Johan Lindgren’s research while affiliated with Lund University and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (102)


Simplified cladogram of mosasaurid relationships. See text for details.
Mosasaurid δ¹³C values by taxon. Color coding denotes subfamily membership: yellow = Halisaurinae; red = Mosasaurinae; green = Plioplatecarpinae; blue = Tylosaurinae. See Appendix A for details.
Temporal distribution of mosasaurs, tooth guild occupation, and isotope values by taxon. Geographic distribution of mosasaurs through time after [1]; horizontal tan bands span 15° to 30° north and south latitude. Tooth-morphology-based guild membership is subjectively assessed following previous research [8,17,77]. Color denotes subfamily membership: yellow = Halisaurinae; red = Mosasaurinae; green = Plioplatecarpinae; blue = Tylosaurinae.
δ¹³C by select geographic region. Color coding denotes subfamily membership: yellow = Halisaurinae; red = Mosasaurinae; green = Plioplatecarpinae; blue = Tylosaurinae.
δ¹³C by select geographic region and body length. Size data taken from [1].
The Evolution of Mosasaurid Foraging Behavior Through the Lens of Stable Carbon Isotopes
  • Article
  • Full-text available

April 2025

·

69 Reads

·

·

Anne S. Schulp

·

[...]

·

A large data set of new and previously published measurements of δ¹³C values derived from tooth enamel (n = 223, of which 93 are new) are compiled to explore patterns of foraging area preferences of Late Cretaceous mosasaurid squamates over evolutionary time scales (~93–66 Ma). Our results indicate that small-bodied halisaurines are restricted to a relatively nearshore range, overlapping the lower end of the range of plioplatecarpines and some mosasaurine taxa. Most moderately sized plioplatecarpines occupy a relatively narrow foraging area in much of the nearshore and proximal offshore marine foraging area for the majority of their existence. Tylosaurines exhibit a greater offshore marine range than plioplatecarpines, consistent with their large body size and the robustness of their feeding apparatus. The largest tylosaurine taxa are replaced by Mosasaurus in the Late Campanian–Maastrichtian in the offshore foraging range. Mosasaurine taxa are found to occupy the broadest range of foraging areas, but their ranges are taxonomically segregated, consistent with adult body size and the diversity of feeding adaptations such as tooth morphologies and skull architecture seen in that subfamily. Where foraging areas of multiple taxa overlap, differences are typically in tooth form, reflecting prey preference or feeding niche. Foraging area occupation by multiple taxa with similar tooth forms suggests that other factors such as body size and prey acquisition style may have allowed for the finer partitioning of resources. Deep diving and long submergence may have also contributed to the depleted signals recovered for some of the large-bodied durophages and the largest of the macrophagous apex predators.

Download

A new specimen of Plesiopterys wildi reveals the diversification of cryptoclidian precursors and possible endemism within European Early Jurassic plesiosaur assemblages

March 2025

·

209 Reads

Background A virtually complete and articulated plesiosaur skeleton (MH 7) is described from the Lower Jurassic (Toarcian) Posidonienschiefer Formation near Holzmaden in southern Germany. Plesiosaur remains are rare in this rock unit compared to those of other marine reptiles, such as ichthyosaurs and thalattosuchian crocodylomorphs. The new specimen offers an opportunity to assess the biodiversity of Early Jurassic plesiosaurs documented from what is now Central Europe. Methods The osteology of MH 7 is described and compared with other Early Jurassic plesiosaurs based on first-hand observations. Phylogenetic analyses using both equal weighting and weighted parsimony determined phylogenetic placement within Plesiosauria. Results Plesiopterys wildi is an early-diverging plesiosauroid and a sister taxon to Franconiasaurus brevispinus and Cryptoclidia. MH 7 represents a subadult individual, providing an updated character state diagnosis of Plesiopterys wildi , which has hitherto only been known from the osteologically immature holotype SMNS 16812. The presence of multiple regionally distinct plesiosaur genera and species within the European epicontinental marine basins suggests possible paleobiogeographical segregation during the Toarcian.



