Creation Exhibit to Open at World Headquarters: Just in Time for Creation Sabbath

In preparation for Creation Sabbath on October 28, 2017, the Geoscience Research Institute (GRI) is creating a series of scientifically accurate and faith building displays. The exhibit will be opened during this year’s Autumn Council of the General Conference Executive Committee, held from October 5-11 at the world headquarters of the Seventh-day Adventist Church in Silver Spring, Maryland.

“The displays will feature physical evidence pointing to design in nature and catastrophe in the rock record,” says Dr. Jim Gibson, GRI Director. “The Scriptures provide a cogent explanation for this evidence. These displays are a testimony to both the Church’s allegiance to the biblical creation and to the scientific study of origins.”

Trilobites, extinct arthropods, illustrate both mass burial and rapid fossilization when found in groups like those on this slab of rock.

The exhibit will show examples of biological beauty and other evidence of design, such as irreducible complexity. Other examples of design will include the way fish are engineered for swimming, birds for flying, eyes for seeing, and fossil ammonite shells for movement in water.

Several displays will feature some of the abundant evidence of the worldwide flood recorded in the Bible. Most scientists agree on the occurrence of past global catastrophes, such as extraterrestrial impacts and gigantic lava flows, but many deny that these could be associated with the flood recorded in Genesis and elsewhere, according to Dr. Tim Standish, senior scientist at GRI. “This evidence of global catastrophe will be included in the displays.”

Trilobites are not the only example of rapid mass burial. This is a pattern repeated for many other organisms including these Knightia fish fossils from the Green River Formation in Wyoming, USA.

“The question of time is one in which the most widely accepted scientific explanations espousing millions of years disagree with the clear record given in Scripture of thousands of years since creation,” says Standish. “Adventists don’t ignore this tension and this will be reflected in the displays.” However, the record of Scripture is robust. For example, one display will examine several patterns in the fossil record that show God’s activity in nature, irrespective of the time assigned to the fossils involved.

The Seventh-day Adventist Church has a long history of interest in the relationship between history recorded in the Bible and the study of nature using the methods of science. Church pioneer, Ellen G. White explained the Adventist approach over a century ago:

Since the book of nature and the book of revelation bear the impress of the same master mind, they cannot but speak in harmony. By different methods, and in different languages, they witness to the same great truths. Science is ever discovering new wonders; but she brings from her research nothing that, rightly understood, conflicts with divine revelation. The book of nature and the written word shed light upon each other. They make us acquainted with God by teaching us something of the laws through which He works” (Education, p. 130).

Creation Sabbath, designated for October 28, is an opportunity to celebrate this Bible-inspired approach to the study of nature, according to Dr. Ted N. C. Wilson, president of the Seventh-day Adventist Church. “The creation story and global flood explain so much, and yet we still have questions that need to be answered. Nevertheless, God’s word is sure!” Wilson affirms.

Faith in the biblical record leading to discoveries using the methods of science has been a hallmark of Adventists’ contribution to understanding nature. Appreciating that many questions remain to be answered has proven a productive incentive to do science, according to Standish. In the sphere of medical science, this motivation has led to the pioneering work of Dr. Harry Miller in nutrition, innovations in neurosurgery by Dr. Ben Carson and Dr. Melvin P. Judkins’ groundbreaking heart catheterization technique using catheters of his design.

In the sciences of paleontology and geology, the Adventist approach, inspired by confidence in the Bible, motivated Dr. Harold Coffin’s study of fossil forests in Yellowstone National Park, says Standish. This led to a new and more comprehensive model explaining their formation.

Dr. Leonard Brand has been inspired to examine the evidence of widespread rock layers that appear to have been rapidly laid down by water across North America. Also featured in the displays at the Adventist world headquarters will be research by Dr. Arthur Chadwick showing worldwide movement of water in distinct patterns.

The creation displays are free and open to the public. They will be on display at the world headquarters through March, 2018, and are designed to illustrate how faith in the biblical record of history has productively inspired science.

Ammonites were named after the Egyptian god Amun. They are beautiful examples of design for living in water. Even though they are now extinct, we can learn much about how wonderfully designed they were from their abundant fossils.

“By showing some of the abundant evidence that points toward a Creator God and a global flood, these displays will encourage confidence in the biblical record of history,” says Gibson. “In addition, the fossils and other evidence presented are intrinsically fascinating, revealing that ‘The works of the Lord are great, studied by all who have pleasure in them’” (Psalm 111:2 NKJV).

For more information and resources for Creation Sabbath, visit

News Release by Timothy G. Standish, PhD
Senior Scientist
Geoscience Research Institute

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North Pacific Union Conference Opens Creation Study Center

Christians believe in the biblical creation described throughout the Bible, yet a great need exists to be better educated about the creation. In response to this need, and also to share the creation with those not yet Christian, the North Pacific Union Conference of the Seventh-day Adventist Church in North America (NPUC) has initiated a Creation Study Center outreach service. This center is led by Dr. Stan Hudson, a pastor with training in geology, a life-long interest in nature and extensive experience successfully educating others about the creation.


Dr. Stan Hudson standing next to a large fossilized femur of the dinosaur genus Camarasaurus, on display at the Creation Study Center.

Jim Gibson, director of the General Conference Geoscience Research Institute (GRI), was on hand for the opening ceremonies. He commented that, “It’s really impressive to see what has been done with this resource center, and it reminds me of the significance of the creation in the life of a Christian… it’s the creation story that gives us confidence in His [Christ’s] salvation; it tells us that He is able to create in us a clean heart.”

Max Torkelsen II, recently retired President of the NPUC, whose vision lies behind the Creation Study Center, said: “When you look at the biblical record, there’s nothing more foundational than the creation story and it effects everything that we believe. … [T]he reason for the establishment of this Creation Study Center is to provide a place where people can come and get reliable, academic, scientific information that supports the biblical view.”

The NPUC Creation Study Center is headquartered in the NPUC offices in Ridgefield Washington. The study center contains exhibits with some amazing fossil specimens, including a dinosaur leg bone almost as tall as Stan Hudson. There is also beautiful artwork illustrating how the fossil record was formed and other resources to teach about the sciences of geology and paleontology from a biblical worldview. But the Creation Study Center will be more than a physical location with fascinating things for visitors to examine. There are plans for printed resources and a dynamic website where there will be more resources and videos. In addition to this, Dr. Hudson is also available to go out on visits to schools and churches. He will be a busy man this coming Creation Sabbath, October 28, 2017, when the entire Seventh-day Adventist Church celebrates the biblical doctrine of Creation.

Speaking for the Geoscience Research Institute, Dr. Gibson saluted the North Pacific Union Conference “for their vision of creating a creation resource center.” Adding, “I certainly would invite everyone to come and take a look at it.” Creation resource centers are something that the Geoscience Research Institute has worked to develop with Church entities around the world. Currently, there are GRI affiliated resource centers in South America, Europe, and Asia, with plans developing them on the African continent. Information about some of these can be found at:

The NPUC Creation Study Center, along with other creation resource centers, serves as a positive affirmation of the Seventh-day Adventist Church’s firm commitment to biblical creation. More information about the NPUC Creation Resource Center can be seen in the short videos below:

Virtual tour of the center

Dedication of the center

Mission of the center

News Release by Timothy G. Standish, PhD
Senior Scientist
Geoscience Research Institute

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Preservation of Dinosaur Soft Tissue: An Update

“You are dust, and to dust you shall return.” This verse from Genesis 3 captures very well the fate of beautifully designed organisms after the entrance of sin into the world. But how long does it take for the organic molecules we are made of to break down after death? In general, the longer the time from death, the larger the amount of decay that should be observed. This is particularly true for soft tissue, the parts of an organism that are not mineralized (such as skin, muscles, or blood vessels). In 1993, Mary Schweitzer, then affiliated with the Museum of the Rockies, shared data suggesting the possibility of soft tissue and biomolecules preservation in a bone of Tyrannosaurus rex supposedly 68 Ma old [1]. Her findings were met with great resistance and skepticism. Similar observations of blood vessels, collagen, and osteocytes from dinosaur bone had been published by Roman Pawlicki and his colleagues since 1966 [2], but had not stirred much debate, probably because Jurassic Park, which popularized the subject, had not been written and filmed yet.

