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Coprolite

A coprolite is the fossilized or mineralized excrement of ancient organisms, preserving traces of their intestinal contents and serving as a valuable trace fossil in paleontology.^[1] These structures typically form when fecal matter, rich in indigestible remnants such as bones, scales, shells, or plant material, undergoes rapid burial and mineralization, often through phosphatization, before decomposition can occur.^[1] Coprolites are relatively rare due to the perishable nature of organic waste, but they are more commonly preserved in marine environments from organisms like fish, reptiles, and invertebrates, appearing as nodular, contorted, or spiral-shaped masses.^[1]^[2] The recognition of coprolites as fossil feces dates to the early 19th century, when fossil collector Mary Anning discovered specimens in the Jurassic strata of Lyme Regis, England, prior to 1824, initially describing them as "bezoar stones."^[3] In 1829, geologist William Buckland coined the term "coprolite" from Greek roots meaning "dung stone" and confirmed their identity as fossilized excrement through detailed analysis, revolutionizing the understanding of prehistoric biology.^[4] Buckland's work, including his identification of coprolites from ichthyosaurs and plesiosaurs containing undigested prey remains, established coprolites as key evidence for reconstructing ancient ecosystems.^[1] Coprolites hold significant paleontological value by revealing the diets, health, behaviors, and environmental conditions of extinct species, often providing direct evidence unavailable from body fossils.^[2] For instance, they can contain identifiable fragments like fish scales, bone shards, or pollen, allowing scientists to infer trophic relationships, such as carnivorous reptiles preying on belemnites or herbivorous dinosaurs consuming wood during seasonal shortages.^[1]^[5] Modern analyses employ techniques like computed tomography (CT) scanning and chemical isotope studies to extract detailed information on nutrition, parasitism, and even gut microbiomes from these fossils.^[6] Despite challenges in attributing coprolites to specific producers, ongoing research continues to uncover their role across the Phanerozoic eon, from Paleozoic invertebrates to Cenozoic mammals.^[6]

Overview

Definition and Etymology

A coprolite is a fossilized specimen of feces or dung produced by ancient animals, serving as a trace fossil that records behavioral evidence such as diet and ecology rather than the physical structure of the organism itself.^[7] Unlike body fossils, which preserve skeletal or soft tissue remains, coprolites fall under the broader category of ichnofossils, including bromalites—fossilized digestive residues—that provide indirect insights into prehistoric life without representing the animal's morphology.^[8] The term "coprolite" was coined in 1829 by the English geologist and paleontologist William Buckland, who introduced it in his seminal work on fossil discoveries near Oxford, England, to describe mineralized dung concretions initially linked to extinct reptiles like Megalosaurus.^[9] Buckland derived the name from the Ancient Greek words kopros (κόπρος), meaning "dung" or "excrement," and lithos (λίθος), meaning "stone," aptly capturing the petrified nature of these specimens.^[10] This etymology reflected Buckland's recognition of coprolites as biogenic structures formed through diagenetic processes, distinguishing them from inorganic concretions. While coprolites are biogenic and primarily associated with animal producers, they are not limited to vertebrates; examples include those from invertebrates such as insects, like opalized termite coprolites from Cretaceous deposits, and even early arthropod feces containing plant material from Siluro-Devonian strata.^[10]^[11]

Physical Characteristics

Coprolites exhibit a wide array of shapes influenced by the digestive systems of their producers, including elongated rod-like or cylindrical forms, spirals with coiled internal structures, discoidal or kidney-shaped variants, and more amorphous or irregular masses.^[12] These morphologies aid in preliminary recognition; for instance, spiral coprolites often derive from animals like sharks possessing spiral valves in their intestines.^[1] Sizes vary dramatically based on the organism, ranging from a few millimeters in length for coprolites produced by small invertebrates such as insects to over 40 centimeters for those from large carnivorous dinosaurs like Tyrannosaurus rex.^[13]^[14] In terms of composition, coprolites are predominantly mineralized remnants of organic fecal matter, with calcium phosphate (in the form of apatite) as the most common mineral, though silica or calcium carbonate replacements also occur depending on the depositional environment.^[15] Embedded inclusions frequently preserve undigested dietary elements, such as bone fragments in carnivore coprolites, seeds or plant material in herbivore specimens, and pollen grains in various types, reflecting the original meal contents.^[12] These inclusions are often pulverized and integrated into the mineral matrix, distinguishing coprolites from similar sedimentary structures. Color variations in coprolites typically span brown to black hues, resulting from organic carbon residues and iron oxides, while lighter shades like yellowish-brown, pinkish, or whitish tones arise from phosphate enrichment or specific mineralization processes.^[16]^[17] Textures externally appear nodular, contorted, or polished smooth, with internal cross-sections revealing concentric layering from successive depositions in the gut or voids created by escaping gases during early decay.^[1]^[18] These features contribute to their distinctive, often lumpy appearance compared to other fossilized concretions.

