Peter Evennett's Course Oct 09
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==Peter Evennett's Course Oct 09 == | ==Peter Evennett's Course Oct 09 == | ||
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=== Friday 16th Oct === | === Friday 16th Oct === | ||
Setup - all lmf staff move stuff to galleria | Setup - all lmf staff move stuff to galleria | ||
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* Optical bench | * Optical bench | ||
* Spinning disk gadget | * Spinning disk gadget | ||
+ | * Polarazing sheets | ||
+ | * Diffraction Grids | ||
+ | * Fluorescent samples | ||
+ | * Fluorescent Beads (Prepare slides) | ||
+ | * First day Handout for students | ||
+ | * Light torches | ||
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− | | 9:30|| | + | | 9:30||11:05||align="center"|INTRODUCTION||align="center" | COURSE PRESENTATION <br> GROUP PRESENTATION||align="center" |LMF TEAM |
|- | |- | ||
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− | | | + | | style="background:DarkKhaki;"|'''11:05''' |
+ | | style="background:DarkKhaki;"|'''11:20''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK'''||align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
|- | |- | ||
| |||||||| | | |||||||| | ||
|- | |- | ||
+ | | 11:20||13:00||align="center"|SESSION 1 <br>Theory & Practice|| align="center" |PRINCIPLES OF LIGHT MICROSCOPY<br> Historical aspects of microscopy<br>Introduction to lenses<br>Lens aberrations<br>Magnification<br> Numerical aperture<br>Microscope illumination<br>Conjugate planes<br>Koehler illumination||align="center" |PETER EVENNETT <br>LMF TEAM | ||
|- | |- | ||
− | | style="background:DarkKhaki;"|''' | + | | |||||||| |
− | | style="background:DarkKhaki;"|''' | + | |- |
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''13:00''' | ||
+ | | style="background:DarkKhaki;"|'''14:00''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''LUNCH''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''LUNCH'''||align="center" style="background:DarkKhaki;"|'''LUNCH''' | ||
+ | |- | ||
+ | | |||||||| | ||
+ | |- | ||
+ | | 14:00||15:30||align="center"|SESSION 2<br>Theory & Practice|| align="center" |PRINCIPLES OF LIGHT MICROSCOPY <br> Demo||align="center" |PETER EVENNETT <br>LMF TEAM | ||
+ | |- | ||
+ | | |||||||| | ||
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''15:30''' | ||
+ | | style="background:DarkKhaki;"|'''15:45''' | ||
|align="center" style="background:DarkKhaki;"|'''BREAK''' | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
− | |align="center" style="background:DarkKhaki;"|''' | + | |align="center" style="background:DarkKhaki;"|'''BREAK'''||align="center" style="background:DarkKhaki;"|'''BREAK''' |
|- | |- | ||
| |||||||| | | |||||||| | ||
|- | |- | ||
− | | | + | | 15:45||18:00||align="center"|SESSION 3<br>Theory & Practice|| align="center" |PRINCIPLES OF LIGHT MICROSCOPY||align="center" |PETER EVENNETT <br>LMF TEAM |
|- | |- | ||
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|} | |} | ||
− | |||
=== DAY TWO (October 20th)=== | === DAY TWO (October 20th)=== | ||
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− | | 9:30||10: | + | | 9:30||10:45||align="center"|SESSION 1 <br>Theory & Practice||align="center" | Resolution<br>Diffraction ||align="center" |PETER EVENNETT <br>LMF TEAM |
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|-- | |-- | ||
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− | |||
| style="background:DarkKhaki;"|'''10:45''' | | style="background:DarkKhaki;"|'''10:45''' | ||
+ | | style="background:DarkKhaki;"|'''11:00''' | ||
|align="center" style="background:DarkKhaki;"|'''BREAK''' | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
− | |align="center" style="background:DarkKhaki;"|''' | + | |align="center" style="background:DarkKhaki;"|'''COFFEE BREAK'''|| style="background:DarkKhaki;"|''' ''' |
|- | |- | ||
− | | | + | | 11:00||13:00||align="center"|DEMONSTRATION || align="center"|Abbe´s diffraction experiments<br>||align="center"|PETER EVENNETT <br>LMF TEAM |
