Actually what is interesting for me is how all the plant life is sorted into specific layers as if they have evolved over time.
Plants don't run around or swim to higher ground.
The trees and grasses we see since the K-T layer are not the plant life that coal is made from, and don't appear in lower layers.
quote:
Timeline of plant evolutionPlant evolution is an aspect of the study of biological evolution, predominantly involving evolution of plants suited to live on land, greening of various land masses by the filling of their niches with land plants, and diversification of groups of land plants.
Fossil evidence of plants begins around 3000 Ma with indirect evidence of oxygen-producing photosynthesis in the geological record, in the form of chemical and isotopic signatures in rocks and fossil evidence of colonies of cyanobacteria, photosynthesizing prokaryotic organisms. Cyanobacteria use water as a reducing agent, producing atmospheric oxygen as a byproduct, and they thereby profoundly changed the early reducing atmosphere of the earth to one in which modern aerobic organisms eventually evolved. This oxygen liberated by cyanobacteria then oxidized dissolved iron in the oceans, the iron precipitated out of the sea water, and fell to the ocean floor to form sedimentary layers of oxidized iron called Banded Iron Formations (BIFs). These BIFs are part of the geological record of evidence for the evolutionary history of plants by identifying when photosynthesis originated. This also provides deep time constraints upon when enough oxygen could have been available in the atmosphere to produce the ultraviolet blocking stratospheric ozone layer. The oxygen concentration in the ancient atmosphere subsequently rose, acting as a poison for anaerobic organisms, and resulting in a highly oxidizing atmosphere, and opening up niches on land for occupation by aerobic organisms.
Cambrian flora
Early plants were small, unicellular or filamentous, with simple branching. .... Other major groups of green algae had been established by this time, but there were no land plants with vascular tissues until the mid-Silurian.
Ordovician flora
The evidence of plant evolution changes dramatically in the Ordovician with the first extensive appearance of spores in the fossil record (Cambrian spores have been found, also). The first terrestrial plants were probably in the form of tiny plants resembling liverworts when, around the Middle Ordovician, evidence for the beginning of the terrestrialization of the land is found in the form of tetrads of spores with resistant polymers in their outer walls. These early plants did not have conducting tissues, severely limiting their size. ... With spores, plants on land could have sent out large numbers of spores that could grow into an adult plant when sufficient environmental moisture was present.
Silurian flora
The first fossil records of vascular plants, that is, land plants with vascular tissues, appeared in the Silurian period. The earliest known representatives of this group (mostly from the northern hemisphere) are placed in the genus Cooksonia. They had very simple branching patterns, with the branches terminated by flattened sporangia. By the end of the Silurian much more complex vascular plants, the zosterophylls, had diversified[3] and primitive lycopods, such as Baragwanathia (originally discovered in Silurian deposits in Victoria, Australia),[4] had become widespread.
Devonian flora
By the Devonian Period, the colonization of the land by plants was well underway. The bacterial and algal mats were joined early in the period by primitive plants that created the first recognizable soils and harbored some arthropods like mites, scorpions and myriapods. Early Devonian plants did not have roots or leaves like the plants most common today, and many had no vascular tissue at all.... They probably spread by a combination of vegetative reproduction forming clonal colonies, and sexual reproduction via spores and did not grow much more than a few centimeters tall.
By the Late Devonian, forests of large, primitive plants existed: lycophytes, sphenophytes, ferns, and progymnosperms had evolved. Most of these plants have true roots and leaves, and many were quite tall.... By the end of the Devonian, the first seed-forming plants had appeared. This rapid appearance of so many plant groups and growth forms has been called the "Devonian Explosion". The primitive arthropods co-evolved with this diversified terrestrial vegetation structure. The evolving co-dependence of insects and seed-plants that characterizes a recognizably modern world had its genesis in the late Devonian. The development of soils and plant root systems probably led to changes in the speed and pattern of erosion and sediment deposition.
The 'greening' of the continents acted as a carbon dioxide sink, and atmospheric concentrations of this greenhouse gas may have dropped.[6] This may have cooled the climate and led to a massive extinction event. see Late Devonian extinction.
Also in the Devonian, both vertebrates and arthropods were solidly established on the land.
Carboniferous flora
Early Carboniferous land plants were very similar to those of the preceding Latest Devonian, but new groups also appeared at this time.
The main Early Carboniferous plants were the Equisetales (Horse-tails), Sphenophyllales (scrambling plants), Lycopodiales (Club mosses), Lepidodendrales (arborescent clubmosses or scale trees), Filicales (Ferns), Medullosales (previously included in the "seed ferns", an artificial assemblage of a number of early gymnosperm groups) and the Cordaitales. These continued to dominate throughout the period, but during late Carboniferous, several other groups, Cycadophyta (cycads), the Callistophytales (another group of "seed ferns"), and the Voltziales (related to and sometimes included under the conifers), appeared.
