reached. For stopping condition (a), the user will be prompted if they would like to end the test or override the previous value. When 'Override' is selected, the user will have the opportunity to either increment the stage displacement limit or reverse the direction of the stage displacement step in order to continue collecting data as the spicule is unloaded. The stage displacement increment direction can also be changed by clicking the "Reverse Loading" button at any point during the test. The bending test output file has the same structure as the voltage-displacement interpolation output file generated in step 4.6 of the protocol. That is, it is a tab delimited list of the mean of 100 FODS output voltage readings and the standard deviation of those readings along with the figure-protocol-20618-axis stage position at every stage displacement increment. The Representative Results section describes how this data file is used along with the voltage-displacement interpolation file to compute the cantilever displacements and stage displacements during the bending test. Subsequently, the cantilever stiffness is used to compute the force applied by the LPT on the spicule.
  9. After the test is complete, turn the FODS micrometer counter-clockwise until the FODS is at least 5 mm from the LPT mirror. Then, carefully remove the stage from the stage base plate.

figure-protocol-21343
Figure 5: Procedure for aligning the LPT with the trench's mid span and performing a bending test. (A) The LPT is positioned below the top surface of the trench ridge at the end of step 5.1 of the protocol, but it is not yet positioned at mid span. (B) The position of the LPT after the centering procedure described in steps 5.2 and 5.3 of the protocol are completed. (C) A micrograph of a spicule taken during the bending test. The displacement of the spicule cross-section beneath the LPT, figure-protocol-22048, is marked schematically. Scale bars = 250 µm (A-C). Please click here to view a larger version of this figure.

결과

The most basic outputs of any mechanical test are the magnitude of the force applied to the specimen and the displacement at the location where the force is applied. In the case of a three-point bending test, the goal is to obtain the magnitude of the force applied by the LPT, figure-results-336, and the displacement of the specimen's cross-section beneath the LPT in the

토론

Several steps of the protocol are particularly important for ensuring that forces and displacements are measured accurately. While some of these critical steps are universal to all three-point bending tests, others are unique to this mechanical testing device.

In step 1.2 of the protocol the LP mirror is cleaned and inspected for scratches, and in step 1.6 of the protocol the FODS gain is set. It is important for the gain and the LP mirror reflectance to be co...

공개

The authors have nothing to disclose.

감사의 말

This work was supported by National Science Foundation [Mechanics of Materials and Structures Program, grant number 1562656]; and the American Society of Mechanical Engineers [Haythornthwaite Young Investigator Award].

자료

NameCompanyCatalog NumberComments
TMC 36" x 48" isolation table with 4" CleanTop breadboardTMC63-563Isolation Table
Diffeential Screw AdjusterThorlabsDAS110For stage leveling plate
1" Travel Micrometer Head with 0.001" GraduationsThorlabs150-801MEFor stage leveling plate
Right-Angle Bracket for PT Series Translation Stages, 1/4"-20 Mounting HolesThorlabsPT102For microscope mount
1" Dovetail Translation Stage, 1/4"-20 TapsThorlabsDT25For microscope mount
1" Translation Stage with 1/4"-170 Adjustment Screw, 1/4"-20 TapsThorlabsPT1BFor microscope mount
12" Length, Dovetail Optical RailEdmund Optics54-401For microscope mount
2.5" Width, Dovetail CarrierEdmund Optics54-404For microscope mount
0.5" Width, Dovetail CarrierEdmund Optics54-403For microscope mount
InfiniTube Mounting C-Clamp with ¼-20Edmund Optics57-788Microscope component
Standard (with no In-Line Attachment), InfiniTubeEdmund Optics56-125Microscope component
Standard In-Line Attachment (Optimized at 2X-10X), InfiniTubeEdmund Optics56-126Microscope component
Mitutoyo/Achrovid Objective Adapter (M26 to M27)Edmund Optics53-787Microscope component
5X Infinity Achrovid Microscope ObjectiveEdmund Optics55-790Microscope component
0.316" ID, Fiber Optic Adapter SX-6Edmund Optics38-944Microscope component
¼" x 36", Flexible Fiber Optic Light GuideEdmund Optics42-347Microscope component
115V, MI-150 Fiber Optic Illuminator w/IR Filter and HolderEdmund Optics55-718Microscope component
Allied Vision Manta G-223 2/3" Color CMOS CameraEdmund Optics88-452Microscope component
Power Supply for Manta/ Guppy Pro/ Stingray/ PikeEdmund Optics68-586Microscope component
1/4" Travel Single Axis Translation StageThorlabsMS1SFODS micrometer
Analog Reflectance Dependent Fiber Optic Displacement SensorPhiltecD20FODS
30V, 3A DC Power SupplyAgilentU8001APower supply for DAQ and FODS
14-Bit, 48 kS/s Low-Cost Multifunction DAQNational InstrumentsUSB-6009DAQ for FODS
Three Axis Motorized Translation StageThorlabsThorlabs T25 XYZ-E/MTranslation stage
T-Cube DC Servo Motor ControllerThorlabsTDC001Motor controller for stage
T-Cube Power SupplyThorlabsTPS001Power supply for motor controller
National Instruments LabVIEW (2013 SP1)National InstrumentsUsed for running software
National Instruments LabVIEW Vision Acquisition Software (2016)National InstrumentsUsed for running software
Nikon Eclipse Ci-POL Main BodyMVIMDA96000Polarized light microscope
Nikon Pi Intermediate Tube with Analyzer SliderMVIMDB45305Polarized light microscope
Nikon Dia-PolarizerMVIMDN11920Polarized light microscope
Power Cord - 7'6"MVI79035Polarized light microscope
Nikon P-Amh Mechanical StageMVIMDC45000Polarized light microscope
Nikon Lwd Achromat CondenserMVIMBL16100Polarized light microscope
Nikon LV-NBD5BD-CH Manual Quint Nosepiece ESDMVIMBP60125Polarized light microscope
Nikon C-TF Trinocular Tube FMVIMBB93100Polarized light microscope
Nikon CFI 10X Eyepiece FN 22mm NCMVIMAK10110Polarized light microscope
Nikon TU Plan Flour BD 10x ObjectiveMVIMUE42100Polarized light microscope
Venus Flower Basket SpongeDenis BrandN/ASponge skeleton
3.5X Headband Flip-Up MagnifierMcMaster Carr1490T5Used for spicule sectioning
Ø1" Silicon Wafer, Type P / <100>Ted Pella16011Used for load point mirror
Low Lint Tapered Tip Cotton SwabMcMaster Carr71035T31Used for cleaning LP mirror
Rubber grip precision knifeMcMaster Carr35575A68Used for sectioning spicules
Microscope Slides, frosted end, 75 x 25 x 1mmTed Pella260409Used for sectioning spicules
Sable Brushes, #00000, 0.08mm W x 4.0mm LTed Pella11806Used for handling spicules
PELCO Pro High Precision Tweezers, extra fine tips, superior finishTed Pella5367-5NMUsed for handling spicules
Dual Axis Linear Scale MicrometerEdmund Optics58-608Used for calibrating the microscopes
FLEX-A-TOP FT-38 CASESD Plastic ContainersFT-38-CASUsed for storing spicules
Plastic Vial Bullseye LevelMcMaster Carr2147A11Used for leveling the stage
Analytical BalanceMettler ToledoMS105DUUsed to mass calibration weights

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