DENDROLOGY WOOD ANATOMY LAB I

I. Make freehand transverse sections midway between successive bud scale scars on one

of the three year Angiosperm twigs you collected. Examine these sections in developmental

sequence using a binocular dissecting microscope. Note the transverse relationships

between successive annual growth rings in each section. Identify as many tissues as you

can in your sections.

II. Obtain a compound light microscope and learn how to establish Kohler illumination. This

procedure, named after August Kohler who developed the theory and procedure in 1894,

should be preliminary to each exercise involving the compound light microscope in order

to optimize resolution and avoid eye strain.

NEW Olympus Microscope 12 Step Instructions for Kohler Illumination.

1. Make sure a) ocular, b) objective, and c) condenser lens are clean.

2. Put the 10X objective in the viewing position.

3. Place a prepared slide on the microscope stage.

4. Bring the image of the prepared slide into sharp focus.

5. Adjust interpupillary distance of oculars. [Make a note of your interpupillary distance on the scale for future rapid adjustment]

6. Adjust the Diopter to compensate for any differences in vision between your right and left eyeballs: A. While looking through the right ocular with your right eye, and with your left eye closed, adjust course and fine foci to bring specimen into sharp focus. B. Then, while looking through the left ocular with your left eye, and with your right eye closed, rotate the diopter adjustment ring on the left ocular to bring the specimen into sharp focus - without adjusting the course and fine focus of the microscope.

7. Open condenser iris diaphragm.

8. Close the lamp diaphram 90%.

9. Focus the image of the edge of the lamp diaphram [fake lamp diaphragm] using the condenser focusing knob - NOT the course/fine foci knobs. If you accidently change the course/fine foci, refocus the specimen, before adjusting the condeser focus.

10. Open the field iris so that the edges of the diaphram are just beyond the field of view of the objective lens.

11. Set the condenser diaphram to the opening that corresponds to the objective lens that you are using. NOTE: You have to adjust the condenser diaphram EACH time you change the objective lens to maintain optimum resolution!

12. Adjust the lamp voltage control for comfortable viewing.

OLD Olympus Microscope 12 Step Instructions for Kohler Illumination.

1. Make sure a) ocular, b) objective, and c) condenser lens are clean.

2. Put the 10X objective in the viewing position.

3. Place a prepared slide on the microscope stage.

4. Bring the image of the prepared slide into sharp focus.

5. Adjust interpupillary distance of oculars. [Make a note of your interpupillary distance on the scale for future rapid adjustment]

6. Adjust ocular focus of each ocular to correspond with your interpupillary distance.

7. Open condenser iris diaphragm.

8. Put the fake lamp diaphragm over half the lamp housing.

9. Focus the image of the edge of the fake lamp diaphragm.

10. Remove the fake lamp diaphragm.

11. Remove one ocular.

12. Peer down the ocular tube and adjust the condenser diaphragm so that ca. 80% of the

objective lens is illuminated.

13. Replace ocular.

14. Adjust the lamp voltage control for comfortable viewing.

NOTE: When the objective lens is changed it is necessary to adjust the condenser

diaphragm to 80% illumination as in steps 10-13. You will use small strips of time tape to

mark the appropriate condenser diaphragm positions to facilitate these adjustments. Also

use a piece of time tape to place your initials on the microscope you will be using each

laboratory.

III. Study in chronological sequence the prepared light microscope cross sections of the 1,

2, and 3 year old Tilia stems. Relate your observations to what you observed in your

freehand sections. Identify: annual rings, pith, primary and secondary xylem, ray

parenchyma, cambium, primary and secondary phloem, dilated ray parenchyma, cortex,

phellum (cork), phellogen (cork cambium), phelloderm. Note if there are any lenticels

present.

IV. Make a freehand longitudinal section of the other Angiosperm twig you collected. Section

through the pith throughout three years of stem growth. Examine your section using a

binocular dissecting microscope. Note the longitudinal relationships between the

successive annual growth rings. Relate these to your transverse observations in I. and III.

above.