Exploring Georgia's Natural History
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  • 1: Georgia's Oldest Fossils; Archaeocyathids, At 513 Million Years Old
  • 2: Trilobites; 500 Million Years Ago
    • 2A; Murray County Stromatolites
    • 2B; A Trilobite Nest in Georgia
  • 3: Geologic Time
  • 4: Our Oldest Vertebrate?
  • 5: Georgia Before the Dinosaurs
    • 5A; Georgia’s Pennsylvanian Plant Fossils
    • 5B: Carpentertypus durhami, Georgia’s Giant Insect, 315 Million Years Ago
  • 6: 200 Million Years Ago
    • 6A: Birth of the Atlantic Ocean
  • 7: Cretaceous Georgia, Dinosaurs & more
    • 7A: Georgias Pterosaur
    • 7C: Coelecanths
    • 7B: So Many Sharks
    • 7D: Xiphactinus vetus
    • 7E: Side-necked turtles
    • 7F: Marine Reptiles
    • 7G: Dinosaurs in Georgia
    • 7I; The Blufftown Formation
    • 7L: Bill Montante's Mega "Gator" Tooth Discovery
    • 7K: The Pio Nono Formation
    • 7J: The Eutaw Formation
    • 7H: Deinosuchus schwimmeri in Recognition of Dr. David Schwimmer
  • 8: Suwannee Current, Gulf Trough, & Bridgeboro Limestone
  • 9: The Clayton Formation Report; By Hank Josey
    • 9A: The Georgia Turtle
  • 10: The Eocene; Georgia's Oldest Mammals
    • 10A: The Origins of Whales
  • 11: A Whale For Georgia
  • 12: Basilosaurids; The First Modern Whales
    • 12A: Basilosaurus cetoides
    • 12B: Basilotritus
    • 12C: Cynthiacetus (Revised)
    • 12D: Chrysocetus
    • 12E: The Redmond Mandible of Albany Ga
    • 12F; Houston County, GA Basilosaurus to the Smithsonian
  • 13: Ziggy and The Museum of Arts & Sciences, Macon, GA
  • 14: Late Eocene
    • 14A: Eocene Fossils & Stratigraphy
    • 14B; Fossils, Impacts, & Tektites Dating the Clinchfield Formation
    • 14C: The Tivola Limestone
    • 14D: Twiggs Clay Vertebrates
    • 14F; Sandersville Limestone, By Hank Josey
    • 14E: Ocmulgee Formation Vertebrates
    • 14I: Dating Late Eocene Sediments
    • 14J: Georgia's Tektites; Georgiaites
    • 14K; Shell Bluff; Georgia's Most Historic Paleontology Site
    • 14L; Taylors Bluff, Paleo Paddling the Ocmulgee River
    • 14M; Eocene Terrestrial Mammals From Gordon, GA
    • 14N: Fossil Ridge, A Stratigraphic Study in Oaky Woods Wildlife Management Area
    • 14O; Georgia's First Entelodont
    • 14P: Historic Rich Hill
    • 14Q; Bibb County's Christy Hill, Clinchfield Formation Hilltop
  • 15: Early Oligocene
    • 15A: The Marianna Limestone
    • 15B; The Glendon Limestone
    • 15C: Undiffereniated Oligocene Residuum
    • 15D; Brissus bridgeboroensis; A New Echinoid Species From Georgia’s Bridgeboro Limestone
    • 15E: The Curious Steinkern Sea Biscuits of Red Dog Farm Road
    • 15F: Early Oligocene Gordian Knot
  • 16: Bonaire GA Entelodont
  • 17: The Whale Eating Shark
  • 18: Miocene Epoch; 23.3 to 5.3 Million Years Ago
    • 18A; Miocene Terrestrial Vertebrates
    • 18B; Paul Fell, Rockhouse Cave
    • 18C: The Marks Head Formation
    • 18D: Miocene Terrestrial Vertebrates of the Marks Head Formation
    • 18E: The Statenville Formation
    • 18F: South Georgia’s Dugong Metaxytherium calvertense
  • 19: Pliocene Epoch; 5.3 to 2.5 Million years Ago
    • 19A; Two Small Primitive Horses from Taylor County
  • 20: The Ice Ages; Pleistocene & Holocene Epochs
    • 20A; Clark Quarry's Mammoths & Bison
    • 20B: Pleistocene Vertebrate List
    • 20C: Georgia’s Eolian Dunes
    • 20D: Georgia’s Carolina Bays
    • 20E: Late Pleistocene Significant Events
    • 20F: Southeastern Thermal Enclave
    • 20G; Diamond Back Terrapins
    • 20H; A Kaolin Mine Beaver Dam
    • 20I; Pleistocene Vertebrate Fossils On Georgia’s Piedmont
    • 20J; Watkins Quarry Pleistocene Vertebrates, Glynn County, GA
  • *NEW* 20K: Pleistocene Vertebrates from Coastal Georgia
  • 21: Humans in Georgia
  • 22: Geology of the Coastal Plain, 1911
    • 22A: 1911 Cretaceous Fossil Locations
    • 22B: 1911 Eocene Fossil Locations
  • 23: Coastal GA Locations (1957)
  • 24: Needed; The Georgia Geologic Survey
  • Building This Site
    • Origins Of This Site
    • Contributing Artists
    • Black & White Sketches

