Hammerschmiede Clay Pit | |
Type: | Fossil site |
Period: | Miocene |
Prilithology: | Silts, sandstone and claystone |
Country: | Germany |
Unitof: | Upper Freshwater Molasse |
Thickness: | 25.7 m |
The Hammerschmiede clay pit (German: Tongrube Hammerschmiede) is a fossil bearing locality in Pforzen, Bavaria, Germany most well known for the discovery of Danuvius guggenmosi, the potentially earliest known bipedal ape. With an age of 11.66-11.42 Ma the site dates to the transition between the Middle and Late Miocene epoch, providing an important window into the faunal changes taking place during this time. This correlates to the time just after the Serravallian-Tortonian boundary, and the MN zones 7/8. It is one of the most well-known Miocene sites, with over 15,000 individual fossils and 117 species having been discovered as of 2020. It has been called "the most important German paleontological discovery of the last decades".
Hammerschmiede's first fossils were first discovered by the hobby archaeologist Siegulf Guggenmos in 1965.[1] The site became known in academic circles following publications on its rich fauna of micromammals in 1975.[2] Since 2011, the excavations are led by a collaboration between the University of Tübingen and the Senckenberg Museum, and led by Madelaine Böhme, with the help of local volunteers. Excavations were intensified in 2015, following the discovery of a variety of scientifically significant finds. Media attention increased following the description of Danuvius guggenmosi in 2019, its name honoring the discoverer of the site.[3] Nicknamed "Udo", the discovery was described as the oldest known example of an upright ape in Hominidae, with some media even going so far as to call it proof that the cradle of humanity was located in Bavaria.[4] The site is threatened by clay mining.[5]
The Hammerschmiede clay pit is located within the eastern Allgäu region of Bavaria, within the municipality of Pforzen, at a height above sea level of almost 700 m. It is located just west of the district Hammerschmiede, after which it is named, and lies between the stream Riedgraben to its south, and the river Wertach to its East. Furthermore, the locality Irsee, where fossil plant remains had already been discovered in the 1950s, is located 4.3 km to its southwest. The closest town is Kaufbeuren to its south-east.
The Hammerschmiede locality is part of the Upper Freshwater Molasse within the North Alpine foreland Basin. It is part of the Obere Serie, which includes Germany's youngest Molasse sediments. The 25.7 m thick section is best exposed at the southern end of the clay pit.
The horizontally bedded layers are mostly grey-colored, carbonatic and fine-grained silts, fine sands and claystone. The sedimentary succession can be traced over 150 m in a northern direction, with seven marker beds being traceable across the whole distance. These are three lignite horizons, three sand horizons and one marlstone. The circa 0.45 m thick homogeneous silty-clayey marlstone contains a variety of terrestrial gastropods, and is located in the basal part of the northern profile. Meanwhile, up to 10 mm thick pedogenic carbonate concretions are abundant in the upper 20 cm. A 20 cm thick blackish lignite horizon occurs 1.5 m above this horizon, overlaying 70 cm of yellowish and brownish mottled dark-grey clay. The color of this lignite is platy, it is partly xylitic and can be horizontally replaced by carbonatic peat clay. This succession may be viewed as a complete calcic paleosol, with the marlstone representing the Bk-horizon, the mottled clay the Bt-horizon, and the lignite the A-horizon. Three horizontally continuous bodies of fine-sand are located between the upper and lower lignite horizons, with the lower one being 1.05 m thick, greenish-grey, showing no bedding structures, but containing iron-hydroxide stains. The middle sand horizon, made up of mica rich grey-blue to greyish sand and containing iron-hydroxide stains, is 2.8 m thick at the southern part of the clay pit, and develops into an up to 4 m deep channel at its erosional base in the North. The upper sand horizon, consisting of grey silty fine-sand showing iron-hydroxide stains, is 1.4 m thick and is divided by a 20 cm thick pedogenic bed 0.70 m above its base. This bed, which includes small fossilised roots, consists of mottled clayey and sandy silts. Reworked pedogenic carbonates clay pebbles with a diameter of up to 3 cm occur 30 cm above the base of the horizon.