|- | |- | ||
| |||||||| | | |||||||| | ||
|- | |- | ||
− | + | | style="background:DarkKhaki;"|'''13:00''' | |
− | | style="background:DarkKhaki;"|''' | + | | style="background:DarkKhaki;"|'''14:00''' |
− | | style="background:DarkKhaki;"|''' | + | |
|align="center" style="background:DarkKhaki;"|'''BREAK''' | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
|align="center" style="background:DarkKhaki;"|'''LUNCH'''|| style="background:DarkKhaki;"|''' ''' | |align="center" style="background:DarkKhaki;"|'''LUNCH'''|| style="background:DarkKhaki;"|''' ''' | ||
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| |||||||| | | |||||||| | ||
|- | |- | ||
− | | | + | | 14:00||16:00||align="center"|SESSION 2<br>Theory & Practice|| align="center"|Bright Field<br> Dark Field<br> Phase Contrast microscopy ||align="center" |PETER EVENNETT <br>LMF TEAM |
+ | |- | ||
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''16:00''' | ||
+ | | style="background:DarkKhaki;"|'''16:15''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''COFFEE BREAK'''|| style="background:DarkKhaki;"|''' ''' | ||
+ | |- | ||
+ | | 16:15|18:00||align="center"|SESSION 2<br>Theory & Practice|| align="center"|Bright Field<br> Dark Field<br> Phase Contrast microscopy ||align="center" |PETER EVENNETT <br>LMF TEAM | ||
|- | |- | ||
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|- | |- | ||
− | | 9:30|| | + | | 9:30||11:30||align="center"|SESSION 1<br>Theory & Practice||align="center" | Objective reading<br> Objective cleaning||align="center" |PETER EVENNETT <br>LMF TEAM |
|- | |- | ||
| |||||||| | | |||||||| | ||
− | |||
|- | |- | ||
+ | | style="background:DarkKhaki;"|'''11:30''' | ||
+ | | style="background:DarkKhaki;"|'''11:45''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK'''|| align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
|- | |- | ||
− | | style="background:DarkKhaki;"|''' | + | | |||||||| |
− | | style="background:DarkKhaki;"|''' | + | |- |
+ | | 11:45||13:00||align="center"|SESSION 2<br>Theory & Practice||align="center" | Polarized light microscopy<br>Differential Interference Contrast (DIC)||align="center" |PETER EVENNETT <br>LMF TEAM | ||
+ | |- | ||
+ | | |||||||| | ||
+ | |- | ||
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''13:00''' | ||
+ | | style="background:DarkKhaki;"|'''14:00''' | ||
|align="center" style="background:DarkKhaki;"|'''BREAK''' | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
|align="center" style="background:DarkKhaki;"|'''LUNCH'''|| style="background:DarkKhaki;"|''' ''' | |align="center" style="background:DarkKhaki;"|'''LUNCH'''|| style="background:DarkKhaki;"|''' ''' | ||
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|- | |- | ||
− | | | + | | 14:00||15:15||align="center"|SESSION 3<br>Theory & Practice|| align="center"|Differential Interference Contrast (DIC)<br>Objective cleaning<br>Digital photomicrography<br>Introduction to Confocal Microscopy ||align="center" |PETER EVENNETT <br>LMF TEAM |
− | + | |- | |
+ | | |||||||| | ||
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''15:15''' | ||
+ | | style="background:DarkKhaki;"|'''15:30''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK'''|| align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |- | ||
+ | | |||||||| | ||
+ | |- | ||
+ | | 15:30||18:00||align="center"|SESSION 4<br>Theory & Practice|| align="center"|Differential Interference Contrast (DIC)<br>Objective cleaning<br>Digital photomicrography<br>Introduction to Confocal Microscopy ||align="center" |PETER EVENNETT <br>LMF TEAM | ||
|- | |- | ||
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| align="center" style="background:#f0f0f0;"|'''TOPICS''' | | align="center" style="background:#f0f0f0;"|'''TOPICS''' | ||
| align="center" style="background:#f0f0f0;"|'''Responsible person(s)''' | | align="center" style="background:#f0f0f0;"|'''Responsible person(s)''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''DEMO Activities''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''DEMO materials''' | ||
