Tag Archives: paleontology

June 28, 2013 · 6:13 pm

The NMNH fossil halls, circa 1963

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A revamp for the dinosaur displays in Hall 2. Courtesy of the Smithsonian Institution Archives.

Since the NMNH building opened in 1910 as the United States National Museum, the east wing has been home to fossil displays. Although there have been many small adjustments and additions to the exhibits over the years, we can separate the east wing’s layout into three main periods. From 1910 t0 1945, the exhibits were primarily under the stewardship of Charles Gilmore. Called the “Hall of Extinct Monsters”, this iteration was somewhat haphazard in its layout and generally resembled a classic “cabinet of curiosity” approach to exhibit design. Gilmore’s version of the east wing remained in place until 1963, when the space was redesigned as part of the Smithsonian-wide modernization project. In the updated halls, there was a directed effort to compartmentalize exhibits based on the subdivisions of the Museum’s research staff, with each area of the gallery becoming the responsibility of a different curator. A second renovation was carried out in several stages starting in 1980. This version, which was open until 2014, was part of the new museology wave that started in the late 1970s. As such, the exhibits form a more cohesive narrative of the history of life on earth, and much of the signage carries the voice of educators, rather than curators.

Of course, the field of paleontology has advanced by leaps and bounds since the early 1980s, and NMNH staff have made piecemeal updates to the galleries when possible, including restorations of deteriorating mounts, and additional signage that addresses the dinosaurian origin of birds and the importance of the fossil record for understanding climate change. A third renovation is currently underway and will be completed in 2019.

But I’m getting ahead of myself. The purpose of this post is to provide an overview of the NMNH fossil halls as they stood in 1963, after the first major renovation. This iteration of the east wing was long gone before I was born, so this information is pieced together from historic photographs, archived exhibit scripts, and correspondence among the individuals involved in the modernization project (my thanks to the staff of the Smithsonian Institution Archives for their assistance in accessing these materials). Perhaps unsurprisingly, records of the dinosaur gallery are by far the most thorough. Information on the other halls is considerably harder to come by, so if any readers who saw the older exhibits in person remember any details, it would be fantastic if you could share them.

Layout of the USNM east wing, circa 1963.

Layout of the USNM east wing, circa 1963.

As mentioned, the Smithsonian underwent a thorough modernization project in the middle of the 20th century. The modernization committee, chaired by Frank Taylor (the eventual director-general of Smithsonian museums), was established in 1948. Under the committee’s guidance, most of the institution’s exhibits were redesigned between 1953 and 1963. Keep in mind that at the time, the United States National Museum was the only Smithsonian museum – it would not be divided into the National Museum of Natural History and the National Museum of History and Technology (now the National Museum of American History) until 1964.

Completed in 1963, the USNM fossil exhibits were among the last to be modernized. Only a small number of specimens were added that had not already been on view in the previous version of the space – in fact, many specimens were removed. The changes primarily focused on the layout of the exhibit, turning what was a loosely organized set of displays into a series of themed galleries. The east wing included four halls in 1963, the layout of which can be seen in the map above. Each hall was the responsibility of a particular curator. Nicholas Hotton oversaw Paleozoic and Mesozoic reptiles in Hall 2. David Dunkle was in charge of fossil fish in Hall 3. Porter Kier oversaw fossil invertebrates and plants in Hall 4. Finally, Charles Gazin, head curator of the Paleontology Division, was responsible for Cenozoic mammals in Hall 5. Each curator had a central role in selecting specimens for display and writing accompanying label copy.

Invertebrates and Fossil Plants

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Echinoderm fossil display in Hall 4. Courtesy of the Smithsonian Institution Archives.

It is likely that part of the reason the fossil halls were late on the modernization schedule was that the curators of the Paleontology Division were not terribly interested in exhibits or outreach. There were no staff members in the division exclusively devoted to exhibit work, so the task of designing the new exhibit space was an added burden for the research staff. As invertebrate paleontology curator G. Arthur Cooper put it in a 1950 memo, “all divisions of Geology at present are in an apathetic state toward exhibition.”

Nevertheless, work on the east wing halls had begun by 1957, if not a bit earlier. The first of the new exhibits to be worked on was Hall 4, featuring fossil invertebrates and plants. The long and narrow space was divided into four sections: the first introduced the study of fossils and how they are preserved, the second was devoted to paleobotany, the third contained terrestrial and marine invertebrates, and the forth provided an overview of geological time. Cooper described the new exhibit as a progressive story of the expansion of life, “its stem connecting all life which is now culminating in man.”

Carboniferous coal swamp fossils in Hall 4. Photo courtesy of the Smithsonian Institution Archives.

In addition to a variety of fossil specimens, Hall 4 featured a series of dioramas built by George Merchand, an exhibit specialist from Ann Arbor, Michigan. Merchand built at least 4 dioramas between 1957 and 1958, each depicting representative invertebrate marine fauna from a different Paleozoic period. Most, if not all, of these dioramas were retained during the 1980s renovation and remained on view through 2014.

Fossil Fishes and Amphibians

Fossil fishes in Hall 3. Photo courtesy of the Smithsonian Institution Archives.

Fossil fish and a smattering of amphibians were located in Hall 3, on the far east side of the wing. This space would be converted into “Mammals in the Limelight” in the 1980s. David Dunkle, for whom everyone’s favorite placoderm Dunkleosteus is named, was in charge of this gallery during his tenure at USNM between 1946 and 1968. The specimens on view were arranged temporally, starting with placoderms on the south side and progressing into actinopterygians and basal amphibians on the north end. Among the more prominently displayed specimens were Xiphactinus, Seymouria, and “Buettneria” (=Koskinonodon). The hall also contained a replica of the recently discovered modern coelacanth, and small diorama of a Carboniferous coal swamp.

Dinosaurs and Other Reptiles

Dinosaurs in Hall 2, as seen facing west. Photo courtesy of the Smithsonian Institution Archives.

Hall 2, featuring dinosaurs and other reptiles, was the main draw for most visitors. It was not, however, a major priority for the Smithsonian research staff. The museum had not had a dinosaur specialist since Gilmore passed away in 1945 and indeed, dinosaurs were not an especially popular area of study among mid-century paleontologists in general. As such, responsibility for Hall 2 fell to Nicholas Hotton, at the time a brand-new Associate Curator. Later in his career, Hotton would be best known as an opponent to the dinosaur endothermy movement, but in the early 1960s he was most interested in early amniotes and the origin of mammals.

Hotton’s display of South African synapsids and amphibians. Photo courtesy of the Smithsonian Institution Archives.

Perhaps due to the general disinterest among USNM curators, changes to the dinosaur exhibits were mostly organizational. Most of the free-standing dinosaur mounts built by Gilmore and his team were collected on a single central pedestal. Preferring not to tackle the massive undertaking of disassembling and remounting the 70-foot Diplodocus skeleton, the exhibit designers left the sauropod in place and clustered the smaller moutns around it. In the new arrangement, the Diplodocus was flanked by the two Camptosaurus and prone Camarasaurus on its right and by Triceratops and “Brachyceratops“ on its left. The Stegosaurus stenops holotype, splayed on its side in a recreation of how it was first discovered, was placed behind the sauropods at the back of the platform.

Close up of Thescelosaurus on the south wall. Photo courtesy of the Smithsonian Institution Archives.

 The north and south walls of Hall 2 were lined with additional specimens. On the south side, Gilmore’s relief mounts of Ceratosaurus and Edmontosaurus (called “Anatosaurus” in this exhibit) were joined by the gallery’s one new dinosaur, a relief mount of Gorgosaurus in a death pose. The north wall featured a long, narrow, glass-enclosed case illustrating the basics of dinosaur classification. In addition to saurischian and ornithischian pelves, the case featured skulls representing most of the major dinosaur groups. Amusingly, all but two of these skulls (Triceratops and Diplodocus) were labeled with names that are no longer considered valid. These skulls included “Antrodemus” (Allosaurus), “Trachodon” (Edmontosaurus) “Procheneosaurus” (probably Corythosaurus)  and “Monoclonius” (Centrosaurus).

In the southwest corner of Hall 2 (where FossiLab is today), visitors could see the Museum’s two free-standing Stegosaurus: the fossil mount constructed by Gilmore in 1913 and the charmingly ugly papier mache version, which had received a fresh coat of paint. Finally, the rear (east) wall of Hall 2 held Gilmore’s relief mounted Tylosaurus.

Mammals

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Brontotherium and Matternes’ Oligocene mural in Hall 5. Photo courtesy of the Smithsonian Institution Archives.

Fossil mammals were exhibited in Hall 5, a corridor-like space accessible from the main rotunda and via two doorways on the north side of Hall 2. After 1990, this space would house the “Life in the Ancient Seas” exhibit. Charles Gazin, head curator of the Division of Paleontology, was in charge of this space on paper, but my impression is that his attention was elsewhere during its design and construction. Gazin was apparently approached by the modernization committee several times during the 1950s, but was reluctant to commit his time to a major renovation project. Gazin had been spending a great deal of time at a Pliocene dig site in Panama, and the collection of new fossils proved more interesting than designing displays. As Gazin tersely explained, “It is a little difficult to concentrate objectively on exhibition problems here in the interior of Panama.”

Basilosaurus and Cenozoic reptiles in Hall 5. Photo courtesy of the Smithsonian Institution Archives.

Nevertheless, Gazin’s interest in Cenozoic mammals ensured that his gallery was exceptionally thorough. Thanks to Gazin’s own collecting expeditions throughout the 1950s, the new fossil mammals galleries contained representatives of nearly all major mammal groups, from every epoch from the Paleocene through the Pliocene (the Pleistocene was deliberately excluded, as a separate ice age exhibit was also in the works). Classic mounts from the Gilmore era like Basilosaurus and Teleoceras were joined by dozens of less showy specimens like rodents, small perissodactyls, and early primates. The new exhibit also introduced the first wave of Jay Matternes’ much-beloved murals, illustrating the changing flora and fauna in North America over the course of the Cenozoic.

