The DOI matches its Crossref record; 82 of the 84 references it cites were found in a registry or an index.
The Mesozoic marine revolution: evidence from snails, predators and grazers
Abstract
Tertiary and Recent marine gastropods include in their ranks a complement of mechanically sturdy forms unknown in earlier epochs. Open coiling, planispiral coiling, and umbilici detract from shell sturdiness, and were commoner among Paleozoic and Early Mesozoic gastropods than among younger forms. Strong external sculpture, narrow elongate apertures, and apertural dentition promote resistance to crushing predation and are primarily associated with post-Jurassic mesogastropods, neogastropods, and neritaceans. The ability to remodel the interior of the shell, developed primarily in gastropods with a non-nacreous shell structure, has contributed greatly to the acquisition of these antipredatory features. The substantial increase of snail-shell sturdiness beginning in the Early Cretaceous has accompanied, and was perhaps in response to, the evolution of powerful, relatively small, shell-destroying predators such as teleosts, stomatopods, and decapod crustaceans. A simultaneous intensification of grazing, also involving skeletal destruction, brought with it other fundamental changes in benthic community structure in the Late Mesozoic, including a trend toward infaunalization and the disappearance or environmental restriction of sessile animals which cannot reattach once they are dislodged. The rise and diversification of angiosperms and the animals dependent on them for food coincides with these and other Mesozoic events in the marine benthos and plankton. The new predators and prey which evolved in conjunction with the Mesozoic reorganization persisted through episodes of extinction and biological crisis. Possibly, continental breakup and the wide extent of climatic belts during the Late Mesozoic contributed to the conditions favorable to the evolution of skeleton-destroying consumers. This tendency may have been exaggerated by an increase in shelled food supply resulting from the occupation of new adaptive zones by infaunal bivalves and by shell-inhabiting hermit crabs. Marine communities have not remained in equilibrium over their entire geological history. Biotic revolutions made certain modes of life obsolete and resulted in other adaptive zones becoming newly occupied.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The Permian-Triassic extinction (∼251 Ma), the biggest in the history of Earth, saw the extinction of nearly 96% of marine and 70% of terrestrial multicellular species (Benton, 2005) and paved the way for the Mesozoic marine revolution, which fundamentally restructured marine ecosystems (Stanley, 1974; Vermeij, 1977).”
From The Astrobiology Primer v2.0 (2016) · cites this paper as Vermeij, 1977
Citations
Cites
BUTTERFLIES AND PLANTS: A STUDY IN COEVOLUTION
Ehrlich, P. R., & Raven, P. H. (1964) · Evolution · doi:10.1111/j.1558-5646.1964.tb01674.x · Cited by 4,501
Estes, R., & Romer, A. S. (1967) · Copeia · doi:10.2307/1441916 · Cited by 1,207
Treatise on Invertebrate Paleontology
Hallam, A. (1972) · Earth-Science Reviews · doi:10.1016/0012-8252(72)90072-4 · Cited by 1,106
Fishes of the Western North Atlantic
(1966) · BioScience · doi:10.1093/bioscience/16.10.752-a · Cited by 759
Experimental Evaluation of Ecological Dominance in a Rocky Intertidal Algal Community
Dayton, P. K. (1975) · Ecological Monographs · doi:10.2307/1942404 · Cited by 713
A theory of evolution above the species level.
Stanley, S. M. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.2.646 · Cited by 705
Ecological Relationships of the Fish Fauna on Coral Reefs of the Marshall Islands
Hiatt, R. W., & Strasburg, D. W. (1960) · Ecological Monographs · doi:10.2307/1942181 · Cited by 700
Taxonomic Diversity during the Phanerozoic
Raup, D. M. (1972) · Science · doi:10.1126/science.177.4054.1065 · Cited by 590
EVOLUTIONARY AND ECOLOGIC SIGNIFICANCE OF OXYGEN‐DEFICIENT MARINE BASINS
Rhoads, D. C., & Morse, J. W. (1971) · Lethaia · doi:10.1111/j.1502-3931.1971.tb01864.x · Cited by 578
Evolution and Extinction Rate Controls.