In the last two decades, Mary Schweitzer and her group found additional examples and used a widening array of analytical techniques to document their findings [3-9]. Consequently, the possibility of preservation of original dinosaur soft tissue and biomolecules is becoming more accepted, and this blog post reviews some of what has been published on the subject in the last year and a half.

Dinosaur specimens with soft tissue preservation reported in 2016-2017

Three different dinosaur skeletons, with bones in articulation or association, were described in the literature with special mention of or an emphasis on the presence of soft tissue.

The first, a ceratopsian ornithischian (Psittacosaurus sp.) from the Lower Cretaceous of China (Fig. 1), has skin preserved as a compressed film with characteristic pigmentation patterns [10]. The pigments are thought to represent original organic matter, more specifically melanin residues. This interpretation was based on SEM microscopy, showing ovoid impressions similar to melanosomes (melanin-bearing organelles).

Fig. 1: The specimen of Psittacosaurus sp. (A) and interpretative drawing showing different skeletal elements and skin with pigment patterns (B). Image from Vinther et al. (2016), (CC BY).

The second, an ankylosaurine dinosaur (Zuul crurivastator) from the Upper Cretaceous of Montana, preserves integumentary structures such as osteoderms, with dark sheaths probably consisting of original keratin [11]. The paper describing the fossil does not present a chemical or microscopic analysis of the soft tissue, but mentions it as the subject for further future investigation.

The third dinosaur skeleton is also of an ankylosaur (Borealopelta markmitchelli), from the Lower Cretaceous of Alberta [12]. This articulated skeleton was found in marine deposits, in a formation where ichthyosaurs and plesiosaurs had been recovered but never a dinosaur. The encasing sediments show evidence of rapid burial of the carcass, with absence of scavenging in spite of some burrows in the surrounding deposits. The exceptional preservation of the fossil encompasses the molecular level, with remnants of organic matter in scales and horn sheaths of the body armor. Chemical analysis through mass spectroscopy indicated the presence of melanin in the organic residue, especially pheomelanin (a reddish-brown pigment). Melanosomes do not appear to have been preserved in this specimen.

Perhaps less impressive than soft tissue preservation, but equally interesting, is the evidence for preservation in dinosaur bone tissue of original molecular components that have a distinct chemical composition. This chemical signature was used to substantiate the presence of medullary bone (a type of bone produced by mature female birds during ovulation) in T. rex remains from the Upper Cretaceous of Montana [13].

Mark Armitage provided new documentation [14] of the exquisite preservation of blood vessels, osteocytes, and collagen at the submicron level in the Triceratops horridus horn and rib bones he discovered in Upper Cretaceous deposits of Montana [15]. The observations are based on microscopy and mostly from dissolved bone material. The next step in this project should be chemical analysis of the material. This example of soft tissue preservation is particularly stunning, given the relatively strong weathering of the horn (roots, fungal hyphae, and insect remains were found traversing the horn).

Mary Schweitzer and colleagues published a new study [16] on the remains of the hadrosaur Brachylophosaurus canadensis (Upper Cretaceous of Montana) that had previously yielded evidence for preservation of endogenous biomolecules [6]. Using a more rigorous protocol for sample preparation and higher resolution mass spectrometry techniques, they recovered 8 peptide sequences of collagen from the hadrosaur bone. Two of the sequences identified replicated some found in the previous study, whereas the other six were new.

Fig. 2: Vascular canal from rib bone of Lufengosaurus showing protein infilling material (transparent), partly outside of the cut canal (red arrow), and microcrystals of hematite (dark) within the canal. Image from Lee et al. (2017), (CC BY 4.0).

An important study presented results obtained on a sauropodomorph dinosaur (Lufengosaurus) from the Lower Jurassic of China [17]. Flat, transparent fragments of soft tissue located along and inside vascular canals in a rib bone (Fig. 2) were analyzed with infrared spectroscopy directly applied in situ and not on processed samples of bone. This non-destructive technique prevents the possibility of sample contamination during dissolution. The absorption spectrum observed was distinctive and typical of collagen. Moreover, particles of hematite (an iron oxide) were found in the vascular canals (Fig. 2) and lacunae left by osteocytes. The particles were interpreted as forming from iron ions attached to blood cells and iron-binding proteins. In the words of the authors, this study provided “undeniable, clear evidence that collagen and protein remains were preserved inside the osteonal central vascular canals of this early dinosaur.”

Finally, an intriguing abstract was presented at the 2017 meeting of the Canadian Society of Vertebrate Paleontology [18]. Fossils from the Upper Cretaceous Dinosaur Park Formation of Alberta showed an unexpectedly high rate of soft tissue preservation. A collection of bone samples from 25 specimens (16 of which dinosaurs), representing different degree of articulation and preserved either in sandstone or in mudstone, were dissolved and searched for soft tissue preservation. Of the 22 samples that successfully dissolved, 20 (including the dinosaur specimens) tested positive for soft tissues. It appears that soft tissue preservation in the Dinosaur Park Formation might be more common than expected, irrespective of the type of embedding sediment or degree of articulation of a specimen.

Recent papers discussing the preservation process

Understanding the pathway through which organic molecules can be preserved for tens to hundreds of millions of years is a significant challenge for those who subscribe to a “deep time” chronology. Proteins, for example, are thought to significantly degrade in shorter time frames of a few tens of thousands of years [19]. Therefore, several studies are attempting to explore potential mechanisms that could result in exceptional preservation of soft tissue in dinosaur remains.

Some have suggested that perhaps the blood vessels and osteocyte-like structures in dinosaur bones do not represent original organic material but are mimics created by bacterial biofilms colonizing the cavities of the bone [20]. However, Schweitzer et al. [21] presented data from actualistic experiments with bacterial biofilms to discard this hypothesis as inadequate. Interestingly, in the preparation of bone samples for their experiments they observed that removal of organics from bone is not easy, even with harsh treatment including repeated cycles of extreme heat, bleach, and enzyme treatment. Their suggestion is that when encased in dense cortical bone, labile organics can persist longer.

In their paper on preserved collagen from a Lufengosaurus bone, Lee et al. found that collagen was preserved only in the vascular canals, not in the bone matrix [17]. Given that the interior of the vascular canals often contained hematite particles, the authors suggested the collagen was preserved because it remained trapped between hematite concretions inside the vessels and the surrounding carbonated apatite minerals in the bone matrix.

Finally, some are still questioning the reliability of the results published by Mary Schweitzer and her group. For example, Buckley et al. [22] demonstrated that all the published putative dinosaur peptide sequences from T. rex and B. canadensis are matched by sequences of collagen from ostrich bone. Their suggested implication is that cross-contamination of the dinosaur samples with ostrich material in the lab cannot be ruled out.

Conclusive considerations

The discussion surrounding the preservation of dinosaur soft tissue is a fascinating example of a paradigm shift in science. Although still met with certain resistance, the evidence for endogenous biomolecular material in fossils has led to a proliferation of new observations and an openness to search for data that were previously overlooked, just because they were considered beyond the realm of possibility. It is clear that this field has a great potential for growth, including a better systematization of the type of molecules that are more commonly preserved in the fossil record and of possible differential levels of degradation and decay observed in these biomolecules at different stratigraphic levels.