A 35 cm thick lignite horizon marks the top of the presently exposed sedimentary succession in the Hammerschmiede outcrop. Its basal 25 cm are platy colored and rarely contain xylit, while the upper 10 cm are blackish carbonatic organic clay instead of lignite. It overlays about 10 cm of carbonate-free, grey-greenish and rusty-yellowish mottled sandy and clayey slits. As a 40 cm thick rooted silt horizon, containing abundant powdery, whitish soft carbonate occurs below it, the topmost succession can be interpreted as an immature calcic paleosol.
Directly below this, another, shjallower calcic paleosol is developed. Its A-horizon is formed by 7 cm thick blackish carbonatic peat clay, overlaying the Bt-horizon (5 cm thick grey clay) and Bk-horizon (8 cm thick whitish clay horizon with abundant powdery carbonate). The paleosols rooting system reaches 50 cm below the A-horizon.
Furthermore, several truncated paleosols, which either completely or partly lack the A-horizon, occur especially between the two lower sand horizons. Those are characterized by up to 0.60 m thick grey green-yellowish mottled clayey marls, which contain matrix-supported pedogenic carbonate concretions. Two less developed calcic-paleosols, which are completely lacking A-horizons but clay-rich Btk horizons, make up the basal 4 meters of the succession in the southern profile.
The locality is divided into six stratigraphic layers.
The environment of Hammerschmiede was a seasonally dry floodplain of meandering rivers and streams flowing from south to north. HAM 5 represents a rivulet of local origin, with a width of four to five meters, a channel fill thickness of 0.8–1 meter and a mean water depth of ≤ 0.8 m. HAM 4 was a medium-sized river, with a width of roughly 50 m, a channel fill thickness of 4–5 m and a mean water depth of ≤ 4 m. Both channels are asymmetric in cross-section, with a more deeply incised outer bank and a shallower slip-off slope. Based on grain sizes, the flow velocity of both channels has been estimated as low to very low. However, the presence of an autochthonous freshwater mollusc fauna made up out of Pisidium, Margaritifera, Sphaerium and Bithynia suggests well-oxygenated waters, with moderate flow. The presence of considerable amounts of water are furthermore supported by the abundance of fish and turtle fossils, as well as swamp plants.[9] Pebbles of alpine origin are not present, but reworked marine plankton from the Upper Marine Molasse is. Therefore, the catchment area of these rivers did not include alpine areas. Instead, they likely had their source in the Faltenmolasse just a few kilometers south of Hammerschmiede.
The paleoclimate of the locality was subtropical and considerably warmer and drier than that of the region today, with annual average temperatures of perhaps over 20 °C. Estimates based on the herpetofauna suggest mean annual precipitation (MAP) of 974 ± 256 mm for HAM 1, 1008 ± 257 mm for HAM 2 and 1196 ± 263 mm for HAM 3, while a MAP of 858 ± 147 mm has been estimated for the calcic paleosol with an estimated age of 11.64 ma. Another study estimates mean warm month temperatures of 24.7-27.9 °C, warm month precipitation of 79–172 mm and an average Köppen Aridity Index of 25.4.[10]
All this suggests a seasonally dry climate, with swamps developing in the riparian regions during wetter periods. The high temperatures and comparatively low precipitations suggest a significant seasonal water stress, which is furthermore supported by the abundant pedogenic carbonate concretions, indications of forest fires and an as of yet unpublished stable isotope analysis, which showcases the enriched δ13C values of a C3 vegetation under very strong water stress. The large number of scansorial species suggests that the site was forested.[11]
