Do mudskippers and lungfishes elucidate the early evolution of four-limbed vertebrates?
© Kutschera and Elliott; licensee Springer. 2013
Received: 30 January 2013
Accepted: 30 January 2013
Published: 26 March 2013
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© Kutschera and Elliott; licensee Springer. 2013
Received: 30 January 2013
Accepted: 30 January 2013
Published: 26 March 2013
Recently, the origin of four-limbed vertebrates (tetrapods) was re-assessed, based on footprints and trackways that were made by early land animals almost 400 million years (my) ago. That is 18 my earlier than the oldest known tetrapod body fossils, such as Acanthostega and Ichthyostega from Greenland, and 10 my older than the earliest ‘tetrapodomorph fishes’ (Panderichthys, Tiktaalik etc.). These and other facts suggest that the first tetrapods may have thrived in the marine-influenced intertidal and/or lagoon zone as well as in brackish and freshwater environments associated with land vegetation, as previously thought.
Here, we discuss the controversial question whether or not extant air-breathing fishes, such as mudskippers, amphibious gobioids that inhabit mangrove swamps, can be interpreted as living model organisms, with reference to the earliest land plants. In addition, recent developmental and behavioural studies on lungfishes (Dipnoi) are summarized and evaluated.
We conclude that mudskipping ‘walking fishes’ (Periophthalmus sp.) and Dipnoi (Protopterus sp.) shed light on the gradual evolutionary transition of ancient fishes to early tetrapods that occurred during the Devonian in muddy, salty waters. However, they are not the ancestors of tetrapods, because extant organisms cannot be progenitors of other living beings.
Over the last two decades, the fossil record of the earliest tetrapods (defined here as vertebrates with digit-bearing limbs rather than paired fin-like limbs) has been considerably expanded. Several books (Clack 2002; Benton 2005; Shubin 2008) and an excellent review article published in this journal (Clack 2009) cover this topic in detail, so that the “fish to amphibian-transition” is one of the best documented macro-evolutionary processes elucidated so far. Can this key event in the history of life be illustrated in biology classes on extant vertebrates? No one knows the ecology and behaviour of the earliest tetrapods that made the transition from water to land, but it is possible that some extant fishes illustrate how the ecological challenges were met.
Fifty years ago, Osche (1962) proposed that mudskippers, extant amphibious fishes that inhabit tropical mangrove swamps, may be regarded as “model organisms” to elucidate the transition from water to land. However, the “mudskipper-as-extant-model system-hypothesis” is still controversial. In the present article, which is in part based on our original studies on mudskippers and other teleost fishes (Elliott 1994; Kutschera 2005, 2006; Kutschera et al. 2008) we summarize some basic facts and definitions pertinent to the key question of whether or not some extant fishes elucidate processes that took place millions of years ago.
There is only one extant species in the first sarcopterygian order, the Crossopterygii, and that is the famous coelacanth, Latimeria chalumnae, which was first caught off the coast of East London, South Africa, in 1938 and described by J. L. B. Smith (1939). Until then, only fossils had been found in this order which was thought to have been extinct for 60 million years. This “living fossil” uses its heavy pectoral and pelvic fins to stir up the mud on the sea floor in search of prey, but does not use these paired fins to move against the substratum, as once proposed. There are six extant species in the second sarcopterygian order, the Dipnoi or lungfishes (Figure 2). They are found in fresh water in Australia, South America and Africa. As their name indicates, they can obtain their oxygen from the air and water, and are best described as “dual breathers”; hence Dipnoi, Dipnoans or Dipneusti (Carvalho and Goncalves 2011). It is unlikely that any extant lungfish was present when the first tetrapods invaded land. Lungfishes have evolved in parallel with terrestrial vertebrates and the extant species are well adapted to a highly specialised ecological niche. As will be shown later, air breathing has evolved independently in many species of Actinopterygii and one group, the mudskippers in the family Gobiidae, function well in a terrestrial environment and thus serve as possible “model organisms” to elucidate the transition from water to land. Therefore, all extant and extinct tetrapods belong to a once comprehensive group of vertebrates that are summarized under the taxon Sarcopterygii, with three extant taxonomic groups: the coelacanths, the lungfishes and the tetrapods (Benton 2005).
