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TISSUES A TISSUE IS A GROUP OF CELLS ORGANIZED INTO A STRUCTURAL AND FUNCTIONAL UNIT. SIMPLE TISSUES CONSIST OF SINGLE CELL TYPES, BUT MAY BE INTERSPERSED WITH OTHER ISOLATED CELL TYPES – IDIOBLASTS (A CELL IN A TISSUE THAT DIFFERS MARKEDLY IN FORM, SIZE OR CONTENTS FROM THE OTHER CELLS IN THE SAME TISSUE – SCLEREIDS ARE AN EXAMPLE). COMPLEX TISSUES CONSIST OF MULTIPLE CELL TYPES AND MAY INCLUDE ELEMENTS OF SEVERAL DIFFERENT SIMPLE TISSUE TYPES. TISSUES CAN ALSO BE DIVIDED INTO TWO GROUPS DEPENDING ON THEIR ORIGIN. 1 PRIMARY TISSUES ARE DERIVED FROM APICAL MERISTEMS; SECONDARY TISSUES ARE DERIVED FROM LATERAL MERISTEMS. FOR NOW, WE ARE TALKING ABOUT PRIMARY TISSUES. SIMPLE TISSUES PARENCHYMA PARENCHYMA CELLS ARE USUALLY THIN WALLED AND POLYHEDRAL. THEY ARE THE LEAST SPECIALIZED CELLS OF THE PLANT BODY. THEY MIGHT BE TIGHTLY PACKED TOGETHER OR INTERSPERSED WITH INTERCELLUAR AIR SPACES. THIS IS THE MOST 2 COMMON TISSUE. SPECIALIZED TYPES INCLUDE SECRETORY TISSUES AND CHLORENCHYMA – WHICH CONTAINS LOTS OF CHLOROPLASTS. AERENCHYMA THIS IS A SPECIALIZED PARENCHYMATOUS TISSUE THAT IS USUALLY FOUND IN AQUATIC PLANTS. IT HAS A REGULAR, WELLDEVELOPED SYSTEM OF LARGE INTERCELLULAR AIR SPACES THAT ALLOWS INTERNAL DIFFUSION OF GASSES (O2 AND CO2) THROUGHOUT THE PLANT. IT IS USUALLY ASSOCIATED WITH A SYSTEM OF TRANSVERSE SEPTA OR DIAPHRAGMS THAT PROVIDE MECHANICAL RESISTENCE TO COMPRESSION AND TO BLOCK WATER FLOW IF THE SYSTEM 3 IS BROKEN. THE SEPTA ARE LAYERS OF PARENCHYMA CELLS THAT HAVE THICKER WALLS THAN NEIGHBORING AERENCHYMA CELLS. COLLENCHYMA THIS CONSISTS OF AXIALLY ELONGATED, TIGHTLY PACKED CELLS WITH UNEVENLY THICKENED PRIMARY WALLS. THIS TISSUE HAS A STRENGHTENING FUNCTION. IT IS OFTEN FOUND IN THE ANGLES OF YOUNG STEMS AND THE MIDRIBS OF LEAVES. THESE ARE LIVING CELLS; THEIR WALLS USUALLY DO NOT BECOME LIGNIFIED. SCLERENCHYMA THIS IS A SUPPORTING OR PROTECTIVE TISSUE, CONSISTING OF CELLS WITH 4 THICKENED, OFTEN LIGNIFIED, SECONDARY WALLS. THE CELLS ARE USUALLY DEAD AT MATURITY. THERE ARE TWO TYPES OF SCLERENCHYMA: FIBERS THESE ARE LONG SLENDER CELLS AND OFTEN OCCUR ALONGSIDE VASCULAR TISSUE PROVIDING PROTECTION AND SUPPORT. THEY ARE ELONGATED ALONG THE LONG AXIS OF THE ORGAN AND USUALLY OCCUR IN GROUPS. THE WALL CONTAINS SIMPLE PITS. FIBERS TEND TO BE FLEXIBLE WITH TENSILE STRENGTH , ALLOWING BENDING WITHOUT BREAKING OF PLANT