SEM images of vessels recovered from non-avian dinosaur and ostrich bone. a–d, MOR 2598, B. canadensis, e–h, MOR 10857, ceratopsian, i–l, MOR 555/USNM 555000, T. rex, m–p, MOR 1125, T. rex, q–t, MOR 1126, T. rex; u–x, MOR 1128, T. rex, y–bb, extant ostrich. Asterisks (*) denote accessory vessel, arrows mark apparent osteocytes on external vessel surfaces. Note that all vessels show a branching pattern and open lumen. Scale bars are as indicated.
TEM images of a,b; MOR 2598; c,d; MOR 10857; e,f; MOR 555/USNM 555000; g,h; MOR 1125; i,j; MOR 1126; k,l; MOR 1128; m,n; S. camelus (ostrich). L, Lumen; NB, Nuclear bulge. Arrow in j shows fibers in the layer adjacent to lumen. Scale bar as indicated.
Representative nano-CT images of dinosaur vessels. a–c, MOR 2598. a, overview, shown with a smaller vessel containing abundant rounded spheres. b, Cross-section, taken at the level of dashed line in a. c, vascular inclusions from MOR 2598. d, MOR 10857 showing heterogeneous surface texture and branching of vessels; e, MOR 555/USNM 555000 shows complex vessel walls with varying density; f, MOR 1125 vessels are long, hollow and show branch points for smaller vessels; g, MOR 1126 has dense outer layer, perhaps indicating encrustation; h, MOR 1128 vessels are highly fractured, with vessel on lower left containing dense, spherical vascular inclusions; i Vessels liberated from extant ostrich (S. camelus) show greater interconnectivity and more branching of vascular network. Scale bars are as indicated.
In situ immunohistochemistry (IHC) data taken in dual channels (transmitted light and FITC) where antibody–antigen complexes are visualized by fluorescence and localized to vessel walls. a–d, MOR 2598; e–h, MOR 10857; i–l, MOR 555/USNM 555000; m–p, MOR 1125; q–t, MOR 1126; u–x MOR 1128; y–bb, ostrich. Column 1, tissues exposed to elastin antibodies (see Supplementary Information for description and characterization); Column 2, exposed to antibodies to tropomyosin; Column 3, exposed to laminin antibodies, and Column 4, exposed to anti-ostrich hemoglobin antibodies. All fossil data collected under the same parameters, allowing direct comparison of binding strength/avidity. Arrows show regions of crystallinity. Scale bars 20 μm.
Detection of proteins in fossil vessels by ToF-SIMS. Overlay TOF-SIMS image of MOR 1126 (a,b) showing the added intensity of ions representing proteins in green and iron phosphate in red. (b) Superimposed ToF-SIMS image (as in (a)) and SEM micrograph of the same area on the vessel surface. (c) SEM image as in (b). Arrowheads indicate structures resembling osteocytes and the yellow box indicates the area magnified in (d). (d) Magnified SEM micrograph highlighting various microstructures: flat, protein-containing layer (*) located below a porous inorganic layer (Δ), porous inorganic layer infiltrated with structureless deposit (+), and filaments resembling collagen fibers (arrowheads). (e) Score plot from spectrum PCA that includes fragment ion intensities in positive ToF-SIMS spectra of four reference proteins and protein-rich ROIs on the fossil vessel surfaces. Labels of specific data points indicate spectra from ROIs displayed in Fig. 5a and Supplementary Information, Fig. S8–12, as marked by green dotted lines. (f) PC1 (upper) and PC3 (lower) loadings from PCA as in (e), for included protein fragment ions (associated amino acids are indicated). Scale bars are 10 μm in (a–c) and 1 μm in (d).
Taphonomic variation in vascular remains from Mesozoic non-avian dinosaurs

