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  • TITLE
  • DEDICATION
  • DECLARATION
  • CERTIFICATE
  • PREFACE
  • ACKNOWLEDGEMENT
  • CONTENTS
  • I. INTRODUCTION
  • II. MATERIALS AND METHODS
  • PREPARATION OF PEELINGS FOR THE EPIDERMAL STUDIES
  • CLEARING TECHNIQUES FOR THE STUDY OF LEAF ARCHITECTURE AND PALISADE RATIO
  • HISTOCHEMICAL TECHNIQUES FOR THE LOCALIZATION OF METABOLITES ON THE FOLIAR EPIDERMIS
  • MACERATION FOR VESSEL ELEMENT STUDIES
  • PREPARATION OF POLLEN FOR PALYNOLOGICAL STUDIES
  • SEED MORPHOLOGY
  • DRAWINGS AND PHOTOGRAPHY
  • SCANNING ELECTRON MICROSCOPY
  • CALCULATIONS
  • CLUSTER ANALYSIS
  • TABLE 1 NAME OF THE TAXA INVESTIGATED AND PLACE OF COLLECTION
  • TABLE: 2 - STAINING METHODS EMPLOYED FOR THE LOCALIZATION OF DIFFERENT CELL METABOLITES
  • III. OBSERVATIONS
  • 1. FOLIAR FEATURES
  • 1.1 a MATURE STOMATA
  • Stomatal Abnormalities
  • Guard Cell Size
  • 1.1b STOMATAL INDEX
  • 1.1 c STOMATAL FREQUENCY
  • TABLE: 3. DATA ON STOMATAL INDEX. STOMATAL FREQUENCY AND GUARD CELL SIZE (WITH STANDARD DEVIATION)
  • Fig.1 EPIDERMAL PEELS OF LAMINA SHOWING STOMATAL DlVERSlTY
  • Fig. 2 EPIDERMAL PEELS OF LAMINA SHOWING STOMATAL DIVERSITY
  • PLATE - 1 LIGHT MICROGRAPHS SHOWING THE ABNORMAL STOMATA - [A-l x 1000)
  • PLATE - 2 LIGHT MICROGRAPHS SHOWING THE ABNORMAL STOMATA (A-1 x 1000; H x 1550)
  • 1.2 LEAF ARCHITECTURE
  • Qualitative Features
  • Venation
  • Major Venation Pattern
  • Primary Veins
  • Secondary Veins
  • Tertiary Veins
  • Minor Venation Pattern
  • Marginal Ultimate Venation
  • lntramarginal Vein
  • Areolation
  • Veinlets
  • Tracheids
  • Isolated Tracheids
  • Extension CelIs
  • Bundle Sheath
  • Hydathodes
  • Table 4. Qualitative Features of Leaf
  • TABLE: 5. Quantitative Features of Leaf
  • Fig. 3 CLEARED LEAVES SHOWING VENATION PATTERN
  • Fig. 4 CLEARED LEAVES SHOWING VENATION PATTERN
  • Fig. 5 CLEARED LEAF TIPS AND MARGINS SHOWING VENATION PATTERN AND HYDATHODE VEIN ENDINGS (A - I x 20)
  • Fig. 6 CLEARED LEAF AND MARGINS SHOWING VENATION PATTERN AND HYDATHODE VEIN ENDINGS [A - K x 20)
  • Fig. 7 CLEARED LEAF TIPS AND MARGINS SHOWING VENATION PATTERN AND HYDATHODE VEIN ENDINGS (A - H x 20)
  • Fig. 8 CLEARED LEAF TIPS AND MARGINS SHOWING VENATION PATTERN AND HYDATHODE VEIN ENDINGS (A - J x 20)
  • Fig. 9 CLEARED LEAF TIPS AND MARGINS SHOWING VENATION PATTERN AND HYDATHODE VEIN ENDINGS (A - K x 25)
  • Fig. 10 CLEARED LEAF TIPS AND MARGINS SHOWING VENATION PATTERN AND HYDATHODE VEIN ENDINGS (A - L x 25)
  • Fig. 11 CLEARED LEAF TIPS AND MARGINS SHOWING VENATION PATTERN AND HYDATHODE VEIN ENDINGS (A - M x 20)
  • PLATE - 3 DIRECT PHOTOGRAPHS OF CLEARED LEAVES SHOWING LEAF ARCHITECTURE
  • PLATE - 4 DIRECT PHOTOGRAPHS OF CLEARED LEAVES SHOWING LEAF ARCHITECTURE (A - D x 2)
  • PLATE - 5 DIRECT PHOTOGRAPHS OF CLEARED LEAVES SHOWING LEAF ARCHITECTURE (A - E x 2)
  • PLATE - 6 DIRECT PHOTOGRAPHS OF CLEARED LEAVES SHOWING LEAF ARCHITECTURE (A - D x 2)
  • PLATE - 7a MICROPHOTOGRAPHS OF CLEARED LEAVES SHOWING VENATION PATTERN (A - F x 200)
  • PLATE - 7b
  • PLATE - 8 MICROPHOTOGRAPHS SHOWING AREOLATION (A - F x 300)
  • PLATE - 9 MICROPHOTOGRAPHS SHOWING TRACHEIDS (A - I x 1000)
  • 1.3 PALISADE RATIO
  • TABLE 6: PALISADE RATIO OF DIFFERENT TAXA
  • 1.4 HISTOCHEMISTRY OF FOLIAR EPIDERMIS
