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The Mammary Gland and Its Origin During Synapsid Evolution
P1: GMX Journal of Mammary Gland Biology and Neoplasia (JMGBN) pp749-jmgbn-460568 January 9, 2003 17:51 Style file version Nov. 07, 2000 Journal of Mammary Gland Biology and Neoplasia, Vol. 7, No. 3, July 2002 (C 2002) The Mammary Gland and Its Origin During Synapsid Evolution Olav T. Oftedal1 Lactation appears to be an ancient reproductive trait that predates the origin of mammals. The synapsid branch of the amniote tree that separated from other taxa in the Pennsylva- nian (>310 million years ago) evolved a glandular rather than scaled integument. Repeated radiations of synapsids produced a gradual accrual of mammalian features. The mammary gland apparently derives from an ancestral apocrine-like gland that was associated with hair follicles. This association is retained by monotreme mammary glands and is evident as ves- tigial mammary hair during early ontogenetic development of marsupials. The dense cluster of mammo-pilo-sebaceous units that open onto a nipple-less mammary patch in monotremes may reflect a structure that evolved to provide moisture and other constituents to permeable eggs. Mammary patch secretions were coopted to provide nutrients to hatchlings, but some constituents including lactose may have been secreted by ancestral apocrine-like glands in early synapsids. Advanced Triassic therapsids, such as cynodonts, almost certainly secreted complex, nutrient-rich milk, allowing a progressive decline in egg size and an increasingly altricial state of the young at hatching. This is indicated by the very small body size, presence of epipubic bones, and limited tooth replacement in advanced cynodonts and early mammali- aforms. Nipples that arose from the mammary patch rendered mammary hairs obsolete, while placental structures have allowed lactation to be truncated in living eutherians. -
The Mesozoic Era Alvarez, W.(1997)
Alles Introductory Biology: Illustrated Lecture Presentations Instructor David L. Alles Western Washington University ----------------------- Part Three: The Integration of Biological Knowledge Vertebrate Evolution in the Late Paleozoic and Mesozoic Eras ----------------------- Vertebrate Evolution in the Late Paleozoic and Mesozoic • Amphibians to Reptiles Internal Fertilization, the Amniotic Egg, and a Water-Tight Skin • The Adaptive Radiation of Reptiles from Scales to Hair and Feathers • Therapsids to Mammals • Dinosaurs to Birds Ectothermy to Endothermy The Evolution of Reptiles The Phanerozoic Eon 444 365 251 Paleozoic Era 542 m.y.a. 488 416 360 299 Camb. Ordov. Sil. Devo. Carbon. Perm. Cambrian Pikaia Fish Fish First First Explosion w/o jaws w/ jaws Amphibians Reptiles 210 65 Mesozoic Era 251 200 180 150 145 Triassic Jurassic Cretaceous First First First T. rex Dinosaurs Mammals Birds Cenozoic Era Last Ice Age 65 56 34 23 5 1.8 0.01 Paleo. Eocene Oligo. Miocene Plio. Ple. Present Early Primate First New First First Modern Cantius World Monkeys Apes Hominins Humans A modern Amphibian—the toad A modern day Reptile—a skink, note the finely outlined scales. A Comparison of Amphibian and Reptile Reproduction The oldest known reptile is Hylonomus lyelli dating to ~ 320 m.y.a.. The earliest or stem reptiles radiated into therapsids leading to mammals, and archosaurs leading to all the other reptile groups including the thecodontians, ancestors of the dinosaurs. Dimetrodon, a Mammal-like Reptile of the Early Permian Dicynodonts were a group of therapsids of the late Permian. Web Reference http://www.museums.org.za/sam/resource/palaeo/cluver/index.html Therapsids experienced an adaptive radiation during the Permian, but suffered heavy extinctions during the end Permian mass extinction. -
Mammal Evolution
