Three new tanaid species (Crustacea, Peracarida, Tanaidacea) from the Lower Cretaceous Álava amber in northern Spain

2007 ◽  
Vol 81 (6) ◽  
pp. 1502-1509 ◽  
Author(s):  
Ronald Vonk ◽  
Frederick R. Schram

Marine crustaceans were not known as inclusions in amber from upper Aptian–middle Albian deposits in Northern Spain. The publication of a photograph of a purported fossil amphipod (Alonso et al., 2000) among many other arthropods promised to be of high interest because the fossil record of the amphipoda does not extend further than Upper Eocene (Schram, 1986; Coleman and Myers, 2000). The Museum of Natural Sciences of Álava in Vitoria-Gasteiz (AMNS), northern Spain, kindly sent us the material with the presumed amphipods, as our intention was to investigate its affinities to other fossil amphipods. The fossil crustaceans of this assemblage were found among 15 orders of insects, spiders, and mites—i.e., mainly terrestrial arthropods.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Iwona Kania-Kłosok ◽  
Wiesław Krzemiński ◽  
Antonio Arillo

AbstractFirst record of the genus Helius—long-rostrum cranefly from Maestrazgo Basin (eastern Spain, Iberian Penisula) is documented. Two new fossil species of the genus Helius are described from Cretaceous Spanish amber and compared with other species of the genus known from fossil record with particular references to these known from Cretaceous period. Helius turolensis sp. nov. is described from San Just amber (Lower Cretaceous, upper Albian) Maestrazgo Basin, eastern Spain, and Helius hispanicus sp. nov. is described from Álava amber (Lower Cretaceous, upper Albian), Basque-Cantabrian Basin, northern Spain. The specific body morphology of representatives of the genus Helius preserved in Spanish amber was discussed in relation to the environmental conditions of the Maestrazgo Basin and Basque-Cantabrian Basin in Cretaceous.



2019 ◽  
Vol 2 (2) ◽  
pp. 115-118
Author(s):  
PENELOPE CLAISSE ◽  
PATRICK BRISAC ◽  
ANDRÉ NEL

Nemopteridae are a small family of myrmeleontoid lacewings characterized by elongated ribbon- or thread-like hindwings. Extant Nemopteridae comprise two subfamilies, viz. Crocinae (thread-wings) and Nemopterinae (spoon- and ribbon-wings). They are distributed in all zoogeographical regions except the Nearctic region in the extant fauna. However, the major species diversity of Nemopteridae is confined to the southern part of Africa. The fossil record of the family is scarce, with five Lower Cretaceous fossils, one from the lowermost Cenomanian, two fossils from the Upper Eocene, and two from the Oligocene (Lu et al., 2019; Nel & Jarzembowski, 2019). Here we describe a new, nearly complete fossil from the Oligocene of Lubéron in France. It was found in the Konservat Lagerstätte of Céreste, in finely laminated lacustrine limestones. It is the only specimen of this family found in this outcrop, among more than 30000 fossil insects. Neuroptera are extremely rare in this outcrop; only one adult Ascalaphidae (Ascaloptynx oligocenicus Nel, 1991) and two Mantispidae (Prosagittalata oligocenica Nel, 1988 and an undescribed specimen) have been discovered there (Nel, 1988, 1991).



2021 ◽  
Vol 108 (1) ◽  
pp. 129-144
Author(s):  
Ludovic Le Renard ◽  
Ruth A. Stockey ◽  
Garland R. Upchurch ◽  
Mary L. Berbee


2016 ◽  
Vol 283 (1839) ◽  
pp. 20161448 ◽  
Author(s):  
Taiping Gao ◽  
Chungkun Shih ◽  
Conrad C. Labandeira ◽  
Jorge A. Santiago-Blay ◽  
Yunzhi Yao ◽  
...  

