Campbell Biology In Focus, Loose-leaf Edition (3rd Edition)
3rd Edition
ISBN: 9780134895727
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky
Publisher: PEARSON
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Textbook Question
Chapter 31.2, Problem 2CC
WHAT IF? If a plant flowers in a controlled chamber with a daily cycle of 10 hours of light and 14 hours of darkness, is it a short-day plant? Explain.
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Predict whether flowering in a short day plant with a minimum critical length of 14 hours would be expected to occur in the following situations.
The plant is exposed to 15 hours of daylight and 9 hours of darkness uninterrupted.
The plant is exposed to 9 hours of daylight and 15 hours of darkness.
The plant is exposed to 9 hours of daylight and 15 hours of darkness, with 10 minutes exposure to red light in the middle of the night.
Phytochrome, plays an important role in flowering in many plants. It can also be used to determine when lettuce seeds germinate (shown in the figure below
Which scenario(s) above produce large amounts of the active form of phytochrome?
A
B
A & C
B & D
Chapter 31 Solutions
Campbell Biology In Focus, Loose-leaf Edition (3rd Edition)
Ch. 31.1 - Prob. 1CCCh. 31.1 - WHAT IF? If a plant has the double mutation ctr...Ch. 31.1 - Prob. 3CCCh. 31.2 - If an enzyme in field-grown soybean leaves is most...Ch. 31.2 - WHAT IF? If a plant flowers in a controlled...Ch. 31.2 - MAKE CONNECTIONS Plants detect the quality of...Ch. 31.3 - Prob. 1CCCh. 31.3 - Prob. 2CCCh. 31.3 - Prob. 3CCCh. 31.4 - Prob. 1CC
Ch. 31.4 - Chewing insects mechanically damage plants and...Ch. 31.4 - Prob. 3CCCh. 31 - The hormone that helps plants respond to drought...Ch. 31 - Prob. 2TYUCh. 31 - Prob. 3TYUCh. 31 - Prob. 4TYUCh. 31 - Prob. 5TYUCh. 31 - Prob. 6TYUCh. 31 - DRAW IT Indicate the response of Arabidopsis to...Ch. 31 - Prob. 8TYUCh. 31 - FOCUS ON EVOLUTION As a general rule,...Ch. 31 - FOCUS ON INTERACTIONS In a short essay (100-150...Ch. 31 - Prob. 11TYU
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
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- control variable?arrow_forward10°C water 25 °C water 40 °C water Lumes number of bubbles released number of bubbles released number of bubbles released 0 3 7 3 1000 11 23 11 2000 17 35 17 3000 19 39 19 Why are bubbles counted in this experiment, and what do they represent? make a line graph showing the difference in the number of oxygen gas bubbles released by the plant under different light intensities and water temperatures. Which light intensity and water temperature caused the plant to produce the most amount oxygen gas during the process of photosynthesis? Why Which light intensity and water temperature caused the plant to produce the least amount oxygen gas during the process of photosynthesis? Why?arrow_forwardWhat preliminary conclusions can you draw from the results of the experiment and what is the independent and dependent variable ?arrow_forward
- QUESTION 10 Which is true regarding plant reproduction? Self-pollination produces offspring genetically identical to the parent modified organs, such as corms and bulbs, are produced as a result of sexual reproduction cross-pollination allows plant populations to survive in unstable environments plants do not reproduce asexually vectors such as flies carry plant spores to new locationsarrow_forwardA long-day plant will flower if Select one: O the duration of continuous light is less than a critical length. O the duration of continuous light exceeds a critical length. O the duration of continuous darkness is less than a critical length O it is kept in continuous far-red light. O the duration of continuous darkness exceeds a critical length.arrow_forwardEXPERIMENT 4: INDUCTION OF CALLUS SOMATIC EMBRYOGENESIS OF HAPLOID PLANTS Objective: To prepare anther as a source of explant To induce callus somatic embryogenesis of haploid plants Procedure: Cut off the buds and sort them into 3 developmental stages based on length of buds Surface sterilize the buds in 70% ethanol for 2-3 minutes, making sure the entire bud is immersed in the alcohol. Drain off excess alcohol from the buds and aseptically excise the anthers from each bud. Remove the filaments and culture the anther on one of the agar media provided. Label the stage of development of the bud on each petri dish as the anthers are cultured. Seal the Petri dishes with parafilm. Incubate in the dark at 26 to 28ºC for 4 to 8 weeks or until small plants can be seen growing out of the anthers. Then transfer to diffuse light. Record the results of the experiment in table form and submit the report. Observation: The culture was contaminated after 8 weeks of incubation…arrow_forward
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