This area of research is very relevant for origins model, because it has implications for the discussion on a long vs short chronology of life on the earth. Is it realistic to think that these original tissues were indeed preserved for tens of millions of years? Are they rather evidence for a much shorter time elapsed since the death of a fossilized organism, in the order of thousands of years? My impression is that the answer to these questions will not depend much on the evidence itself. When it comes to origins and historical sciences, “silver bullets” or unassailable proof of a model tend to be elusive. Those committed to a long chronology will probably attempt to normalize something that was formerly considered exceptional, presenting numerous scenarios of how preservation through “deep time” could be possible. Perhaps, a positive outcome of these efforts will be a better understanding of biomolecular structure, thermodynamics, decay pathways, and interaction with the surrounding chemical environment. However, those who subscribe to a biblical chronology will also have the opportunity to point out possible inadequacies of postulated mechanisms of preservation through “deep time.” Moreover, if soft tissue preservation turns out to be more common than previously thought, instead of “exceptional,” this line of evidence would also fit well with a short chronology and flood model of origins, not necessarily “proving” but being certainly compatible with a biblical worldview. Indeed, the most exquisite and pristine examples of original soft tissue preservation will likely remain a challenging puzzle for those who assign them ages covering periods of time so immense to be even hard to conceptualize.



[1] Schweitzer, M.H., Biomolecule preservation in Tyrannosaurus rex. Journal of Vertebrate Paleontology, 1993. 13(Supplement to n. 3): p. 56A.
[2] Pawlicki, R., A. Korbel, and H. Kubiak, Cells, Collagen Fibrils and Vessels in Dinosaur Bone. Nature, 1966. 211(5049): p. 655-657.
[3] Schweitzer, M.H., et al., Soft-tissue vessels and cellular preservation in Tyrannosaurus rex. Science, 2005. 307(5717): p. 1952-1955.
[4] Asara, J.M., et al., Protein sequences from Mastodon and Tyrannosaurus rex revealed by mass spectrometry. Science, 2007. 316(5822): p. 280-285.
[5] Organ, C.L., et al., Molecular phylogenetics of Mastodon and Tyrannosaurus rex. Science, 2008. 320(5875): p. 499.
[6] Schweitzer, M.H., et al., Biomolecular characterization and protein sequences of the Campanian Hadrosaur B. canadensis. Science, 2009. 324(5927): p. 626-631.
[7] San Antonio, J.D., et al., Dinosaur Peptides Suggest Mechanisms of Protein Survival. PLoS One, 2011. 6(6): p. e20381.
[8] Schweitzer, M.H., et al., Molecular analyses of dinosaur osteocytes support the presence of endogenous molecules. Bone, 2013. 52(1): p. 414-423.
[9] Schweitzer, M.H., et al., A role for iron and oxygen chemistry in preserving soft tissues, cells and molecules from deep time. Proceedings of the Royal Society B: Biological Sciences, 2014. 281(1775).
[10] Vinther, J., et al., 3D Camouflage in an Ornithischian Dinosaur. Current Biology, 2016. 26(18): p. 2456-2462.
[11] Arbour, V.M. and D.C. Evans, A new ankylosaurine dinosaur from the Judith River Formation of Montana, USA, based on an exceptional skeleton with soft tissue preservation. Royal Society Open Science, 2017. 4(5): p. 161086.
[12] Brown, C.M., et al., An Exceptionally Preserved Three-Dimensional Armored Dinosaur Reveals Insights into Coloration and Cretaceous Predator-Prey Dynamics. Current Biology, 2017.
[13] Schweitzer, M.H., et al., Chemistry supports the identification of gender-specific reproductive tissue in Tyrannosaurus rex. 2016. 6: p. 23099.
[14] Armitage, M.H., Preservation of Triceratops horridus tissue cells from the Hell Creek Formation, MT. Microscopy Today, 2016. 24: p. 18-23.
[15] Armitage, M.H. and K.L. Anderson, Soft sheets of fibrillar bone from a fossil of the supraorbital horn of the dinosaur Triceratops horridus. Acta Histochemica, 2013. 115(6): p. 603-608.
[16] Schroeter, E.R., et al., Expansion for the Brachylophosaurus canadensis Collagen I Sequence and Additional Evidence of the Preservation of Cretaceous Protein. Journal of Proteome Research, 2017. 16(2): p. 920-932.
[17] Lee, Y.-C., et al., Evidence of preserved collagen in an Early Jurassic sauropodomorph dinosaur revealed by synchrotron FTIR microspectroscopy. 2017. 8: p. 14220.
[18] van der Reest, A.J. and P.J. Currie, Preliminary results of an investigation into the preservation of soft tissue structures in bone from the Dinosaur Park Formation. Vertebrate Anatomy Morphology Palaeontology, 2017. 4: p. 49.
[19] Wadsworth, C. and M. Buckley, Proteome degradation in fossils: investigating the longevity of protein survival in ancient bone. Rapid Communications in Mass Spectrometry, 2014. 28: p. 605-615.
[20] Kaye, T.G., G. Gaugler, and Z. Sawlowicz, Dinosaurian soft tissues interpreted as bacterial biofilms. PLoS One, 2008. 3(7): p. e2808.
[21] Schweitzer, M.H., A.E. Moyer, and W. Zheng, Testing the Hypothesis of Biofilm as a Source for Soft Tissue and Cell-Like Structures Preserved in Dinosaur Bone. PLoS One, 2016. 11(2): p. e0150238.
[22] Buckley, M., et al., A fossil protein chimera; difficulties in discriminating dinosaur peptide sequences from modern cross-contamination. Proceedings of the Royal Society B: Biological Sciences, 2017. 284(1855).

Ronny Nalin, PhD, Geoscience Research Institute

Posted in Chemistry, Dating and the Age of the Earth, Dinosaurs, Fossils, Molecular, Uncategorized | Tagged , , , , , , , | 2 Comments

Homo naledi: An update

This blog post complements a piece written for the GRI blog on October 2015, linked here.

Two important papers were published in May 2017, warranting an update on the subject of Homo naledi.

Fig. 1: “Neo,” the partial skeleton recovered from the Lesedi chamber. Image from Hawks et al. (2017) (CC BY 4.0)

The first publication [1] reports the discovery of hominin remains from a different location in the Rising Star cave system. These include a partial skeleton (with a near complete cranium) (Fig. 1) and remains from at least two other individuals. The morphologic characteristics are “indistinguishable” from the H. naledi sample from the Dinaledi chamber published in 2015. The upper range of cranial capacity, when the latest specimen of H. naledi is included, increases to 610 ml.

The second publication [2] expands upon the initial description of the stratigraphy of the Dinaledi chamber deposits, and presents an estimated age for the H. naledi remains found there. The estimate is based on a variety of methods, with different degrees of reliability, but the authors converge on a period between 236 ka and 335 ka as their best age estimate.


The intentional disposal hypothesis

The discovering team has strongly advocated this hypothesis for the accumulation of the H. naledi remains in the Dinaledi chamber, especially in non-academic media outreach. The idea conveyed is some sort of funerary practice, with caching of carcasses in the same specific chamber in different occasions, possibly using torches to light the way to this remote location. However, the new discoveries show that remains of H naledi are not confined to the Dinaledi chamber. Also, the most recent results indicate that fossils found in the Dinaledi chamber are not from multiple levels, but they are all from the same level. This is a significant correction, because in the original paper [3] the H. naledi remains were described as coming from two separate layers. This evidence had been used to imply repeated events of “disposal” of carcasses and to exclude the mass mortality/death trap scenario.

