[return to lab schedule] [home] [class schedule] [BioPort] [contents]
(keeping in mind that
traditionally introductory biology labs require
memorization of specimens for
identification at a later date).
[Front of Room]
|
1A, 1B, 1C |
2A, 2B, 2C |
3A, 3B, 3C |
4A, 4B, 4C |
5A, 5B, 5C |
|
6A, 6B, 6C |
7A, 7B, 7C |
8A, 8B, 8C |
9A, 9B, 9C |
10A, 10B, 10C |
|
11A, 11B, 11C |
12A, 12B, 12C |
13A, 13B, 13C |
14A, 14B, 14C |
15A, 15B, 15C |
|
16A, 16B, 16C |
17A, 17B, 17C |
18A, 18B, 18C |
19A, 19B, 19C |
20A, 20B, 20C |
[Back of Room]
Boxes in above
table refer to desks.
Materials
should be arranged in the order presented in your lab text.
Please let us
know if there is a discrepancy or other problems.
Please be
aware that you don’t necessary have to begin at station 1.
Please pay
attention to suggested microscope magnifications (below)
(too-high
magnification can be as misleading as too-low magnification).
|
Page |
Sect. |
Section
Title |
Specimen |
State |
Container |
Scope |
Comments |
|
|
397 |
15.1.A |
Division
Bryophyta |
1A |
Moss |
Living |
Large culture dish |
None |
|
|
397 |
15.1.A |
Same
as above |
1C |
Antheridial
head ( #B361B) |
Slide |
Prepared |
Compound |
|
|
397 |
15.1.A |
Same
as above |
2A |
Archegonial
head ( #B363) |
Slide |
Prepared |
Compound |
|
|
397 |
15.1.A |
Same
as above |
2C |
Mnium
life cycle (#PB383) |
Preserved |
Bottle |
None |
Don’t
remove from bottle; don’t draw |
|
399 |
15.1.B |
Division
Hepatophyta |
3A |
Marchantia |
Living |
None |
None |
|
|
399 |
15.1.B |
Same as above |
3B |
Liverwort types (#PB350) |
Preserved |
None |
None |
Don’t remove from bottle; don’t draw; lab prep person:
please do not put out liverwort life cycle sheet since it confusingly
contradicts the lab text |
|
399 |
15.1.B |
Same
as above |
3C |
Ricciocarpus,
Marchantia, Porella, Anthoceros (#POM 16510) |
Lucite
|
None |
Dissecting or None |
Don't
draw |
|
404 |
15.2.B |
Division Pterophyta (formerly Division Psilophyta) |
4A |
Whiskfern |
Living |
None |
None |
Keep in mind that your text mostly discusses the regular
ferns (below), not the whiskferns… you will become confused if you attempt
to locate division Pterophyta anatomy while observing these plants |
|
402 |
15.2.A |
Division
Lycophyta |
5A |
Lycopodium
lucidulum (or equivalent) |
Living |
None |
None |
|
|
402 |
15.2.A |
Same
as above |
5B |
Lycopodium complanatar
|
Preserved |
None |
None |
Don’t
remove from bottle; don’t draw |
|
402 |
15.2.A |
Same as above |
5C |
Selaganella (resurrection plant) |
Living |
None |
None |
Don’t draw |
|
404 |
15.2.B |
Division
Sphenophyta |
6A |
Equisetum
hyemale |
Living |
None |
None |
|
|
404 |
15.2.B |
Same as above |
6C |
Equisetum hyemale L. “common field horsetail” |
Preserved |
Herbarium Sheet |
None |
Please be very careful with these preserved specimens |
|
404 |
15.2.B |
Division
Pterophyta |
7A |
Fern
sorus |
Preserved |
None |
Dissecting |
Note
sori; draw at level-2 zoom |
|
404 |
15.2.B |
Same as above |
7C |
Fern |
Living |
None |
None |
Don’t draw; sori may not yet be present on living fern
leaves |
|
406 |
15.2.C |
Same
as above |
8A |
Fern
sporangia (#B431) |
Slide |
Prepared |
Compound |
Note
that fern sori are bundles of these sporangia; view/draw at 100x power; see
poster immediately behind table (i.e., table 13); note that the Fiddler fern
leaf is not a fern sporangia (i.e., it is shown in the poster
approximately real size… it is not microscopic) |
|
406 |
15.2.C |
Same
as above |
8C |
Fern
leaflet indusium (fern sorus cross section) (#B432a) |
Slide |
Prepared |
Compound |
Note
that sori are bundles of sporangia; sketch with detail only down to the
outlines of sporangia; view/draw at lower power |
|
406 |
15.2.C |
Same as above |
9A |
Fern prothallium archegonia (fern gametophyte) (#B407) |
Slide |
Prepared |
Compound |
View/draw at low power |
|
406 |
15.2.C |
Same as above |
9C |
Fern prothallium antheridia (fern gametophyte) (#B405) |
Slide |
Prepared |
Compound |
View/draw at 100x power; note antheridia (these are where the sperm come from) |
|
406 |
15.2.C |
Same as above |
10A |
Fern prothallium with young sporophyte (fern gametophyte with young sporophyte) (no number—Frey Scientific) |
Slide |
Prepared |
Dissecting |
Use 1x power to view; don’t draw |
|
406 |
15.2.C |
Same
as above |
10C |
Ferm
gametophyte |
Living |
Petri dish |
Dissecting |
Don’t
draw |
|
409 |
15.2.D |
Fossils |
11A |
Stigmaria |
mold??? |
None |
None |
=underground
stem |
|
409 |
15.2.D |
Fossils |
11C |
Lepidodendron |
mold |
None |
None |
Don’t
draw |
|
409 |
15.2.D |
Fossils |
11C |
Lepidodendron |
cast |
None |
None |
Don’t
draw |
|
409 |
15.2.D |
Fossils |
12A |
Calamite
(Sphenopsids?) |
cast |
None |
None |
Don’t
draw |
|
409 |
15.2.D |
Fossils |
12A |
Calamite |
crushed
cast |
None |
None |
Don’t
draw |
|
409 |
15.2.D |
Fossils |
12C |
Fossil of extinct fern |
??? |
None |
None |
Don’t draw |
Choice of containers:
· Concave slide: Use a concave slide when a normal slide will crush the specimen (e.g., Volvox)
· Dish (observe in): Many specimens will need to be removed from their containers to observe; an appropriate dish will be supplied for pouring the specimen into; please use a dish for this purpose only if you are instructed to (Laboratory prep person: please supply dishes and label specimens that should or should not be observed in dishes)
· Dissection pan: Any dissections will be done in a dissection pan; you will obtain specimens for dissections from stations then bring those specimens, in a dissection an, back to your desk; if the specimen is presented to you in a dissection pan, then that specimen should be observed at the station but not extensively dissection (i.e., poking and otherwise manipulating is OK, but cutting, etc., is not)
· Petri dish: Normally a petri dish will be employed if that is what the specimen is supplied in
· Slide (microscope): Use a slide when the specimen is relative small and will be observed using a compound scope
· No container: Some items are suffiently large or are already mounted such that a container is not necessary
Choice of microscopes:
· Compound microscope: Use for observing relatively small specimens
· Dissecting (stereoscopic) microscope: Use for observing the fine structure of relatively large specimens
· Phase-contrast microscope: Use for observing especially living bacteria
· No microscope: Some items are sufficiently large or its fine structure sufficiently inaccessible that we will not employ microscopic observation