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Late Cretaceous neornithine from Europe illuminates the origins of crown birds – Nature.com

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  • 1.

    Prum, R. O. et al. A comprehensive phylogeny of birds (Aves) using targeted next-generation DNA sequencing. Nature 526, 569–573 (2015).

  • 2.

    Jarvis, E. D. et al. Whole-genome analyses resolve early branches in the tree of life of modern birds. Science 346, 1320–1331 (2014).

  • 3.

    Claramunt, S. & Cracraft, J. A new time tree reveals Earth history’s imprint on the evolution of modern birds. Sci. Adv. 1, e1501005 (2015).

  • 4.

    Field, D. J. et al. Early evolution of modern birds structured by global forest collapse at the end-Cretaceous mass extinction. Curr. Biol. 28, 1825–1831 (2018).

  • 5.

    Larson, D. W., Brown, C. M. & Evans, D. C. Dental disparity and ecological stability in bird-like dinosaurs prior to the end-Cretaceous mass extinction. Curr. Biol. 26, 1325–1333 (2016).

  • 6.

    Mayr, G. Avian higher level biogeography: Southern Hemispheric origins or Southern Hemispheric relicts? J. Biogeogr. 44, 956–958 (2017).

  • 7.

    Saupe, E. E. et al. Climatic shifts drove major contractions in avian latitudinal distributions throughout the Cenozoic. Proc. Natl Acad. Sci. USA 116, 12895–12900 (2019).

  • 8.

    Ksepka, D. T. & Phillips, M. J. Avian diversification patterns across the K–Pg boundary: influence of calibrations, datasets, and model misspecification. Ann. Mo. Bot. Gard. 100, 300–328 (2015).

  • 9.

    Berv, J. S. & Field, D. J. Genomic signature of an avian Lilliput effect across the K–Pg extinction. Syst. Biol. 67, 1–13 (2018).

  • 10.

    Field, D. J. et al. Timing the extant avian radiation: the rise of modern birds, and the importance of modeling molecular rate variation. PeerJ Preprints 7, e27521v1 (2019).

  • 11.

    Mayr, G. Avian Evolution (Wiley, 2016).

  • 12.

    Clarke, J. A., Tambussi, C. P., Noriega, J. I., Erickson, G. M. & Ketcham, R. A. Definitive fossil evidence for the extant avian radiation in the Cretaceous. Nature 433, 305–308 (2005).

  • 13.

    Dyke, G. J. et al. Europe’s last Mesozoic bird. Naturwissenschaften 89, 408–411 (2002).

  • 14.

    Xing, L., Stanley, E. L., Bai, M. & Blackburn, D. C. The earliest direct evidence of frogs in wet tropical forests from Cretaceous Burmese amber. Sci. Rep. 8, 8770 (2018).

  • 15.

    Simões, T. R. et al. The origin of squamates revealed by a Middle Triassic lizard from the Italian Alps. Nature 557, 706–709 (2018).

  • 16.

    Evers, S. W., Barrett, P. M. & Benson, R. B. J. Anatomy of Rhinochelys pulchriceps (Protostegidae) and marine adaptation during the early evolution of chelonioids. PeerJ 7, e6811 (2019).

  • 17.

    Bi, S. et al. An Early Cretaceous eutherian and the placental–marsupial dichotomy. Nature 558, 390–395 (2018).

  • 18.

    Lee, M. S. Y. & Yates, A. M. Tip-dating and homoplasy: reconciling the shallow molecular divergences of modern gharials with their long fossil record. Proc. R. Soc. Lond. B 285, 20181071 (2018).

  • 19.

    Hope, S. in Mesozoic Birds: Above the Heads of Dinosaurs (eds Chiappe, L. M. & Witmer, L. M.) 339–388 (Univ. California Press, 2002).

  • 20.

    Longrich, N. R., Tokaryk, T. & Field, D. J. Mass extinction of birds at the Cretaceous–Paleogene (K–Pg) boundary. Proc. Natl Acad. Sci. USA 108, 15253–15257 (2011).

  • 21.