Unveiling and Reactions

The new east wing galleries officially opened on June 25, 1963. According to the press release, “the new exhibit features in colorful and dramatic settings more than 24 skeletons and skulls of the largest land animals the world has ever known.” The exhibits were officially unveiled with a late afternoon ceremony, in which Carol Hotton (Nicholas Hotton’s daughter) cut the ribbon and the lights to Hall 2 were suddenly turned on to dramatic effect.

Unfortunately, the new exhibits were not universally loved by the museum staff. The wing had been planned a set of compartmentalized exhibits, each corresponding to a subdivision of the Division of Paleontology, with a different curator taking responsibility for each hall. While seeming sensible on paper, this plan turned out to be a logistical nightmare, and a common cause for complaint among Division staff for the next decade. In addition, Gazin in particular voiced concerns as early as January 1964 that the design of the new halls was entirely inadequate for preventing accidental or deliberate damage to specimens by visitors. The mounts in Hall 2 were raised only about a foot off the ground, and were not protected by any sort of guard rail or barrier. As a result, within a few months of the exhibit’s unveiling, several ribs and vertebral processes had been broken off or stolen from Camarasaurus, Gorgosaurus, Ceratosaurus and others.

With the notable caveat that I never saw the 1963 exhibits in person, I would say that this is aesthetically my least favorite iteration of the east wing. The grandiose, institutional Greco-Roman architecture originally displayed in the Hall of Extinct Monsters was replaced with what can only be described as extremely 1960s design. Solid earth-tone colors, wood paneling and wall-to-wall carpeting gave the halls a much more austere character. While the efforts to categorize specimens into thematic zones was commendable for a museum of that era, the label copy (written by the curators) was still highly pedantic and verbose. As such, the 1963 fossil halls seem to have been very much of their time. While the designers were working to avoid the overt religiosity and grandeur of turn of the century museums, they had not yet reached the point of developing truly audience-centered educational experiences. The result was an exhibit that was humble, yet still largely inacessible. Perhaps for this reason, the 1963 fossil halls were the shortest-lived at NMNH to date, being replaced within 20 years of their debut.

This post was updated and edited on January 8, 2018.

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May 25, 2013 · 9:27 pm

A Triceratops for Lawrence

In an earlier post, I described how the Smithsonian’s Triceratops was the first free-standing mount of this animal ever created, and the eccentricities of its proportions and posture would define how the species would be depicted in artwork and other reconstructions for the better part of a century. I should have clarified, however, that this was not the first time Triceratops fossils were put on public exhibit. That honor goes to the University of Kansas Natural History Museum, which was founded in 1864 and is still operational today.

Among the Museum’s basement paleontology exhibits is a case of dinosaur fossils that has literally gone unchanged since the 1950s. Although this time capsule of mid-century museum design is of some historical interest, it would be nice if those sauropod limb bones weren’t labeled “Brontosaurus” (to be clear, the whole museum doesn’t look like this, the staff has been slowly but surely modernizing the exhibits). Of particular importance is the Triceratops skull (specimen 422) on the left side of the case. While there is no historical information on its label, this specimen has been with the museum for over 115 years, having been unearthed and put on display only six years after O.C. Marsh first named and described Triceratops.

The dinosaur case at the KU Natural History Museum, untouched since the 1950s.

The dinosaur case at the KU Natural History Museum, untouched since the 1950s.

The story of the KU Triceratops is not well-known, although it is the subject of the somewhat hard-to-find book (neither the Museum nor the KU library has a copy) A Triceratops Hunt in Pioneer Wyoming. In the summer of 1895, a team from the University ventured into the frontier lands of of eastern Wyoming with the explicit goal of finding a Triceratops for display at the young Natural History Museum. The team was led by Samuel Wendell Williston, founder of the University’s geology department. Although Williston’s specialty was entomology, he had previously worked under Marsh at Yale and was well-acquainted with the plethora of dinosaurs on which his mentor had published. Also on the expedition were KU Regent James Polk Sams, and two individuals whose names are quite familiar to anyone with an interest in the history of paleontology, Barnum Brown and Elmer Riggs. Brown would, of course, go on to be the star fossil hunter at the American Museum of Natural History, while Riggs would become a curator at the Field Museum of Natural History. In 1895, however, both were students, and not especially interested in fossil collecting or paleontology. 

The team found the Triceratops they were looking for on July 9, near the confluence of Lightning and Lance Creeks. By July 22, the skull was fully excavated and crated for a journey by train back to Lawrence. The fossil apparently garnered a fair amount of attention on the journey; while Triceratops is well known today, in 1895 few had any idea that animals such as this had ever walked the Earth. And yet, here was clear, physical evidence of an extinct animal like nothing alive in the modern world, and it would soon be displayed for all to see in the University of Kansas Museum.

Triceratops skull retrieved by the 1895 Wyoming expedition.

Triceratops skull retrieved by the 1895 Wyoming expedition.

The 1895 expedition was not tremendously productive scientifically, the fossils found that summer resulting in only three short papers. However, the journey, and the Triceratops skull that was brought back, did end up being quite important for paleontology. The expedition inspired Brown and Riggs to pursue careers in paleontology, and as Brinkman and colleagues write in A Triceratops Hunt in Pioneer Wyoming, “they would hunt bones for the rest of their lives, to the great benefit of science, and might never have done so had not circumstances landed them in the circle of Williston’s influence in the summer of 1895.”

Furthermore, by setting out with the clear goal to find a dinosaur for display, the University of Kansas team were trailblazers in a movement that would lead to the inseparable connection between dinosaurs and museums in popular culture today. In the first decade of the 20th century, newly burgeoning large urban museums openly competed to find and display the largest and most spectacular dinosaurs. Exhibits like the AMNH Brontosaurus, the Carnegie Museum of Natural History Diplodocus and, of course, the Smithsonian Triceratops brought millions of Americans into museums, ensuring that to this day, when we think of museums, we think of dinosaur skeletons (and vice versa). In spite of the somewhat dingy basement display it currently finds itself in, the University of Kansas Triceratops was an early trendsetter and a profound example of the intersection of science and history.

Reference

Kohl, M.F., Martin, L.D. and Brinkman, P., eds. (2004). A Triceratops Hunt in Pioneer Wyoming: The Journals of Barnum Brown and J.P. Sams. Glendoo, WY: High Plains Press.

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March 18, 2013 · 4:45 pm

A Visit to the Academy of Natural Sciences

I spent yesterday in Philadelphia, my first visit in at least 10 years, and of course made a point of visiting the Academy of Natural Sciences. Founded in 1812, the Academy is the oldest natural science research institution and museum in North America, established “for the encouragement and cultivation of the sciences, and the advancement of useful learning.” Initially formed as a hub for research on the American frontier, the Academy has sponsored scientific expeditions across the world and has amassed a collection of 17 million specimens that is still actively used 200 years after its founding.

In 1868, the Academy museum made a landmark contribution to paleontology by hosting the first mounted dinosaur skeleton ever constructed. The mount, the work of paleontologist Joseph Leidy and sculptor Benjamin Waterhouse Hawkins, depicted Hadrosaurus foulki, the first dinosaur discovered in North America and at the time the most complete dinosaur ever found. With only two limbs, a section of the spinal column and some other odds and ends to work with, Hawkins invented many of the mounting techniques that are still in use today. For instance, Hawkins created mirrored duplicates of the left limb bones for use on the animal’s right side, and reconstructed best-guess stand-ins for the skull, scapulae and most of the vertebrae using extant animals as reference. By modern standards, the Leidy-Hawkins Hadrosaurus mount wasn’t especially accurate (the sculpted scapulae and vertebrae resemble those of a mammal, not a reptile; the skull, based on that of an iguana, turned out to be completely off the mark; the fully upright, kangaroo-like posture is now known to be anatomically implausible), but it nevertheless presented the first-ever opportunity to stand in the presence of a dinosaur. Extinct animals were already known to the public, and some had even been mounted, but the Hadrosaurus was so bizarre,  so utterly unlike anything alive today, that it really opened people’s eyes to the unexplored depths of the Earth’s primordial history.

Original 1868 Hadrosaurus mount.

Original 1868 Hadrosaurus mount.

The Hadrosaurus display caused public visitation to skyrocket, prompting the Academy to relocate in 1876 to a larger building in central Philadelphia, where it remains today. I haven’t been able to find any photographs or detailed information about it, but for much of the 20th century the Academy had a fossil exhibit with a Corythosaurus mount as its centerpiece. This was replaced in 1986 with an expanded “Discovering Dinosaurs” exhibit, which apparently was among the first to showcase the discoveries of the dinosaur renaissance. This exhibit has just about zero web presence, as well (seriously, any help tracking down details about it would be greatly appreciated). The current version of the Dinosaur Hall opened in 1998, and is what I will discuss below.

This cast of the AMNH Tyrannosaurus is the centerpiece of the Dinosaur gallery. Source: Wikipedia Commons.

What’s Cool

Although crammed into a fairly small space, the Academy’s two-level Dinosaur Hall is packed with mounts of North American fossil reptiles, including Tyrannosaurus, Chasmosaurus, Deinonychus, Tylosaurus, Pachycephalosaurus and many more. Compared to the sterile and coldly scientific displays at larger museums like the American Museum of Natural History, the Academy’s exhibit designers clearly put an emphasis on accessibility, particularly for younger visitors. Signs are attractive, colorful and use simple language, but do not sacrifice scientific accuracy. Although “Do Not Touch” notices abound, guardrails are low and allow visitors to view the mounts up close. Even the fossil prep lab, a staple in paleontology exhibits, is not behind glass but is separated from visitors by a low wall, allowing guests to converse freely with the preparators if they so choose (This might not be so fun for the preparators; I’ve worked in a couple of these labs and I’ll be the first to admit that our conversations are not always for public ears).

