MICROFIBER-PAM

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Product

Probing of Cells and Tissue in Microbial Mats and Leaves

The MICROFIBER-PAM employs thin (100 µm) optical fibers for fluorescence excitation and detection. The thin fiber allows probing of small spots of heterogeneous photosynthetic surfaces like soil crusts.

A “working fiber” (MF-F, accessory), which is inserted into a leaf or a photosynthetic mat, measures photosynthetic gradients inside the sample. For easier penetration, the working fiber can be pulled out to a tapered tip of 10 to 30 μm.

Fiber optic coupler consisting of a central beam splitter (black elongated central part) and four multi-mode optical fibers (orange lines) with ST (straight tip) connectors. Grey box: Photomultiplier.

Outstanding Properties of the MICROFIBER-PAM

PAM fluorometer with the thinnest fiberoptics cable

Ultrahigh sensitivity

Four measuring light colors available

Measurement of light attenuation
 

The fiberoptics system of the MICROFIBER-PAM consists of two pairs of optical fibers. A fiberoptics coupler optically connects the fibers. Two fibers link the light source and the photomultiplier, respectively, to one end of the fiberoptics coupler. The two other fibers link the sample to the opposite end of the fiberoptics coupler.

For fluorescence measurements, the fiber optic coupler guides light from the LED via a single fiber to the sample, and it transmits the fluorescence emitted by the sample to the photomultiplier. Color filters prevent LED light from reaching the photomultiplier. To measure light attenuation, the two sample fibers are placed at opposite sides of the object of study and color filters are removed (see Figs. 1 and 2 below).

Fluorescence excitation and detection are controlled by the PAM-CONTROL unit, which allows stand-alone operation of the MICROFIBER-PAM but also functions as an interface for operation of the system by a Windows computer.

The PAM-CONTROL unit can be operated by the WinControl software versions 2 or 3. The system includes, an RS-232 cable, a USB-RS-232 adapter (when an RS-232 port is not available), a charger MINI-PAM/L, a cable to connect a chart recorder, a transport box, and a stand (ST-101).

Functional Diagram MICROFIBER-PAM

Fluorescence measurement (Fig. 1): Blue light passes through a short-pass filter transmitting light only at wavelengths smaller than 600 nm (MF-L470). A fiber guides the LED light to the four-port fiberoptic coupler, MF-2-2-100. Another fiber directs the LED light from there to the sample, and guides fluorescence back to the fiberoptic coupler. LED light and fluorescence are then transmitted fiberoptically to the photomultiplier (PM-MF).

Only fluorescence light reaches the photomultiplier because it is protected against the blue LED light by long-pass filters transmitting light only at wavelength longer than 640 nm. The fiber adapter for the photomultiplier is part of the MICROFIBER-PAM adapter set, MF-A. The MF-A adapter set also includes a holder for the blue LED and three additional LEDs.

Light attenuation measurement (Fig. 2): Without the color filters in front  of the LED and the photomultiplier, and with face-to-face orientation of the tips of the two sample fibers, the MICROFIBER-PAM detects the blue measuring light transmitted by the fiberoptics system to the photomultiplier. A sample placed between the fiber tips reduces the blue light intensity reaching the photomultiplier. The degree of light attenuation by a sample can be derived from the photomultiplier signal.

PAM-CONTROL Universal Control Unit

The PAM-CONTROL unit can be used to carry out PAM fluorescence measurements independently of a computer but it also acts as interface between fluorometer and a Windows computer running the version 2 or 3 of the WinControl software.

The PAM-CONTROL unit is part of several PAM systems, which all employ a highly sensitive photomultiplier tube for fluorescence detection: the MICROSCOPY-PAM, the MICROFIBER-PAM, and the WATER-PAM FIBER Version. In all three systems, an automatic shutdown procedure protects the photomultiplier tube against damage by high fluorescence levels or external light.
The memory of the unit can store 4000 data sets. An extensive menu provides full control of instrumental settings and a variety of measuring protocols.

An option that the MICROFIBER-PAM offers is the investigation of gradients of photosystem II characteristics within the leaf. For such investigations, the pointed tip of a working fiber (MF-F) is advanced into the leaf tissue by a micromanipulator, and saturation pulse analysis is carried out at defined depths of penetration.
Using this strategy, Terashima and his colleagues have analyzed how strong light of different colors damages photosystem II at various distances from the leaf surface. By measuring the maximum photochemical quantum yield of photosystem II (FV/FM), the authors demonstrated that amplitude as well as leaf gradients of photoinhibition depend on the color of photoinhibitory light.

