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1.
J Evol Biol ; 24(11): 2505-19, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21910777

ABSTRACT

Biogeographic boundaries are the meeting zone of broadly distributed faunas, or the actual cause of a faunal break. In the latter case, closely related sister species should be found across such a boundary. To achieve such a situation, preliminary stages are expected, where phylogeographic breaks followed by genetic cryptic speciation would be observed. Biogeographic boundaries, in the Cape Point/Cape Agulhas region of southern Africa, offer an ideal system to test such predictions. Here, we studied two intertidal clinid fish species that are endemic to southern Africa, Clinus superciliosus (n = 127) and Muraenoclinus dorsalis (n = 114). Using mitochondrial control region, 16S rRNA, 12S rRNA and NADH2 genes and the nuclear rhodopsin and the first intron of the S7 ribosomal protein gene, we show both phylogeographic breaks and likely cryptic speciation in each species. Pairwise Φ(st) results suggest population genetic structuring for both species, with higher levels for M. dorsalis (Φ(st) = 0.34-0.93) than for C. superciliosus (Φ(st) = 0.1-0.74). Further, we recover two and three distinct lineages within M. dorsalis and C. superciliosus, respectively. Phylogenetic topologies, concordance between nuclear and mitochondrial markers and levels of sequence divergence, which are consistent with closely related sister species pairs, suggest the presence of cryptic species. Our results therefore meet the expectation for reduced gene flow at a biogeographic barrier, which translates into significant genetic breaks and cryptic sister species.


Subject(s)
Demography , Genetic Speciation , Genetic Variation , Perciformes/genetics , Phylogeny , Animals , Base Sequence , Cluster Analysis , DNA, Mitochondrial/genetics , Gene Flow/genetics , Genetics, Population , Likelihood Functions , Locus Control Region/genetics , Models, Genetic , Molecular Sequence Data , Multienzyme Complexes/genetics , NADH, NADPH Oxidoreductases/genetics , Oceans and Seas , Phylogeography , RNA, Ribosomal/genetics , RNA, Ribosomal, 16S/genetics , Rhodopsin/genetics , Sequence Analysis, DNA , South Africa , Species Specificity
2.
J Acoust Soc Am ; 100(3): 1878-86, 1996 Sep.
Article in English | MEDLINE | ID: mdl-8817910

ABSTRACT

Sound production of gray whales was investigated to determine their acoustic repertoire along the migration route, and to compare sound production in deep and shallow water. Recording was conducted off Monterey Bay and Carmel Bay, California, during the annual migrations of 1988 through 1991. Sounds were analyzed through digital signal processing. Six acoustic variables were measured. Three variables were used for final classification, chosen for their clarity in the presence of high levels of ambient noise (poor signal-to-noise ratio). These variables were 3-dB bandwidth, center frequency, and harmonic/sideband interval. Q ratio was used as an indicator of how broadband or narrow band a signal was relative to other gray whale signals. Four categories of signals were determined: M1, M3, M4, and M5. All signal types were concentrated below 1500 Hz. M3 signals had the lowest center frequency, averaging below 100 Hz. M1 were pulses and bonging signals, M3 were low-frequency moans, M4 were grunts, and M5 were subsurface exhalations. The rate of sound production was lower when whales traveled over deep water than over shallow water. Rate of sound production was less along the migration route compared to the lagoons. M3 signals were the most common, comprising 46.6% of the repertoire along the migration route, with M1 signals comprising 37.4%.


Subject(s)
Vocalization, Animal , Whales , Acoustics , Animals , Sound Spectrography
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