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How did photosynthesis change conditions on earth
early photosynthetic organism used sunlight to make organic molecules, in the process they split water and released O2
initially a lot of this O2 reacted with dissolved iron in the oceans, producing iron oxides, eventually around 2.2 billion years ago oxygen began to accumulate in the atmosphere
photosynthesis → O2 production → oxygen-rich atmosphere
Great oxidation event
the major accumulation of free O2 in Earth’s atmosphere due to photosynthetic organisms
O2 began accumulating about 2.2 billion years ago, and atmospheric increased substantially afterward
completely changed what kind of organisms could survive and evolve
ultimately caused by oxygen-producing photosynthesis
formation of the Ozone layer
once enough atmospheric O2 accumulated, some O2 molecules in the upper atmosphere were converted into ozone (O3)
ozone absorbs harmful UV radiation from sunlight
by approximately 450 million years ago, the ozone layer provided enough UV protection for organisms to survive at the surface and helped make the colonization of land possible
O2 accumulation → O3 formation → UV protection → life on land becomes possible
Aerobic respiration possible through what
increasing atmospheric oxygen also allowed organisms to use aerobic respiration
aerobic respiration uses oxygen to break down energy-rich organic molecules
aerobic respiration can extract far more energy from organic molecules than anaerobic processes
photosynthesis → O2 → aerobic respiration → much more efficient energy extraction
limiting factors in the aquatic environment
early photosynthetic organism lived in water, as their populations increased they used up resources (Carbon, Hydrogen, Oxygen, essential minerals/nutrients, light limited in deeper water)
encouraged organisms to become more abundant near shorelines, where rivers and streams continuously supplied minerals and nutrients
challenges of the terrestrial environment
land provided abundant light, CO2, O2, and mineral-rich soil, but the major problem was water
water is the critical factor in the transition from water to land
plants needed ways to obtain water → transport water → prevent water loss
needed structural support because water was no longer supporting their bodies
adaptations to terrestrial life
structures evolved to solve these problems
roots: anchor the plant and collect water and minerals from soil
stems: provide structural support and raise photosynthetic organs toward sunlight
leaves: became the major organs for photosynthesis
vascular tissue: transports substances throughout the plant
epidermis: covers the aboveground plant
waxy cuticle: covers the epidermis and reduces water loss
stomata: pores controlled by guard cells that allow gas exchange while helping regulate water loss
xylem vs. phloem
both vascular tissues used for transport of substances
xylem: water and minerals primarily upward from roots
phloem: products of photosynthesis such as sugars throughout the plant
reproductive adaptations to land
drought resistant spores: one of the earliest reproductive adaptations to land
multicellular reproductive structures: games/reproductive cells were protected from drying by surrounding sterile cells
later seeds provided even greater protection (embryo, stored food, seed coat)
water balance challenges and adaptations
plants face a trade off: they need to conserve water but they also need to exchange gases with the atmosphere
cuticle: reduces water loss but a completely sealed surface would prevent gas exchange necessary for photosynthesis and respiration
stomata is the solution, with guard cells for regulation
cuticle → conserve water
stomata → controlled gas exchange
guard cells → open/close stomata
Phylogenetic trees/cladograms
represents evolutionary relationships and common ancestry
node: represents a common ancestor/branching event (speciation event)
clade: branch on tree of life with original taxon and all descendent taxa
monophyletic: an ancestor and all descendants
polyphyletic: descendants from multiple branches, not ancestor
paraphyletic: includes common ancestor and some descendants
asexual reproduction
involves one parent and does not involve fusion of gametes, offspring are generally genetically identical to the parent so they are essentially clones
ex: vegetative growth (through stolons and rhizomes, strawberries and aspens), plantlets developing along leaf margins (mother of thousands), apomixis (asexual production of seeds)
advantages: fast, requires one parent, uses less energy/resources, offspring suited to parents environment