Mammal Evolution Geology 331 Paleontology Triassic synapsid reptiles: Therapsids or mammal-like reptiles. Note the sprawling posture. Mammal with Upright Posture From Synapsids to Mammals, a well documented transition series Carl Buell Prothero, 2007 Synapsid Teeth, less specialized Mammal Teeth, more specialized Prothero, 2007 Yanoconodon, Lower Cretaceous of China Yanoconodon, Lower Cretaceous of China, retains ear bones attached to the inside lower jaw Morganucodon Yanoconodon = articular of = quadrate of Human Ear Bones, or lower reptile upper reptile Auditory Ossicles jaw jaw Cochlea Mammals have a bony secondary palate Primary Palate Reptiles have a soft Secondary Palate secondary palate Reduction of digit bones from Hand and Foot of Permian Synapsid 2-3-4-5-3 in synapsid Seymouria ancestors to 2-3-3-3-3 in mammals Human Hand and Foot Class Mammalia - Late Triassic to Recent Superorder Tricodonta - Late Triassic to Late Cretaceous Superorder Multituberculata - Late Jurassic to Early Oligocene Superorder Monotremata - Early Cretaceous to Recent Superorder Metatheria (Marsupials) - Late Cretaceous to Recent Superorder Eutheria (Placentals) - Late Cretaceous to Recent Evolution of Mammalian Superorders Multituberculates Metatheria Eutheria (Marsupials) (Placentals) Tricodonts Monotremes . Live Birth Extinct: . .. Mammary Glands? Mammals in the Age of Dinosaurs – a nocturnal life style Hadrocodium, a lower Jurassic mammal with a “large” brain (6 mm brain case in an 8 mm skull) Were larger brains adaptive for a greater sense of smell? Big Brains and Early Mammals July 14, 2011 The Academic Minute http://www.insidehighered.com/audio/academic_pulse/big_brains_and_early_mammals Lower Cretaceous mammal from China Jawbones of a Cretaceous marsupial from Mongolia Mammal fossil from the Cretaceous of Mongolia Reconstructed Cretaceous Mammal Early Cretaceous mammal ate small dinosaurs Repenomamus robustus fed on psittacosaurs. -
A New Mammaliaform from the Early Jurassic and Evolution Of
R EPORTS tary trough with a shelflike dorsal medial ridge, and all other nonmammalian mamma- A New Mammaliaform from the liaforms have a medial concavity on the man- dibular angle (8–14, 23), as in nonmamma- Early Jurassic and Evolution of liaform cynodonts (9, 14, 24–27). The post- dentary trough and the medial concavity on Mammalian Characteristics the mandibular angle respectively accommo- dated the prearticular/surangular and the re- Zhe-Xi Luo,1* Alfred W. Crompton,2 Ai-Lin Sun3 flected lamina of the angular (9, 25–27) that are the homologs to the mammalian middle A fossil from the Early Jurassic (Sinemurian, ϳ195 million years ago) represents ear bones (9, 14, 16–21, 23, 26). The absence a new lineage of mammaliaforms, the extinct groups more closely related to of these structures indicates that the postden- the living mammals than to nonmammaliaform cynodonts. It has an enlarged tary bones (“middle ear ossicles”) must have cranial cavity, but no postdentary trough on the mandible, indicating separation been separated from the mandible (Fig. 3). of the middle ear bones from the mandible. This extends the earliest record of Hadrocodium lacks the primitive meckelian these crucial mammalian features by some 45 million years and suggests that sulcus of the mandible typical of all nonmam- separation of the middle ear bones from the mandible and the expanded brain maliaform cynodonts (24–27), stem groups vault could be correlated. It shows that several key mammalian evolutionary of mammaliaforms (8, 9, 14, 23, 26, 27), innovations in the ear region, the temporomandibular joint, and the brain vault triconodontids (28, 29), and nontribosphenic evolved incrementally through mammaliaform evolution and long before the therian mammals (30). -
Mesozoic: the Dark Age for Mammals!
