2022 Solved Old Paper (BOT-102)
Apomixis:- When embryo is produced from the parent plant without fertilization, it is called asexual reproduction. Any vegetative cell acts as a zygote. The resulting seedlings are clones of their parents. It is of three types -
i. Adventive Embryony
ii. Apospory
iii. Diplospory
Telome concept:-
Telomes:-
> The name telome has been given to the simple ultimate terminal portions of dichotomously branched axis.
> These axes are undifferentiated and single nerved.
> Two telomes of a dichotomizing axis are united below the point of dichotomy to form a fused structure, called mesome.
> There are two types of telomes on the basis of their function:
i. Vegetative or sterile telomes:- These telomes are without sporangia and they are also called phylloids.
ii. Fertile telomes:- Those telomes which bore terminal sporangia are called fertile telomes.
Origin of Bryophytes (including fossil record) ब्रायोफाइट्स की उत्पत्ति (जीवाश्म रिकॉर्ड सहित):-
> Bryophytes are small, non vascular land plants, that require water for reproduction.
(ब्रायोफाइट्स छोटे, असंवहनी स्थलीय पौधे हैं, जिन्हें जनन के लिए जल की आवश्यकता होती है।)
> The defining features of bryophytes are that their life cycle featuring alternating haploid and diploid generations with a dominant, branched gametophyte stage.
(ब्रायोफाइट्स की परिभाषित विशेषताएं यह हैं कि उनके जीवन चक्र में एक प्रभावी, शाखित युग्मकोदभिद पीढ़ी के साथ एकांतरित अगुणित और द्विगुणित पीढ़ियाँ शामिल होती हैं।)
> The term "bryophyte” has its origin in the Greek language, referring to plants that swell upon hydration.
("ब्रायोफाइट" शब्द की उत्पत्ति ग्रीक भाषा से हुई है, जो उन पौधों को संदर्भित करता है जो जलयोजन पर फूल जाते हैं।)
> The bryophytes are quite soft and delicate and, therefore, they lack fossil records.
(ब्रायोफाइट्स काफी नरम और नाजुक होते हैं और इसलिए, इनके जीवाश्म रिकॉर्ड की कमी होती है।)
> All the views based on the evidence under the following three heads:-
(निम्नलिखित तीन शीर्षकों के अंतर्गत साक्ष्यों पर आधारित सभी विचार हैं:-)
i. Evidence from comparative morphology of the living plants
(जीवित पौधों की तुलनात्मक आकारिकी से साक्ष्य)
ii. Evidence from ontogeny of the living plants
(जीवित पौधों की ओंटोजेनी से साक्ष्य)
iii. Evidence based on analogies with the living plants of other groups
(अन्य समूहों के जीवित पौधों के साथ समानता पर आधारित साक्ष्य)
> Bryologists are divided into two concepts on the origin of bryophytes. One concept support Algal hypothesis and another one support Pteridophytean hypothesis of the origin of bryophytes.
(ब्रायोफाइट्स की उत्पत्ति पर ब्रायोलॉजिस्ट दो अवधारणाओं में विभाजित हैं। एक अवधारणा शैवालीय परिकल्पना का समर्थन करती है और दूसरी ब्रायोफाइट्स की उत्पत्ति की टेरिडोफाइटियन परिकल्पना का समर्थन करती है।)
1. Algal hypothesis (शैवालीय परिकल्पना):-
> Similarities (समानताएं):-
i. Amphibian nature
(उभयचर प्रकृति)
ii. Presence of flagellated spermatozoid
(कशाभ युक्त पुमणुओं की उपस्थिति)
iii. Presence of free water at the time fertilization
(निषेचन के समय मुक्त जल की उपस्थिति)
iv. Alga like protonema
(शैवाल की तरह प्रोटोनिमा)
> Bower (1908):- Bryophytes show resemblance with green algae (Chlorophyceae)
[ब्रायोफाइट्स हरे शैवाल (क्लोरोफाइसी) से समानता दर्शाते हैं]
i. Photosynthetic pigments like chlorophyll a, Chlorophyll b, Carotene, leutine and violaxanthin
(प्रकाश संश्लेषक वर्णक जैसे क्लोरोफिल a, क्लोरोफिल b, कैरोटीन, ल्यूटिन और वायोलाग्जैन्थिन)
ii. Starch as reserve food materials
(संग्रहित खाद्य सामग्री के रूप में स्टार्च)
iii. Filamentous protonema in the juvenile stage
(तरुण अवस्था में तंतुमय प्रोटोनिमा)
> Fritsch’s view (1916, 1945):- It is based on comparative study of various algal groups:
(यह विभिन्न शैवाल समूहों के तुलनात्मक अध्ययन पर आधारित है:)
i. Gradual reduction of conductive tissue in aerial plants (as in Sargassum)
[वायवीय पौधों में संवहनी ऊतक की धीरे-धीरे कमी (जैसे कि सारगासम में)]
ii. Heterotrichous habit (as in chaetophorales)
[विषमतंतुक प्रकृति (कीटोफोरेल्स की तरह)]
iii. Parenchymatous structure of erect filaments ( as in Laminariales and Fucales)
[स्तंभित तंतुओं की मृदूतकीय संरचना (लैमिनेरिएल्स और फ्यूकेल्स में)]
> Smith (1955):-
- Bryophytes have originated from chlorophyceae, primitive form established in area having plenty of water and gradual changes from aquatic to terrestrial, this led to the establishment of more massive plant body and abundance of moisture.