AXES. FIBERS ARE THE SOURCE OF TEXTILES SUCH AS LINEN & HEMP. 5 SCLEREIDS THESE CELLS ARE SHORT AND OF VARIABLE SHAPES –OFTEN IDIOBLASTS. THEY FORM STONE CELLS IN PEARS AND THE SHELL OF WALNUTS. SCLEREIDS MAY CONTAIN A PROTOPLAST. BRACHYSCLEREIDS ARE ISODIAMETRIC CELLS DISPERSED AMONG PARENCHYMA CELLS – STONE CELLS OF PEARS. ASTROSCLEREIDS ARE HIGHLY BRANCHED CELLS WITH PROJECTIONS THAT GROW INTRUSIVELY INTO SURROUNDING INTERCELLULAR SPACES – COMMON IN LEAVES. 6 MACROSCLEREIDS ARE COLUMNAR OR ROD SHAPED AND ARE COMMON IN THE EPIDERMIS OF SEEDS AND ENDOCARPS OF FRUITS. COMPLEX TISSUES GROUND TISSUE THIS TISSUE FORMS THE BULK OF THE PLANT. IT TYPICALLY CONSISTS OF PARENCHYMA, SCLERENCHYMA OR COLLENCHYMA, OFTEN WITH IDIOBLASTS. IT FORMS THE CORTEX (THE TISSUE REGION BETWEEN THE VASCULAR SYSTEM AND THE EPIDERMIS IN STEMS AND ROOTS) AND THE PITH (THE TISSUE REGION IN THE CENTER OF THE STEM & ROOT). 7 THE MESOPHYLL OF LEAVES – BETWEEN THE UPPER AND LOWER EPIDERMIS (EXCLUDING THE VASCULAR BUNDLES) IS GROUND TISSUE IMPORTANT IN PHOTOSYNTHESIS. EPIDERMAL TISSUES THE EPIDERMIS IS A CONTINUOUS PROTECTIVE LAYER OF CELLS ON THE OUTER SURFACES OF ROOTS, STEMS & LEAVES. ITS PRIMARY FUNCTION IS TO LIMIT WATER LOSS, PROTECT THE PLANT FROM PATHOGENS, MITIGATE THE EFFECTS OF SOLAR RADIATION AND TO STRENGTHEN & SUPPORT THE PLANT BODY. AT THE SAME TIME IT MUST ALLOW O2 AND CO2 TO ENTER & LEAVE THE PLANT. 8 THE CELLS ARE USUALLY COATED WITH A WAXY LAYER OF CUTIN (LIPIDS & WAXES) – THE CUTICLE. THIS IS USUALLY THIN AND TRANSPARENT. XERIC PLANTS MAY HAVE A VERY THICK CUTICLE. IT IS LARGELY BUT NOT TOTALLY IMPERMEABLE TO THE PASSAGE OF WATER & OTHER SMALL MOLECULES. IT PLAYS A MAJOR ROLE IN THE RESTRICTION OF WATER LOSS FROM THE PLANT. EPICUTICULAR WAX – THE OUTER SURFACE OF THE CUTICLE CONSISTS OF SCALE LIKE PLATELETS OF VARIOUS FORMS. THESE PLAY A MAJOR ROLE IN RELFECTING LIGHT, WHICH REDUCES THE CHANCE OF OVERHEATING AND EXCESSIVE WATER LOSS THROUGH TRANSPIRATION. IT ALSO SERVES TO “WATER9 PROOF” THE PLANT AND MAKES IT “SELFCLEANING” –DURING RAINFALL WATER AND CONTAMINATING PARTICLES FLOW OFF THE LEAF, ETC. THE EPIDERMIS IS USUALLY JUST ONE CELL LAYER THICK, LACKS CHLOROPLASTS AND IS TRANSPARENT (BUT THEIR VACUOLES MAY CONTAIN OTHER PIGMENTS – ANTHOCYANINS). IT CONSISTS MOSTLY OF LIVING PARENCHYMA CELLS – TYPICALLY TABULAR (NARROW RADIAL DIMENSION AND LARGE INNER AND OUTER SURFACE AREAS). IN MANY MONOCOTS EPIDERMAL CELLS ARE ELONGATE WITH THE LONG AXIS PARALLEL TO THE LONG AXIS OF THE PLANT STRUCTURE. 