Ed’s Simplified History of the Mammals Note progression from Pelycosaurs (1) to Therapsids and Cynodonts (2) in Triassic. Stem mammals appeared in Late Triassic and Early Jurassic (3). Relationships among the Middle Jurassic forms (4) are controversial (see handout). Therian clade, identified by the tribosphenic molar (5), emerged at the end of the Jurassic, Early Cretaceous. A slightly more detailed version… in case you like something that looks more slick From Pough et al. 2009. Vertebrate Life, 8th ed. Pelycosaurs Dominated the late Permian, gave rise to therapsids Therapsids Rapid radiation in late Permian, around 270 MYA Still “mammal-like reptiles” The mass extinction at the end of the Permian was the greatest loss of diversity ever with >80% of all known genera and about 90% of all species going extinct, both terrestrial and marine. Cynodonts Late Permian to mid Triassic Last remaining group of therapsids, survived mass extinction at the end of the Permian. Persisted well Only 1 lineage of into Triassic and developed cynodonts survived many features associated through the late Triassic, with mammals. and this group became ancestors of mammals. Mesozoic: the Dark Age for Mammals! multituberculate Morganucodon, one of the earliest mammals (What else was happening in the Late Triassic and Jurassic Hadrocodium that may have contributed to mammals becoming small and Most were very small with nocturnal?) conservative morphology ...but new fossil finds indicate more diversity than we thought Repenomanus Still, largest known mammal during Mesozic Most were shrew to is no larger than a mouse sized, for 125 woodchuck million years! Some Mesozoic events and mammals you should know 1. -
The Mesozoic Mesozoic Things to Think About
The Mesozoic Mesozoic Things to think about • Breakup of Pangea and its relationship to sealevel and climate • Dominance of reptiles • Origin of birds • Origin of mammals • Origin of flowers (angiosperms) • Expansion of insects • Life in the seas assumes an (almost) modern form 1 2 3 4 5 Triassic Period 248 to 206 Million Years Ago 6 The Connecticut River Valley 7 Dinosaur Footprints of the Connecticut Valley Edward Hitchcock Fossil Fish of the Connecticut Valley 8 Jurassic Period 206 to 144 Million Years Ago 9 Cretaceous Period 144 to 65 Million Years Ago 10 11 Mesozoic Ammonites 12 Cretaceous Heteromorph Ammonites Nipponites mirabilis Kamchatka, Russia Macroscaphites sp. Baculites sp. Didymoceras stevensoni Rudistid Bivalves: Jurassic- Cretaceous 13 Durania cornupastoris at Abu Roash, Western Desert near Gizah, Egypt Fringing Upper Cretaceous rudist reef reservoirs flanking basement highs, Augila oil field, eastern Libya Reef-forming rudist (Radiolites) from Sarvak Formation, Cenomanian, south Iran. 14 Biostrome of hippuritid rudists at Montagne des Cornes; Santonian, Pyrenees, France Rudistid Buildups 15 Biostrome of Vaccinites vesiculosus (Woodward, 1855); Campanian of Saiwan, Oman Monopleura marcida Albian, Viotía, Greece 16 Chalk 17 Pterosaurs Mosasaurs 18 Plesiosaurs Ichthyosaurs 19 A Dinosaur Family Tree (aka Phylogeny) 20 Sauropods Theropods 21 Dilong paradoxus Early Cretaceous, China A feathered tyrannosaurid? 22 A Dinosaur Family Tree (aka Phylogeny) Ornithopods (aka Hadrosaurs) 23 Thyreophorans (aka Ankylosaurs, etc) Margincephalians (aka Ceratopsians) 24 A Dinosaur Family Tree (aka Phylogeny) The Liaoning Fauna: An early Cretaceous Lagerstatten Some highlights: -- feathered dinosaurs -- preserved internal organs -- oldest placental mammal 25 The Liaoning Fauna The Liaoning Fauna Caudipteryx. Microraptor gui MICRORAPTOR zhaoianus. -
Mammal Disparity Decreases During the Cretaceous Angiosperm Radiation