The Academy’s Dinosaur Hall is also filled with interactive activities. I question the educational value of a green-screen that places visitors into a scene with dinosaurs running around (the last thing we need is to encourage more people to think humans and dinosaurs coexisted), but many of the other interactives are quite inspired. In one corner, children are encouraged to climb inside a Tyrannosaurus skull cast to find evidence for its diet and lifestyle. Crouching between its jaws, kids find partially-erupted teeth, evidence that the predator broke and regrew teeth throughout its life. My favorite interactive, however, featured parallel rows of theropod and crocodile footprints on the floor. Visitors were directed to walk down each trackway, comparing how it felt different to move with an upright or sprawling gait. At the end, a sign explained that it’s harder, and less energy efficient, to move like a crocodile. I loved this activity because it was simple (just images on the floor, no technology required) and yet conveyed a clear explanation of biomechanics. Visitors use their own bodies to reach the conclusion, finding the answer in a tactile and experiential way that is more memorable than just being told that a sprawling posture is inefficient.

Overall, the Dinosaur Hall is a great overview of dinosaur science. It focuses on the biology of dinosaurs, emphasizing their similarity to animals we know today, and how scientists can draw conclusions about past life by studying the modern world. This content is communicated in a way that is clear and engaging for visitors of all ages, making this exhibit a good example of the old adage that all good science can be explained in simple terms. When I visited, there were a couple children using the open exhibits like a playground, but for the most part I think this highly accessible dinosaur exhibit is quite successful.

What’s Not So Cool

The Academy’s Dinosaur Hall is 15 years old, and is in some places showing its age. Some of the exhibit content is not entirely up-to-date; for instance, a display on the relationship between birds and dinosaurs leaves the question completely open ended. I also saw at least two invalid names, “Majungatholus” and “Ultrasauros”, used on labels. Probably more obvious to most visitors is the general wear and tear visible in certain parts of the exhibit. Some labels, particularly those facing large windows, are badly faded. The Elasmosaurus mount was moved from the Dinosaur Hall proper to the entrance lobby at some point, but Elasmosaurus signage, now labeling an empty space, is still in place in the exhibit. I got the impression that the Academy, like much of Philadelphia, is hurting for funding.

Corythosaurus and Chasmosaurus mounts. Source: TravelMuse.

The story of Leidy’s Hadrosaurus appears in several places throughout the museum. Casts of the original fossil material are displayed over a silhouette of the dinosaur toward the back of the Dinosaur Hall. Elsewhere , there is a new full casted mount of Hadrosaurus (signs explain that it is filled in with Maiasaura material), and the original tibia is displayed as part of a rather cool 200th Anniversary special exhibit. At the time, I wished that these displays were consolidated in one place, since the Hadrosaurus story is an important chapter in the history of science and of museums that can be seen exclusively at the Academy. I later found out that in 2008, the Academy had a major temporary exhibit commemorating the 150th anniversary of the original Hadrosaurus mount, which featured, among other things, a recreation of the victorian-era exhibit and the workshop of Benjamin Waterhouse Hawkins (great videos and interviews about the exhibit here). I wish I had been able to see that, because it blends the scientific, cultural and historic value of fossil mounts in a way that only this museum can.

The sadly closed Hadrosaurus Anniversary exhibit. Note Hawkins’ original sculpted head on the red pillow. Source: The Art Blog.

The current centerpiece of the Dinosaur Hall is a cast of the AMNH Tyrannosaurus. It’s neat, but I imagine most visitors would be more enthused to see the real one just a couple hours down the road. Indeed, most of the dinosaurs on display at the Academy are casts from other institutions. I have no problem with displaying casts, but I can’t help but feel that this generalized dinosaur exhibit is underselling the Academy’s own fossil collections, not to mention its contributions to paleontology. Should the Academy renovate this space again, I’d love to see the institutions’ unique history play a more prominent role, as well as the work that Academy-affiliated researchers are doing today.

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January 8, 2013 · 8:28 pm

Extinct Monsters: Murals and Dioramas

Click here to start the Extinct Monsters series from the beginning.

Fossils are the hard evidence behind paleontology. They tell us not only that prehistoric organisms existed, but hold clues as to how they lived and behaved. However, it is only through  artwork that extinct animals and ecosystems can be brought back to life. Since Benjamin Waterhouse Hawkins built the first life-sized dinosaur sculptures in 1842, skilled artists have played a critical role in visualizing the results of paleontological research and making that information available to a wider audience.

At the National Museum of Natural History, spectacular works of art have always appeared alongside displays of original fossils, firing up the viewer’s imagination and inviting them to visualize the world of prehistory. Although many of these pieces are now scientifically dated, they were on the cutting edge in their time. These artworks remain exquisite works of craftsmanship, invaluable for their decades of contribution to science education.

The Life-Sized Models

The charmingly ugly Stegosaurus is one of the oldest fixtures of the Smithsonian fossil exhibits. F.A.L. Richardson created this model for the the Smithsonian’s exhibition at the St. Louis, Missouri World’s Fair in 1904. Made from papier mâché with a foam skin, the Stegosaurus was based on small sculpture produced by Charles Gilmore. With its sagging belly, sprawling forelimbs, and head held well below the horizontal plane, this Stegosaurus is typical of reconstructions from the early to mid 20th century.

As legend had it, the paper used to fabricate the Stegosaurus was ground-up money from the National Treasury. The model had even earned the nickname “Mr. Moneybags” among some of the museum staff. Curator Emeritus Ray Rye got to the bottom of this in 1981. He contacted the Treasury to find out what was done with worn-out paper money at the turn of the century – apparently it was burned at a plant in Maryland. Nevertheless, at Rye’s request a group of historians from the Treasury took a sample of the Stegosaurus while the hall was closed for construction, and confirmed that it was made from regular paper.

This pudgy papier mache Stegosaurus has been a fixture at the Smithsonian since 1904.

This pudgy Stegosaurus has been a fixture at the Smithsonian since 1904. Photo courtesy of the Smithsonian Institution Archives.

When the Hall of Extinct Monsters opened in 1910, the Stegosaurus was given a spot of honor right in the center of the room. In 1913, a real Stegosaurus skeleton was placed alongside it. Both dinosaurs would remain in place until the exhibit was renovated in 1963. In the reconfigured and renamed Hall of Fossil Reptiles, the model Stegosaurus was relocated to a corner display.  Most recently, the 1981 renovation saw the Stegosaurus model moved to the south side of the gallery, protected by a low plexiglass barrier. This time, it was given a cycad replica for company, and a mural of lush Jurassic jungle behind it. The Stegosaurus remained in this position until the fossil halls closed in 2014.

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The NMNH exhibits team with their nearly-finished Quetzalcoatlus. Image from Thomson 1985.

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The Quetzalcoatlus survived a 2010 earthquake, although the plaster molding above it was damaged. Photo by the author.

The 1981 renovation also saw the introduction of a life-sized model of the pterosaur Quetzalcoatlus. Having been discovered in 1971, the largest flying animal that ever lived was big news at that time. In-house modelmakers spent two years on the project, first sculpting the animal in clay, then casting it in lightweight fiberglass with a steel armature. Paleontologist Nicholas Hotton served as the scientific consultant. Although he was dubious that pterosaurs had any sort of soft body covering, he okayed the use of deer fur to give the model believable texture. However, Hotton nixed the idea of placing a dangling fish in the mouth of the Quetzalcoatlus. Contemporary wisdom was that even giant pterosaurs were extremely light, weighing as little as 75 pounds, so even a 5-pound fish was thought to be enough to disrupt a Quetzalcoatlus in flight.

The Stegosaurus and Quetzalcoatlus both now reside at the Museum of the Earth in Ithaca, New York.

The Murals

The first dedicated prehistoric mammal exhibit at NMNH opened in the summer of 1961. Alongside the array of Cenozoic fossil mounts, the exhibit featured four brand new murals created by paleoartist Jay Matternes (he painted two more for the Ice Age hall several years later). Still active today, Matternes is a prolific artist of both modern and prehistoric wildlife. In addition to the NMNH murals, Matternes has contributed to exhibits at the American Museum of Natural History and the Cleveland Museum of Natural History, as well as numerous publications including National Geographic Magazine.

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Matternes’ Oligocene mural as first exhibited in the 1960s. Photo courtesy of the Smithsonian Institution Archives.

Oligocene and early Miocene murals, as seen in the 1985-2014 iteration of the exhibit, Mammals in the Limelight. Photo by the author.

Each of the murals Matternes contributed to the exhibit depicts North America during an epoch of the Cenozoic, and is displayed behind corresponding fossil mounts. Most of the animals on display coincide with life reconstructions in the murals, so visitors can match the skeletons to images of how they may have looked in life. Matternes’ hyper-detailed style is particularly striking. The environments look nearly photo-real, and not too far removed from the world today. Likewise, the artist’s knowledge of anatomy plainly shows in the utterly lifelike appearances of the animals. I particularly like Matternes’ use of familiar color patterns on the relatives of modern taxa. The Pliocene and Pleistocene murals will be returning in 2019.