Eldredge, N., & Boucot, A. J. (1975) · Systematic Zoology · doi:10.2307/2412728 · Cited by 566
Research works printed but not linked: 19
- Newell, 1971, An outline history of tropical organic reefs, Am. Mus. Novit., 2465, 1
- Woodward, 1892, On the mode of growth and the structure of the shell in Velates conoideus, Lamk., and other Neritidae, 528
- Waller T. R. 1972. The functional significance of some shell microstructures in the Pectinacea (Mollusca: Bivalvia). Pp. 48–56. Int. Geol. Congr. 24th Session, Montreal, Can. Sect. 7, Paleontol.
- Stanley, 1977, Patterns of Evolution
- Fischer, 1977, Secular variation in pelagic realms, Soc. Econ. Petr. Mineral. Special Publ., 25
- Crosse, 1882, Note complémentaire sur la resorption des parois internes du teste chèz Olivella, J. Conchyliol., 30, 181
- 10.2307/2412837 · DOI
- Fischer, 1881, Note sur le genre Olivella, J. Conchyliol., 29, 31
- Earle, 1972, The influence of herbivores on the marine plants of Great Lameshur Bay, with an annotated list of plants, Nat. Hist. Mus. Los Angeles County Sci. Bull., 14, 17
- Glaessner, 1969, Treatise on Invertebrate Paleontology, R399
- Kauffman, 1974, Structure and evolution of Antillean Cretaceous rudist frameworks, Verhandl. Naturf. Ges. Basel., 84, 399
- Copper, 1974, Structure and development of Early Paleozoic reefs, Second Int. Coral Reef Symp., 1, 365
- Kauffman, 1960, An Upper Cretaceous ammonite bitten by a mososaur, Contrib. Mus. Paleontol. Univ. Mich., 15, 193
- Vermeij, 1971, The geometry of shell sculpture, Forma et Functio., 4, 319
- Riegraf, 1973, Biszspuren auf Jurassischen Belemniten-rostren, N. Jb. Geol. Palaontol. M.H., 8, 494
- Bright, 1970, Food of deep-sea bottom fishes, Texas AandM Univ. Oceanogr. Studies., 1, 245
- Rex, 1976, Open coiling in Recent gastropods, Malacologia., 15, 289
- Rhoads, 1970, Mass properties, stability, and ecology of marine muds related to burrowing activity, Trace Fossils, 3, 391
- Yochelson, 1971, A new Late Devonian gastropod and its bearing on problems of open coiling and septation, Smithson. Contrib. Paleobiol., 3, 231
Cited by
Sorted by citations
Items 701–800 of 1,000
Mallick, S., Bardhan, S., Paul, S., Goswami, P., & Das, S. S. (2016) · Ichnos/Ichnos : an international journal for plant and animal traces · doi:10.1080/10420940.2015.1126584 · Cited by 8
Late Cretaceous gastropod dominated communities of the Western Tarim Basin, Southern Xinjiang, China
Hua‐Zhang, P. (1990) · Lethaia · doi:10.1111/j.1502-3931.1990.tb01453.x · Cited by 8
Onshore-offshore trend in the evolution of calliotropid gastropods expressed in shell morphology
Ferrari, M., & Kaim, A. (2018) · Journal of Systematic Palaeontology · doi:10.1080/14772019.2017.1407371 · Cited by 8
Forel, M., & Moix, P. (2020) · Bulletin de la Société Géologique de France · doi:10.1051/bsgf/2020035 · Cited by 8
Comparative Paleoecology of Fossils and Fossil Assemblages
Bush, A. M., & Daley, G. M. (2008) · The Paleontological Society Papers · doi:10.1017/s108933260000173x · Cited by 8
Benthic invertebrates of a modern carbonate ramp: a preliminary survey
Ivany, L. C., Newton, C. R., & Mullins, H. T. (1994) · Journal of Paleontology · doi:10.1017/s0022336000025828 · Cited by 8
Impact of early Toarcian climatic changes on marine reptiles: Extinction and recovery