Antennae are important, insect sensory organs that are used principally for communication with other insects and the detection of environmental cues. Some insects independently evolved ramified (branched) antennae, which house several types of sensilla for motion detection, sensing olfactory and chemical cues, and determining humidity and temperature levels. Though ramified antennae are common in living insects, occasionally they are present in the Mesozoic fossil record. Here, we present the first caddisflies with ramified antennae, the earliest known fossil sawfly, and a scorpionfly also with ramified antennae from the mid-Lower Cretaceous Yixian Formation of Northeastern China, dated at 125 million years ago (Ma). These three insect taxa with ramified antennae consist of three unrelated lineages and provide evidence for broad structural convergence that historically has been best demonstrated by features such as convergent mouthparts. In addition, ramified antennae in these Mid-Mesozoic lineages likely do not constitute a key innovation, as they are not associated with significantly increased diversification compared with closely related lineages lacking this trait, and nor are they ecologically isolated from numerous, co-occurring insect species with unmodified antennae.



Zootaxa ◽  
2016 ◽  
Vol 4200 (2) ◽  
pp. 327 ◽  
Author(s):  
PEDRO S. R. ROMANO

Pelomedusoides is the most diverse clade of side-necked turtles and there is an extensive fossil record (de Broin, 1988; Lapparent de Broin, 2000; Gaffney et al., 2006, 2011) that dates back at least to the Barremian (Lower Cretaceous) (Romano et al., 2014). Its large fossil record evidences a greater diversity in the past, particularly at the end of the Mesozoic, and exhibits a good sampling of species that are represented by skull material (Gaffney et al., 2006, 2011). As a consequence, the most complete and recent phylogenetic hypotheses for this clade (e.g. Romano et al., 2014; Cadena, 2015) are based on matrices comprising a great amount of cranial characters derived largely from Gaffney et al. (2006, 2011). In addition, it is well established that shell characters show a lot of phenotypic plasticity, even in the fossil species (Romano, 2008; Gaffney et al., 2006, 2011). In most cases it consequently is not justified to rely on “diagnostic features” of poorly informative shell-only material for describing a new species. Because of that, most authors remark new morphotypes in the literature when such aberrant specimens are recovered, but do not make any nomenclatural act by proposing a new yet poorly supported species (e.g. Romano et al., 2013; Ferreira & Langer, 2013; Menegazzo et al., 2015). Unfortunately, such a supposedly new bothremydid turtle (Pleurodira: Bothremydidae) from the Early Paleocene of Brazil was recently described based on poorly diagnostic remains (Carvalho et al., 2016; hereafter CGB, for the authors initials) and a correction of this unfounded nomenclatural act is required. In addition I present some comments on shell only material from Brazil in order to guide splitter-taxonomists to stop describing poorly preserved fossil specimens as new species. 



2015 ◽  
Vol 152 (6) ◽  
pp. 1123-1136 ◽  
Author(s):  
ELADIO LIÑÁN ◽  
JOSÉ ANTONIO GÁMEZ VINTANED ◽  
RODOLFO GOZALO

AbstractThe type material ofAgraulos antiquusSdzuy, 1961 from the La Herrería Formation, northern Spain, is revised together with additional material and included in the new genusLunagraulos. The stratigraphical range ofLunagraulos antiquus(Sdzuy, 1961) – occurring below that of the trilobite species of the generaLunolenus,MetadoxidesandDolerolenusin the type locality of Los Barrios de Luna in the province of León, northern Spain – and the accompanying ichnofossil assemblage demonstrate an Ovetian age (lower part of Cambrian Stage 3, currently being discussed by the International Subcommission on Cambrian Stratigraphy) for this species. Moreover, the trilobiteLunagraulos tamamensisn. gen. n. sp. is found in the Tamames Sandstone near the village of La Rinconada in the province of Salamanca, central Spain. The biostratigraphical position of this new taxon and its accompanying ichnoassemblage is also analysed and assigned to the lowermost Ovetian Stage. The genusLunagraulosis therefore the oldest agraulid found in the fossil record. The exceptional presence ofLunagraulosin a marine coarse siliciclastic succession – a facies rather typical for the ichnofossilsCruzianaandRusophycus, some of the oldest signs of trilobite activity – suggests that first trilobite representatives may have inhabited high- to middle-energy, marine environments. This hypothesis may also explain both the taxonomic and biostratigraphic heterogeneity of the first trilobite genera appearing across the world, due to preservation problems in this type of facies. Comparison of theLunagraulos biostratigraphy with other coeval Spanish fossil assemblages allows us to propose its intercontinental correlation with the oldest records of currently known trilobites.