disadvantages: low genetic diversity
sexual reproduction
the production and combination of gametes, an egg and sperm joining during fertilization
advantages: high genetic diversity
disadvantages: requires time and resources and specialized reproductive structures (flowers, fruits, cones, nectar), offspring may be small and vulnerable
alternation of generations
plants alternate between two multicellular generations (gametophyte = haploid (1n), sporophyte = diploid (2n))
the cycle repeatedly switches between the two
sporophyte (2n) → (meiosis) spores (1n) → (mitosis/growth) gametophyte (1n) → (mitosis) gametes (1n) → (fertilization) zygote (2n) → (mitosis/growth) sporophyte (2n)
gametophyte generation
haploid (1n) gamete-producing generation, developed from a haploid spore
because the gametophyte is already haploid, it produces gametes through mitosis not meiosis
Archegonium → produces egg
Antheridium → produces sperm
combined creates the zygote which grows through mitosis into the sporophyte
sporophyte generation
diploid (2n) spore-producing generation, which develops from the 2n zygote
sporophyte contains structures called sporangia, where spores are produced
sporophyte (2n) → sporangium → (meiosis) spores (1n) (then grow through mitosis into haploid gametophytes)
gametophyte → gametes by mitosis
sporophyte → spores by meiosis
moss alternation of generations
mosses are different from vascular plants
gametophyte (1n) dominant
sporophyte (2n), short lived and attached/dependent on the gametophyte
water dependent fertilization because sperm must travel through water to reach the egg
fern alternation of generations
ferns show an evolutionary shift
sporophyte (2n) dominant, free living and can persist for many years
gametophyte (1n) free living but much smaller and short lived (1-12 months)
water dependent fertilization
gymnosperm alternation of generations
includes pines, cycads, ginkgo. even greater shift towards sporophyte
sporophyte dominant (2n)
gametophyte (1n) greatly reduced and are no longer large, independent plants, they remain associated and dependent on the sporophyte
fertilization is not water dependent, sperm reach the egg through the pollen system/pollen tube
angiosperm alternation of generations
angiopserms are flowering plants
sporophyte (2n) is dominant
gametophytes are greatly reduced
fertilization is not dependent on external water because pollen allows sperm to reach the egg
dioecious
male and female reproductive structures occur on different individual plants
ex. Ginkgo, cycads, aspen
monoecious
a single plant produces both male and female reproductive structures
ex. oaks and pines
bisexual
a single flower contains both male and female reproductive structures
occurs in many angiosperms
bryophytes vs. polysporangiophytes (vascular plants)
bryophytes: gametophyte dominant, sporophyte is small and nutritionally dependent, usually one sporangia, no true xylem/phloem, no true roots/ stems/ leaves, little structural support
polysporangiophytes: sporophyte dominant, sporophyte is large (branched) and free-living, many sporangia, xylem and phloem present, true roots/stems/leaves, lignin in cell walls provides support and allows taller growth
vascular tissue organization
protostele: solid central core of vascular tissue, no pith, found in roots and lycophytes
siphonostele: vascular tissue surrounds a central pith, leaf traces may leave leaf gaps which are common in ferns
eustele: separate vascular bundles arranged in a ring around a pith, found in seed plants
leaf evolution
microphylls: usually small leaves with one unbranched vein and no leaf gap, characteristic of lycophytes, likely evolved as small stem outgrowths called enations
megaphylls: generally larger leaves with branched veins and leaf gaps, evolved from branching systems through overtopping, plantation, and webbing. found in ferns, horsetails, and seed plants
reproductive systems
oogamy: large nonmotile egg is fertilized by a small motile sperm
heteromorphic alternation of generations: multicellular haploid gametophyte and multicellular diploid sporophyte which look different
sporophyte is dominant in vascular plants ; gametophytes are reduced
fertilization still requires water because flagellated sperm must swim to the egg
homospory vs heterospory
homosporous: one type of spore; usually produces a bisexual gametophyte with both antheridia and archegonia
heterosporous: two spore types, microspores (male gametophytes) and megaspores (female gametophytes that are smaller, unisexual, and usually develop inside the spore wall)
