Lepas australis, Darwin, 1851

Schiffer, Philipp H. & Herbig, Hans-Georg, 2016, Endorsing Darwin: global biogeography of the epipelagic goose barnacles Lepas spp. (Cirripedia, Lepadomorpha) proves cryptic speciation, Zoological Journal of the Linnean Society 177 (3), pp. 507-525 : 516

publication ID

https://doi.org/10.1111/zoj.12373

persistent identifier

https://treatment.plazi.org/id/666987EE-CF43-F211-FE8F-FEEAFB8CFB8F

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Marcus (2021-08-29 14:11:31, last updated by Plazi 2023-11-05 15:14:57)

scientific name

Lepas australis
status

 

LEPAS AUSTRALIS

It is most surprising to find a geographic pattern in L. australis that is even supported by the slowly evolving nuclear locus. The species in general is restricted to cold-water masses linked with Antarctica, an area where longitudinal landmasses that could impede gene flow, and thus lead to the evolution of geographically confined populations, are missing. In contrast, the westerly wind-driven Antarctic Circumpolar Current (ACC) effectively mediates the transport of organisms around Antarctica. Within the ACC the Antarctic Polar Front (APF, or Antarctic Convergence; U.S. Geological Survey 2010 /2012), which coincides approximately with the edge of the winter sea ice, and a sudden change in seawater surface temperature, acts as an effective latitudinal barrier between water masses, and also between marine organisms ( Thornhill et al., 2008). Further north, the Subantarctic Front (or Subtropical Convergence; U.S. Geological Survey, 2010 /2012), i.e. the northern boundary of the ACC, is a second major latitudinal water-mass barrier. The effectiveness of these fronts as barriers to gene flow has already been demonstrated, e.g. in the chaetognath Eukrohnia hamata (Mobius, 1875) ( Kulagin et al., 2014) .

All our sampling sites are situated north of the ACC. There, we recognize a common population of L. australis in the cool to temperate waters north of the Subantarctic Front, herein termed the ‘Southern Ocean subgroup’. This population of L. australis is obviously caught in the current system adjoining north of the Subtropical Convergence, albeit also circling eastwards around Antarctica, and in the northeast deviating current systems, which sweep up the coasts of Western Australia and New Zealand (South Indian Current s.l.), respectively, Argentina (Falkland Current), and South Africa (Benguela Current) ( Fig. 6).

The ‘coastal Chilean subgroup’ differs from all other sampling sites. It matches biogeographic results of a separate eastern Pacific/Chilean province from other pelagic organisms. Examples are the copepod Rhincalanus nasutus ( Goetze, 2003) , which has a sister group along the North American coast, the rafting bryozoan Membranipora ( Schwaninger, 2008) , the giant kelp Macrocystis ( Coyer, Smith & Andersen, 2001) , or, most evident, the bull kelp Durvillaea antarctica (Chamisso) Hariot 1892 ( Fraser et al., 2009). The latter shows distinct haplotypes along the central and northern Chilean coast. In analogy to results from New Zealand, they are most probably related to the continuous warming of seawater ( Fraser et al., 2009; Fraser, Nikula & Waters, 2011). The observations on D. antarctica are consistent with further zoogeographic studies of littoral benthic and pelagic organisms, which provide evidence for three distinct, most probably SSTrelated, zoogeographical regions along the Chilean coast ( Escribano, Fernandez & Aranıs, 2003; Hinojosa et al., 2006). As goose barnacles from the southern hemisphere are abundantly rafting on detached Macrocystis and D. antarctica ( Thiel & Gutow, 2004; Hinojosa et al., 2006), the coastal Chilean subgroup appears to be very plausible.

In addition to extreme genetic divergence between populations of the bull kelp D. antarctica from Chile and New Zealand, and further genetic differentiation within both regions, a genetically homogeneous population exists further south within the ACC ( Fraser et al., 2009, 2011). Unified Antarctic genotypes were also described for the chaetognath Eukrohnia hamata and the Antarctic krill Euphausia superba Dana, 1850 ( Bortolotto et al., 2011; Kulagin et al., 2014). Therefore, it might be hypothesized that a third, truly subantarctic L. australis subtype might exist south of the Subtropical Convergence. One tiny L. australis specimen collected from floating Durvillaea kelp at around 50 ° S off the Chilean coast does not belong to the postulated Subantarctic subgroup, nor to the coastal Chilean subgroup, but to the Southern Ocean subgroup.

Bortolotto E, Bucklin A, Mezzavilla M, Zane L, Patarnello T. 2011. Gone with the currents: lack of genetic differentiation at the circum-continental scale in the Antarctic krill Euphausia superba. BMC Genetics 12: 32.

Coyer JA, Smith GJ, Andersen RA. 2001. Evolution of Macrocystis spp. (Phaeophyceae) as determined by ITS 1 and ITS 2 sequences. Journal of Phycology 37: 574 - 585.

Escribano R, Fernandez M, Aranis A. 2003. Physical-chemical processes and patterns of diversity of the Chilean eastern boundary pelagic and benthic marine ecosystems: an overview. Gayana 67: 190 - 205.

Fraser CI, Nikula R, Spencer HG, Waters JM. 2009. Kelp genes reveal effects of Subantarctic sea ice during the Last Glacial Maximum. Proceedings of the National Academy of Sciences of the United States of America 106: 3249 - 3253.

Fraser CI, Nikula R, Waters JM. 2011. Oceanic rafting by a coastal community. Proceedings of the Royal Society of London B: Biological Sciences 278: 649 - 655.

U. S. Geological Survey (2010, update 2012). Antarctic convergence. Available at: www. eoearth. org / view / article / 150096 /.

Goetze E. 2003. Cryptic speciation on the high seas; global phylogenetics of the copepod family Eucalanidae. Proceedings of the Royal Society of London B: Biological Sciences 270: 2321 - 2331.

Hinojosa I, Boltana S, Lancellotti D, Macaya E, Ugalde P, Valdivia N, Vasquez N, Newman W, Thiel M. 2006. Geographic distribution and description of four pelagic barnacles along the south east Pacific coast of Chile - a zoogeographical approximation. Revista Chilena de Historia Natural 79: 13 - 27.

Kulagin DN, Stupnikova AN, Neretina TV, Mugue NS. 2014. Spatial genetic heterogeneity of the cosmopolitan chaetognath Eukrohnia hamata (Mobius, 1875) revealed by mitochondrial DNA. Hydrobiologia 721: 197 - 207.

Schwaninger HR. 2008. Global mitochondrial DNA phylogeography and biogeographic history of the antitropically and longitudinally disjunct marine bryozoan Membranipora membranacea L. (Cheilostomata): another cryptic marine sibling species complex? Molecular Phylogenetics and Evolution 49: 893 - 908.

Thiel M, Gutow L. 2004. The ecology of rafting in the marine environment. I. The floating substrata. Oceanography and Marine Biology Annual Review 42: 181 - 263.

Thornhill DJ, Mahon AR, Norenburg JL, Halanych KM. 2008. Open-ocean barriers to dispersal: a test case with the Antarctic Polar Front and the ribbon worm Parborlasia corrugatus (Nemertea: Lineidae). Molecular Ecology 17: 5104 - 5117.

Kingdom

Animalia

Phylum

Arthropoda

Class

Maxillopoda

Order

Pedunculata

Family

Lepadidae

Genus

Lepas