1964 ◽  
Vol S7-VI (3) ◽  
pp. 305-308
Author(s):  
Jean Claude Griffon ◽  
J. Magne ◽  
Jacques Sigal

Abstract The limestone dorsal of the northern part of the Rif mountains near Tetuan, Morocco, exposes Permian clastics, Triassic dolomite, Jurassic and lower Cretaceous limestone, upper Cretaceous to Eocene marl, transgressive upper Eocene conglomerate, and Oligocene flysch. The microfauna of the upper Cretaceous and the Paleogene formations are particularly useful in correlations. Major tectonic movements occurred in the Miocene.



1992 ◽  
Vol 66 (6) ◽  
pp. 958-972 ◽  
Author(s):  
Robert W. Wieder ◽  
Rodney M. Feldmann

Nine species of fossil isopods have been studied from Cretaceous to Pleistocene rocks of North America. This represents all known species from the Mesozoic and Cenozoic fossil record on this continent. Four species of Palaega were studied. Palaega goedertorum Wieder and Feldmann, 1989, from upper Eocene to lower Miocene rocks of Washington state, has served recently as the basis for restructuring the genus. Emendations are made to species descriptions of Palaega guadalupensis and P. williamsonensis from the Cretaceous rocks of Texas. The fourth species of Palaega, P. lamnae, also from the Cretaceous rocks of Texas, although of doubtful affinities with this genus, was not removed due to lack of sufficient information to reassign it. Two new species are described, Cirolana enigma, from Lower Cretaceous rocks of South Dakota, and Archaeoniscus texanus, from the Cretaceous of Texas. This is the first report of Cirolana from the fossil record. Two sphaeromatid isopods were included: one, Sphaeroma burkartii from Tertiary rocks of Mexico, was not located for study; the other, Eocopea oculata, is from Miocene rocks of southern California. Two specimens of the valviferan genus Saduria, from Pleistocene deposits in Canada, were also studied.



2009 ◽  
Vol 83 (6) ◽  
pp. 994-997 ◽  
Author(s):  
Julián F. Petrulevičius

The order Mecoptera is represented on all continents, albeit with an uneven distribution. Mecoptera includes about 34 families (Labandeira, 1994, p. 34), only four of them, until now, represented in South America: Permochoristidae Tillyard, 1917 (†) (Pinto, 1972); Bittacidae Handlirsch, 1906 [and stem-group “Neorthophlebinae” (†)] (Petrulevičius, 2001a, 2003, 2007); Nannochoristidae Tillyard, 1917; and Eomeropidae Cockerell, 1909. The two latter families have a present relict distribution in southern South America but without fossil record, obviously an artifact due to few studies of fossil insects in the subcontinent. The diversity of recent Bittacidae is high in South America with respect to other continents. Thirty-five percent of recent genera of Bittacidae come from South America, and 80% of these genera are endemic (extracted from Penny, 1997). Bittacidae is well represented in the fossil record, with species from the Jurassic of Patagonia (Petrulevičius, 2007), Lower Cretaceous of Brazil (Petrulevičius and Martins-Neto, 2001), to the late Paleocene of Argentina (Petrulevičius, 1998, 1999, 2001b, 2003). This contribution reports a specimen belonging to the Panorpoidea, a group with no recent species in South America and very few species in the entire Southern Hemisphere.



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