Fossil Seahorses

 

 

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A head of a fossil baby seahorse, 1cm.

 

 

 



One complete baby seahorse, 1cm.

 

 

 


Another head of a fossil baby seahorse, 1cm.

 

 

 


A detail of the photo on the right.

 

 

 

 


These macroalgae could represent the first habitat where Middle Miocene seahorses lived.

 

 

 


A fossil insect found accompanied with the seahorses.

 

 

 

 

 

 

 

Of all the mysterious, secretive creatures in the ocean, the seahorse is probably the most legendary. It looks like a creature that could only exist in someone's imagination.

 Hippocampus, photo by Seahorse.org

 

Seahorses and pipefish belong to the Syngnathidae, a teleost family whose oldest fossils date back to the Eocene (Lutetian: 52 mya; cf. Teske et al. 2004)*. The family also includes the pygmy pipehorses (grouped with seahorses in the subfamily Hippocampinae), pipehorses and seadragons (Solegnathinae), flag-tail pipefishes (Doryrhamphinae), and pipefishes (Syngnathinae).

 

Till recently little was known about their origin. When, how and where did they originated? For several decades fossil seahorses have been known only from the 5 million years old, Lower Pliocene (and perhaps also Upper Miocene)* Merecchia River Formation, Poggio Berni, Rimini Province in Italy. However, in the year 2005 much older fossils of these amazing and exotic animals have been found in the Tunjice hills (Slovenia). They are of the Middle Miocene age (Lower Sarmatian, 13 million years), therefore representing the oldest known seahorse fossils.

 

Seahorses appear quite often in the beds of the Coproltic Horizon - a Konservat - Lagerstätte, where also several fossil insects and medusae fossils have been found. Most specimens are juvenile and therefore very small, however adult specimens can be found as well. Most often only the head and the spine are preserved. Some specimen show that juvenile seahorses might have been almost transparent.

In last year we have spent considerable time comparing these fossil seahorses to other related fish, such as pipefish and pipehorses. Luckily, one specimen has been recovered, which still has bony plates preserved, covering the body. All important macroscopic features are well visible, which allow to reconstruct this seahorse species with relatively high accuracy. Taking this specimen into consideration, it is clear that the seahorses, we are finding in the Tunjice Hills, represent a relatively well developed seahorse species.

 

 

This fossil seahorse specimen is the most important fossil found in the beds of Coprolitic Horizon and perhaps represents the most recognizable Slovenian fossil. It is excellently preserved. Even the smallest features are visible, allowing to reconstruct all macroscopic characteristics of this ancient seahorse species.

 

 

When did the seahorses originated in the Earth history?

 

As Teske et al. (2004) write, the world's tropical marine faunas can be divided into those associated with an Atlantic Ocean biome (including the Caribbean and Mediterranean), and those associated with an Indo-Pacific biome. It has been suggested that this pattern arose after the closure of the Tethyan seaway, a tectonic event that resulted from the convergence of the African and Eurasian plates during the late Oligocene and Miocene. Seahorses are found throughout the tropical and temperate regions of both the Atlantic and Indo-Pacific biomes, but their origin and evolutionary history are not well understood.

 

In a study on cytochrome b sequences, Casey (1999) (cf. Teske et al. 2004) concluded that the genus Hippocampus probably evolved in the Atlantic biome. An Atlantic origin is also supported by the fact that most species of the closely related pipefish genus Syngnathus are associated with the Atlantic biome, as well as the fact that to date the only known seahorse fossils have been found in Italy. On the other hand, it is interesting to note that the majority of seahorse species are found in the Indo-West Pacific region (>27 species).  

 

Several small seahorses Hippocampus sp. and their oldest known ancestor. (photo on the right by Robert Pearce)

 

Based on the study of RP1 and 16S rRNA sequences Taske et al. (2004) have proposed a different hypothesis. The large genetic distance of the pygmy seahorse, H. bargibanti, to all other seahorses suggests an ancient divergence of this group from the main clade of seahorses. H. bargibanti is widely distributed throughout the western Pacific, but the fact that this species is highly adapted to parasitise a certain species of Muricella gorgonian coral suggests that it is unlikely to disperse readily beyond the region where this species occurs. Among the species associated with the main clade of seahorses, the most basal positions are occupied by H. breviceps and H. abdominalis. Both species are associated with the Australian continent, suggesting that this may be the region from which seahorses originated. An Australian or south-west Pacific origin of seahorses is also supported by the distributions of the three possible sister genera of the genus Hippocampus. Pygmy pipehorses of the genus Amphelikturus are restricted to the Atlantic biome, the genus Acentronura is widely distributed throughout the Indo-Pacific, and all known specimens of Idiotropiscis have been found in Australian waters. Among these three genera, the species of the genus Idiotropiscis, and particularly a recently discovered species from southern New South Wales, are most seahorse-like in appearance.

 

 

Where did the seahorses originated?

 

Based on the present-day evidence it is diffucult to decide, where seahorses originated (Peter Taske, personal communication). Fossil seahorses found in the Tunjice hills (Slovenia) and also the Italian fossil seahorses confirm the presence of these seahorses in the Paratethys and Mediterranean close to the time when the Tethyan seaway closed. The Paratethys and Mediterranean were once probably species-rich, and it is possible that the ancestors of all of the extant forms of pygmy pipehorses, pygmy seahorses and proper seahorses were once present there, and then spread towards the Indopacific. Likewise, it is possible that the form we are finding in the Tunjice Hills, was once present in the Indopacific and then colonised the Paratethys and perhaps also the Meditrranean (Peter Taske, personal comunication). This could happen already before the Early Sarmatian, because the migration paths connecting Paratehys and Mediterranean with the Indopacific existed till the Late Badenian (Roegel 1999). Later in the Early Sarmatian, the seaway into the Indopacific closed, and another opened, connecting Paratethys and Mediterranean.

 

Paleogeographic map, seacurrents and possible migration paths for the seahorses in the Late Badenian. (After Roegel 1999).

Paleogeographic map, seacurrents and possible migration paths for the seahorses in the Early Sarmatian. (After Roegel 1999).