Mammal disparity decreases during the Cretaceous angiosperm radiation David M. Grossnickle1 and P. David Polly2 1Department of Geological Sciences, and 2Departments of Geological Sciences, Biology, and Anthropology, rspb.royalsocietypublishing.org Indiana University, Bloomington, IN 47405, USA Fossil discoveries over the past 30 years have radically transformed tra- ditional views of Mesozoic mammal evolution. In addition, recent research provides a more detailed account of the Cretaceous diversification of flower- Research ing plants. Here, we examine patterns of morphological disparity and functional morphology associated with diet in early mammals. Two ana- Cite this article: Grossnickle DM, Polly PD. lyses were performed: (i) an examination of diversity based on functional 2013 Mammal disparity decreases during dental type rather than higher-level taxonomy, and (ii) a morphometric analysis of jaws, which made use of modern analogues, to assess changes the Cretaceous angiosperm radiation. Proc R in mammalian morphological and dietary disparity. Results demonstrate a Soc B 280: 20132110. decline in diversity of molar types during the mid-Cretaceous as abundances http://dx.doi.org/10.1098/rspb.2013.2110 of triconodonts, symmetrodonts, docodonts and eupantotherians dimin- ished. Multituberculates experience a turnover in functional molar types during the mid-Cretaceous and a shift towards plant-dominated diets during the late Late Cretaceous. Although therians undergo a taxonomic Received: 13 August 2013 expansion coinciding with the angiosperm radiation, they display small Accepted: 12 September 2013 body sizes and a low level of morphological disparity, suggesting an evol- utionary shift favouring small insectivores. It is concluded that during the mid-Cretaceous, the period of rapid angiosperm radiation, mammals experi- enced both a decrease in morphological disparity and a functional shift in dietary morphology that were probably related to changing ecosystems. -
HISTORIA NATURAL Tercera Serie Volumen 2 (2) 2012/5-30
ISSN (impreso) 0326-1778 / ISSN (on-line) 1853-6581 HISTORIA NATURAL Tercera Serie Volumen 2 (2) 2012/5-30 DISCOVERIES IN THE LATE TRIASSIC OF BRAZIL IMPROVE KNOWLEDGE ON THE ORIGIN OF MAMMALS Descubrimientos en el Triásico tardío de Brasil perfeccionan nuestro conocimiento sobre el origen de los mamíferos José F. Bonaparte1, 2, Marina B. Soares3, and Agustín G. Martinelli4 1Museo Municipal de Ciencias Naturales “Carlos Ameghino”, Calle 26 512 (6600), Mercedes, Buenos Aires, Argentina. 2Departamento de Ciencias Naturales y Antropología, Fundación de Historia Natural Félix de Azara, Universidad Maimónides, Hidalgo 775 piso 7 (C1405BDB), Ciudad Autónoma de Buenos Aires, República Argentina. [email protected] 3Departamento de Paleontologia e Estratigrafia, Instituto de Geociências, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9500, Caixa Postal (15.001, 91501-970), Porto Alegre, RS, Brasil. 4Centro de Pesquisas Paleontológicas L. I. Price, Complexo Cultural e Científico Petrópolis (CCCP/UFTM), BR-262, Km 784, Bairro Peirópolis, 755, Uberaba, Minas Gerais, Brazil. 5 Bonaparte J. F., Soares M. B. and Martinelli A. G. Abstract. A new specimen of Brasilitherium riograndensis, which includes complete skull, lower jaws, dentition and some postcranial bones, is described, along with a redescription of the skull, lower jaws and dentition of Minicynodon maieri, both derived eucynodonts from the Late Triassic of Southern Brazil. The anatomical comparison confirms the close relationships of both genera with the Morganucodonta and suggest that the Tritheledontidae is the sister group of the Brasilodontidae. Some comments after the anatomical information from the brasilodontids are developed on the following subjects: the sister group of mammals, the interpterygoid vacuity, and on Adelobasileus, Hadrocodium and Microconodon. -