February 2025

·

144 Reads

The identity and source of flexible, semi-transparent, vascular-like components recovered from non-avian dinosaur bone are debated, because: (1) such preservation is not predicted by degradation models; (2) taphonomic mechanisms for this type of preservation are not well defined; and (3) although support for molecular endogeneity has been demonstrated in select specimens, comparable data are lacking on a broader scale. Here, we use a suite of micromorphological and molecular techniques to examine vessel-like material recovered from the skeletal remains of six non-avian dinosaurs, representing different taxa, depositional environments and geological ages, and we compare the data obtained from our analyses against vessels liberated from extant ostrich bone. The results of this in-depth, multi-faceted study present strong support for endogeneity of the fossil-derived vessels, although we also detect evidence of invasive microorganisms. Supplementary Information The online version contains supplementary material available at 10.1038/s41598-025-85497-y.



Fig. 1. Bornholm and the Hasle Formation. a, Overview map of northern Germany and southern Scandinavia. Note the location of the Danish Island of Bornholm in the southern part of the Baltic Sea. b, Simplified geological map of Bornholm, Denmark, with the location of the town of Hasle and type locality of the Hasle Formation indicated by a red star (modified from Graversen 2009, fig. 1). c, Middle to Upper Jurassic stratigraphy of Bornholm (modified from Sandersen et al. 2014, fig. 3.2). The Hasle Formation is marked by a red star.
Fig. 2. Descriptive terminology of a left lower tritylodontid postcanine (modified from Panciroli et al. 2017, fig. 1). Abbreviations: AIA, anterior interlocking area; b, buccal cusp; l, lingual cusp; PIA, posterior interlocking area.
Fig. 3. Photographs of NHMD 1725979. a, Occlusal view (stereo pair). Note slightly offset cusp rows and embayments (arrows) representing the PIA. b, Crown base (stereo pair). Note ridged, "enamel-covered" projection (arrow) representing the AIA. c, d, NHMD 1725979 in c, lingual and d, buccal views, respectively.
Fig. 4. Digital reconstruction and CT slice data of NHMD 1725979. a, Oblique posterolingual view of the tooth. Arrows mark the PIA. b, Buccal view of the fossil. The dotted line marks the pseudo-cingulid, while the solid line indicates the orientation of the CT slice depicted in panel i. c, The tooth depicted in lingual view. d, Anterior view of NHMD 1725979. Arrow indicates the AIA. e, The fossil in occlusal view. Note shallow depressions on the anterior face of b2 and l2 (arrowheads). Arrow denotes the PIA, while the lines indicate the orientation of the CT slice data depicted in panel h and j, respectively. f, Base of the crown. Arrow marks the AIA. g, Posterior view of NHMD 1725979. Arrow denotes the PIA. h, Longitudinal CT slice through cusp b2 and parts of b1, showing the pulp cavity of b2. Striations radiating from the pulp cavity likely represent growth lines, and are indicated by an arrow. i, Section placed transversely through the cusp bases. The pulp cavities of l2 and b2 can be seen, as well as the beginning of this cavity in b1. j, Buccolingual section through b2 and l2. Note prominent pulp cavities.
The first tritylodontid (Synapsida, Cynodontia) fossil from Scandinavia

December 2024

·

120 Reads

Bulletin of the Geological Society of Denmark

Lower Jurassic (Pliensbachian) sand- and siltstones of the Hasle Formation on the Danish Island of Bornholm have yielded a diverse invertebrate and vertebrate assemblage dominated by marine taxa. Recently, dental and skeletal remains of terrestrial animals have also been collected from this rock unit, including the first tritylodontid tooth from Scandinavia. Here we describe the new fossil (NHMD 1725979), identified as a left lower postcanine. Even though precise taxonomic placement within Tritylodontidae is difficult, the preserved morphological characters are shared to varying extent with the Middle Jurassic – Lower Cretaceous genera Polistodon, Montirictus, Nuurtherium, Stereognathus, Xenocretosuchus, and Shartegodon. Hence, NHMD 1725979 may represent the stratigraphically oldest occurrence of a derived tritylodontid.