(ब्रायोफाइट्स की उत्पत्ति क्लोरोफाइसी से हुई है, जो प्रचुर मात्रा में जल वाले क्षेत्र में स्थापित आदिम रूप है और धीरे-धीरे जलीय से स्थलीय में परिवर्तन होता है, इससे अधिक विशाल पादप शरीर की स्थापना हुई और नमी की प्रचुरता हुई।)
- As per Smith, Fritschiella; a member of chaetophorales may be probable nearer to the primitive ancestor for bryophytes.
(स्मिथ के अनुसार, फ्रिट्स्चिएला; कीटोफोरेल्स का एक सदस्य संभवतः ब्रायोफाइट्स के आदिम पूर्वज के निकट हो सकता है।)
> Again the supporters of this hypothesis also believed that sex organs of Bryophytes have been evolved from Ectocarpus algae.
(पुनः इस परिकल्पना के समर्थकों का यह भी मानना था कि ब्रायोफाइट्स के लैंगिक अंगों का विकास एक्टोकार्पस शैवाल से हुआ है।)
2. Pteridophytean hypothesis (टेरिडोफाइटियन परिकल्पना):- According to this the bryophytes have been descended from pteridophytes by means of reduction. They formulated their argument on the basis of the following two features:
(इसके अनुसार ब्रायोफाइट्स कमी द्वारा टेरिडोफाइट्स से उत्पन्न हुए हैं। उन्होंने निम्नलिखित दो विशेषताओं के आधार पर अपना तर्क तैयार दिया:)
i. Close similarity between the sex organs of the two groups.
(दोनों समूहों के लैंगिक अंगों के बीच घनिष्ठ समानता।)
ii. Resemblance between sporogonium of Anthocerose, Sphagnum and terminal sporangium of fossil pteridophytes – Sporogonites and Horneophyton.
(स्फेगनम व एन्थोसिरोस के स्पोरोगोनियम की जीवाश्म टेरिडोफाइट्स (स्पोरोगोनाइट्स और हॉर्नियोफाइटन) के शीर्षस्थ बीजाणुधानियों से समानता।)
> This theory is strongly supported by some of the scientists such as Lang(1917), Kidston (1917), Scott(1923), Haskell(1949) and Kashyap (1919).
[इस सिद्धांत को लैंग (1917), किडस्टन (1917), स्कॉट (1923), हास्केल (1949) और कश्यप (1919) जैसे कुछ वैज्ञानिकों ने पुरजोर समर्थन दिया है।]
> Affinities (समानताएं):-
i. Similarity of their pigments
(उनके वर्णकों की समानता)
ii. Structure of cell wall
(कोशिका भित्ति की संरचना)
iii. Food reserves
(खाद्य सामग्री)
iv. Reproductive methods
(जनन विधियाँ)
v. Life cycle
(जीवन चक्र)
> Scott introduce the idea (1911):-
i. Presence of chlorophyll and plastids in the sporogonium of mosses and Anthoceros.
