Abstract The latest early Campanian archipelago deposits of the Kristianstad Basin, southern Sweden, yield one of the most diverse Cretaceous chondrichthyan faunas collected from a narrow stratigraphical interval. Building on previous descriptions of various selachians, squatiniform and synechodontiform sharks are added to the faunal list. Squatinidae is represented by Squatina ( Squatina ) lundegreni sp. nov. and Squatina ( Squatina ) fortemordeo sp. nov. The poorly preserved type specimens of the nominal Squatina hassei from the Maastrichtian of The Netherlands were recently regarded conspecific with better preserved Santonian–Maastrichtian teeth of Squatina ( Cretascyllium ) from the Anglo-Paris Basin. This appears to have been based largely on the assumption that the nominal S . hassei was the only Squatina present in NW Europe during the Santonian–Maastrichtian. The Swedish material indicates a greater diversity of squatinoids, and the nominal S . hassei is here regarded as a nomen dubium of uncertain subgeneric affinity. Two types of synechodontid teeth with a tall central cusp co-occur in the Campanian of the Kristianstad Basin. Based on articulated jaws of the markedly dignathic S . dubrisiensis from the Cenomanian of England, the two morphs are regarded as upper and lower anterior teeth of the single species S . filipi sp. nov.

Abstract A partial exoccipital–opisthotic from the uppermost lower Campanian (Upper Cretaceous) of the Åsen locality, Kristianstad Basin, southernmost Sweden, is described and illustrated. The fossil represents the first braincase element of a plesiosaur found in Sweden. It includes the chamber for the ampulla and utriculus, openings for the caudal vertical and horizontal semicircular canals, and four foramina for cranial nerves. The incomplete braincase can be referred to an elasmosaurid plesiosaur, and closely resembles the exoccipital–opisthotic of Libonectes morgani and a referred specimen of Aristonectes parvidens . Although we discuss putative postcranial material of the elasmosaurid subfamily Aristonectinae in the uppermost lower Campanian of southernmost Sweden, the exoccipital–opisthotic from Åsen most likely belongs to a juvenile individual of a non-aristonectine elasmosaur.

Abstract An assemblage of the burrowing ghost shrimp, Protocallianassa faujasi , is described, providing the first evidence of this decapod species from Sweden. The fossils occur in successions of the informal earliest late Campanian Belemnellocamax balsvikensis zone at Åsen and the latest early Campanian B. mammillatus zone at Ivö Klack, both in the Kristianstad Basin of NE Skåne. Numerous, heavily calcified chelipeds were found within a restricted bed at Åsen that was rich in carbonate-cemented nodules. Based on the burrowing lifestyle of modern mud shrimps, we interpret these nodules as infilled burrow chambers. The low abundance of molluscs within the Protocallianassa beds is also consistent with analogous extant communities, indicating that a similar ecologically exclusive relationship ruled within the Late Cretaceous shallow-marine ecosystems.

Abstract Mesozoic dinosaur fossils are exceptionally rare in Scandinavia. The Swedish record is typically depauperate, with the Kristianstad Basin of Skåne (Scania) yielding all of the known fossils from Swedish Cretaceous strata. Although highly fragmentary, these body remnants are important because they provide evidence of a relatively diverse fauna, including previously recognized hesperornithiform birds and leptoceratopsid ceratopsians, as well as indeterminate ornithopods that are confirmed here for the first time. In this paper, we describe three phalanges (from Åsen) and an incomplete right tibia (from Ugnsmunnarna) from the Kristianstad Basin. One of the phalanges appears to pertain to a leptoceratopsid ceratopsian, providing further evidence of these small ornithischians in the Cretaceous sediments of Sweden. The other two phalanges are interpreted as deriving from small ornithopods similar to Thescelosaurus and Parksosaurus . The tibia appears to represent the first evidence of a non-avian theropod dinosaur in the Cretaceous of Sweden, with a previous report of theropod remains based on fish teeth having been corrected by other authors. The remains described herein provide important additions to the enigmatic dinosaurian fauna that inhabited the Fennoscandian archipelago during the latest Cretaceous.

Abstract Although a diverse range of aquatic vertebrates are documented from the Upper Cretaceous (mid-Campanian) marine strata of the Kristianstad Basin in southern Sweden, only chondrichthyans and marine amniotes have been described in detail to date. In contrast, coeval actinopterygians are virtually unreported, yet their remains are extremely abundant at most sampled localities. A comprehensive assessment of these fossils has identified the first Late Cretaceous actinopterygian fauna from the Fennoscandian Shield, incorporating indeterminate lepisosteids, the durophagous pycnodontid Anomoeodus subclavatus , the predatory pachycormid Protosphyraena sp., a large ichthyodectid, pachyrhizodontids resembling Pachyrhizodus , the enchodontid Enchodus cf. gladiolus and indeterminate small teleosts. These taxa are diagnosed mainly from isolated teeth and scales, implying substantial taphonomic loss prior to burial. Moreover, the prolific recovery of actinopterygian skeletal remnants in recent excavations suggests that historical collecting biases, rather than ecological paucity, have contributed to their under-representation in the Swedish Cretaceous record. Palaeobiogeographically, the Kristianstad Basin actinopterygians show compositional resemblance to assemblages from the Northern European Platform and the Western Interior Seaway of North America, advocating distributional communication across the Boreal proto-Atlantic Ocean.

