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GEOL 331 Principles of Paleontology

Fall 2016

Paleobotany II: Flowering plants

fromCornell University BIOG1445

• Theovule: The derived sporangium of seed plants in whichmegaspores are produced and retained.
• The haploid femalegametophyte develops inside the ovule, producing ova.
• Fertilization by sperm produces azygote that develops into anembryo.
• After fertilization, the ovule develops into a seed, and haploid cells of the ovule develop into"endosperm", nutritional tissue for the embryo.

• Anthophyta: Flowering plants and their kin
• Acrgymnoseprmae: The traditional - "Gymnospermae" (naked seed) - non-flowering seed plants.

Acrogymnospermae: (Devonian - Quaternary) Deemed paraphyletic in earlier literature, the traditional "gymnosperms" have emerged from recent molecular analyses as a monophyletic group. An interesting fact for its own sake, but also because it implies that the evolutionary "roots" of flowering plants go back to the mid-Paleozoic.

Dioon spinulosum
Cycadophyta: (Cycads) CarboniferousPermian - Quaternary Shrub-sized superficially fern or palm-like plants with short trunks and very tough pinnate leaves. They are very slow-growing and long-lived. Like conifers, they producemale andfemale strobili. In this case, however, the plants aredioecious i.e., each individual plant is fully male or female, producing cones of only one sex. Cycads were very commonunderstory plants during the Mesozoic but are uncommon today.


Ginkgo biloba
Ginkgoales (Ginkgos) Permian - Quaternary Common in theMesozoic and Paleogene, they are now reduced to a single species,Ginkgo biloba. Like cycads, ginkgos aredioecious - have separate male and female individuals. The ovule is enclosed in a malodorous fleshy capsule.

Represented by a single species,Ginkgo biloba, butmore speciose during the Mesozoic. Ginkgoes began to decline during the Cretaceous and were significantly reduced by the end of the Paleocene. (Possibly because the animals on which they depended to disperse their seeds had also declined.)

With the exception of a small region of southwestern China, ginkgoes are extinct in the wild. Thankfully, they are common under cultivation.



Pinus nigra
Pinophyta: (Devonian - Quaternary) carry their seeds on the scales of cones. Most conifers are tree-sized and produce both male (pollen bearing) and female (seed bearing) cones. In many cases, their leaves are reduced to needles, allowing them to withstand cold and dry conditions. This ability allows many to retain their leaves year-round. Earliest known representative belonged to"Cordaitanthales" (Devonian - Jur.), trees with whorls of strap-like leaves superficially like modernPandanus. Paraphyletic.

Crown-group Pinophyta includes of thePinales (Carboniferous - Quaternary) Important canopy trees of late Paleozoic andMesozoic forests. Representatives include:

• Araucarians
• Podocarpus
• Yews
• Pines
• Cypress

A fourth group requires notice:

Welwitschia mirabili fromNature Hills Nursery

Until recently, we would have presented Gnetophyta as close relatives of flowering plants, however strong recent molecular evidence indicates that they are actually nested within Pinales - counterintuitive but strongly supported.

Anthophyta: Carboniferous - Quaternary) The total group of flowering plants and their kin. The familiar termAngiopspermae refers to the crown-group.

fromHMH School Publishers

• Unlike other seed plants, in which pollen and ovule producing structures are completely separate,flowers combine them in a single complex structure.
  • The pollen-organ is thestamen
  • The ovulate organ is thepistil, a composite containing:
    • One or morecarpels - the specialized leaves from which the ovules are suspended (homologous with the scales of a conifer ovulate cone.)
    • Thestigma, to which pollen grains attach
    • Thestyle, with guides the pollen tube to the ovule.
  • Perianth, the circle of specialized leaves (petals and sepals) inclosing the pistil and stamens.

• Unlike in other seed plants, the ovule is completely concealed by htecarpel. When the ovule is fertilized, the carpel of many species swells to form a fruit, whose primary purpose seems to be to intice animals into consuming the seed. This allows the seed to hitch a ride in the animal's gut and insures that it will be deposited with a blob of fertilizer. Indeed, some seeds can't germinate without first passing through someone's gut.

• The specialized leaves (petals,sepals) of the perianth along with secretions of nectar function to attract pollinators, usually insects. In the latter two adaptations, the plant "pays" animals to transport pollen directly to other flowers, and to disperse seeds, resulting in an increase in reproductive efficiency.
  

• 
  fromDJ's Science Page
  But that is tame. The angiosperm seed is derived in that theendosperm - the tissue that nourishes the embryo - forms from the fusion of sperm with a specialdiploid cell of the ovule. After fertilization, thistriploid cell develops into the endosperm. (Think of it as if everyone shared the womb with a fraternal twin whom they were supposed to eat.) In non-anthophytes, this nutrient tissue is haploid.
  
  
  Nymphaea sp.
• Angiosperms tend to have broad leaves with branching venation, in which the veins show multiple orders of branching, cross veins, and

Anthophyte Evolution:

• 
  Delnortea abbottiae fromgigantopteroid.org
  Gigantopteridales: (Permian) Major portion of Late Paleozoic and Triassic Gondwanan flora. These bore distinct ovulate and stamenate reproductive structures on separate specialized leaves - the ancestral lignophyte pattern. Were derived in their development of broad non-pinnate leaves.

  
  

• 
  Glossopteris fromFurman University
  Glossopteridales: (Permian - Triassic) Major portion of Late Paleozoic and Triassic Gondwanan flora. These, again, bore distinct ovulatte and stamenate reproductive structures on separate specialized leaves. Note, the PermianGlossopteris was a particularly significant member of theGondwanan flora.
  