Hammerschmiede dates to the latest stages of MN7/8, overlapping with the Astaracian-Vallesian boundary. Notable is the presence of Kretzoiarctos beatrix and Sinohippus sp., which link it with the slightly older locality Nombrevilla 2. Another taxon connecting Hammerschmiede to this Spanish locality is Galerix cf. exilis, thought to have gone extinct in Central Europe during earlier in the Middle Miocene, which likely reemmigrated from the Iberian peninsula to Germany during this time. Species such as these suggest that Hammerschmiede, and contemporary sites, may represent the last European faunas with Middle Miocene character. In slightly younger deposits, for example those correlating to the Mytilopsis ornitopsis zone (11.5 to 11.4 Ma, Vienna Basin) many lineages of large middle Miocene mammals have already been replaced with new immigrants, such as Hipparionine horses which define the MN9 zone. However, more typical Late Miocene taxa such as the large bovid Miotragocerus and the cricetid Microtocricetus molassicus are also present. Indeed, the occurrence of this cricetid originally led researchers to the conclusion that Hammerschmiede should be dated to MN9. Furthermore, Hammerschmiede shows both the first and last occurrences of a number of taxa, such as Eomellivora and Laphyctis, respectively.[12]
The carnivoran assemblage of Hammerschmiede is the third richest known from Miocene Europe, with 28 different species. 13 sympatric small carnivorans are known from HAM 5 alone, a diversity comparable with the African tropics. The comparison with six other fossil assemblages (Sansan, Steinheim, La Grive-Saint Alban, Rudabánya, Can Ponsic and Can Llobateres 1) shows some marked differences between the carnivoran guild of those sites and Hammerschmiede. Amphicyonids, extremely common at the other localities, and barbourofelids, which are a regular presence, are only known from infrequent and fragmentary material at Hammerschmiede. Herpestids and lophocyonids, which are known from Sansan and La Grive, are completely absent, while Potamotherium and phocids are not known from the other localities. Mustelids are the most diverse family, with 11 species, making up 39% of all Carnivora present at the locality. Viverrids are only presented by 3 species (11%), but make up 21% of all individuals found. However, there is a marked difference between their abundance in HAM 4 (36%) and HAM 5 (4%). HAM 4 generally shows a lower diversity of large, scansorial and hypercarnivorous carnivorans in comparison with HAM 5, although the number of semiaquatic species is much higher with four. Notably, it is the only locality in which Lartetictis and Paralutra are known to have coexisted, despite the suggestion that the latter genus gradually replaced the former. Other likely competitors include Viverrictis-Circamustela and Semigenetta sansaniensis-"Martes" sansaniensis. Larger species with overlapping ecological roles include the metailurine and barbourofelid. The latters shows more derived sabertooth features, suggesting it likely preyed on larger animals than the felid, which probably attacked medium-sized prey from trees. The coexistence of all these competing taxa can be explained by the existence of significant resources. Niche partitioning is also seen among the proboscideans, with Tetralophodon being a mixed feeder, and Deinotherium a browser. As Gomphotherium is absent from this locality, it has been suggested that it correlates to the transition period from Middle Miocene faunas dominated by trilophodont gompothere taxa to the Late Miocene ones dominated by tetralophodont species.[13]
