Distribution of Diploid and Tetraploid Species of Gray Tree Frogs (Hyla chrysoscelis and Hyla versicolor) in Kansas

1987 ◽  
Vol 117 (1) ◽  
pp. 214 ◽  
Author(s):  
David M. Hillis ◽  
Joseph T. Collins ◽  
James P. Bogart
2011 ◽  
Vol 279 (1733) ◽  
pp. 1583-1587 ◽  
Author(s):  
Mitch A. Tucker ◽  
H. C. Gerhardt

For polyploid species to persist, they must be reproductively isolated from their diploid parental species, which coexist at the same time and place at least initially. In a complex of biparentally reproducing tetraploid and diploid tree frogs in North America, selective phonotaxis—mediated by differences in the pulse-repetition (pulse rate) of their mate-attracting vocalizations—ensures assortative mating. We show that artificially produced autotriploid females of the diploid species ( Hyla chrysoscelis ) show a shift in pulse-rate preference in the direction of the pulse rate produced by males of the tetraploid species ( Hyla versicolor ). The estimated preference function is centred near the mean pulse rate of the calls of artificially produced male autotriploids. Such a parallel shift, which is caused by polyploidy per se and whose magnitude is expected to be greater in autotetraploids, may have facilitated sympatric speciation by promoting reproductive isolation of the initially formed polyploids from their diploid parental forms. This process also helps to explain why tetraploid lineages with different origins have similar advertisement calls and freely interbreed.


Genome ◽  
2020 ◽  
Vol 63 (11) ◽  
pp. 547-560 ◽  
Author(s):  
James P. Bogart ◽  
Patrick Burgess ◽  
Jinzhong Fu

Hyla chrysoscelis and H. versicolor are common treefrogs in eastern North America and are a cryptic diploid–tetraploid species pair. They are morphologically identical but H. versicolor is a tetraploid. They can be identified acoustically by the male’s advertisement mating call, which has a pulse repetition rate that has twice as many pulses per second in the diploid species, H. chrysoscelis. We used isozymes, microsatellite DNA alleles, and mitochondrial cytochrome b sequences to test the hypothesis that gene exchange occurs between the diploid and tetraploid species in sympatric populations. Each method provided results that are best explained by occasional hybridization of female H. versicolor and male H. chrysoscelis. We propose that H. versicolor first arose from an autotriploid H. chrysoscelis female that produced unreduced triploid eggs. After H. versicolor became established, genes could be passed from H. chrysoscelis to H. versicolor in sympatric populations when these species hybridize. Their F1 female progeny produce unreduced triploid eggs that are fertilized by haploid H. chrysoscelis sperm to reconstitute H. versicolor. Genes can be passed from diploid H. chrysoscelis to tetraploid H. versicolor in sympatric populations.


1982 ◽  
Vol 60 (6) ◽  
pp. 1441-1445 ◽  
Author(s):  
Brian O. Reilly ◽  
P. T. K. Woo

Laboratory-raised grey tree frogs, Hyla versicolor LeConte, infected with either Trypanosoma andersoni Reilly and Woo or Trypanosoma grylli Nigrelli were fed on by laboratory-raised leeches, Batracobdella picta (Verrill). Trypanosoma andersoni multiplied by binary fission as sphaeromastigotes and epimastigotes in the gut of B. picta at 22 ± 1 °C. Some sphaeromastigotes and epimastigotes contained yellow granules. Two types of metatrypanosomes were found in the digestive tract of the leech at 24 days. Trypanosomes from leeches which had infected blood meals 35 days earlier were not infective when inoculated intraperitoneally or by the leeches feeding on laboratory raised H. versicolor. Trypanosoma grylli did not develop in B. picta at 22 ± 1 °C


Genetics ◽  
1983 ◽  
Vol 103 (4) ◽  
pp. 753-769
Author(s):  
Roy G Danzmann ◽  
James P Bogart