2B: A Trilobite Nest in Georgia  
By Thomas Thurman
Filed 26/July/2019
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At 500 million years ago there was a trilobite nest in Northwest Georgia. The implications for that statement are simply staggering, but it’s true. (1) This shows that nesting behavior is at least 500 million years old. 
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The specimen seen above shows both nesting and homing behavior and came from the bank of the Conasauga River in Murray County of northwestern Georgia. It’s actually a small fossiliferous rock slab roughly 6cm (2.36”) square.

​Questions persist, in general, over when and where various behaviors emerged. Trilobites have been recently shown to be oviparous, meaning they laid eggs which hatched later. When this behavior emerged in the animal kingdom is unknown.

It was discovered in the field by William (Bill) M. Montante  of Tellus Science Museum who's a well-seasoned amateur knowledgeable over these NW Georgia sediments. Recognizing that he had something interesting, he took the slab to Dr. David Schwimmer at Columbus State University, his old friend and a long time Georgia trilobite researcher. 

Upon review Schwimmer concluded that Montante had indeed found an important fossil which dramatically added to the scientific body of knowledge. They decided to pursue peer-review publication (Schwimmer & Montante have published multiple  peer-reviewed papers together). They succeeded and their research appears in Volume 24 of the highly regarded Palaios, no small feat.  
 

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​The slab has been dated by Schwimmer and Montante to the early Paibian Stage of the Upper Cambrian. The Paibian Stage spans from 501 to 496 million years ago, so early Paibian would be right around 500 million years ago.

​As a reminder; 500 million years ago Georgia was the floor of a shallow sea and there were no bones, trees, insects or enameled teeth (such as ours) on all the Earth.
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The slab reveals a cluster of juvenile (larval) trilobites of the genus; Aphelaspis, and the molted parts of a shell from an adult Aphelaspis brachyphasis. The molted shell seems to be from a single individual. 
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At least 113 individual juveniles are present. Juveniles which would have been highly mobile in life.

Most individuals are so poorly preserved that they offer little further information. However, at least 29 are at the same stage of development (meraspid degree 5), suggesting they’re the same age. There are 27 individuals which are complete, suggesting rapid buried and that this is a death assemblage. There are two individuals which are probably older (meraspid degree 6), one individual at meraspid degree 2, and one at meraspid degree 3 or 4.

​In a moment we’ll discuss what “meraspid” means, it's a term used to described stages of juvenile trilobite growth.
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​The molted shell from the adult is roughly 2cm (.8”) long and 1.6cm (.6”) wide. The mass of 100+ juveniles is roughly 2.5cm X 2.8cm (1” X 1.1”), so this is a large group of tiny individuals. 

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What the fossils on the slab show is larval aggregation, basically large numbers of larva coming together. Why larva gather together isn’t fully understood. It’s seen today in several species of insects.

​One research abstract from 2018 on the fruit fly Bactrocera tryoni (2) states that larval aggregation consistently gave body mass benefits to individuals. Since larger larva generally lead to adults who are more fit, individuals clearly benefitted from group behavior.​

Trilobite Molting
To understand what Schwimmer & Montante are reporting, we must understand a bit about the stages of molting in trilobites. Like all arthropods trilobites molt. They had a hard segmented shell, an exoskeleton which couldn’t grow. When they outgrew it, they shed their shell and a new exoskeleton was exposed and hardened. Today we see this in crabs, shrimp, scorpions, centipedes, spiders, insects and many more.
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This means that you might find fossils of either cast-off molts and bodies. For researchers, telling the difference is straightforward. The first give-away is the presence of free cheeks (or librigenae), these are very easily carried away by currents. If the librigenae are present it’s the fossil of a body. As stated above, at leave 27 of the larva were body fossils made by living animals. 
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Paleontologists have learned that juvenile trilobites add body segments when molting, but adults do not. So Paleontologists divide the development of trilobites into three stages, protaspid, meraspid, & holaspid. (3)
  1. Protaspid; the earliest form of trilobite where no segments are present.
  2. Meraspid; Once molts have produced two or more segments trilobites reach the meraspid stage. We have no information about the frequency of molts or how fast segments are added; one segment per molt? Two segments per molt? It may even be variable.
  3. Holaspid; Once the addition of segments has reached the adult stage the trilobite has matured to the holaspid stage, all the adult parts are in place, the animal is sexually mature, growth and molting continues but only results in an increase of size.​ ​

​The meraspid stage is further subdivided into degrees by how many segments have been added. Interestingly, at least 29 juveniles present in the slab are at meraspid degree 5, they show the same number of body segments. It is assumed that they’re all at the same age. However, we have no information about their rate of growth or what their age is beyond juveniles of meraspid degree 5.


