MAMMALS FROM THE AGE OF DINOSAURS—ORIGINS, EVOLUTION, AND STRUCTURE

By Ian J. Corfe. 2007

405 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Paleontology

View Paper: https://www.semanticscholar.org/paper/2e64f1991d61b5f2fbb66ffdd2c307587eca3811

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology, Evolution, Behavior and Systematics

1. J. Wible
2. R. Asher
3. C. McCain
4. M. Novacek
5. G. Rougier
6. John‐Arvid Grytnes
7. Ellen I. Damschen
8. P. Donoghue

In Paleontology

1. J. Wible
2. M. Novacek
3. P. Mannion
4. R. Asher
5. G. Rougier
6. Paul Upchurch
7. C. McCain
8. M. Friedman

Citations in the corpus

• On the Cranial Osteology of the Hispaniolan Solenodon, Solenodon paradoxus Brandt, 1833 (Mammalia, Lipotyphla, Solenodontidae) (2008, background): “The extra premolar of the five is in the middle of the series, and some authors (e.g., Cifelli 2000; Kielan-Jaworowska et al. 2004) number the five as P1, P2, Pc, P3, P4 to avoid confusion with the older literature, whereas others (e.g., Nessov et al. 1998; Wible et al. 2007, in press; this report)…”
• Revision of the sauropod dinosaur Diamantinasaurus matildae Hocknull et al. 2009 from the mid-Cretaceous of Australia: Implications for Gondwanan titanosauriform dispersal (2015, background): “…affinities of these fossils have generated much debate, though the relationship of ausktribosphenids to monotremes has garnered wider acceptance (Woodburne et al., 2003; Kielan-Jaworowska et al., 2004; Rich and Vickers-Rich, 2004, 2012b; Martin and Rauhut, 2005; Rich, 2008; Phillips et al., 2009).”
• A multivariate approach to infer locomotor modes in Mesozoic mammals (2015, background): “…have been inferred for the Metatheria (arboreal, scansorial, terrestrial, and possibly semiaquatic [Szalay 1994; Luo et al. 2002; Horovitz 2003; Kielan-Jaworowska et al. 2004; Longrich 2004; Chester et al. 2010, 2012]), and only two for the Docodonta (semiaquatic and semifossorial [Ji et al.…”
• Mammals across the K/Pg boundary in northeastern Montana, U.S.A.: dental morphology and body-size patterns reveal extinction selectivity and immigrant-fueled ecospace filling (2013, background): “Kielan-Jaworowska et al. (2004) outlined three major morphological associations of lower premolars and incisors and their functional implications.”
• Constraints on the timescale of animal evolutionary history (2015, background): “Tooth-based mammal taxa from the early Jurassic of India (Kotatherium, Nakundon) and North America (Amphidon) that might be spalacotheroids (Kielan Jaworowska et al., 2004) are not convincingly members of the clade (Averianov, 2002) and are ignored here.”
• Different evolutionary histories underlie congruent species richness gradients of birds and mammals (2012, background): “metatherians and eutherians) in the Late Jurassic and Cretaceous (Kielan-Jaworowska et al., 2004); and (4) the many northern clades able to colonize and radiate in tropical South America during the Great American Biotic Interchange (Vaughan, 1986; Webb, 2006).”
• The Eutherian Mammal Maelestes gobiensis from the Late Cretaceous of Mongolia and the phylogeny of cretaceous eutheria (2009, methodology): “Although not carbon copies, the skulls of the Mongolian asioryctitheres Kennalestes, Asioryctes, and Ukhaatherium are generally similar to one another (fig. 35; Novacek et al., 1997; Kielan-Jaworowska et al., 2004) as are the skulls of the zalambdalestids Zalambdalestes and Barunlestes to each other”
• Developmental Patterns in Mesozoic Evolution of Mammal Ears (2012, background): “Multituberculates are omnivorous to herbivorous mammals with a long history from the Middle Jurassic to the late Eocene; they are also abundant in some fossil assemblages of the Late Jurassic and the Late Cretaceous (Kielan-Jaworowska et al. 2004).”