(मॉस और एन्थोसिरोस के स्पोरोगोनियम में क्लोरोफिल और प्लास्टिड की उपस्थिति।)
ii. Presence of stomata on the sporogonium of Anthoceros and the apophysis region of capsule of mosses.
(एन्थोसिरोस के स्पोरोगोनियम और मॉस के कैप्सूल के एपोफाइसिस क्षेत्र पर रंध्रों की उपस्थिति।)
> Kashyap (1919):- Order Equisetales gives 3 orders:-
(गण इक्विसेटेल्स 3 गण देता है:-)
i. Marchantiales (मारकेंशिएल्स)
ii. Jungermanniales (जंगरमेनिएल्स)
iii. Anthocerotales (एंथोसिरोटेल्स)
> Haskell (1949):- He advanced the origin of the bryophytes from the algae through the Psilophytales by simplification.
(उन्होंने सरलीकरण द्वारा साइलोफाइटेल्स के माध्यम से शैवाल से ब्रायोफाइट्स की उत्पत्ति को आगे बढ़ाया।)
Evolution of stele:-
Stele:- The central cylinder or core of vascular tissue, consisting of xylem, phloem, pericycle and sometimes medullary rays and pith, is technically called stele.
Stelar theory:-
> Van Tieghem and Douliot (1886) developed this theory.
> They used the term stele in collective sense and mentioned that the stele is not only made up of xylem and phloem, but the tissue like pericycle, vascular rays and pith are also associated with it.
> According to them the cortex and the stele are the fundamental parts of a shoot and both these parts are separated from each other by the endodermis.
> According to stellar theory, primarily there is no fundamental difference in the gross anatomy of stem and roots, because in both of them a stele is surrounded by the cortex is present.
> Foster and Gifford (1959) have mentioned that the most debated and controversial aspect of “stellar theory is the nature of the anatomical boundaries which separate the cortex from the stele”.
> According to Van Tieghem and Douliot (1886) the endodermis represents the inner boundary of the cortex. The cells of the endodermal layer have the characteristic casparian strip strips.
> But in the stems of many seed plants, the characteristic endodermal layer is not present. Some have mentioned that in such cases the pericycle serves as separating layer between the stele and the cortex.
Types of stele:- 7 types of steles are found in the whole plant kingdom -
1. Protostele
2. Siphonostele
3. Solenostele
4. Dictyostele
5. Polycyclic stele
6. Eustele
7. Atactostele
Note:- Out of these the first 5 types of steles are found only in the stem of pteridophytes. Eusteel is found in the stem of gymnosperms and dicots. Atactostele is found in the stem of monocots.
Note:- The development of stele has also happened in this sequence. Atactosteel is considered to be the most advanced type of stele.
1. Protostele:- This is the most primitive type of stele in which the pith is completely absent and the phloem surrounds the xylem. According to Jeffrey (1898), the protostele is primitive type of stele in vascular plants.
On the basis of the shape of the xylem in the cross section, it is of 4 types -
i. Haplostele:- The xylem appears circular in cross section. It has been observed in fossil genera like Rhynia, Horneophyton and living genera like Selaginella chrysocaulos, S. kraussiana, S. selaginoides, S. willdenowi, Gleichenia dichotoma, Lygodium and Cheiropleuria.
ii. Actinostele:- The xylem appears star shaped in cross section. Brebner (1902) named such a protostele as actinostele. Eg.- Asteroxylon, Psilotum, Lycopodium serratum and Sphenophyllum.
iii. Plectostele:- In cross section, the xylem appears as parallel plates. Eg.- Lycopodium clavatum and L. volubile.
iv. Mixed protostele:- In cross section, the xylem is seen scattered in the form of segments. Eg.- Lycopodium cernuum
2. Siphonostele:- In this, pith or pith cavity is found in the center around which vascular tissues are found.
Origin of siphonostele:- There are different views among scientists regarding the origin of siphonostele. But they all agreed that the siphonostele originated from protostele by the formation of a pith in the center. Here, the centrally placed xylem core is replaced with a parenchymatous pith.
Different stages of changing protostele to siphonostele can be observed in the T.S. at different levels in Gleichenia, Osmunda, and Anemia.
There are two views regarding the origin of pith in the siphonostele.
i. Jeffrey’s theory:-
- According to this theory, the pith is formed as a result of the invasion of cortical parenchymatous cells into the stele. The invasion of the pith occurs through the leaf gap or branch gap.