Cenozoic

The Cenozoic section of Kish’s 130-foot magnum opus. Source

The “Life in the Ancient Seas” exhibit debuted in 1990 with a monumental 130-foot mural by Eleanor Kish. From the explosion of invertebrate diversity in the Cambrian to the proliferation of aquatic mammals in the recent past, the mural spans 541 years of deep time. The project took Kish two years to complete and is, simply put, a masterpiece. Within the exhibit, this meticulously crafted image defines the space’s layout and color palate. It visually separates concepts and themes, and even directs visitor traffic with its strong leftward momentum.

The Dioramas

The dinosaur dioramas were one of my favorite parts of the old NMNH fossil halls. Norman Neal Deaton created three dioramas, representing North America during the Triassic, Jurassic, and Cretaceous. The Mesozoic dioramas were commissioned for the 1963 exhibit renovation, and were on display until 2014. Each 1″:1′ scale diorama is set into a recessed space in the wall and is protected by glass.  The scenes are populated by a menagerie of outdated but gorgeously detailed dinosaurs and contemporary reptiles, set among dense forests of ferns and craggy rock formations. The complexity of the dioramas allows viewers to get lost in them as their eye wanders from one static encounter to the next. I’ve been admiring these scenes since literally before I could talk and I still notice minute details I hadn’t seen before.

The diorama project began in 1963 and took four years to complete. The scenes were initially blocked out by Jay Matternes and Nicholas Hotton, the Curator of Vertebrate Paleontology at the time. Matternes and Hotton worked together on anatomical drawings for each of the animals to be reconstructed, and planned the basic layout of the dioramas. Deaton created the final dioramas at his studio in Newton, Iowa. Deaton had been previously employed at the Smithsonian as an exhibits specialist, but had left to found his own studio in the late 1950s, where he continued to work on projects for the Smithsonian as a contractor. In addition to the dinosaur dioramas, Deaton led the creation of the iconic Fénykövi elephant that stands in the NMNH rotunda today, and has created sculptures and dioramas for dozens of other museums. Deaton is still active today, and much of his 2-D and 3-D work can be seen at his website.

Deaton mailed these slides of his unpainted models to Hotton for approval. Photos courtesy of the Smithsonian Institution Archives.

Deaton mailed these slides of his unpainted models to Hotton for approval. Photos courtesy of the Smithsonian Institution Archives.

Deaton sculpted each of the animals in clay based on the drawings provided by Matternes and Hotton. Nearly every model went through a few incremental adjustments based on notes from Hotton, changing things like the bulk of the muscles or how visible the scapula or pelvis would be under the skin. The soft anatomy was based on modern reptiles, particularly crocodiles, although Deaton found that some of the animals had no obvious analogs. Once the clay models were approved, they were casted in rubber, then painted. Deaton also created the miniature worlds inhabited by the animals, including foliage, muddy riverbanks, and sheer cliffs. The backdrops, however, were painted by Matternes.

The completed dioramas represented the most up-to-date knowledge of the Mesozoic world at that time. Of course, our understanding of dinosaurs has been overhauled significantly since then. Compared to the active, fleet-footed, and often feathered dinosaurs we know today, the inhabitants of the NMNH dioramas at first look a bit ponderous and inert. Inaccuracies are easy to point out: the Ankylosaurus has a weird clubless armadillo tail, the torso of the Diplodocus is much too long, the Cretaceous diorama mixes Hell Creek and Belly River dinosaurs that were separated by at least 20 million years, and there are sprawly tail-draggers aplenty.

Cretaceous diorama by Norman Deaton. Source: flickr.

Cretaceous diorama by Norman Deaton. Photo by the author.

Triassic diorama

Triassic diorama by Norman Deaton. Source

Still, these issues are easy to overlook when one appreciates just how engaging these scenes are. Little details like footprints behind each animal and mud splattered on their feet fill the motionless dioramas with life and the possibility of more adventures in the imagination of the viewer. And several of the models are surprisingly energetic for 60’s dinosaurs. The Ceratosaurus face-biting the Camptosaurus (above) is full of energy, and the Elphrosaurus  is running full-tilt with its tail in the air (and even has propatagia for some reason).

Many of the works of art in the NMNH fossil halls are no longer appropriate as literal representations of prehistoric animals. But that does not mean they are irrelevant relics of mid-century science. Each model and painting is a stunning example of artistry, and more to the point, every inaccuracy is an opportunity to start up a conversation about what we know about prehistory and how we know it. These pieces are time capsules in the history of science, representing different eras of understanding and the researchers that took part in them. I, for one, would hate to see them forgotten.

A big thank you  to Norman Deaton and Raymond Rye for their assistance with this article.

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January 1, 2013 · 4:00 pm

Beating the orthogenetic horse

According to the rad personalized 2012 review provided by WordPress, the top search engine terms leading people here over the last year were dinosours, horse evolutionary tree, horse evolution tree, horse phylogenetic tree and Daspletosaurus. It’s not too difficult to pick out the pattern there – horse evolution seems to be a major draw, even though I only mentioned it in a single post back in June. I aim to please, so I suppose a more detailed discussion of horse phylogeny is in order. First off, let me recommend Brian Switek’s thorough and thoughtful take on the subject. If you stick around here, you’re going to get more of a tirade.

Most depictions of horse evolution available online, including the one I posted a few months ago that is luring people to this site, are terrible. The typical linear presentation of horses progressively increasing in size from Eohippus to modern Equus, losing toes along the way, misrepresents not only what we know about horses as a group, but how evolution works in general.

This didn’t happen.

Evolution is, of course, neither linear nor progressive: it is primarily the result of populations adapting to thrive in their particular environments. As environments change over time species may evolve or go extinct, but there is no predetermined goal that lineages are reaching for. Modern Equus is not the most “highly evolved” horse – this is, in fact, a misleading if not meaningless concept, because a species’ success is dependent on its ability to thrive in that specific time and place. A modern horse is well adapted for grazing and running fast on open plains, but relocate one to the Eocene cloud forests where Eohippus thrived and it would do very badly.

Furthermore, it has been known for over a century that horses as a group did not consistently grow larger over time or otherwise become more Equus-like. Instead, horses diversified into a variety of forms over the group’s 55 million year existence, each group adapting to different environmental niches across the northern hemisphere. Large and small, forest-dwelling browsers and plains-dwelling grazers, these and all manner of other horses overlapped in time and space over the course of the Cenozoic. As J.W. Gidley of the American Museum of Natural History had worked out as early as 1907, horse evolution was not a linear progression but a tangled bush (just like the evolution of most other clades).

A modern horse phylogeny. From Macfadden 2005, via Laelaps.

A modern horse phylogeny. From MacFadden 2005, via Laelaps.

So where did the orthogenetic depiction of horse evolution come from, and why is it still with us today? The answer highlights the importance of museum exhibits and specimen provenance in the public’s understanding of paleontology, with a dose of jealous personalities for good measure.

In 1859, Charles Darwin published On the Origin of Species, in which he articulated the process of evolution by natural selection virtually exactly as we understand it today. Darwin’s book incited a whirlwind of debate in both scientific and public circles because of its implication that the diversity of life could be attributed to natural forces, rather than an unknowable divine power. Within a decade, however, the vast majority of the scientific community was convinced by the soundness of Darwin’s theory, and to this day billions of individual observations of the natural world tell us that evolution is assuredly true.

One of the many lines of evidence covered in On the Origin of Species is the fossil record, with which we can trace the evolution and extinction of organisms over time, including the ancestors of modern life. However, Chapter 9 of Darwin’s book, “On the Imperfection of the Geological Record” (full text pdf) reads like like a lengthy apology for the incomplete nature of fossil preservation. Today, the use of organized, cladistic methodologies allow paleontologists to piece together detailed phylogenies from fossils, but in Darwin’s day, the evidence was patchier, and he opted to de-emphasise the fossil record’s usefulness to avoid such criticism. As Darwin put it, “we have no right to expect to find in our geological formations an infinite number of of those fine transitional forms.” Unfortunately for paleontology specialists, this led other biologists to believe that fossils could not make any independent contribution to the understanding of evolution. Largely shut out of the biggest biological discovery of all time, paleontologists became stewards of a “second-class discipline” (Sepkoski 2012, 9).

Paleontologists in the late 19th century.

Since biologists interested in evolution considered paleontology mostly irrelevant, late 19th-century paleontologists were left with three options. They could support evolution as best they could and accept that other biologists might not take notice, they could ignore theoretical discussion entirely and focus on purely descriptive studies of morphology, or they could be spiteful and seek alternatives to Darwinian evolution. The second course of action was the most popular well into the 20th century. E.D. Cope seems to be  an example of the third approach, favoring an odd sort of neo-Lamarckism in his book The Origin of the Fittest. Such conceptions of directional change, such as Cope’s Law, are counter to evolution as proposed by Darwin and as understood today. However, a handful of paleontologists stuck with it and endeavored to provide meaningful fossil evidence for evolutionary theory.

Throughout the 1860’s, paleontologist O.C. Marsh amassed an impressive array of fossil horses from Wyoming and elsewhere in the American west. Horse fossils had been found in Europe much earlier, but Marsh’s horse collection was much more complete, and was probably the best fossil record compiled for any vertebrate group at the time. In 1870, the influential British naturalist Thomas “Darwin’s Bulldog” Huxley visited Marsh in New Haven and was suitably impressed: Marsh’s fossils ranged from the Eocene up until the Pleistocene, providing a clear picture of how the horse family had evolved over time. While Darwin had been hesitant to make too big a deal about the fossil record as evidence for evolution, the horse fossils were blatant examples of animals changing over time.