Skin Anatomy, Bone Histology and Taphonomy of a Toarcian (Lower Jurassic) Ichthyosaur (Reptilia: Ichthyopterygia) from Luxembourg, with Implications for Paleobiology

August 2024

·

171 Reads

A partial ichthyosaur skeleton from the Toarcian (Lower Jurassic) bituminous shales of the ‘Schistes Carton’ unit of southern Luxembourg is described and illustrated. In addition, associated remnant soft tissues are analyzed using a combination of imaging and molecular techniques. The fossil (MNHNL TV344) comprises scattered appendicular elements, together with a consecutive series of semi-articulated vertebrae surrounded by extensive soft-tissue remains. We conclude that TV344 represents a skeletally immature individual (possibly of the genus Stenopterygius) and that the soft parts primarily consist of fossilized skin, including the epidermis (with embedded melanophore pigment cells and melanosome organelles) and dermis. Ground sections of dorsal ribs display cortical microstructures reminiscent of lines of arrested growth (LAGs), providing an opportunity for a tentative age determination of the animal at the time of death (>3 years). It is further inferred that the exceptional preservation of TV344 was facilitated by seafloor dysoxia/anoxia with periodical intervals of oxygenation, which triggered phosphatization and the subsequent formation of a carbonate concretion.



Eumelanin and phaeomelanin molecules and their respective constituent monomers
Key eumelanin monomer units are 5,6-dihydroxyindole (DHI) and 5,6-dihydroxyindole-2-carboxylic acid (DHICA); phaeomelanin monomer units are benzothiazine (BT) and benzothiazole (BZ). Chemical degradation of these units by alkaline hydrogen peroxide oxidation (AHPO) generates PDCA (pyrrole-2,3-dicarboxylic acid), PTCA (pyrrole-2,3,5-tricarboxylic acid), PTeCA (pyrrole-2,3,4,5-tetracarboxylic acid), TTCA (thiazole-2,4,5-tricarboxylic acid) and TDCA (thiazole-4,5-dicarboxylic acid) markers. Hydroiodic acid (HI) hydrolysis generates 4-AHP (4-amino-3-hydroxyphenylalanine), BZ-AA (benzothiazole amino acid) and 3-AHP (3-amino-4-hydroxyphenylalanine; see Supplementary Fig. 16)33–36,40,41.
AHPO-HPLC data for black, rufous and white feathers from extant birds with, and without, thermal treatment
Bar charts show melanin marker concentrations in black and rufous (each n = 5; Gallus gallus) and white (n = 4; Egretta garzetta) feathers; data are shown for untreated feathers and feathers thermally matured at 200 °C and 250 °C. Melanin markers are generated during alkaline hydrogen peroxide oxidation (AHPO) and hydroiodic (HI) acid hydrolysis. Data are presented as mean ± SD. PTCA pyrrole-2,3,5-tricarboxylic acid, PDCA pyrrole-2,3-dicarboxylic acid, PTeCA pyrrole-2,3,4,5-tetracarboxylic acid, TTCA thiazole-2,4,5-tricarboxylic acid, 4-AHP 4-amino-3-hydroxyphenylalanine, TDCA thiazole-4,5-dicarboxylic acid, BZ-AA benzothiazole amino acid. Source data are provided as a Source Data file.