Furthermore, in the original description of the Dinaledi chamber deposits, it was reported that the only macroscopic remains found in the sediments were from H. naledi. The new paper [2] specifies that two long bones (unidentified, but not hominin) are present in the cave deposits and also a baboon tooth has been found. These remains are interpreted as older than the H. naledi fossils. This is also an important correction because it was suggested that only very fine grained sediment could get into the chamber through sedimentary transport, but apparently other macroscopic remains (different from H. naledi fossils) found their way to deposition in the chamber.

The “young” age estimate

The mixture of “archaic” and “modern” characters in H. naledi had sparked some hopes that this form could fill the gap in the poorly documented early stages of the evolution of the genus Homo. This expectation was well exemplified by the PBS-NOVA documentary “Dawn of Humanity,” which ended with the assertion: “the tantalizing gap in the fossil record at the beginning of our genus is being slowly filled in. Finally, there is light at the dawn of humanity.” However, the age estimate places H. naledi more towards the dusk than dawn of humanity. In the words of Schroeder et al. (2017) [4], it represents another example “where species with small brains and H. erectus-like morphology persisted into more recent times, creating a profound disjunction between geological and morphological age.” Therefore, H. naledi complicates the attempts of creating an evolutionary sequence in the hominin fossil record and reinforces the conclusion of a mosaic distribution of characters in fossil forms. Interestingly, hybridization between different types is presented more and more as a possible explanation for this mosaic combinations of characters. Berger et al. (2017) [5], for example, explicitly mention the possibility that “H. naledi resulted from the hybridization of a more human-like population and a late-surviving australopith,” even if they see this as a currently untestable hypothesis.


[1] Hawks, J., et al., New fossil remains of Homo naledi from the Lesedi Chamber, South Africa. eLife, 2017. 6: p. e24232.
[2] Dirks, P.H.G.M., et al., The age of Homo naledi and associated sediments in the Rising Star Cave, South Africa. eLife, 2017. 6: p. e24231.
[3] Berger, L.R., et al., Homo naledi, a new species of the genus Homo from the Dinaledi Chamber, South Africa. eLife, 2015. 4.
[4] Schroeder, L., et al., Skull diversity in the Homo lineage and the relative position of Homo naledi. Journal of Human Evolution, 2017. 104: p. 124-135.
[5] Berger, L.R., et al., Homo naledi and Pleistocene hominin evolution in subequatorial Africa. eLife, 2017. 6: p. e24234.

Ronny Nalin, PhD, Geoscience Research Institute

Posted in Anatomy and Physiology, Evolutionary Theory, Fossils, Hominids, Uncategorized | Tagged , , , , , , | Leave a comment

Would You Move to an Exoplanet?

If given the choice where in our Milky Way galaxy you would prefer to live, where would you go? To one of those newly-discovered extra-solar planets the media get enthusiastic about when water has been detected there?

Before you answer these questions remember that, beyond the presence of water, many other conditions must be fulfilled before any planet can support the continued existence of life as-we-know-it, human life.

Over the last 40 years or so, astronomical studies have taught us that our life on Earth is dependent on a number of physical and other conditions far beyond just the presence of water. The majority of almost two hundred conditions refer to the necessary characteristics of our planet itself (temperature, chemical composition, stability, etc.) as well as to the properties of, and our location in, our Milky Way galaxy (are there nearby planets, sources of harmful radiation, etc.?).

These conditions include the following: Life on Earth requires a “just right” distance from our reliable source of energy, the sun. Earth’s chemical composition must contain those chemicals that are the main building blocks of human life: oxygen to breath, calcium to build skeletons, carbon to build carbohydrates and, together with hydrogen, nitrogen, oxygen and phosphorus, to make DNA. Earth needs a reasonably stable climate to allow food production to proceed along largely predictable lines; our Moon provides that stability for Earth’s rotation axis and its seasons. Our planet must not be too close to the centre of the Milky Way where deadly high-energy radiation would destroy life.

In fact, even the universe as a whole plays an important role in the habitability of our planet. This includes the almost perfect electrical balance between positively and negatively charged particles to ensure that the universe does not expand too fast for stars and planets to form. The word “perfect” in this sentence means an accuracy of 1 in 1037 [this is a 1 followed by 37 zeroes!]. A similar balance governs the mass density of the universe which should not vary by more than 1 in 1060; too high and the universe would have collapsed long ago, too low and the universe would expand too fast for galaxies, stars and planets to form. No wonder we talk about these specific conditions as ‘fine-tuning’!

The large number of requirements and their often narrow limits outside of which life could not exist already tell us that it may be difficult to find all of them fulfilled at a large number of different locations in the Milky Way. Add to this the fact that what we know about any extrasolar planets is still very rudimentary, and our search becomes like the one for a needle in a haystack.

Since Earth offers a successful habitat for many life forms, in a first approach we should focus on Earth-size planets in extrasolar planetary systems: the distance from their star, the presence of water, the nature of its atmosphere, etc. For each host star these conditions are only fulfilled in a fairly narrow zone around it inside of which the planet must be revolving. This zone is called the Circumstellar Habitable Zone (CHZ) of that star. It will be farther from a hotter star and closer to a cooler star (Fig. 1).

Fig. 1: CHZ (green) around three different stars; red zones are too hot, blue zones are too cold for life (courtesy NASA).

Thus, our search for suitable planets must first focus on finding suitable host stars, preferable a little less massive than the sun. Such stars are known as red dwarf stars, which constitute the overwhelming majority of stars in the Milky Way. The next step is to find small, i.e., Earth-size planets that are most likely to be rocky and have a suitable atmosphere. However, small planets are much harder to detect than their giant gaseous neighbours.

The temperature of the star and its planet’s distance from it tell us whether we can expect to find liquid water. In a few cases the planet’s atmospheric composition can be derived. Surely, before moving to any exoplanet, we want to know many more details that are not easily obtained. Therefore, even the simple question about the number of possible exoplanets fit for human life will probably not be answered today or tomorrow.

Because of the number of conditions to occur simultaneously, we do not expect to find many habitable exoplanets. The universe may turn out to be a rather inhospitable place for human life. Earth, if not unique, could well be one of a very small number of favourable planets. Considering the huge amount of fine-tuning required for a liveable planet, we should contemplate the possibility that the Creator of the universe has had a special purpose for creating Earth and its inhabitants, and that Earth’s uniqueness is a result of design rather than of accident.

Mart de Groot, PhD,  has been both an astronomer with 40 years of research experience and a pastoral minister for 16 years thereafter

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What is the evidence for a large asteroid impact at the Cretaceous-Paleogene (K-Pg) boundary?

The hypothesis of a large meteorite impacting the surface of the Earth at the end of the Cretaceous was introduced almost four decades ago.[1] In the ensuing years, the geologic community gathered a large body of data in support of this hypothesis, elevating it to the status of a universally accepted fact of Earth history. However, competing models and lively discussions are still unfolding over the dynamics and environmental consequences of this large impact. This short article attempts to a) summarize the evidence that led to the acceptance of the hypothesis; b) assess current areas of uncertainty related to the impact hypothesis; and c) consider ways in which this event is relevant for creationist thinking.