During the same visit, Huxley gave a lecture in New York in which he cited the horse fossils as a fantastic new line of evidence in support of evolution. Unfortunately, Huxley’s lecture (while admittedly aimed at a general audience) tread into some severely teleologic territory. As quoted in The Gilded Dinosaur (Jaffe 2000, 162), Huxley told his audience that “the horse is in many ways a most remarkable animal in as much as it presents us with an example of one the most perfect pieces of machinery in the animal kingdom.” He went on to explain how horse ancestors, from the little four-toed Hyracotherium in the Eocene to increasingly large horses like Merychippus and Pliohippus, gradually perfected the design of the modern horse. According to Huxley, over the course of the Cenozoic horses got bigger, faster, leggier, and generally better at being horses as we know them today. Problematically, this essentialist narrative rather misses the point of evolution as described by Darwin. 

Marsh, like Huxley, was an early advocate of evolution,  but his narrative of horse evolution was more on the mark. Marsh concluded that the smaller early horses with brachydont teeth were well suited for life in the rainforests that covered the western United States 50 million years ago. Horses like we know them today emerged as a direct result of the Earth getting cooler and drier over the course of the Cenozoic, and by the end of the Pleistocene the lineages of forest horses were completely extinct. Equus is with us today not because it is the best horse for any circumstance, but because it was most successful during the ice ages that shaped the modern flora and fauna (it also helped that humans figured out that horses are useful and ensured their survival through domestication).

Unfortunately, Marsh was never enthusiastic about public education, and so the progressive view of horse evolution was the one that made it into the public sphere. The history of horses remained a popular example of evidence for evolution, trotted out over the years by prominent biologists like George Simpson and Stephen Gould. Indeed, it was the first good evolutionary story known from fossils, although by no means the last or the best. In the earliest 1900s, Henry Osborn had a major role in solidifying the orthogenetic horse evolution story in the public eye when he curated the exhibit on the subject at the American Museum of Natural History. It is on the basic premise of this exhibit that the textbook, museum, and web descriptions of linear horse evolution that persist to this day are based.

Photo by the author.

The fossil horses of AMNH. Photo by the author.

After the modern biological synthesis, paleontologists realigned with the rest of biology, and the odd pseudo-evolutionary ideas that persisted in paleontological circles began to fall by the wayside. However, orthogenetic ideas remain common in natural history exhibits on horse evolution to this day (in about 62% of them, according to MacFadden et al. 2012). The reason these exhibits have stuck around isn’t entirely clear. MacFadden and colleagues suggest suggest a lack of inertia or funding for the renovation of exhibits is a factor, but they also point out that even some newer exhibits fall back on linear horse evolution.

The biggest problem is that orthogenetic evolution makes more intuitive sense to non-specialists. We often use the word “evolution” to imply improvement, so it would follow that horses should get bigger and better over time. This is an important misconception to overcome, because, as if we need a reminder, only 15% of Americans believe humans evolved from other animals via strictly natural processes, and an even smaller number can correctly articulate how evolution works. Evolution is the fundamental principle underlying everything we see in the natural world, and it is imperative that a correct understanding of how it works is the basis of any biology education. With the proper background, the real story of horse evolution is a great example of how changing climates effect organisms and ecosystems over time. This is helpful for interpreting the ever-important subject of climate change, but it won’t click until the linear horse evolution story is trampled out for good.

References

Jaffe, M. 2000. The Gilded Dinosaur: The Fossil War Between E.D. Cope and O.C. Marsh and the Rise of American Science. New York, NY: Three Rivers Press.

MacFadden, B.J., Oviedo, L.H., Seymour, G.M. and Ellis, S. 2012. “Fossil Horses, Orthogenesis and Communicating Evolution in Museums.” Evolution, Education and Outreach 5:29-37.

Sepkoski, D. 2012. Rereading the Fossil Record: The Growth of Paleobiology as an Evolutionary Discipline. Chicago, IL: University of Chicago Press.

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December 23, 2012 · 8:58 pm

Fossil mounts: specimens, showpieces, art and more

A few days ago, Andy Farke posed the following question on twitter:

If fossils are part of our planet’s heritage, and belong to all of us, are museum restrictions on photos ethical?

Farke clarified that he was referring specifically to fossils held in collections, especially those collected on federal land and/or with public funding. Following the same sound logic that makes open access scientific publication a necessity, any scientific work using public resources should be accessible to everyone, including objects in collections.* The question had arisen because some museums bar researchers utilizing collections from using photographs in their published articles (or charge a fee for the privilege). This is a valid concern, but I don’t have enough experience with scientific publishing to explore it properly. Instead, I’d like to hijack the question in order to discuss the murky identity of fossil mounts.

*I’m going to disregard for-profit museums for the time being, suffice it to say such collections exist and can be useful for research as well.

A sampling of fossil collections and curators at the National Museum of Natural History. Source: http://paleobiology.si.edu.

As was already pointed out in response to Farke’s initial question, the public’s right to access photographs of some fossil collections should not necessarily extend to museum exhibits. Any modern museum exhibit worth its salt is far more than specimens on shelves. Exhibits are immersive experiences that use specimens to illustrate a story. A great deal of creative work goes into designing and fabricating an exhibit, and it is not unreasonable for museums to claim ownership of any reproductions, including photographs, if they so choose.

Allosaurus and Barosaurus mount in the Roosevelt rotunda of the American Museum of Natural History. Source: http://www.ourtravelpics.com.

Allosaurus and Barosaurus mounts in the Roosevelt rotunda of the American Museum of Natural History. Source: http://www.ourtravelpics.com.

Fossil mounts, however, are a different beast. These structures are difficult to categorize because they are intended both to educate and to entertain. They may incorporate real fossils, or casts taken directly from them, but I would argue that fossil mounts are primarily constructed pieces. With the exception of some more recently extinct mammal taxa, most mounts are composites of casts, sculpted elements and original fossils collected in different places at different times. Steel armatures are custom-made not only to support the specimens but to appropriately fill the exhibit space. Mounts like the striking Barosaurus and Allosaurus encounter in the Roosevelt rotunda at AMNH (above) are designed to make an aesthetic impression as well as to inform. Overall, mounts require a substantial investment of time, labor, money and artistic skill to create and maintain. Experienced researchers typically guide the construction process and the contributions of knowledgeable scientists cannot be overstated, but fossil specimens certainly do not come out of the ground mount-ready. There is a great deal more to making a good mount than stringing vertebrae together in the right order.

A direct comparison can be made between fossil mounts and the taxidermied animals that are also a staple at natural history museums. A taxidermy mount also incorporates a scientific specimen, the animal’s skin, which if collected using public resources should be accessible to all. Like fossil mounts, however, taxidermy pieces require extensive artistic and technical skill to create, from the steel or wood armature to the clay model that build’s out the animal’s musculature to the eyes and mouth, which are typically sculpted from scratch. It is worth quoting Rachel Poliquin’s excellent The Breathless Zoo at length:

As dead and mounted animals, [taxidermy mounts] are thoroughly cultural objects; yet as pieces of nature, [they] are thoroughly beyond culture. Animal or object? Animal and object? This is the irresolvable tension that defines all taxidermy. (Poliquin 2012, 5-6)

I firmly believe that the results of scientific inquiry belong in the public domain, and it follows that restrictions on the photographic reproduction of collections specimens are inappropriate. Nevertheless, fossil mounts and taxidermied animals are the products of artisans as much as of researchers, and the right to credit and control over this work ought to be respected. This middle ground is awkward to negotiate, and as Poliquin puts it, a means to please all parties might be “irresolvable.”

Robert Rockwell sculpts the internal model for AMNH's taxidermied brown bear. Source: Scientific American.

Robert Rockwell sculpts the internal model for AMNH’s taxidermied brown bear. Source: Scientific American.

To make a non-committal final point, I’d like to mention that it is tempting to be too uptight about copyright, particularly in a museum setting. This past October, I had the pleasure to give a presentation with Alexis Fekete at the Kansas Museum Association’s annual conference. The most interesting part of our session (which was about how web 2.0 tools can help museums) was when audience members, mostly representing small history museums, voiced concerns over making their photography collections available online. There was apprehension about making it too easy for people to copy and sell pictures without permission, which I assume is the primary reasoning behind other museums’ policies prohibiting the publication of fossil images. I’m skeptical, however, that this is the most pressing concern. Perhaps I’m being naïve, but I have no problem with getting information disseminated to genuinely interested people. Creating awareness and enthusiasm for content is part of the general mission of museums, and I’d hate to see overzealous copyright barriers get in the way of that.

References

Poliquin, R. 2012. The Breathless Zoo: Taxidermy and the Cultures of Longing. University Park, PA: Pennsylvania State University Press.

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July 20, 2012 · 12:09 pm

Extinct Monsters: Ice Age Giants

Click here to start the NMNH series from the beginning.

The old fossil mammal exhibits at the National Museum of Natural History were notable for their sheer diversity. From rabbits to elephants and from bats to whales, virtually every major group of North American mammals, particularly eutherian (placental) mammals, was represented. By my count, there were no less than 48 mounted mammal skeletons on display (not including individual skulls and other parts) in 2014, arranged by time period and distributed across three sizable halls.

The comprehensive nature of these exhibits was largely thanks to C.L. Gazin, head curator of the Division of Vertebrate Paleontology in the 1950s and 60s. During the modernization of the fossil halls in the early 1960s, Gazin focused his efforts on assembling a complete narrative of Cenozoic mammal evolution. The six-part exhibit debuted in 1961 in Hall 5, and was relocated two decades later to Hall 3. Gazin also initiated the construction of the adjacent Ice Age exhibit, although it would not be permanently opened to the public until 1974.

Now that the fossil halls are being renovated, NMNH staff face the enormous task of disassembling and restoring the dozens of historic mammal skeletons. Many will return when the exhibit reopens in 2019, but others may be retired to the collections if they are deemed too fragile for continued display, or if they are not illustrative of the story being told in the new exhibit.

The Megaloceros

This Megaloceros

This Megaloceros has the distinction of being the Smithsonian’s first mounted skeleton composed of original fossils. Photo by the author.

