Specific examples from speciation: fossils
editLimitations exist within the fossil record when considering the concept of what constitutes a species. Paleontologists largely rely on a different framework: the morphological species concept.[1] Due to the absence of information such as reproductive behavior or genetic material in fossils, paleontologists distinguish species by their phenotypic differences.[1] Extensive investigation of the fossil record has led to numerous theories concerning speciation (in the context of paleontology) with many of the studies suggesting that stasis, punctuation, and lineage branching are common. In 1995, D. H. Erwin, et al. published a major work—New Approaches to Speciation in the Fossil Record—which compiled 58 studies of fossil speciation (between 1972 and 1995) finding most of the examples suggesting stasis (involving anagenesis or punctuation) and 16 studies suggesting speciation.[1] Despite stasis appearing to be the predominate conclusion at first glance, this particular meta-study investigated deeper, concluding that, "...no single pattern appears dominate..." with "...the preponderance of studies illustrating both stasis and gradualism in the history of a single lineage".[2] Many of the studies conducted utilize seafloor sediments that can provide a significant amount of data concerning planktonic microfossils.[1] The succession of fossils in stratigraphy can be used to determine evolutionary trends among fossil organisms. In addition, incidences of speciation can be interpreted from the data and numerous studies have been conducted documenting both morphological evolution and speciation.
Globorotalia
editExtensive research on the planktonic foraminifer Globorotalia truncatulinoides has provided insight into paleobiogeographical and paleoenvironmental studies alongside the relationship between the environment and evolution. In an extensive study of the paleobiogeography of G. truncatulinoides, researchers found evidence that suggested the formation of a new species (via the sympatric speciation framework). Cores taken of the sediment containing the three species G. crassaformis, G. tosaensis, and G. truncatulinoides found that before 2.7 Ma, only G. crassaformis and G. tosaensis existed. A speciation event occurred at that time, whereby intermediate forms existed for quite some time. Eventually G. tosaensis disappears from the record (suggesting extinction) but exists as an intermediate between the extant G. crassaformis and G. truncatulinoides. This record of the fossils also matched the already existing phylogeny constructed by morphological characters of the three species.[3] See figure 6a.
Radiolaria
editIn a large study of five species of radiolarians (Calocycletta caepa, Pterocanium prismatium, Pseudoculous vema, Eucyrtidium calvertense, and Eucyrtidium matuyamai), the researchers documented considerable evolutionary change in each lineage. Alongside this, trends with the closely related species E. calvertense and E. matuyamai showed that about 1.9 Mya E. calvertense invaded a new region of the Pacific, becoming isolated from the main population. The stratigraphy of this species clearly shows that this isolated population evolved into E. Matuyamai. It then reinvaded the region of the still-existing and static E. calvertense population whereby a sudden decrease in body size occurred. Eventually the invader E. matuyamai disappeared from the stratum (presumably due to extinction) coinciding with a desistance of size reduction of the E. calvertense population. From that point on, the change in size leveled to a constant. The authors suggest competition-induced character displacement.[4][5]
Rhizosolenia
editResearchers conducted measurements on 5,000 Rhizosolenia (a planktonic diatom) specimens from eight sedimentary cores in the Pacific Ocean. The core samples spanned two million years and were chronologized using sedimentary magnetic field reversal measurements. All the core samples yielded a similar pattern of divergence: with a single lineage (R. bergonii) occurring before 3.1 Mya and two morphologically distinct lineages (daughter species: R. praebergonii) appearing after. The parameters used to measure the samples were consistent throughout each core.[6] An additional study of the daughter species R. praebergonii found that, after the divergence, it invaded the Indian Ocean.[1][7]
Turborotalia
editA recent study was conducted involving the planktonic foraminifer Turborotalia. The authors extracted “51 stratigraphically ordered samples from a site within the oceanographically stable tropical North Pacific gyre”. Two hundred individual species were examined using ten specific morphological traits (size, compression index, chamber aspect ratio, chamber inflation, aperture aspect ratio, test height, test expansion, umbilical angle, coiling direction, and the number of chambers in the final whorl). Utilizing multivariate statistical clustering methods, the study found that the species continued to evolve non-directionally within the Eocene from 45 Ma to about 36 Ma. However, from 36 Ma to approximately 34 Ma, the stratigraphic layers showed two distinct clusters with significantly defining characteristics distinguishing one another from a single species. The authors concluded that speciation must have occurred and that the two new species were ancestral to the prior species.[8] Just as in most of evolutionary biology, this example represents the interdisciplinary nature of the field and the necessary collection of data from various fields (e.g. oceanography, paleontology) and the integration of mathematical analysis (e.g. biometry).
