Leptictidium

Leptictidium (a Latinized diminutive of the name of its close relative Leptictis, which means "graceful weasel" in Ancient Greek) is an extinct genus of small mammals that were likely bipedal. Comprising eight species, they resembled today's elephant shrews. They are especially interesting for their combination of characteristics typical of primitive eutherians with highly specialized adaptations, such as powerful hind legs and a long tail which aided in locomotion. They were omnivorous, their diet a combination of insects, lizards and small mammals. One of the first branches to split from basal eutherians,[1] they appeared in the Lower Eocene, a time of warm temperatures and high humidity, roughly fifty million years ago. Although they were widespread throughout Europe, they became extinct around thirty-five million years ago with no descendants,[2] probably because they were adapted to live in forest ecosystems and were unable to adapt to the open plains of the Oligocene.

Leptictidium Temporal range: Early to Late Eocene, 50–35 Ma PreꞒ Ꞓ O S D C P T J K Pg N
Fossil L. auderiense skeleton, Muséum national d'histoire naturelle
Scientific classification
Kingdom:	Animalia
Phylum:	Chordata
Class:	Mammalia
Order:	†Leptictida
Family:	†Pseudorhyncocyonidae
Genus:	†Leptictidium Tobien, 1962
Type species
†Leptictidium auderiense Tobien, 1962
Species
L. auderiense Tobien, 1962 L. nasutum Lister & Storch, 1985 L. tobieni Koenigswald & Storch, 1987 L. ginsburgi Mathis, 1989 L. sigei Mathis, 1989 L. listeri Hooker, 2013 L. prouti Hooker, 2013 L. storchi Hooker, 2013

Description

Illustration

Leptictidium is a special animal because of the way its anatomy combines quite primitive elements with elements which prove a high degree of specialization. It had small fore legs and large hind legs, especially at the distal side (that further from the body). The lateral phalanges of its forelegs (fingers I and V) were very short and weak, finger III was longer and fingers II and IV were roughly equal in size, and slightly shorter than finger III. The tips of the phalanges were elongated and tapered.[1]

Artist's impression of a Leptictidium

The ankles and the sacroiliac joint were quite loosely fixed, while the pelvis had a flexible joint with only one coccygeal vertebra. The anteorbital muscle fenestrae in their crania suggest they probably had a long and mobile snout, similar to that of elephant shrews.

Leptictidium had wide diastemata in the antemolar row,[3] its upper molar teeth were more transverse than those of the North American leptictids and its fourth premolars were molariform.[4] Its C1 canines were incisiviform. Its dentition was quite small in comparison to the size of the mandible and the animal as a whole.[3]

It varied between 60 and 90 cm (24–36 in) in length[5] (more than half of which belonged to the tail),[6] and 20 cm (8 in) in height. It weighed a couple of kilograms.[7] These sizes could vary from one specimen to another.

Locomotion

L. nasutum fossil

One of the mysteries about Leptictidium is whether it moved by running or by jumping. Because there are very few completely bipedal mammals, it is difficult to find an appropriate living model to compare it with. If the kangaroo is used, it is probable that Leptictidium hopped along with its body tilted forward, using its tail as a counterweight.[7] On the other hand, elephant shrews combine both types of locomotion; they usually move on four legs, but they can run on two legs to flee from a predator.[6] Studies of the bone structure of Leptictidium have yielded contradicting information: its leg articulations appear too weak to have supported the shock of repeated jumps, but its long feet were obviously adapted for jumping rather than running.

Kenneth D. Rose compared the species L. nasutum with the leptictid Leptictis dakotensis. L. dakotensis had a series of traits which show it was a running animal which sometimes moved by jumping. Despite the marked similarities between Leptictis and Leptictidium, there are certain differences in their skeletons which prevent the example of Leptictis from being used to determine with certainty the way Leptictidium moved: the most important being that, unlike Leptictis, the tibia and the fibula of Leptictidium were not fused together.[8]

Behaviour

Perfectly preserved fossils of three different species of Leptictidium have been found in the Messel pit in Germany. The marks on their fur have been preserved, as well as their stomach contents, which reveal Leptictidium were omnivores which fed on insects, lizards and small mammals.[9] The holotype of L. tobieni also had pieces of leaves and notable amounts of sand in its abdomen, but it cannot be determined with certainty if the animal swallowed it.[3]

Habitat

Leptictidium and Gastornis as shown in Walking With Beasts on exhibition in Horniman Museum, London

Leptictidium lived in the European subtropical forests of the Eocene. From the beginning of this period, the temperature of the planet rose in one of the quickest (in geological terms) and most extreme episodes of global warming in the geological record, termed Paleocene–Eocene Thermal Maximum. It was an episode of quick and intense (of up to 7 °C in high latitudes) warming which lasted less than 100,000 years.[10] The thermal maximum caused a great extinction which is used to distinguish the Eocene fauna from that of the Paleocene.