Formation

Biological Origin

Coprolites originate from the feces produced by animals through their digestive systems, which process ingested food, extract nutrients, and expel undigested residues as waste. In vertebrates, the digestive tract—comprising the mouth, stomach, intestines, and cloaca or anus—breaks down food via enzymatic and mechanical actions, resulting in feces that vary in composition based on diet. Carnivorous vertebrates, such as ancient sharks or dinosaurs, produce feces rich in undigested bone fragments, scales, or feathers due to incomplete digestion of protein-rich prey, while herbivorous vertebrates like titanosaurs yield feces containing plant fibers, seeds, pollen, or bark remnants from cellulose-heavy diets.^[19]^[12]^[20] Invertebrates also contribute to coprolite formation through analogous digestive processes, though their systems are simpler and often segmented. For instance, annelids and arthropods like insects process food in a foregut, midgut, and hindgut, excreting compact fecal pellets or castings that preserve undigested organic matter, such as wood particles in termite coprolites from the Eocene-Oligocene. Coprolites are categorized by their producers, including those from fish (e.g., spiral forms from spiral valve intestines in sharks), dinosaurs (e.g., bone shards indicating carnivory in theropods), mammals (e.g., hair inclusions in therapsid feces), insects, and even ancient humans, with dietary indicators like bone fragments in carnivore examples highlighting trophic levels.^[21]^[12]^[20] Immediately after excretion, several pre-fossilization factors influence the potential for feces to persist long enough for fossilization. High moisture content promotes rapid bacterial decomposition of organic components, accelerating breakdown, while drier conditions slow this process and enhance preservation chances. Bacterial activity, particularly in phosphate-rich carnivore feces, can create microenvironments that inhibit further decay through early mineralization, and exposure to environmental elements like oxygen and temperature fluctuations determines initial stability before burial.^[12]^[20]^[22]

Fossilization Process

The fossilization of coprolites begins with taphonomic pathways that prioritize rapid burial in fine-grained sediments to shield the fecal material from scavengers, weathering, and aerobic decay. This initial entombment, often occurring within hours to days after deposition, limits bacterial decomposition and oxidation, allowing organic components to persist long enough for mineralization to commence.^[23] In many cases, permineralization follows, where minerals such as apatite (calcium phosphate) infiltrate and replace the original organic matrix, transforming the soft, amorphous feces into a durable phosphatic structure. This process replicates the internal textures and inclusions, preserving evidence of undigested remains while gradually recrystallizing the material over geological timescales.^[24] Environmental conditions play a crucial role in favoring coprolite preservation, particularly anaerobic settings that inhibit oxidative breakdown. Low-oxygen environments, such as stagnant lagoons, lake bottoms, or cave floors, promote the accumulation of phosphate-rich pore waters derived from decaying organic matter, creating ideal conditions for phosphatization—the precipitation of calcium phosphate minerals like fluorapatite directly onto or within the coprolite.^[25] These settings often feature microbial mats or biofilms that accelerate burial and provide a geochemical barrier, with low pH (below 6.38) and high phosphate availability driving the carbonate-phosphate switch essential for mineral authigenesis.^[23] In lacustrine or wetland systems, for instance, seasonal anoxia enhances this process, as seen in Early Cretaceous deposits where microbial coverage ensured rapid encapsulation.^[7] The overall fossilization of coprolites typically unfolds over millions of years through diagenetic and lithification stages, with early mineralization stabilizing the structure within weeks to months before sedimentary compaction and cementation complete the transformation. However, rare instances of accelerated preservation occur in exceptional media like amber, where coprolites entomb insects with amber-like fidelity over thousands to millions of years, or in tar pits, where asphaltic impregnation halts decay almost immediately, as evidenced by 50,000-year-old coprolites retaining cellulosic material.00674-6)^[26]