10 THE EPIDERMIS MAY CONTAIN IDIOBLASTS: 1. CORK CELLS – NON-LIVING, WITH SUBERIZED WALLS, UNKNOWN FUNCTION. 2. SILICA CELLS – CONTAIN DEPOSITS OF SiO2, ABRASIVE NATURE OF GRASS LEAVES 3. BULLIFORM CELLS – IN GRASSES, LARGE THIN WALLED CELLS, CONTRIBUTE TO THE UNROLLING OF GRASS LEAVES; IN MATURE LEAVES DURING DROUGHT PARTICIPATE IN INVOLUTION – THE ROLLING UP OF THE LEAVES BY BECOMING FLACCID (LOSE WATER). 4. OTHER CELLS MAY CONTAIN PIGMENTS, OILS, CRYSTALS, TANNINS, ETC. MULTIPLE EPIDERMIS – MULTILAYERED EPIDERMIS FOUND IN SOME PLANTS (FICUS, 11 PIPERACEAE). THE VELAMEN OF THE AERIAL ROOTS OF ORCHIDS IS A MULTIPLE EPIDERMIS. THE CELLS ARE ADAPTED FOR WATER STORAGE. TRICHOMES THESE ARE OUTGROWTHS OF THE EPIDERMIS – INCLUDE HAIRS, SCALES, ETC. AND MAY BE GLANDULAR. THEY MAY BE ALIVE OR DIE FOLLOWING DEVELOPMENT, MAY BE UNI- OR MULTI-CELLULAR, UNBRANCHED OR BRANCHED OR PELTATE. HAIRS MAY BE FOUND ON ALL PARTS OF THE PLANT. THEIR FUNCTION IS POORLY UNDERSTOOD: 1. DENSE COVERINGS MAY HOLD A LAYER OF VAPOR FILLED AIR ON THE SURFACE OF THE LEAF, REDUCING TEMPERATURE 12 2. MAY INHIBIT WATER LOSS 3. REFLECT LIGHT, PREVENT OVER HEATING 4. PREVENT OR RESTRICT INSECT PREDATION 5. SPECIALIZED HAIRS OF SALT MARSH PLANTS ARE REPOSITORIES OF SALT, PREVENT THE BUILD UP OF TOXIC LEVELS OF SALT IN THE PLANT RHIZODERMIS THIS IS THE ROOT EPIDERMIS AND DIFFERS FROM THE EPIDERMIS OF STEMS AND LEAVES. 1. CUTICLE ABSENT 2. NO STOMATA 3. ABSORPTION OCCURS THROUGH ALL OUTER SURFACES OF EPIDERMAL CELLS 4. ROOT HAIRS ARE SIMPLE EXTENSIONS FROM SINGLE EPIDERMAL CELLS. THEY INCREASE 13 THE ABSORPTIVE SURFACE. THEY DEVELOP FROM SPECIALIZED CELLS IN THE EPIDERMIS CALLED TRICHOBLASTS. THEY GENERALLY OCCUPY AN AREA JUST BEHIND THE ROOT TIP AND AREA WHERE THE PERIDERM DEVELOPS – A SECONDARY PROTECTIVE TISSUE THAT CAN REPLACE THE EPIDERMIS. STOMATA (plural) STOMA (singular) THESE ARE SPECIALIZED PORES IN THE EPIDERMIS THROUGH WHICH GASEOUS EXCHANGE TAKES PLACE (O2, CO2, H2O). THEY OCCUR ON MOST PLANT SURFACES ABOVE GROUND, BUT ESPECIALLY ON PHOTOSYNTHETIC STEMS AND LEAVES. IN DICOTS MOST ABUNDANT ON LOWER 14 SURFACE, IN MONOCOTS MORE EVENLY DISTRIBUTED. THE STOMA CAN REFER TO THE APERTURE OR PORE ONLY OR THE PORE PLUS THE STOMATAL APPARATUS (GUARD CELLS, SUBSIDARY CELLS). THE STOMATA OF ALL PLANTS ARE VERY SIMILAR – THE