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trends in reproduction
alternation of generations
sporophyte is dominant
all are oogamous
oogamous
large eggs and small sperm
egg stays in place, sperm moves
homosporous
1 type of spore by meiosis
most non-vascular and lower vascular plants
bisexual gametophyte
bisexual gametophyte
bear both sperm producing antheridia and egg producing antheridia
heterosporous
2 types of spores in 2 different kinds of sporangia
all seed plants and a few others
microspores in microsporangia
megaspores in megasporangia
unisexual or gametophyte
life cycle of SVPs
sporophyte is dominant
gametophyte is significantly reduced in physical size
both sporophyte and gametophyte are independent at maturity
most are homosporous, some are hetersporous
gametophytes can be male, female, or bisexual
rely on water for fertilization
Have archegonia (egg) and antheridia (sperm)
SVPs
evolution is uncertain, fossil record is incomplete
postulated that vascular tissue, waxy epidermis and others evolved over millions of years in freshwater algae
Dominated landscape around 350 mya, for ~100 million years
today only ~5% of living plant species
living phyla of SVPs
Phylum Lycopodiophyta and Monilophyta
hypothesis of the origins of SVPs
2 extinct phyla appear in the fossil record 450 mya: Rhyniophytes, Zonterophylls, and Trimerophytes
All had branching photosynthetic stems without roots or leaves
Phylum lycopdiophyta families
Lycopodiacease, Selaginellaceae, and Isoetaceae
microphylls
leaves with a single vascular trace or leaf vein
In all lycophytes
two hypothesis for origination enation theory and telome theory
enation theory
holds that microphylls developed when a vascular trace gradually extended into an enation, a non-vascular flap of tissue
telome theory
holds that microphylls evolved as a result of existing telomes
Lycopodiaceae
club mosses
15 genra, 400 species
8 species in WV
mostly tropical
epiphytes
evergreen
Lycopodiaceae physical structure
rhizome
vegetative propagation
sessile microphylls
branching: dichotomous and pseudo-monopodial
homosporous, spores produced in sporangium which group into stobilus
bisexual gametophyte
Selaginellaceae
spike mosses
1 genus, 700 species
2 species in WV
scattered around the world
wet areas
highly diverse in form
Selaginellaceae physical structure
have a ligule
heterospory -> 2 types of spores -> unisexual gametophyte
can produce microspores in microsporangium or megaspores in megasporangium
Isoetaceae
Quillworts
1 genus, 150 species
2 species in WV
Aquatic, seasonal pools
Corm
Long narrow sporophylls
have peculiarity
Isoetaceae reproduction
Heterosporous with micro and megasporangium
Phylum monilophyta
Mostly what people will look at and call a fern
12000 species, 75% in tropics
1000 in costa rica, ~61 in WV
Characteristics used to identify ferms
megaphylls
sporangium- eusporangium and leptosporangium
Sorus and indusium traits
homosporous vs heterosporous
megaphylls
leaves with more than 1 vascular trace
Eusporangiate sporangia
large, thick sporangium wall
produce large numbers of spores (100-1000)
Leptosporangia sporangia
Smaller, thin capsule wall
produce fewer spores (16, 32, 64, 128, etc)
Sorus and indusium traits
Sporangia usually borne in clusters called sori
Located on the under side of the blade or borne on fertile leaflets
Some sori have a protective covering (indusium)
homosporous ferns
produce only one type of spore which produce bisexual gametophytes
Heterosporous ferns
produce both megaspores and microspores; unisexual gametophytes (separate male and female gametophytes)
Classes of phylum monilophyta
psilotopsida, marattiopsida, polypodiopsida, and equisetopsida
Orders of psilotopsida
Ophioglossales and psilotales
eusporangiate, homosporous ferns
Ophioglossales
eusporangiate
homosporous
1 leaf/rhizome per year
Psilotales
whisk ferns
2 living genra: Psilotum and Tmesipteris
homosporous
bisexual gametophytes
simple habit=derived condition
Psioltales physical characteristics
no leaves and no roots
hair-like rhizoids
underground rhizomes
photosynthetic stem