The global climate of the Eocene was probably the most homogeneous of the Cenozoic; the temperature gradient from the equator to the poles was half that of today's, and the deep ocean currents were exceptionally warm. The polar regions were much warmer than today, possibly as warm as the present-day Pacific Northwest of North America. Temperate forests reached the poles themselves, while rainy tropical climates reached 45° N. The greatest difference was in temperate latitudes; nevertheless, the climate at the tropics was probably similar to today's.[11]

In the Eocene, most of what is now Europe, the Mediterranean and south-west Asia was submerged under the Tethys Sea. These two continents were separated by the Turgai Strait (an epeiric sea).[12] Due to high humidity and temperatures, most of the European continent was covered in vegetation.

Lake Nyos, Cameroon, a volcanic lake saturated with reactive gases similar to the one once found in the Messel pit zone.

The region which today is Germany was in a volcanically active zone during the Eocene. It is thought that the Messel pit could have been the old location of a volcanic lake saturated with CO₂. The lake would periodically release the gas it contained, creating a lethal cloud which would asphyxiate any animal in its path. This would explain the great number of non-aquatic species which have been found in the old lake-bed of the Messel pit.

In the lush forests of this region, Leptictidium shared its habitat with animals such as Godinotia, Pholidocercus, Palaeotis or Propalaeotherium. There were also predators, the crocodilian Asiatosuchus, the hyaenodont Lesmesodon, and the Messel giant ant.[13]

Species

The genus Leptictidium includes eight species. These include:

Leptictidium auderiense

L. auderiense

Described by Heinz Tobien in 1962 based on a series of lower jaws from the Lutetian faunal stage. Tobien also uncovered a small skeleton he defined as a paratype of the species, but Storch and Lister proved in 1985 that, in fact, the skeleton did not even belong to the genus Leptictidium.[3] It was the smallest species of all and was only sixty centimetres long. Several skeletons have been found at the Messel pit.[14] Mathis remarks the exceptional development of the paraconid (or mesiobucal cusp) of the lower P4 premolar.[15] Its premolars and molars were quite small in comparison to the dentition as a whole. The name of the species refers to the Roman settlement of Auderia.

Leptictidium ginsburgi

Described by Christian Mathis in 1989. Fossils have been found in the lagerstätte at Robiac, Le Bretou, Lavergne, La Bouffie, Les Clapiès, Malpérié and Perrière (France), in Upper Ludian strata. The mesostyle typical of the genus Leptictidium is not developed in this species.[15] The species is dedicated to Léonard Ginsburg, French paleontologist and deputy director of the Muséum national d'histoire naturelle in París.

Leptictidium nasutum

L. nasutum

Described by Adrian Lister and Gerhard Storch in 1985. It was a middle-sized species which was seventy-five centimeters long. Several skeletons have been found in the Messel pit,[14] in Lower Lutetian strata. The tail of this species had 42-43 vertebrae,[1] a number surpassed among mammals solely by the long-tailed pangolin. Its premolar and molar teeth were quite small in comparison to the dentition as a whole. The name of the species refers to the nose of the animal. The holotype is the complete skeleton of an adult specimen kept in the Forschungsinstitut Senckenberg in Frankfurt am Main.[1]

Leptictidium sigei

Described by Christian Mathis in 1989. Fossils have been found in the lagerstätte at Sainte-Néboule, Baby, Sindou and Pécarel (France), and it has a more primitive appearance than L. nasutum. It is known mainly from isolated teeth. It has a P4 with a much reduced paraconid, as well as very distinct entoconids and hypoconulids on M1 and M2.[15] The species is dedicated to Bernard Sigé, French paleontologist.

Leptictidium tobieni

Fossil of L. tobieni at the Hessisches Landesmuseum, Darmstadt.