GUARD CELLS ARE KIDNEY SHAPED AND THE CELL WALLS IN THE POLAR REGIONS (WHERE THE ENDS OF THE PAIR OF CELLS ARE ATTACHED) ARE THICKER THAN OTHER PARTS OF THE CELL WALL. THE GUARD CELLS CONTAIN CHLOROPLASTS. ADJACENT TO THE GUARD CELLS ARE SUBSIDARY CELLS (2 OR 4) THAT USUALLY ARE DIFFERENT MORPHOLOGICALLY FROM OTHER 15 EPIDERMAL CELLS. SUBSIDARY CELLS MAY BE DEVELOPMENTALLY RELATED TO GUARD CELLS AND ARE INVOLVED IN THE PROCESS OF STOMATAL OPENING. IMMEDIATELY BELOW THE STOMA THERE IS A LARGE AIR SPACE IN THE LEAF MESOPHYLL CALL THE SUBSTOMAL CHAMBER. AT MATURITY THE GUARD CELLS MAY BE MAY BE AT THE SAME LEVEL IN THE EPIDERMIS AS THE SUBSIDARY CELLS, RAISED ABOVE THEM OR SUNKEN BELOW THEM. GUARD CELLS OPEN AND CLOSE IN RESPONSE TO TURGOR PRESSURE IN THE CELLS; AS TURGOR INCREASES THE GUARD CELLS EXPAND AWAY FROM EACH OTHER OPENING THE PORE, SINCE THE ENDS OF THE GUARD CELLS ARE ATTACHED THEY BULGE AWAY 16 FROM EACH OTHER; LOSS OF TURGOR AND THE APERTURE CLOSES. POTASSIUM IONS ARE IMPORTANT IN CONTROLLING THE TURGOR PRESSURE AND SUBSIDARY CELLS ARE THE SOURCE OF THE WATER AND IONS DURING THE PROCESS OF STOMATAL OPENING. IN THE POACEAE AND CYPERACEAE THE GUARD CELLS ARE VERY DIFFERENT – RESEMBLING A DUMB-BELL. THE ENDS OF THE GUARD CELLS ARE THIN WALLED AND BULBOUS WITH THE CENTRAL REGION NARROW AND THICKER WALLED. WHEN THE BULBOUS ENDS ARE TURGID AND EXPANDED THE APERTURE IS OPEN, WHEN NOT EXPANDED IT IS CLOSED. 17 VASCULAR TISSUE THIS TISSUE SERVES TO TRANSPORT SUBSTANCES THROUGHOUT THE PLANT BODY. IT IS COMPOSED OF XYLEM, WHICH CONDUCTS WATER & MINERALS, AND PHLOEM, WHICH DISTRIBUTES SUGAR AND MINERALS THAT ARE DISSOLVED IN WATER. VASCULAR SYSTEMS OF PLANTS IS NOT A CIRCULATORY SYSTEM LIKE THAT FOUND IN ANIMALS. WATER & MINERALS ENTER THE XYLEM IN THE ROOTS AND ARE CONDUCTED UPWARD TO THE STEMS & LEAVES. XYLEM SAP TRAVELS THROUGH DEAD CELLS; WATER & MINERALS ARE ABSORBED BY SURROUNDING CELLS, WATER EVAPORATES FROM THE LEAVES AND IS LOST. PHLOEM CELLS ARE 18 LIVING. THEY GET SUGAR FROM WHERE IT IS ABUNDANT – LEAVES IN SUMMER, TUBERS OR RHIZOMES IN SPRING – AND TRANSPORT IT TO AREAS WHERE IT IS NEEDED – GROWING TIPS OF ROOTS, SHOOTS & LEAVES, FLOWERS, FRUITS, ETC. BOTH XYLEM AND PHLOEM ARE COMPLEX TISSUES WITH SEVERAL DIFFERENT CELL TYPES. TYPICALLY XYLEM & PHLOEM OCCUR TOGETHER IN A COLUMN CALLED A VASCULAR BUNDLE. XYLEM THE CONDUCTING CELLS OF XYLEM ARE CALLED TRACHEARY ELEMENTS