Identification

Morphological Features

Coprolites display a range of diagnostic shapes and patterns that facilitate preliminary field identification of their producers, often reflecting the anatomy of the digestive tract. Reptilian coprolites frequently exhibit segmented forms characterized by circumferential constrictions, as seen in crocodilian specimens with rounded ends and periodic narrowing along their length. Spiral patterns are common in coprolites from reptiles and certain fish, resulting from the spiral valve in their intestines; these heteropolar structures feature tight coils at one end tapering to an exposed edge, with coil widths varying from 3-4 mm in larger examples. Cross-sections of such coprolites reveal internal layering, where longitudinal and transverse views show stacked spirals or continuous wrappings of material, providing clues to the producer's gut morphology. Surface features further aid in distinguishing coprolites during initial assessment. Desiccation cracks often appear as fine, irregular fissures on the exterior, particularly in exposed specimens, while longitudinal zones of rough texture may indicate areas where fecal material adhered to intestinal walls before expulsion. Impressions from surrounding tissues or ingested items, such as shell fragments, can be visible on the surface, and embedded fossils like parasite eggs—such as cestode ova with distinct morphological traits resembling modern forms—may protrude or be discernible without dissection. Size and weight of coprolites correlate with the body size of the producer, offering proportional insights for identification. For instance, sauropod dinosaur coprolites can reach up to 40 cm in diameter, reflecting the massive scale of their herbivores, whereas smaller reptiles produce specimens under 10 cm. These dimensions, combined with density variations, help estimate the original animal's mass without invasive analysis.

Analytical Techniques

Non-destructive methods, such as X-ray computed tomography (CT) scanning, allow researchers to visualize the internal structures of coprolites without causing damage, enabling the identification of inclusions like bone fragments, plant material, or entire organisms. For instance, synchrotron phase-contrast microtomography has revealed articulated fish skeletons and insect remains within Triassic coprolites, providing insights into predator-prey relationships while preserving the specimen for further study.^[27] This technique produces high-resolution 3D reconstructions, distinguishing coprolites from similar sedimentary structures by highlighting voids and textures indicative of digestive processes.^[27] Destructive analytical approaches, including thin-section microscopy and chemical assays like Fourier transform infrared (FTIR) spectroscopy, provide detailed examinations of coprolite microstructure and composition. Thin-section preparation involves slicing and polishing coprolites to 30 μm thickness for petrographic analysis under transmitted light, revealing microcrystalline calcium phosphate groundmasses and inclusions such as fish scales or decapod cuticles that indicate dietary habits and diagenetic history.^[28] FTIR spectroscopy, applied to powdered samples, identifies mineral components by measuring infrared absorption spectra; for example, the presence of apatite (absorption at 580–600 cm⁻¹) in coprolites suggests carnivorous producers, while carbonates and silicates point to herbivores.^[29] Biomolecular techniques further enhance coprolite studies by targeting ancient genetic and isotopic signatures. Ancient DNA (aDNA) extraction, often using phenol-chloroform methods followed by PCR amplification, has successfully recovered human mitochondrial DNA from coprolites up to 14,000 years old,^[30] confirming species origin and detecting parasites like Enterobius vermicularis even in microscopically negative samples.^[31] Stable isotope analysis measures ratios such as δ¹³C in coprolite collagen or apatite to distinguish dietary contributions from C₃ (e.g., temperate grasses, δ¹³C ≈ -27‰) versus C₄ plants (e.g., maize, δ¹³C ≈ -13‰), offering quantitative insights into plant-based diets without relying on macroscopic remains.^[32] Metagenomics, via shotgun sequencing of aDNA, reconstructs gut microbiomes by classifying bacterial taxa; analyses of Late Pleistocene coprolites from megafauna show reduced diversity compared to modern feces, with elevated Actinobacteria and diminished Firmicutes, reflecting preservation biases and host-specific communities.^[33] Tools like CoproID leverage these metagenomic data to predict coprolite sources (e.g., human vs. canine) based on microbiome composition and host DNA proportions.