|- | |- | ||
− | | |||||||| | + | | |||||||||||| |
|- | |- | ||
− | | 9:30||10: | + | | 9:30||10:20||align="center"|SESSION 1<br>Theory||align="center" | Question session <br> Fundamentals concepts of fluorescence ||align="center" |LMF TEAM<br>Dan||align="center" |- ||align="center" |- |
|- | |- | ||
− | | | + | | |||||||||||| |
|- | |- | ||
− | | |||||||| | + | | style="background:DarkKhaki;"|'''10:20''' |
+ | | style="background:DarkKhaki;"|'''10:55''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK'''|| align="center" style="background:DarkKhaki;"|'''BREAK'''||align="center" style="background:DarkKhaki;"|'''BREAK'''||align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |- | ||
+ | | |||||||||||| | ||
+ | |- | ||
+ | | 10:55||13:15||align="center"|SESSION 2<br>Theory & Practice||align="center" | Fluorescence Microscopy||align="center" |LMF TEAM<br>Humberto||align="center" |• Mercury lamp<br>• Lamp houses <br>• Spectra <br>• Filters <br> • Filter cubes <br>• Fluorescent-labeled samples <br> • Filter spectral charts of each microscope (laminated)||align="center" | • Spare lamp houses <br> • Lamps <br> • Ocean optics equipment<br> • Different filters<br> • Four (4) different Filter-sets (cubes), with the appropriate descriptions | ||
+ | |- | ||
+ | | |||||||||||| | ||
|- | |- | ||
|- | |- | ||
− | | style="background:DarkKhaki;"|''' | + | | style="background:DarkKhaki;"|'''13:15''' |
− | | style="background:DarkKhaki;"|''' | + | | style="background:DarkKhaki;"|'''14:15''' |
|align="center" style="background:DarkKhaki;"|'''BREAK''' | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
− | |align="center" style="background:DarkKhaki;"|'''LUNCH'''|| style="background:DarkKhaki;"|''' | + | |align="center" style="background:DarkKhaki;"|'''LUNCH'''|| align="center" style="background:DarkKhaki;"|'''LUNCH'''||align="center" style="background:DarkKhaki;"|'''LUNCH'''||align="center" style="background:DarkKhaki;"|'''LUNCH''' |
|- | |- | ||
− | | |||||||| | + | | |||||||||||| |
|- | |- | ||
− | | | + | | 14:15||15:45||align="center"|SESSION 3<br>Theory & Practice|| align="center"|Imaging with CCD ||align="center" |LMF TEAM<br> Britta||align="center" | • CCD<br> • Cameras || align="center" |• CCD chip <br> • Cameras |
|- | |- | ||
− | | style="background:DarkKhaki;"|'''15: | + | | style="background:DarkKhaki;"|'''15:45''' |
− | | style="background:DarkKhaki;"|''' | + | | style="background:DarkKhaki;"|'''16:00''' |
|align="center" style="background:DarkKhaki;"|'''BREAK''' | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
− | |align="center" style="background:DarkKhaki;"|''' | + | |align="center" style="background:DarkKhaki;"|'''BREAK'''|| style="background:DarkKhaki;"|''' '''|| style="background:DarkKhaki;"|''' '''|| style="background:DarkKhaki;"|''' ''' |
|- | |- | ||
− | | | + | | 16:00||18:00||align="center"|SESSION 4<br>Practice|| align="center"|Imaging with CCD cameras using LMF systems ||align="center" |LMF TEAM<br>Jan / Peter / Dan / Britta (*)||align="center"|• Displaying <br>• Pixel size<br>• Look up table<br>• Binning<br>• Exposure time<br>• Saturation<br>• Signal to noise <br>• ROI<br>• Bit depth<br>• Auto map<br>• Auto contrast || align="center"|• Microscopes (4) <br>• Sample slides |
|} | |} | ||
+ | '' | ||
=== DAY FIVE (October 23th)=== | === DAY FIVE (October 23th)=== | ||
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| align="center" style="background:#f0f0f0;"|'''TOPICS''' | | align="center" style="background:#f0f0f0;"|'''TOPICS''' | ||
| align="center" style="background:#f0f0f0;"|'''Responsible person(s)''' | | align="center" style="background:#f0f0f0;"|'''Responsible person(s)''' | ||
+ | |- | ||
+ | | 9:30||10:20||align="center"|SESSION 1<br>Theory & Demo||align="center" | Optical sectioning methods<br>Pros&Cons ||align="center" |LMF TEAM <br> Dan / Jan | ||
|- | |- | ||
| |||||||| | | |||||||| | ||
|- | |- | ||