    Mayr, G. Paleogene Fossil Birds (Springer, 2009).

  • 22.

    Clyde, W. C., Ramezani, J., Johnson, K. R., Bowring, S. A. & Jones, M. M. Direct high-precision U–Pb geochronology of the end-Cretaceous extinction and calibration of Paleocene astronomical timescales. Earth Planet. Sci. Lett. 452, 272–280 (2016).

  • 23.

    Gauthier, J. A. & de Queiroz, K. in New Perspectives on the Origin and Early Evolution of Birds: Proceedings of the International Symposium in Honor of John H. Ostrom (eds Gauthier, J. & Gall, L. F.) 7–41 (Peabody Museum of Natural History, Yale University, 2001).

  • 24.

    Keutgen, N. A bioclast-based astronomical timescale for the Maastrichtian in the type area (southeast Netherlands, northeast Belgium) and stratigraphic implications: the legacy of PJ Felder. Neth. J. Geosci. 97, 229–260 (2018).

  • 25.

    Field, D. J., Lynner, C., Brown, C. & Darroch, S. A. F. Skeletal correlates for body mass estimation in modern and fossil flying birds. PLoS One 8, e82000 (2013).

  • 26.

    Olson, S. L. & Feduccia, A. Presbyornis and the origin of the Anseriformes (Aves: Charadriomorphae). Smithson. Contrib. Zool. 323, 1–24 (1980).

  • 27.

    Elzanowski, A. & Stidham, T. A. Morphology of the quadrate in the Eocene anseriform Presbyornis and extant galloanserine birds. J. Morphol. 271, 305–323 (2010).

  • 28.

    Worthy, T. H., Degrange, F. J., Handley, W. D. & Lee, M. S. Y. The evolution of giant flightless birds and novel phylogenetic relationships for extinct fowl (Aves, Galloanseres). R. Soc. Open Sci. 4, 170975 (2017).

  • 29.

    Tambussi, C. P., Degrange, F. J., De Mendoza, R. S., Sferco, E. & Santillana, S. A stem anseriform from the early Palaeocene of Antarctica provides new key evidence in the early evolution of waterfowl. Zool. J. Linn. Soc. 186, 673–700 (2019).

  • 30.

    Mayr, G., De Pietri, V. L., Love, L., Mannering, A. & Scofield, R. P. Oldest, smallest and phylogenetically most basal pelagornithid, from the early Paleocene of New Zealand, sheds light on the evolutionary history of the largest flying birds. Pap. Palaeontol. https://doi.org/10.1002/spp2.1284 (2019).

  • 31.

    Budd, G. E. & Mann, R. P. The dynamics of stem and crown groups. Sci. Adv. 6, eaaz1626 (2020).

  • 32.

    Ksepka, D. T. & Clarke, J. Phylogenetically vetted and stratigraphically constrained fossil calibrations within Aves. Palaeontologia Electronica 18, 18.1.3FC (2015).

  • 33.

    Mayr, G., De Pietri, V. L., Scofield, R. P. & Worthy, T. H. On the taxonomic composition and phylogenetic affinities of the recently proposed clade Vegaviidae Agnolín et al., 2017 – neornithine birds from the Upper Cretaceous of the Southern Hemisphere. Cretaceous Research 86, 178–185 (2018).

  • 34.

    Clarke, J. A. et al. Fossil evidence of the avian vocal organ from the Mesozoic. Nature 538, 502–505 (2016).

  • 35.

    Agnolín, F. L., Egli, F. B., Chatterjee, S., Marsà, J. A. G. & Novas, F. E. Vegaviidae, a new clade of southern diving birds that survived the K/T boundary. Naturwissenschaften 104, 87 (2017).

  • 36.

    O’Connor, J. K., Chiappe, L. M. & Bell, A. in Living Dinosaurs: The Evolutionary History of Modern Birds (eds Dyke, G. & Kaiser, G.) 39–114 (Wiley-Blackwell, 2011).

  • 37.

    Cracraft, J. in The Phylogeny and Classification of the Tetrapods Vol. 1 (ed. Benton, M. J.) 339–361 (Oxford Univ. Press, 1988).