History

Early Discovery and Studies

The initial scientific recognition of coprolites as fossilized feces occurred in the early 19th century, primarily through the work of English geologist William Buckland. In 1829, Buckland published a seminal paper describing spiral-shaped fossils from the Lias formations near Lyme Regis, England, which he identified as the excrement of ichthyosaurs based on their contents, including undigested fish bones and scales. This marked the first systematic study of coprolites, distinguishing them from previously misinterpreted objects like bezoar stones or plant cones, and he coined the term "coprolite" from the Greek words for dung and stone.^[34]^[35] Mary Anning, a renowned fossil collector from Lyme Regis, played a crucial role in these early discoveries by excavating numerous coprolites and supplying them to Buckland for analysis. Her observations of inclusions such as fish remains within the fossils provided key evidence supporting Buckland's interpretations, and her correspondence with him in 1829 included detailed descriptions that advanced the understanding of coprolite morphology and association with marine reptiles. Anning's contributions extended the scope of coprolite studies beyond mere collection, emphasizing their potential for revealing dietary habits of extinct animals.^[36]^[37] During the 19th and early 20th centuries, coprolite research evolved amid debates over their origins, with some paleontologists proposing they were bezoar stones or plant cones rather than fecal matter. Buckland's findings countered these views by highlighting organic inclusions incompatible with such interpretations, but the controversy persisted. Classifications based on shape, composition, and stratigraphic context to differentiate them from other concretions helped standardize identification, shifting focus from curiosity to structured analysis.^[38] Key milestones in the 1920s included Otto Abel's studies on coprolite inclusions, which integrated them into paleobiological reconstructions of ancient ecosystems and behaviors. Abel examined fossil feces from various formations to infer predator-prey relationships and digestive processes, promoting coprolites as vital for holistic paleontology rather than isolated oddities. This period marked a transition to systematic research, laying groundwork for mid-20th-century advancements in trace fossil analysis.^[8]

Commercial Mining

The commercial mining of coprolites emerged in the mid-19th century as a significant industry driven by the demand for phosphate-rich fertilizers to boost agricultural productivity. In England, particularly in Suffolk, Essex, and Cambridgeshire, extraction began in the late 1820s following the recognition of coprolites—fossilized nodules high in phosphate—as a viable alternative to bone meal and guano.^[39] The boom intensified during the 1840s to 1860s, coinciding with post-Napoleonic War food shortages and advancements in soil chemistry.^[40] Similarly, in the United States, coprolite mining took off in South Carolina around 1867, centered in the Charleston Basin along rivers such as the Ashley and Cooper, where phosphate deposits including coprolitic nodules were abundant and linked to post-Civil War agricultural recovery.^[41] Mining operations typically involved open-pit excavation, with workers using picks, shovels, and later steam-powered dredgers to remove shallow deposits from chalk, gravel, or riverbed layers.^[39] Extracted nodules were processed at nearby washmills—often horse- or steam-operated—where they were crushed, washed to remove impurities, and treated with sulfuric acid to produce "coprolite manure," a soluble superphosphate fertilizer.^[40] The scale was substantial: in the UK, annual production peaked at over 258,000 tons by 1876, generating economic value exceeding £1 million yearly and royalties averaging £100 per acre for landowners.^[39] In South Carolina, the industry yielded $300,000 to $400,000 annually in the early 1880s, with state royalties reaching $250,000 per year by 1890, employing thousands and spurring investments of millions in equipment and land.^[41] The coprolite trade declined sharply by the 1890s and had largely ended by 1900, supplanted by cheaper imports of guano (until its exhaustion around 1872), vast rock phosphate discoveries in South Carolina and Florida, and the rise of synthetic fertilizers like those developed by John Bennet Lawes.^[39] This shift was accelerated by regulatory measures, such as the UK's 1894 Quarries Act, and economic pressures from weather-related farm failures.^[39] The legacy includes profound environmental alterations, with extensive pits, ponds, and lowered fields scarring landscapes in eastern England and South Carolina's Lowcountry, some of which persist as wetlands or archaeological sites today.^[40]^[41]

