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Xylem
-One direction
-water and minerals
-has tracheids, vessel elements, and xylarly fibers
Tracheids
-Dead at maturity
-within xylem
-thinner than vessels
-capillary action
-found in every secondary growth plant
-secondary cell walls for support
Vessel elements
-Secondary cell walls for support
-dead at maturity
-ONLY FOUND IN ANGIOSPERMS
-stacked atop each other to create vessels
-has perforation plate
Xylarly fibres
-No cell membrane, just cell walls
-FOUND IN ANGIOSPERMS
Phloem tissue
-Transports sugars, hormones, proteins, etc.
-Multidirectional, from source to sink.
-Has sieve cells, sieve tube elements, albuminous cells, companion cells, and phloem fibres
Sieve cells
-Like tracheids
-alive at maturity but NO NUCLEUS
-no pits but has sieve spots for sugars to go in and out
Albuminous cells
Acts to load and unload sugars from sieve cells,
Sieve tube elements
-Alive at maturity
-NO NUCLEUS
-ONLY IN ANGIOSPERMS
-stacked to create sieve tubes which are more efficient and can start and stop sugar flow themselves
Companion cells
Do basically the same as albuminous cells
Phloem fibres
-Thick cell walls
-dead at maturity
-ONLY IN ANGIOSPERMS
-provide support
Secondary growth
-Increases girth of plant
-creates wood
-needs vascular cambium to be continuous
Hardwood
Angiosperms, complex, has holes for water + air,
Softwood
Gymnosperms, less complex
Vascular cambium
- Developed from procambium
- wedged between the xylem and phloem
- needs to be continuous for secondary growth
- interfascicular cambium bridges gaps between facicular cambium - why damage to tree can inhibit secondary growth, a lateral meristem
Fusiform + ray initials
- Ray initial through xylem + phloem
- divide inwards (XYLEM) and outwards (PHLOEM)
- called periclinal division - parallel to stem growth
Secondary phloem
- Produces inner bark
- gets pushed to outer edges from fusiform + ray initials so needs to be replaced in annual growth
Secondary xylem
- grows inwards
- differs based on tree type
- angiosperms : tracheids, vessel elements(pores), fibers, ray parenchyma
- gymnosperms : tracheids, rays, sometimes resin canals
Annual growth
- Can be seen in the rings - categorized by early wood and late wood
- needs time of little to no growth
Early wood
- formed early in the growth year
- xylem formed early
- tracheids and vessel elements (lumens) long to maximize water transport
Late wood
- smaller lumens (tracheids + vessel elements)
Sapwood
- xylem that is actively transporting water
- closest to surface
- ray parenchyma still alive (xylem dead tho womp womp, think cheeky quirky little living mole inside husk of dead xylem)
Heartwood
- not transporting water actively
- ray parenchyma dead
- stores compounds to drive off fungi, virus, etc
Reaction wood
- uneven vascular cambium growth in response to gravitropism
- 2 types - tension wood (angiosperms) and compression wood (gymnosperms)
Tension wood
- Angiosperms
- pulls the stem up, on upper side of tree
- tension strength high
Compression wood
- Gymnosperms
- on lower side to push stem upright
Root secondary growth
- no rings
- pericycle cells complete vascular cambium
Taproot system
- One main vertical root that grows more lateral roots off it
- primary flow
- big ol anchor
- goes deep
- will take a taproot in me to pass this
Flatroot system
- slow taproot growth, lateral roots go brrr
- shallow roots
- adapted for shallow or poor soils
Heartroot system
- mix of taproot and flatroot
- all moderately deep
Root buttressing (ha)
- if vascular cambium not even around root and root not stable, can make i - beam looking construct to limit horizontal motion
Bark
- epidermis from primary growth not ****ing good enough get your shit together epidermis more like epidernotgonnamis it when its gone
- needs more support, tree makes second better child with the cork cambium
Cork cambium
- shoved in just below epidermis
- divides inward AND outward
- when inwards - makes phelloderm
- when outwards makes cork / phellem
- divides sideways
- makes more cork to keep up with stem girth (i wish haha am i right haha)
Cork / phellem
- cells filled with wax to prevent water loss
- dead at maturity
- trees such as the cork oak have single periderm with extra thick cock i mean cock i mean cock i mean cork so taking layers off does not kill the tree
Phelloderm
- made of parenchyma cells
- alive at maturity
Lenticel development
- cork cambium divides enough to create bulges underneath stomata
- growth causes bulge to split
- allows for passive gas exchange
- maintained throughout life cycle of the plant
Bark development
- made of periderm and secondary phloem
In young trees
- smooth bark - periderm continuous, bark stretching with annual growth
In mature trees
- periderm splits, can be discontinuous
- cork cambium arising continuously from old secondary phloem
