Gomphotherium land bridge

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The Gomphotherium land bridge was a land bridge that connected Eurasia to Afro-Arabia between approximately 19 and 15 million years ago (Ma) during the Burdigalian stage of the Early Miocene. [1] More recent analysis found that the Gomphotherium land bridge may have formed slightly earlier, around 20 Ma. [2] It is believed that the connection between the Mediterranean and Indian oceans was temporarily re-established during the Langhian stage of the Middle Miocene, before reclosing, and has remained closed to present day. [1]

Contents

Similar interchanges of have happened occurred throughout the Cenozoic, such and the collision between insular India and Asia. [3] [4] As well as the collision of the Americas, which resulted in the Great American Interchange. [5] [6]

Before the interchange

Isolation of Afro-Arabia

Apterodon langebadreae, a apterodontine hyaenodont Apterodon langebadreae.jpg
Apterodon langebadreae , a apterodontine hyaenodont

During the Early Cretaceous (Aptian-Albian), Africa became isolated from the rest of Gondwana and Laurasia, spending the rest of the Cretaceous and most of the Cenozoic as an island continent. [7] Mammalian fauna endemic to the continent primarily consisted of Afrotheria (proboscideans, sirenians, embrithopods, hyracoids, and several other groups), metatherians (herpetotheriids), and hyaenodonts (hyainailouroids and several unranked clades). [8] [9] [10] [7]

Barytherium, a basal proboscidean Barytherium graveDB1.jpg
Barytherium , a basal proboscidean

Proboscideans, the order that contains modern elephants, first evolved in Africa around 60 Ma, during the Selandian stage of the Paleocene; with Eritherium being the earliest known proboscidean, which weighed 3–8 kilograms (6.6–17.6 lb). [11] By the Early Eocene, proboscideans began growing in size. Daouitherium , the earliest known elephantiform, may have weighed 200 kg (440 lb). [12] This would make it the earliest known large mammal within Africa. [13] By the Late Eocene, some taxa began to reach notable sizes such as Barytherium , which could’ve weighed 2 tonnes (2.0 long tons; 2.2 short tons). [12] Some proboscideans during this time, such as Barytherium and Moeritherium , were semi-aquatic. [14] Elephantimorphs, a clade of proboscideans that includes mastodons and modern elephants, first appeared in the Late Oligocene. [15] [16]

Arsinoitherium, a derived embrithopod Arsinoitherium hharder.png
Arsinoitherium , a derived embrithopod

Embrithopods are a enigmatic order of afrotherian mammals that arose in the Early Eocene. The earliest known embrithopod was Stylolophus . [17] Arsinoitheriids were a highly successful group of large herbivores that were widespread in Africa. [18] Arsinoitherium , the most well known taxon, was rhino-like in appearance. [19] The largest species could’ve stood 1.75 m (5.7 ft) at the shoulders and measured 3 m (9.8 ft) in length. [20] [21] One of its defining features was a pair of enormous horns on its head, which was structured similarly to the horns of modern bovids. [22] Embrithopods were last recorded in latest Oligocene. [23]

Within the carnivore guild, hyaenodonts were the dominant carnivores of Africa. [24] Hyaenodonts were consisted of groups such as hyainailouroids, boualitominae, and the Lahimia clade. Hyainailouroids, the most notable group, were one of the three superfamilies of Hyaenodonta, an extinct order of carnivorous mammals, and were thought to have originated from Afro-Arabia, evolving during the Late Paleocene, despite the oldest fossils of hyainailourids being found in Asia. [9] [25] [26] The hyainalourids were ecologically diverse, while hyainailourines were terrestrial predators, [27] apterodontines had otter-like adaptations suggesting they were semi-aquatic predators. [28]

Non-mammalian predators included reptiles such as the large madtsoiid Gigantophis . [29]