- Thus pith and cortex are homogeneous structures according to this theory.
- This theory is not accepted by most of the authors since in many pteridophytes there is a stele without leaf gaps but having siphonostele.
ii. Boodle’s theory:- According to the theory proposed by Boodle (1901), and Gwynne Vaughan, the siphonostele has evolved from the protostele by a transformation of the inner vascular tissue into the parenchyma.
On the basis of the location of phloem it is of two types –
i. Ectophloic siphonostele:- Phloem is found around the xylem. Eg.- Osmunda, Schizaea, etc.
ii. Amphiphloic siphonostele:- Phloem is found at both outside and inside the xylem. Eg. Rhizome of Marsilea, Adiantum, Dipteris.
3. Solenostele:- The vascular tissue in the ectophloic siphonostele forms a leaf gap when it enters the leaf as a leaf trace.
4. Dictyostele:- When the leaves are found densely, many leaf gaps come together causing the vascular tissue of the amphipholic siphonostele to break into many pieces. Each piece is called a meristele and each meristele is a haplostele. In this way many merysteles are found in the form of a circle.
5. Polycyclic stele:- When 2 or more cycles of meristeles are found.
6. Eustele:- When vascular bundles are found in a circle.
7. Atactostele:- When vascular bundles remain scattered throughout the ground tissue.
Soral evolution:-
Sorus:- It is brownish or yellowish cluster of spore-producing structures (sporangia) usually located on the lower surface of fern leaves. A sorus may be protected during development by a scale or flap of tissue called an indusium.
Types of sorus:-
i. Simple sorus:-
> The Simplices are primitive and extend to the Paleozoic.
> All sporangia within a sorus may be at the same stage of development (Simplices).
> The sporangia in such a sorus development simultaneously and all of them mature together.
> Eg.- Ophioglossum and Osmunda.
ii. Gradate sorus:-
> In such cases the internal space within the radial sorus gets filled by overlapping sporangia.
> Overcrowding results and there is no space for the proper dehiscence of sporangia and consequently some of them do not dehisce.
> The Gradate with an oblique annulus, occupy a middle position and have been discovered in the Mesozoic.
> Eg.- Dicksonia, Loxosoma, Trichomanes, Cyathea, Alsophila etc.
iii. Mixed sorus:-
> The spores are released in a staggered fashion and even if the environmental conditions are not favorable when the spores are initially released; this problem is solved by a constant crop of spores over a given length of time.
> Mixtae annulus is present but in a vertical fashion.
> Eg.- Polypodiaceae (Adiantum, Pteris, Pteridium, Davallia) Polypodiaceae
Indusial protection:- The indusium may be formed as an epidermal outgrowth covering receptacle and sporangia (true indusium) or it may merely be the in turning of the margin of the leaf to protect the sporangia (pseudo indusium or false indusium).
Position of sorus in ferns:- The Ophioglossales are group of interesting ferns in which the sporangia are marginal in position.
> In Maeattia, Angiopteris, Danaea etc. the sori are elongagated and are situated below the lateral veins.
> In christensia the sori are naked, circular and are irregular arranged between the lateral veins.
> In Adiantum the sporangia develop on the underside of special marginal flaps of lamina that become reflexed and protect the sorus
> The sori in Mattoniaceae are ventral in position and are usually arranged in two rows on either side of the midrib.
> In Glecheniaceae, the sporangia from distinct sori on the ventral surface of the leaves.
> The sporangia in Osmunda, Davalia, Trivhomanes and many other ferns are also marginal in position.
> In Marsileales and the Salviniales the sporangia develop in sori that are borne within distinct structure called the Sporocarp.
- In Salviniales the smaller sporocarp contain many microsporangia each and the larger ones contain one or more megasporangia per sporocarp.
- The sporocarp in Marsilea enclose sori that contain both micro and megasporongia.
Classification of Bryophytes (ब्रायोफाइट्स का वर्गीकरण):- According to the newest classification, Bryophyta is split into three classes:
(नवीनतम वर्गीकरण के अनुसार, ब्रायोफाइटा को तीन वर्गों में विभाजित किया गया है:)
1. Hepaticopsida (Liverworts)
2 Anthocerotopsida (Hornworts)
3. Bryopsida (Mosses)
1. Hepaticopsida (Liverworts):-
> The name hepaticopsida comes from the word “hepatic” which means liver.