HCl-AHPO-HPLC data for black, rufous and white feathers from extant birds with, and without, thermal treatment
Bar charts show melanin marker concentrations for untreated feathers and feathers thermally matured at 200 °C and 250 °C. Melanin markers are generated during HCl-alkaline hydrogen peroxide oxidation (AHPO). Filled bars indicate the mean values per treatment; floating bars indicate standard deviation per treatment. Black and rufous feathers are from the domestic chicken (each n = 5; Gallus gallus) and white feathers are from the little egret (n = 4; Egretta garzetta). Data are presented as mean ± SD. PTCA pyrrole-2,3,5-tricarboxylic acid, PDCA pyrrole-2,3-dicarboxylic acid, PTeCA pyrrole-2,3,4,5-tetracarboxylic acid, TTCA thiazole-2,4,5-tricarboxylic acid, TDCA thiazole-4,5-dicarboxylic acid. Source data are provided as a Source Data file.
HCl-AHPO-HPLC data for fossil melanins
Eumelanin (a) and phaeomelanin (b) marker concentrations in samples of melanosomes. Fossil feathers are from the early bird Confuciusornis and the feathered dinosaur Sinornithosaurus from the Jehol biota. Fossil frog samples are of internal melanosomes from Pelophylax pueyoi from the Libros biota. PTCA pyrrole-2,3,5-tricarboxylic acid, PDCA pyrrole-2,3-dicarboxylic acid, PTeCA pyrrole-2,3,4,5-tetracarboxylic acid, BZ benzothiazole, TTCA thiazole-2,4,5-tricarboxylic acid, TDCA thiazole-4,5-dicarboxylic acid. Source data are provided as a Source Data file. Sinornithosaurus and Confuciusornis silhouettes by Conty (modified by T. Slater). Used under an Attribution 3.0 Unported (CC by 3.0) license. https://creativecommons.org/licenses/by/3.0/.
Authentic chemical signals for fossil melanins
Schematic showing chemical degradation of eumelanin and phaeomelanin during fossilisation based on AHPO-HPLC analysis of experimentally matured black and rufous (Gallus gallus) and white (Egretta garzetta) feathers. Dashed line separates data with, and without, HCl treatment. The long horizontal arrows illustrate the relative concentrations of melanin markers before treatment (left-hand margin of arrow) and after maturation at 250 °C (right-hand margin (point) of arrow) without HCl treatment. The short horizontal arrows (on the right) depict the relative concentrations of markers following HCl treatment and maturation at 250 °C. Concentration values (in ng/mg) indicate absolute concentrations of melanin markers. PTCA pyrrole-2,3,5-tricarboxylic acid, PDCA pyrrole-2,3-dicarboxylic acid, PTeCA pyrrole-2,3,4,5-tetracarboxylic acid, 4-AHP 4-amino-3-hydroxyphenylalanine, BZ-AA benzothiazole amino acid, TTCA thiazole-2,4,5-tricarboxylic acid, TDCA thiazole-4,5-dicarboxylic acid. Egretta garzetta by Punnawich Limparungpatanakij (modified by T. Slater). Used under a Royalty Free license. https://dreamstime.com.
Taphonomic experiments reveal authentic molecular signals for fossil melanins and verify preservation of phaeomelanin in fossils