• 
  fromSystematic Biology - Susquehanna University
  Bennettitales: (Triassic - Cretaceous) (Sometimes called "Cycadeoids.") Superficially resembling cycads with short trunks covered by leaf scars and pinnate leaves. Theirreproductive structures are different. First, like most flowering plants, they are hermaphrodites. Second, some displayflower-like cones in which the ovule is contained in a central recepticle surrounded by specialized leaves (bracts) that might be homologous to petals. In some, microspore (pollen) producing structures are arrayed radially around it, like stamens - a truly flower-like arrangement. Alas, not all bennettitaleans show this, so this bisexual reproductive structure seems to be convergent with angiosperms.
  

• 
  Sanmiguelia lewisii fromUC Berkeley Museum of Paleontology
  Sanmiguelia lewisii: (Triassic) Described byCornet 1986 as having:
  • Separate stamenate and ovulate reproductive structures in which the latter were very similar to those of angiosperms.
  • Leaf venation patterns similar to those of angiosperms.
  Some have putSanmiguelia forward as "the earliest angiosperm." Probably not, but it is getting very close.

  
  

• 
  Archaefructus eoflora fromPaleobiology of Angiosperms - A General account
  Archaefructus eoflora: (Early Cretaceous): An aquatic plant. In contrast toSanmiguelia which seems to have male and female structures on distinct branches,Archaefructus eoflora is described byJiet al., 2004 as having a single enflorescences (branches covered with small reproductive structures) in which:
  • the distal structures were stamenate
  • the proximal ones were ovulate
  • But where they met were a few rows of composite bisexual structures.

  
  

Angiospermae:

Angiosperms appear unambiguously in the fossil record in the Early Cretaceous. Today, they are the dominant plant type, with over 200,000 known species (compared to 550 species of gymnosperms).

Both the ecologies of their fossil relativesSanmiguelia andArchaefructus, and of their basal living members suggest that they inhabited wetlands.

Lichnomesopsyche gloriae fromSmithsonian Science

Angiosperm partners:

Fruit eaters:

Arthropods might like to eat the fleshy parts of fruit, but they destroy them in the process. Plants develop fruit to select for something that can eat the whole fruit and spread the seeds. During the Mesozoic, that could only be a vertebrate.

• Herbivorous mammals and squamates of the Early Cretaceous were mostly small, but could have eaten berry-sized fruit.
• Herbivorous crocodyliforms were rare, but did exist
• But herbivorous dinosaurs werequite common, and could easily eat and transport a plenty of fruit! Since most early angiosperms were built low to the ground, it would be small and/or low-browsing forms that would have been the main agents of transportation for fruit.

Flower sniffers:

• No Early Cretaceous archosaur shows nectar-eating adaptations.
• Mammals were small, and may have been pollinators, but bats - the great modern mammalian pollinators - did not exist.
• Insects (including beetles, dipterans (flies), lepidopterans (butterflies and moths), and hymenopterans (wasps, bees, and ants)) were present, and were almost certainly the main pollinators in the Mesozoic just as they are today.
• In fact, the major groups of holometabolous insects that are the major pollinators today tend todiversify greatly around the time ofangiosperm origins.

Was anyone else on the scene to fill this role? In fact, mecopteran insects (today represented byscorpionflies) appear to haveserved that role. Rather than being predators, like the living members, fossil Cretaceous scorpionflies did not have biting jaws, but insteadbutterfly-like probing snouts.

fromEffective and creative lesson plans!

Angiosperm diversity:

• Traditionally, flowering plants have been divided intoDicotyledonae andMonocotyledonae (commonly dicots and monocots). Although there are many morphological distinctions (see today's lab) the names derive from a major difference in their embryos:
  • Dicots embryos have twocotyledons - embryonic first leaves.
  • Monocots have one cotyledon.

  Great. Now forget it! "Dicots" are paraphyletic.

Yellow stargrass -Hypoxis hirsuta

• Phylogentic systematists have confirmed thatMonocotyledonae is monophyletic, however dicots are not.
• Most "dicots" do fall within a monophyletic "Eudicotyledonae", however some, including:
  • water-lillies
  • star anise
  • Amborella
  • magnolias
  fall outside these groups.

• Monocotyledonae appear in the Cretaceous and include lillies (right), orchids, grasses, palms, etc. Note thatgrasses appeared in the Eocene and proliferated during the Oligocene, transforming much of the world by converting arid and semi-arid regions to grasslands.

  C₃ and C₄ plants: Depending on the plant, two distinct photosynthetic pathways are employed by plants, termed C₃ and C₄. Most plants use C₃. The C₄ pathway conserves water and it present in arid adapted plants and grasses.

Amborella trichopoda male flower fromDavid Tng

• Amborella trichopoda most primitive. Although weird for being dioecious (plesiomorphy?), otherwise suggests the structure of the ancestral flower:
  • very small
  • petals and sepals undifferentiated
  • ovum development resembles that of nonflowering plants
  Other basal angiosperm groups:
  • Nymphaeaceae Water lilies.
  • Austrobaileyales including star anise.
  • Magnoliidae: Including magnolias and laurels.
  • Chloranthales
• Sister taxon to Eudicotyledonae:Ceratophyllaceae - Fresh water aquatic plants.
  

But we note that water-lilies have endosperm that is merely diploid - a plesiomorphy or autapomorphy?