(हिपेटिकोप्सिडा नाम "हिपेटिक" शब्द से आया है जिसका अर्थ है यकृत।)
> The most basic bryophytes are liverworts.
(सबसे आधारभूत ब्रायोफाइट्स लिवरवॉर्ट्स हैं।)
> They prefer moist rocks and wet soil to live in.
(वे रहने के लिए नम चट्टानें और गीली मिट्टी पसंद करते हैं।)
> Because they dwell near water, their chances of drying are much reduced.
(क्योंकि वे जल के पास रहते हैं, उनके सूखने की संभावना बहुत कम हो जाती है।)
> The gametophyte plant is either thalloid or foliose.
(युग्मकोदभिद पौधा या तो थैलॉइड या पत्तेदार होता है।)
> Thalloid forms are dorsiventral, lobed, and dichotomously branched.
(थैलॉइड रूप पृष्ठाधरी, पालित और द्विभाजित शाखा वाले होते हैं।)
> Rhizoids are unicellular, unbranched and of 2 type:
(मूलाभास एककोशिकीय, अशाखित और 2 प्रकार के होते हैं:)
> Sex organs are borne dorsally embedded in gametophytic tissues.
(लैंगिक अंग युग्मकोदभिद ऊतकों में पृष्ठीय रूप से धँसे होते हैं।)
> The sporophyte is a compilation of only capsule (in Riccia) or foot, seta, and capsule (in Marchantia).
The columella is absent in the capsule.
(बीजाणुदभिद केवल कैप्सूल (रिक्सिया में) या फुट, सीटा और कैप्सूल (मार्केन्शिया में) का संकलन है। कैप्सूल में कोल्यूमेला अनुपस्थित होता है।)
> Sporogenous tissues develop from endothecium.
(बीजाणुजनित ऊतक एन्डोथेसियम से विकसित होते हैं।)
> Hepaticopsida is further divided into 5 orders:
(हेपेटिकॉप्सिडा को आगे 5 गणों में विभाजित किया गया है:)
a. Sphaerocarpales:- 2 families: (2 कुल)
i. Sphaerocarpaceae:- Eg.- Sphaerocarpos, Geothallus
ii. Riellaceae:- Eg.- Riella
b. Marchantiales:- 4 families: (4 कुल)
i. Ricciaceae:- Eg.- Riccia, Ricciocarpus, Tesselina (Oxymitra)
ii. Targionaceae:- Eg.- Targionia, Cyathodium, Aitchisoniella
iii. Monocleaceae:- Eg.- Monoclea
iv. Marchantiaceae:- Eg.- Marchantia, Plagiochasma, Dumortiera, Lunularia, Reboulia, Grimaldia, Monoselenium
c. Jungermanniales:- 3 families: (3 कुल)
i. Ricardiaceae (Aneuraceae):- Eg.- Ricardia (Aneura)
ii. Blyttiaceae (Pallavaciniaceae):- Eg.- Blyttia
iii. Codoniaceae:- Eg.- Pellia, Petalophyllum, Fossombronia
d. Calobryales:- 1 family: (1 कुल)
i. Calobryaceae:- Eg.- Calobryum, Haplomitrium
e. Takakiales:- 1 family: (1 कुल)
i. Takakiaceae:- Eg.- Takakia
2. Anthocerotopsida (Hornworts):-
> They are commonly known as hornworts.
(इन्हें आमतौर पर हॉर्नवॉर्ट्स के नाम से जाना जाता है।)
> The gametophytic body is flat, dorsiventral, simple thalloid, and has no internal differentiation.
(युग्मकोदभिद शरीर चपटा, पृष्ठीय, सरल थैलॉइड होता है और इसमें कोई आंतरिक विभेदन नहीं होता है।)
> Rhizoids are unicellular, unbranched and smooth-walled.
(मूलाभास एककोशिकीय, अशाखित और चिकनी भित्ति वाले होते हैं।)
> Each cell has one chloroplast with a pyrenoid.
(प्रत्येक कोशिका में पाइरेनॉइड के साथ एक क्लोरोप्लास्ट होता है।)
> Sex organs are present dorsally embedded in the thallus.
(लैंगिक अंग थैलस में पृष्ठीय रूप से धँसे होते हैं।)
> Sporogenous tissues develop from amphithecium.
