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late 1990s a new fossil bearing locality 300 metres 980 ft from the village of basturs catalonia as the village already lent its name to a locality where dinosaur eggs had been found it was named the basturs poble bp locality poble derived from the word for village the locality belongs to the conques formation of the tremp group dated to the late early maastrictian 1 over ten years from 2001 through 2011 field work was done at this site and a massive bonebed consisting of some one thousand skeletal elements was discovered 1 2 the discovery was first reported in the literature in an abstract at the 55th symposium for vertebrate palaeontology and comparative anatomy and the 16th meeting of the symposium for palaeontological preparation and conservation conference in 2007 the authors then approached the bonebed under the hypothesis of a single species being present at the site it was reported that all ontogenetic stages were present 3 the stratigraphic layer where the bonebed was found is 1 5 metres 4 9 ft in thickness around 95 of all remains from the site belong to dinosaurs nearly all identified specimens from this sample belong to hadrosaurs of prepared material 270 skeletal elements can confidently be identified as belonging to hadrosauroids 1 2 the number of hadrosaur specimens from the site in total could number over 500 and possibly as much as 900 2 4 in addition to the large numbers of fossils of the animals themselves the bp locality is one of many sites from the tremp syncline where hadrosaurs tracks have been found at least one track is preserved at the site in a sandstone block from a stratigraphic level similar to that of the bonebed 2 5 it is the richest hadrosaur bonebed ever found in europe and the largest ever found in one palaeoinsular locale as such it is the most important hadrosauroid site of the eastern tremp syncline 1 2 number of species present edit a selection of dentary material from the basturs poble bonebed the primary subject of research regarding the bonebed has been the taxonomic identity of the hadrosaurs there namely whether only one taxon or multiple taxa are present the question has been complicated by a rarity of cranial elements in the sample since they are the most taxonomically informative areas of the skeleton in hadrosaurs 1 initially it was assumed that only a single species was present in the sample 3 in 2015 a study by alejandro blanco and colleagues performed multiple types of morphometric analysis to investigate hadrosaur diversity in from the pyrenees using dentaries the number of alveolar positions in the dentary was the primary metric for distinctiveness as more basal taxa possess less though it was noted this can also increase with age as an individual grows three morphotypes groupings of specimens with a distinct anatomy from the other groupings were found in the sample of which two numbers two and three were present in the bp bonebed growth trajectory analysis of the different morphotypes supported their separation sexual dimorphism being the reason for different anatomy was considered unlikely due to different results in regression analysis morphotype three was interpreted as belonging to dwarf potentially relictual hadrosauroids and morphotype two was considered to represent larger lambeosaurine animals it was stressed each morphotype was not necessarily just one species but merely representative of a distinct lineage of hadrosaurs 4 in 2018 a more extensive study of the material was conducted by víctor fondevilla and colleagues and the question of how many taxa were present of the sample was investigated using specimens from multiple parts of the body as opposed to just the dentaries overall a large amount of variation was noted in the specimens but as it was gradual rather than a case of two obvious morphotypes the authors attributed it to individual variation regarding the dentaries they too were not found to obviously sort into multiple morphotypes due to a high amount of variation between all of them one particular dentary was noted to be rather distinct from the rest but taphonomic damage or improper restoration during preparation of the fossil were considered possible explanations as opposed to taxonomic distinctiveness the authors favored identification of the hadrosaurs present in the bonebed as a singular taxon of lambeosaurine 1 size and age of the individuals edit growth trajectories of several tibiae taken from a 2018 study of the taxonomy and ontogeny of the specimens an intertwined subject to the taxonomy which has been noted and studied has been the size and ontogeny growth and development of the individuals represented individuals of multiple sizes are represented in the sample but overall they represent smaller animals than the hadrosaurs known from asia and north america despite this a small number of individuals falling into the adult size ranges of other hadrosaurs are indicated by isolated elements such