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Muttaburrasaurus
The plants, animals and climate of the Australian continent have changed dramatically over long periods of time. Imagine this giant creature roaming the luxuriant wet forests that covered parts of the continent in the Cretaceous period, about 100-110 million years ago. The Muttaburrasaurus ambled along on all four legs or stood on its hind legs. Its large teeth were well adapted to eat tough vegetation such as the leathery foliage of the evergreen forests of Araucaria trees, ancient relatives of the bunya pine of south-eastern Queensland.
In 1963, grazier Doug Langdon discovered the fossilised bones of a dinosaur on his property near Muttaburra in central-west Queensland. It was one of the most complete dinosaur skeletons found in Australia. The bones belonged to a new species of ornithopod and palaeontologists named it Muttaburrasaurus langdoni.

Cast of Muttaburresaurus langdoni 1987 made by Queensland Museum, Brisbane National Museum of Australia
Taxa Muttaburrasaurus

Muttaburrasaurus The plants, animals and climate of the Australian continent have changed dramatically over long periods of time. Imagine this giant creature roaming the luxuriant wet forests that covered parts of the continent in the Cretaceous period, about 100-110 million years ago. The Muttaburrasaurus ambled along on all four legs or stood on its hind legs. Its large teeth were well adapted to eat tough vegetation such as the leathery foliage of the evergreen forests of Araucaria trees, ancient relatives of the bunya pine of south-eastern Queensland. In 1963, grazier Doug Langdon discovered the fossilised bones of a dinosaur on his property near Muttaburra in central-west Queensland. It was one of the most complete dinosaur skeletons found in Australia. The bones belonged to a new species of ornithopod and palaeontologists named it Muttaburrasaurus langdoni. Cast of Muttaburresaurus langdoni 1987 made by Queensland Museum, Brisbane National Museum of Australia

bone museum Australia Cretaceous +5
Life restoration of the small German Jurassic ichthyosaur Hauffiopteryx typicus.
References
Maxwell, E. E.; Cortés, D. (2020). "A revision of the Early Jurassic ichthyosaur Hauffiopteryx (Reptilia: Ichthyosauria), and description of a new species from Southwestern Germany". Palaeontologia Electronica 23: 1–43. Archived from the original on 2022-07-06. Retrieved on 2022-03-15.
Note: This image is currently uncolored
Taxa Hauffiopteryx

Life restoration of the small German Jurassic ichthyosaur Hauffiopteryx typicus. References Maxwell, E. E.; Cortés, D. (2020). "A revision of the Early Jurassic ichthyosaur Hauffiopteryx (Reptilia: Ichthyosauria), and description of a new species from Southwestern Germany". Palaeontologia Electronica 23: 1–43. Archived from the original on 2022-07-06. Retrieved on 2022-03-15. Note: This image is currently uncolored

description Germany Early Jurassic Jurassic +3
Life restoration of the Triassic ichthyosaur Callawayia neoscapularis. Three specimens of this ichthyosaur are known, the holotype, ROM 41993, and two referred specimens, TMP 94.380.11 and 94.382.2. The skull is primarily based on ROM 41993, cross-checked against TMP 94.380.11 and TMP 94.382.2. The vertebral column is based primarily on TMP 94.382.2 as it is the most complete of these specimens, while the ribs were based on ROM 41993. The forelimbs were mainly based on those of ROM 41993, with TMP 94.380.11 used to determine their breadth. The hindlimbs were based on TMP 94.380.11, especially the more complete right hindlimb.
ROM 41993 was cross-scaled with TMP 94.380.11 by the dimensions of the forelimb epipodials, which produced similar vertebral dimensions. The two TMP specimens were cross-scaled based on femoral length, also producing similar vertebral dimensions. Nicholls & Manabe (2001) stated that no wedge-shaped caudal centra supporting a tailbend were found and that there was no evidence of a bend being present, though considered that they might have existed in the gap in the preserved caudals. Since various other Triassic ichthyosaurs have since been found to have tail bends, one was illustrated here. A modest downturn of roughly 15° was illustrated, comparable to that in Guanlingsaurus, and the location of the bend within the gap in the preserved vertebrae matches well with the location of the bend in Guizhouichthyosaurus.