Reolid, M., Ruebsam, W., Reolid, J., & Benton, M. J. (2024) · Earth-Science Reviews · doi:10.1016/j.earscirev.2024.104965 · Cited by 8
Brownstein, C. D., Near, T. J., & Dearden, R. P. (2024) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2024.1824 · Cited by 7
Kashiyama, Y., Ozaki, K., & Tajika, E. (2011) · Paleontological Research · doi:10.2517/1342-8144-15.2.089 · Cited by 7
Robin, N., Noirit, F., Chevrinais, M., Clément, G., & Olive, S. (2022) · Papers in Palaeontology · doi:10.1002/spp2.1460 · Cited by 7
A new index for quantifying the ornamentational complexity of animals with shells
Miao, L., Dai, X., Song, H., Backes, A. R., & Song, H. (2022) · Ecology and Evolution · doi:10.1002/ece3.9247 · Cited by 7
Zhang, Z., & Sun, Y. (2023) · Geological Magazine · doi:10.1017/s0016756822001236 · Cited by 7
Kolmann, M. A., Grubbs, R. D., Shah, S., Patel, H., & Lovejoy, N. R. (2023) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2023.151939 · Cited by 7
The Ecology of Biotic Interactions in Echinoids
Petsios, E., Farrar, L. E., Tennakoon, S. D., Jamal, F., Portell, R. W., Kowalewski, M., & Tyler, C. L. (2023) · Cambridge University Press eBooks · doi:10.1017/9781108893510 · Cited by 7
Fossil evidence for the escalation and origin of marine mutualisms
Forsey, G. F. (2013) · Journal of Natural History · doi:10.1080/00222933.2013.766276 · Cited by 7
Quantifying Seafood Through Time: Counting Calories in the Fossil Record
Finnegan, S. (2013) · The Paleontological Society Papers · doi:10.1017/s1089332600002679 · Cited by 7
Saupe, E. E., & Myers, C. (2021) · Springer eBooks · doi:10.1007/978-3-319-32979-6_126 · Cited by 7
The Origins and Diversification of Coral Reef Butterflyfishes
Bellwood, D. R., & Pratchett, M. S. (2013) · CRC Press eBooks · doi:10.1201/b15458-2 · Cited by 7
Vörös, A. (2014) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2014.03.030 · Cited by 7
Takeda, Y., & Tanabe, K. (2014) · Acta Palaeontologica Polonica · doi:10.4202/app.00131.2014 · Cited by 7
Testing the Predation-Diversification Hypothesis for the Cambrian—Ordovician Radiation
López-Villalta, J. S. (2016) · Paleontological Research · doi:10.2517/2016pr022 · Cited by 7
Keeping a lid on it: muscle scars and the mystery of the Mobergellidae
Topper, T. P., & Skovsted, C. B. (2017) · Zoological Journal of the Linnean Society · doi:10.1093/zoolinnean/zlw011 · Cited by 7
The many shapes of diversity: ecological and evolutionary determinants of biodiversity through time
Castiglione, S., Mondanaro, A., Carotenuto, F., Passaro, F., Fortelius, M., & Raia, P. (2017) · Florence Research (University of Florence) · Cited by 7
GASTROPOD DRILLING PREDATION IN THE UPPER JURASSIC OF KUTCH, INDIA
Saha, R., Paul, S., Mondal, S., Bardhan, S., Das, S. S., Saha, S., & SARKAR, D. (2021) · Palaios · doi:10.2110/palo.2020.072 · Cited by 7
Uribe, J. E., Fedosov, A. E., Murphy, K. R., Sei, M., & Harasewych, M. G. (2021) · Mitochondrial DNA Part B · doi:10.1080/23802359.2021.1889408 · Cited by 7
Treatise Online no. 72: Part N, Revised, Volume 1, Chapter 19: Evolutionary Ecology of the Bivalvia
Stanley, S. M. (2015) · Treatise Online · doi:10.17161/to.v0i0.5055 · Cited by 7
A fresh look at macroalgal-coral interactions: are macroalgae a threat to corals?