Applications in Paleontology

Dietary Reconstruction

Coprolites serve as direct evidence for reconstructing ancient animal diets by preserving undigested inclusions that reflect the consumed food sources and trophic habits. These inclusions often include plant microfossils such as pollen grains, starch granules, and phytoliths, which indicate herbivorous or omnivorous diets dominated by vegetation; bone fragments and tooth pieces, signaling carnivory through predation or scavenging; and fish scales or spines, pointing to piscivorous feeding in aquatic or semi-aquatic environments.^[25] Such macroscopic and microscopic remains provide high-resolution snapshots of individual meals, allowing paleontologists to infer seasonal variations and resource availability without relying solely on skeletal evidence.^[42] Notable examples illustrate the diversity of dietary insights from coprolites. In Late Cretaceous tyrannosaurid coprolites from western Canada, crushed bone fragments constitute 30–50% of the volume, demonstrating a carnivorous diet that included large vertebrates, with the fragmentation patterns suggesting bone-crushing behavior consistent with scavenging or active predation.^[43] Similarly, Pleistocene coprolites attributed to herbivores like horses in South America contain evidence indicating a grazing diet focused on C3 and C4 grasses in open grasslands, which aligns with dental wear patterns observed in associated Equus fossils.^[44] These cases highlight how coprolites reveal specific foraging strategies, such as opportunistic scavenging in apex predators or specialized grazing in ungulates. Quantitative methods enhance dietary reconstructions by estimating proportions of food types and trophic positions. Pollen concentration analysis, for instance, quantifies plant intake by counting grains per gram of coprolite material, enabling estimates of dietary breadth—such as high concentrations of herb pollen (114,000–138,000 grains/ml) indicating dominant herbivory in moa coprolites from New Zealand.^[45] Stable isotope ratios, particularly δ15N values, further delineate trophic levels, with enrichments of 3–5‰ per level signaling shifts from primary producers to carnivores, as seen in coprolite associations from Miocene ecosystems where higher δ15N confirmed top-predator status.^[46] These approaches, often integrated with techniques like mass spectrometry from the identification section, provide robust, proportional models of ancient diets.^[47] A 2024 analysis of over 500 coprolites from the early Jurassic in Poland revealed dietary flexibility in early dinosaurs, contributing to understanding their ecological dominance.^[48]

Parasite and Pathogen Studies

Coprolites serve as exceptional repositories for preserved parasite remains, particularly the eggs and cysts of helminths such as nematodes and trematodes, which can endure mineralization or desiccation processes over millennia. These structures are often identified through microscopic examination, revealing intact or partially degraded forms that indicate infection intensity and host-parasite dynamics in ancient populations. For instance, in human coprolites from Hinds Cave in Texas, dating to the Archaic period (approximately 4,000–8,000 years ago), pinworm eggs (Enterobius vermicularis) have been documented, suggesting endemic parasitism among prehistoric hunter-gatherers in arid environments where dry conditions favored preservation.^[49] Such findings highlight how coprolites capture snapshots of parasitic burdens without relying on skeletal evidence. Pathogen detection in coprolites has advanced through ancient DNA (aDNA) analysis, enabling the recovery of bacterial spores and viral genetic material that illuminate infectious disease histories. Metagenomic sequencing of coprolites has identified diverse microbial communities, including potential zoonotic agents like those from Salmonella or hepatitis viruses, providing evidence of disease transmission between humans and animals in prehistoric settings. A notable example is the extraction of viral DNA from a 14th-century coprolite in Belgium, which revealed a diverse virome including bacteriophages and giant viruses such as Mimiviridae, offering insights into ancient microbial diversity in human guts.^[50] These studies, often employing polymerase chain reaction (PCR) and next-generation sequencing on rehydrated samples, underscore coprolites' utility in tracing pathogen evolution and public health challenges in early human societies.^[51] The evolutionary implications of parasite findings in coprolites extend to tracking co-evolution between hosts and parasites across geological timescales, particularly in non-human contexts. In Mesozoic coprolites, helminth eggs, including those of acanthocephalans (thorny-headed worms), have been preserved, indicating ancient infections in reptilian hosts and shedding light on parasite diversification during the age of dinosaurs. For example, putative acanthocephalan eggs recovered from Late Cretaceous coprolites in Brazil, likely from crocodyliform producers, represent some of the earliest direct evidence of these parasites, suggesting their adaptation to vertebrate intermediate hosts predated the K-Pg extinction event.^[52] Such discoveries facilitate reconstructions of parasite-host phylogenies and ecological roles in prehistoric ecosystems.

