C, H, O - fixed as sugars by photosynthesis (H2O+CO2)
P, K, N, S, Ca, Mg - all come from the soil (1-4% dry weight)
Micronutrients
Required in small amounts, mostly as enzymatic co-factors
Too much can be a bad thing
Cl, Cu, Fe, Mn, Zn, Mo, B, Ni
If your houseplant is looking poorly, it may need more nutrients
How water and minerals get from the soil into the vasculature
Travel through the symplast (cytosol connected by plasmodesmata)
Travel through the apoplast (cell walls and intercellular spaces)
Substances can pass between symplast and apoplast via the plasma membrane (transmembrane route)
How other substances (or too much of certain nutrients) are kept from entering the vasculature
Water and substances moving by the symplast can pass by plasmodesmata through the endodermis to the vasculature
Water and substances moving by the apoplast get blocked from entering the vasculature at the endodermis cell wall by the Casparian strip (waxy layer)
Substances in the apoplast still can get into the cytosol of endodermal cells via the transmembrane route
The Casparian strip minimizes leakage of accumulated solutes out of the vasculature
Impacts of the root-soil interface
Evolution/Ecology: Plants often locally adapt to difficult soil conditions
Agriculture: Soil quality decreases when crops are poorly managed, requiring more fertilizer
Health: We (and other animals) obtain many nutrients from plants, which may also take up toxic minerals
Environment: Phytoremediation / Phytomining
Intersection with climate change: As CO2 increases, plants fix more carbon but don't take up proportional amounts of nutrients, leading to poorer food quality
Shoot apical meristem (SAM)
Organ primordia form on the margins, producing leaf primordia and axillary buds with their own apical meristems
If the shoot apex is removed, growth proceeds from the apical meristems of axillary buds
Phyllotaxy
The non-random order and arrangement of organ primordia initiation, often in a spiral pattern to avoid self-shading
Basic leaf types
Simple
Compound
Tendrils
Storage leaves
Spines
Reproductive leaves
Leaf anatomy
Dermal tissue: upper and lower epidermis with waxy cuticle and stomatal pores
Ground tissue: palisade and spongy mesophyll
Vascular tissue: xylem and phloem
Phyllotaxy
The non-random order and arrangement of primordia initiation
In the form of phyllotaxy shown here (spiral), each successive leaf emerges ~137.5º from the site of the previous one
Phyllotaxy
Averts self-shading, also maximizing leaf coverage of ground area + shading shorter competitors
Basic Leaf Types
simple
compound
tendrils
storage leaves
spines
reproductive leaves
Dermal Tissue
Upper and lower epidermis are lawns of pavement cells coated in waxy cuticle that prevents water loss
Stomatal pores (stomata) opened and closed for gas exchange by guard cells (CO2 in, H2O and O2 out)
Vascular Tissue
Xylem and phloem networked throughout in veins
Xylem brings water to photosynthetic cells
Phloem carries photosynthate back to rest of plant
Monocots and dicots differ in venation pattern
Mesophyll
Palisade mesophyll consists of elongated chloroplast-rich cells specialized for light capture
Spongy mesophyll form a porous space with high surface area : volume ratio that allows for gas circulation
Stomata are only on the lower epidermis to facilitate gas exchange with spongy mesophyll
Bundle sheath cells
Surround veins and regulate transfer of substances between mesophyll and vasculature
Leaf Diversity
succulent leaves
tendrils
storage leaves
spines
reproductive leaves
Vascular bundles
In monocots they are dispersed throughout, while in eudicots they form a large ring
Phloem is peripheral to the xylem
Secondary Growth
1. Vascular cambium forms cylindrical bands that add more xylem and phloem
2. Cork cambium forms a tough, thick, waxy covering called cork that protects stem
Secondary growth drives the thickening of plant stems (or roots) and mostly occurs only in eudicots and conifers, not in monocots