October 2023

·

257 Reads

·

6 Citations

Melanin pigments play a critical role in physiological processes and shaping animal behaviour. Fossil melanin is a unique resource for understanding the functional evolution of melanin but the impact of fossilisation on molecular signatures for eumelanin and, especially, phaeomelanin is not fully understood. Here we present a model for the chemical taphonomy of fossil eumelanin and phaeomelanin based on thermal maturation experiments using feathers from extant birds. Our results reveal which molecular signatures are authentic signals for thermally matured eumelanin and phaeomelanin, which signatures are artefacts derived from the maturation of non-melanin molecules, and how these chemical data are impacted by sample preparation. Our model correctly predicts the molecular composition of eumelanins in diverse vertebrate fossils from the Miocene and Cretaceous and, critically, identifies direct molecular evidence for phaeomelanin in these fossils. This taphonomic framework adds to the geochemical toolbox that underpins reconstructions of melanin evolution and of melanin-based coloration in fossil vertebrates.


Preservational modes of some ichthyosaur soft tissues (Reptilia, Ichthyopterygia) from the Jurassic Posidonia Shale of Germany

July 2023

·

218 Reads

·

5 Citations

Palaeontology

Konservat-Lagerstätten, such as the Toarcian (Early Jurassic) Posidonia Shale of southwestern Germany, are renowned for their spectacular fossils. Ichthyosaur skeletons recovered from this formation are frequently associated with soft tissues; however, the preserved material ranges from three-dimensional, predominantly phosphatized structures to dark films of mainly organic matter. We examined soft-tissue residues obtained from two ichthyosaur specimens using an integrated ultrastructural and geochemical approach. Our analyses revealed that the superficially-looking ‘films’ in fact comprise sections of densely aggregated melanosome (pigment) organelles sandwiched between phosphatized layers containing fibrous microstructures. We interpret this distinct layering as representing condensed and incompletely degraded integument from both sides of the animal. When compared against previously documented ichthyosaur fossils, it becomes readily apparent that a range of preservational modes exists between presumed ‘phosphatic’ and ‘carbonized’ soft-tissue remains. Some specimens show high structural fidelity (e.g. distinct integumentary layering), while others, including the fossils examined in this study, retain few original anatomical details. This diversity of soft-tissue preservational modes among Posidonia Shale ichthyosaurs offers a unique opportunity to examine different biostratinomic, taphonomic and diagenetic variables that potentially could affect the process of fossilization. It is likely that soft-tissue preservation in the Posidonia Shale was regulated by a multitude of factors, including decay efficiency and speed of phosphatic mineral nucleation; these in turn were governed by a seafloor with sustained microbial mat activity fuelled by high organic matter input and seasonally fluctuating oxygen levels.


Citations (72)


... Paleontology is a multidisciplinary analytical eld that studies ancient organisms by developing and applying modern advanced technology to analyze fossils, both at the physical and chemical levels. [1][2][3][4] Fossils preserving non-biomineralized tissues, i.e. so tissues (e.g., skin, eyespot and various internal organs) and in particular those preserved as carbonaceous lms (organic preservation 5 ) are of great importance for the research on the preservation of biomolecules, such as melanins, [6][7][8][9] keratins 10,11 and other biomolecules. [12][13][14] These fossils are usually analyzed using a range of analytical methods, encompassing scanning electron microscopy (SEM) and transmission electron microscopy (TEM), gas chromatography-mass spectrometry (GC-MS), Fourier-transform infrared (FTIR) spectroscopy, Raman spectroscopy, synchrotron radiation macro-X-ray uorescence (SR-MA-XRF) spectroscopy, and X-ray absorption (XAS) spectroscopy. ...

Reference:

Application of mobile-macroscale scanning X-ray fluorescence (mobile-MA-XRF) imaging in paleontology: analyses of vertebrate fossil specimens from Messel conserved in different solid and liquid media
Taphonomic experiments reveal authentic molecular signals for fossil melanins and verify preservation of phaeomelanin in fossils

... The abundant Mn-and Fe-oxides occurring in the skeletal elements and their surrounding calcareous sediment matrix demonstrate they were strongly oxidized by recent weathering (Fig. 7A). Articulated and sub-articulated ichthyosaur specimens found in the coeval organic-rich shale and calcareous concretions of the Posidonia Shale in SW Germany regularly show phosphatized and pyritized soft tissues as well as body outlines preserved as organic films (Martill, 1993;Lindgren et al., 2018;De La Garza et al., 2023). The almost total TOC loss documented for the sediment surrounding the ichthyosaurs from Beaujolais implies that such organic films, if any, would have very likely been removed totally by recent weathering. ...

Preservational modes of some ichthyosaur soft tissues (Reptilia, Ichthyopterygia) from the Jurassic Posidonia Shale of Germany

Palaeontology

... In all samples, peptides/proteins were detected by the presence of typical protein-related secondary ions ( Supplementary Information, Fig. S7a-c). These N-containing fragment ions occur at high signal intensities in positive ion spectra of pure proteins and peptides [117][118][119] , and usually comprise the side group of a specific amino acid together with the C-N portion of the peptide backbone 117 . These same ions also occur in ToF-SIMS spectra of free amino acids but, importantly, free amino acids also generate comparably intense peaks corresponding to intact molecular ions 133 , which are notably lacking in spectra of peptides/proteins. ...