Intra-leaf profiles of FV/FM in leaves of Capsicum annuum measured by a MICROFIBER-PAM having an optical microfiber of 30 μm diameter. The micro fiber was inserted into the leaf tissues with the aid of a three-dimensional water-pressure micromanipulator (WR-60, Narishige, Tokyo, Japan). Prior to FV/FMmeasurements, leaf discs were treated with lincomycin, an inhibitor of protein synthesis, and then photoinhibited at 2000 μmol photons m-2 s-1 at room temperature for 60 min by broad-band blue (400–500 nm, blue symbols), or red light (600–700 nm, red symbols). Measurements with non-irradiated control disks are shown as open symbols. Data from Terashima I, Fujita T, Inoue T, Chow WS, Oguchi R (2009) Plant Cell Physiology 50: 684–697. Original data were kindly provided by Prof. Ichiro Terashima.

Scientific Publications using Walz Devices

Source: Google Scholar.
Keywords: (Walz OR Waltz) Effeltrich.
Date: June 22, 2026.

Ʃ = 19642

Per Year

Source: Google Scholar.
Keywords: (Walz OR Waltz) Effeltrich.
Date: June 22, 2026.

Ʃ = 19642

Year

Selected Publications

Fluorescence and electron transfer of Limnospira indica functionalized biophotoelectrodes.

Ryzhkov N, Colson N, Ahmed E, Pobedinskas P, Haenen K, Janssen PJ, Braun A

Photosynthesis Research 162, 29-45

Go to publication

Light environment within a leaf. II. Progress in the past one-third century.

Terashima I, Ooeda H, Fujita T, Oguchi R

Journal of Plant Research 129: 353-363

Go to publication

Photosynthetic acclimation of Symbiodinium in hospite depends on vertical position in the tissue of the scleractinian coral Montastrea curta

Lichtenberg M, Larkum AWD, Kühl M

Frontiers in Microbiology 7: 230

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Pronounced gradients of light, photosynthesis and O2 consumption in the tissue of the brown alga Fucus serratus

Lichtenberg M, Kühl M

New Phytologist 207: 559-569

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Gradients of photoinhibition in the interior of a leaf induced by photoinhibition lights of different colors

Oguchi R, Douwstra P, Fujita T, Chow WS, Terashima I

Photosynthesis Research for Food, Fuel and the Future. Advanced Topics in Science and Technology in China. Springer, Berlin, Heidelberg

Go to publication

Intra-leaf gradients of photoinhibition induced by different color lights: implications for the dual mechanisms of photoinhibition and for the application of conventional chlorophyll fluorometers

Oguchi R, Douwstra P, Fujita T, Chow WS, Terashima I

New Phytologist 191: 146-159

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Green light drives leaf photosynthesis more efficiently than red light in strong white light: revisiting the enigmatic question of why leaves are green

Terashima I, Fujita T, Inoue T, Chow WS, Oguchi R

Plant and Cell Physiology 50: 684-697

Go to publication

Inter-polyp genetic and physiological characterisation of Symbiodinium in an Acropora valida colony

Ulstrup KE, van Oppen MJH, Kühl M, Ralph PJ

Marine Biology 153: 225-234

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Photobiology of endolithic microorganisms in living coral skeletons: 1. Pigmentation, spectral reflectance and variable chlorophyll fluorescence analysis of endoliths in the massive corals Cyphastrea serailia, Porites lutea and Goniastrea australensis

Ralph PJ, Larkum AWD, Kühl M

Marine Biology 152: 395-404

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Intra-colonial variability in light acclimation of zooxanthellae in coral tissues of Pocillopora damicornis

Ulstrup KE, Ralph PJ, Larkum AWD, Kühl M

Marine Biology 149: 1325-1335

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Impact of the wasting disease pathogen, Labyrinthula zosterae, on the photobiology of eelgrass Zostera marina

Ralph PJ, Short FT

Marine Ecology Progress Series 226: 265-271

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Spatial heterogeneity in active chlorophyll fluorescence and PS II activity of coral tissues

Ralph PJ, Gademann R, Larkum AWD, Kühl M

Marine Biology 141: 639-646

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Bio-optical characteristics and the vertical distribution of photosynthetic pigments and photosynthesis in an artificial cyanobacterial mat

Kühl M, Fenchel T

Microbial Ecology 40: 94-103

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Measurement of chlorophyll fluorescence within leaves using a modified PAM fluorometer with a fiber-optic microprobe.

