The ecology of invasion: acquisition and loss of the siphonal canal in gastropods

Paleobiology ◽  
2007 ◽  
Vol 33 (3) ◽  
pp. 469-493 ◽  
Author(s):  
Geerat J. Vermeij

AbstractMost evolutionary innovations—power-enhancing phenotypes previously absent in a lineage—have arisen multiple times within major clades. This repetition permits a comparative approach to ask how, where, when, in which clades, and under which circumstances adaptive innovations are acquired and secondarily lost. I use new and literature-based data on the phylogeny, functional morphology, and fossil record of gastropods to explore the acquisition and loss of the siphonal canal and its variations in gastropods. The siphonal indentation, canal, notch, or tube at the front end of the shell is associated in living gastropods with organs that detect chemical signals directionally and at a distance in an anteriorly restricted inhalant stream of water.Conservative estimates indicate that the siphonate condition arose 23 times and was secondarily lost 17 times. Four siphonate clades have undergone prodigious diversification. All siphonate gastropods have a shell whose axis of coiling lies at a low angle above the plane of the aperture (retroaxial condition). In early gastropods, the siphonal canal was short and more or less confined to the apertural plane. Later (mainly Cretaceous and Cenozoic) variations include a dorsally deflected canal, a long canal, and a closed canal. The closed siphonal canal, in which the edges join to form a tube, arose 15 times, all in the adult stages of caenogastropods with determinate growth.Gastropods in which the siphonate condition arose were mobile, bottom-dwelling, microphagous animals. Active predaceous habits became associated with the siphonate condition in the Mesozoic and Cenozoic Purpurinidae-Latrogastropoda clade. Loss of the siphonate condition is associated with nonmarine habits, miniaturization, and especially with a sedentary or slow-moving mode of life.The siphonate condition arose seven times each during the early to middle Paleozoic, the late Paleozoic, and the early to middle Mesozoic, and only once each during the Late Cretaceous and Cenozoic. Well-adapted incumbents prevented most post-Jurassic clades from evolving a siphonal indentation and its associated organs. Dorsally deflected, long, and closed canals are known only from Cretaceous and Cenozoic marine gastropods, and represent improvements in sensation and passive armor.In a discussion of contrasting ecologies of clades that gained and lost the siphonate condition, I argue that macroevolutionary trends in the comings and goings of innovations and clades must incorporate ecological and functional data. Acquisitions of energy-intensive, complex innovations that yield greater power have a greater effect on ecosystems, communities, and their resident clades than do reversals, which generally reflect energy savings.

Paleobiology ◽  
2007 ◽  
Vol 33 (3) ◽  
pp. 469-493 ◽  
Author(s):  
Geerat J. Vermeij

AbstractMost evolutionary innovations—power-enhancing phenotypes previously absent in a lineage—have arisen multiple times within major clades. This repetition permits a comparative approach to ask how, where, when, in which clades, and under which circumstances adaptive innovations are acquired and secondarily lost. I use new and literature-based data on the phylogeny, functional morphology, and fossil record of gastropods to explore the acquisition and loss of the siphonal canal and its variations in gastropods. The siphonal indentation, canal, notch, or tube at the front end of the shell is associated in living gastropods with organs that detect chemical signals directionally and at a distance in an anteriorly restricted inhalant stream of water.Conservative estimates indicate that the siphonate condition arose 23 times and was secondarily lost 17 times. Four siphonate clades have undergone prodigious diversification. All siphonate gastropods have a shell whose axis of coiling lies at a low angle above the plane of the aperture (retroaxial condition). In early gastropods, the siphonal canal was short and more or less confined to the apertural plane. Later (mainly Cretaceous and Cenozoic) variations include a dorsally deflected canal, a long canal, and a closed canal. The closed siphonal canal, in which the edges join to form a tube, arose 15 times, all in the adult stages of caenogastropods with determinate growth.Gastropods in which the siphonate condition arose were mobile, bottom-dwelling, microphagous animals. Active predaceous habits became associated with the siphonate condition in the Mesozoic and Cenozoic Purpurinidae-Latrogastropoda clade. Loss of the siphonate condition is associated with nonmarine habits, miniaturization, and especially with a sedentary or slow-moving mode of life.The siphonate condition arose seven times each during the early to middle Paleozoic, the late Paleozoic, and the early to middle Mesozoic, and only once each during the Late Cretaceous and Cenozoic. Well-adapted incumbents prevented most post-Jurassic clades from evolving a siphonal indentation and its associated organs. Dorsally deflected, long, and closed canals are known only from Cretaceous and Cenozoic marine gastropods, and represent improvements in sensation and passive armor.In a discussion of contrasting ecologies of clades that gained and lost the siphonate condition, I argue that macroevolutionary trends in the comings and goings of innovations and clades must incorporate ecological and functional data. Acquisitions of energy-intensive, complex innovations that yield greater power have a greater effect on ecosystems, communities, and their resident clades than do reversals, which generally reflect energy savings.