The Carboniferous lycophytes of the order Lepidodendrales, which were cousins (but not ancestors) of the tiny club-mosses of today, were huge trees with trunks 30 meters high and up to 1.5 meters in diameter. These included Lepidodendron (with its fruit cone called Lepidostrobus), Halonia, Lepidophloios and Sigillaria. The roots of several of these forms are known as Stigmaria.
The fronds of some Carboniferous ferns are almost identical with those of living species. Probably many species were epiphytic. Fossil ferns include Pecopteris and the tree ferns Megaphyton and Caulopteris. Seed ferns or Pteridospermatophyta include Cyclopteris, Neuropteris, Alethopteris, and Sphenopteris.
Cordaites, a tall plant (6 to over 30 meters) with strap-like leaves, was related to the cycads and conifers; the catkin-like inflorescence, which bore yew-like berries, is called Cardiocarpus. These plants were thought to live in swamps and mangroves. True coniferous trees (Walchia, of the order Voltziales) appear later in the Carboniferous, and preferred higher drier ground.
Permian flora
The Permian began with the Carboniferous flora still flourishing. About the middle of the Permian there was a major transition in vegetation. The swamp-loving lycopod trees of the Carboniferous, such as Lepidodendron and Sigillaria, were replaced by the more advanced conifers, which were better adapted to the changing climatic conditions. Lycopods and swamp forests still dominated the South China continent because it was an isolated continent and it sat near or at the equator.
Triassic flora
On land, the holdover plants included the lycophytes, the dominant cycads, Ginkgophyta (represented in modern times by Ginkgo biloba) and glossopterids. The spermatophytes, or seed plants came to dominate the terrestrial flora: in the northern hemisphere, conifers flourished. Dicroidium (a seed fern) was the dominant southern hemisphere tree during the Early Triassic period.
Jurassic flora
The arid, continental conditions characteristic of the Triassic steadily eased during the Jurassic period, especially at higher latitudes; the warm, humid climate allowed lush jungles to cover much of the landscape.[7] Conifers dominated the flora, as during the Triassic; they were the most diverse group and constituted the majority of large trees. Extant conifer families that flourished during the Jurassic included the Araucariaceae, Cephalotaxaceae, Pinaceae, Podocarpaceae, Taxaceae and Taxodiaceae.[8] The extinct Mesozoic conifer family Cheirolepidiaceae dominated low latitude vegetation, as did the shrubby Bennettitales.[9] Cycads were also common, as were ginkgos and tree ferns in the forest. Smaller ferns were probably the dominant undergrowth. Caytoniaceous seed ferns were another group of important plants during this time and are thought to have been shrub to small-tree sized.[10] Ginkgo-like plants were particularly common in the mid- to high northern latitudes. In the Southern Hemisphere, podocarps were especially successful, while Ginkgos and Czekanowskiales were rare.[9][11]
Cretaceous flora
Flowering plants, also known as angiosperms, spread during this period[12], although they did not become predominant until near the end of the period (Campanian age). Their evolution was aided by the appearance of bees; in fact angiosperms and insects are a good example of coevolution. The first representatives of many modern trees, including figs, planes and magnolias, appeared in the Cretaceous. At the same time, some earlier Mesozoic gymnosperms, like Conifers continued to thrive, although other taxa like Bennettitales died out before the end of the period.
Cenozoic flora
The Cenozoic began at the Cretaceous–Paleogene_extinction_event with a massive disruption of plant communities. It then became just as much the age of savannas, or the age of co-dependent flowering plants and insects. At 35 Ma, grasses evolved from among the angiosperms. About ten thousand years ago, humans in the Fertile Crescent of the Middle East develop agriculture. Plant domestication begins with cultivation of Neolithic founder crops. This process of food production, coupled later with the domestication of animals caused a massive increase in human population that has continued to the present. In Jericho (modern Israel), there is a settlement with about 19,000 people. At the same time, Sahara is green with rivers, lakes, cattle, crocodiles and monsoons. At 8 ka, Common (Bread) wheat (Triticum aestivum) originates in southwest Asia due to hybridisation of emmer wheat with a goat-grass, Aegilops tauschii. At 6.5 ka, two rice species are domesticated: Asian rice, Oryza sativa, and African rice Oryza glaberrima.
Why are there no grasses below the Cretaceous–Paleogene_extinction_event layers?
Why do all these plant fossils form a consistent pattern within the geographical/geological/temporal matrix, a pattern that seemingly shows new groups evolving from existing groups?
More preposterous things have been suggested.
Why are the Banded Iron Formations (BIFs) only found in the same age/stratigraphic layers around the world?
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