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In February 1971, a meteorite fell on the roof of a barn belonging to Mr. E. Schmitz in Tintigny, a village in southern Belgium. Upon its recovery, its meteoritic origin was confirmed by the schoolteacher, Mr. A. Rossignon who then looked after the sample. In 2017, for the first time, the meteorite was given to specialists for a detailed examina-tion and classification. We used various analytical techniques to characterize its mineralogy, elemental, and isotopic composition. Based on the obtained data, we classified it as a polymict eucrite, a meteorite originating from 4 Vesta, and named it Tintigny [1]. Tintigny is partly covered by shiny black fusion crust. Its interior mainly exhibits a light grey color and shows a brecciated texture composed of a fine-grained matrix, hosting darker crystals and cm-sized dark grey clasts. Under the microscope, a brecciated sub-ophitic basaltic texture mainly composed of plagioclase/maskelynite and clinopy-roxene is dominant. In addition to the dominant sub-ophitic texture, at least three distinct textures exposed in clasts are observable. At least two generations of shock effects (such as fractures), are present in the sample: those limited to clasts and large crystals, and those that crosscut both the large grains and the matrix. The accessory minerals include troilite, ilmenite, chromite, FeNi metal, and silica. Mineral chemistry calculations of pyroxene end-members show ranges from 8.5 to 60.7 mol% for enstatite, 30.1–70.0 mol% for ferrosilite, and 2.6–38.4 mol% for wollastonite. Based on these values, most pyroxenes in Tintigny are pigeonite and augite [2]. The Fe/Mn ratios of pyroxenes range from 27.1 to 39.3, with the highest ratio observed in pyroxene from the symplectitic clast. Fe/Mn and Fe/Mg ratios in low-Ca pyroxene (Wo<10) are 30.2±4.4 and 0.8±0.3, respectively. These ratios in high-Ca pyroxene (n=8) are 34.3±3.7 for Fe/Mn and 2.6±2.4 for Fe/Mg. The average pyroxene Fe/Mn ratio for all pyroxene is 32.5±4.4 (SD, n=14). Fe/Mg ranges from 0.6 to 8.2, with an average value of 1.8±2.0 (SD, n±14). Considering pyroxene Fe/Mn ranges of 40±11, 62±18, 32±6, and 30±2 for basaltic rocks from the Earth, Moon, Mars, and 4 Vesta (eucrites), respectively, and based on our data, particularly those of low-Ca py-roxene, Tintigny falls in the range of basaltic eucrites [3]. The bulk rock Fe/Mn and Fe/Mg ratios of Tintigny are 33.9 and 3.1, respectively. These values overlap with those measured for howardite-eucrite-diogenite (HED) and martian meteorites [4]. With a Ga/Al ratio of 4.17×10-5, Tintigny falls within the range of those of eucrites. Using the CI-normalized elemental concentration, we can see strong simi-larities between Tintigny and noncumulate eucrites, which is also reflected based on the abundance of TiO2 (0.63) and FeO/MgO ratio (2.66) in Tintigny. The bulk oxygen isotopic composition of Tintigny, as determined by laser fluorination, is also consistent with it being an HED (δ17O=1.72±0.04 ‰; δ18O=3.76±0.08‰; Δ17O=-0.25±0.01 ‰ (n=2, errors 2SD)), with a composition that plots close to the Eucrite Fractionation Line [5]. Based on the Meteoritical Bulletin Database, only 70 HED falls have been reported so far. Including Tintigny, only 39 eucrite falls are known to date, 11 of them occurred in Europe, with Tintigny being the only one from Belgium. In addition to the scientific importance of studying a eucrite fall like Tintigny, we emphasize the significance of the discovery of a historical meteorite fall by drawing attention to national scientific heritage that must be properly un-derstood and safeguarded for generations of scientists, scholars, and amateurs to come. Nowadays, together with four other meteorites from Belgium (Hautes Fagnes LL5, Lesves L6, St. Denis Westrem L6, and Tourinnes-la-Grosse L6), the Tintigny achondrite is exhibited in the meteorite gallery of the Institute of Nat-ural Sciences in Brussels and is open to the public for visits.

