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See below, because I'm not sure how you arrived at those numbers but they don't jive with studies I've read.
That doesn't conflict with evolutionary laws. In truth that isn't thought to be the prevalent factor though. The largest factor was predatory pressure from what I've been reading. The food rich environment simply allowed for runaway growth. We've never since seen that amount of flaura rich environments. Humans don't, and haven't really, increase in height because there's no selective pressure where a gain in height or mass would be advantageous. Also, there also seems to a be a mass where an animal couldn't, in a land environment, move enough heat from its core to its outer body fast enough to stop overheating and subsequent death, so the largest sauropods might have hit an upper limit but this is still being studied.
Yep, that's what I found too, about one third of the current land mass. Obviously this is enough land mass to support large populations.
Actually, I think your mixing up the tracks.
http://www2.brevard.edu/reynoljh/FTWeb/Ass...lenRoseDino.jpgSame site. You can see the sauropod tracks on the right. The three toed tracks in the pic you linked to are the therapod. As you can see the sauropod tracks are quite similar to an elephant as they are broad and flat. Here's some pics of trackways:
http://palaeo.gly.bris.ac.uk/Palaeofiles/T...5/egtracks.htmlHere's a cool little paper comparing sauropods to elephants:
http://www.projectexploration.org/jobaria/...TheElephant.pdfThe largest factor in Sauropod locomotion is the ridiculous mass of their bones which allowed such size:
"The faster an animal runs, the greater the forces its feet exert on the ground and the stronger its legs need to be. The reason is, at higher speeds each foot is on the ground for a smaller fraction of the stride, so it has to exert peak force - the maximum force that occurs while the foot is on the ground - to make a complete stride balance and carry the body weight. The forces exerted by the feet of various creatures led to a greater understanding of dinosaur motion. The use of a force plate to measure the forces on the feet of people, dogs etc enabled us to calculate the stresses imposed on the animals' leg bones. The same approach used for dinosaurs would have involved elaborate calculations and a good deal of imagination. As a result, a quicker and easier way, using the concept of dynamic similarity and insights from structural engineering is preferred.
Forces that act on the ends of bones setting up stresses can be broken down into their components : axial force (Fax), acts along the long axis of the bone, and transverse force (Ftrans) acts at right angles to it. Fax sets up a uniform stress, -Fax/ A, where A is a cross section of the bone and the minus sign indicates a compressive stress. Added to this force are the stresses caused by F trans. These transverse stresses vary across the thickness of the bone from -Ftrans x /Z at one end of the bone to +Ftransx /Z at the other. x is the distance of the cross section from the end of the bone, and Z is the section modulus. Calculations for the leg bones of running and jumping modern animals showed that the stress Fax x/ Z was generally much greater than the stress Faxx/A. This difference tells us that transverse forces are a much more serious threat to bones than axial ones. So the less important Fax can be ignored.
For animals running dynamically in a similar fashion, the forces on the bones are proportional to body weight, W. The stresses they cause (Ftrans x/Z) are proportional to W x/Z. The stresses in the leg bones of two similar animals of different sizes in comparison, will be less in whichever animal has lower values of W x/Z, indicating that its bones are stronger than the other animals' bones.
By changing the expression just slightly, the reciprocal Z/Wx, a value for a strength indicator can be arrived at. The greater the value of Z/Wx, the more athletic an animal can be expected to be. More precisely, the expression, Z/aWx can be used, where a is the fraction of body weight supported by the forelegs or hindlegs, as is appropriate. This weight distribution enables comparison between elephants and dinosaurs. Once the strength indicator is determined, we could conclude that a dinosaur could have been as athletic as any modern mammal with similar strength indicators. The conclusion depended on the assumption that the bones of different animals can stand about the same stresses. It also depended on the assumption that evolution has adjusted the strengths of bones of different animals to give them equal safety factors. The process of arriving at the values for the strength indicators for the dinosaurs is not as straight forward as the conclusions imply. The first step is to calculate the value of the section modulus, or Z, of their bones. Detailed measurements of cross sections at known distances, x, from the end of the bones was obtained from accurate drawings published by earlier paleontologists. The calculation of the strength indicators becomes complete with the weight, W, of the dinosaur and if quadruped, the fraction, a, of that weight carried by each pair of feet. To calculate the distribution of weight between the feet, centre of gravity of each dinosaur must be found. In the real animals, the bones are distributed along the whole length of the body, which did not affect the centre of gravity too much. The models that were selected for studying had to contain a hole, bored through, representing the approximate volume where the lungs would have been.
The above procedures and data supplied the information needed to calculate the strength indicators. Z/aWx for different dinosaur limbs. Obtaining large values to compare elephants and Apatosaurus, commonly known as brontosaur, suggests that despite Apatosaurus' huge size, it could have been about as athletic as an elephant. Diplodocus, a more slender sauropod, seems to have a lower strength indicator and was therefore probably less agile, able to walk on land, possibly unable to run. Considerable doubt exists about the mass of Diplodocus and Triceratops because measurements have been made in each case on a skinny model and a stout one - it seems uncertain which model is more accurate. The higher values of strength indicators of Triceratops suggests it may have been more athletic. The conclusions reached for Apatosaurus, Diplodocus and Triceratops are tentative, and more so, for Tyrannosaurus, because all modern bipeds are so very much smaller.
Finally, the calculations that allowed us to assess the agility of dinosaurs are firmly based on physics and engineering. Although large dinosaurs walked slowly, most were capable of quite a quick run and none needed to live in water or to rely on buoyancy for support.