When palaeontologists discuss fossils from the Devonian period (ca. 416 to 359 mllion years ago, mya), they sometimes refer to the “Age of Fishes”, because fish-like creatures represent the most abundant vertebrates of this geological time period (Gradstein et al. 2004). Fossil evidence documents that towards the end of the Devonian, the “fish-to-tetrapod transition” occurred between about 385 and 360 mya (Coates 1996; Clack 2002; Benton 2005; Ahlberg and Clack 2006; Coates et al. 2008; Shubin 2008), and today the “four-limbed vertebrates” are defined as follows. Tetrapods are vertebrate animals with four limbs bearing digits (fingers and toes), such as amphibians (salamanders etc.), reptiles (lizards etc.) and mammals (mice, apes, men etc.). In addition, the Tetrapoda include vertebrates that have reduced, modified or lost their limbs in the course of evolution, such as whales (mammals), snakes (reptiles) and birds (extant relatives of the extinct theropod dinosaurs) (Buergin 1998; Coates et al. 2008; Clack 2009).
Molecular data document that the Sarcopterygii, but not the coelacanth, are the closest living relatives of the Tetrapoda (Brinkmann et al. 2004). Extinct relatives of these fleshy-limbed vertebrates (Figure 1b), such as the ca. 380 my old fossil Dipterus, are the ancestors of the four-limbed vertebrates. Two years ago, well-preserved and dated tetrapod tracks were documented from Polish marine tidal flat sediments of early Middle Devonian age (ca. 398 mya). These tracks predate the oldest tetrapod skeletal remains by 18 my and the earliest “tetrapodomorph” (elpistostegalian) fishes, such as Kenichthys, by ca 10 my (Janvier and Clément 2010; Niedźwiedzki et al. 2010). These data indicate that the first tetrapods, from which no fossils have yet been found, may have evolved in marine-influenced settings and invaded the mud of brackish lagoons.
In numerous earlier reconstructions of the fish-to-tetrapod transition, it has been suggested that this macroevolutionary process took place over a time period of ca. 16 to 20 my in the vegetated margins or surrounding seasonal ‘flooded forest’ environments of rivers, and, hence, in freshwater ecosystems (Romer 1941; Jarvik 1980; Schmalhausen 1968; Clack 2002). Moreover, it was proposed that early land plants were associated with this evolutionary step on land. Recent analyses of the colonization of the terrestrial landscape by green, multicellular plants (embryophytes), a process that pre-dated the early evolution of tetrapods, revealed the following insights Niklas and Kutschera (2009, 2010). The embryophytes (Kingdom Plantae) represent a monophyletic group of photosynthetic eukaryotes that today comprise the non-vascular plant lineage (bryophytes), and the tracheophytes (i. e., lycophytes, ferns, horsetails and seed plants). The earliest embryophytes descended in freshwater environments from charophyte-like ancestors during the late Silurian (ca. 420 mya), and the earliest fossilized land plants (stems etc. with stomata) are ca. 410 my old (Cooksonia, Rhynia, Zosterophyllum). Hence, the water-to-land transition in the plant kingdom pre-dated the evolution of the earliest tetrapods by at least 10, possibly by 50 my (Gensel 2008; Niklas and Kutschera 2009, 2010).
It is, therefore, likely that these key events in the history of life on Earth occurred independently in different environments (freshwater ecosystems vs. marine intertidal or lagoon zones in plants and animals, respectively). The finding that the earliest tetrapods may have thrived in the “mud of a shallow marine lagoon” (Janvier and Clément 2010) is of importance with respect to the “mudskippers-as-model organisms” question that is discussed below.
