Cenizo et al.—Pseudo-toothed birds from Eocene of Antarctica
879
Figure 7. Temporal distribution, phylogenetic affinities, and size-types in selected pelagornithid species (modified from Mayr et al., 2013). The internal nodes are supported by the following presumable derived features (Mayr et al., 2013, and present work): Clade 1 (humerus with ventral portion of proximal end narrow and tuberculum dorsale strongly projected, ulna with very short olecranon, trochlea metatarsi II at the same level or slightly more plantarly projected than the trochlea IV); Clade 3 (femur with trochlea fibularis lacking sulcus). The Clade 2 is still uncertain, but according to general similarities it considered by Mayr et al. (2013) as Pelagornis s.l. (a presumable derived character noted here is the presence of the transverse furrow near the tip of the rostrum). The size-types represent the wingspan inferred by extrapolated dimensions of the known elements in incomplete specimens compared with the homologous elements in the P. chilensis holotype, the most completely known pelagornithid specimen. The gray areas indicate possible cladogenetic event. (Af) Africa, (E) Europe, (NA) North America, (Ant) Antarctica, (NZ) New Zealand, (SA) South America, (Au) Australia.
in Antarctica (Acosta Hospitaleche, 2013, 2015; Acosta Hospitaleche and Reguero, 2015), and the late Oligocene in New Zealand (Ksepka and Ando, 2011). After that, giant penguins disappear from the fossil record, suggesting an important ecological segregation favoring medium and small penguins, in contrast with pseudo-toothed birds, in which giant size was maintained until their extinction in the late Neogene.
Highlights in pelagornithid evolution.—The phylogenetic affi- nities within Pelagornithidae are not well understood, and thus, reliable conclusions are difficult to assess. The following inferences about the evolutionary history of the group should be considered as
the younger Mio/Pliocene taxa in a highly specialized group of forms (Clade 3, Fig. 7), that probably constituted the third and more recent evolutionary event in pelagornithids.
Acknowledgments
preliminary, and must be confirmed with new and more complete findings. On this basis, and having in mind that the pelagornithid record is patchy, three main evolutionary events can be recognized. MLP 12-I-20-4, assigned to morphotype 1, is the oldest
pseudo-toothed birds from Antarctica, and is more derived than Dasornis in several features. It indicates in the middle Ypresian, the presence of a more specialized ‘clade’ than that of Dasornis. This first event probably includes the disappearance of Dasornis and would be the starting point of the dominance of more advanced forms (“Clade” 1, Fig. 7) with a trend toward the extreme specialization of soaring capacity. The second event would be linked to the origin of the
Pelagornis s.l. species (hypothetical Clade 2, Fig. 7; see Mayr et al., 2013). It would have occurred during the early Oligocene, although unfortunately, the fossil record of pseudo-toothed birds is very scarce for that time. Finally, Mayr et al. (2013) recognized some presumable synapomorphies that allow to join
We thank the logistic support of the Dirección Nacional del Antártico and Fuerza Aérea Argentina during field work in Antarctica. Especially to Cecilia Deschamps and Federico Agnolin for their assistance with English version. The sugges- tions and comments provided by the associate editor Daniel Ksepka, Estelle Bourdon and an anonymous reviewer improved the quality of the manuscript and are appreciated. The Instituto Antártico Argentino supported this project along with grants from the Consejo Nacional de Investigaciones Científicas y Técnicas, Agencia Nacional de Promoción Científica y Tecno- lógica, and Universidad Nacional de La Plata.
References
Acosta Hospitaleche, C, 2015, New penguin giant bones from Antarctica: systematic and paleobiological significance: Comptes Rendus Palevol, v. 13, p. 555–560.
Acosta Hospitaleche, C., and Haidr, N., 2011, Penguin (Aves, Sphenisciformes) cranial remains from the La Meseta Formation (Eocene) of Antarctic Peninsula (Antarctica): Antarctic Sciences, v. 23, p. 369–378.