Schreiber U, Kühl M, Klimant I, Reising H

Photosynthesis Research 47: 103-109

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MICROFIBER-PAM

Features
Data memory
128 kB CMOS RAM providing memory for 4000 data sets
Microcontroller
CMOS 80C52
Display
2 x 24 character alphanumerical LC-display with backlight
User interface
2 x 4 touch-sensitive keys to operate the internal mode
Measured parameters
F0, FM, FM', F, FV/FM (max. Yield), ΔF/FM' (Yield), qP, qN, NPQ, PAR (using special micro quantum sensor), ETR (i.e. PAR x ΔF/FM')
Power supply
Internal rechargeable battery 12 V/2 Ah, providing power for at least 10 000 Yield measurements, automatic power off, battery charger MINI-PAM/L (100 to 240 V AC)
Dimensions
17.6 cm x 11.5 cm x 9.5 cm (L x W x H)
Weight
2 kg (incl. battery)
Operating temperature
-5 to +45 °C
Connectors
Actinic light
Drives up to three actinic LEDs
AUX input
Receives signals from temperature and light sensors
AUX output
Sends control signals to external LED drivers
Charge
Socket for battery charger
Far-red light
Up to three far-red LEDs can be driven
Measuring light
Capacity to drive up to three LEDs, both as measuring and actinic light sources, 12 LED intensity and 12 pulse frequency settings are available, automatic change of measuring light frequency
Output
Provides analog signal to chart recorder
Photomultiplier
Full control of photomultiplier PM-MF
RS232
Communication with Windows Computer
Computer-controlled Operation
Software
WinControl-3 System Control and Data Acquisition Program (Microsoft Windows 10 and 11) for operation of measuring system via PC, data acquisition and analysis. Not compatible with Windows 10 on ARM
Input
100 to 240 V AC, 47 to 63 Hz
Output
19 V DC, 3.7 A
Operating temperature
0 to 40 °C
Dimensions
15 cm x 6 cm x 3 cm (L x W x H)
Weight
300 g
Design
100/140 μm (core/cladding diameters) step index fibers, 2 input and 2 output arms with ca. 1.2 m lengths and ST-connectors at all ends, PVC-adapter to connect photomultiplier PM-MF
Weight
85 g
Design
Based on photosensor module H-6779-01 (Hamamatsu) with pulse preamplifier and automatic overload switch-off, aluminum housing with mounting rod to be fixed on Stand ST-101
Signal detection
Miniature photomultiplier with high red sensitivity (type H6779-01, Hamamatsu)
Dimensions
110 mm x 65 mm x 78 mm (H x W x D)
Weight
520 g (incl. 1.4 m cable)
Emission peak
470 nm
Short-pass filter
λ < 600 nm
Detector-filterset
λ > 640 nm
Dimensions
Ø 25 mm, length 112 mm
Weight
115 g (incl. 1.4 m cable)
Design
Consisting of filter holder, to be mounted on Photomultiplier-Detector PM-MF, with adapter for fiber coupler MF-2-2-100, and a holder for mounting up to four LED light sources for the MICROFIBER-PAM, to be fixed on stand ST-101
Dimensions

Base plate, 40 cm x 30 cm

Height

73.5 cm, diameter 1.5 cm

Weight

2.8 kg

Design
Aluminum box with custom foam packing for PAM-CONTROL and accessories
Dimensions
60 cm x 40 cm x 25 cm (L x W x H)
Weight
5 kg

Accessories

Design
Single 100/140 μm step index fiber with ST-connector on one end and free fiber on other end, including connector to link with Multimode Fibercoupler MF-2-2-100
Total length
2 m
Emission peak
520 nm
Short-pass filter
λ < 600 nm
Detector-filterset
λ > 640 nm
Dimensions
Ø 25 mm, length 112 mm
Weight
115 g (incl. 1.4 m cable)
Emission peak
630 nm
Short-pass filter
λ < 680 nm
Detector-filterset
λ > 710 nm
Dimensions and weight
See Green LED MF L470
Emission peak
650 nm
Short-pass filter
λ < 680 nm
Detector-filterset
λ > 710 nm
Dimensions and weight
See Green LED MF L470

WinControl-3 Software

General Features and Graphical User Interface

The MICROFIBER-PAM can be operated by Windows computers running the WinControl-3 software. The same software operates the fluorometers DIVING-PAM-II, MICRO-PAM, MINI-PAM-II, MONITORING-PAM, and JUNIOR-PAM, PAM fluorometers operated via the PAM-CONTROL interface (MICROSCOPY-PAM, MICROFIBER-PAM and WATER-PAM FIBER-Version) as well as the Universal Light Meter ULM-500.

WinControl-2 Software

General Features and Graphical User Interface

The software WinControl-2 was developed for on-line operation via the interface PAM-CONTROL of the fluorometers MICROSCOPY-PAM, MICROFIBER-PAM, and WATER-PAM FIBER Version. WinControl-2 logs fluorescence data and automatically calculates fluorescence ratio parameters derived from saturation pulse analysis.

The WinControl-2 software runs only on Windows 7 32 bit or older Windows 32 bit operating systems.