History of the hypothesis and geologic evidence

Fig. 1: Physicist Luis Alvarez and his geologist son Walter, next to the thin dark clay layer (above Walter’s right hand) sandwiched between limestone beds, outcropping near Gubbio, Italy. This is one of the initial localities where the iridium anomaly was first detected. Image courtesy of Berkeley Lab (CC BY-NC-ND 2.0)

The original physical evidence that led Alvarez et al.[1] to suggest the impact hypothesis was an anomalously high content of the heavy element iridium in thin clay deposits stratigraphically placed at the so-called K-Pg boundary (Fig. 1), the contact between Cretaceous and Paleogene rocks.[2] Iridium is much more abundant in meteorites than in the rocks of Earth’s crust. Therefore, Alvarez et al.[1] concluded that all the extra iridium found in the clay boundary layer must have come from the impact of a large extraterrestrial bolide, the dust of which settled after being projected and dispersed through the Earth’s atmosphere. The theory gained strength because the iridium anomaly was detected at the K-Pg boundary in many localities around the globe, a prediction of the impact hypothesis.[3] It was also noted that K-Pg boundary clays were enriched not only in iridium but also in other noble metals more abundant in meteorites than on Earth’s crust.[4] Furthermore, numerous tiny spherules of glass and other minerals were discovered in the boundary layer and interpreted as droplets of melt and vaporized rock, ejected after the impact and solidified during fallout.[5-7] K-Pg boundary deposits were also found to contain shocked grains, which are small mineral granules showing features diagnostic of shock-induced deformation (Fig. 2). Such shock features were expected to form in crystals of target rock hit by the impactor and ejected from the crater area.[8] Finally, a surprisingly large amount of soot, a form of elemental carbon produced in the burning of flames, was also detected in some boundary clay deposits, leading to the suggestion that the impact had ignited global wildfires.[9,10]

Microphotograph of shocked quartz grain with two sets of planar deformation features (PDFs) in impact melt rock. This example comes from the Suvasvesi South impact structure, Finland. Image courtesy of Martin Schmieder (CC BY 3.0)

In their 1980 paper,[1] Alvarez et al. had already made an estimate of the size of the asteroid (~10km), predicting a diameter for the impact crater of about 200 km. However, ten years after the publication of their paper no crater structure had yet been found. It seemed that the thickness of ejecta deposits (the material expelled from the crater after the impact) decreased away from North-Central America, an area where there was also evidence of tsunami-related deposition thought to have occurred near the impact site.[11,12] Therefore, the crater had to be located somewhere between North and South America. Eventually, Hildebrand et al.[13] localized a subsurface circular structure in the Yucatán Peninsula (Mexico) of matching size, expected stratigraphic position (at the top of Cretaceous strata), and with the right type of impact-related rocks and deposits to be identified as the impact crater. This structure was given the name of Chicxulub Crater. Finding that the last missing piece of the puzzle fulfilled former predictions helped to settle the case in favor of the impact hypothesis.

Developments and open questions

Since its discovery, the Chicxulub Crater has been studied with geophysical methods and wells have been drilled to better characterize the structure and its deposits.[14-19] It appears that the crater is a multi-ring structure, with large concentric fault systems and tilted blocks around its rim, and a central uplift where deep crust and even upper mantle material was upwarped by several kilometers. Impact-related deposits include impact melt, melt-bearing breccias, and large uplifted blocks of granitic basement with pervasive evidence of shock features. The thickness of these deposits varies, but can reach up to several km within the crater. Uncertainties remain about the specific dynamics that generated the multi-ring structure during the impact, the reason for asymmetries observed in the structure, and the lithology and horizontal and vertical distribution of different impact-related deposits in the crater.

Fig. 3: An example of distal ejecta deposits. In the Agost section (Spain), the K-Pg boundary is at the base of a dark, several cm-thick, clay layer (indicated by the arrow). Photo courtesy of Dr. Raul Esperante.

The study of the ejecta deposits has also significantly advanced after the discovery of the Chicxulub Crater. Their thickness, composition, and sedimentology seem to correspond well with the location of the impact at Chicxulub.[20] Proximal deposits are thicker (from meters to hundreds of meters thick) and generally indicative of more energetic deposition, whereas distal deposits are thin (from cm to mm thick) and deposited through settling (Fig. 3). Early reports had already suggested the possibility of tsunami-related deposition caused by the impact in proximal areas.[11] However, high-quality geophysical data have revealed the truly astonishing proportions of sedimentation processes triggered by the event.[21,22] For example, in the Gulf of Mexico, a region close to the impact site, the boundary layer can be very thick (up to 400m) and is traceable all across the basin. It appears to consist of debris flows and turbidites generated by earthquakes and tsunamis, causing significant erosion and resuspension of unconsolidated sediment. Not all the sediment in this boundary deposit, considered the most voluminous event deposit known to date in the geologic record, was derived from the impact crater. A substantial component was sourced from slope instability and erosion of shelf platforms close to the impact site.

However, a dissenting interpretation of the ejecta deposits has been strongly advocated by Gerta Keller (Princeton University) and colleagues.[23-27] This alternative view suggests that some of the deposits usually interpreted as forming rapidly by sediment gravity flows related to the impact formed instead over a prolonged period of time after the impact. Therefore, they do not represent the actual K-Pg boundary. The evidence in support of this view is based on detailed sedimentological and paleontological analyses, showing a more complex picture than usually assumed. It includes the presence of distinct and multiple spherule layers, occurrence of burrowing and sedimentary structures in the boundary deposits requiring a certain amount of time to form, and erosion and reworking at the K-Pg boundary that may impede precise age attribution. If the Chicxulub Crater predates the K-Pg boundary, it could be possible that a different, subsequent impact caused the iridium anomaly, and some possibilities for multiple impact scenarios have been discussed in the literature, although they have not gained much traction.[28-30] Most importantly, if the impact precedes the K-Pg boundary by a substantial amount of time, it cannot be the direct cause for the remarkable disappearance of many groups of fossils (including the famous extinction of the dinosaurs) observed across the boundary. The link between the impact and patterns of extinctions observed in sedimentary layers spanning the K-Pg boundary has always been the most controversial aspect of the hypothesis.[3] Many paleontologists believe that the distribution of different groups of organisms in the layers below and above the K-Pg boundary was not caused by the impact, and favor more gradualistic models of extinction caused by progressive deterioration of environmental conditions, perhaps aggravated by the impact.[31] The most commonly invoked alternative as the cause for mass extinction is large scale volcanism recorded in the Deccan Large Igneous Province (India), which also spans the K-Pg boundary.[31,32]

Modelling and reconstruction of the environmental effects of the impact is also an area where considerable differences in view have emerged. The original scenario proposed by Alvarez et al. [1] of ejected dust obscuring the sky for years and shutting down photosynthesis was found to overestimate the dust load in the ejecta plume,[33] but variants of the “impact winter” hypothesis are commonly discussed in the literature.[34,35] The hypothesis of global wildfires was also reconsidered, because levels of charcoal in the boundary layer are low and soot probably derived from the ignition of organic matter in the target rocks rather than from burning forests.[36,37] Models also show that the thermal radiation caused by reentry of ejecta particles in the atmosphere was probably not sufficient to cause global wildfires.[38,39] Other suggested effects in the aftermath of the impact include acid rains and absorption of solar radiation by sulfur aerosols produced by the vaporization of sulfur-bearing sediments in the impact target rocks.[20]

Finally, an important focus of research on the impact hypothesis has been the characterization of the type of impactor, based on geochemical signatures left in the ejecta deposits, with the consensus seeming to indicate a carbonaceous chondrite.[40,41]

Implications for creationist thinking

Philosophical implications: The impact hypothesis has been instrumental in breaking the mold of gradualistic thinking in geology, spurring a new way of looking at geologic data, with renewed openness to and interest in large scale and catastrophic processes. Although this trend had already been signaled by the acceptance of Bretz’s megaflood hypothesis, the exponential growth of publications addressing catastrophes in the Earth systems[42] was certainly favored by a change in the cultural milieu where the impact hypothesis of Alvarez et al. played an important role. Creationist thinking is sympathetic to the development of catastrophic models, because a short chronology requires a great amount of geologic activity to occur over a short amount of time and because the biblical account mentions a short but globally cataclysmic flood. Therefore, creationists have benefited and will continue to benefit from the development of neocatastrophist hypotheses, with increased possibilities for common interests in research projects and collaborations with secular scholars.