Abstract A Late Cretaceous (Campanian) leaf megaflora from the Vomb Trough in southern Skåne, Sweden, has been investigated on the basis of collections held at the Swedish Museum of Natural History. The main plant-bearing locality is Köpinge, but single specimens originate from Högestad, Ingelstorp, Rödmölla, Svenstorps mölla and Tosterup. The fossil flora is dominated by the angiosperm (eudicot) Debeya ( Dewalquea ) haldemiana (Debey ex de Saporta & Marion) Halamski. Other dicots are cf. Dryophyllum sp., Ettingshausenia sp., Rarytkinia ? sp., Dicotylophyllum friesii (Nilsson) comb. nov. and Salicites wahlbergii (Nilsson) Hisinger. Conifers are represented by cf. Aachenia sp. (cone scales), Pagiophyllum sp. and Cyparissidium sp. (leaves). Single poorly preserved specimens of ferns and monocots have also been identified. The terrestrial palynomorphs (the focus herein) clearly link to the megaflora, although with different relative abundances. The fern spore Cyathidites dominates along with the conifer pollen Perinopollenites elatoides and Classopollis . Angiosperm pollen comprise up to 15% of the assemblage, represented by monocolpate, tricolpate and periporate pollen and the extinct Normapolles group. The spores in the kerogen residue show a thermal alteration index (TAI) of 2+. The flora probably represents mainly a coastal lowland Debeya /conifer forest, and is similar to approximately coeval assemblages from analogous palaeo-communities described from eastern Poland, western Ukraine and Westphalia.

Abstract The Bothnia–Skellefteå lithotectonic unit is dominated by turbiditic wacke and argillite (Bothnian basin), deposited at 1.96 (or older)–1.86 Ga, metamorphosed generally under high-grade conditions and intruded by successive plutonic suites at 1.95–1.93, 1.90–1.88, 1.87–1.85 and 1.81–1.76 Ga. In the northern part, low-grade and low-strain, 1.90–1.86 Ga predominantly magmatic rocks (the Skellefte–Arvidsjaur magmatic province) are enclosed by the basinal components. Subduction-related processes in intra-arc basin and magmatic arc settings, respectively, are inferred. Changes in the metamorphic grade and the relative timing of deformation and structural style across the magmatic province are linked to major shear zones trending roughly north–south and, close to the southern margin, WNW–ESE. Zones trending WNW–ESE and ENE–WSW dominate southwards. Slip along the north–south zones in an extensional setting initiated synchronously with magmatic activity at 1.90–1.88 Ga. Tectonic inversion steered by accretion to a craton to the east, involving crustal shortening, ductile strain and crustal melting, occurred at 1.88–1.85 Ga. Deformation along shear zones under lower-grade conditions continued at c. 1.8 Ga. Felsic volcanic rocks (1.90–1.88 Ga) host exhalative and replacement-type volcanogenic massive sulphide deposits (the metallogenic Skellefte district). Other deposits include orogenic Au, particularly along the ‘gold line’ SW of this district, porphyry Cu–Au–Mo, and magmatic Ni–Cu along the ‘nickel line’ SE of the ‘gold line’.

Abstract During the Cretaceous (145.5-65.5 Ma; Gradstein et al. 2004 ). Central Europe was part of the European continental plate, which was bordered by the North Atlantic ocean and the Arctic Sea to the NW and north, the Bay of Biscay to the SW, the northern branch of the Tethys Ocean to the south, and by the East European Platform to the east ( Fig. 15.1 ). The evolution of sedimentary basins was influenced by the interplay of two main global processes: plate tectonics and eustatic sea-level change. Plate tectonic reconfigurations resulted in the widening of the Central Atlantic, and the opening of the Bay of Biscay. The South Atlantic opening caused a counter-clockwise rotation of Africa, which was coeval with the closure of the Tethys Ocean. Both motions terminated the Permian-Early Cretaceous North Sea rifting and placed Europe in a transtensional stress field. The long-term eustatic sea-level rise resulted in the highest sea level during Phanerozoic times ( haq et al. 1988;Hardenbol et al. 1998 ). Large epicontinental shelf areas were flooded as a consequence of elevated spreading rates of mid-ocean ridges and intra-oceanic plateau volcanism, causing the development of extended epicontinental shelf seas and shelf-sea basins ( Hays & pitman 1973 ; Larson 1991 ). A new and unique lithofacies type, the pelagic chalk, was deposited in distal parts of the individual basins. Chalk deposition commenced during middle Cenomanian-early Turanian times. Chalk consists almost exclusively of the remains of planktonic coccolithophorid algae and other pelagic organisms, and its great thickness reflects a high rate of production of the algal tests. The bulk of the grains are composed of lowmagnesium calcite, representing coccolith debris with a subordinate amount of foraminifers, calcispheres, small invertebrates and shell fragments of larger invertebrates ( Håkansson et al. 1974 ; Surlyk & Birkelund 1977 ; Nygaard et al. 1983 ; Hancock 1975 , 1993 ).