Vieira, C., Payri, C. E., & Clerck, O. D. (2016) · Perspectives in Phycology · doi:10.1127/pip/2016/0068 · Cited by 7
DUROPHAGOUS FISH PREDATION TRACES VERSUS TUMBLING-INDUCED SHELL DAMAGE—A PALEOBIOLOGICAL PERSPECTIVE
Salamon, M. A., Brachaniec, T., & Gorzelak, P. (2020) · Palaios · doi:10.2110/palo.2019.091 · Cited by 7
Distribution of gastropods within the Cretaceous Tethyan realm
Kollmann, H. A. (1992) · Springer eBooks · doi:10.1007/978-3-7091-5644-5_7 · Cited by 7
Bardhan, S., & Halder, K. (2000) · Historical Biology · doi:10.1080/10292380009380564 · Cited by 7
SIGNS OF BORING PREDATION ON MIDDLE DEVONIAN HYOLITHIDS FROM THE MICHIGAN BASIN
Baumiller, T. K., MARINOVIC, J. C., Tuura, M. E., DAMSTRA, E. S., & MILLER, D. J. (2010) · Palaios · doi:10.2110/palo.2010.p10-044r · Cited by 7
Kase, T. (1988) · Journal of Geography (Chigaku Zasshi) · doi:10.5026/jgeography.97.6_623 · Cited by 7
Hoffman, A. (1984) · Springer eBooks · doi:10.1007/978-1-4615-6977-0_1 · Cited by 7
The demise of large tropical brachiopods and the Mesozoic marine revolution
Harper, E. M., & Peck, L. S. (2024) · Royal Society Open Science · doi:10.1098/rsos.231630 · Cited by 7
Peterman, D., Hebdon, N., Lusch, M., Byron, M., Panah, A. E., & Ritterbush, K. A. (2025) · Paleobiology · doi:10.1017/pab.2025.10053 · Cited by 6
Бакаев, А. С., Johanson, Z., & LeBlanc, A. R. H. (2023) · Papers in Palaeontology · doi:10.1002/spp2.1512 · Cited by 6
Biology of Brazilian Benthic Reef Builders and Dwellers
Mies, M., Banha., T. N. S., Castro, C. B., Cordeiro, R. T. S., Lotufo, T. M. D. C., & Bianchini, A. (2024) · Brazilian marine biodiversity · doi:10.1007/978-3-031-59152-5_4 · Cited by 6
Tajika, A., Rashkova, A., Landman, N. H., & Klompmaker, A. A. (2025) · Swiss Journal of Palaeontology · doi:10.1186/s13358-024-00341-6 · Cited by 6
Brittle-star mass occurrence on a Late Cretaceous methane seep from South Dakota, USA
Thuy, B., Landman, N. H., Larson, N. L., & Numberger-Thuy, L. D. (2018) · Scientific Reports · doi:10.1038/s41598-018-27326-z · Cited by 6
Wilmsen, M., & Nagm, E. (2019) · Acta Palaeontologica Polonica · doi:10.4202/app.00637.2019 · Cited by 6
Niebuhr, B., & Wilmsen, M. (2022) · Paläontologische Zeitschrift · doi:10.1007/s12542-022-00615-9 · Cited by 6
‘Arm brains’ (axial nerves) of Jurassic coleoids and the evolution of coleoid neuroanatomy
Klug, C., Hoffmann, R., Tischlinger, H., Fuchs, D., Pohle, A., Rowe, A., Rouget, I., & Kruta, I. (2023) · Swiss Journal of Palaeontology · doi:10.1186/s13358-023-00285-3 · Cited by 6
Mollusca: Bivalvia and Gastropoda
Quiroz-Barroso, S. A., Guerrero-Arenas, R., García-Barrera, P., & Sánchez‐Beristain, F. (2024) · Springer geology · doi:10.1007/978-3-031-51034-2_4 · Cited by 6
Irwin, A. R., Roberts, N. W., Strong, E. E., Kano, Y., Speiser, D. I., Harper, E. M., & Williams, S. T. (2024) · Systematic Biology · doi:10.1093/sysbio/syae063 · Cited by 6
Tyler, C. L., & Schiffbauer, J. D. (2012) · Palaios · doi:10.2110/palo.2012.p12-014r · Cited by 6
Gorzelak, P., Rahman, I. A., Zamora, S., Gąsiński, A., Trzciński, J., Brachaniec, T., & Salamon, M. A. (2017) · Evolutionary Biology · doi:10.1007/s11692-017-9411-1 · Cited by 6
Iterative ontogenetic development of ammonoid conch shapes from the Devonian through to the Jurassic
