Historically, creationists have explained the diversity in created
kinds primarily in terms of initial created variability, Mendelian
inheritance, chance deleterious mutations, and natural selection. Baraminology
research suggests that some animal kinds represented by a
single pair on the ark less than 4500 years ago have diversified significantly and are now represented by entire families. This suggests that
other mechanisms are present that generate diversity to allow animals
to adapt. Research on the RNASE gene in Old World monkeys suggests
that programmed adaptive genetic changes were involved in gene
duplication and subsequent nonrandom adaptive mutations.
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Article: [PDF]
The Universal Deluge:
Alternative Hypotheses for Hardground Origins
John Woodmorappe
Transport processes can potentially account for in situ hardgrounds
in the sedimentary record. Steadily accumulating evidence undermines
the certitude of life-position inferences of at least certain fossils.
Some turbidity currents and debris fl ows allow for the contemplation
of large-scale transport, imbrication, and coplanar deposition of large,
flat slabs of antediluvian hardground origin. Modern volcanoes demonstrate
that released gas can cause the flotation of large rock slabs.
Finally, many in situ hardgrounds show evidences at least suggestive of
a composite, allochthonous origin. A hardground-conduit hypothesis
posits that hardgrounds formed in pseudokarstic-submarine (underwater
cavelike) structures. This solves the apparent problems of time and
stratigraphically superposed hardgrounds. The hardiness of hardground
organisms is just one factor consistent with this hypothesis.
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Can Evolution Make New Biological Software?
Richard W. Stevens
The modern theory of biological evolution focuses almost entirely
on how random mutation (including recombination) with natural
selection could produce all of the physical features and functions
that appear in plants and animals. Yet, how do new species of animals
obtain the knowledge (the software) to operate the new limbs, organs,
and other features (the hardware) that evolution produces? This article
will look at reptile-bird evolution and the need for the simultaneous
evolution of fl ying software to support the evolution of the fl ying hardware
(the wings). Next, the article addresses whether random mutation
and natural selection can modify software to achieve any new useful
functions. Using the InforMutation simulation system, the analysis
shows that random modifi cations to computer software yield broken
programs, not improved software. By analogy, biological control systems
cannot be modifi ed randomly and then be able to operate new biological
hardware.
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Can Recolonization Explain the Rock Record?
John K. Reed, Andrew S. Kulikovsky, and Michael J. Oard
The recolonization model is a recently proposed diluvial solution to
many enigmas of the rock record. Working within the framework
of the global stratigraphic succession developed by uniformitarian geologists
over the past two centuries, it seeks to reconcile it with Biblical
history by moving the Flood event to the very base of the stratigraphic
record. Thus the Flood is represented by that section that extends
from the oldest crustal rocks (Hadean) up into the Carboniferous. The
post-Carboniferous record refl ects a sequential terrestrial recolonization
by Flood survivors, preserved as a series of historical snapshots by
post-Flood catastrophes. Although appealing in its attempt to merge
the geologic column with Genesis, the model’s positive arguments are
unconvincing. An evaluation of Biblical, axiomatic, logical, and geological
issues reveals significant weaknesses. Two of its greatest flaws lie
in its two key assumptions: 1) the veracity of the geologic timescale’s
relative chronology, and 2) the validity of uniformitarian depositional
models.
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Article:
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