Lesson 2 bio101 (c)Dr. Evangelista

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Lecture #2 The Development of the Plant body

Transcript of Lesson 2 bio101 (c)Dr. Evangelista

Page 1: Lesson 2 bio101 (c)Dr.  Evangelista

Lecture #2

The Development of the Plant body

Page 2: Lesson 2 bio101 (c)Dr.  Evangelista

Parts of a flower The four kinds of floral organs are the sepals, petals, stamens, and carpels.

 Sepals and petals are nonreproductive organs.

 Stamens and carpels are the male and female reproductive organs, respectively.

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The stamen

  made up of anther and filament

 The microsporangia/pollen sacs contain the pollen grains

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The stamen: tissue differentiation

Archesporial layer

*

*periclinal division

**in eudicots originate from outer parietal layer; in monocots from inner parietal layer

***cytokinesis is usually simultaneous in dicots and successive in monocots

10 parietal layer

endothecium

**middle layer

Tapetum (nourishment of the developing PMC)

10 sporogenous tissue

Micro sporocytes

Meiosis*** microspores

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Illustration of a new models for plant archesporial initiation in the ovule and anther. Cells colored in red, blue, yellow, magenta, orange and green indicate archesporial cells, sporogenous cells (sc), primary parietal cells, tapetal cells, middle layer cells and endothecium cells, respectively.

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Development of male gametophyte

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The ovule

 Consists of the:

  nucellus – the megasporangium

  integuments

 funiculus – the stalk

 chalaza- the region where the integuments fuse with the funiculus

nucellus

micropyle

chalaza

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Megasporogenesis

Archesporial cell

Sporogeous cell

10 sporogenous cell

Parietal cell Megaspore mother cell

meiosis 4 Megaspores

(3 degenerate)

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Pollination and Fertilization

Pollination – is the transfer of the pollen to the stigma of the flower

Self pollination – transfer within the same flower or between flowers of the same plant

Cross pollination –transfer to a genetically distinct flower

Double fertilization gives rise to the zygote and endosperm

• Endosperm development usually precedes embryo development.

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 The endosperm is rich in nutrients, which it provides to the developing embryo.

 In most monocots and some eudicots, the endosperm also stores nutrients that can be used by the seedling after germination.

 In many eudicots, the food reserves of the endosperm are completely exported to the cotyledons before the seed completes its development, and consequently the mature seed lacks endosperm.

Endosperm

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Embryo and suspensor  The first mitotic division of the zygote is transverse, splitting the fertilized egg into a basal cell, and a terminal cell which gives rise to most of the embryo.

 The basal cell continues to divide transversely, producing a thread of cells, the suspensor, which anchors the embryo to its parent.

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 The suspensor may develop into a large haustorium which draws nutrients to the embryo from the parent

 The terminal cell divides several time and forms a spherical proembryo attached to the suspensor.

 Cotyledons begin to form as bumps on the proembryo. -A eudicot, with its two cotyledons, is heart- shaped at this stage. -Only one cotyledon develops in monocots.

Embryo and suspensor

 The suspensor pushes the embryo into the endosperm

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  After the cotyledons appear, the embryo elongates. -Cradled between cotyledons is the apical meristem of the embryonic

shoot. -At the opposite end of the embryo axis, is the apex of the embryonic root,

also with a meristem.

  After the seed germinates, the apical meristems at the tips of the shoot and root will sustain growth as long as the plant lives. -The three primary meristems - protoderm, ground meristem, and

procambrium - are also present in the embryo.

  During the last stages of maturation, a seed dehydrates until its water content is only about 5-15% of its weight. - The embryo stops growing until the seed germinates. - The embryo and its food supply are enclosed by a protective seed coat

formed by the integuments of the ovule.

The embryo

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  In the seed of a common bean, the embryo consists of an elongate structure, the embryonic axis, attached to fleshy cotyledons. - Below the point at which the fleshy cotyledons are attached, the

embryonic axis is called the hypocotyl and above it is the epicotyl/ plumule, consisting of the shoot tip with a pair of miniature leaves.

- The hypocotyl terminates in the radicle, or embryonic root.

The Seed

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  While the cotyledons of the common bean supply food to the developing embryo, the seeds of some dicots, such as castor beans, retain their food supply in the endosperm and have cotyledons that are very thin.

- The cotyledons will absorb nutrients from the endosperm and transfer them to the embryo when the seed germinates.

The Seed

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  The seed of a monocot has a single cotyledon. - Members of the grass family, including maize and wheat, have a

specialized cotyledon, a scutellum. - The scutellum is very thin, with a large surface area pressed

against the endosperm, from which the scutellum absorbs nutrients during germination.

  The embryo of a grass seed is enclosed by two sheaths, a coleorhiza, which covers the young root, and a coleoptile, which cover the young shoot.

The Seed

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Typesofseedgermination

1. Hypogealgermination

2. Epigealgermination

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Life cycle of angiosperms