Acosta Hospitaleche, C., and Reguero, M., 2010, Taxonomic notes about Ich- tyopteryx gracilis Wiman, 1905 and Orthopteryx gigas Wiman, 1905 (Aves, Spheniscidae): Alcheringa, v. 35, p. 463–466.
Page 1 |
Page 2 |
Page 3 |
Page 4 |
Page 5 |
Page 6 |
Page 7 |
Page 8 |
Page 9 |
Page 10 |
Page 11 |
Page 12 |
Page 13 |
Page 14 |
Page 15 |
Page 16 |
Page 17 |
Page 18 |
Page 19 |
Page 20 |
Page 21 |
Page 22 |
Page 23 |
Page 24 |
Page 25 |
Page 26 |
Page 27 |
Page 28 |
Page 29 |
Page 30 |
Page 31 |
Page 32 |
Page 33 |
Page 34 |
Page 35 |
Page 36 |
Page 37 |
Page 38 |
Page 39 |
Page 40 |
Page 41 |
Page 42 |
Page 43 |
Page 44 |
Page 45 |
Page 46 |
Page 47 |
Page 48 |
Page 49 |
Page 50 |
Page 51 |
Page 52 |
Page 53 |
Page 54 |
Page 55 |
Page 56 |
Page 57 |
Page 58 |
Page 59 |
Page 60 |
Page 61 |
Page 62 |
Page 63 |
Page 64 |
Page 65 |
Page 66 |
Page 67 |
Page 68 |
Page 69 |
Page 70 |
Page 71 |
Page 72 |
Page 73 |
Page 74 |
Page 75 |
Page 76 |
Page 77 |
Page 78 |
Page 79 |
Page 80 |
Page 81 |
Page 82 |
Page 83 |
Page 84 |
Page 85 |
Page 86 |
Page 87 |
Page 88 |
Page 89 |
Page 90 |
Page 91 |
Page 92 |
Page 93 |
Page 94 |
Page 95 |
Page 96 |
Page 97 |
Page 98 |
Page 99 |
Page 100 |
Page 101 |
Page 102 |
Page 103 |
Page 104 |
Page 105 |
Page 106 |
Page 107 |
Page 108 |
Page 109 |
Page 110 |
Page 111 |
Page 112 |
Page 113 |
Page 114 |
Page 115 |
Page 116 |
Page 117 |
Page 118 |
Page 119 |
Page 120 |
Page 121 |
Page 122 |
Page 123 |
Page 124 |
Page 125 |
Page 126 |
Page 127 |
Page 128 |
Page 129 |
Page 130 |
Page 131 |
Page 132 |
Page 133 |
Page 134 |
Page 135 |
Page 136 |
Page 137 |
Page 138 |
Page 139 |
Page 140 |
Page 141 |
Page 142 |
Page 143 |
Page 144 |
Page 145 |
Page 146 |
Page 147 |
Page 148 |
Page 149 |
Page 150 |
Page 151 |
Page 152 |
Page 153 |
Page 154 |
Page 155 |
Page 156 |
Page 157 |
Page 158 |
Page 159 |
Page 160 |
Page 161 |
Page 162 |
Page 163 |
Page 164 |
Page 165 |
Page 166 |
Page 167 |
Page 168 |
Page 169 |
Page 170 |
Page 171 |
Page 172 |
Page 173 |
Page 174 |
Page 175 |
Page 176 |
Page 177 |
Page 178 |
Page 179 |
Page 180 |
Page 181 |
Page 182 |
Page 183 |
Page 184 |
Page 185 |
Page 186 |
Page 187 |
Page 188 |
Page 189 |
Page 190 |
Page 191 |
Page 192 |
Page 193 |
Page 194 |
Page 195 |
Page 196 |
Page 197 |
Page 198 |
Page 199 |
Page 200 |
Page 201 |
Page 202 |
Page 203 |
Page 204 |
Page 205 |
Page 206 |
Page 207 |
Page 208 |
Page 209 |
Page 210 |
Page 211 |
Page 212