ABSTRACT Intra- and interspecific cross combinations between the tetraploid treefrog Hyla versicolor, and between H. versicolor and the diploid treefrog Hyla chrysoscelis were performed. Progeny phenotypes resulting from these crosses were examined electrophoretically using a polymorphic glutamate oxaloacetic transminase (GOT-1) locus, to determine the mechanism of chromosome segregation in H. versicolor, and to test theoretical expectations for isozyme expression in interspecific (2n × 4n or 4n × 2n) hybrids. In some intraspecific tetraploid crosses progeny phenotypes fit a disomic mode of segregation, whereas in other crosses a tetrasomic mode of segregation was the most probable. Additional crosses produced phenotypic ratios that conformed to either a disomic or tetrasomic mode of segregation. These results suggest that a polymorphism, with respect to segregation of gametes, exists in H. versicolor, resulting from differences in chromosome pairings during meiosis I. This polymorphism in gametic segregation occurred in both sexes. Certain crosses, however, produced phenotypic ratios that did not conform to any chromosome segregation model. Progeny phenotypes observed from most interspecific crosses conformed to expected interspecific isozyme staining intensity models. Symmetrical heterozygotes, representing either a single dose for both alternate alleles or double doses for both alternate alleles, were also observed. Such phenotypes are unexpected in triploid progeny. A null allele was postulated to account for the aberrant segregation ratios and phenotypes observed in certain intra- and interspecific crosses.


1995 ◽  
Vol 198 (7) ◽  
pp. 1527-1538 ◽  
Author(s):  
D McLister ◽  
E D Stevens ◽  
J P Bogart

Isometric twitch and tetanus parameters, force-velocity curves, maximum shortening velocity (Vmax) and percentage relaxation between stimuli (%R) across a range of stimulus frequencies were determined for a muscle used during call production (the tensor chordarum) and a locomotor muscle (the sartorius) for three species of hylid frogs, Hyla chrysoscelis, H. versicolor and H. cinerea. The call of H. chrysoscelis has a note repetition rate (NRR) approximately twice as fast as the call of H. versicolor (28.3, 42.5 and 56.8 notes s-1 for H. chrysoscelis and 14.8, 21.1 and 27.4 notes s-1 for H. versicolor at 15, 20 and 25 degrees C, respectively). Hyla cinerea calls at a very slow NRR (Approximately 3 notes s-1 at 25 degrees C). Hyla versicolor evolved from H. chrysoscelis via autopolyploidy, so the mating call of H. chrysoscelis is presumably the ancestral mating call of H. versicolor. For the tensor chordarum of H. chrysoscelis, H. versicolor and H. cinerea at 25 degrees C, mean twitch duration (19.2, 30.0 and 52.9 ms, respectively), maximum isometric tension (P0; 55.0, 94.4 and 180.5 kN m-2, respectively), tetanic half-relaxation time (17.2, 28.7 and 60.6 ms, respectively) and Vmax (4.7, 5.2 and 2.1 lengths s-1, respectively) differed significantly (P < 0.05) among all three species. The average time of tetanic contraction to half-P0 did not differ significantly between H. chrysoscelis (14.5 ms) and H. versicolor (15.8 ms) but was significantly longer for H. cinerea (52.6 ms). At 25 degrees C, Vmax differed significantly among the sartorius muscles of H. chrysoscelis, H. versicolor and H. cinerea (5.2, 7.0 and 9.8 lengths s-1, respectively) but mean twitch duration (29.5, 32.2 and 38.7 ms, respectively), P0 (252.2, 240.7 and 285.1 kN m-2, respectively) and tetanic half-relaxation time (56.3, 59.5 and 60.7 ms, respectively) did not differ significantly. The average time of contraction to half-P0 did not differ significantly between H. chrysoscelis (23.7 ms) and H. versicolor (22.9 ms) but was significantly shorter for H. cinerea (15.6 ms). The only consistent contractile differences found in this study between the calling muscle and locomotor muscle of H. chrysoscelis, H. versicolor and H. cinerea were that the calling muscles generated less tension and their force-velocity relationship was much more linear. These differences may be attributable to ultrastructural differences between calling and locomotor muscles.(ABSTRACT TRUNCATED AT 400 WORDS)


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