Walton, S. A., & Korn, D. (2017) · Palaeontology · doi:10.1111/pala.12308 · Cited by 6
Key, M. M., & Schweitzer, C. E. (2019) · Lethaia · doi:10.1111/let.12350 · Cited by 6
Phanerozoic shallow water diversity driven by changes in sea-level
Wyatt, A. R. (1993) · International Journal of Earth Sciences · doi:10.1007/bf00191826 · Cited by 6
Tomášových, A. (2008) · Evolutionary ecology research · Cited by 6
Konieczyński, K., Pisera, A., Bitner, M. A., & Galácz, A. (2013) · Swiss Journal of Geosciences · doi:10.1007/s00015-013-0128-6 · Cited by 5
Record of Foraminifera test composition throughout the Phanerozoic
Faulkner, K., Lowery, C. M., Martindale, R. C., Simpson, C., & Fraass, A. J. (2025) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2025.0221 · Cited by 5
Tongue-bite apparatus highlights functional innovation in a 310-million-year-old ray-finned fish
Giles, S., Kolmann, M. A., & Friedman, M. (2025) · Biology Letters · doi:10.1098/rsbl.2025.0270 · Cited by 5
Multiple paths to recovery after the Permian-Triassic mass extinction
Liu, X., Song, H., Chu, D., Dai, X., Tian, L., Wu, Y., Wang, F., & Silvestro, D. (2026) · Current Biology · doi:10.1016/j.cub.2025.11.065 · Cited by 5
Revealing the hidden patterns of shark and ray diversity over the past 145 million years
Gardiner, A. M., Mathes, G., Cooper, R., Kocáková, K., Villafaña, J. A., Silvestro, D., & Pimiento, C. (2026) · Current Biology · doi:10.1016/j.cub.2025.12.017 · Cited by 5
Jurassic paleosurfaces with fecal mounds reveal the last supper of arenicolid worms
Mángano, M. G., Buatois, L. A., Piñuela, L., Volkenborn, N., Rodríguez-Tovar, F. J., & García-Ramos, J. C. (2024) · Scientific Reports · doi:10.1038/s41598-023-51103-2 · Cited by 5
Early evolution of the ecdysozoan body plan
Wang, D., Qiang, Y., Guo, J., Vannier, J., Song, Z., Peng, J., Zhang, B., Sun, J. Y., Yu, Y., Zhang, Y., et al. (2024) · eLife · doi:10.7554/elife.94709 · Cited by 5
García-Penas, Á., Baumiller, T. K., Aurell, M., & Zamora, S. (2024) · Geology · doi:10.1130/g52179.1 · Cited by 5
Functional diversity and resilience of bivalves after the Permian-Triassic mass extinction
Wang, Y., Huang, Y., Song, H., Tian, L., Chu, D., & Tong, J. (2024) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2024.112581 · Cited by 5
Prickly Defenders: A Review of Venomous Sea Urchins (Echinoidea)
Ehlert-Flaskämper, S., Motti, C. A., & Harris, R. J. (2025) · Marine Drugs · doi:10.3390/md23060253 · Cited by 5
Evangelisti, F., Albano, P. G., & Sabelli, B. (2012) · Marine Biology · doi:10.1007/s00227-012-2019-1 · Cited by 6
McIntire, L. C., Kotas, T., Flagor, T. E., & Bourdeau, P. E. (2021) · Marine Biology · doi:10.1007/s00227-021-03860-9 · Cited by 5
Karapunar, B., Werner, W., Simonsen, S., Bade, M., Lücke, M., Rebbe, T., Schubert, S. D., & Rojas, A. (2023) · Paleobiology · doi:10.1017/pab.2023.6 · Cited by 5
Anatomy and size of Megateuthis, the largest belemnite
Klug, C., Schweigert, G., Hoffmann, R., Fuchs, D., Pohle, A., Weis, R., & Baets, K. D. (2024) · Swiss Journal of Palaeontology · doi:10.1186/s13358-024-00320-x · Cited by 5
Palaeoenvironment of the Upper Cretaceous (Coniacian) concretion-bearing Lagerstätten from Poland
Trzęsiok, D., Krzykawski, T., Niedźwiedzki, R., Brom, K. R., Gorzelak, P., & Salamon, M. A. (2014) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2014.02.030 · Cited by 5