− | | | + | | style="background:DarkKhaki;"|'''10:20''' |
+ | | style="background:DarkKhaki;"|'''10:35''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK'''||align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
|- | |- | ||
+ | | |||||||| | ||
|- | |- | ||
− | | style="background:DarkKhaki;"|''' | + | | 10:35||13:00||align="center"|SESSION 1<br>Theory & Demo||align="center" | Optical sectioning methods<br>Pros&Cons ||align="center" |LMF TEAM <br> Dan / Jan |
− | | style="background:DarkKhaki;"|''' | + | |- |
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''13:00''' | ||
+ | | style="background:DarkKhaki;"|'''14:00''' | ||
|align="center" style="background:DarkKhaki;"|'''BREAK''' | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
|align="center" style="background:DarkKhaki;"|'''LUNCH'''|| style="background:DarkKhaki;"|''' ''' | |align="center" style="background:DarkKhaki;"|'''LUNCH'''|| style="background:DarkKhaki;"|''' ''' | ||
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| |||||||| | | |||||||| | ||
|- | |- | ||
− | | | + | | 14:00||15:15||align="center"|SESSION 2<br>Theory & Demo|| align="center"|Basics of Quantitative Image Analysis <br> (Image Processing) ||align="center" |LMF TEAM<br>Dan |
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''15:15''' | ||
+ | | style="background:DarkKhaki;"|'''15:30''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''BREAK'''|| align="center" style="background:DarkKhaki;"|'''BREAK''' | ||
+ | |- | ||
+ | | |||||||| | ||
+ | |- | ||
+ | | 15:30||16:30||align="center"|SESSION 3|| align="center"|Course evaluation ||align="center" |LMF TEAM | ||
+ | |} | ||
+ | |||
+ | === OFFICE DUTIES=== | ||
+ | ==== - LMF Members available for users (19th Oct to 23rd Oct) - ==== | ||
+ | |||
+ | {| border="4" cellpadding="2" cellspacing="8" {| {{table}} | ||
+ | |- style="; color:MidnightBlue;" | ||
+ | | align="center" style="background:#f0f0f0;"|'''FROM''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''TO''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''MONDAY''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''TUESDAY''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''WEDNESDAY''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''THURSDAY''' | ||
+ | | align="center" style="background:#f0f0f0;"|'''FRIDAY''' | ||
+ | |- | ||
+ | | |||||||| |||| | ||
+ | |- | ||
+ | | 9:30||12:30||align="center"| - ||align="center" | Britta ||align="center" |Peter ||align="center" |Peter ||align="center" |Silke | ||
+ | |- | ||
+ | | style="background:DarkKhaki;"|'''12:30''' | ||
+ | | style="background:DarkKhaki;"|'''13:30''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''L''' | ||
+ | |align="center" style="background:DarkKhaki;"|'''U'''|| align="center" style="background:DarkKhaki;"|''' N '''||align="center" style="background:DarkKhaki;"|''' C '''||align="center" style="background:DarkKhaki;"|''' H ''' | ||
+ | |- | ||
+ | | |||||||||||| | ||
|- | |- | ||
− | | | + | | 13:30||18:00||align="center"|Britta|| align="center"|Dan ||align="center" |Silke ||align="center" |(*)Silke <br> Humberto||align="center" |- |
|} | |} | ||
+ | (*) Silke and Humberto will be cleaning and reorganizing the Galeria |
Latest revision as of 15:50, 6 November 2009
Contents |
[edit] Peter Evennett's Course Oct 09
[edit] Friday 16th Oct
Setup - all lmf staff move stuff to galleria Equipment needed
- Microscopes
- Optical bench
- Spinning disk gadget
- Polarazing sheets
- Diffraction Grids
- Fluorescent samples
- Fluorescent Beads (Prepare slides)
- First day Handout for students
- Light torches
[edit] DAY ONE (October 19th)
FROM | TO | ACTIVITY | TOPICS | Responsible person(s) |
9:30 | 11:05 | INTRODUCTION | COURSE PRESENTATION GROUP PRESENTATION |
LMF TEAM |
11:05 | 11:20 | BREAK | BREAK | BREAK |
11:20 | 13:00 | SESSION 1 Theory & Practice |
PRINCIPLES OF LIGHT MICROSCOPY Historical aspects of microscopy Introduction to lenses Lens aberrations Magnification Numerical aperture Microscope illumination Conjugate planes Koehler illumination |