as femurs 1 2 multiple hypotheses have been put forward to explain this firstly juvenile individuals may have been the dominant life stage living in the area where the bonebed was preserved due to ecological differences over lifespan secondly it s possible they represent dwarfed animals dominating the environment relative to rare a larger species lastly it s possible the large individuals were comparative giants of a single dwarfed species near the extreme end of individual variation in the species 2 the 2015 analysis of hadrosaur dentaries from the pyrenees found two morphotypes to be present in the bonebed so they favored the second hypothesis 4 the more in depth 2018 study used histological analysis in order to assess the age of different individuals using tibiae of the several tibiae tested four between 390 450 millimetres 15 18 in long were identified as juveniles between the ages of one and three based on comparisons to tissue patterns in other ornithopods and three more were found to likely be juveniles based on similarities to the former four the eighth 550 millimetres 22 in long and ninth 720 millimetres 28 in long were found to belong to an early adult and subadult individual respectively a 720 millimetres 28 in femur was found to share subadult growth features with the subadult tibia three tibiae 550 millimetres 22 in 600 millimetres 24 in and around 900 millimetres 35 in respectively were found to belong to adult individuals growth trajectory was found to be consistent between the tibiae supporting the idea that the site represents a large variety of age stages of a single species 1 taxonomic identity edit holotype dentary of koutalisaurus kohlerorum a species the bonebed material was once assigned to a poster presentation and abstract at a conference suggested the specimens may have belonged to koutalisaurus kohlerorum but they cautioned an adult dentary from the bonebed would need to be discovered to test the hypothesis 6 this was later rejected as koutalisaurus was found to be an invalid nomen dubium 7 fondevilla et al 2018 compared to the material from basturs poble to recognized species of lambeosaurine from geographically and temporally similar locations in the pyrenees the jugals from the sample were found to be distinct from those known from blasisaurus and arenysaurus possible synonyms of pararhabdodon and the frontals were also distinguishable from the latter identity as specimens as either of those taxa was therefore ruled out overlapping taxonomically informative material with pararhabdodon was not found from the bonebed excepting a maxilla too fragmentary for use in referral however both the type locality of sra and the locality of the referred maxilla mcd 4919 are close to the area the bonebed was found as such it was considered most likely the basturs poble hadrosaurs are members of the species p isonensis but the poor state of preservation of the only comparable material in the bonebed prevented a secure referral 1 later a 2019 study by prieto márquez et al described a new genus and species of spanish lambeosaurine adynomosaurus arcanus they compared the material of their species to that of the bonebed and though similarities were found their tooth crowns and ilia had different shapes and the scapulae from the site lacked the distinct shallow nature that characterizes a arcanus accordingly they considered it unlikely the bonebed belonged to their species additionally they commented on the lack of tsintaosaurin synapomorphies in the bonebed material and so kept a referral as indeterminate lambeosaurines rather than considering it to represent pararhabdodon 8 references edit 1 2 3 4 5 6 7 8 9 fondevilla v dalla vecchia f m gaete r galobart à moncunill solé b köhler m 2018 ontogeny and taxonomy of the hadrosaur dinosauria ornithopoda remains from basturs poble bonebed late early maastrichtian tremp syncline spain plos one 13 10 e0206287 bibcode 2018ploso 1306287f doi 10 1371 journal pone 0206287 pmc 6209292 pmid 30379888 1 2 3 4 5 6 7 dalla vecchia fm gaete r riera v oms o prieto márquez a vila b et al the hadrosauroid record in the maastrichtian of the eastern tremp syncline northern spain in eberth da evans dc editors hadrosaurs bloomington indiana university press 2014 pp 298 314 1 2 martín m gaete r galobart à riera v oms o a new hadrosaurian bonebed in the maastrichtian of the southern pyrenees a stratigraphic and taphonomic approach in liston j editor 55th symposium of vertebrate palaeontology and comparative anatomy and the 16th symposium of palaeontological preparation and conservation glasgow 2007 p 40 1 2 3 blanco alejandro prieto márquez albert de esteban trivigno soledad 2015 diversity of hadrosauroid dinosaurs from the late cretaceous ibero armorican island european archipelago assessed from dentary morphology cretaceous research 53 447 457 doi 10 1016 j cretres 2015 04 001 vila bernat oms oriol fondevilla victor gaete rodrigo galobart àngel riera violeta ignacio canudo josé 2013 the latest