Trilobite Clusters
Now, there are many reports of trilobite clusters. Two types of clusters are known, molt and body clusters. Molt clusters are preserved empty shells, since they’re very lightweight they’re easily moved about by currents until they’re dropped in an eddy and buried by sediments. It's believed that shed clusters are simply formed by currents.
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Body clusters are different. These were living animals which came together intentionally; perhaps a feeding group, or for mating or collective defense. They died together and were preserved together.
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More importantly, 27 of these are well enough preserved to see that they still possessed their free cheeks at the time of preservation. This cluster of trilobites was rapidly buried & killed.
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Now comes the interesting part. Those 27 complete, juvenile Aphelaspis trilobite found along the Conasauga River are not newly hatched. Nor are they adults. They are at the meraspid stage, they’re juveniles.
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Why were so many juvenile trilobites, of the same apparent age, still together? The first instinct is to assume protection; but the geology of the claystone strongly suggest that these trilobites were exposed on the sea bottom. They weren’t hiding under anything.
  

Horseshoe crabs are probably the closest living relative to trilobites and they are well known to gather in great numbers for molting, mating, and to deposit eggs. These massed horseshoe crabs are well document feeding opportunities for predators, so protection isn’t a motive for the individuals.
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Those meraspid Aphelaspis trilobites were juveniles so they weren’t mating or depositing eggs. The attached free cheeks show this wasn’t a molting assemblage.
 

When these trilobites lived the claystone matrix of the slab would have been a soft substrate of fine-grained sediments representing a quiet marine environment. But the muddy, silty bottom would have been unsuitable for eggs. Eggs would have been easily buried by silt disturbed by another passing animal.  However, there was a molted shell of an adult trilobite nearby. This shell would have made a good, fairly hard surface site for eggs.
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Schwimmer & Montante’s Theory
I’m proud to say I know both Schwimmer and Montante, they’re both respected scientists, especially here in the Southeast and Georgia.

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They noted that the fine-grained muddy bottom was probably unsuitable for egg laying but the nearby molted shell of the adult is a different matter. It’s been established that trilobites very likely laid eggs. Schwimmer & Montante theorize that the eggs were laid in the molted shell.
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To quote their research;
“We hypothesize, therefore, that these sclerites (molted shells) comprise the egg deposition site that originated this meraspid assemblage. It is recognized that this hypothesis assumes there was some form of homing or kin-affiliative behavior in meraspid trilobites which would explain how mobile, and likely planktonic, individuals re-associated after some developmental stages.”
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Schwimmer and Montante further, and successfully, argue that some sort of homing behavior, larval aggregation, would explain the behavior recorded in the slab. That such an assemblage of same-age individuals “…would be improbable as a random event.”
They argue that these trilobites hatched in the nest of the discarded shell and returned, or homed, after multiple molts to the nest site.

We cannot currently know how much time passed between hatching and homing back to the nest. We don't know why they returned.
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The location where the small slab was collected contains many Aphelaspis brachyphasis at all stages of development; “… and there are other specimens from the site which may represent additional occurrences of larval clustering.”
 
Schwimmer and Montante close by acknowledging that the preserved juvenile trilobites’ behavior may well be a feeding mass or a herd-protection mass, but the question of why and how a larval aggregation of juveniles came together persist… 
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References
​1)      A Cambrian Meraspid Cluster: Evidence of Trilobite Egg Deposition in a Nest Site; By David R. Schwimmer & William M. Montante, PALAIOS, 2019, v. 34, 254–260, Research Article
2)     Social and nutritional factors shape larval aggregation, foraging, and body mass in a polyphagous fly; by, Juliano Morimoto, Binh Nguyen, Shabnam Tarahi Tabrizi, Fleur Ponton & Phillip Taylor, published; Scientific Reports, volume 8, Article number: 14750 (2018)
3)     Molting in Trilobites; Trilobiteseas.com, Paleobiology of a Paleozoic Icon for the Collector and Enthusiast, by; Christopher R. Cunningham, copyright 2016-2017