References
McGowan, C. (1994). "A new species of Shastasaurus (Reptilia: Ichthyosauria) from the Triassic of British Columbia: The most complete exemplar of the genus". Journal of Vertebrate Paleontology 14 (2): 168–179. DOI:10.1080/02724634.1994.10011550.
Nicholls, E. L.; Manabe, M. (2001). "A new genus of ichthyosaur from the Late Triassic Pardonet Formation of British Columbia: Bridging the Triassic-Jurassic gap". Canadian Journal of Earth Sciences 38 (6): 983–1002.
Ji, C.; Jiang, D.Y.; Hao, W.; Sun, Y. (2011). "True tailbend occurred in the Late Triassic: Evidence from ichthyosaur skeletons of South China". Acta Scientiarum Naturalium Universitatis Pekinensis 47 (2): 309–314.
Shang, Q. H.; Li, C. (2009). "On the occurrence of the ichthyosaur Shastasaurus in the Guanling biota (Late Triassic), Guizhou, China". Vertebrata PalAsiatica 47 (3): 178–193.
Taxa Guanlingsaurus

Life restoration of the Triassic ichthyosaur Callawayia neoscapularis. Three specimens of this ichthyosaur are known, the holotype, ROM 41993, and two referred specimens, TMP 94.380.11 and 94.382.2. The skull is primarily based on ROM 41993, cross-checked against TMP 94.380.11 and TMP 94.382.2. The vertebral column is based primarily on TMP 94.382.2 as it is the most complete of these specimens, while the ribs were based on ROM 41993. The forelimbs were mainly based on those of ROM 41993, with TMP 94.380.11 used to determine their breadth. The hindlimbs were based on TMP 94.380.11, especially the more complete right hindlimb. ROM 41993 was cross-scaled with TMP 94.380.11 by the dimensions of the forelimb epipodials, which produced similar vertebral dimensions. The two TMP specimens were cross-scaled based on femoral length, also producing similar vertebral dimensions. Nicholls & Manabe (2001) stated that no wedge-shaped caudal centra supporting a tailbend were found and that there was no evidence of a bend being present, though considered that they might have existed in the gap in the preserved caudals. Since various other Triassic ichthyosaurs have since been found to have tail bends, one was illustrated here. A modest downturn of roughly 15° was illustrated, comparable to that in Guanlingsaurus, and the location of the bend within the gap in the preserved vertebrae matches well with the location of the bend in Guizhouichthyosaurus. References McGowan, C. (1994). "A new species of Shastasaurus (Reptilia: Ichthyosauria) from the Triassic of British Columbia: The most complete exemplar of the genus". Journal of Vertebrate Paleontology 14 (2): 168–179. DOI:10.1080/02724634.1994.10011550. Nicholls, E. L.; Manabe, M. (2001). "A new genus of ichthyosaur from the Late Triassic Pardonet Formation of British Columbia: Bridging the Triassic-Jurassic gap". Canadian Journal of Earth Sciences 38 (6): 983–1002. Ji, C.; Jiang, D.Y.; Hao, W.; Sun, Y. (2011). "True tailbend occurred in the Late Triassic: Evidence from ichthyosaur skeletons of South China". Acta Scientiarum Naturalium Universitatis Pekinensis 47 (2): 309–314. Shang, Q. H.; Li, C. (2009). "On the occurrence of the ichthyosaur Shastasaurus in the Guanling biota (Late Triassic), Guizhou, China". Vertebrata PalAsiatica 47 (3): 178–193.

China Jurassic Late Triassic Triassic +12
A figure from Notes on Osteology of Baptanodon. With a Description of a New Species.
Taxa Baptanodon

A figure from Notes on Osteology of Baptanodon. With a Description of a New Species.

description Baptanodon new species
New species of Mesozoic benthic foraminifera from the former British Petroleum micropalaeontology collection, Ophthalmidium dracomaris n. sp.
(1) holotype (NHMUK PM PF 74496); (2–5) paratypes (NHMUK PM PF 74497–74500). (8–9) Eobigenerina calloviensis n. sp.: (8) holotype (NHMUK PM PF 74504); (9) paratype (NHMUK PM PF 74505). (10–12) Trochammina fordonensis n. sp.: (10) holotype (NHMUK PM PF 74501); (11–12) paratype (NHMUK PM PF 74502–74503). (13–15) Arenoturrispirillina swiecickii n. sp.: (13) holotype (NHMUK PM PF 74506); (14–15) paratype (NHMUK PM PF 74507 + NHMUK PM PF 74552). (16–17) Ataxophragmium mariae n. sp.: (16) holotype (NHMUK PM PF 74553); (17) paratype (NHMUK PM PF 74554).

New species of Mesozoic benthic foraminifera from the former British Petroleum micropalaeontology collection, Ophthalmidium dracomaris n. sp. (1) holotype (NHMUK PM PF 74496); (2–5) paratypes (NHMUK PM PF 74497–74500). (8–9) Eobigenerina calloviensis n. sp.: (8) holotype (NHMUK PM PF 74504); (9) paratype (NHMUK PM PF 74505). (10–12) Trochammina fordonensis n. sp.: (10) holotype (NHMUK PM PF 74501); (11–12) paratype (NHMUK PM PF 74502–74503). (13–15) Arenoturrispirillina swiecickii n. sp.: (13) holotype (NHMUK PM PF 74506); (14–15) paratype (NHMUK PM PF 74507 + NHMUK PM PF 74552). (16–17) Ataxophragmium mariae n. sp.: (16) holotype (NHMUK PM PF 74553); (17) paratype (NHMUK PM PF 74554).

Mesozoic holotype new species

News

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