Environmental Insights

Coprolites serve as valuable archives for reconstructing past vegetation and climates through pollen and spore analysis, which reveals the floral composition of ancient environments ingested by their producers. Pollen grains preserved within coprolites can indicate dominant plant communities, such as grasslands or forests, and shifts between arid and humid conditions based on the ratios of drought-tolerant versus moisture-dependent species. For instance, analysis of Late-Glacial coprolites from the giant ground sloth Mylodon darwinii in Mylodon Cave, southern Chile, identified pollen from grasses, shrubs, and herbaceous plants like Fragaria and Azorella, suggesting a transitional landscape with both open, dry steppes and wetter, forested patches during the Pleistocene-Holocene boundary around 10,530 BP.^[53] This approach complements stable isotope techniques by providing direct botanical evidence of seasonal or regional climate variability.^[25] Faunal interactions within ecosystems are illuminated by coprolites through traces of coprophagy, the consumption of feces, which highlights nutrient recycling and trophic dynamics. Invertebrate borings, such as tunnels made by insect larvae, observed in approximately one-third of Late Triassic coprolites from the Chinle Formation in Petrified Forest National Park, Arizona, demonstrate rapid post-depositional exploitation by coprophagous organisms, fostering energy transfer across trophic levels in swampy habitats.^[54] Similarly, packrat middens—accumulations of fecal pellets from Neotoma rodents—preserve macrofossils and pollen that track biodiversity fluctuations and vegetation succession in arid environments, such as expansions of woodlands during Marine Isotope Stage 3 (~50,000 years BP) in southern California lowlands. The spatial distribution of coprolites aids in habitat reconstruction, particularly by inferring migration routes and resource availability like water sources. Concentrations of coprolites in Permian deposits, such as the "Coproland" site in the Rio do Rasto Formation of the Paraná Basin, Brazil, with over a thousand specimens featuring flat undersurfaces indicative of submersion, point to persistent aquatic environments that attracted aggregations of fish and reptiles, suggesting reliable freshwater availability in a Middle to Upper Permian floodplain.^[55] In Early Permian sites like Arroyo del Agua, New Mexico, clustered coprolites from diverse vertebrates imply seasonal gatherings around water bodies, informing on migration patterns driven by hydrological features in semi-arid landscapes.^[56]

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Instead of isolated individual examples, we explore herein a coprolite association to reconstruct the food-web structure of an ancient ecosystem. The ...Missing: methods | Show results with:methods
[46]
Dietary interpretations for extinct megafauna using coprolites ...
Jun 15, 2016 · Stable isotopes (e.g. δ13C and δ15N) in animal tissues exhibit variations reflecting dietary sources and trophic level, but can also be ...
[47]
Oxyuridae) in the Prehistoric Americas
Oct 31, 2016 · The coprolites were recovered from a cave and exhibited good preservation. No pinworm eggs were encountered although other helminth species were ...
[48]
Viruses in a 14th-Century Coprolite - PMC - NIH
Coprolites are fossilized fecal material that can reveal information about ancient intestinal and environmental microbiota. Viral metagenomics has allowed ...
[49]
Human Coprolites as a Source for Paleomicrobiology - ASM Journals
Microscopic observations can reveal helminths eggs and protozoa cysts (14, 34). These microbial residues can remain uncollapsed for at least 11,000 years inside ...
[50]
First record of Acanthocephala parasites eggs in coprolites ...
This study presents the oldest record of Acanthocephala parasite eggs in coprolites preliminary assigned to Crocodyliformes, recovered in the region of ...Missing: dinosaur infections
[51]
Diet and environment of Mylodon darwinii based on pollen of a Late ...
Pollen analysis confirms earlier findings that the Mylodon was a grazer, but the discovery of large amounts of Fragaria and Azorella pollen in the faeces may ...Missing: arid | Show results with:arid
[52]
Vertebrate coprolites and coprophagy traces, Chinle Formation ...
Coprolites also contain traces of coprophagy (consumption of the original feces), which provides further information about coprolite taphonomy and nutrient ...Missing: chains | Show results with:chains
[53]
Exceptionally preserved asphaltic coprolites expand the ... - Nature
Mar 19, 2020 · The coprolites are cylindrical pellets that represent terrestrial mammal feces (“group III” characterization) found in a context of plant ...<|control11|><|separator|>
[54]
Paleobiology of a unique vertebrate coprolites concentration from ...
Aug 7, 2025 · In southern Brazil, a unique locality provides a record of more than a thousand coprolite specimens. This 'Coproland' is an outcrop of the Morro ...
[55]
(PDF) Early Permian vertebrate coprolites from north-central New ...
Sep 8, 2015 · Abstract—Many Early Permian vertebrate fossils are found in the vicinity of Arroyo del Agua in the Chama. Basin of northern New Mexico.