  • 38.

    Livezey, B. C. A phylogenetic analysis of basal Anseriformes, the fossil Presbyornis, and the interordinal relationships of waterfowl. Zool. J. Linn. Soc. 121, 361–428 (1997).

  • 39.

    Cracraft, J. & Clarke, J. The basal clades of modern birds. In New Perspectives on the Origin and Early Evolution of Birds: Proceedings of the International Symposium in Honor of John H. Ostrom (eds Gauthier, J. & Gall, L. F.) 143–156 (Peabody Museum of Natural History, Yale University, 2001).

  • 40.

    Felice, R. N. & Goswami, A. Developmental origins of mosaic evolution in the avian cranium. Proc. Natl Acad. Sci. USA 115, 555–560 (2018).

  • 41.

    Field, D. J. Endless skulls most beautiful. Proc. Natl Acad. Sci. USA 115, 448–450 (2018).

  • 42.

    Huxley, T. H. On the classification of birds; and on the taxonomic value of the modifications of certain of the cranial bones observable in that class. Proc. Zool. Soc. Lond. 1867, 415–472 (1867).

  • 43.

    Ericson, P. G. P. Systematic relationships of the Palaeogene family Presbyornithidae (Aves: Anseriformes). Zool. J. Linn. Soc. 121, 429–483 (1997).

  • 44.

    Cooney, C. R. et al. Mega-evolutionary dynamics of the adaptive radiation of birds. Nature 542, 344–347 (2017).

  • 45.

    Bright, J. A., Marugán-Lobón, J., Rayfield, E. J. & Cobb, S. N. The multifactorial nature of beak and skull shape evolution in parrots and cockatoos (Psittaciformes). BMC Evol. Biol. 19, 104 (2019).

  • 46.

    Field, D. J. & Hsiang, A. Y. A North American stem turaco, and the complex biogeographic history of modern birds. BMC Evol. Biol. 18, 102 (2018).

  • 47.

    Mourer-Chauviré, C. Les oiseaux fossiles des phosphorites du Quercy (Éocène supérieur a Oligocène supérieur): implications paléobiogéographiques. Geobios 15, 413–426 (1982).

  • 48.

    Mayr, G. Two-phase extinction of “Southern Hemispheric” birds in the Cenozoic of Europe and the origin of the Neotropic avifauna. Palaeobiodivers. Palaeoenviron. 91, 325–333 (2011).

  • 49.

    O’Connor, J. K. & Zhou, Z. The evolution of the modern avian digestive system: insights from paravian fossils from the Yanliao and Jehol biotas. Palaeontology 63, 13–27 (2020).

  • 50.

    Feduccia, A. Explosive evolution in tertiary birds and mammals. Science 267, 637–638 (1995).

  • 51.

    Clarke, J. A. Morphology, phylogenetic taxonomy, and systematics of Ichthyornis and Apatornis (Avialae: Ornithurae). Bull. Am. Mus. Nat. Hist. 286, 1–179 (2004).

  • 52.

    Field, D. J. et al. Complete Ichthyornis skull illuminates mosaic assembly of the avian head. Nature 557, 96–100 (2018).

  • 53.

    Mayr, G. & Weidig, I. The early Eocene bird Gallinuloides wyomingensis – a stem group representative of Galliformes. Acta Palaeontol. Pol. 49, 211–217 (2004).

  • 54.

    Ksepka, D. T. Broken gears in the avian molecular clock: new phylogenetic analyses support stem galliform status for Gallinuloides wyomingensis and rallid affinities for Amitabha urbsinterdictensis. Cladistics 25, 173–197 (2009).

  • 55.

    Mayr, G. & Rubilar-Rogers, D. Osteology of a new giant bony-toothed bird from the Miocene of Chile, with a revision of the taxonomy of Neogene Pelagornithidae. J. Vertebr. Paleontol. 30, 1313–1330 (2010).

  • 56.

    Bourdon, E. Osteological evidence for sister group relationship between pseudo-toothed birds (Aves: Odontopterygiformes) and waterfowls (Anseriformes). Naturwissenschaften 92, 586–591 (2005).