There are different kinds of air-breathing fishes. Aquatic air-breathing fishes remain in water and surface periodically to gulp air. This behaviour may be continuous in some species subjected to low oxygen concentrations and high water temperatures, or facultative in species subjected to occasional conditions unfavourable for aquatic respiration. In contrast, amphibious air-breathers emerge from the water to feed, rest, escape predators, find a mate and defend territories. Some species are active on land, such as the mudskippers that are the subject of the next section. Other species are inactive on land and become air-breathers when their aquatic habitat disappears during the tropical dry season. Some lungfishes are in this category and are confined in mud burrows until the rains return. They are without food and enter a hypometabolic state or even aestivate (see Figure 2).
Mudskippers are probably the most studied of air-breathing fishes and their biology has been reviewed by Clayton (1993), who noted the problems with their identification to species. As many as 100 species were once named but these have now been reduced considerably by the taxonomic revision by Murdy (1989). He recognized four mudskipper genera and 24 species: Periophthalmus (12 species), Periophthalmodon (3 species), Boleophthalmus (5 species) and Scartelaos (4 species).
The skin of a mudskipper is highly vascularised and this facilitates cutaneous respiration in both air and water. For the species of Periophthalmus in Figure 6, cutaneous respiration accounts for 50 to 60% of total aerial respiration and about 40% of total aquatic respiration (Graham 1997). As well as the sucker formed by the pelvic fins, mudskippers have well-developed pectoral fins that assist in their locomotion. They are capable of jumping and skipping across tidal mud flats, but also crawl with their body held stiff and pulled along by the alternate anterior extension and adduction of their large, highly dextrous, pectoral fins (Figure 6b,c). They also have well-developed turreted eyes and are active carnivores that can climb up rocks and even up the roots, trunk and lower branches of mangrove trees.
In an experimental study, prey recognition in P. barbarus was found to be similar to that in the European toad, Bufo bufo, when both species were offered small earthworms as food (Kutschera et al. 2008). Therefore, mudskippers may be regarded as “extant model organisms” to elucidate the vertebrate transition from water to land, and are intermediate forms that display a number of anatomical and physiological macro-modifications of their body plan that enable them to live and forage for food on land. In other words, these fishes, that primarily seek food out of water and detect their prey organisms entirely by sight, are examples of macroevolution in progress (Kutschera 2006; Kutschera et al. 2008).
As noted earlier, there are only seven extant species in the lobe-finned Sarcopterygii (exclusive of the Tetrapoda, Benton 2005). The deep sea coelacanth is obviously not an air-breather but does use its paired fins for slow swimming with alternating gaits similar to those seen in terrestrial amphibians. It was once assumed that coelacanths walked across the sea bottom because of the similarity between their fin morphology and the limbs of the early fossil tetrapods, but this is now considered incorrect (see Brinkmann et al. 2004). The remaining six species of sarcopterygians are all lungfishes in the Dipnoi and, as their name indicates, they can obtain oxygen from both air and water.
The species Neoceratodus forsteri has large fleshy fins and thick scales. This species is restricted to a small area of eastern Australia, is nocturnal, and lives in open waters and deep pools. It is mainly carnivorous with a maximum length of about 1.5 m, and, unlike other lungfishes, it does not burrow or aestivate. Breathing in air is fairly continuous at low frequencies and its lung is ventilated by the same buccal force-pump mechanism found in other lungfishes (Graham 1997). It is the only extant lungfish with well-developed pectoral and pelvic fins that are greatly reduced in all the other species of lungfishes. Lepidosiren paradoxa has an eel-like shape and attains a length of about 1 m. It is restricted to the Amazon and Pirana river basins of South America where it lives in swamps and shallow water where low oxygen concentrations are common, and seasonal droughts are frequent. It feeds on a mixture of invertebrates and small vertebrates, and its reduced limbs have tactile and chemosensory uses in orientation and prey detection in turbid water, but are of little use in locomotion (Graham 1997). L. paradoxa does not actively leave the water and during the dry season it lives in a moist burrow where it can survive for several months.