COMPOSED OF TRACHEIDS AND VESSELS. BOTH HAVE TWO FUNCTIONS: SUPPORT AND TRANSPORT OF WATER AND MINERALS. THE TRACHEID IS THE 19 OLDER OF THE CELL TYPES; ALMOST ALL NON-ANGIOSPERMS (CONIFERS & FERNS) HAVE XYLEM COMPOSED OF TRACHEIDS ONLY. VESSELS EVOLVED FROM TRACHEIDS RELATIVELY RECENTLY AND OCCUR ALMOST EXCLUSIVELY IN ANGIOSPERMS (BUT MOST ANGIOSPERMS ALSO HAVE TRACHEIDS). BOTH TRACHEIDS AND VESSELS HAVE A PRIMARY WALL AND A SECONDARY WALL. THE SECONDARY WALL IS THICK WITH LOTS OF LIGNIN. THE SECONDARY WALL IS DISCONTINUOUS BEING DEPOSITED ON THE PRIMARY WALL IN HELICAL, RETICULATE, ANNULAR OR SCALARIFORM PATTERNS. THE SECONDARY WALL IS IMPERMEABLE TO WATER; THE PRIMARY WALL IS PERMEABLE 20 TO WATER ALLOWING WATER TO ENTER THE CELLS. BOTH HAVE PITS (WELL DEFINED AREAS LACKING A SECONDARY WALL). THE PIT-PAIRS IN THE CELL WALLS ALLOW FOR THE TRANSPORT OF WATER FROM ONE CELL TO ANOTHER. THE PRIMARY WALL OF THE TWO CELLS AND THE MIDDLE LAMELLA LIE BETWEEN THE TWO PITS OF A PAIR AND FORM THE PIT MEMBRANE. THIS IS HIGHLY POROUS AND FACILITATES THE TRANSPORT OF WATER & MINERALS FROM ONE CELL TO THE ADJACENT ONE. THE TRACHEID IS A LONG NARROW CELL WITH POINTED ENDS THAT OVERLAP THE ENDS OF OTHER TRACHEIDS. 21 VESSELS ARE SHORT, WIDE CELLS USUALLY WITH FLAT ENDS. THEY HAVE PERFORATE END WALLS. IN XYLEM THE VESSELS ARE STACKED END TO END FORMING LONG TUBES – AT MATURITY THE ENTIRE END WALL MAY BE REMOVED OR A PERFORATION PLATE MAY EXIST – A WALL WITH HOLES IN IT. WATER CAN MOVE MORE EFFECIENTLY THROUGH VESSELS – THE PERFORATIONS ALLOW WATER TO FLOW SMOOTHLY WITHOUT GOING THROUGH PIT MEMBRANES. VESSELS ALSO FORM LONG TUBES SO THE WATER FOLLOWS A STRAIGHT PATH RATHER THAN A HELICAL ONE IN TRACHEIDS. THE LARGER DIAMETER OF THE VESSEL ALSO IMPROVES TRANSPORT EFFECIENCY. IT IS 22 THOUGHT THAT THE EVOLUTION OF VESSELS IN ANGIOSPERMS AND THEIR GREATER WATER TRANSPORT CAPACITY IS A MAJOR REASON ANGIOSPERMS DOMINATE THE LANDSCAPE. XYLEM ALSO HAS PARENCHYMA, SCLERENCHYMA, SCLEREIDS AND FIBERS IN IT. PHLOEM PHLOEM IS A COMPLEX TISSUE WITH PARENCHYMA, FIBERS, SCLERENCHYMA AND SCLEREIDS. THE CONDUCTING CELLS OF PHLOEM ARE THE SIEVE ELEMENTS COMPOSED OF SIEVE CELLS AND SIEVE TUBE MEMBERS. BOTH ARE COMPOSED OF LIVING CELLS WITH PRIMARY WALLS ONLY. 23 SIEVE CELLS ARE LONG AND NARROW WITH POINTED ENDS THAT OVERLAP THE ENDS OF OTHER SIEVE CELLS. SIEVE AREAS ARE SPECIALIZED PERFORATE REGIONS (CLUSTERS OF PORES) ON