  • 57.

    Mayr, G. Cenozoic mystery birds – on the phylogenetic affinities of bony-toothed birds (Pelagornithidae). Zool. Scr. 40, 448–467 (2011).

  • 58.

    Goloboff, P. A. & Catalano, S. A. TNT version 1.5, including a full implementation of phylogenetic morphometrics. Cladistics 32, 221–238 (2016).

  • 59.

    Ronquist, F. et al. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst. Biol. 61, 539–542 (2012).

  • 60.

    Miller, M. A., Pfeiffer, W. & Schwartz, T. Creating the CIPRES Science Gateway for inference of large phylogenetic trees. In Gateway Computing Environments Workshop (GCE 2010) 45–53 (IEEE, 2010).

  • 61.

    Lewis, P. O. A likelihood approach to estimating phylogeny from discrete morphological character data. Syst. Biol. 50, 913–925 (2001).

  • 62.

    Heath, T. A., Huelsenbeck, J. P. & Stadler, T. The fossilized birth–death process for coherent calibration of divergence-time estimates. Proc. Natl Acad. Sci. USA 111, E2957–E2966 (2014).

  • 63.

    Zhang, C., Stadler, T., Klopfstein, S., Heath, T. A. & Ronquist, F. Total-evidence dating under the fossilized birth–death process. Syst. Biol. 65, 228–249 (2016).

  • 64.

    Kealy, S. & Beck, R. Total evidence phylogeny and evolutionary timescale for Australian faunivorous marsupials (Dasyuromorphia). BMC Evol. Biol. 17, 240 (2017).

  • 65.

    Vinther, J., Parry, L., Briggs, D. E. & Van Roy, P. Ancestral morphology of crown-group molluscs revealed by a new Ordovician stem aculiferan. Nature 542, 471–474 (2017).

  • 66.

    Gill, F., Donsker, D & Rasmussen, P. (eds) IOC World Bird List (v.10.1) https://www.worldbirdnames.org/ioc-lists/crossref/ (2020).

  • 67.

    Field, D. J., LeBlanc, A., Gau, A. & Behlke, A. D. B. Pelagic neonatal fossils support viviparity and precocial life history of Cretaceous mosasaurs. Palaeontology 58, 401–407 (2015).

  • 68.

    Ericson, P. G. P. et al. Diversification of Neoaves: integration of molecular sequence data and fossils. Biol. Lett. 2, 543–547 (2006).

  • 69.

    Jetz, W., Thomas, G. H., Joy, J. B., Hartmann, K. & Mooers, A. O. The global diversity of birds in space and time. Nature 491, 444–448 (2012).

  • 70.

    Phillips, M. J. Geomolecular dating and the origin of placental mammals. Syst. Biol. 65, 546–557 (2016).

  • 71.

    He, H. Y. et al. Timing of the Jiufotang Formation (Jehol Group) in Liaoning, northeastern China, and its implications. Geophys. Res. Lett. 31, (2004).

  • 72.

    Wang, X. et al. The earliest evidence for a supraorbital salt gland in dinosaurs in new Early Cretaceous ornithurines. Sci. Rep. 8, 3969 (2018).

  • 73.

    Musser, G., Ksepka, D. T. & Field, D. J. New material of Paleocene-Eocene Pellornis (Aves: Gruiformes) clarifies the pattern and timing of the extant Gruiform radiation. Diversity 11, 102 (2019).

  • 74.

    Ksepka, D. T., Stidham, T. A. & Williamson, T. E. Early Paleocene landbird supports rapid phylogenetic and morphological diversification of crown birds after the K–Pg mass extinction. Proc. Natl Acad. Sci. USA 114, 8047–8052 (2017).

  • 75.

    Parham, J. F. et al. Best practices for justifying fossil calibrations. Syst. Biol. 61, 346–359 (2012).

  • 76.

    Püschel, H. P., O’Reilly, J. E., Pisani, D. & Donoghue, P. C. J. The impact of fossil stratigraphic ranges on tip-calibration, and the accuracy and precision of divergence time estimates. Palaeontology 63, 67–83 (2020).