Vertebrates
editThere exists evidence for vertebrate speciation despite limitations imposed by the fossil record. Studies have been conducted documenting similar patterns seen in marine invertebrates.[1] For example, extensive research documenting rates of morphological change, evolutionary trends, and speciation patterns in small mammals[9] has significantly contributed to the scientific literature; once more, demonstrating that evolution (and speciation) occurred in the past and lends support common ancestry.
A study of four mammalian genera: Hyopsodus, Pelycodus, Haplomylus (three from the Eocene), and Plesiadapis (from the Paleocene) found that—through a large number of stratigraphic layers and specimen sampling—each group exhibited, "gradual phyletic evolution, overall size increase, iterative evolution of small species, and character divergence following the origin of each new lineage".[10] The authors of this study concluded that speciation was discernible. In another study concerning morphological trends and rates of evolution found that the European arvicolid rodent radiated into 52 distinct lineages over a time frame of 5 million years while documenting examples of phyletic gradualism, punctuation, and stasis.[11]
- ^ a b c d e f Michael J. Benton; Paul N. Pearson (2001), "Speciation in the Fossil Record", Trends in Ecology and Evolution, 16 (7)
- ^ Erwin, D. H.; Anstey, R. L. (1995), New Approaches to Speciation in the Fossil Record, Columbia University Press, p. 22
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suggested) (help) - ^ David Lazarus; et al. (1995), "Sympatric Speciation and Phyletic Change in Globorotalia truncatulinoides", Paleobiology, 21 (1): 28–51
- ^ Davida E. Kellogg; James D. Hays (1975), "Microevolutionary Patterns in Late Cenozoic Radiolaria", Paleobiology, 1 (2): 150–160, doi:10.1017/s0094837300002347
- ^ James D. Hays (1970), "Stratigraphy and Evolutionary Trends of Radiolaria in North Pacific Deep-Sea Sediments", Geological Society of America Memoirs, 126: 185–218
- ^ Ulf Sörhannus; et al. (1998), "Cladogenetic and anagenetic changes in the morphology of Rhizosolenia praebergonii Mukhina", Historical Biology: 185–205
- ^ Ulf Sörhannus; et al. (1991), "Iterative evolution in the diatom genus Rhizosolenia Ehrenberg", Lethaia, 24 (1)
- ^ Paul N. Pearson; Thomas H. G. Ezard (2014). "Evolution and speciation in the Eocene planktonic foraminifer Turborotalia". Paleobiology. 40: 130–143. doi:10.1666/13004.
- ^ P. D. Gingerich (1985), "Species in the Fossil Record: Concepts, Trends, and Transitions", Paleobiology, 11: 27–41
- ^ P. D. Gingerich (1976), "Paleontology and Phylogeny: Patterns of Evolution at the Species Level in Early Tertiary Mammals", American Journal of Science, 276: 1–28, doi:10.2475/ajs.276.1.1
- ^ J. Chaline; et al. (1993), "Morphological Trends and Rates of Evolution in Arvicolids (Arvicolidae, Rodentia): Towards a Punctuated Equilibria/Disequilibria Model", Quarternary International, 19: 27–39, doi:10.1016/1040-6182(93)90019-c