| Feature | Prophase | Telophase |
|---|---|---|
| Nuclei Count | One single nucleus area | Two distinct nuclei areas |
| Chromosome State | Condensing into visible threads | Decondensing/becoming fuzzy |
| Cell Plate | Absent | Often visible as a line between nuclei |
Magnification: Always start at low power to find the meristematic zone, then switch to high power ( or with oil immersion) to identify specific stages.
Artifacts: Be aware that the 'squashing' process can sometimes overlap cells or break nuclei; only analyze cells that are clearly separated and intact.
Quantitative Analysis: Exams often require calculating the Mitotic Index, which is the ratio of cells undergoing mitosis to the total number of cells observed:
Confusing Interphase with Prophase: Students often mistake the granular appearance of a nucleus in late interphase for the early condensation of prophase. Look for distinct, individual 'worm-like' threads to confirm prophase.
Incorrect Pressure: Applying sideways pressure during the squash technique will cause cells to slide over each other rather than flatten, resulting in a blurred image where stages cannot be identified.
Sampling the Wrong Area: Taking a sample from the very tip (the root cap) will show dead or differentiated cells that are not dividing; the sample must include the tissue behind the tip.