  • 77.

    Worthy, T. H. et al. Osteology supports a stem-galliform affinity for the giant extinct flightless bird Sylviornis neocaledoniae (Sylviornithidae, Galloanseres). PLoS One 11, e0150871 (2016).

  • 78.

    Benton, M. J. & Donoghue, P. C. J. Paleontological evidence to date the tree of life. Mol. Biol. Evol. 24, 26–53 (2007).

  • 79.

    Reddy, S. et al. Why do phylogenomic data sets yield conflicting trees? Data type influences the avian tree of life more than taxon sampling. Syst. Biol. 66, 857–879 (2017).

  • 80.

    Hackett, S. J. et al. A phylogenomic study of birds reveals their evolutionary history. Science 320, 1763–1768 (2008).

  • 81.

    Kimball, R. T. et al. A phylogenomic supertree of birds. Diversity 11, 109 (2019).

  • 82.

    Dunning, J. B. CRC Handbook of Avian Body Masses 2nd edn (CRC Press, 2007).

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    SpaceX launch marks 300th successful booster landing – Phys.org

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    Credit: Unsplash/CC0 Public Domain

    SpaceX sent up the 30th launch from the Space Coast for the year on the evening of April 23, a mission that also featured the company’s 300th successful booster recovery.

    A Falcon 9 rocket carrying 23 of SpaceX’s Starlink internet satellites blasted off at 6:17 p.m. Eastern time from Cape Canaveral Space Force Station’s Space Launch Complex 40.

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    The first-stage booster set a milestone of the 300th time a Falcon 9 or Falcon Heavy booster made a successful recovery landing, and the 270th time SpaceX has reflown a booster.

    This particular booster made its ninth trip to space, a resume that includes one human spaceflight, Crew-6. It made its latest recovery landing downrange on the droneship Just Read the Instructions in the Atlantic Ocean.

    The company’s first successful booster recovery came in December 2015, and it has not had a failed booster landing since February 2021.

    The current record holder for flights flew 11 days ago making its 20th trip off the .

    SpaceX has been responsible for all but two of the launches this year from either Kennedy Space Center or Cape Canaveral with United Launch Alliance having launched the other two.

    SpaceX could knock out more launches before the end of the month, putting the Space Coast on pace to hit more than 90 by the end of the year, but the rate of launches by SpaceX is also set to pick up for the remainder of the year with some turnaround times at the Cape’s SLC-40 coming in less than three days.

    That could amp up frequency so the Space Coast could surpass 100 launches before the end of the year, with the majority coming from SpaceX. It hosted 72 launches in 2023.

    More launches from ULA are on tap as well, though, including the May 6 launch atop an Atlas V rocket of the Boeing CST-100 Starliner with a pair of NASA astronauts to the International Space Station.

    ULA is also preparing for the second launch ever of its new Vulcan Centaur rocket, which recently received its second Blue Origin BE-4 engine and is just waiting on the payload, Sierra Space’s Dream Chaser spacecraft, to make its way to the Space Coast.

    Blue Origin has its own it wants to launch this year as well, with New Glenn making its debut as early as September, according to SLD 45’s range manifest.

    2024 Orlando Sentinel. Distributed by Tribune Content Agency, LLC.

    Citation:
    SpaceX launch marks 300th successful booster landing (2024, April 24)
    retrieved 24 April 2024
    from https://phys.org/news/2024-04-spacex-300th-successful-booster.html

    This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
    part may be reproduced without the written permission. The content is provided for information purposes only.

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    Wildlife Wednesday: loons are suffering as water clarity diminishes – Canadian Geographic

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    The common loon, that icon of northern wilderness, is under threat from climate change due to declining water clarity. Published earlier this month in the journal Ecology, a study conducted by biologists from Chapman University and Rensselaer Polytechnic Institute in the U.S. has demonstrated the first clear evidence of an effect of climate change on this species whose distinct call is so tied to the soundscape of Canada’s lakes and wetlands.