(बीजाणुजनित ऊतक एम्फ़िथेशियम से विकसित होते हैं।)
> Pseudoelaters are present in the capsule.
(कैप्सूल में कूटइलेटर्स पाये जाते हैं।)
> The columella is present within the capsule, which originates from the endothecium.
(कोल्यूमेला कैप्सूल के भीतर मौजूद होता है, जो एंडोथेसियम से उत्पन्न होता है।)
> It has only one order:
(इसका केवल एक ही गण है:)
a. Anthocerotales:- 2 families: (2 कुल)
i. Anthocerotaceae:- Eg.- Anthoceros, Paeoceros, Dendroceros, Megaceros
ii. Notothylaceae:- Eg.- Notothylas
3. Bryopsida (Mosses):-
> They are commonly called mosses.
(इन्हें आम तौर पर मौस कहा जाता है।)
> The gametophyte is divided into protonema and foliose gametophore.
(युग्मकोदभिद को प्रोटोनिमा और पर्णीय गैमेटोफोर में विभाजित किया गया है।)
> Foliose gametophore is formed of the stem as an axis and leaves without a midrib.
(पर्णीय गैमेटोफोर एक अक्ष के रूप में तने और मध्यशिरा रहित पत्तियों से बना होता है।)
> Rhizoids are multicellular with oblique septate.
(मूलाभास तिरछे पट्ट युक्त बहुकोशिकीय होते हैं।)
> Sex organs are borne apically on the stem.
(लैंगिक अंग शीर्षस्थ रूप से तने पर उत्पन्न होते हैं।)
> Elaters are absent.
(इलेटर अनुपस्थित होते हैं।)
> The sporophyte is differentiated into foot, seta and capsule.
(बीजाणुदभिद को फुट, सीटा और कैप्सूल में विभेदित किया जाता है।)
> Sporogenous tissues develop from endothecium.
(बीजाणुजनित ऊतक एन्डोथेसियम से विकसित होता है।)
> The columella is present.
(कोल्यूमेला उपस्थित होता है।)
> Separation of the lid is the result of the Dehiscence of the capsule.
(ढक्कन का अलग होना कैप्सूल के फूटने का परिणाम है।)
> Bryopsida is further divided into 3 sub-classes:
(ब्रायोप्सिडा को आगे 3 उप-वर्गों में विभाजित किया गया है:)
a. Sphagnidae:- 1 order: (1 गण)
I. Sphagnales:- 1 family: (1 कुल)
i. Sphagnaceae:- Eg.- Sphagnum
b. Andreidae:- 1 order: (1 गण)
I. Andreales:- 1 family (1 कुल)
i. Andreaceae:- Eg.- Andrea (Granite moss)
c. Eubryidae (Bryidae):- 3 orders: (3 गण)
I. Polytrichales:- 1 family: (1 कुल)
i. Polytrichaceae:- Eg.- Polytrichum, Pogonatum, Atrichium, Oligotrichum, Lyellia
II. Funariales:- 5 families (5 कुल)
i. Gigaspermaceae
ii. Funariaceae:- Eg.- Funaria
iii. Disceliaceae
iv. Oedipodiaceae
v. Splachaceae
III. Buxbaumiales:- 1 family:
i. Buxbaumiaceae:- Eg.- Buxbaumia, Diphyscium
Heterospory:- The phenomenon of the development of two types of spores (differing in size, structure and function) by the same species is known as heterospory.
> The two different sizes are smaller spores also known as microspores and the larger spores also known as megaspores.
> Rashid (1999) listed nine genera as living examples of heterosporous pteridophytes. e.g. Selaginella, Isoetes, Stylites, Marsilea, Pilularia, Regnellidium, Salvinia, Azolla and Platyzoma.
Origin of Heterospory:- The origin of heterospory can be better discussed on the basis of evidences from paleobotany, developmental and experimental studies.
1. Palaeobotanical evidences:-
- It has been suggested that heterospory arose due to degeneration of some spores in a few sporangia. As more nutrition becomes available to less number of spores, the surviving spore grow better, hence increase in their size.
- Palaeobotanical evidences show that the earlier vascular plants were all homosporous and the heterosporous condition appeared subsequently in the lowermost upper Devonian.
