The Pelecaniformes /pɛlɪˈkænɪfɔːrmiːz/ are an order of medium-sized and large waterbirds found worldwide. As traditionally—but erroneously—defined, they encompass all birds that have feet with all four toes webbed. Hence, they were formerly also known by such names as totipalmates or steganopodes. Most have a bare throat patch (gular patch), and the nostrils have evolved into dysfunctional slits, forcing them to breathe through their mouths. They also have a pectinate nail on their longest toe. This is shaped like a comb and is used to brush out and separate their feathers. They feed on fish, squid, or similar marine life. Nesting is colonial, but individual birds are monogamous. The young are altricial, hatching from the egg helpless and naked in most. They lack a brood patch.
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Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Aves |
| Clade: | Pelecanes |
| Order: | Pelecaniformes Sharpe, 1891 |
| Suborder and Families | |
The pelicans, shoebill and hamerkop form a clade within the order (suborder Pelecani). The relationships between Pelecani, herons (Ardeidae) and ibises and spoonbills (Threskiornithidae) are unclear. The Fregatidae (frigatebirds), Sulidae (gannets and boobies), Phalacrocoracidae (cormorants and shags), Anhingidae (darters), and Phaethontidae (tropicbirds) were traditionally placed in the Pelecaniformes, but molecular and morphological studies indicate they are not such close relatives. They have been placed in their own orders, Suliformes and Phaethontiformes, respectively.[3]
Systematics and evolution
editClassically, bird relationships were based solely on morphological characteristics. The Pelecaniformes were traditionally, but erroneously, defined as birds that have feet with all four toes webbed (totipalmate), as opposed to all other birds with webbed feet where only three of four were webbed. Hence, they were formerly also known by such names as totipalmates or steganopodes. The group included frigatebirds, gannets, cormorants, anhingas, and tropicbirds.[4]
Sibley and Ahlquist's landmark DNA-DNA hybridisation studies (see Sibley-Ahlquist taxonomy) led to them placing the families traditionally contained within the Pelecaniformes together with the grebes, cormorants, ibises and spoonbills, New World vultures, storks, penguins, albatrosses, petrels, and loons together as a subgroup within a greatly expanded order Ciconiiformes, a radical move which by now has been all but rejected: their "Ciconiiformes" merely assembled all early advanced land- and seabirds for which their research technique delivered insufficient phylogenetic resolution.
Morphological study has suggested pelicans are sister to a gannet-cormorant clade, yet genetic analysis groups them with the hamerkop and shoebill, though the exact relationship between the three is unclear.[5] Mounting evidence pointed to the shoebill as a close relative of pelicans.[4] This also included microscopic analysis of eggshell structure by Konstantin Mikhailov in 1995, who found that the shells of pelecaniform eggs (including those of the shoebill but not the tropicbirds) were covered in a thick microglobular material.[6] Reviewing genetic evidence to date, Cracraft and colleagues surmised that pelicans were sister to the shoebill with the hamerkop as the next earlier offshoot.[7] Ericson and colleagues sampled five nuclear genes in a 2006 study spanning the breadth of bird lineages, and came up with pelicans, shoebill and hamerkop in a clade.[8] Hackett and colleagues sampled 32 kilobases of nuclear DNA and recovered shoebill and hamerkop as sister taxa, pelicans sister to them, and herons and ibises as sister groups to each other, with the heron and ibis group a sister to the pelican/shoebill/hamerkop clade.[9]
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The current International Ornithological Committee classification has pelicans grouped with the shoebill (Balaenicipitidae), hamerkop (Scopidae), ibises and spoonbills (Threskiornithidae), and herons, egrets and bitterns (Ardeidae). The IOC considers Threskiornithidae and Ardeidae to from a clade, citing Hackett et al. 2008 ([9]). [10]
Another hypothesis is that Threskiornithidae is sister to the rest of Pelecaniformes, and Ardeidae and Pelecani form a clade. [11][12]
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Recent research strongly suggests that the similarities between the Pelecaniformes as traditionally defined are the result of convergent evolution rather than common descent, and that the group is polyphyletic.[13] All families in the traditional Pelecaniformes except the Phalacrocoracidae have only a few handfuls of species at most, but many were more numerous in the Early Neogene. Fossil genera and species are discussed in the respective family or genus accounts; one little-known prehistoric Pelecaniforms, however, cannot be classified accurately enough to assign them to a family. This is "Sula" ronzoni from Early Oligocene rocks at Ronzon, France, which was initially believed to be a sea-duck and possibly is an ancestral Pelecaniform.
The pelecaniform lineages appear to have originated around the end of the Cretaceous. Monophyletic or not, they appear to belong to a close-knit group of "higher waterbirds" which also includes groups such as penguins and Procellariiformes. Quite a lot of fossil bones from around the Cretaceous–Paleogene boundary cannot be firmly placed with any of these orders and rather combine traits of several of them. This is, of course, only to be expected, if the theory that most if not all of these "higher waterbird" lineages originated around that time is correct. Of those apparently basal taxa, the following show some similarities to the traditional Pelecaniformes:
- † Lonchodytes (Lance Creek Late Cretaceous of Wyoming, US)
- † Torotix (Late Cretaceous)
- † Tytthostonyx (Late Cretaceous/Early Palaeocene)
- † Cladornis (Deseado Early Oligocene of Patagonia, Argentina)
- † "Liptornis"—a nomen dubium
The proposed Elopterygidae—supposedly a family of Cretaceous Pelecaniformes—are neither monophyletic nor does Elopteryx appear to be a modern bird.[14]
References
edit- ^ Mayr, G.; De Pietri, V. L.; Scofield, R. P.; Smith, T. (2018). "A fossil heron from the early Oligocene of Belgium: the earliest temporally well-constrained record of the Ardeidae". Ibis. 161 (1): 79–90. doi:10.1111/ibi.12600.