Geological implications: A first consideration about the impact hypothesis is that its development and corroboration attest to the reliability of the discipline of stratigraphy. It was stratigraphy that led geochemists in their search around the world for a peak in the concentration of iridium, a peak that, in most disparate places, was where the work of stratigraphers had previously located the K-Pg boundary. This impressive example of the power and high resolution of stratigraphic correlation counters the arguments of those who are skeptical about the reliability of stratigraphy and about the value of the geologic column as a framework to spatially organize rock units.[43]

Secondly, impact-related processes and deposits are an open window to the remarkable signature of catastrophic events in the rock record and have the potential to revolutionize the gradualistic interpretive approach. In sedimentology, impact-related deposits provide an example of rapid (hours to days) basin-scale deposition of hundreds of meters of sediment.[21] and basin-scale erosion and remobilization of unconsolidated sediment.[22] In structural geology, crater formation requires extreme rock weakening, to the point of fluidization,[15] offering instructive scenarios for crust and mantle softening that could help model plate tectonic processes within a catastrophist framework. Cratering also offers an example of almost instantaneous formation of faults and tectonic features.[19] In igneous geology, models have shown that large impacts can produce massive amounts of melts almost instantaneously, leading to the suggestion that impacts might even have been responsible for the emplacement of some large igneous provinces.[44-46] At the same time, not everything in the geologic record of impacts is massive or disruptive. For example, some distal ejecta layers are only mm thin and often found sandwiched in relatively undisturbed fine grained marine deposits. Therefore, impact deposition epitomizes well the formidable complexity of the geologic record. The same event that accounts for hundreds of meters of sediment and complete disruption in one area is expressed elsewhere by a perfectly identifiable thin layer within hundreds of meters of unrelated rocks.

Finally, the physical evidence attributed to the impact is a prime example of how the rocks have a story to tell. There are indeed large shocked blocks of basement and tens of meters of breccia in the subsurface of the Yucatán Peninsula, tiny spherules forming thin layers can be found near or at the K-Pg boundary in several locations around the world, and an anomalously high concentration of iridium can be globally detected in a very precise stratigraphic interval. These observations, and many others more, can be placed together in a coherent picture.[47] in spite of all the uncertainties and limitations intrinsic to the practice of historical sciences. The reconstruction of what occurred might not be exactly right in all of its aspects, but the rocks are indeed there to challenge and alert us that something did happen.

Biblical implications: Perhaps, the most obvious question for creationists is where does the timing of the impact event fit within the framework of Earth history presented in the Scriptures. Historical narratives in the Bible do not contain a description of an impact event.[48] Consequently, we should be cautious when advocating for a specific position in the absence of explicit biblical references. The Bible does mention the global flood of Genesis as a time of major geologic activity, with the chiastic structure of Genesis 7:11 indicating the involvement of both endogenic and exogenic forces. Among the latter, signified by the “opening of the windows of heaven,” one could fit collisions of extraterrestrial objects. Indeed, in the creationist literature large meteoritic impacts on the Earth are most commonly associated with the flood event.[49-56]

Theological implications: The destructive and catastrophic nature of a large impact event has the potential to raise questions about God’s interaction with the creation and about the nature of His character. One could ask if meteoritic impacts are contingencies allowed to occur within a complex created universe or if they are a direct expression of God’s plan.

In particular, if God oversaw the unfolding of the impact event during the Genesis flood, was that accomplished through direct or secondary causation? Was there design and divine intent in the specifics of the location, energy, and timing of the impact? Answers to these questions can be placed on a spectrum between the two extremes of hyperdeterminism, where every minimal detail of geological phenomena has a predetermined purpose, and a naturalistic-like “closed system” view, where God is excluded from any further interaction with the world after the setting in motion of its laws. More significantly, one could ask how the God of love, the giver and protector of life,[57] could be so intimately associated with an utterly destructive event. In searching for answers to these difficult questions, the Genesis narrative clearly describes how the flood and its geologic processes occurred after the entrance of evil into the world and as a consequence of the total corruption of God’s original creation. The textual evidence powerfully presents the flood as the “undoing of creation.”[58] Therefore, God’s action can be seen as a withdrawal of His sustaining, ordering, and life-giving power, an expression of how things dissolve when we reject His presence. And yet, at the acme of the chiastic structure of the Genesis flood narration,[59] we are told that “God remembered Noah, and every living thing, and all the animals that were with him in the ark” (Gen 8:1). It is hard to imagine a way short of God’s miraculous protection that could preserve a human-made wood vessel and its passengers in the midst of such cataclysmic forces, of which the Chicxulub impact might have been just a small component. However, instead of taking our everyday existence as a granted necessity of nature, we should recognize behind its sustenance the same miraculous grace and mercy that carried the ark and its occupants through a perilous journey.

Ronny Nalin, PhD, Geoscience Research Institute



[1]Alvarez, L.W., et al., Extraterrestrial Cause for the Cretaceous-Tertiary Extinction. Science, 1980. 208(4448): p. 1095-1108.

[2]Originally, this stratigraphic boundary was referred to in the literature as the K-T (Cretaceous-Tertiary) boundary, a notation that was subsequently abandoned for K-Pg (Cretaceous-Paleogene), which better reflects current conventions in stratigraphic nomenclature.

[3]Alvarez, L.W., Experimental evidence that an asteroid impact led to the extinction of many species 65 million years ago. Proceedings of the National Academy of Sciences, 1983. 80(2): p. 627-642.

[4]Ganapathy, R., A Major Meteorite Impact on the Earth 65 Million Years Ago: Evidence from the Cretaceous-Tertiary Boundary Clay. Science, 1980. 209(4459): p. 921-923.

[5]Smit, J. and G. Klaver, Sanidine spherules at the Cretaceous–Tertiary boundary indicate a large impact event. Nature, 1981. 292(5818): p. 47-49.

[6]Montanari, A., et al., Spheroids at the Cretaceous-Tertiary boundary are altered impact droplets of basaltic composition. Geology, 1983. 11(11): p. 668-671.

[7]Sigurdsson, H. and S.D. Hondt, Glass from the Cretaceous/Tertiary boundary in Haiti. Nature, 1991. 349(6309): p. 482.

[8]Bohor, B.F., et al., Mineralogic evidence for an impact event at the Cretaceous-Tertiary boundary. Science, 1984. 224: p. 867-870.

[9]Wolbach, W.S., et al., Global fire at the Cretaceous-Tertiary boundary. Nature, 1988. 334(6184): p. 665-669.

[10]Wolbach, W.S., R.S. Lewis, and E. Anders, Cretaceous extinctions: evidence for wildfires and search for meteoritic material. Science, 1985. 230: p. 167-171.

[11]Bourgeois, J., et al., A tsunami deposit at the Cretaceous-Tertiary boundary in Texas. Science, 1988. 241(4865): p. 567.

[12]Hildebrand, A.R. and W.V. Boynton, Proximal Cretaceous-Tertiary boundary impact deposits in the Caribbean. Science, 1990. 248(4957): p. 843.

[13]Hildebrand, A.R., et al., Chicxulub Crater: A possible Cretaceous/Tertiary boundary impact crater on the Yucatán Peninsula, Mexico. Geology, 1991. 19(9): p. 867-871.