Early Dispersals

Pterodon dasyuroides Pterodon Life Reconstruction.png
Pterodon dasyuroides

Afro-Arabian origin

Hyainailourids had dispersed into Europe at least three times during the Paleogene via the Iberian Peninsula. [27] [30] Hyainailourines made their first appearance in at MP16, with the appearance of Paroxyaena galliae and Kerberos . [31] [27] The second dispersal was during the Late Eocene, being represented by Pterodon and Parapterodon . [27] Hyainailourines would later go extinct in Europe which was contemporary with Grande Coupure, the result of the turnover saw a 60% extinction rate for West European mammalian lineages. [31] [32] Originally it was thought that competition with carnivorans played a role in the extinction of Pterodon, [33] however more recent analysis found no evidence of competitive displacement between carnivorans and hyaenodonts. In addition, immigrant carnivorans dispersed into Western Europe after the extinction of the hyainailourines. [31]

The third dispersal was during the Oligocene, represented by Apterodon gaudryi. [30] [34] MP23 marked the last occurrence of European Apterodon, with their extinction likely being the result of global cooling. [35] Hyainailourines also dispersed into Asia at least once during the Paleogene, which led to the evolution of Maocyon and Orienspterodon . [25] [26]

Embrithopods dispersed into Eurasia during the Late Paleocene, represented by Palaeoamasia and Hypsamasia . [23] In addition, embrithopods were found in Western Europe during the Early Eocene. [23] [36] They may have been able to disperse into Eurasia via rafting or island hopping. [37] Compared to arsinoitheriids, palaeoamasiids had more conservative dentitions. [18]

Eurasian origins

Anthropoid primates were originally thought to have evolved in Africa, however more recent evidence now suggests they evolved in Asia. [38] Fossil evidence suggests at least two Asian anthropoids colonized Africa. Because of the similarity between Afrasia and Afrotarsius , the colonization of eosimiiforms anthropoids must’ve occurred shortly before 38 Ma. [38] [39] On the other hand, most of the early African anthropoids belonged to the Simiiformes clade. [39] Anthracotheres were thought to have evolved in Asia before dispersing into Africa during the Late Eocene, with Bothriogenys representing the earliest African anthracothere. North Africa was the primary area of their evolution. By the Early Oligocene, anthracotheres diversified into two genera: Bothriogenys and Qatraniodon . However, the former would still be more abundant and would later give rise to Brachyodus . [40]

Effects and aftermath

The formation of the Gomphotherium land bridge marked the end of Africa’s biogeographic isolation, which lasted for 75 million years. [2] Passage of fauna between Eurasia and the Arabian Plate and thus Africa was largely hindered before the Early Miocene, as many animals could not cross the open Tethyan seaway, with a few exceptions. [1] [30] However, during the mid-Burdigalian, the tectonic plates of Afro-Arabia and Eurasia collided, creating a terrestrial isthmus connecting the two landmasses. This faunal exchange that resulted is known as the Proboscidean Datum Event or the Great Old World Biotic Interchange (GOWBI). [1] [2]

The land bridge allowed the elephantine gomphotheres and other proboscideans to migrate out of Africa and into Eurasia. [41] [1] Ungulates, who dominated the large herbivore fauna in Eurasia since the start of the Cenozoic, were able to disperse into Africa due to the formation of the land bridge. [42] Fossil evidence also showed dispersal between mammalian predators. Hyainailouroids such as Hyainailouros , Dissopsalis , Metapterodon , and possibly Megistotherium dispersed into Eurasia. [27] [43] [26] [44] While carnivorans, such as amphicyonids, dispersed into Afro-Arabia. [26] [45]

The mammalian exchange between the two continents was asymmetrical with most mammals originating from Asia. [2] Ungulates saw an increase in diversification and explored new functional spaces. [42] The arrival of mammals from Eurasia coincided with the extinction of the embrithopods, many hyracoids, and other afrotherian mammals, as well as several endemic lineages of rodents. [2] Hyracoids probably couldn’t compete with the diversifying ungulates due to their inefficiency in feeding, low metabolic rate, and short plantigrade feet made them less effective competitors against ungulates in open environments. [24] [46] However, some animals endemic to Afro-Arabia have been proven to be successful in Eurasia such as hyaenodonts and proboscideans, [2] with the latter showing an increase in diversity and would later disperse into North America via the Bering land bridge. [47]

