Supplement to Lab Topic 18: Animal Diversity II

 

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Map of Stations

 

[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).

 

Specimen List

 

Page

Sect.

Section Title

Stat.

Specimen

State

Container

Scope

Comments

467

18.1

Phylum Mollusca

1

Clams

Preserved

Dissection pan

None

Follow directions in text

467

18.1

Same as above

6A

Various gastropods

Preserved

None

None

Observe diversity; do not draw

467

18.1

Same as above

6C

Snail radula w.m. Z1410

Slide

None

Compound

Observe (100x); don’t draw; what does the snale use its radula for?

467

18.1

Same as above

11A

Various Polyplachophorans

Preserved

None

None

Observe diversity; do not draw

467

18.1

Same as above

11B

Various bivalves

Preserved

None

None

Observe diversity; do not draw

467

18.1

Same as above

11C

Various cephalopods

Preserved

None

None

Observe diversity; do not draw

471

18.2.A

Phylum Arthropoda

2

Crayfish

Preserved

Dissecting pan

None

Follow directions in text

471

18.2.A

Same as above

9A

Crustaceans

Preserved

None

None

Observe diversity; do not draw

471

18.2.A

Same as above

9C

Daphnia w.m. Z1655

Slide

None

Compound

Observe; do not draw; 100x

474

18.2.B

Same as above

12

Grasshopper

Preserved

Dissecting pan

None

Follow directions in text

474

18.2.B

Same as above

17A

Uniramians

Preserved

None

None

Observe diversity; do not draw

474

18.2.B

Same as above

17B

Chelicerates

Preserved

None

None

Observe diversity; do not draw

474

18.2.B

Same as above

17C

Tick and Mite w.m. Z1790

Slide

None

Dissecting

Observe; do not draw

---

---

Phylum Echinodermata

3A

Various echinoderms

Preserved

None

None

Observe diversity; do not draw

477

18.3

Phylum Chordata

3C

Various tunicates

Preserved

None

None

Observe diversity; do not draw

477

18.3

Same as above

8A

Lancelet x.s. amphioxus

Slide

None

Dissecting

Draw

477

18.3

Same as above

8B

Lancelet Z1217 Amphioxus

Slide

None

Dissecting

Follow directions in text for observing preserved whole; feel free to observe preserved whole under scope

477

18.3

Same as above

8C

Angnathans

Preserved

None

Dissecting?

Observe and compare to lancelets; note how the agnathans are barely vertebrates

---

---

Same as above

4

Chondricthyes

Preserved

None

None

Observe diversity; do not draw

---

---

Same as above

9

Osteichthyes

Preserved

None

None

Observe diversity; do not draw

---

---

Same as above

14a

Amphibians

Preserved

None

None

Observe diversity; do not draw

---

---

Same as above

14b

Reptiles

Preserved

None

None

Observe diversity; do not draw

---

---

Same as above

19A

Aves

Preserved

None

None

Observe diversity; do not draw

---

---

Same as above

19C

Mammals

Preserved

None

None

Observe diversity; do not 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

·         Dissection (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