[14]Urrutia‐Fucugauchi, J., et al., The Chicxulub scientific drilling project (CSDP). Meteoritics & Planetary Science, 2004. 39(6): p. 787-790.

[15]Gulick, S., et al., Expedition 364 Preliminary Report: Chicxulub: Drilling the K-Pg Impact Crater. International Ocean Discovery Program, 2017.

[16]Christeson, G.L., et al., Mantle deformation beneath the Chicxulub impact crater. Earth and Planetary Science Letters, 2009. 284(1–2): p. 249-257.

[17]Morgan, J., et al., Size and morphology of the Chicxulub impact crater. Nature, 1997. 390(6659): p. 472-476.

[18]Morgan, J. and M. Warner, Chicxulub: The third dimension of a multi-ring impact basin. Geology, 1999. 27(5): p. 407-410.

[19]Gulick, S., et al., Geophysical characterization of the Chicxulub impact crater. Reviews of Geophysics, 2013. 51(1): p. 31-52.

[20]Schulte, P., et al., The Chicxulub Asteroid Impact and Mass Extinction at the Cretaceous-Paleogene Boundary. Science, 2010. 327(5970): p. 1214-1218.

[21]Sanford, J.C., J.W. Snedden, and S.P.S. Gulick, The Cretaceous-Paleogene boundary deposit in the Gulf of Mexico: Large-scale oceanic basin response to the Chicxulub impact. Journal of Geophysical Research: Solid Earth, 2016. 121(3): p. 1240-1261.

[22]Denne, R.A., et al., Massive Cretaceous-Paleogene boundary deposit, deep-water Gulf of Mexico: New evidence for widespread Chicxulub-induced slope failure. Geology, 2013. 41(9): p. 983-986.

[23]Mateo, P., et al., Mass wasting and hiatuses during the Cretaceous-Tertiary transition in the North Atlantic: Relationship to the Chicxulub impact? Palaeogeography, Palaeoclimatology, Palaeoecology, 2016. 441, Part 1: p. 96-115.

[24]Keller, G., et al., Chicxulub impact spherules in the North Atlantic and Caribbean: age constraints and Cretaceous–Tertiary boundary hiatus. Geological Magazine, 2013. 150(5): p. 885-907.

[25]Keller, G., et al., Cretaceous Extinctions: Evidence Overlooked. Science, 2010. 328(5981): p. 974-975.

[26]Keller, G., et al., Chicxulub impact predates K–T boundary: New evidence from Brazos, Texas. Earth and Planetary Science Letters, 2007. 255(3-4): p. 339-356.

[27]Keller, G., et al., Chicxulub impact predates the K-T boundary mass extinction. Proceedings of the National Academy of Sciences of the United States of America, 2004. 101(11): p. 3753-3758.

[28]Jolley, D., et al., Two large meteorite impacts at the Cretaceous-Paleogene boundary. Geology, 2010. 38(9): p. 835-838.

[29]Lerbekmo, J.F., The Chicxulub-Shiva extraterrestrial one-two killer punches to Earth 65 million years ago. Marine and Petroleum Geology, 2014. 49: p. 203-207.

[30]Archibald, J.D., et al., Cretaceous Extinctions: Multiple Causes. Science, 2010. 328(5981): p. 973-973.

[31]Courtillot, V. and F. Fluteau, Cretaceous Extinctions: The Volcanic Hypothesis. Science, 2010. 328(5981): p. 973-974.

[32]Keller, G., J. Punekar, and P. Mateo, Upheavals during the Late Maastrichtian: Volcanism, climate and faunal events preceding the end-Cretaceous mass extinction. Palaeogeography, Palaeoclimatology, Palaeoecology, 2016. 441, Part 1: p. 137-151.

[33]Pope, K.O., Impact dust not the cause of the Cretaceous-Tertiary mass extinction. Geology, 2002. 30(2): p. 99-102.

[34]Vellekoop, J., et al., Evidence for Cretaceous-Paleogene boundary bolide “impact winter” conditions from New Jersey, USA. Geology, 2016. 44(8): p. 619-622.

[35]Kaiho, K., et al., Global climate change driven by soot at the K-Pg boundary as the cause of the mass extinction. Scientific Reports, 2016. 6: p. 28427.

[36]Harvey, M.C., et al., Combustion of fossil organic matter at the Cretaceous-Paleogene (K-P) boundary. Geology, 2008. 36(5): p. 355-358.

[37]Belcher, C.M., et al., Fireball passes and nothing burns—The role of thermal radiation in the Cretaceous-Tertiary event: Evidence from the charcoal record of North America. Geology, 2003. 31(12): p. 1061-1064.

[38]Goldin, T.J. and H.J. Melosh, Self-shielding of thermal radiation by Chicxulub impact ejecta: Firestorm or fizzle? Geology, 2009. 37(12): p. 1135-1138.

[39]Morgan, J., N. Artemieva, and T. Goldin, Revisiting wildfires at the K-Pg boundary. Journal of Geophysical Research: Biogeosciences, 2013. 118(4): p. 1508-1520.

[40]Trinquier, A., J.-L. Birck, and C. Jean Allègre, The nature of the KT impactor. A 54Cr reappraisal. Earth and Planetary Science Letters, 2006. 241(3–4): p. 780-788.

[41]Goderis, S., et al., Reevaluation of siderophile element abundances and ratios across the Cretaceous–Paleogene (K–Pg) boundary: Implications for the nature of the projectile. Geochimica et Cosmochimica Acta, 2013. 120: p. 417-446.

[42]Marriner, N., C. Morhange, and S. Skrimshire, Geoscience meets the four horsemen?: Tracking the rise of neocatastrophism. Global and Planetary Change, 2010. 74(1): p. 43-48.

[43]Reed, J., P. Klevberg, and C. Froede Jr, Towards a diluvial stratigraphy, in The geologic column: Perspectives within diluvial geology, J. Reed and M.J. Oard, Editors. 2006, Creation Research Society Books. p. 31-51.

[44]Jones, A.P., et al., Impact induced melting and the development of large igneous provinces. Earth and Planetary Science Letters, 2002. 202(3): p. 551-561.

[45]Elkins-Tanton, L.T. and B.H. Hager, Giant meteoroid impacts can cause volcanism. Earth and Planetary Science Letters, 2005. 239(3–4): p. 219-232.

[46]Ingle, S. and M.F. Coffin, Impact origin for the greater Ontong Java Plateau? Earth and Planetary Science Letters, 2004. 218(1–2): p. 123-134.

[47]However, some do not find the evidence for an impact at Chicxulub convincing. See for example the recent in depth analysis by Clarey, T.L., Do the data support a large meteorite impact at Chicxulub? Answers Research Journal, 2017. 10: p. 71-88.

[48]Some of the language in Revelation 8:8-11 could be compatible with the description of the impact of extraterrestrial objects, but most modern commentators agree that the context of John’s vision is prophetic and presented in apocalyptic style. See, for example, J. Paulien, The End of Historicism? Reflections on the Adventist Approach to Biblical Apocalyptic—Part One. Journal of the Adventist Theological Society, 2003. 14(2): p. 15–43. It should also be noted that as of May 8, 2017, the Earth Impact Database  listed 190 confirmed impact structures identified on Earth, of which Chicxulub is listed as the second largest in diameter. This article focuses only on the K-Pg impact event, but biblical and theological considerations similar to those expressed for this specific event can also apply to the larger phenomenon of large meteoritic impacts on Earth.

[49]Gibson, L.J., A catastrophe with an impact. Origins, 1990. 17(1): p. 38-47.

[50]Oard, M.J., An impact Flood submodel—dealing with issues. Journal of Creation, 2012. 26(2): p. 73-81.