Described by Wighart von Koenigswald and Gerhard Storch in 1987. It was the largest species of all at ninety centimetres long. It is one of the species found in the Messel pit,[14] in Lutetian strata. The species is dedicated to Heinz Tobien, descriptor of the genus Leptictidium and promoter of research in the Messel pit during the 1960s. The holotype is a complete and perfectly preserved skeleton of an adult specimen which was uncovered in September 1984 and which can be found at the Hessisches Landesmuseum Darmstadt.[3] There is also a paratype; a non-complete and badly preserved specimen which can be found at the Institut Royal des Sciences Naturelles de Belgique.

It has a relatively robust mandible with a relatively large mesostyle. The molariform premolar teeth are a characteristic of the genus Leptictidium as a whole which is very marked in the P4 premolars of L. tobieni. The well-developed mesostyle and the transversal configuration of the upper molars are other typical traits of this species.[3]

Comparison of the Messel species

By observing the clear morphological differences in the dentition of the three species found in Messel, the possibility can be discarded that either the discovered fossils are specimens of the same species but of different age, or that two of these forms belonged to the same species with a marked sexual dimorphism.[3]

The Messel species developed very quickly a series of characteristic evolutionary traits, common to all of them, which separate them from the lagerstätte of Quercy.[15]

This table compares the size of different specimens of each species found in the Messel pit (sizes in millimetres).

Messel species comparison[3]
species	L. auderiense		L. nasutum			L. tobieni
specimens	LNK Me 418a	SMF 78/1	SMF ME 1143	LNK Me 576	HLMD Me 8059	HLMD Me 8011a	I. R. Sc. N. B. M1475
Cranium	67.4	67.2	88.2	89.8	88.6	101.1	-
Head+torso	220	215	300	295	328	375	-
Tail	(340)	375	450	445	454	500	-
Humerus	31.8	32.3	41.9	41.9	43.1	45.7	46.6
Ulna	29.4	31.8	45.6	44.2	45.3	51.2	-
Radius	21.5	23.9	31.7	31.1	33.2	37.0	36.2
Pelvis	54.5	56.5	77.8	77.1	-	85.7	(82)
Femur	54.2	57.5	75.3	71.5	75.1	84.8	(82)
Tibia	64.4	66.3	79.7	79.0	80.1	91.6	90.5
Fibula	57.4	58.7	75.2	72.3	-	86.6	-
Calcaneus	22.3	22.6	25.3	25.2	-	26.7	25.4
Neurocranium †	33.0	31.6	38.7	39.3	37.5	42.2	42.5
Height of the lower jaw below M2	5.7	5.6	6.9	6.6	6.4	9.0	9.5
Height of the mandibular ramus ††	14.3	-	20.8	23.3	23.0	29.2	28.5

† From the front edge of the orbit.
†† Above the incisura praeangularis.

Evolutionary tendencies

Restoration

In his work Quelques insectivores primitifs nouveaux de l'Eocène supérieur du sud de la France (1989), French paleontologist Christian Mathis studied the evolutionary tendencies of the genus Leptictidium, based on comparison of the most primitive and the most recent species. From his observations, Mathis remarks:[15]

• an increase in size;
• a precocious merging of the hypoconulid and the entoconid on M3;
• a slight reduction of the width of the talonid on M3 in comparison to the anterior molars;
• the formation and development of a mesostile on the molariform jugal teeth P4-M3;
• the reduction of the parametastylar and metastylar regions of these same teeth (with some exceptions), in particular with a reduction of the parastylar lobe which rises less in the anterior part of M3 and possibly P4;
• a transverse shortening of the upper molarised teeth, which become more square;
• the development of accessory conuli on the preprotocrista and postprotocrista;
• the development of the postcingulum.

Bibliography

In English

• Benton, M. (2000). Vertebrate Palaeontology. Oxford: Blackwell Publishers. ISBN 0-632-05614-2.
• Frey, E.; Herkner, B.; Schrenk, F.; Seiffert, C (1993). Reconstructing organismic constructions and the problem of Leptictidium's locomotion. Darmstadt: Kaupia Darmstädter Beiträge zur Naturgeschichte.
• Rose, K. (2006). The Beginning of the Age of Mammals. The Johns Hopkins University Press. ISBN 0-8018-8472-1.

In French

• Mathis, C. (1989). Quelques insectivores primitifs nouveaux de l'Eocène supérieur du sud de la France. Paris: Bulletin du Muséum national d'histoire naturelle.