  • Table 7.Showing the distribution of different histochemical metabolites in the foliar epidermis
  • PLATE - 10 LIGHT MICROGRAPHS OF STOMATA SHOWING THE DISTRIBUTION OF STARCH GRAINS (Iodine - Potassium iodide test: Fig. A - l x. 550)
  • PLATE - 11 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF CELLULOSE[Iodine - Potassium iodide - Sulphuric acid Test: A - F x 450)
  • PLATE - 12 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF INSOLUBLE POLYSACCHARIDES (PAS reaction: A - C x 800)
  • PLATE - 13 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF INSOLUBLE POLYSACCHARIDES (PAS reaction: A - C x 8001
  • PLATE - 14 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF POLYPHENOLS, SULPHATED AND CARBOXYLATED POLYSACCHARIDES (TBO Test: A - C x 800)
  • PLATE - 15 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF POLYPHENOLS, SULPHATED AND CARBOXYLATED POLYSACCHARIDES (TBO Test: A - C x 800)
  • PLATE - 16 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF PROTEINS[Mercuric Brornophenol Blue Test: A - D x 450)
  • PLATE - 17 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF PROTEINS (Mercuric Bromophenol Blue Test: A - D x 450)
  • PLATE - 18 LIGHT MICROGRAPHS SHOWING THE LOCALISATION OF LIPIDS (Sudan Black Method: A - C x 800)
  • 2. NODAL, INTERNODAL AND ROOT VESSEL ELEMENTS
  • Shape
  • Size
  • Perforation Plate
  • Pitting
  • Tail
  • TABLE 8: SHOWING THE LENGTH OF NODAL VESSELS ELEMENTS WITH STANDARD DEVIATION
  • TABLE: 9 SHOWING THE LENGTH OF INTER NODAL VESSEL ELEMENTS WITH STANDARD DEVIATION
  • TABLE: 10 SHOWlNG THE LENGTH OF ROOT VESSEL ELEMENTS WITH STANDARD DEVIATION
  • TABLE 11: CLASSIFICATION SHOWING THE BREADTH OF NODAL VESSEL ELEMENTS WlTH STANDARD DEVIATIONS
  • TABLE 12: SHOWING THE BREADTH OF INTER NODAL VESSEL ELEMENTS WITH.STANDARD DEVIATION
  • TABLE 13: SHOWING THE BREADTH OF ROOT VESSEL ELEMENTS WITH STANDARD DEVIATION
  • TABLE 14: SHOWING THE TYPE AND NUMBER OF PERFORATON PLATES, NATURE OF INTER-VESSEL PITS, AND DISPOSITION OF PERFORATION PLATES OF NODA.L VESSEL ELEMENTS
  • TABLE 15: SHOWING THE TYPE AND NUMBER OF PERFORATION PLATES, TYPE OF INTER-VESSEL PITS, AND DISPOSITION OF PERFORATION PLATES OF INTER-NODAL VESSEL ELEMENTS
  • TABLE 16: SHOWING THE TYPE AND NUMBER OF PERFORATION PLATES, NATURE OF INTER-VESSEL PITS, AND DlSPOSlTlON OF PERFORATION PLATES OF ROOT VESSEL ELEMENTS
  • Fig. 12 NODAL VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 - 96 x 200)
  • Fig. 13 NODAL VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 - 75 x 200)
  • Fig. 14 NODAL VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 - 74 x 200)
  • Fig. 15 INTERNODAL VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 - 32 x 200)
  • Fig. 16 INTERNODAL VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 - 35 x 200)
  • Fig. 17 INTERNODAL VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 -31 x 200)
  • Fig. 18 INTERNODAL VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES[ I - 51 x 200)
  • Fig. 19 ROOT VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 - 47 x 200)
  • Fig. 20 ROOT VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES (1 - 53 x 200)
  • Fig. 21 ROOT VESSEL ELEMENTS SHOWING STRUCTURAL FEATURES11-49 x 200)