- flakey or scaly
Girdling
- kills trees cause cuts off phloem + sugar transport
- prevents new cork cambium
Root grafting
- friction between roots of same species can damage root vascular cambium, graft the two roots together
Active growing season
- Shoot apical meristem produces phytomers, increases height
- axillary meristems create branches
Syllaptic branches
- buds that grow in SAME season they were produced
- if you can see a leaf below the branch it is a syllaptic branch
Proleptic branches
- from lateral buds
- branches NOT grown in same season ie no leaf underneath
- has bud scale scars
Lateral buds
- follow leaf arrangement - grown at nodes
- can remain for multiple growing seasons
- can take over should damage occur to canopy
Determinate growth
- bud set occurs early
- creates all the growth for the following season
- cue for bud set is developmental
Indeterminate growth
- bud set later
- creates only some of the growth for the next season
- cue for bud set is environmental
Growing season order ++++++++COME BACK TO+++++++++
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- bud set
- cold hardiness develops
- leaf senescence
- chilling requirement
- quiescence
- heat sum requirement
Environmental cues that cause bud set
- extreme heat
- drought
- nutrient stress
- cold
- pathogen/herbivory
- changing daylength ie CRITICAL PHOTOPERIOD
Phytochrome in bud set role
- Pfr = active phytochrome, under high quality red light
- Pr = inactive, under far red or darkness
- sets threshold of critical photoperiod
Critical photoperiod
- determined genetically
- the amount of daytime vs CONTINUOUS nighttime a plant needs to realize its gotta set that bud
- also differs based on latitude
- plants in north / high elevations set bud early
- generally tracks timing of frost, highly selective
Lammas growth
- a second growth after bud set before full dormancy if conditions are insanely good
- adds itty bitty little smidge of more growth as a treat
- both terminal and lateral buds can undergo Lammas growth, can create forking by making another leader
Leaf senescence
- deciduous canopy would lose too much water in winter so the tree axes it
- induced by long nights too BUT critical photoperiod for this is shorter ie happens later in the year
- controlled via hormones
- nutrients like nitrogen and chlorophyll broken down in leaf and reabsorbed into inner bark by phloem
Colour change in leaf cause
- senescence causes chlorophyll to stop getting produced and get yoinked back up
- carotenoids are unmasked, thats what the point of the mask is, shows the yellows and oranges
- anthocyanin, the red, is produced
Anthocyanin
- the red pigment
- like sunblock
- produced in exposed canopy
Abscission zone
- base of petiole
- split into two layers - the separation layer and the protective layer
Separation layer
- starts outside, progresses inwards, girdling leaf
- cuts off tissues ending with the xylem
Protective layer
- on the tree
- suberin / wax seals off tissues
- forms waterproof barrier to keep innards in, plugging xylem
Abscission process
- middle lamella (gunk made of pectin) between separation and protective layers is digested
- cells in separation layer expand
- zone is weakened so gravity or wind or anything can yank that shit off
Cladoptosis
Whole branch abscission, tree just says **** this whole ass thing
- when a branch is no longer considered useful, ever look up and see where branches were on a tall tree but aren't anymore? Yea its this
Cold hardiness
- resistance to damage from freezing
- develops right after bud set pre leaf senescence
- induced by photoperiod
- begins with sugar content in bud GOING UP
- highly selective cause only plants that survive winter can reproduce
LT50
- the measurement for cold hardiness
- lethal temp at which 50% of tissue is injured or 50% of species dies
- LT50 decreases as cold hardiness increases (ie can withstand colder temps)
- max LT50 through Jan - Feb
Extraorgan freezing
- ice created around bud by bud scales + stem tissue
- protective ice
- keeps tissues inside from freezing
Deep supercooling
- most common in milder areas
- functional down to -40 degrees C
- water remains in cell below freezing point
- plant INCREASES solute concentration in cell, isolating cell from cell nucleating agents
Freeze dehydration
- water yoinked out of cells
- makes ice in controlled way between cells outside cell walls
- means no ice can be made within cell
- most common in areas with severe winters
Chilling requirement
- amount of time at cool temps, approx 1.5 C
- differs by species / population
- goes into quiescence (like the snooze button)
Heat sum requirement
- ends quiescence
- certain number of days above about 5 degrees C
Interaction of chilling + heat sum
- buds need both + respond to both
- warmer winters means longer time taken to hit chilling req so therefore higher heat sum req needed