Operculum regeneration following failed predation in the Silurian gastropod O riostoma
Peel, J. S. (2015) · Palaeontology · doi:10.1111/pala.12154 · Cited by 5
PASSIVE DEFENSIVE TRAITS ARE NOT GOOD PREDICTORS OF PREDATION FOR INFAUNAL REEF BIVALVES
Martinelli, J., Kosnik, M. A., & Madin, J. S. (2016) · Palaios · doi:10.2110/palo.2016.018 · Cited by 5
Seike, K., Shiino, Y., & Suzuki, Y. (2020) · Spanish Journal of Palaeontology · doi:10.7203/sjp.29.1.17487 · Cited by 5
Crinoid respiration and the distribution of energetic strategies among marine invertebrates
Saulsbury, J. G. (2019) · Biological Journal of the Linnean Society · doi:10.1093/biolinnean/blz167 · Cited by 5
Diversity of vertebrate remains from the Lower Gogolin Beds (Anisian) of southern Poland
Antczak, M., Ruciński, M., Stachacz, M., Matysik, M., & Król, J. J. (2020) · Annales Societatis Geologorum Poloniae/Rocznik Polskiego Towarzystwa Geologicznego · doi:10.14241/asgp.2020.22 · Cited by 5
Komatsu, T. (2013) · Palaeontology · doi:10.1111/j.1475-4983.2012.01206.x · Cited by 5
Evolutionary Trends within Jurassic Ammonoids
Neige, P., & Rouget, I. (2015) · Topics in geobiology · doi:10.1007/978-94-017-9633-0_3 · Cited by 5
Brom, K. R., & Szopa, K. (2016) · Contemporary Trends in Geoscience · doi:10.1515/ctg-2016-0008 · Cited by 5
Deciphering deterministic factors of predation pressures in deep time
Ishikawa, M., Kase, T., & Tsutsui, H. (2018) · Scientific Reports · doi:10.1038/s41598-018-35505-1 · Cited by 5
Boulding, E. G., Yamada, S. B., Schooler, S. S., & Shanks, A. L. (2020) · Canadian Journal of Zoology · doi:10.1139/cjz-2019-0250 · Cited by 5
Anti-predator adaptations in a great scallop (Pecten maximus) – a palaeontological perspective
Brom, K. R., Szopa, K., Krzykawski, T., Brachaniec, T., & Salamon, M. A. (2015) · Geoscience Records · doi:10.1515/georec-2015-0002 · Cited by 5
Functional Morphology of Gastropods and Bivalves
Sälgeback, J. (2006) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 5
Yoshida, K. (2006) · Ecological Modelling · doi:10.1016/j.ecolmodel.2005.11.036 · Cited by 5
Macroevolution: Predation by drilling gastropods
Benton, M. J. (1986) · Nature · doi:10.1038/321110a0 · Cited by 5
Fish–sea lily interactions as observed from a submersible: Paleoecological implications
Gorzelak, P., Salamon, M. A., Messing, C. G., & Baumiller, T. K. (2025) · Ecology · doi:10.1002/ecy.70092 · Cited by 4
Tyler, C. L., & Kowalewski, M. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2405727122 · Cited by 4
Earliest octopuses were giant top predators in Cretaceous oceans
Ikegami, S., Mutterlose, J., Sugiura, K., Takeda, Y., Derin, M. O., Kubota, A., Tainaka, K., Harada, T., Nishida, H., & Iba, Y. (2026) · Science · doi:10.1126/science.aea6285 · Cited by 4
The evolution and diversification of life
Awramik, S. M., & McNamara, K. J. (2007) · Cambridge University Press eBooks · doi:10.1017/cbo9780511812958.018 · Cited by 4
The Fractional MacroEvolution Model: a simple quantitative scaling macroevolution model
Lovejoy, S. M., & Spiridonov, A. (2024) · Paleobiology · doi:10.1017/pab.2023.38 · Cited by 4