  • PLATE - 19 VESSEL ELEMENTS OF VARIOUS TAXA STUDIED
  • 3. PALYNOLOGY
  • TABLE 17. QUALITATIVE FEATURES OF POLLEN GRAIN
  • TABLE: 18 QUANTITATIVE DATA OF POLLEN GRAINS OF DIFFERENT TAXA WITH STANDARD DEVIATION
  • Fig. 22 PALYNOGRAM (C - J x 3750; C1 - J1 x 12001
  • Fig. 23 PALYNOGRAM (A - J x 3750; Al - J, x 1200)
  • Fig. 24 PALYNOGRAM (A - J x 3750: Al - J1 x 1200)
  • Fig. 25 PALYNOCRAM (A - H x 3750; Al - H x 1200)
  • PLATE - 20 LIGHT MICROGRAPHS OF POLLEN GRAINS (A - P x 800)
  • PLATE - 21 SCANNING ELECTRON MICROGRAPHS OF POLLEN GRAINS (A - E x 5000; F x 5500)
  • PLATE - 22 SCANNING ELECTRON MICROGRAPHS OF POLLEN GRAINS (A x 6500; B - F x 50001
  • PLATE - 23 SCANNING ELECTRON MICROGRAPHS OF POLLEN GRAINS
  • PLATE - 24 SCANNING ELECTRON MICROGRAPHS OF POLLEN GRAINS (A - F x 5000)
  • PLATE - 25 SCANNING ELECTRON MICROGRAPHS OF POLLEN GRAINS
  • PLATE - 26 SCANNING ELECTRON MICROGRAPHS OF POLLEN GRAINS (A - D x 5000)
  • PLATE - 27 SCANNING ELECTRON MICROGRAPHS OF POLLEN GRAINS (A - C x 5000)
  • 4. ACHENE MORPHOLOGY
  • TABLE 19: DATA ON ACHENE MORPHOLOGICAL CHARACTERS OF THE TAXA STUDIED
  • TABLE 20: DATA ON ACHENE MEASUREMENTS OF THE TAXA STUDIED
  • Fig. 26 DlAGRAMMATIC REPRESENTATION OF ACHENES SHOWING THE POSITION OF THE ATTACHMENT POINT 11-sox101
  • PLATE - 28 SCANNING ELECTRON MICROGRAPHS OF ACHENE SURFACE (A - I x 5001
  • PLATE - 29 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • PLATE - 30 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • PLATE - 31 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • PLATE - 32 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • PLATE - 33 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • PLATE - 34 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • PLATE - 35 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • PLATE - 36 SCANNING ELECTRON MICROGRAPHS OF ACHENES
  • IV. DISCUSSIONS
  • 1. SIGNIFICANCE OF STOMATAL STUDIES
  • Stornatal index
  • Stomatal frequency
  • 2. DIVERSITY IN LEAF ARCHITECTURE AND ITS SIGNIFICANCE
  • Hydathodes
  • 3. VARIATIONS IN PALISADE RATIO AND TAXONOMY
  • 4. SIGNIFICANCE OF HISTOCHEMISTRY
  • 5. STRUCTURAL VARIATION IN VESSEL ELEMENTS AND ITS SIGNIFICANCE
  • Scanning electron micrograph of the pollen grain of Melampodiumpaludosum B.H.K. (X55.000)
  • 6. PALYNOLOGY AND ITS TAXONOMIC SIGNIFICANCE
  • KEY TO THE SPECIES
  • Scanning electron micrograph of the achene of Calinsoga parviflora Cav. (X1000)
  • 7. DIVERSITY IN ACHENE MORPHOLOGY AND ITS TAXONOMIC IMPORTANCE
  • V. TAXONOMIC HISTORY OF THE TRIBE HELIANTHEAE
  • VI. PHYLOGENETIC AND SYSTEMATIC CONSIDERATION OF THE TRIBE HELIANTHEAE - AN ANALYSIS
  • VII. CLASSIFICATION OF THE TRIBE HELIANTHEAE - A NUMERICAL APPROACH
  • Cluster Analysis - Numerical technique used in the present study
  • 1. Average Linkage Method
  • 2. Complete Linkage (farthest neighbour) Method
  • 3. Centroid Linkage Method
  • 4.Median Method (Central or nodal clustering)
  • DISCUSSION
  • TABLE 21: SHOWING MATRIX OF CORRELATION
  • TABLE 22a: INPUT DATA FOR CLUSTER ANALYSIS
  • TABLE: 22b ASSIGNMENT OF CODES
  • Vlll. SUMMARY AND CONCLUSION
  • IX. REFERENCES
  • X. APPENDIX
  • APPENDIX 1. CLASSIFICATIONS OF THE TRIBE HELIANTHEAE
  • APPENDIX 2. TERMINOLOGIES USED
  • APPENDIX 3. ABBREVIATIONS USED IN THE THESIS