primary vs secondary growth
primary: lengthening of roots and shoots, occurs at apical meristems
secondary: thickening of roots and stems, occurs at lateral meristems (vascular cambium makes secondary xylem and phloem, cork cambium produces periderm which replaces the epidermis)
Lycopodiacea, Phylum Lycopodiophyta
club mosses
Homosporous
Microphylls
sporophylls may form a cone called strobilus
gametophytes are often bisexual and may be underground/mycorrhizal
Selaginellaceae, Phylum Lycopodiophyta
spike mosses
Heterosporous
produce microspores and megaspores
have a ligule, small scale-like outgrowth near the upper surface of each microphyll
Isoetaceae, Phylum Lycopodiophyta
quillworts
Heterosporous
often aquatic or grow in seasonally wet soil
have a corm and quill like microphylls
also have ligules
Phylum Monilophyta classes
class Psilotopsida: whisk ferns and adders tongue ferns, eusporangiate
Marattiopsida: large tropical eusporangiate ferns
Equisetopsida: horsetails, joined stems, whorled branches, and strobili
eusporangia vs leptosporangia
eusporangia: develop from several initial cells, have thick walls and produce many spores
leptosporangia: develop from one initial cell, have one cell thick wall, usually produce 64 spores, and often contain annulus for spore release
seed definition and advantages
a mature ovule containing a diploid embryo (young sporophyte), stored food, and a protective seed coat
seeds are better than spores because they protect and nourish the embryo, allow dormancy until conditions are good, and disperse the developing sporophyte instead of only one cell
key evolutionary changes that produced seeds
all seeds are heterosporous: produce microspores and megaspores
the megaspore is retained within the megasporangium
only one of the four megaspores survives
the female gametophyte develops within the retained megaspore and is not free-living
embryo develops within the female gametophyte
integument surrounds the megasporangium, leaving an opening called the micropyle
the megasporangium/ovule evolves to receive pollen, allowing fertilization without free water
the dispersal unit becomes a seed, not a spore
progymnosperms
extinct seedless vascular plants considered precursors to gymnosperms, they had secondary growth from a bifacial vascular cambium, producing secondary xylem inside and secondary phloem outside, but reproduced using freely dispersed spores rather than seeds
Phylum Coniferophyta
leaf: needle or scale-like leaves, sex arrangement: mostly monoecious, sperm: nonmotile, ex: pines, firs, spruces, redwoods
Phylum Cycadophyta
leaf: large, pinnately compound leaves, sex: dioecious, sperm: motile multiflagellated, ex: cycads
Ginkgophyta
leaf: fan shaped leaves with open dichotomous veins, sex: dioecious, sperm: motile multiflagellated, ex: ginkgo biloba only
Gnetophyta
leafs: variable, often broad leaves or scale-like leaves, sex: usually dioecious, sperm: non-motile, ex: Ephedra, Gnetum, and Welwitschia
pine reproduction
pines are monoecious (the same tree makes pollen cones and ovulate cones)
a pollen cone produces microspores which develop into pollen grains (male gametophytes)
pollen reaches an ovulate cone by wind pollination
in the ovule a megaspore mother cell undergoes meiosis making four megaspores, three degenerate and one survives
surviving megaspore undergoes mitosis and develops into the female gametophyte/megagametophyte which contains archegonia and eggs
the pollen grain grows a pollen tube through the nucellus to the egg
the generative cell forms two nonmotile sperm, one fertilizes the egg and the other degenerates
zygote becomes an embryo, the mature seed contains the embryo, female gametophyte food tissue, and seed coat (it takes about two years for pines to produce a mature seed)
major conifer families
Pinaceae: pines, needles usually occir in fasicles/bundles
Taxaceae: yews, seeds are surrounded by a fleshy red aril not a typical woody cone
Cupressaceae: cypresses, junipers, redwoods, scale like or awl like leaves are common
Araucariaceae: includes wollemia nobilis, primarily southern hemisphere
Phylum Cycadophyta, Cycads
cycads are dioecious plants with palm-like pinnately compound leaves, they produce motile, multiflagellated sperm, their seeds are often toxic, and some are pollinated by beetles, male cones resemble corn cobs
Phylum Ginkgophyta, Ginkgos
Ginkgo biloba is the only living Ginkgo species, it is dioecious, has fan-shaped leaves, and produces motile multiflagellated sperm, female plants make fleshy seeds that smell bad because of butyric acid, male trees are usually preffered for landscaping