[51]Spencer, W.R., Geophysical effects of impacts during the Genesis Flood, in Proceedings of the Fourth International Conference on Creationism, R.E. Walsh, Editor. 1998, Creation Science Fellowship. p. 567-579.

[52]Spencer, W.R., Catastrophic impact bombardment surrounding the Genesis Flood, in Proceedings of the Fourth International Conference on Creationism: , R.E. Walsh, Editor. 1998, Creation Science Fellowship. p. 553-566.

[53]Oard, M.J., Precambrian impacts and the Genesis Flood. Journal of Creation 2014. 28(3): p. 99–105.

[54]Spencer, W.R., Impacts and Noah’s Flood—how many and other issues. Journal of Creation, 2013. 27(1): p. 85-89.

[55]Unfred, D.W., Asteroidal impacts and the Flood-judgment Creation Research Society Quarterly 1984. 21: p. 82-87.

[56]Froede, C.R.J. and D.B. DeYoung, Impact events within the young-earth Flood model. Creation Research Society Quarterly, 1996. 33: p. 23-34.

[57]See Gen.4:10,17; Gen 9:5; Ex 20:13.

[58]For a summary of scholarly work supporting the “undoing of creation” motif, see Davidson, R.M., The Genesis flood narrative: Crucial issues in the current debate. Andrews University Seminary Studies, 2004. 42(1): p. 49-77.

[59]Shea, W.H., The structure of the Genesis Flood narrative and its implications. Origins, 1979. 6(1): p. 8-29.

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Organisms in their niche: passive modeling clay or problem-solving entities?

One person’s cultural background can bias their view about people from other cultures…even before they have ever met. Could people also have a bias about how they think about other creatures? It may even be possible that scientific culture could prejudice the way researchers see creature-environmental relations with the potential to bias whole research programs.

Last November, Great Britain’s prestigious Royal Society held a conference to deliberate if evolutionary theory needed an “extension” to accommodate fresh ideas from new discoveries. Nature had also opened the question for debate (Fig. 1). Supporters of status quo evolutionary theory held that new findings could readily be explained within the current structure. While an advocate of the new “Extended Evolutionary Synthesis,” Gerd Muller of the University of Vienna had previously stated that one value of the extension would overcome the “restrictions” of “externalism.”[1] Externalism is principally a way to think about how organisms formed, yet it may bias how we think and write about a creature’s behavior. What is externalism supposed to explain for evolutionary theory and what elements of it does Muller hope to escape?

Fig. 1: Nature recognized the growing number of researchers dissenting from aspects of the Darwinian model and opened a discussion in 2014. Laland, K. et al. 2014. Does evolutionary theory need a rethink? Nature. 514 (7521):161-164.

As it turns out, disputes over whether the source of an organism’s form derives from external or internal causes have been longstanding. Stephen Jay Gould frames this historical discussion: “The designation of one principle or the other [internalism/structuralism or externalism/functionalism] as the causal foundation of biology virtually defines the position of any scientist towards the organic world and its causes of order. Shall we regard the plan of high-level taxonomic form as primary, with local adaptations viewed as a set of minor wrinkles (often confusing) upon an abstract majesty? Or do local adaptations build the entire system from the bottom up?…This dichotomy continues to define a major issue in modern evolutionary debates: does functional adaptation or structural constraint maintain priority in setting evolutionary pathways and directions?”[2]

In this case, the phenomenon most in need of explanation is: why do organisms appear to fit their environments so well? They have traits that seem to precisely relate to, and even exploit properties of nature (e.g., inertia and gravity) and other external conditions. Externalists, see these traits as imposed on organisms from the outside. This generally happens by the very external conditions, designated as “selective pressures,” which match so well to the trait. Michael Denton explains that according to the paradigm “often referred to as functionalism, the main designs of life (pentadactyl limb, body plans, etc.) are not the result of physical law, that is, not immanent in nature or arising from intrinsic physical constraints inherent in biological matter, but rather the result of specific adaptations built additively by selection during the course of evolution, to serve particular functional ends, ends that are imposed by the environment and that are external to the organism itself.”[3]

Few people recognize that in the externalist approach organisms are viewed essentially as passive lumps of clay being molded by their environment. In fact, two researchers stated that is exactly how Charles Darwin’s theory encapsulates the organism-environment relationship, “He [Darwin] accepted the view that the environment directly instructs the organism how to vary, and he proposed a mechanism for inheriting those changes…The organism was like modeling clay, and remolding of the clay meant that each of the billions of little grains was free to move a little bit in any direction to generate new form…If an organism needed a wing, an opposable thumb, longer legs, webbed feet, or placental development, any of these would emerge under the proper selective conditions with time.”[4] Which Marta Linde Medina, another leading theoretician in this field, sums up, “as a result, organisms are as passive as the matter that forms them.”[5]

Externalism has a strong philosophical appeal to those who advocate for explanations of biological phenomena that are fully naturalistic. It is certainly not teleological. Externalism also can feed into the view that if God didn’t create nature, nature can somehow create itself—including crafting living things. Interestingly, externalism is analogously central to both Darwin’s theory of evolution and influential psychologist B.F. Skinner’s theory of human behavior. “First, both theories draw on an externalist or ‘outside-in’ pattern of explanation, in which the structure or behaviour of living things is seen as a consequence of their environments. Second, both rely on a process that can be described loosely as ‘trial and error.’”[6]

Externalism is currently the dominant view in biology. Denton elaborates on the probability that any view other than externalism would be “very alien” and essentially “inconceivable to most English-speaking biologists.”[7] But what if it is wrong in the sense that it has identified causality backwards? This updated insight may be indicated by waves of discoveries documented by Gerd Muller and others. They’ve found a principal role for internal factors.

What if populations of organisms could be seen from a design-based perspective as traveling through diverse environments just as human-designed vehicles do? Designed capacity of an entity is always an internal feature as designers build into their craft the ability to successfully engage all anticipated external conditions. Similarly, innate self-adjusting capacity should be true for organisms. Thus, intrinsic design could control both its basic body plan and 100% of its ability to adapt itself to external conditions. Internal programming also specifies certain external conditions to be a stimulus or a cue for both man-made things and organisms. Inherently designed systems control detection of challenging exposures and would specify internally driven self-adjustments primarily as targeted solutions to environmental challenges and rarely, if ever, by “trial-and-error.” Individuals (or populations over multiple generations) could actively detect environmental conditions and could express a spectrum of phenotypes from a relatively stable genotype controlled by innate systems.

Enriching the phenotypic panoply is the capacity of several biological systems to “learn” from environmental interactions by processes similar to IBM’s “Watson” computing system; meaning, organisms are designed with a nature already devised to be nurtured. It may be demonstrated that organisms are causal for the successful fit of their traits-to-exposures, rather than externalism’s notion of personified environments seeing, selecting, and saving traits to build organisms.

Perhaps, the tight organism-environment relationship may be explained by populations of active, problem-solving organisms continuously tracking environmental changes via innate mechanisms to express heritable phenotypes bearing problem solving potential—which already precede environmental challenges. This is worth thinking about as an internalist approach may well be confirmed by continuing research.

Randy J. Guliuzza, P.E., M.D. is a licensed professional engineer and medical doctor previously Board Certified in Aerospace Medicine who now specializes in researching engineering principles of biological adaptation.



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[3]Denton, M. J. 2013. The Types: A Persistent Structuralist Challenge to Darwinian Pan-Selectionism. BIO-Complexity, (3):1−18. doi:10.5048/BIO-C.2013.3

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[7]Denton, M. Two Views of Biology: Structuralism vs. Functionalism. Posted on February 3, 2016 accessed on March 28, 2017.

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