Ephemeroptera indet. | Larvae |
Margaritifera/Pseudunio[14] | M. flabellata | HAM 4HAM 5 | Unionid freshwater mussel, the most abundant bivalve of the Upper Freshwater Molasse, forming dense, monospecific communities in clean sand or gravel bottoms. | |||
Sphaerium | S. rivicola | HAM 4 | fragmentary valves | First record from the Upper Freshwater Molasse. Inhabits muddy sand near riverbanks, with moderately strong currents, well-oxygenated water, but little submerged vegetation. | ||
Pisidium | P. amnicum | HAM 4 | Two contiguous and a great number of individual valves | Inhabits sand in well-oxygenated waters, preferring strong currents and hard water |
Bithynia | C. sp. 1 | HAM 4 | Four shells of sub-adult individuals and asingle operculum. | Generalist inhabiting limnic and fluval waters. | ||
B. sp. 2 | HAM 4 | Over 70 opercula | ||||
Borysthenia | B. sp. | HAM 4 | two almost complete shells | Earliest record of the genus. Inhabits sandy and muddy substrate near river banks. | ||
Triptychia | Terrestrial snail belonging to the family Filholiidae | |||||
Helicoidea indet. | Terrestrial snail, possibly belonging to the genus Pseudochloritis |
Esox | E. sp. | HAM 1 HAM 3 HAM 5[15] | ||||
Silurus | S. joergi[16] | HAM 1 HAM 3 HAM 5[17] | Medium-sized catfish, the oldest member of the genus in Europe | |||
Cobitis | C. sp. | HAM 1 HAM 3 HAM 5 | ||||
Tinca | T. sp. | HAM 1 HAM 3 HAM 5 | ||||
Palaeoleuciscus | P. sp. | HAM 1 HAM 3 HAM 5 | ||||
Leuciscus | L. sp. | HAM 1 HAM 3 HAM 5 | ||||
Barbus | B. sp. | HAM 5 | ||||
Gobius | G. sp. | HAM 1 HAM 3 HAM 5 | ||||
Perca | P. sp. | HAM 1 HAM 3 HAM 5 | ||||
Sciaenidae indet. | HAM 5 |
Eopelobates | E. sp. | HAM 3HAM 5 | ||||
Palaeobatrachus[18] | P. sp. | HAM 3HAM 5 | ||||
Latonia | L. gigantea | HAM 1HAM 3 HAM 5 | ||||
Pelophylax | P. sp. | HAM 1HAM 3 HAM 5 | ||||
Hyla | H. sp. | HAM 1HAM 5 | ||||
Bufotes | B. cf. viridis | HAM 3HAM 5 | Referred to as Bufo cf. viridis |
Batrachosauroididae indet. | HAM 1HAM 3[19] HAM 5 | Occasionally spelled "Batrachosauroidae" | |||
aff. Palaeoproteus | aff. P. sp. | HAM 1HAM 3 | Batrachosauroidid salamander | ||
Scapherpetontidae indet. | HAM 3HAM 5 | ||||
Andrias | A. scheuchzeri | HAM 4HAM 5 | Giant salamander | ||
Mioproteus | M. aff. weizei | HAM 1HAM 3 HAM 5 | Fossil salamander related to the olm | ||
Chelotriton | C. paradoxus | HAM 1HAM 3 HAM 5 | A newt | ||
Triturus | T. roehrsi | HAM 1HAM 3 HAM 5 | A newt | ||
T. aff. montadoni | HAM 3HAM 5 |
Lazarussuchus | L. sp. | HAM 2HAM 3 HAM 5 | The youngest fossils referred to this taxon |
Trionyx | T. sp. | HAM 1HAM 5 | Plate fragments[20] | A softshell turtle | ||
Chelydropsis | C. sp. | HAM 1HAM 4 HAM 5 | Over a thousand remains, including eggs and a well-preserved skull. | Most commonly found tetrapod at the locality. With a length of 70 cm the largest European turtle of its time. Likely molluscivorous chelydrid[21] | ||
Titanochelon | T. sp. | HAM 5 | A large tortoise | |||
Testudo | T. sp. | HAM 1HAM 5 | A tortoise | |||
Clemmydopsis | C. sp. | HAM 1HAM 4 HAM 5 | Carapace of a juvenile | A swamp turtle | ||
Mauremys | M. sarmatica | HAM 5 | A swamp turtle |
Lacerta[22] | L. sp. 1 | HAM 1HAM 2 HAM 3 HAM 5 | ||||
L. sp. 2 | HAM 1HAM 5 | |||||
Pseudopus | P. pannonicus | HAM 1HAM 2 HAM 3 HAM 5 | A great number of scales. | Anguid, with a length of up to two meters the largest lizard present[23] | ||