Fig. 1. Hadrocodium Wui Gen. Et Sp. Nov. (IVPP 8275). (A) Lateral and (B) Ventral Views of Restored Skull
Fig. 1. Hadrocodium wui gen. et sp. nov. (IVPP 8275). (A) Lateral and (B) ventral views of restored skull. (C) Dentition (lateral view restoration). (D) Occlusion [based on scanning electron microscope (SEM) photos]. (E) Wear of molars (shaded areas are wear facets). The main cusp A of the upper molar occludes in the embrasure between the opposite lower molars. Abbreviations.: an, angular process (dentary); bo, basioccipital; bs, basisphenoid; c, canine; ce, cavum epiptericum; co, coronoid process (of dentary); dc, dentary condyle; er, epitympanic recess; f, frontal; fc, foramen cochleare ("perilymphatic foramen"); fst, fossa for stapedial muscle; fv, fenestra vestibuli; hp, hamulus (of pterygoid); I/i, upper and lower incisors; in, internal nares; iof, infraorbital foramen; J, jugal; jf, jugular foramen; L, lacrimal; lt, lateral trough; M, molar; mx, maxillary; n, nasal; oc, occipital condyle; P, premolar; Pa, parietal; pcd, postcanine diastema; pgd, postglenoid degression; pr, promontorium (petrosal); ptc, posttemporal canal (between petrosal and squamosal); px, premaxillary; sm, septomaxillary; so, supraoccipital; sof, spheno-orbital fissure; sq, squamosal; tmj, temporomandibular joint (dentary/squamosal jaw hinge); v3, foramen for the mandibular branch of the trigeminal nerve (v); xii, hypoglossal nerve (xii). Molar cusps following (11): A, B, and C, main cusps of upper molars; a, b, c, d, and e, cusps of the lowers Fig. 5. (A) Scaling of brain vault size (width measured at the level of anterior squamosal/parietal suture) relative to skull size (measured at the distance between the left versus right temporomandibular joints). This shows that allometry of small size of Hadrocodium, by itself, is not sufficient to account for its very large braincase. -
Redalyc.New Information on Riograndia Guaibensis Bonaparte
Anais da Academia Brasileira de Ciências ISSN: 0001-3765 [email protected] Academia Brasileira de Ciências Brasil SOARES, MARINA B.; SCHULTZ, CESAR L.; HORN, BRUNO L.D. New information on Riograndia guaibensis Bonaparte, Ferigolo & Ribeiro, 2001 (Eucynodontia, Tritheledontidae) from the Late Triassic of southern Brazil: anatomical and biostratigraphic implications Anais da Academia Brasileira de Ciências, vol. 83, núm. 1, marzo, 2011, pp. 329-354 Academia Brasileira de Ciências Rio de Janeiro, Brasil Available in: http://www.redalyc.org/articulo.oa?id=32717681018 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative “main” — 2011/2/12 — 13:39 — page 329 — #1 Anais da Academia Brasileira de Ciências (2011) 83(1): 329-354 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 www.scielo.br/aabc New information on Riograndia guaibensis Bonaparte, Ferigolo & Ribeiro, 2001 (Eucynodontia, Tritheledontidae) from the Late Triassic of southern Brazil: anatomical and biostratigraphic implications MARINA B. SOARES, CESAR L. SCHULTZ and BRUNO L.D. HORN Departamento de Paleontologia e Estratigrafia, Instituto de Geociências, Universidade Federal do Rio Grande doSul Av. Bento Gonçalves, 9500, Caixa Postal 15.001, 91501-970 Porto Alegre, RS, Brasil Manuscript received on December 20, 2010; accepted for publication on January 24, 2011 ABSTRACT The tritheledontid Riograndia guaibensis was the first cynodont described for the “Caturrita Formation” fauna from the Late Triassic of southern Brazil (Santa Maria 2 Sequence). -
The Role of Miniaturisation in the Evolution of the Mammalian Jaw and Middle Ear
