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ANSWERS
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1.
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B
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The embryo
is where the first shoot apical meristem and the first root apical
meristem appear. From these the entire shoot, and root, systems emerge.
Because of repeated organogenesis, new shoot apices arise in the axils
of leaves (A) and new root apices arise buried in the root axis from
the pericycle (C), so a branching system appears. A leaf primordium
grows into a leaf; no apices form from it. |
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ANSWERS
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2.
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B
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It is the leaf that is an appendage that is determinate
in growth. The shoot apex also produces a stem (C) but that is not
an appendage. The lateral shoot (A) which is the same as the axillary
shoot (D) are appendages of the shoot apex, but they are indeterminate
in growth.
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ANSWERS
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3.
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D
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The way roots provide sufficient surface area, and
one that can increase, by a system of cylinders that grow from their
tips and branch by producing more cylinders that grow from their
tips. The root system provides good anchorage (C) but that is not
its main or primary purpose. The system does allow roots to go deeper
(B) but this is not the driving force--plants produce roots in all
directions and many need not go deeper for water, just further out
in all directions.
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ANSWERS
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4.
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A
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The principal role of cotyledons is nutrition, both
the absorption of nutrients late in embryo and seed development
and the provision of nutrients during germination. The seed coats
(B) form from the integuments of the ovule; the root is protected
by the root cap (C) and leaf primordia (D) form from the shoot apex
in the embryo.
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ANSWERS
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5.
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B
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Secondary growth, and in particular the vascular
cambium, produces more conducting tissue, both xylem and phloem.
The cork cambium adds cork cells to replace the epidermis, which
has to the pushed off by the new tissue forming inside. Secondary
growth does make the stem thicker and stronger (A) but that is not
its first function. Leaves and flowers (C) come from the shoot apex--they
are primary growth, not secondary. The stem tissue between leaves
(D) comes from growth of that region and is primary growth.
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ANSWERS
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6.
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A
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When you peel bark, you are breaking the tissue at
its weakest point, where the vascular cambium is. (The cells are
dividing and meristematic and very thin walled and easily broken.)
Outside the vascular cambium includes all the phloem and all the
periderm, or corky, layers. Since the phloem tissues carry the nutrients
from the leaves to the roots, if you peel off a strip of bark around
the entire diameter of a tree, the roots will starve and the tree
will die. Deer often do this in the winter.
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ANSWERS
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7.
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A
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By definition, wood is secondary xylem. Phloem is
soft tissue and easy rots away when a tree is cut down; you would
never build anything from phloem tissue.
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ANSWERS
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8.
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B
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It is often called the transpiration-cohesion theory.
The atmosphere is drier than the interior of the leaf and the evaporation
of water from leaves causes the leaf cells to develop a more negative
water potential and pull water from each other and eventually from
the water-containing vessels and tracheids in the xylem tissue.
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ANSWERS
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9.
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C
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Only the sieve cell is alive, functioning and without
a nucleus. The guard cell (D) is alive and has a nucleus. The sieve
cell (C) is dead when mature and lacks a nucleus and everything
else except a cell wall. The cork cell (B) may or may not be dead
when mature; if alive, it has its nucleus.
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ANSWERS
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10.
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D
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The pressure flow theory states that solutes entering
the sieve cell cause water to follow. Pressure builds up and both
water and solute flow along the tube. There is "room" because cells
at some other point, called the sink, are removing compounds/solutes.
For the other choices: (A) guard cells contract and expand when
they lose or gain water from adjacent cells but that water is never
pumped anywhere else. (B) The cell surrounding the sieve cell-companion
cell actively pump the solute into the them; the sieve cells do
not pump. (C) Water does not evaporate at the sink. It enters the
supply of water in the neighboring cells.
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ANSWERS
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11.
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A
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In C-4 plants, the bundle sheath cells have the Calvin
cycle where the radioactive carbon is incorporated into sugars.
The carbon dioxide is first trapped in the mesophyll cells (B) by
the Hatch and Slack cycle, but that generates only organic acids.
It is these organic acids that travel to the bundle sheath and give
up the carbon dioxide to the Calvin cycle. The sieve cells (C) receive
the sugar after the Calvin cycle has manufactured it and the epidermal
cells (D) never photosynthesize.
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