Science ◽  
2018 ◽  
Vol 362 (6413) ◽  
pp. 460-464 ◽  
Author(s):  
Lauren Sallan ◽  
Matt Friedman ◽  
Robert S. Sansom ◽  
Charlotte M. Bird ◽  
Ivan J. Sansom

Ancestral vertebrate habitats are subject to controversy and obscured by limited, often contradictory paleontological data. We assembled fossil vertebrate occurrence and habitat datasets spanning the middle Paleozoic (480 million to 360 million years ago) and found that early vertebrate clades, both jawed and jawless, originated in restricted, shallow intertidal-subtidal environments. Nearshore divergences gave rise to body plans with different dispersal abilities: Robust fishes shifted shoreward, whereas gracile groups moved seaward. Fresh waters were invaded repeatedly, but movement to deeper waters was contingent upon form and short-lived until the later Devonian. Our results contrast with the onshore-offshore trends, reef-centered diversification, and mid-shelf clustering observed for benthic invertebrates. Nearshore origins for vertebrates may be linked to the demands of their mobility and may have influenced the structure of their early fossil record and diversification.


Geosciences ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 397
Author(s):  
Przemysław Sztajner

The paper is an attempt to reconstruct the mode of life of Pholadomya bivalves, very common in the fossil record, particularly that of the Jurassic. The only extant representative of the genus is extremely rare and very poorly known. Materials from the Polish Jurassic deposits (Bajocian–Kimmeridgian; Western Pomerania and Polish Jura) and literature data were used for the reconstruction. Specifically, observations on the anatomy, taphonomy, and diagenesis of the specimens examined as well as lithology of the deposits housing the specimens were used. Shell anatomy characteristics are known for their particular utility in mode of life reconstructions, although the extremely thin-shelled and coarsely sculpted bivalves, such as the Pholadomya examined, have not been studied so far. The reconstruction suggest a diversity of the mode of life, coincident with the morphological differences between the Pholadomya species. At least the adults of anteriorly flattened species are inferred to have lived extremely deeply buried in the sediment, and were hardly mobile. The smaller, more oval in shape, species were more mobile, and some of them are thought to have preferred life in shelters, should those be available. In addition, the function of the cruciform muscle, other than that considered so far, is suggested.


2021 ◽  
Vol 15 (2) ◽  
pp. 153
Author(s):  
Marcello Guimarães Simões ◽  
Antonio Carlos Marques ◽  
Luiz Henrique Cruz de Mello ◽  
Renato Pirani Ghilardi

The Megadesmidae (Bivalvia, Anomalodesmata) fossil record was examined in order to assess the role of taphonomy in cladistic analysis. Megadesmids are thick-shelled, infaunal, suspension-feeding bivalves. Our data indicate that their fossil record seems biased in favor of thick-shelled, shallow-burrowing genera and/or deep­burrowing forms. Consequently, there is a relation between the mode of life (shallow versus deep) and the resolution and quality of the fossil record. Deep-burrowers (Vacunella) are often preserved in life position offering a more accurate (temporal and spatial) fossil record, adequate for paleoecological inferences, while shallow-burrower shells (Plesiocyprinella), that are more prone to post-mortem transport and temporal mixing, offer a record with poor spatial and temporal resolution. The identification of homoplasy among infauna! bivalves constitutes a major challenge for their cladistic analysis. Within Megadesmidae intrinsic (bauplan limitations) and extrinsic (better preservational potential) factors favor the occurrence and preservation of homoplasy among the deep-burrowers. The implications are: a) clustering of deep-burrowing bivalves (Vacunella, Roxoa) due to parallel homoplasies, forming "adaptive", not necessarily "evolutive" taxa, and b) lower consistency indices in their cladistic analysis. 


