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Lecture #2
  The Development of the Plant body

 

Parts of a flower
The four kinds of
floral organs are
the sepals,
petals, stamens,
and carpels.
  epals and petals are
 S
nonreproductive organs.
  tamens and carpels
 S
are the male and female
reproductive organs,
respectively.
The stamen




                          he microsporangia/pollen
                         T
                        sacs contain the pollen grains



 made up of
anther and filament
The stamen: tissue differentiation

                                                         endothecium

                         10 parietal layer
                                                       **middle layer
                                                         Tapetum
Archesporial     *                                       (nourishment of the developing
                                                         PMC)
    layer
                                                        Meiosis***
                        10 sporogenous         Micro                 microspores
                        tissue                 sporocytes

 *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
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.
Development of male gametophyte
The ovule


  onsists of the:
 C                                   chalaza
                                      nucellus
  nucellus – the
      megasporangium
 integuments
 uniculus – the stalk
 f
  halaza- the region where
 c
       the integuments fuse      micropyle
with the funiculus
Megasporogenesis




                    Sporogeous cell


Archesporial cell

                    Parietal cell
                                                      meiosis
                     10   sporogenous   Megaspore          4 Megaspores
                             cell       mother cell
                                                          (3 degenerate)
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

 •  ndosperm development usually
  E
 precedes embryo development.
Endosperm

  he endosperm is rich in nutrients, which it provides to
 T
the developing embryo.

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

    n many eudicots, the food reserves of the endosperm
    I
   are completely exported to the cotyledons before the
   seed completes its development, and consequently the
   mature seed lacks endosperm.
Embryo and suspensor
  he first mitotic division of the zygote is transverse, splitting the
  T
fertilized egg into a basal cell, and a terminal cell which gives
rise to most of the embryo.
     he basal cell continues to divide transversely, producing a
     T
   thread of cells, the suspensor, which anchors the embryo to
   its parent.
Embryo and suspensor

  he suspensor pushes the embryo into the endosperm
 T
      he suspensor may develop into a large haustorium which
     T
    draws nutrients to the embryo from the parent
  he terminal cell divides several time and forms a spherical
 T
proembryo attached to the suspensor.

     otyledons begin to form as bumps on the proembryo.
    C
              -A eudicot, with its two cotyledons, is
       heart- shaped at this stage.

             -Only one cotyledon develops in monocots.
The embryo
  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 Seed

  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

  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
  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.
Types
of
seed

      germination

1.  ypogeal
germination

  H
2.  pigeal
germination

  E
Life cycle of angiosperms

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Lesson 2 bio101 (c)Dr. Evangelista

  • 1. Lecture #2 The Development of the Plant body 
 

  • 2. Parts of a flower The four kinds of floral organs are the sepals, petals, stamens, and carpels.   epals and petals are S nonreproductive organs.   tamens and carpels S are the male and female reproductive organs, respectively.
  • 3. The stamen   he microsporangia/pollen T sacs contain the pollen grains  made up of anther and filament
  • 4. The stamen: tissue differentiation endothecium 10 parietal layer **middle layer Tapetum Archesporial * (nourishment of the developing PMC) layer Meiosis*** 10 sporogenous Micro microspores tissue sporocytes *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
  • 5. 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.
  • 6.
  • 7.
  • 8. Development of male gametophyte
  • 9. The ovule   onsists of the: C chalaza nucellus   nucellus – the megasporangium  integuments  uniculus – the stalk f   halaza- the region where c the integuments fuse micropyle with the funiculus
  • 10. Megasporogenesis Sporogeous cell Archesporial cell Parietal cell meiosis 10 sporogenous Megaspore 4 Megaspores cell mother cell (3 degenerate)
  • 11.
  • 12.
  • 13. 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 •  ndosperm development usually E precedes embryo development.
  • 14.
  • 15. Endosperm   he endosperm is rich in nutrients, which it provides to T the developing embryo.  n most monocots and some eudicots, the endosperm I also stores nutrients that can be used by the seedling after germination.  n many eudicots, the food reserves of the endosperm I are completely exported to the cotyledons before the seed completes its development, and consequently the mature seed lacks endosperm.
  • 16. Embryo and suspensor   he first mitotic division of the zygote is transverse, splitting the T fertilized egg into a basal cell, and a terminal cell which gives rise to most of the embryo.   he basal cell continues to divide transversely, producing a T thread of cells, the suspensor, which anchors the embryo to its parent.
  • 17. Embryo and suspensor   he suspensor pushes the embryo into the endosperm T   he suspensor may develop into a large haustorium which T draws nutrients to the embryo from the parent   he terminal cell divides several time and forms a spherical T proembryo attached to the suspensor.   otyledons begin to form as bumps on the proembryo. C -A eudicot, with its two cotyledons, is heart- shaped at this stage. -Only one cotyledon develops in monocots.
  • 18. The embryo   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.
  • 19. The Seed   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.
  • 20. The Seed   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.
  • 21. The Seed   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.
  • 22. Types
of
seed
 germination
 1.  ypogeal
germination
 H 2.  pigeal
germination
 E
  • 23.
  • 24. Life cycle of angiosperms