An ancestral hard-shelled sea turtle with a mosaic of soft skin and scutes

... Sclerites can preserve fine morphological details and colour patterns and are known to last for several million years under the right conditions (e.g. Heingard et al. 2022). The recovery of sclerites from archaeological excavations is a delicate procedure that entails paraffin floatation and sieving through a 300 µm mesh (Coope & Osborne 1968). ...

Preservation and Taphonomy of Fossil Insects from the Earliest Eocene of Denmark

... The collaboration between virtual paleontology and paleoart, through digital reconstructions, can effectively communicate ancient life to a wide range of audiences (Hochadel, 2022). The rapid development of novel analytical techniques and artistic outlets has exponentially increased our understanding of ancient life, making reconstructive prospects significantly brighter (Eriksson et al., 2022). Digitalization has fundamentally changed paleoart. ...

A review of ichthyosaur (Reptilia, Ichthyopterygia) soft tissues with implications for life reconstructions
  • Citing Article
  • February 2022

Earth-Science Reviews

... In addition, we could consider the potential role of prior information on other parameters. For example, fossil-based estimates of sampling probability can be used to inform the sampling rate (Wagner and Marcot 2010;O'Reilly and Donoghue 2020;Wright et al. 2021;Thuy et al. 2022). Any implications of prior choice for the reliability of the results are rarely discussed in the literature. ...

Miniaturization during a Silurian environmental crisis generated the modern brittle star body plan

Communications Biology

... There have only been two documented examples of melanophore preservation in the fossil record; an approximately 10 million year old fossil snake (McNamara, Orr, et al., 2016) and a 180-million-year-old ichthyosaur (Lindgren et al., 2018). The preservation of both melanophores and melanosomes in F. brocksi presents a rare opportunity to examine the coloration of extinct fish species (Heingård et al., 2021;McNamara, Van Dongen, et al., 2016;Rossi et al., 2022;Tanaka et al., 2014). Melanosomes, rather than melanophores have been found in a variety of species, including teleosts such as Mene rhombea from the Eocene (Rossi et al., 2022) and Acanthodes bridge from the Carboniferous (Tanaka et al., 2014). ...

Crypsis in the pelagic realm: evidence from exceptionally preserved fossil fish larvae from the Eocene Stolleklint Clay of Denmark

Palaeontology

... Additionally, despite the perceived low stiffness when compared with those of non-marine turtles, the sea turtle shell has still served as a protective structure for millions of years. Fossilized remnants of carapacial and plastral bones from Paleogene and Cretaceous turtles show evidence of predation by sharks and crocodilians (Shimada and Hooks, 2004;Myrvold et al., 2018;Garza et al., 2021). The degree of protection afforded to these ancestral turtles by their shells remains unknown, but evidence of partially healed bite marks on the carapace indicates that some turtles survived these attacks (Garza et al., 2021). ...

A fossil sea turtle (Reptilia, Pan-Cheloniidae) with preserved soft tissues from the Eocene Fur Formation of Denmark

... Our phylogenetic analyses were conducted using the dataset of Sachs et al. (2021) which is a substantially modified version of the data first assembled by Benson and Druckenmiller (2014). The taxon sampling was modified with addition of firsthand scores for Franconiasaurus brevispinus, obtained from BT 011224.00 ...

Cranial osteology of the mid-Cretaceous elasmosaurid Thalassomedon haningtoni from the Western Interior Seaway of North America
  • Citing Article
  • February 2021

Cretaceous Research

... The second-order peaks of the carbonaceous material emerged after the absence of C-H peaks, implying the transformation of proteins to carbonized material, which occurred at 150- 175°C in our experiments. Moreover, the noise of the Raman signal was the most intense ( Figure 1w), with increased fluorescence intensity due to the decarboxylation or dihydroxylation of proteins during heating (Ito et al., 2013;Jarenmark et al., 2020). This was accompanied by morphological damage to the hair shape and keratinous fibers (Figures 1d, 1e, 1k, and 1l). ...

Chemical Evaluation of Eumelanin Maturation by ToF-SIMS and Alkaline Peroxide Oxidation HPLC Analysis