succession of dinosaur tracksites in europe hadrosaur ichnology track production and palaeoenvironments plos one 8 9 e72579 bibcode 2013ploso 872579v doi 10 1371 journal pone 0072579 pmc 3760888 pmid 24019873 prieto márquez a gaete r galobart a riera v new data on european hadrosauridae dinosauria ornithopoda from the latest cretaceous of spain j vertebr paleontol 2007 27 3 131a prieto márquez a dalla vecchia f m gaete r galobart à 2013 diversity relationships and biogeography of the lambeosaurine dinosaurs from the european archipelago with description of the new aralosaurin canardia garonnensis pdf plos one 8 7 e69835 bibcode 2013ploso 869835p doi 10 1371 journal pone 0069835 pmc 3724916 pmid 23922815 prieto márquez albert fondevilla víctor sellés albert g wagner jonathan r galobart àngel 2019 adynomosaurus arcanus a new lambeosaurine dinosaur from the late cretaceous ibero armorican island of the european archipelago cretaceous research 96 19 37 doi 10 1016 j cretres 2018 12 002 portals dinosaurs spain v t e ornithopoda kingdom animalia phylum chordata clade dinosauria clade ornithischia clade neornithischia clade cerapoda avemetatarsalia see avemetatarsalia ornithischia see ornithischia ornithopoda see below ornithopoda ornithopoda burianosaurus callovosaurus thescelosauridae hypsilophodontidae gideonmantellia hypsilophodon vectidromeus elasmaria anabisetia atlascopcosaurus chakisaurus diluvicursor fostoria galleonosaurus gasparinisaura isasicursor kangnasaurus leaellynasaura macrogryphosaurus mahuidacursor morrosaurus muttaburrasaurus notohypsilophodon qantassaurus sektensaurus talenkauen tietasaura trinisaura weewarrasaurus rhabdodontomorpha ampelognathus emiliasaura foskeia fostoria muttaburrasaurus obelignathus tenontosauridae convolosaurus iani tenontosaurus rhabdodontidae matheronodon mochlodon pareisactus rhabdodon transylvanosaurus zalmoxes dryomorpha draconyx hesperonyx owenodon dryosauridae dryosaurus dysalotosaurus elrhazosaurus eousdryosaurus iyuku kangnasaurus valdosaurus ankylopollexia barilium bayannurosaurus calvarius camptosaurus cedrorestes cumnoria dakotadon emiliasaura fukuisaurus hippodraco iguanacolossus istiorachis lanzhousaurus lurdusaurus magnamanus napaisaurus oblitosaurus osmakasaurus planicoxa proa ratchasimasaurus riabininohadros theiophytalia uteodon hadrosauriformes bolong hypselospinus jinzhousaurus mantellisaurus morelladon ouranosaurus iguanodontidae barilium comptonatus iguanodon mantellisaurus hadrosauroidea see below hadrosauroidea hadrosauroidea altirhinus bactrosaurus batyrosaurus brighstoneus cariocecus choyrodon claosaurus comptonatus datonglong eolambia equijubus fylax gilmoreosaurus gobihadros gongpoquansaurus gonkoken haolong huehuecanauhtlus hypsibema jeyawati jintasaurus koshisaurus levnesovia lophorhothon nanningosaurus nanyangosaurus penelopognathus plesiohadros portellsaurus probactrosaurus protohadros qianjiangsaurus shuangmiaosaurus siamodon sirindhorna tanius xuwulong yunganglong zhanghenglong zuoyunlong telmatosauridae kryptohadros telmatosaurus tethyshadros hadrosauridae aquilarhinus eotrachodon hadrosaurus lapampasaurus malefica yamatosaurus lambeosaurinae adynomosaurus ajnabia angulomastacator aralosaurus arenysaurus blasisaurus canardia jaxartosaurus kazaklambia latirhinus minqaria nipponosaurus pararhabdodon taleta tsintaosaurus parasaurolophini adelolophus charonosaurus parasaurolophus plesiolophus tlatolophus lambeosaurini amurosaurus corythosaurus hypacrosaurus lambeosaurus magnapaulia olorotitan velafrons saurolophinae barsboldia brachylophosaurini acristavus brachylophosaurus gongshuilong maiasaura ornatops probrachylophosaurus wulagasaurus austrokritosauria bonapartesaurus huallasaurus kelumapusaura secernosaurus kritosaurini ahshislesaurus anasazisaurus coahuilasaurus gryposaurus kritosaurus naashoibitosaurus rhinorex saurolophini augustynolophus prosaurolophus saurolophus edmontosaurini edmontosaurus kamuysaurus kerberosaurus kundurosaurus laiyangosaurus shantungosaurus related articles ichnotaxa amblydactylus anomoepus bonaparteichnium camptosaurichnus caririchnium dakotasaurus dinehichnus hadrosaurichnus iguanodontipus orcauichnites ornithopodichnites shiraminesauropus sousaichnium staurichnium tetrapodosaurus wintonopus ootaxa guegoolithus nomina dubia arstanosaurus cionodon claorhynchus diclonius eucercosaurus fulgurotherium glishades koutalisaurus loncosaurus mandschurosaurus microhadrosaurus ornithotarsus orthomerus pteropelyx siluosaurus stephanosaurus syngonosaurus thespesius tichosteus trachodon willinakaqe other articles arkharavia basturs poble bonebed dakota fossil hadrosaur diet hypsilophodont list of informal dinosaur names contains hadrosaur nomina nuda timeline of hadrosaur research edmontosaurus mummy amnh 5060 edmontosaurus mummy s m r4036 retrieved from https en wikipedia org w index php title basturs_poble_bonebed oldid 1350882711 categories lambeosaurinae tremp formation dinosaurs of 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