Some experts hypothesized that the arrival of gomphotheres may have resulted in the extinction of the paraceratheres. Much like modern elephants, gomphotheres may have knocked down trees which in turn created open landscapes. Due to being specialized for high browsing, paraceratheres can’t cover their energy loss while browsing lower than 2 m (6 ft 7 in). [43] However, this validity of this hypothesis remains unclear. [48]

Restoration of Hyainailouros sulzeri (far left), Cynelos eurydon, Afrosmilus africanus and Hyainailouros napakensis (far right) Africa - the evolution of a continent and its large mammal fauna (2006) fig. 8.png
Restoration of Hyainailouros sulzeri (far left), Cynelos eurydon , Afrosmilus africanus and Hyainailouros napakensis (far right)

Despite being successful in Eurasia, many experts believe that that hyainailouroids may have experienced their decline and extinction because of competition with carnivorans. [49] [26] The discovery of Pakakali implies small hyainailourines, during the Paleogene, had a diverse diet being similar to that of mesocarnivores such as gray foxes and ringtail. This contrasts small hyainailourines in the Miocene. Miocene hyainailourines similar in size or smaller than Pakakli, such as Isohyaenodon pilgrimi , Mlanyama , and Metapterodon kaiseri, showed high levels of specialization towards hypercarnivory. On the other hand, the abundance of small mesocarnivorous carnivorans present in Afro-Arabia, such as Kichechia zamanae and Leptoplesictis namibiensis , suggests carnivorans quickly dominated this niche after dispersing into the continent. This suggests small hyainailourines may had became hypercarnivorous due to the arrival of the carnivorans. [50] On the other hand, large hyainailourines, such as Hyainailouros and Megistotherium, may have found themselves competing against social, cooperative carnivorans. The larger, more complex brains of the cooperative carnivorans could’ve prevented hyainailourines from effectively defending their kills. [26]

However, studies have found that brain size has no correlation with sociality in carnivorans, [51] instead relative size of the anterior brain within carnivoran families likely played a role in sociality instead. [52] [53]

References

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  50. ↑ Borths, Matthew R.; Stevens, Nancy J. (11 October 2017). Smith, Thierry (ed.). "The first hyaenodont from the late Oligocene Nsungwe Formation of Tanzania: Paleoecological insights into the Paleogene-Neogene carnivore transition". PLOS ONE . 12 (10) e0185301. Bibcode:2017PLoSO..1285301B. doi: 10.1371/journal.pone.0185301 . ISSN   1932-6203. PMC   5636082 . PMID   29020030.
  51. ↑ Finarelli, J. A.; Flynn, J. J (2009). "Brain-size evolution and sociality in Carnivora". Proc. Natl. Acad. Sci. U.S.A. 106 (23): 9345–9349. Bibcode:2009PNAS..106.9345F. doi: 10.1073/pnas.0901780106 . PMC   2695124 . PMID   19474299.
  52. ↑ Vinuesa, Víctor; Iurino, Dawid A.; Madurell-Malapeira, Joan; Liu, Jinyi; Fortuny, Josep; Sardella, Raffaele; Alba, David M. (August 2016). "Inferences of social behavior in bone-cracking hyaenids (Carnivora, Hyaenidae) based on digital paleoneurological techniques: Implications for human–carnivoran interactions in the Pleistocene" . Quaternary International. 413: 7–14. Bibcode:2016QuInt.413....7V. doi:10.1016/j.quaint.2015.10.037.
  53. ↑ Finarelli, J. A.; Flynn, J. J (2009). "Brain-size evolution and sociality in Carnivora". Proc. Natl. Acad. Sci. U.S.A. 106 (23): 9345–9349. Bibcode:2009PNAS..106.9345F. doi: 10.1073/pnas.0901780106 . PMC   2695124 . PMID   19474299.
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