(Condensed From R McNeill Alexander, Sci. Am., 62, (1991))"
Here is a clearer pic of a Sauropod foot print:http://www.dinoruss.com/utah2kweb/morrision_j/morrison_j_sltwashvert3.jpeg
Again what you see here doesnt make sense as the print is believed to be that of a creature weighing some thirty tons but the imprint shows that the size of the pad of the foot to be not much larger than a fully grown Elephant's.
You state that the larger Dinosaurs were agile and capable of running. This indicates a high metabolic rate and if true ,conflicts with the idea that Dinosaurs were reptiles. A high metabolic rate also indicates fast growth which reinforces the research that points to higher oxygen levels during the period of the Jurassic but this research is somewhat in dispute by fresher research that has claimed the opposite to be true - in which case what drove such rapid growth and increased metabolic rate?
"Hundreds of slices from bones of all types of dinosaurs have now been examined and all show:
1) Woven bone typical of rapid bone growth
2) Vascular canals equivalent to those of birds
3) Generally poor growth rings but more obvious in teeth
ie in all regards they resemble warm-blooded rather than cold-blooded animals. However, continuing studies have complicated the interpretation of these results. Many small mammals and birds do not show either Haversian canals or fibrolamellar bone, and at least one turtle has been found with a dense Haversian bone. Dinosaurs do appear to differ from other reptiles in their ability to deposit fibrolamellar bone continuously instead of periodically.
In 1993 a comparative study was made of the long bone growth plate of a chicken (bird), dog (mammal) and monitor lizard (cold-blooded reptile) with juvenile Maiasaura bone. In longitudinal section, the line between cartilage and newly formed bone was straight in the dog and monitor, but undulating in the bird and dinosaur. As well as reinforcing the close relationship between dinosaur and bird, the authors conclude that the different bone formation processes that cause the wavy line indicate rapid growth and are consistent with a high metabolic rate ."
Source:
http://www.dinoruss.com/de_4/5c51dbb.htmSo far as Oxygen levels during the Jurassic:
"Recent evidence suggests that oxygen levels were suppressed worldwide 175 million to 275 million years ago and fell to precipitously low levels compared with today's atmosphere, low enough to make breathing the air at sea level feel like respiration at high altitude.
Now, a University of Washington paleontologist theorizes that low oxygen and repeated short but substantial temperature increases because of greenhouse warming sparked two major mass-extinction events, one of which eradicated 90 percent of all species on Earth.
In addition, Peter Ward, a UW professor of biology and Earth and space sciences, believes the conditions spurred the development of an unusual breathing system in some dinosaurs, a group called Saurischian dinosaurs that includes the gigantic brontosaurus. Rather than having a diaphragm to force air in and out of lungs, the Saurischians had lungs attached to a series of thin-walled air sacs that appear to have functioned something like bellows to move air through the body.
Ward, working with UW biologist Raymond Huey and UW radiologist Kevin Conley, believes that breathing system, still found in today's birds, made the Saurischian dinosaurs better equipped than mammals to survive the harsh conditions in which oxygen content of air at the Earth's surface was only about half of today's 21 percent.
"The literature always said that the reason birds had sacs was so they could breathe when they fly. But I don't know of any brontosaurus that could fly," Ward said. "However, when we considered that birds fly at altitudes where oxygen is significantly lower, we finally put it all together with the fact that the oxygen level at the surface was only 10 percent to 11 percent at the time the dinosaurs evolved.
"That's the same as trying to breathe at 14,000 feet. If you've ever been at 14,000 feet, you know it's not easy to breathe," he said.
Ward believes low oxygen and greenhouse conditions caused by high levels of methane from intense volcanic activity are likely culprits in mass extinctions that occurred about 250 million years ago, at the boundary between the Permian and Triassic periods, and about 200 million years ago, at the boundary between the Triassic and Jurassic periods. He will make a presentation on the topic Tuesday at the American Geological Society annual meeting in Seattle.
The Permian-Triassic extinction is believed to have eradicated 90 percent of all species, including most protomammals, a group of mammal-like reptiles that were the immediate ancestors of true mammals. The Triassic-Jurassic extinction killed more than half the species on Earth, with mammal-like reptiles and true mammals, which evolved during the Triassic Period, hit particularly hard. But dinosaurs, which also evolved between the two extinctions, had little problem with conditions during the Triassic-Jurassic extinction.
"The seminal observation is that dinosaurs skated across the second of these mass extinctions, actually increasing in number as they went along, while everything else was dropping around them," Ward said.
Scientists know of five mass extinction events in Earth's history, but a cause has been widely agreed upon for only one -- the episode at the end of the Cretaceous Period 65 million years ago, when the impact of an asteroid is believed to have brought the demise of the dinosaurs. Such impact also has been suggested as the cause of the Permian-Triassic and Triassic-Jurassic extinctions, but geologists have yet to unearth any indisputable evidence of such an impact, and there is no conclusive evidence of what caused either of the events.
Ward said mass spectrometer readings on fossil material, as well as the extinction pattern for fossils in rock outcrops collected from the time of the two extinctions, indicates the events were drawn-out affairs and did not happen suddenly, as they would have with an asteroid impact.
In addition, he said it is known which types of creatures, and which breathing systems, best survived the extinction events. The same breathing systems are still present in birds, which are known to fare well at high altitudes, where oxygen levels are substantially lower than at the surface.
"The reason the birds developed these systems is that they arose from dinosaurs halfway through the Jurassic Period. They are how the dinosaurs survived," he said.
For more information, contact Ward at (206) 543-2962 or argo@u.washington.edu
Source:
http://uwnews.washington.edu/ni/article.asp?articleID=2205