PETER EVENNETT LMF TEAM |
13:00 | 14:00 | LUNCH | LUNCH | LUNCH |
14:00 | 15:30 | SESSION 2 Theory & Practice |
PRINCIPLES OF LIGHT MICROSCOPY Demo |
PETER EVENNETT LMF TEAM |
15:30 | 15:45 | BREAK | BREAK | BREAK |
15:45 | 18:00 | SESSION 3 Theory & Practice |
PRINCIPLES OF LIGHT MICROSCOPY | PETER EVENNETT LMF TEAM |
[edit] DAY TWO (October 20th)
FROM | TO | ACTIVITY | TOPICS | Responsible person(s) |
9:30 | 10:45 | SESSION 1 Theory & Practice |
Resolution Diffraction |
PETER EVENNETT LMF TEAM |
10:45 | 11:00 | BREAK | COFFEE BREAK | |
11:00 | 13:00 | DEMONSTRATION | Abbe´s diffraction experiments |
PETER EVENNETT LMF TEAM |
13:00 | 14:00 | BREAK | LUNCH | |
14:00 | 16:00 | SESSION 2 Theory & Practice |
Bright Field Dark Field Phase Contrast microscopy |
PETER EVENNETT LMF TEAM |
16:00 | 16:15 | BREAK | COFFEE BREAK | |
18:00 | SESSION 2 Theory & Practice |
Bright Field Dark Field Phase Contrast microscopy |
PETER EVENNETT LMF TEAM | |
[edit] DAY THREE (October 21th)
FROM | TO | ACTIVITY | TOPICS | Responsible person(s) |
9:30 | 11:30 | SESSION 1 Theory & Practice |
Objective reading Objective cleaning |
PETER EVENNETT LMF TEAM |
11:30 | 11:45 | BREAK | BREAK | BREAK |
11:45 | 13:00 | SESSION 2 Theory & Practice |
Polarized light microscopy Differential Interference Contrast (DIC) |
PETER EVENNETT LMF TEAM |
13:00 | 14:00 | BREAK | LUNCH | |
14:00 | 15:15 | SESSION 3 Theory & Practice |
Differential Interference Contrast (DIC) Objective cleaning Digital photomicrography Introduction to Confocal Microscopy |
PETER EVENNETT LMF TEAM |
15:15 | 15:30 | BREAK | BREAK | BREAK |
15:30 | 18:00 | SESSION 4 Theory & Practice |
Differential Interference Contrast (DIC) Objective cleaning Digital photomicrography Introduction to Confocal Microscopy |
PETER EVENNETT LMF TEAM |
[edit] DAY FOUR (October 22th)
FROM | TO | ACTIVITY | TOPICS | Responsible person(s) | DEMO Activities | DEMO materials |
9:30 | 10:20 | SESSION 1 Theory |
Question session Fundamentals concepts of fluorescence |
LMF TEAM Dan |
- | - |
10:20 | 10:55 | BREAK | BREAK | BREAK | BREAK | BREAK |
10:55 | 13:15 | SESSION 2 Theory & Practice |
Fluorescence Microscopy | LMF TEAM Humberto |
• Mercury lamp • Lamp houses • Spectra • Filters • Filter cubes • Fluorescent-labeled samples • Filter spectral charts of each microscope (laminated) |
• Spare lamp houses • Lamps • Ocean optics equipment • Different filters • Four (4) different Filter-sets (cubes), with the appropriate descriptions |
13:15 | 14:15 | BREAK | LUNCH | LUNCH | LUNCH | LUNCH |
14:15 | 15:45 | SESSION 3 Theory & Practice |
Imaging with CCD | LMF TEAM Britta |
• CCD • Cameras |
• CCD chip • Cameras |
15:45 | 16:00 | BREAK | BREAK | |||
16:00 | 18:00 | SESSION 4 Practice |
Imaging with CCD cameras using LMF systems | LMF TEAM Jan / Peter / Dan / Britta (*) |
• Displaying • Pixel size • Look up table • Binning • Exposure time • Saturation • Signal to noise • ROI • Bit depth • Auto map • Auto contrast |
• Microscopes (4) • Sample slides |
[edit] DAY FIVE (October 23th)
FROM | TO | ACTIVITY | TOPICS | Responsible person(s) |
9:30 | 10:20 | SESSION 1 Theory & Demo |
Optical sectioning methods Pros&Cons |
LMF TEAM Dan / Jan |
10:20 | 10:35 | BREAK | BREAK | BREAK |
10:35 | 13:00 | SESSION 1 Theory & Demo |
Optical sectioning methods Pros&Cons |
LMF TEAM Dan / Jan |
13:00 | 14:00 | BREAK | LUNCH | |
14:00 | 15:15 | SESSION 2 Theory & Demo |
Basics of Quantitative Image Analysis (Image Processing) |
LMF TEAM Dan |
15:15 | 15:30 | BREAK | BREAK | BREAK |
15:30 | 16:30 | SESSION 3 | Course evaluation | LMF TEAM |
[edit] OFFICE DUTIES
[edit] - LMF Members available for users (19th Oct to 23rd Oct) -
FROM | TO | MONDAY | TUESDAY | WEDNESDAY | THURSDAY | FRIDAY |
9:30 | 12:30 | - | Britta | Peter | Peter | Silke |
12:30 | 13:30 | L | U | N | C | H |
13:30 | 18:00 | Britta | Dan | Silke | (*)Silke Humberto |
- |
(*) Silke and Humberto will be cleaning and reorganizing the Galeria