CRS Blog

Polystrate fossils are one of numerous evidences for the rapid deposition of strata, as opposed to the uniformitarian belief in slow deposition over millions of years. They are briefly described from the Joggins Formation, Nova Scotia; Yellowstone National Park, Montana and Wyoming; Ginkgo Petrified Forest State Park, Washington; the Geodetic Hills of Axel Heiberg Island; the Lompoc diatomite, California; and a diatomite from Peru. Uniformitarian geologists usually ignore polystrate fossils or claim that they represent only local rapid deposition, but they rarely supply any supporting evidence. A new location with polystrate petrified trees is described from open-pit coal mines in Alaska. About twenty upright trees at many different levels support rapid deposition of the strata there. The upright trees can be explained by the log mat model, and evidence from the coal mines supports that interpretation.

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The biosystematic method of baraminology has grown significantly in the past decade. Its conceptual foundations were discussed in the evolution/creation debates of the nineteenth century, long before Frank Lewis Marsh coined the term baramin in 1941. Currently, baraminology has been applied to dozens of groups, and the results of 66 baraminology studies are summarized and evaluated here. Though bias in group and character selection prevents firm conclusions, it appears at this time that Price’s suggestion that the family is an approximation of the “created kind” may be correct. Criticisms of baraminology from evolutionists and creationists alike can be resolved with further research. Whatever its future, baraminology is at present a useful tool for investigating God’s biological creation.

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A Fresh Look at the Australopithecines and Homo habilis
Patrick H. Young

The australopithecines and Homo habilis have been publicized for years as examples of evolutionary transitional forms that launched our own human lineage. Dogmatic evolutionists have rationalized these claims on the basis of brain expansion, encephalization quotients, and bipedalism. However, any evolutionary justification for brain expansion in these extinct creatures must rest in a precise model for the determination of body mass. To insure an accurate body mass model, one must take into account whether the animal is quadruped, facultative biped, or obligatory biped. Past body mass estimates for the australopithecines and Homo habilis were based on assumptions about their bipedalism that have proven to be erroneous. When a body mass model is used accounting for the facultative bipedalism of the australopithecines and Homo habilis, the data shows that they are not highly encephalized, and hence nothing more than a microevolutionary adaptation of the pan-troglodytes. Read more…

Walter R. Barnhart

Supposed nests of dinosaur eggs are examined for indications that they were laid under normal subaerial conditions. It is shown that when representative clutches of eggs are examined from numerous sites worldwide, they were all laid into a watery environment in which sedimentation was often actively taking place. This leads to the conclusion that dinosaur nests, as they are presently found, cannot represent normal living environments for the dinosaurs and instead show life existed at the survival level under highly stressed conditions. These conditions are consistent with egg laying taking place during a worldwide flood. Read more…