THE LATERAL WALLS – THESE ARE SIEVE PORES. THE PROTOPLASTS OF CONTIGUOUS SIEVE CELLS ARE INTERCONNECTED. THE SIEVE PORES OF ADJACENT CELLS ARE ALIGNED. SIEVE TUBE MEMBER CELLS ARE SHORT AND WIDE WITH FLAT ENDS. THESE CELLS LINE UP END TO END TO FORMING LONG COLUMNS (SIEVE TUBES). ON THE SIDE WALLS THERE ARE SMALL SIEVE AREAS. ON THE END WALLS ARE SIEVE PLATES WITH PORES GENERALLY 24 LARGER THAN THE PORES OF THE SEIVE AREAS. SIEVE ELEMENTS ARE LIVING CELLS BUT ARE DIFFERENT IN THAT THEIR NUCLEI AND TONOPLASTS DEGENERATE AND THEY LACK RIBOSOMES. THEY DO HAVE MITOCHONDRIA AND ER AND SOME PLASTIDS WHICH ARE LOCATED AT THE EDGES OF THE CELLS. SIEVE ELEMENTS ARE UNABLE TO CONTROL THEIR GENETIC AND METABOLIC ACTIVITIES. ASSOCIATED SPECIALIZED CELLS TOOK OVER THESE FUNCTIONS AND ALSO FACILITATE THE TRANSFER OF SUGARS FROM MESOPHYLL CELLS INTO AND OUT OF THE SIEVE ELEMENTS. 25 SIEVE TUBE MEMBER CELLS ARE ASSOCIATED WITH COMPANION CELLS. EACH COMPANION CELL IS DERIVED FROM THE SAME MOTHER CELL AS THE SIEVE TUBE MEMBER CELL WITH WHICH IT IS IN CONTACT. THE COMPANION CELL HAS A DENSE PROTOPLAST WITH A NUCLEUS, MITOCHONDRIA, ER, RIBOSOMES, VACUOLE AND PLASTIDS. THE COMPANION CELLS OF SIEVE TUBE MEMBER CELLS ARE CONNECTED BY PLASMODESMATA TO THE SEIVE TUBE MEMBER CELL. COMPANION CELLS PROVIDES THE SEIVE TUBE MEMBER WITH PROTEINS, SIGNALING MOLECULES AND ATP. SIEVE CELLS ARE ASSOCIATED WITH SPECIALIZED CELLS CALLED STRASBURGER 26 CELLS WHICH PERFORM THE SAME FUNCTION AS COMPANION CELLS BUT DIFFER IN ORIGIN AND STRUCTURE. SIEVE CELLS ARE COMMON IN GYMNOSPERMS AND FERNS, THEY ARE NOT IN ANGIOSPERMS. SEIVE TUBE MEMBERS ARE FOUND INANGIOSPERMS ONLY. VASCULAR BUNDLES XYLEM AND PHLOEM OCCUR TOGETHER AS VASCULAR BUNDLES, USUALLY SURROUNDED BY LAYERS OF PARENCHYMA OR SCLERENCHYMA WHICH FORM THE BUNDLE SHEATH. THERE ARE FOUR TYPES OF BUNDLES: 1. COLLATERAL BUNDLE – PRIMARY XYLEM IS INNERMOST AND THE PRIMARY PHLOEM IS 27 THE OUTER PART; COMMON IN GYMNOSPERMS AND ANGIOSPERMS. 2. BICOLLATERAL BUNDLE – THE PRIMARY XYLEM IS BOUNDED ON BOTH INSIDE AND OUTSIDE BY PRIMARY PHLOEM – EXTERNAL PHLOEM IS ON THE OUTSIDE AND INTERNAL PHLOEM ON THE INSIDE; FOUND ONLY IN SOME ANGIOSPERMS. 3. AMPHIVASAL BUNDLE – THE PRIMARY XYLEM SURROUNDS THE PRIMARY PHLOEM; IN SOME MONOCOTS AND A FEW DICOTS. 4. AMPHICRIBRAL BUNDLE – THE PRIMARY PHLOEM SURROUNDS THE PRIMARY XYLEM; COMMON IN SOME FERNS AND FEW AQUATIC ANGIOSPERMS. 28 29