- A number of heterosporous genera belonging to the Lycopsida, Sphenopsida and Pteropsida were known in the late Devonian and early Carboniferous periods.
2. Evidences from Experimental Studies:-
- Experimental studies on Selaginella (Goebel, 1905) and Marsilea (Shattuck, 1910) suggest that nutritional factors mainly govern the heterospory.
- Under conditions of low light intensity, the photosynthetic activity of Selaginella was retarted and it produced microsporangia.
- By sudden lowering of the temperature, the size of the microspores in the sporocarp of Marsilea increases by six times.
3. Evidences from Developmental Studies:-
- In heterosporous pteridophytes, the development of micro and megasporangia follow the same pattern. While in megasporangia most of the spore mother cells degenerate but in microsporangia only a few mother cells are disorganized.
- The phenomenon of heterospory becomes distinct either before or after meiosis in Selaginella. Isoetes, it is distinct before meiosis.
Importance of heterospory:-
i. The differentiation in the size of the spore is directly related to the differentiation of sex of the gametophyte. Therefore, heterospory is an expression of sex determination in plants.
ii. Because of heterospory, plants become free to grow in varied environmental conditions, instead of only aquatic surroundings.
iii. It ultimately leads to seed development.
iv. The megaspore having female gametophyte derives nourishment from sporophyte and thus remains independent from external factors.
Seed habit:- Because of heterospory, the gametophytic tissue is reduced. Partial or complete retention of megasporangium and female gametophyte on the sporophyte also takes place. They show reduction in megaspores and male gamete. All these characters show a tendency towards seed habit.
Origin of seed habit:- One of the most important advantages of heterospory is the formation of seed habitat. The origin of seed habit is associated with the following:
i. Production of two types of spores (heterospory).
ii. Reduction in the number of megaspores finally to one per megasporangium.
iii. Retention and germination of the megaspores and fertilization of the egg.
iv. Continued development of the fertilized egg into the embryo while still in situ.
Seed habit in Selaginella:- Selaginella exhibits remarkable approach to the seed habit because of the following features:
i. The heterospory occurs in almost all the species of Selaginella.
ii. In most species only one functional megaspore mother cell is produced which by reduction division produces four haploid megaspores. In some species e.g. rupestris and S. monospora only one megaspore is formed in each megasporangium.
iii. Germination of megaspore starts within the megasporangium, but its stage and time of retention within megasporangium differ in different species.
iv. Fertilization and embryo development also takes place within the megasporangium.
Although certain species of Selaginella suggest early stages in the evolution of seed habit, Selaginella should not be considered as an ancestor to seed plants because:
i. Absence of integuments around the megasporangia.
ii. Absence of permanent retention of megaspores within megaspoarangia except a few species.
iii. Absence of complete histological fusion between megasporangium wall and megaspore.
iv. After the development of embryo there is lack of resting period.
Therefore, Selaginella has considerably advanced towards seed habit but it’s approach to true seed is not complete.
Isoetes:-
1. Systematics:-
Division:- Lycophyta
Class:- Ligulopsida
Order:- Isoetales
Family:- Isoetaceae
Genus:- Isoetes
2. Habit and Habitat:-
> Isoetes includes 60 to 70 species and is world wide in distribution. Nearly 10 species are reported
from India, such as:-
i. Isoetes coromandelina:- Reported from Kerala, Tamil nadu, Andhra Pradesh Maharashtra and Gujrat Padampur and Bengal Madhya Pradesh, Uttar Pradesh, Bihar and Orissa.
ii. Isoetes coromandelina Sub Sps. branchyglossa:- West Bengal.
iii. Isoetes bilaspurensis:- Madhya Pradesh.
iv. Isoetes dixitii:- Maharashtra.
v. Isoetes indica:- Uttar Pradesh, Madhya Pradesh and Tamilnadu.
vi. Isoetes panchananii:- Madhya Pradesh and Maharashtra.
5. Phylogeny:-
> Phylogeny:- The history of the evolution of a species or group, especially in reference to lines of descent and relationships among broad groups of organisms.

.png)
.png)


.png)
.png)


.png)
.png)
.png)
.png)














.png)

.jpeg)


.bmp)



















.bmp)