Ophisaurus | O. sp. | HAM 1HAM 2 HAM 3 HAM 5 | Anguid lizard | |||
Chalcides | C. sp. | HAM 1 HAM 5 | A skink | |||
Scincidea indet. | HAM 2HAM 3 | |||||
Amphisbaenidae indet. | HAM 1HAM 5 | |||||
Colubrinae sp. 1 | HAM 1HAM 5 | |||||
Colubrinae sp. 2 | HAM 1HAM 5 | |||||
Natricinae sp. 1 | HAM 1HAM 5 | |||||
Natricinae sp. 2 | HAM 5 | |||||
Erycinae indet. | HAM 5 |
Accipitriformes indet. | HAM 5 | One or two species | ||||
Alcedinidae indet. | About the size of the Collared Kingfisher. First fossil record of the family in Europe. | |||||
Allgoviachen[24] | A. tortonica | HAM 4HAM 5 | Nearly complete leg | Anatid comparable in size to an Egyptian goose | ||
cf. Mioquerquedula | cf. M. sp. | HAM 4 | Three wing and pectoral girdle bones | Tiny anatid even smaller than the smallest extant species | ||
Anatidae sp. 1 | HAM 4 | Undetermined medium-sized anatid | ||||
Anatidae sp. 2 | HAM 4 | Undetermined medium-sized anatid | ||||
Anhinga[25] | A. pannonica | HAM 4HAM 5 | Various postcranial remains | Large sized darter | ||
Galliformes indet. | HAM 5 | |||||
Galliformes indet. 2 | ||||||
Gruidae indet.[26] | HAM 4 | Dorsal portions of beak and neurocranium | Very large crane, with a skull similar in size and shape to the Siberian crane | |||
Passeriformes indet. | About the size of the Eurasian Magpie | |||||
Phalacrocoracidae indet. | HAM 4 | Small cormorant |
Listriodon | L. splendens | HAM 5 | A listriodontine suid | |||
Parachleuastochoerus | P. steinheimensis | HAM 5 | Perfectly preserved skull[27] | A tetraconodontine suid | ||
Dorcatherium | D. naui | HAM 5 | Large tragulid with pronounced sexual dimorphism[28] | |||
Miotragocerus | M. monacensis | HAM 4[29] HAM 5 | Partial skull, postcranial material, teeth, horn cores[30] | Large, boselaphine bovid. Youngest known fossils from this species. | ||
Boselaphinae indet. | HAM 5 | |||||
Euprox | E. furcatus | HAM 5 | A cervid | |||
Muntiacini indet. | HAM 5 | |||||
Moschidae indet. | HAM 5 |
Alopecocyon | A. goeriachensis | HAM 5 | teeth, mandible | Small, scansorial simocyonine ailurid | ||
Simocyoninae indet. | HAM 4 | molar | Rather large possibly belongs to Protursus | |||
Amphicyonidae indet. | HAM 5 | isolated teeth | Considerably larger than Amphicyon major | |||
Kretzoiarctos | K. beatrix | HAM 4HAM 5 | teeth | Ailuropodine ursid, opportunistic feeder weighing around 100 kg | ||
Phocidae indet. | HAM 4HAM 5 | teeth | Piscivore, slightly larger than the harbor seal | |||
Proputorius | P. pusillus | HAM 1 | teeth | Tiny (<1 kg), hypocarnivorous mephitid | ||
P. sansaniensis | HAM 1HAM 5 | teeth | Small (1–3 kg), hypocarnivorous mephitid | |||
Palaeomeles | P. pachecoi | HAM 5 | mandible, teeth | Badger-like mephitid, slightly smaller than Meles | ||
Circamustela | C. hartmanni | HAM 1HAM 4 HAM 5 | mandible, teeth | Small, hypercarnivorous gulonine | ||
"Martes" | M. munki | HAM 4 HAM 5 | right hemimandible | smaller than "M". sansaniensis | ||
M. sansaniensis | HAM 4HAM 5 | skull | Rather large (3 kg) marten | |||
M. sp. | HAM 1 | teeth | Small, <1 kg | |||
Laphyctis | L. mustelinus | HAM 4 | molar | Almost wolverine sized gulonine, potentially belongs to the Genus Ischyrictis | ||
Gulolinae indet. | HAM 5 | left hemimandible and left femur | Hypocarnivore, weighing 5 kg | |||
Eomellivora | E. moralesi | HAM 5 | right hemimandible, teeth | Oldest occurrence of the genus, slightly larger than a wolverine | ||
Lartetictis | L. cf. dubia | HAM 4 | left hemimandible, teeth | Semiaquatic mustelid | ||
Paralutra | P. jaegeri | HAM 4HAM 5 | teeth | Small (<10 kg) otter | ||