The Smithsonian’s first mounted fossil skeletons went on display in 1871 in the building colloquially called “the castle.” The exhibit included plaster casts of the ground sloth Megatherium, the tortoise Colossochelys and the glyptodont Scistopleurum, all made from originals at the British Museum. The following year saw the addition of the giant deer Megaloceros (USNM V 7051) — the Smithsonian’s first mounted skeleton composed of original fossils. The Smithsonian purchased this complete Megaloceros, which was uncovered in an Irish peat bog, from Philadelphia-based antiques dealer Thomas and Sons. The mount was assembled by none other than Benjamin Waterhouse Hawkins, the sculptor who created the famous Crystal Palace dinosaurs.

Note basilo

Megaloceros in the southeast court of the Arts and Industries building, circa 1896. The British Museum Megatherium cast can be seen on the left. Source

When construction of the original United States National Museum (what is now called the Arts and Industries Building) was completed in 1881, all of the fossil displays were moved to the new setting. Vertebrate fossils found a home in the 80,000 square foot southeast court. Gradually, the Megaloceros and British Museum casts were joined by many more crowd-pleasing skeletons, including a copy of the Philadelphia Hadrosaurus, an Edmontosaurus, a Triceratops, and a mastodon (discussed below). By the time the USNM was preparing to move to yet another new building across the national mall in 1910, the southeast court had become quite crowded. Unfortunately, the Megatherium and Collossochelys never made it to the new location. These casts were discarded due to the damage they had accumulated while on display. Although the glyptodont cast was still on exhibit as of 1940, it too was eventually destroyed. Happily, the Megaloceros survived, and has been included in each subsequent iteration of the fossil exhibits.

Starting in 1974, the Megaloceros was displayed alongside the extinct bird Diornis in the Ice Age hall. It’s weight was partially supported by cables descending from the ceiling, which proved to be a problem when it came time to disassemble it in July 2014. Rather than attempting to lift the delicate skull and heavy antlers off the armature, the exhibit team strapped the skull to a mechanical lift so that it could be slowly and gently lowered to the floor. In the new National Fossil Hall, the Megaloceros will be sitting on the ground. This pose was selected in order to bring the spectacular antlers to visitors’ eye level.

The Mastodon

The Indiana mastodon in the Hall of Extinct Monsters. Photo courtesy of the Smithsonian Institution Archives.

In 1901, Michigan farmer Levi Wood found a well-preserved, nearly complete Mammut americanum (USNM 2106) in a peat swamp on his land. The USNM purchased the rights to excavate the skeleton from Wood and began work that same year. The specimen turned out to be virtually complete, save for the forelimbs and left hindlimb. Alban Stewart mounted the skeleton, adding a left hindlimb from another mastodon specimen from Missouri, and filling in other missing elements with plaster replicas. The completed mount was first exhibited at the Louisiana Purchase Exposition in St. Louis, Missouri in 1904.

For a time, there were two mastodon mounts on display in the Hall of Extinct Monsters. Photo courtesy of the Smithsonian Institution Archives.

After the Exposition, the Michigan mastodon was added to the fossil displays in the  southeast court of the Arts and Industries Building. It remained there for four years, before joining the rest of the paleontology exhibits and collections in the move to the new USNM building.

In 1915, a second mastodon (USNM V 8204) from Indiana was added to the Hall of Extinct Monsters. The matching set can be seen on the left side of the image above, with the plaster skull of a Deinotherium (USNM V 1917) positioned between them. The larger Indiana mastodon persisted through the 1963 and 1981 renovations, and will return with an energetic trumpeting pose in 2019. NMNH loaned the Michigan mastodon to the Oregon Zoo for many years. It has since been returned, dismantled, and retired to the collections.

The Stegomastodon

Stegomastodon in 2014. Photo by the author.

Stegomastodon in 2014. Photo by the author.

The young male Stegomastodon (USNM 10707) was collected by James Gidley and Kirk Bryan collected this skeleton in the San Pedro Valley of Arizona. This 1921 collecting trip also produced the museum’s Glyptotherium. While the genus Stegomastodon was erected in 1912, Gidley referred his specimen to a new species, S. arizonae, due to its more “progressive” physiology and slightly younger age. By 1925, the skeleton was mounted and on display in the Hall of Extinct Monsters. While the original mount used the real fossil tusks, these were eventually replaced with facsimiles.

Stegomastodon with

Stegomastodon with its original tusks. Photo from Gidley 1925.

The Stegomastodon will not be returning when the National Fossil Hall reopens in 2019. For one thing, there are already two big elephants on display: the mammoth and the mastodon. Elephants take up a lot of space, and a third proboscidean offers diminishing returns when compared to the amount of floor space it requires. More importantly, the Stegomastodon is a holotype specimen, and the exhibit team elected to remove most of these important specimens from the public halls. This is both to keep them safe from the damaging effects of vibration, humidity, and fluctuating temperature, as well as to make them more accessible to researchers.

The Eremotherium pair

Eremotherium

The unique and impressive Eremotherium pair. Photo by the author.

The immense pair of giant ground sloths (USNM V 20867 and USNM V 20872) are among the most impressive and unique skeletal mounts at NMNH. Many a visitor has ascended the ramp to the Ice Age gallery only to stop and stare at them. Unlike the Megaloceros, mastodon, and many others, these were new additions added during the 1960s modernization. Gazin’s team recovered the fossils in Panama between 1950 and 1951, bringing back over 100 plaster jackets representing at least eight individual sloths of the genus Eremotherium.

sou

John Ott and Gladwyn Sullivan attach the scapula of the standing sloth. Source

Assistant Curator of Cenozoic Mammals Clayton Ray oversaw the assembly of the two Eremotherium mounts in 1969. Both the larger standing sloth and smaller kneeling one are composites of fossils from many individuals (there are also plenty of reconstructed bones, easily spotted by their solid beige coloration). Most of the surplus bones were repatriated to Panama before the mounts went on display. The sloths were originally positioned back-to-back on a central platform, accentuated by an illuminated opening in the ceiling. However, this layout only lasted a few years. In 1974, the Quaternary Hall was completely reorganized into the Hall of Ice Age Mammals and the Age of Man. In the new arrangement, the Eremotherium pair was relocated to a corner at the north end of the gallery. In 2019, only one Eremotherium will be on display.

The Mammoth

Chimera mammoth

This mammoth was assembled from as many as 70 individual specimens. Photo by the author.

Although it was always labeled as a woolly mammoth (Mammuthus primigenius), the Smithsonian’s third proboscidian skeleton (USNM V 23792) is actually a composite of over fifty individual specimens, some of which probably belong to the more southerly Columbian mammoth (Mammuthus columbi). Most of these fossils were acquired in a trade with the American Museum of Natural History in the 1960s, specifically to build a mounted skeleton for the Ice Age hall. Perhaps because they were acquired for display, rather than study, the origin of these fossils was not well-recorded. It is only now that the mammoth has been disassembled that collections staff can begin to to learn more about this iconic chimera. Some of the bones are marked with the year and location of their collection, crucial details for piecing together their provenance.

The mammoth in its new, snow-shoveling pose. Photo courtesy of the Smithsonian Newsdesk.

In the new fossil hall, the mammoth will be leaning forward, pushing its great tusks across the ground as though it were brushing away snow. In the meantime, the original mount was digitally scanned, and the model is freely available from Smithsonian 3D.

References

Carrano, M. 2018. Pers. comm.

Gazin, C.L. 1956.  Exploration for the remains of giant ground sloths in Panama. Smithsonian report, 341-354.

Gidley, J.W. 1925. Fossil Proboscidea and Edentata of the San Pedro Valley, Arizona. Shorter Contributions to General Geology (USGS). Professional Paper 140-B, 83-95.

Gilmore, C.W. 1906. Notes on Some Recent Additions to the Exhibition Series of Vertebrate Fossils. Proceedings of the United States National Museum No. 30.

Gilmore, C.W.  1941. A History of the Division of Vertebrate Paleontology in the United States National Museum. Proceedings of the United States National Museum No. 90.

Marsh, D.E. 2014. From Extinct Monsters to Deep Time: An ethnography of fossil exhibits production at the Smithsonian’s National Museum of Natural History. http://circle.ubc.ca/handle/2429/50177

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July 11, 2012 · 8:56 am

Extinct Monsters: History of Smithsonian Fossil Exhibits

Click here to start the Extinct Monsters series from the beginning.

Upon his death in 1829, British scientist James Smithson left his fortune to the United States government to found “at Washington…an establishment for the increase and diffusion of knowledge.” Congress used Smithson’s estate to establish the publicly funded Smithsonian Institution in 1846, which has since grown into an expansive research institute and museum complex that is recognized the world over. Vertebrate paleontology has been an important part of the Smithsonian’s agenda since the beginning, and this article by Ray Rye provides a compelling history of the scientific staff and their research. This post will take a slightly different approach, summarizing the changing public face of Smithsonian paleontology in the form of its genre-defining exhibits.

In 1847, Joseph Henry, the Smithsonian’s first secretary, started construction on the original Smithsonian building, which today is colloquially known as “the castle.” The first vertebrate paleontology exhibit housed within its walls consisted of a trio of casted skeletons: the ground sloth Megatherium, the glyptodont Scistopleurum, and the tortoise Collossochelys. These exhibits were probably obtained through Ward’s Natural Science Establishment. The Smithsonian’s first skeletal mount made from original fossils was a Megaloceros, purchased from antiquities dealers Thomas and Sons in 1872.

Exhibits like this one at USNM were deemed incomprehensible and inspired early reform

Basilosaurus, Megatherium, and Megaloceros are visible in the southwest court of the first United States National Museum. Image courtesy of the Smithsonian Institution Archives.

