Eleutherodactylus nitidus (Peters, 1870)
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publication ID |
https://doi.org/ 10.5281/zenodo.11265040 |
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publication LSID |
lsid:zoobank.org:pub:9B3E8106-74E8-428F-B0BB-3CCD9EFDF0F3 |
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DOI |
https://doi.org/10.5281/zenodo.11265062 |
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persistent identifier |
https://treatment.plazi.org/id/670387A7-FFB1-FF9D-FF0F-F8B2FC55F9BC |
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treatment provided by |
Felipe |
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scientific name |
Eleutherodactylus nitidus |
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Summary Data for Eleutherodactylus nitidus View in CoL Species Group Members
To help differentiate between the two new species described above, and the related species in the Eleutherodactylus nitidus species group, important morphological, mensural, and call differences of all of the species in this group are collated into a single table ( Table 3 View Table 3 ), and photographs of related species in the E. nitidus species group are provided ( Figs. 9–10 View Fig View Fig ). The distributions of the species in the E. nitidus group are mapped in Figs. 7 View Fig and 13. View Fig
Differentiating the Advertisement Calls of Closely Related Eleutherodactylus nitidus Species Group Members
Recordings were made from 120 calling males of all 24 species of Eleutherodactylus from western Mexico. The calls of the species analyzed were found to fall into five different categories of a rapid burst whistle (trill), a drawn-out whistle (whistle), a strong high-pitched chirp (peep), a soft high-pitched chirp (chirp), and a drawn-out chirp (pipe). Of the species analyzed herein, four ( E. dilatus , E. nebulosus , E. pipilans , E. sentinelus ) produce a strongly high-pitched chirp (peep), four ( E. albolabris , E. nitidus , E. orarius , E. petersi ) produce a drawn-out whistle (whistle), two ( E. maculabialis and E. syristes ) produce multi-note or pulsed calls (trill) of various rates and notes, and one ( E. maurus ) produces a slow and drawn-out chirp (pipe). While a detailed account is given of the calls of the species we describe here, as well as some of their relatives, we refrain from giving detailed descriptions of the calls of E. nitidus , E. albolabris , E. orarius , E. petersi , E. pipilans , E. nebulosus , and “ E. rubrimactulatus ” pending a more detailed taxonomic study of this species complex.
Eleutherodactylus dilatus . The advertisement call of E. dilatus is a single high-pitched “chirp” best described as a “peep” ( Fig. 11C View Fig ). Calls recorded at the type locality consist of a rapid chirp, with an average duration of 110 ms, and a dominant frequency ranging between starting at 2,550 kHz and 2,780 kHz.
Eleutherodactylus maculabialis . The advertisement call of E. maculabialis is a relatively slow multi-note “trill” ( Fig. 3 View Fig ). Calls recorded at the type locality consist of slow six-note trills with a duration of 180–210 ms, and a dominant frequency starting at 2,600 –2,900 kHz and rising to 3,050 –3,200 kHz. The call interval is about 40–55 ms ( Fig. 3A View Fig ). At a nearby locality at 1,320 m asl ( Fig. 3B View Fig ), calls were recorded of two males which varied from the type locality in consisting of five-note trills with an average duration of 230 ms and a dominant frequency starting at 3,630 kHz and reaching 4,000 kHz ( Table 4 View Table 4 ).
Eleutherodactylus maurus . The advertisement call of E. maurus is a single, drawn-out “chirp” best described as a “pipe.” Calls recorded near Ocuilan, in Estado de México, consisted of a single chirp with a duration of 205 ms, and a dominant frequency starting at 2,760 kHz and rising to 3,150 kHz. The amplitude was strongest at the middle of a call ( Fig. 11D View Fig ). At a locality near Taxco, Guerrero, a call of E. maurus was recorded which consisted of a single, drawn-out chirp. However, the call was longer, averaging 275 ms and the amplitude was distributed in three sub-pulses. This indicates a further need to investigate this population.
Eleutherodactylus sentinelus . The advertisement call of E. sentinelus is a single high-pitched “chirp” best described as a “peep” ( Fig. 3 View Fig ). Calls recorded at the type locality consist of a rapid chirp, with an average duration of 160 ms, and a dominant frequency starting at 2,560 kHz and rising to 3,100 kHz ( Fig. 3D View Fig ). Calls recorded above the type locality at 1,900 m asl ( Fig. 3C View Fig ) are slightly shorter and of higher frequency, with an average duration of 120 ms, and a dominant frequency starting at 2,700 kHz and finishing at 3,300 kHz ( Table 4 View Table 4 ).
Eleutherodactylus syristes . The advertisement call of E. syristes is a rapid but long multiple-pulse “trill” ( Fig. 11A–B View Fig ). Calls recorded at two different localities in Guerrero consisted of 49–60 pulses, about 10 ms apart, with a total duration of the call averaging 500– 560 ms. The GoogleMaps dominant frequency at Agua de Obispo GoogleMaps , Guerrero, was between 2,700 –3,170 kHz, starting lower, peaking, and then lowering again ( Fig. 11A View Fig ). At a second locality, slightly lower than Agua de Obispo GoogleMaps , east of Highway GoogleMaps 95, the calls tended to have a dominant frequency ranging between 3,000 –3,390 kHz ( Fig. 11B View Fig ).
Eleutherodactylus albolabris . The advertisement call of E. albolabris is a single, multi-pulsed whistle, with the call continuous amongst the pulses and with a duration of approximately 150–250 ms ( Fig. 11F View Fig ). Calls recorded at the type locality at Agua de Obispo had a duration of 160 ms, and started at a dominant frequency of 2,840 kHz rising to 3,015 kHz. Calls varied between 7–10 continuous pulses. At a second locality, near Vallecitos in the Municipality of José Azueta , Guerrero, the calls had a duration of 240 ms, and started at a dominant frequency of 2,740 kHz which rose to 2,915 kHz. Calls started with a multi-pulsed trill and then ended with several distinct pulses. This population’s call is best described as a combination of a “trill” with a “whistle” ( Fig. 11E View Fig ).
Molecular Analysis of the Eleutherodactylus nitidus View in CoL Species Group
The molecular phylogeny based on the mitochondrial rRNA 16S recovered a well-supported Eleutherodactylus nitidus species group (posterior probability (pp) 1; Figs. 12 View Fig and S 1 View Fig ), which is sister to the E. modestus group as defined by Grünwald et al. (2018). As with previous phylogenies of the group based on 16S, some of the intermediate nodes in the phylogeny are not well supported (pp <0.5), and we have collapsed all nodes below this value.
In the Eleutherodactylus nitidus species group, we recovered two main clades. The first one is composed of E. pipilans , E. erythrochomus , and E. nebulosus , while the second group includes all the other species. In the second group, many of the intermediate nodes have little to no support. However, individual species do show strong support (pp = 1) in most cases, including E. dilatus , E. sentinelus , E. maurus , and E. syristes , while E. maculabialis has a posterior support of 0.86.
All the remaining species in the group form a second, well-supported clade (pp =0.99). In this clade, we recovered an early split between Eleutherodactylus albolabris and the other species, which include E. orarius , E. petersi , E. nitidus , and a hitherto undescribed form from Jalisco and Nayarit ( Fig. 13 View Fig ). We refrain from describing the western-most form at this time, as material from the type locality of E. petersi is unavailable, so the relationship of the western form with E. petersi remains unclear.
We believe that a more detailed study of the taxa related to E. nitidus is needed, when more thorough sampling is available and employing more populationlevel specific tools, such as genome-wide SNP data, in order to better understand the patterns of gene-flow and introgression.
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