Vishnuonyx | V. neptuni | HAM 4 | mandible, teeth | Rather large, piscivorous (10–15 kg) otter[31] | ||
Trocharion | T. albanense | HAM 4HAM 5 | skull, teeth | House cat sized leptarcine, hypocarnivore | ||
Potamotherium | P. sp. | HAM 4HAM 5 | isolated teeth | Semiaquatic, piscivorous carnivoran of unclear taxonomic status, comparable in size to the smooth-coated otter |
Barbourofelidae indet. | HAM 5 | right distal humerus | A very large form (>100 kg). Similar fossils have been found in Spain. | |||
Metailurini indet. | HAM 5 | right upper canine | Potentially a connection between Pseudaelurus and Metailurus. Large, similar in size to M. major. | |||
Pseudaelurus | P. quadridentatus | HAM 5 | teeth | Leopard-sized felid | ||
Leptofelis | L. vallesiensis | HAM 5 | Not mentioned in the review of Hammerschmiede carnivorans | |||
Hyaenidae indet. | incisor | Very large form (>100 kg). Potentially either belongs to Dinocrocuta or an early crocutoid | ||||
Thalassictis | T. montadai | HAM 4?HAM 5 HAM 6 | teeth | Wolf-like ictitheriine hyena | ||
Semigenetta | S. grandis | HAM 4 | teeth | Large (ca. 10 kg) viverrid, hypercarnivore with a similar dietary niche as jackals[32] | ||
S. sansaniensis | HAM 1HAM 4 HAM 5 | various remains | Most common carnivoran present. Scansorial omnivore leaning towards meat, with a dietary niche comparable to the small Indian civet. Weight of 1.5–4 kg, individuals from Hammerschmiede closer towards the lower end. | |||
Viverrictis | V. modica | HAM 4HAM 5 | teeth | Very small (<1 kg), scansorial, insectivorous viverrid |
Chiroptera indet. | various species | HAM 5 |
Plesiosorex | P. schaffneri | HAM 1HAM 5 | A plesiosoricid | |||
Crusafontina | C. exulta | HAM 1HAM 3[33] HAM 5 | Maxilla and teeth | A member of the obscure, highly specialized shrew tribe Anourosoricini[34] | ||
Dinosorex | D. sp. nov. | HAM 5 | A soricid | |||
Paenelimnoecus | P. crouzeli | HAM 5 | A soricid | |||
Soricidae indet. 1 | HAM 5 | |||||
Soricidae indet. 2 | HAM 5 | |||||
Desmanella | D. sp. | HAM 5 | A talpid related to shrew moles | |||
Gehardstorchia | G. quinquecuspidata | HAM 1HAM 5 | A talpid | |||
Proscapanus | P. sp. | HAM 5 | A talpid | |||
Talpa | T. sp. | HAM 5 | A talpid | |||
Erinaceinae indet. | HAM 5 | |||||
Galerix | G. cf. exilis | HAM 3 | molars | A galercine, last known Central European occurrence | ||
Plesiodimylus | P. johanni | HAM 5 | A dimylid | |||
Metacordylodon | M. schlosseri | HAM 5 | A dimylid |
Eurolagus | E. fontannesi | HAM 1HAM 5 | An ochotonid | |||
Prolagus | P. oeningensis | HAM 5 | An ochotonid |
Danuvius | D. guggenmosi | HAM 5 | Partial skeleton, and a variety of additional remains | A small hominoid, potentially capable of bipedalism, although that has been disputed[35] | ||
Pliopithecidae indet. | HAM 5 | Teeth | New species |
Ancylotherium | A. sp. | HAM 5 | A schizotheriine | |||
Aceratherium | A. sp. | HAM 1HAM 4 | A hornless rhinoceros | |||
Hoploaceratherium | H. belvederense | HAM 5 | A one-ton heavy, folivorous rhinoceros with a small horn[36] | |||
Sinohippus | S. sp. | HAM 5 | A folivorous, anchitheriine equid |
Deinotherium | D. levius | HAM 4HAM 5 | Remains of several juveniles and one adult | A deinotheriine proboscidean | ||
Tetralophodon | T.. longirostris | HAM 5HAM 6 | Partial skeleton of an adult, remains of a juvenile[37] | An elephantoid proboscidean |
Anomalomys | A. gaudryi | HAM 1HAM 5 | An anomalomyid rodent | |||
Albanesia | A. grimmi | HAM 5 | A flying squirrel | |||
Blackia | B. miocaenica | HAM 5 | A flying squirrel | |||