1881 saw the completion of the original United States National Museum, next door to the castle (this structure is now called the Arts and Industries Building). The southwest court was dedicated to osteology and paleontology, and the existing skeletal mounts were placed here among rows of cases containing smaller specimens. At this point in time, the Smithsonian had very few permanent staff members, instead relying mostly on scholars serving in unpaid “honorary” positions to curate the growing national collection. Famed paleontologist O.C. Marsh (the beardier half of the “bone wars” rivals) was the honorary curator of vertebrate paleontology. Under contract with the United States Geological Survey, Marsh supervised numerous field expeditions to the American west and oversaw the collection of untold thousands of fossil specimens. When Marsh died in 1899 the fossils he collected for the government were relocated from Yale University (his home institution) to the Smithsonian.

Gilmore and the Hall of Extinct Monsters

Gilmore with Diplodocus vertebrae.

C.W. Gilmore with some Diplodocus vertebrae. Image courtesy of the Smithsonian Institution Archives.

Charles Whitney Gilmore was a student in mine engineering at the University of Wyoming when he became involved in the Carnegie Museum’s fossil hunting expeditions in 1899. Recognizing the young man’s enthusiasm and talent, John Bell Hatcher hired Gilmore immediately after his graduation in 1901. Gilmore worked with Hatcher for two field seasons, but in 1903 he moved to Washington, DC upon being offered a position as a full-time preparator at the USNM. He was promoted to Curator of Vertebrate Paleontology in 1924, and is fondly remembered as an exceptionally modest but extraordinarily productive scientist. As curator, Gilmore led sixteen fossil-hunting expeditions to the western interior. Gilmore’s most enduring contribution to paleontology, however, is his extensive body of descriptive publications on the Marsh fossils. His monographs on Apatosaurus, Camarasaurus, Ceratosaurus, and many others are still regularly cited today.

Along with preparators Norman Boss and James Gidley, Gilmore is responsible for creating most of the mounted dinosaur skeletons that are on display at the Smithsonian. The first dinosaur mount Gilmore and his team completed was Edmontosaurus, which went on display in the original USNM building in 1904. Gilmore would go on to supervise the construction of Triceratops (the first mount of this taxon in the world), Camptosaurus, Stegosaurus, Dimetrodon, Ceratosaurus, Diplodocus, and numerous other displays that have been enjoyed by generations of museum visitors.

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The Hall of Extinct Monsters, sometime before 1929. Image courtesy of the Smithsonian Institution Archives.

Congress authorized the construction of a new United States National Museum on the north side of the National Mall in 1911. In contrast to the Victorian style of the original building, the new museum sported neoclassical granite construction which matched the aesthetic of the other federal buildings. Exactly when the museum opened is the subject of some debate. Collections and offices began moving across the mall via horse and wagon in 1908, and part of the first floor opened to the public on March 17th, 1910. Nevertheless, it was not until 1911 that all the exhibit spaces were ready for visitors, including the evocatively titled “Hall of Extinct Monsters” in the museum’s east wing. This cavernous space devoted to fossil displays was primarily under Gilmore’s stewardship, and generally resembled a classic “cabinet of curiosity” approach to exhibit design. Gilmore and his team would gradually fill the Hall of Extinct Monsters will new specimens over the coming decades, culminating in the towering Diplodocus mount completed in 1932.

Modernization and Renaissance

Gilmore retired in 1945, and vertebrate paleontology research at the USNM, particularly in dinosaurs, quieted in his absence. Charles Gazin, Gilmore’s successor as Curator of Vertebrate Paleontology, specialized in mammals, and the museum remained without a curator specializing in dinosaurs until Matt Carrano was hired in 2003. In 1957, the USNM split into two subdivisions, the Museum of Natural History and the Museum of History and Technology. The Smithsonian’s history collections were moved to a new building next door, now called the National Museum of American History, and other collections gradually dispersed into 20-some other Smithsonian museums. The site of the disbanded USNM was officially renamed the National Museum of Natural History in 1967, and remains the home of natural sciences and anthropology.

The Diplodocus, as it stood from 1963 through 1981. Image courtesy of the Smithsonian Institution Archives.

The Hall of Fossil Reptiles lasted from 1962 to 1981. Image courtesy of the Smithsonian Institution Archives.

The Hall of Extinct Monsters persisted largely unchanged until 1962, when it was finally renovated as part of a Smithsonian-wide modernization project. The fossil exhibits were among the last to be updated, in part due to ambivalence from the paleontology curators. The department did not employ any staff members exclusively devoted to exhibit work, so the task of reinventing the displays was an added burden for the research staff. As such, the changes to the hall ended up being more cosmetic than structural. The largest mount, Gilmore’s Diplodocus, was too difficult to disassemble and move, so the new exhibit was designed around it. Solid earth tones and wall-to-wall carpet replaced the original neoclassical aesthetic. The John Elliot mural Diana of the Tides, positioned high on the east wall, was simply boarded over during construction (and has remained so ever since).

The 1981 renovation saw the addition of a mezzanine over the dinosaur exhibit. Source

In 1974, the addition of the Hall of Ice Age Mammals and the Rise of Man expanded the paleontology display space beyond the east wing. Further renovations took place in three stages starting in 1979. Entitled “Fossils: The History of Life”, the overhauled exhibit complex represented a significant departure from earlier iterations of this space. While the previous renovation arranged specimens according to taxonomy and curatorial specialties, “The History of Life” followed the evolutionary progression of fossil plants and animals through time. The new exhibits also differed from prior efforts in that they were not put together exclusively by curators. Instead, the design process was led by educators and exhibits specialists, who sought curatorial input at all stages. The new specimens and displays also required the once spacious hall to be carved up into a maze of small rooms and narrow corridors. Even with the additional floor space provided by a new balcony over the dinosaurs, the east wing had become quite crowded.

Of course, the science of paleontology has advanced by leaps and bounds since the 1980s, and NMNH staff have made piecemeal updates to the exhibits when possible. These changes include restorations of deteriorating mounts, the addition of a cast of Stan the Tyrannosaurus, and a few revised signs addressing the dinosaurian origin of birds and new dates for geologic time periods. Still, the east wing remained largely the same for over 30 years, and began to look a bit tired next to the brand-new exhibits that have opened at NMNH over the last decade.

Looking Ahead

The NMNH fossil halls closed on April 27th, 2014 for a five year renovation project. For the first time, the east wing was completely gutted and its underlying infrastructure overhauled. Aging specimens like the 1932 Diplodocus and the 1911 Ceratosaurus were be painstakingly disassembled and conserved, and the space itself was restored to its original Beaux Arts splendor. The re-imagined exhibit is arranged in reverse chronological order: visitors  start among mammoths and ground sloths in the Pleistocene and move backward in time through increasingly alien-looking versions of North America. Unlike the present exhibit, however, an open floor plan will allow visitors to get a sense of what they’re in for from the moment they walk into the hall.

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Mesozoic section of the new Hall of Fossils – Deep Time. Concept art on display in the Last American Dinosaurs exhibit at NMNH.

The overall theme is change over geologic time, highlighting the myriad ways that climate, geography, evolution, and other living and nonliving systems interact and shape the world’s environments. Not all the classic mounts will make it into the new space (Brachyceratops, Zygorhiza, and Stegomastodon are among the retirees), but there are many new additions, including the Nation’s T. rex.  The result will be a compelling mix of classic early 20th century museum aesthetics and modern visitor-focused educational strategies.

References

Gilmore, C.W.  (1941). A History of the Division of Vertebrate Paleontology in the United States National Museum. Proceedings of the United States National Museum No. 90.

Rye, R. (2002.) History of the NMNH Paleobiology Department. http://paleobiology.si.edu/history/rye.html

Sues, H. and Marsh, D. (2013). Charles Whitney Gilmore: The Forgotten Dinosaur Hunter. http://paleobiology.si.edu/history/gilmore.html

Yochelson, E.L. (1985). The National Museum of Natural History: 75 Years in the Natural History Building. Washington, DC: Smithsonian Institution Press.

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Aside

Medullary Bone and the Dinosaur-Bird Link

One of the coolest lines of evidence that birds are extant dinosaurs is the presence of medullary bone in multiple dinosaur species. Medullary bone (hereafter referred to as MB, to avoid confusion with the medullary surface) is a temporary tissue that forms on the interior surfaces of the long bones of birds. MB is identified by unique collagen organization: it is both densely mineralized and strongly vascularized. This structure helps MB serve its purpose as a readily retrieved source of calcium for use in forming eggshells, and prevents incapacitating bone resorption during this process. Among extant animals, MB is only found in mature female birds in the process of producing eggs. Its creation is triggered by hormones during the onset of ovulation, and it disappears during the laying process. Among extant animals, MB is only known in birds. However, in 2005 Mary Schweitzer and colleagues reported their discovery of medullary bone in a Tyrannosaurus rex individual. Lee and Werning followed up on this research in 2007 by reporting MB in the theropod Allosaurus and the ornithopod Tenontosaurus.

Medullary bone in modern Gallus and fossil Tyrannosaurus. From http://www.abc.net.au/science.

Since MB is unique to reproductively active females, most popular coverage of dinosaur MB  has focused on its potential use for determining the sex and life stage of individual dinosaur specimens. We shouldn’t, however, lose sight of the fact that MB is an independent line of evidence supporting a close phylogenetic relationship between dinosaurs and birds. Nearly all paleontologists agree that the evidence that birds are dinosaurs is overwhelming, and MB is but a drop in the ocean of shared characters between birds and dinosaurs. Nevertheless, it is noteworthy that few authors have attempted to challenge Schweitzer’s initial publication.