The Messel Pit is a Konservat-Lagerstätte in Germany, representing the deposits of a latest early to earliest middle Eocene maar lake, and one of the first palaeontological sites to be included on the list of UNESCO World Heritage Sites. One aspect of Messel that makes it so extraordinary is that its sediments are rich in different fossilised organisms – microfossils, plants, fungi, invertebrate animals and vertebrates – that are rarely preserved together. We present an updated list of all taxa, named or not, that have been documented at Messel, comprising 1409 taxa, which represent a smaller but inexactly known number of biological species. The taxonomic list of Labandeira and Dunne (2014) contains serious deficiencies and should not be used uncritically. Furthermore, we compiled specimen lists of all Messel amphibians, reptiles and mammals known to us. In all, our analyses incorporate data from 32 public collections and some 20 private collections. We apply modern biodiversity-theoretic techniques to ascertain how species richness tracks sampling, to estimate what is the minimum asymptotic species richness, and to project how long it will take to sample a given proportion of that minimum richness. Plant and insect diversity is currently less well investigated than vertebrate diversity. Completeness of sampling in aquatic and semiaquatic, followed by volant, vertebrates is higher than in terrestrial vertebrates. Current excavation rates are one-half to two-thirds lower than in the recent past, leading to much higher estimates of the future excavation effort required to sample species richness more completely, should these rates be maintained. Species richness at Messel, which represents a lake within a paratropical forest near the end of the Early Eocene Climate Optimum, was generally higher than in comparable parts of Central Europe today but lower than in present-day Neotropical biotopes. There is no evidence that the Eocene Messel ecosystem was a “tropical rainforest.”

We redescribe the type material of Phyllodactylus siamensis Boulenger, 1899, type species of the Southeast Asian gekkonid genus Dixonius Bauer, Good & Branch, 1997, using external morphology and cranial osteology (by Micro-Computed Tomography, µ-CT). There is some evidence that the type series contains more than one species; we hence designate a lectotype in order to stabilize nomenclature and provide more precision on the geographical location of the type locality. Because the current concept of Dixonius siamensis auctorum is incomplete and composite, we provide a revised diagnosis based on the presently designated lectotype and a paralectotype from the same locality, as well as observations on new material from the type locality and the first photographs of live topotypical individuals. We regard Dixonius siamensis as probably geographically restricted to the Dong Phaya Yen mountain range in central Thailand, and the numerous published mentions of this species from outside this range likely refer to other or undescribed taxa. We treat Phyllodactylus burmanicus Annandale, 1905 from Tavoy, southern Myanmar, as a valid species, as Dixonius burmanicus comb. nov.

We here provide a detailed description of the vertebral morphology of the African arboreal viperid snakes of the genus Atheris. Vertebrae of three different species of the genus, i.e., Atheris desaixi, Atheris hispida, and Atheris katangensis, were investigated via the aid of μCT (micro‐computed tomography) scanning. We describe several vertebrae from different regions of the vertebral column for all three species, starting from the atlas‐axis complex to the caudal tip, in order to demonstrate important differences regarding the intracolumnar variation. Comparison of these three species shows an overall similar general morphology of the trunk vertebrae among the Atheris species. We extensively compare Atheris with other known viperids. As the sole arboreal genus of Viperinae the prehensile nature of the tail of Atheris is reflected in its caudal vertebral morphology, which is characterized by a high number of caudal vertebrae but also robust and anteroventrally oriented pleurapophyses as a skeletal adaptation, linked with the myology of the tail, to an arboreal lifestyle. We anticipate that the extensive figuring of these viperid specimens will also aid identifications in paleontology.