Published August 7, 2023 | Version v1
Taxonomic treatment Open

Adenomera guarani Zaracho & Lavilla & Carvalho & Motte & Basso 2023, sp. nov.

  • 1. Laboratorio de Herpetología, Departamento de Biología, Facultad de Ciencias Exactas y Naturales y Agrimensura, Universidad Nacional del Nordeste, Av. Libertad 5470, (3400) Corrientes, Argentina.
  • 2. Unidad Ejecutora Lillo (UEL), CONICET-FML, Miguel Lillo 251, (4000) S. M. Tucumán, Argentina.
  • 3. Departamento de Zoologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • 4. Museo Nacional de Historia Natural del Paraguay, Km 10,5 Ruta Mcal. Estigarribia, San Lorenzo, Paraguay.
  • 5. Instituto de Diversidad y Evolución Austral (IDEAus-CONICET), Bvd. Brown 2915; and Facultad de Ciencias Naturales y Ciencias de la Salud, Universidad Nacional de la Patagonia " San Juan Bosco ", (9120) Puerto Madryn, Chubut, Argentina.

Description

Adenomera guarani sp. nov.

urn:lsid:zoobank.org:act: 13EA7E3F-AFF1-4999-985E-EAB9B45109AA

Figs 9–12; Tables 2–3

Diagnosis

Adenomera guarani sp. nov. is recognized within Adenomera by the following combination of character states: (1) body robust, (2) medium size (adult male SVL = 20.1–26.4 mm); (3) light-colored, broad mid-dorsal stripe with diffuse borders, extending from above the vent to the scapular region; (4) a dark mask-like pattern formed by an inverted triangle in the interorbital region; (5) toe tips unexpanded with tapered point; (6) antebrachial tubercle absent; (7) exotrophic larvae; (8) labial tooth row formula (LTRF): 2(2)/3(1); (9) single-note advertisement call; (10) call notes formed by incomplete pulses; (11) relatively high note repetition rate (73–147 per minute); and (12) low pulse number (4–9 per note).

Etymology

The specific name guarani, used as a noun in apposition and refers to the Guaraní, a native indigenous group that inhabited in the past a vast region in South America, including areas where the new species occurs. Currently, a few indigenous communities still live in wild areas. However, the Guaraní language (Avañe′ẽ), is usually spoken by people in Paraguay and other neighboring countries and also utilized to name innumerous geographical features (e.g., rivers, wetlands, hills), animals, plants, towns, and cities.

Type material

Holotype ARGENTINA • ♂ (Fig. 9); Corrientes Province, Capital Department, Corrientes City, Campus Universitario, Universidad Nacional del Nordeste; 27°28′04″ S, 58°46′53″ W; 60 m a.s.l.; 8 Feb. 2007; V.H. Zaracho leg.; UNNEC 9074.

Paratypes ARGENTINA – Corrientes • 1 ♂; Capital Department, Corrientes City; 27°28′04″ S, 58°46′53″ W; 8 Nov. 2016; V.H. Zaracho leg.; UNNEC 8994 • 1 ♂; same collection data as for preceding; LGE 25740 • 2 ♂♂; same collection data as for preceding; Feb. 2011; F. Abreliano leg.; UNNEC 11977, 11978 • 3 ♀♀; Capital Department, Corrientes City; 27°29′26″ S, 58°50′13″ W; 24 Jun. 2005; V.H. Zaracho, J.A. Ruiz García and J.A. Céspedez leg.; UNNEC 8365 to 8367 • 1 ♀; Capital Department, San Cayetano; 27°33′04″ S, 58°40′37″ W; 18 Mar. 2011; J.L. Acosta and M. Ortiz leg.; LGE 25741 • 1 ♀; San Cosme Department, Paso de la Patria; 27°19′27″ S, 58°34′05″ W; 29 Jul. 2007; J.L. Acosta and S. Palomas leg.; UNNEC 9551 • 1 ♂; same collection data as for preceding; 2 Dec 2006; V.H. Zaracho and M.R. Ingaramo leg.; UNNEC 9003. – Chaco • 1 ♂; San Martin Department, Paraje Las Tablas; 26°11′40″ S, 59°38′45″ W; 13 Dec. 2005; V.H. Zaracho, R.H. Aguirre and J.A. Céspedez leg.; UNNEC 8531. Formosa • 2 ♂♂; Patiño Department, Comandante Fontana; 25°20′19″ S, 59°41′19″ W; 24 Nov. 2007; V.H. Zaracho leg.; UNNEC 9728, 9729 • 3 ♂♂; Pilcomayo Department, Laguna Naick Neck; 25°10′58″ S, 58°07′29″ W; 29 Feb. 2008; V.H. Zaracho and J.L. Acosta leg.; UNNEC 9856 to 9858 • 1 ♂; Pilcomayo Department, Laguna Naick Neck; 25°10′58″ S; 58°07′29″ W; 15 Oct. 2009; V.H. Zaracho leg.; UNNEC 11964.