This is the accepted version of a letter published on 17/9/2018 in Nature at https://doi.org/10.1038/ s41586-018-0521-4 1 The role of miniaturisation in the evolution of the mammalian jaw and middle ear 2 3 Stephan Lautenschlager1,2 *, Pamela Gill1,3, Zhe-Xi, Luo4, Michael J. Fagan5, Emily J. 4 Rayfield1* 5 6 1School of Earth Sciences, University of Bristol, UK 7 2School of Geography, Earth and Environmental Sciences, University of Birmingham, UK 8 3Earth Science Department, The Natural History Museum, London, UK 9 4Department of Organismal Biology and Anatomy, University of Chicago, USA 10 5School of Engineering and Computer Science, University of Hull, UK 11 12 *Corresponding authors: [email protected], [email protected] 13 14 The evolution of the mammalian jaw is one of the most important innovations in 15 vertebrate history, underpinning the exceptional radiation and diversification of 16 mammals over the last 220 million years1,2. In particular the mandible’s transformation 17 to a single tooth-bearing bone and the emergence of a novel jaw joint while 18 incorporating some of the ancestral jaw bones into the mammalian middle ear is often 19 cited as a classic textbook example for the repurposing of morphological structures3,4. 20 Although remarkably well documented in the fossil record, the evolution of the 21 mammalian jaw still poses an intriguing paradox: how could bones of the ancestral jaw 22 joint function both as a joint hinge for powerful load bearing mastication and also as 23 mandibular middle ear that would be delicate enough for hearing? Here, we use new 24 digital reconstructions, computational modelling, and biomechanical analyses to 25 demonstrate that miniaturisation of the early mammalian jaw was the primary driver 26 for the transformation of the jaw joint. -
In Quest for a Phylogeny of Mesozoic Mammals
In quest for a phylogeny of Mesozoic mammals ZHE−XI LUO, ZOFIA KIELAN−JAWOROWSKA, and RICHARD L. CIFELLI Luo, Z.−X., Kielan−Jaworowska, Z., and Cifelli, R.L. 2002. In quest for a phylogeny of Mesozoic mammals. Acta Palaeontologica Polonica 47 (1): 1–78. We propose a phylogeny of all major groups of Mesozoic mammals based on phylogenetic analyses of 46 taxa and 275 osteological and dental characters, using parsimony methods (Swofford 2000). Mammalia sensu lato (Mammaliaformes of some authors) are monophyletic. Within mammals, Sinoconodon is the most primitive taxon. Sinoconodon, morganu− codontids, docodonts, and Hadrocodium lie outside the mammalian crown group (crown therians + Monotremata) and are, successively, more closely related to the crown group. Within the mammalian crown group, we recognize a funda− mental division into australosphenidan (Gondwana) and boreosphenidan (Laurasia) clades, possibly with vicariant geo− graphic distributions during the Jurassic and Early Cretaceous. We provide additional derived characters supporting these two ancient clades, and we present two evolutionary hypotheses as to how the molars of early monotremes could have evolved. We consider two alternative placements of allotherians (haramiyids + multituberculates). The first, supported by strict consensus of most parsimonious trees, suggests that multituberculates (but not other alllotherians) are closely re− lated to a clade including spalacotheriids + crown therians (Trechnotheria as redefined herein). Alternatively, allotherians can be placed outside the mammalian crown group by a constrained search that reflects the traditional emphasis on the uniqueness of the multituberculate dentition. Given our dataset, these alternative topologies differ in tree−length by only ~0.6% of the total tree length; statistical tests show that these positions do not differ significantly from one another.