search.noResults

search.searching

note.createNoteMessage

search.noResults

search.searching

orderForm.title

orderForm.productCode
orderForm.description
orderForm.quantity
orderForm.itemPrice
orderForm.price
orderForm.totalPrice
orderForm.deliveryDetails.billingAddress
orderForm.deliveryDetails.deliveryAddress
orderForm.noItems
Journal of Paleontology, 89(5), 2015, p. 791–801 Copyright © 2016, The Paleontological Society 0022-3360/16/0088-0906 doi: 10.1017/jpa.2015.52


Kooiichthys jono n. gen. n. sp., a primitive catfish (Teleostei, Siluriformes) from the marine Miocene of southern South America


María de las Mercedes Azpelicueta,1 Alberto Luis Cione,2 Mario Alberto Cozzuol,3 and Juan Marcos Mirande4


1División Zoología Vertebrados, Museo de La Plata, 1900 La Plata, Argentina ⟨azpeli@gmail.com⟩ 2División Paleontología Vertebrados, Museo de La Plata, 1900 La Plata, Argentina ⟨acione@museo.fcnym.unlp.edu.ar⟩ 3Departamento de Zoologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627 Pampulha,


31270-910, Belo Horizonte, MG, Brazil ⟨mario.cozzuol@gmail.com⟩ 4Fundación Miguel Lillo, Miguel Lillo 251, San Miguel de Tucumán (4000), Tucumán, Argentina ⟨mcmirande@gmail.com


Abstract.—A specimen of a remarkable new catfish genus and species was collected in middle/late Miocene marine beds of the Puerto Madryn Formation at the base of the marine cliff of the sea lion colony area near Puerto Pirámide, southern coast of Península Valdés, northeastern Patagonia, Argentina. Siluriforms (catfishes) constitute a most important monophyletic ostariophysan group of mainly freshwater fishes that occurs in almost all continents but it is especially diverse in South America. Catfishes are presently distributed in tropical to temperate areas and a small number of species are marine or amphibiotic. The new catfish shows many primitive features for catfishes in the maxilla, autopalatine, hyal elements, and Weberian apparatus. The genus is clearly distinguished by four autapomorphies: sand clock–shaped autopalatine, posterior limb of autopalatine widening strongly, post-articular arm of autopalatine longer, and a metapterygoid longer than broad. One tree was obtained both under equal and implied weighting with the following topology: a basal polytomy in the Siluriformes formed by Diplomystidae, Bachmanniidae, Kooiichthys and the Siluroidei. The new species appears to have been a marine or amphibiotic taxon: it was collected in beds considered to represent the Maximum Flooding Horizon of the transgression that deposited the Puerto Madryn Formation. The coast at this moment was at approximately 90 km to the west. According to faunistic evidence, the sea was warm temperate.


Introduction


Siluriformes (catfishes) comprise one of the most diverse vertebrate groups both morphologically and taxonomically (Fink and Fink, 1996; Nelson, 2006). Presently, there are approximately 37 families with almost 3,400 species in all continents except Antarctica (Ambruster, 2011). However, they inhabited Antarctica at least during the Eocene, when radically climatic conditions prevailed in the world (Grande and Eastman, 1986). Only a small number of catfishes (most of the ariids and many of the plotosids) are marine and some species of other families can enter brackish waters (Nelson, 2006). The most plesiomorphic catfishes in a morphological


sense are the living Diplomystidae of Patagonia and central Chile (Arratia, 1987; Azpelicueta, 1994) and the Eocene Bachmanniidae of Patagonia (Azpelicueta and Cione, 2011). The oldest fossils assignable to Siluriformes occur in the Campanian (late Cretaceous) of southern South America (Cione and Laffite, 1980; Cione, 1987). Moreover, South America is the only continent where catfishes are relatively common in Cretaceous rocks (Argentina: Cione and Lafitte, 1980; Cione et al., 1985; Arratia and Cione, 1996. Bolivia: Gayet and Meunier, 2003.Brazil: Bertini et al., 1993). The only extra–South American Cretaceous records are otoliths in North America


(Nolf and Stringer, 1996) and one spine from India (Cione and Prasad, 2002). South America is the continent where siluriforms are most


diverse and where the most primitive catfishes occur (Azpelicueta and Cione, 2011). Since the Cretaceous, lineage-splitting should have been coupled with many independent evolutionary experi- ments and ecological specializations. They are relatively common in Cenozoic rocks in the continent (Arratia and Cione, 1996; Azpelicueta and Cione, 2011). The discovery of the present catfish in Miocene beds of Patagonia deserves special attention; unfortunately, only the anterior part of the neurocranium, great part of visceral skeleton, anterior vertebrae, and great part of pectoral girdle were preserved. No other material was collected despite repeated collecting visits to the area. In this paper, we describe the new genus and species and


discuss its relationships based on morphological features with the most primitive siluriform taxa and the rest of catfishes.


Stratigraphy


The fossil-bearing bed is formed of muddy sandstones included in the Puerto Madryn Formation (Fig. 1). These beds were deposited during the late part of the extensive marine encroachment that lasted from the late Oligocene until the late


791


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