The only work I have found  that disputes Schweitzer and colleagues is the dissertation of Dr. Devon Quick  (.pdf link), in which Dr. Quick and Dr. John Ruben investigated the reliability of the methods used to recognize MB in the fossil record using extant animals. This is not, incidentally, the only work by Quick and Ruben challenging the dinosaur-bird connection. As a doe-eyed student, I’d like to take a shot at reviewing this paper. And since I’m posting it publicly, I of course welcome anyone who’d be so kind as to call me out for being wrong.

Quick and Ruben looked at cross-sections of the femora and tibiotarsi of a crocodilian (Alligator mississippiensis) and several birds. Scanning electron microscopy revealed that the medullary surfaces of the tibiotarsi of  reproductively active birds displayed the highly contoured and floccular texture that is characteristic of MB. Likewise, the male and non-reproductively active female birds displayed smooth medullary surfaces. In this regard, Quick and Ruben are in agreement with previous work. However, the authors also reported that the medullary cavity of the alligator femur contained “material superficially similar to…avian medullary bone” (Quick and Ruben 2008). This material was limited to the immediate diaphyseal side of the metaphysis, making it much less extensive than what was observed in birds. Since the alligator individual used in the study was a juvenile male, it was almost certainly not producing reproductively-specific MB. From this observation, the authors conclude from these data that a floccular texture may indicate early-stage bone mineralization and is not a reliable indicator of MB.

Quick and Ruben’s results are unconvincing in part due to a weak experimental design. Their conclusions are dependent on observations gleaned from a single alligator specimen, which is not an adequate sample. The authors’ conclusions would carry more weight if they had looked at multiple individuals. It would also be beneficial to compare males, females, adults and juveniles. Ideally, additionally crocodilian species ought to be included in the study, as well. Schweitzer and colleagues carried out a similar investigation, in which they looked for evidence of MB in multiple alligators, including gravid females, males and juveniles (Schweitzer et al. 2007). Schweitzer and colleagues found no evidence of MB, even with estrogen stimulation, and their larger sample size allows their study to carry more weight than that of Quick and Ruben. Furthermore, although Quick and Ruben assert that that “histological aspects of Tyrannosaurus tissues that are supposedly consistent with an avian-style reproductive physiology were not analyzed carefully”, they did not look at the Tyrannosaurus material as part of their study. Accordingly, no evidence is provided that the structures the authors observed on their alligator were synonymous with those observed by Schweitzer and colleagues on Tyrannosaurus. Finally, Quick and Ruben’s observations are focused on the floccular texture used to identify MB, when in fact Schweitzer and colleagues used several other indicators, including extensive vascularization, to identify MB in Tyrannosaurus. It is notable that the structure, thickness and texture of MB in modern birds varies considerably based on the specifics of the animal’s reproductive biology and the size of the taxa. Given that Tyrannosaurus is several orders of magnitude larger than most extant birds, some structural difference is to be expected (wow, that sentence had some serious science snark).

Quick and Ruben suggest that the floccular texture on the alligator bone may be the result of early-stage mineralization, which would be consistent with the sub-adult status of the individual they used in the study. The authors go on to speculate that a similar explanation might account for the evidence of MB in Tyrannosaurus. Again, it would have been helpful if the authors had amassed more examples of sub-adult archosaurs undergoing skeletal mineralization, and compared them directly to the Tyrannosaurus material in question, rather than merely speculating. If the Tyrannosaurus was forming MB, this would be consistent with information from lines of arrested growth in Tyrannosaurus and other dinosaurs, which indicates that dinosaurs became reproductively active before reaching adult size.

Having reached the somewhat tenuous conclusion that texture is not a reliable indicator of MB, Quick and Ruben go on to argue that even if MB is present in dinosaurs, the fact that it has been reported in both saurischians and ornithiscians “offers no particular insight into the phylogenetic origins of birds.” On the contrary, MB is an independently observable feature that unites the crown group Dinosauria with Avialae, and therefore supports the consensus that Avialae is bracketed by Dinosauria. At the very least, MB suggests marked similarity in reproductive strategies employed by birds and dinosaurs. As demonstrated by Schweitzer and colleagues, MB is not known in crocodilians. Quick and Ruben freely admit this, which makes their statement that MB “may well be a plesiomorphic trait that first evolved in basal archosaurs” nonsensical (Quick and Ruben 2008). The authors could theoretically argue that MB production is primitive but was lost in modern crocodilians, but there is no evidence for this.

Overall, Quick and Ruben’s work is hindered by weak experimental design and vague, unsupported conclusions. Given that a similar but more rigorous study regarding MB in crocodilians has already been carried out by Schweitzer and colleagues, Quick and Ruben’s interpretations are not convincing. Even the broadest interpretation of the available evidence indicates that MB originated after the divergence of crocodilymorphs from the main archosaur line. The phylogeny postulated by Schweitzer and colleagues remains most tenable, in which MB originated in early dinosaurs, and was inherited by ornithiscians, tyrannosaurids and modern birds (Schweitzer et al. 2005).

References

Lee, A. H. and Werning, S. “Sexual maturity in growing dinosaurs does not fit reptilian growth models.” 2007. PNAS 105:2:582-587.

Quick, D. E. and Ruben, J. A. “Amniote bone structure and longbone histology in birds, alligators and the theropod Tyrannosaurus rex.” 2008. Oregon State University.

Schweitzer, M. H., Elsey, R. M., Dacke, C. G., Horner, J. R. and Lamm, E. T. “Do egg-laying crocodilian (Alligator mississippiensis) archosaurs form medullary bone?” 2007. Bone 40: 1152-1158.

Schweitzer, M. H., Wittmeyer, J. L. and Horner, J. R. “Gender-Specific Reproductive Tissue in Ratites and Tyrannosaurus rex.”2005. Science 308: 1456-1460.

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January 20, 2012 · 6:26 am
July 28, 2011 · 7:57 am

Jurassic Park is awesome and a milestone for paleontology…

…deal with it.

What follows was partially written several months ago and never finished. I dug it up again due to the resurgence of JP interest with Steven Spielberg’s announcement.

I was six years old when Jurassic Park came out. I was crazy about dinosaurs, but my parents had been told that the movie was way too scary for a kid my age. Since Aliens was already on my short list of favorite films at that point, this seems a moot point, but by the time my parents warmed up to taking me to see JP, it was at a second run theater. I don’t remember seeing it at the theater, but I do remember my endless viewings of my VHS copy, and the tattered box remembers too.

I still enjoy Jurassic Park immensely. It means a lot to me, but surprisingly, that feeling is not shared by the entirety of the paleontological community (as a student/intern, I put myself in a very broad definition of that collective). As an example, take a look at Dr. David Hone’s admittedly 3-year old post about the film. While Dr. Hone is generally positive, he expresses annoyance about the inaccurate portrayals of dinosaurs and paleontologists that have so firmly entrenched themselves in the public consciousness as a result of Jurassic Park. Similar complaints turn up from time to time on the Dinosaur Mailing List as well.

I, for one, have to disagree. When I’m chatting with people about vert paleo, something I genuinely enjoy, I’m thrilled when Jurassic Park enters the conversation. It’s such a genuinely entertaining movie that people remember it well, 18 years after it’s release. What’s more, it’s a movie that made many people think about what they were watching: what dinosaurs were like, and how we know what we do about them. This is an excellent jumping-off point for any discussion about paleontology, because it is a shared frame of reference. At work, I have become well acquainted with the fact that very few people understand Deep Time, or have ever given it any thought at all. But people know Jurassic Park, and I am very grateful for it as a starting point in the education process.

What’s more, we can complain all we like about what Jurassic Park got wrong, but I’m more impressed by how much it got right. Jurassic Park was the first widely disseminated look at believable dinosaurs, and it single-handedly brought post-Dinosaur Renaissance conceptions of dinosaurs to everyone.

Unfortunately, as I mentioned, Jurassic Park is 18 years old now. It took awhile, but it seems to no longer be the go-to source of dinosaur knowledge for many Americans. The seemingly endless parade of shitty “documentaries” on cable TV, as well as fare like Dinosaur Train, are crowding Jurassic Park off its perch. And that is why I’m optimistic about the announcement of Jurassic Park 4. The original film was a fantastic resource not only for paleontology education, but science education in general. If a new sequel can match or approach that level of quality, then our job as educators will be much easier.

I also have a bunch of thoughts about Jurassic Park that I feel like sharing but don’t really have a place for above. Read on at your own risk.

  • One time when I was watching Jurassic Park with friends, somebody commented that Grant’s jaw dropping and staggering about at the sight of the Brachiosaurus was really bad acting. I beg to differ…I imagine I would do much the same thing.
  • The CGI dinosaurs get all the credit, but they are on screen for less than two minutes. Stan Winston’s flawless puppets and animatronics are the real stars of the show.
  • In fact, the dinosaurs as a whole don’t get much screen time. There’s barely a dinosaur to be seen for the first hour. Credit to Spielberg for great pacing and constructing fantastic set-piece sequences that get the most out of very few dinosaur scenes.
  • Grant’s dig site at the beginning of the film cracks me up. Putting aside the completely articulated skeleton for the moment, the rag-tag assortment of people present doesn’t make much sense, and the assortment of clutter in the trailer seems rather useless too.
  • Jurassic Park can (and has) be used as a basic introduction to cloning, genetics and chaos theory. Molecular biologists and mathematicians can nit-pick the movie as much or more as paleontologists can, but at the end of the day it’s an effective way to introduce the public to ideas they might not otherwise be exposed to.
  • It’s kind of funny that the idea of cloning was science fiction in the late 1980s when Michael Crichton wrote the book.
  • What was Gennaro asking Hammond about “auto-erotica?” What could that possibly mean besides what I think it means? Seriously, I would love an explanation.

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