Miopetaurista | M. crusafonti | HAM 1 | A flying squirrel, synonymous with M. albanensis | |||
Petauristinae indet. | HAM 5 | |||||
Spermophilinus | S. bredai | HAM 1HAM 3[38] HAM 5 | A xerine squirrel | |||
Chalicomys | C. jaegeri | HAM 4HAM 5 | A semiaquatic castorid[39] | |||
Steneofiber[40] | S. depereti | HAM 4HAM 5 | Teeth | A medium sized, semiaquatic castorid | ||
Trogontherium | T. minutus | HAM 1HAM 4 HAM 5 | A semiaquatic castorid, with similarities to Ondatra[41] Also known as Euroxenomys | |||
Eliomys | E. sp. | HAM 5 | A glirid rodent | |||
Glirulus | G. conjunctus | HAM 5 | A glirid rodent | |||
Microdyromys | M. complicatus | HAM 5 | A glirid rodent, synonymous with M. miocaenicus[42] | |||
Muscardinus | M. hispanicus | HAM 5 | A glirid rodent | |||
Myoglis | M. meini | HAM 1HAM 5 | A glirid rodent | |||
Eomyops | E. catalaunicus | HAM 1HAM 2 HAM 3[43] HAM 5 | great number of isolated teeth | An eomyid rodent | ||
Keramidomys | K. sp. | HAM 5 | An eomyid rodent | |||
Collimys | C. hiri | HAM 1HAM 3HAM 5 | Great number of isolated teeth | A cricetid rodent | ||
C. dobosi | Isolated teeth | A cricetid rodent | ||||
Democricetodon | D. nov. sp. | HAM 1HAM 5 | A cricetid rodent | |||
Eumyarion | E. latior | HAM 5 | A cricetid rodent | |||
Megacricetodon | M. minutus | HAM 1HAM 5 | A cricetid rodent | |||
Microtocricetus | M. molassicus | HAM 5 | A cricetid rodent |
Alnus[44] | A. sp. | |||
Asteraceae | ||||
Betula | B. sp. | |||
Buxus | B. sp. | |||
Caldesia | ||||
Carex | ||||
Carpinus | A. sp. | |||
Carya | C. sp. | |||
Celtis | C. sp. | |||
Ceratophyllum | ||||
Decodon | ||||
Ephedripites | E. sp. | |||
Ericaceae | ||||
Extrapunctatosporis | E. miocaenicus | |||
Fagus | F. sp. | |||
Foveotriletes | F. sp. | |||
Hydrosporis | H. levis | |||
Ilex | I. sp. | |||
Inaperturopollenites | I. concedipites | |||
Juglans | J. sp. | |||
Laevigatosporites | L. sp. | |||
Leiotriletes | L. sp. L. neddenioides L. wolffi brevis L. wolffi wolffi | |||
Liquidambar | L. sp. | |||
Lonicera | L. sp. | |||
Magnoliaepollenites | M. sp. | |||
Mneme | ||||
Momipites | M. punctatus | |||
Monogemmites | M. pseudosetarius | |||
Monoleiotriletes | M. gracilis | |||
Myrica | M. sp. | |||
Nymphaea | ||||
Nyssa | ||||
Oleaceae | ||||
Onagraceae | ||||
Perinomonoletes | P. sp. | |||
Piceapollis | P. sp. | |||
Pityosporites | P. alatus P. insignis P. labdacus P. pristinipollinius | |||
Platycarya | P. sp. | |||
Poaceae | ||||
Podocarpidites | P. sp. | |||
Polycolpopollenites | P. hexaradiatus | |||
Potamogeton | ||||
Proserpinaca | ||||
Pterocarya | ||||
Quercoidites | Q. henrici Q. microhenrici | |||
Quercus | Q. sp. | |||
Retitriletes | R. sp. | |||
Salix | S. sp. | |||
Sambucus | ||||
Sapotaceae | ||||
Sciadopitys | S. sp. | |||
Sequoiapollenites | S. sp. | |||
Sparganiaceaepollenites | S. polygonalis | |||
Sparganium | ||||
Spirematospermum | Belongs to the order Zingiberales and inhabited water-associated habitats[45] | |||
Sphagnum | S. sp. | |||
Stratiotes | ||||
Swida | Junior synonym of Cornus | |||
Tiliaceae | ||||
Tricolpopollenites | T. sp. T. liblarensis fallax T. cingulum T. cingulum pusillus T. megaexactus bruehlensis T. megaexactus exactus T. pseudocingulum T. pulcher T. wackersdorfensis T. multivallatus | |||
Tsuga | T. sp. | |||
Ulmus | U. sp. | |||
Verrucatosporites | V. sp. | |||
Vitis | ||||
Zelkova | Z. sp. |
Madelaine Böhme et al.: Reply to: Reevaluating bipedalism in Danuvius. In: Nature. Band 586, 2020, S. E4–E5, .
Fossils suggest tree-dwelling apes walked upright long before hominids did. Auf: sciencenews.org vom 6. November 2019.