Phylum Gnetophyta, Gnetophytes
non-motile sperm delivered through a pollen tube, some including Ephreda show a form of double fertilization but it does not produce true triploid endosperm like in angiosperms
basal grade angiosperms
earliest diverging groups, including Amborella, water lillies, and Austrobaileyales. They are called a grade because they are not one single clade
Magnoliids
include magnolias, laurels, pepper plants, and relatives. Many retain ancestral-looking traits such as numerous floral parts
Monocots
one cotyledon, parallel leaf veins, scattered vascular bundles, fibrous roots, flower parts usually in multiples of 3, and pollen with one opening
dicots (eudicots)
two cotyledons, netted leaf veins, vascular bundles in a ring, usually a taproot, flower parts usually in multiples of 4 or 5, and pollen with three openings
Perianth
the nonreproductive outer flower parts
calyx: all sepals, usually green and protective
corolla: all petals, often colored and attracts pollinators
Gynoecium
the female reproductive whorl; all carpels of a flower
carpel
female reproductive structure consisting of 4 parts
stigma: sticky tip that receives pollen
style: stalk through which the pollen tube grows
ovary: enlarged base containing ovules
ovules: develop into seeds after fertilization
Androecium
the male reproductive whorl; all stamens of a flower
stamen
male reproductive structure consisting of 2 parts
anther: produces pollen
filament: stalk supporting the anther
microsporogenesis
meiosis occurs in the anther’s microsporangia. a diploid microsporocyte produces four haploid microspores
microgametogensis
each microspore develops by mitosis into a pollen grain, the male gametophyte
a pollen grain contains a vegetative/tube cell and a generative cell, the generative cell divides to form two sperm cells
megasporogensis
meiosis occurs in the ovule, one diploid megasporocyte produces four haploid megaspores; usually three degenerate
megagametogensis
the remaining functional megaspore undergoes mitosis and develops into the embryo sac, the female gametophyte
the typical mature embryo sac has seven cells and eight nuclei (one egg cell, two synergids, three antipodal cells, one central cell with two polar nuclei)
pollination
transfer of pollen from an anther to a stigma
after pollen reaches a compatible stigma it germinates and grows a pollen tube down the style to an ovule
the tube delivers two sperm cells into the embryo sac
double fertilization
one sperm fertilizes the egg → diploid zygote which becomes the embryo
the other sperm fuses with the two polar nuclei → triploid endosperm which nourishes the embryo
the ovule becomes a seed and the ovary becomes a fruit
5 trends in floral evolution
flowers changed from many, indefinite parts to fewer parts in definite numbers
the floral axis became shorter, placing flower parts closer together
ovaries often became inferior instead of superior
radial symmetry often changed to bilateral symmetry
floral parts frequently became fused or specialized for particular pollinators
floral traits and pollination vectors (8)
beetles: open bowl shaped flowers, often strong fruity, spicy, yeasty odors, provide pollen and or nectar
flies: dark red or purple or brown, may smell like rotting meat or carrion, some mimic places where flies lay eggs
bees: blue, yellow, UV marked nectar guides, landing platforms, sweet scents and nectar
butterflies: bright colored flowers, often with a landing platform and nectar in narrow tube
moths: pale or white flowers that commonly open at night, strong sweet scent, long floral tubes or spurs
birds: usually red, orange, or brightly colored tubular flowers with lots of nectar, little odor
bats: large, sturdy, pale flowers that open at night, strong odor and abundant thin nectar
wind: small inconspicuous flowers with no scent or nectar, produce huge amounts of lightweight pollen, exposed anthers and feathery stigmas
fruit traits and dispersal vectors (6)
autochory (self-dispersal)
barochory (dispersal by gravity, heavy round fruits) or ballochory ballistic (explosion of fruit)
Allochory
wind (anemochory): small lightweight fruits or seeds with wings, hairs, plumes, or parachute-like structures
water (hydrochory): floating fruits (coconuts), waterproof skin
animals (zoochory): epizoochory (external): dry fruits with hooks, spines, barbs, or sticky structures that attach to fur or feathers, endozoochory (internal, eaten): fleshy, colorful, sweet, nutritious fruits; animals eat them and disperse seeds in droppings
caching: gather seeds and store them underground/surface/ground