The remaining four species of lungfishes are all in the genus Protopterus, P. annectens (Figures 2a,d; maximum length 0.8 m), P. dolloi (0.3 m), P. amphibius (0.4 m) and P. aethiopicus (1.8 m). They are found in tropical Africa and live in swamps, shallow pools, deep lakes and rivers. They are active predators but are also eaten by humans. All species develop like amphibians, i.e., they ontogenetically re-capitulate a “newt/salamander”-stage of gill development (Figure 2b). Finally, they become obligatory air-breathers at a young age and this enables them to survive low oxygen concentrations in many of their natural habitats (Graham 1997). When its habitat is subject to seasonal drying, the lungfish lives in a vertical burrow, constructs a mucous cocoon to prevent dehydration, and aestivates in dry mud for up to four years in the wild and six years in the laboratory. This survival strategy is depicted schematically in Figure 2c and described in detail by Greenwood (1986).
In the early evolution of tetrapods, forelimbs and skulls became modified earlier than hind limbs so that the head and anterior of the body could be raised out of the water for air breathing, as seen in present-day mudskippers (Figure 6b). As noted above, the early tetrapods did not originate from mudskippers, which are teleosts (Actinopterygii) (Figure 1a), but from ancient lobe-finned sarcopterygians. Current views are that the lungfishes are more closely related to early tetrapods than the coelacanth, despite the latter being once regarded as an iconic “tetrapod ancestor” (Clack 2009).
The fins of P. annectens are long and slender (Figures 2a,d). A detailed experimental study by King et al. (2011) has shown that when this species is in an aquatic environment, it uses a range of pelvic fin-driven, tetrapod-like gaits, including walking and bounding, and is able to lift its body clear of the substratum by using its pelvic fins. These authors conclude that some basic features of tetrapod locomotion, including pelvic limb gait patterns, probably arose in sacopterygians before the origin of digital limbs and the invasion of land. The bipedal pelvic-driven gait produced patterns similar to those shown by some of the early fossil trackways, discussed above and previously attributed to tetrapods (Janvier and Clément 2010). King et al. (2011) conclude that trackways lacking unambiguous evidence of digits are now open to question, especially those from the Devonian when sarcopterygian fishes were diverse and abundant.
Five decades ago, when Osche (1962) wrote his theoretical paper, it was still suggested that the coelacanth, and not lungfishes, were the next living relatives of the Tetrapoda. Therefore, Osche (1962) discussed this topic from the “Latimeria-perspective” and did not take into account our modern view of this topic (Brinkmann et al. 2004). The “mudskipper-hypothesis” has remained controversial over the past five decades (Kutschera 2006; Kutschera et al. 2008). Here we show how mudskippers and lungfishes have coped with the ecological challenge of the water-to-land transition (Figures 2, 5, 6). It is possible that similar mechanisms enabled the gradual evolutionary transition of Devonian fishes to early tetrapods. Moreover, extant lungfishes (Figure 2) display a number of features that are reminiscent of those of the earliest tetrapods from the Devonian. The evidence is clearly circumstantial and assumes that convergent evolution occurred in mudskippers, lungfishes and the early tetrapods, an assumption that cannot be verified for the latter from the fossil record.
However, we must emphasise that neither mudskippers nor lungfishes are the ancestors of the Tetrapoda - extant organisms cannot be ancestral forms of other living beings. In other words, there exists no “Great Chain of Beings” in nature, and hence no “higher vs. lower organisms” or “advanced vs. primitive” can be distinguished. To make this point clear, men did not evolve from living chimpanzees, but from extinct hominoids, such as Sahelanthropus and related “ape-like bipedals” (Shubin 2008). We conclude that all extant species are of the same rank (Kutschera 2009; Kutschera 2011a, b) and represent the tips of one large tree of life that Darwin (1859) envisioned, and biologists of the 20th century corroborated using the techniques of DNA-sequence-based reconstructions of phylogenetic trees.
million years ago.
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