Klug, C., Sivgin, T., Miedema, F., Scheffold, B., Reisdorf, A. G., Stössel, I., Maxwell, E. E., & Scheyer, T. M. (2024) · Swiss Journal of Palaeontology · doi:10.1186/s13358-024-00327-4 · Cited by 4
Karapunar, B., Höhna, S., & Nützel, A. (2024) · Journal of Systematic Palaeontology · doi:10.1080/14772019.2024.2384141 · Cited by 4
Attila, V., & Szives, O. (2025) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2025.112788 · Cited by 4
The Revolution of Small Snails and the Early Modern Evolutionary Fauna
Dominici, S. (2025) · Diversity · doi:10.3390/d17020120 · Cited by 4
Krawczyński, W. (2013) · Annales Societatis Geologorum Poloniae/Rocznik Polskiego Towarzystwa Geologicznego · Cited by 4
Nearshore articulate crinoid from the Albian of Alberta, Canada (Early Cretaceous, Echinodermata)
Ausich, W. I., Buckley, R. A., & Plint, A. G. (2011) · Canadian Journal of Earth Sciences · doi:10.1139/e10-094 · Cited by 4
Salamon, M. A., & Gorzelak, P. (2011) · Paleontological Research · doi:10.2517/1342-8144-15.1.023 · Cited by 4
Stilwell, J. D., & Zinsmeister, W. J. (2003) · Cretaceous Research · doi:10.1016/s0195-6671(03)00035-1 · Cited by 4
Kondo, Y., & Sano, S. (2009) · Paleontological Research · doi:10.2517/1342-8144-13.1.039 · Cited by 4
Rantuch, J. (2021) · Historical Biology · doi:10.1080/08912963.2020.1867124 · Cited by 4
Love, not war, drove the Mesozoic marine revolution
Novack‐Gottshall, P. M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617404113 · Cited by 4
Niche partitioning among the Mesozoic echinoderms: biotic vs abiotic traits
Abdelhady, A. A., & Elshekhipy, A. A. (2020) · Arabian Journal of Geosciences · doi:10.1007/s12517-020-05908-4 · Cited by 4
Geologic controls on phytoplankton elemental composition
Sharoni, S., & Halevy, I. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2113263119 · Cited by 4
A Historical Conspiracy: Competition, Opportunity, and the Emergence of Direction in History
Vermeij, G. J. (2011) · Cliodynamics The Journal of Quantitative History and Cultural Evolution · doi:10.21237/c7clio21211 · Cited by 4
Self-citationRos-Franch, S., Renzi, M. D., Damborenea, S. E., & Aliaga, A. M. (2012) · Treatise Online · doi:10.17161/to.v0i0.4271 · Cited by 4
Metadata
- Authors
- Vermeij, G. J.
- Affiliations
- University of Maryland, College Park (US)
- Corresponding author
- Vermeij, Geerat J.
- ORCID
- Vermeij, Geerat J.
- Venue
- Paleobiology
- Publisher
- Cambridge University Press (CUP)
- Published
- 1977
- Volume
- 3
- Issue
- 3
- Pages
- 245-258
- ISSN
- 0094-8373 (ISSN-L)
- 1938-5331
- OpenAlex
- W2336345527
- Cited by
- 1,043
- References
- 84
- Citations by year
- 2026: 37 · 2025: 32 · 2024: 47 · 2023: 37 · 2022: 29 · 2021: 39 · 2020: 45 · 2019: 46 · 2018: 33 · 2017: 34 · 2016: 37 · 2015: 41 · 2014: 37 · 2013: 36 · 2012: 34
- FWCI
- 6.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Paleobiology (publishedVersion)
- Topics
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Paleontology and Stratigraphy of Fossils
- Physical Sciences › Earth and Planetary Sciences › Oceanography › Marine Biology and Ecology Research
- Keywords
- Mesozoic Marine Revolution, teleosts, mantis shrimp, Decapoda, grazing, benthic community structure, angiosperm diversification, continental breakup, adaptive zones, hermit crabs, Bivalvia
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review