In German

• Christian, A. (1999). Zur Biomechanik der Fortbewegung von Leptictidium (Mammalia, Proteutheria). Frankfurt am Main: Courier Forschungsinstitut Senckenberg.
• Maier, W.; Richter, G.; Storch, G. (1986). Leptictidium nasutum - ein archaisches Säugetier aus Messel mit außergewöhnlichen biologischen Anpassungen. Frankfurt am Main: Natur und Museum.
• Storch, G. (1987). Leptictidium - ein archaischer Säuger. Naturwissenschaftliche Rundschau.
• Storch, G.; Lister, A. (1985). Leptictidium nasutum - ein Pseudorhyncocyonide aus dem Eozän der Grube Messel bei Darmstadt (Mammalia, Proteutheria). Frankfurt del Main: Senckenbergiana lethaea.
• Tobien, H. (1962). Insectivoren (Mammalia) aus dem Mitteleozän (Lutetium) von Messel bei Darmstadt. Wiesbaden: Notizbl. hess. Landesamt. Bodenforsch.
• von Koenigswald; W.; Storch, G. (1987). Leptictidium tobieni n sp., ein dritter Pseudorhyncocyonide (Proteutheria, Mammalia) aus dem Eozän von Messel. Frankfurt del Main: Courier Forschungsinstitut Senckenberg.
• von Koenigswald, W.; Wuttke, M. (1987). Zur Taphonomie eines unvollständigen Skelettes von Leptictidium nasutum aus dem Ölschiefer von Messel. Wiesbaden: Geol. Jb. Hessen.

References

1. Adrian Lister; Gerhard Storch (July 22, 1985). "Leptictidium nasutum n sp., ein Pseudorhyncocyonide aus dem Eozän der "Grube Messel" bei Darmstadt (Mammalia, Proteutheria)". Senckenbergiana Lethaea (in German). 66.
2. McKenna, M. C; S. K. Bell (1997). Classification of Mammals Above the Species Level. Columbia University Press. ISBN 0-231-11012-X.
3. Wighart von Koenigswald; Gerhard Storch (March 16, 1987). "Leptictidium tobieni n sp., ein dritter Pseudorhyncocyonide (Proteutheria, Mammalia) aus dem Eozän von Messel". Courier Forschungsinstitut Senckenberg (in German). 91: 107–116, 9 Abb.
4. D. Rose, Kenneth; Archibald, J. David (2006). The Beginning of the Age of Mammals. The Johns Hopkins University Press. ISBN 978-0-8018-8472-6. Retrieved 2008-01-20.
5. Chaisson, Eric J. (2001). "Leptictidium wildfacts". Animal wildfacts. BBC. Retrieved 2007-12-30.
6. Jehle, Martin (2007). "Insectivore-like mammals: Tiny teeth and their enigmatic owners". Paleocene Mammals. Martin Jehle. Retrieved 2007-12-30.
7. "Leptictidium". Leptictidium bij Kenozoicum.nl (in Dutch). Kenozoicum.nl. 2007. Archived from the original on 2007-09-09. Retrieved 2007-12-30.
8. Rose, Kenneth D. "The postcranial skeleton of early Oligocene Leptictis (Mammalia: Leptictida), with preliminary comparison to Leptictidium from the middle Eocene of Messel". Cite journal requires |journal= (help)
9. Haines, Tim (2001). "New Dawn". Walking with Beasts. Londres: BBC Books. ISBN 0563537639.
10. Gavin A. Schmidt & Drew T. Shindell; Shindell (2003). "Atmospheric composition, radiative forcing, and climate change as a consequence of a massive methane release from gas hydrates" (PDF). Paleoceanography. 18: n/a. Bibcode:2003PalOc..18.1004S. doi:10.1029/2002pa000757. Archived from the original (PDF) on 2011-10-20.
11. Stanley, Steven M. (1999). Earth System History. New York: W.H. Freeman and Company. ISBN 0716728826.
12. Scotese, Christopher (2002). "Paleomap project". Paleomap project. Christopher Scotese. Retrieved 2008-01-23.
13. Walking with monsters
14. Morlo, Michael; Stephan Schaal, Gerald Mayr & Christina Seiffert (2004). "An annotated taxonomic list of the Middle Eocene (MP 11) Vertebrata of Messel" (PDF). Cour. Forsch.-Inst. Senckenberg. 252: 95–108.
15. Mathis, C. (1989). "Quelques insectivores primitifs nouveaux de l'Eocène supérieur du sud de la France". Bulletin du Muséum National d'Histoire Naturelle de Paris. 11: 33–64.