    Through the course of their research, the scientists found that July rainfall results in reduced July water clarify in loon territories in Northern Wisconsin. In turn, this makes it difficult for adult loons to find and capture their prey — mainly small fish — underwater, meaning they are unable to meet their chicks’ metabolic needs. Undernourished, the chicks face higher mortality rates. The consistent foraging techniques used by loons across their range means this impact is likely echoed wherever they are found — from Alaska to Canada to Iceland.

    The researchers used Landsat imagery to find that there has been a 25-year consistent decline in water clarity, and during this period, body weights of adult loon and chicks alike have also declined. With July being the month of most rapid growth in young loons, the study also pinpointed water clarity in July as being the greatest predictor of loon body weight. 

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    One explanation for why heavier rainfall leads to reduced water clarity is the rain might carry dissolved organic matter into lakes from adjacent streams and shoreline areas. Lawn fertilizers, pet waste and septic system leaks may also be to blame.

    The researchers, led by Chapman University professor Walter Piper, hope to use these insights to further conservation efforts for this bird Piper describes as both “so beloved and so poorly understood.”

    Return of the king

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    Giant prehistoric salmon had tusk-like teeth for defence, building nests

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    The artwork and publicity materials showcasing a giant salmon that lived five million years ago were ready to go to promote a new exhibit, when the discovery of two fossilized skulls immediately changed what researchers knew about the fish.

    Initial fossil discoveries of the 2.7-metre-long salmon in Oregon in the 1970s were incomplete and had led researchers to mistakenly suggest the fish had fang-like teeth.

    It was dubbed the “sabre-toothed salmon” and became a kind of mascot for the Museum of Natural and Cultural History at the University of Oregon, says researcher Edward Davis.

    But then came discovery of two skulls in 2014.

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    Davis, a member of the team that found the skulls, says it wasn’t until they got back to the lab that he realized the significance of the discovery that has led to the renaming of the fish in a new, peer-reviewed study.

    “There were these two skulls staring at me with sideways teeth,” says Davis, an associate professor in the department of earth sciences at the university.

    In that position, the tusk-like teeth could not have been used for biting, he says.

    “That was definitely a surprising moment,” says Davis, who serves as director of the Condon Fossil Collection at the university’s Museum of Natural and Cultural History.

    “I realized that all of the artwork and all of the publicity materials and bumper stickers and buttons and T-shirts we had just made two months prior, for the new exhibit, were all out of date,” he says with a laugh.

    Davis is co-author of the new study in the journal PLOS One, which renames the giant fish the “spike-toothed salmon.”

    It says the salmon used the tusk-like spikes for building nests to spawn, and as defence mechanisms against predators and other salmon.

    The salmon lived about five million years ago at a time when Earth was transitioning from warmer to relatively cooler conditions, Davis says.

    It’s hard to know exactly why the relatives of today’s sockeye went extinct, but Davis says the cooler conditions would have affected the productivity of the Pacific Ocean and the amount of rain feeding rivers that served as their spawning areas.

    Another co-author, Brian Sidlauskas, says a fish the size of the spike-toothed salmon must have been targeted by predators such as killer whales or sharks.

    “I like to think … it’s almost like a sledgehammer, these salmon swinging their head back and forth in order to fend off things that might want to feast on them,” he says.

    Sidlauskas says analysis by the lead author of the paper, Kerin Claeson, found both male and female salmon had the “multi-functional” spike-tooth feature.

    “That’s part of our reason for hypothesizing that this tooth is multi-functional … It could easily be for digging out nests,” he says.

    “Think about how big the (nest) would have to be for an animal of this size, and then carving it out in what’s probably pretty shallow water; and so having an extra digging tool attached to your head could be really useful.”

    Sidlauskas says the giant salmon help researchers understand the boundaries of what’s possible with the evolution of salmon, but they also capture the human imagination and a sense of wonder about what’s possible on Earth.

    “I think it helps us value a little more what we do still have, or I hope that it does. That animal is no longer with us, but it is a product of the same biosphere that sustains us.”

    This report by The Canadian Press was first published April 24, 2024.

    Brenna Owen, The Canadian Press

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