- ^ Kuhl, H.; Frankl-Vilches, C.; Bakker, A.; et al. (2020). "An unbiased molecular approach using 3'UTRs resolves the avian family-level tree of life". Molecular Biology and Evolution. 38: 108–127. doi:10.1093/molbev/msaa191. PMC 7783168. PMID 32781465.
- ^ Jarvis, Erich D.; et al. (2014). "Whole-genome analyses resolve early branches in the tree of life of modern birds". Science. 346 (6215): 1320–1331. Bibcode:2014Sci...346.1320J. doi:10.1126/science.1253451. hdl:10072/67425. PMC 4405904. PMID 25504713.
- ^ a b Hedges, S. Blair; Sibley, Charles G. (1994). "Molecules vs. morphology in avian evolution: the case of the "pelecaniform" birds". PNAS. 91 (21): 9861–65. Bibcode:1994PNAS...91.9861H. doi:10.1073/pnas.91.21.9861. PMC 44917. PMID 7937906.
- ^ Mayr, G. (2007). "Avian higher-level phylogeny: Well-supported clades and what we can learn from a phylogenetic analysis of 2954 morphological characters". Journal of Zoological Systematics and Evolutionary Research. 46: 63–72. doi:10.1111/j.1439-0469.2007.00433.x. S2CID 59486699.
- ^ Mikhailov, Konstantin E. (1995). "Eggshell structure in the shoebill and pelecaniform birds: comparison with hamerkop, herons, ibises and storks". Canadian Journal of Zoology. 73 (9): 1754–70. doi:10.1139/z95-207.
- ^ Cracraft, Joel; Barker, F. Keith; Braun, Michael J.; Harshman, John; Dyke, Gareth J.; Feinstein, Julie; Stanley, Scott; Cibois, Alice; Schikler, Peter; Beresford, Pamela; García-Moreno, Jaime; Sorenson, Michael D.; Yuri, Tamaki & Mindell, David P. (2004): Phylogenetic Relationships Among Modern Birds (Neornithes): Toward an Avian Tree of Life. In: Cracraft, J. & Donoghue, M.J. (eds.): Assembling the Tree of Life: 468–489. Oxford University Press, New York. ISBN 0-19-517234-5 PDF fulltext Archived 2013-05-14 at the Wayback Machine
- ^ Ericson, P. G. P.; Anderson, C. L.; Britton, T.; et al. (2006). "Diversification of Neoaves: integration of molecular sequence data and fossils". Biology Letters. 2 (4): 543–547. doi:10.1098/rsbl.2006.0523. PMC 1834003. PMID 17148284.
- ^ a b Hackett, Shannon J.; Kimball, Rebecca T.; Reddy, Sushma; et al. (2008). "A Phylogenomic Study of Birds Reveals Their Evolutionary History". Science. 320 (5884): 1763–68. Bibcode:2008Sci...320.1763H. doi:10.1126/science.1157704. PMID 18583609. S2CID 6472805.
- ^ International Ornithological Committee (2 January 2012). "Ibises to Pelicans & Cormorants". IOC World Bird Names: Version 2.11. WorldBirdNames.org. Archived from the original on 1 March 2012. Retrieved 30 April 2012.
- ^ Reddy, S.; Kimball, R.T.; Pandey, A.; et al. (2017). "Why do phylogenomic data sets yield conflicting trees? Data type influences the avian tree of life more than taxon sampling". Systematic Biology. 66 (5): 857–879. doi:10.1093/sysbio/syx041. PMID 28369655.
- ^ Kuhl, H.; Frankl-Vilches, C.; Bakker, A.; et al. (2021). "An unbiased molecular approach using 3′-UTRs resolves the avian family-level tree of life". Molecular Biology and Evolution. 38 (1): 108–127. doi:10.1093/molbev/msaa191. PMC 7783168. PMID 32781465.
- ^ Mayr, Gerald (2003). "The phylogenetic affinities of the Shoebill (Balaeniceps rex)" (PDF). Journal für Ornithologie. 144 (2): 157–175. Bibcode:2003JOrni.144..157M. doi:10.1007/BF02465644 – via senckenberg.de.
- ^ Mortimer, Michael (2004). "Phylogeny of taxa". archosaur.us. The Theropod Database. Archived from the original on 2013-05-16.
Further reading
edit- Bourdon, Estelle; Bouya, Baâdi & Iarochene, Mohamed (2005): Earliest African neornithine bird: A new species of Prophaethontidae (Aves) from the Paleocene of Morocco. J. Vertebr. Paleontol. 25(1): 157–170. DOI: 10.1671/0272-4634(2005)025[0157:EANBAN]2.0.CO;2 HTML abstract
External links
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