1992 ◽  
Vol 6 ◽  
pp. 75-75
Author(s):  
Rex E. Crick

The historical and prevailing view regarding the distribution of nautiloid cephalopods is one of cosmopolitanism. There are several objections to such a sweeping view of this major group of marine invertebrates, but only the most significant are addressed here. First, unlike endemism, there is no clear agreement on the meaning of the term cosmopolitanism as used in biogeography. It is thus extremely difficult to gain a historical perspective without access to original data. I have found the term used for as few as four occurrences on four modern landmasses without reference to the paleogeographic relationships of these landmasses. Second, while a few nautiloid groups did compile impressive dispersal statistics, the fossil record clearly reveals that such periods of dispersal were generally brief in geological terms and that the group or groups involved did not colonize all available landmasses. Third, nautiloids were incapable of developing cosmopolitan distributions unless climatic constraints were removed by changes in the global system or by positioning all landmasses within the sub-tropical to tropical latitudes. Since there is no convincing evidence that either event occurred during the 520 million years of nautiloid evolution, it is perhaps more appropriate to view the distribution of nautiloids in terms of the number of landmasses colonized relative to the number of landmasses available for colonization. For nautiloids, the number of landmasses available for colonization was always fewer than the number of landmasses comprising the global paleogeography during any one slice of geologic time. Nautiloid genera restricted to one landmass are considered endemic, a condition exhibited by 65% of the Ordovician and Silurian genera and 81% of the Devonian genera. The maximum number of landmasses colonized by any one nautiloid genus for any one particular period of time was four, two fewer than the six available landmasses.The basic biogeographic unit for nautiloid cephalopods is the genus. This is so because the dispersive potential of nautiloids was low when compared with true pelagic groups such as conodonts. Thus for nautiloid groups capable of dispersal among landmasses, the time needed to effect dispersal and insure permanence in the stratigraphic record was something greater than the longevity of the typical nautiloid species but less than the longevity of most genera. It seems reasonable that the best chance for the occurrence of cosmopolitan nautiloid genera would be at or near the zenith of those groups with attributes most suitable for dispersal. However, the fossil record for nautiloids shows that such periods rarely coincide with the peak intervals of total nautiloid diversity for the Lower and Middle Paleozoic (Arenig, Wenlock and Eifelian) occurring instead during succeeding intervals of time. Such events are generally confined to periods of modal diversity within each group. The lowest percentages of endemic genera and the intervals in which they occurred for the major nautiloid groups are: Ellesmerocerida (57%) and Endocerida (60%) for the Llanvirn, Actinocerida (36%) and Tarphycerida (45%) in the Llandeilo, Orthocerida (52%, 47%, 55%) and Oncocerida (66%, 66%, 75%) for the Caradoc, Ludlow, and Givetian, Discosorida (67%) in the Wenlock and Nautilida (62%) for the Givetian. While the low percentage of endemics for the Actinocerida and Tarphycerida translate into the highest percentages of genera found on more than three separate landmasses (20%), similar percentages of endemics for the Orthocerida do not. Nonendemic members of the Orthocerida are more common to two or three of the available landmasses with approximately 20% occurring in either of these configurations. The fossil record also shows that Devonian nautiloids were the most restricted with the majority occurring on no more than two landmasses.These and other criteria indicate that the distributions of nautiloid cephalopods do not conform to the general perception of cosmopolitanism. At the generic level the group is largely endemic with reasonably large numbers of genera occurring on two or three landmasses with no genus occurring on all available landmasses during a given interval of time. Because of the type and manner of biogeographic barriers imposed on nautiloids, their distributions or patterns tend to have well defined limits with considerable predictive powers.


Paleobiology ◽  
1979 ◽  
Vol 5 (1) ◽  
pp. 31-39 ◽  
Author(s):  
Stanley C. Finney

An unusual isolated specimen representing an immature rhabdosome of Dicellograptus sp. from the Middle Ordovician Athens Shale of Alabama has a flattened sphere attached to the distal end of the nema. The flattened sphere can be interpreted as a float that probably conferred buoyancy on the rhabdosome. Such floats, which became detached in mature rhabdosomes, may be common in the fossil record. The presence of nematophorous siculae in all planktonic graptolites suggests that for immature rhabdosomes a passive, buoyant mode of life, attained by means of a float, might have been widespread taxonomically. This mode of life is compatible with the theory of passive response for the mode of life of mature rhabdosomes, but it is difficult to reconcile with the theory of automobility.


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