dichotomous branching
two kinds of appendages in psilotales
enations and synangium
enations
no vascular tissue
synangium
groups of 3 sporangia
on ends of short, lateral branches
psilotales gametophytes
subterranean
devoid of chlorophyll
symbiosis with mycorrhizal fungi
rhizoids
bisexual
Marattiopsida
euosporangiate, homosporous ferns
polypodiopsida
35 families, 320 genera, 10,500 species
leptosporangiate ferns
leptosporangiate ferns
order filicales (filicalian ferns)
orders marsileales and salviniales (water ferns)
filicalian ferns
homosporous
water ferns
salvinia and azolla
heterosporous ad aquatic
heterosporous sporocarps are modified sori
feathery pinnae
fronds
ferns leaves that are megaphylls
filicales
fiddleheads
a large diversity in the sporophyll
different morphologies of sporophylls
little or no difference in form between sterile and fertile fronds
large difference between the two stages
only distal pinnae are fertile
different morphologies of sori
with or without an indusium
bare
margins of the blade rolled back a false indusium
covered by kidney-shaped indusia
growth of the prothallus
generally one cell layer thick except at apical sinus
no vascular tissues
bisexual
sequential differentiation of sex organs
major steps in polypodium lifecycle
1. differentiation of sporangia
2. release and germination of spores
3. growth of prothallus
4. fertilization and formation of the zygote
5. development of the embryo
6. growth into a mature sporophyte
Marsilea
Water Clover
shallow ponds
compound leaves
stolon-like stem
leaves alternately arranged, in 2 rows
sporocarps
heterosporous sporocarp is a modified pinna
have a gelatinous ring
Asexually reproducing ferns
water ferns
in some species, the gametophyte stage persists indefinitely without ever producing sporophytes
reproduce by gemmae
sporophytes never induced
populations estimated to be over 1000 years old
extinction of sporophytes possibly result of glaciation cycles
Equisetopsida
horsetails or scouring rushes
only one living genus Equisetum
indistinguishable from fossils 300 million years old
whorled microphylls at nodes
historically used to clean pots
good at vegetative propagation
poisonous livestock because of enzyme thiaminase
Equisetopsida reproduction
homosporous
gametophyte is photosynthetic and bisexual or male
practically
sporophyte has a hollow, jointed stem
fertile and sterile stems
has a strobilus with spores and elaters
Equisetum gametophyte
free-living
photosynthetic
no vascular tissue
no stomata
bisexual or male
Challenges of land plants
1. harvesting light energy
2. staying wet when things get dry
3. dealing with gravity
4. divide or be conquered
5. leveraging resources
solution of SVPs to harvesting light energy
evolution of leaves
lycopodiophyta, psilotopsida, and equisetopsida have microphylls
ferns have megaphylls
solution of ferns to staying wet when things get dry
conductive tissues (vasculature)
solution of ferns to dealing with gravity
strengthens cell walls
lignin
principle building block of plant cell walls is cellulose
lignin strengthens cell walls by replacing water and coating or encrusting cellulose
no seen in bryophytes
lignin
substance in vascular plants that makes cell walls rigid
allows for increases in size and height
solution of ferns to divide or be conquered
homospory vs. heterospory
significance of heterospory is associated with:
Reduction of the gametophyte
Almost complete retention of the gametophyte in the spore wall
No need to develop large vegetative bodies
Reduced risk of damage and/or death
Rapid production of gametes because of precocious germination
Difference in spore size results because of the greater demands on the female gametophyte and therefore on the megaspore
evolutionary process resulting in increased efficiency
benefits of leaves
increased photosynthetic surfaces, increased food and energy
benefits of vascular tissue
increased ability to move water and increase in range
benefits of lignin
stronger cells, get to greater heights and out compete neighbors
benefits of heterospory
lead to an increase in reproductive efficiency