PARAGUAY – Concepción • 4 ♂♂; 85 km NE of Concepción, Arroyo Capitigo; 22°46′30″ S, 56°47′56″ W; 11 Nov. 1981; L. Fitzgerald, A.L. Aquino and N.J. Scott leg.; MNHNP 0413, 0415, 0421, 0436. – Presidente Hayes • 1 ♀; Ea. La Golondrina; 24°57′02″ S, 57°42′07″ W; 9 Sep. 1982; A.L. Aquino and D. Norman leg.; MNHNP 0783. – Central • 1 ♂; Villeta; 25°30′48″ S, 57°33′30″ W; 31 Aug. 1982; A.L. Aquino and D. Norman leg.; MNHNP 0417. Amambay • 1 ♂; Parque Nacional Cerro Corá; 22°39′56″ S, 56°00′24″ W; 13 Oct. 2009; V.H. Zaracho and M. Motte leg.; MNHNP 11333. Alto Paraguay • 3 ♀♀; Ea. Doña Julia, 5 km N of Bahía Negra; 20°15′34″ S, 58°12′02″ W; 1 Oct. 1984; A.L. Aquino and D. Norman leg.; MNHNP 0784 to 0786. Ñeembucú • 1 ♂; 19.8 km SSW of Pilar; 26°58′47″ S, 58°22′52″ W; 20 Feb. 1996; P. Freed leg.; MNHNP 10046 • 1 ♂; same collection data as for preceding; UNNEC 13938.

Description

Holotype

Body small, robust; head nearly as broad as long (HW/HL = 1.1); snout sub-elliptical dorsally and acuminate laterally; canthus rostralis round; loreal region slightly concave; eye dorsolateral, its diameter about 32% of head length; pupil horizontal, elliptical; palpebral membrane translucent, bordered in its upper edge by a black streak; tympanum distinct, its diameter about 63% of the eye diameter. Tympanic membrane translucent, with some melanophores on the central region; supratympanic fold well developed, extending from the back of the eye to arm insertion; nostrils anterolateral, closer to the tip of the snout than to the eye, flanged in almost all their extension, except on the inner edge; internarial distance about 26% of head width; triangular postcommissural gland; lower lip with a medial projection that fits into a notch in the upper lip; tongue ovoid; vocal sac subgular with a fold parallel to jaw extending to the forearm; maxillary and premaxillary teeth present; vomerine teeth located posterior to and between choanae, arranged in straight transverse rows. Dorsum glandular, with more conspicuous glands placed on the posterior region. A pair (dorsal and lateral) of glandular rows formed by small segments starting behind the eyes and running towards the posterior part of the dorsum; ventral surface of the body smooth, with a distinct discoidal fold (pectoral few distinctive in the specimen in conservation); an axillary gland behind each arm insertion. Arms short and robust; fingertips rounded, not expanded (character state A); relative finger length IV <II ≤ I <III; nuptial asperities absent; inner metacarpal tubercle oval and ½ smaller than the outer, rounded; palmar tubercles present; prominent, rounded and entire subarticular tubercles on fingers, those on the base of each finger the most noticeable. Shank slightly longer than the thigh; thigh length about 43% SVL; relative toe lengths I <II <V <III <IV, with rounded tip, neither expanded nor flattened (character state A); toes without webbing or lateral fringing; metatarsal tubercles oval, not keratinized; outer tubercle smaller than the inner; subarticular tubercles present; plantar and supernumerary tubercles absent; posterior part of dorsum and ventral surface of both heel and metatarsals with dispersed, small and white-tipped tubercles; distinct inner tarsal fold with a single row of small, white-tipped tubercles on the edge, running for about two-thirds of the tarsus length. Ventral surfaces of the legs smooth, except the ventral surface of thighs, which is areolate. Vent fold distinct on the upper anus. A cream, rounded and small paracloacal gland is present on each side of the vent.

Measurements of the holotype (mm)

SVL = 21.6, HL = 7.3, HW = 8.3, ED = 2.4, TD = 1.2, EN = 1.9, IOD = 2.2, IND = 2.2, UAL = 3.1, LAR = 4.3, HAL = 5.2, THL = 9.2, TIL = 9.7, TAL = 5.6 and FL = 11.2.

Coloration of the holotype

In life, dorsum medium grayish-brown, with a black mask-like patch on the interorbital region; chevron shaped mark on the scapular area, and several smaller spots on dorsum. Broad, light mid-dorsal stripe with diffuse borders, running from the chevron-shaped mark to the vent fold. Dorsal glandular row mainly highlighted in dark; lateral glandular row and paracloacal glands cream. Faded orange patches on elbows and heels. Distinct dark longitudinal bars on the dorsal region of lower arms, thighs, and shanks. Dark marks on lateral upper lip and behind nostrils. Posterior part of the supratympanic fold and the border of the upper eyelids highlighted with dark brown coloration. Body ventrally whitish, immaculate; gular region and ventral surface of thighs faded pink; lateral fold of the vocal sac black. In preservative, color patterns as in life, except for a duller coloration.

Comparisons with congeners

Adenomera guarani sp. nov. (robust body shape) is distinguished from three congeners with slender body shapes (A diptyx, A. martinezi, and A. saci). The body size of A. guarani (male SVL = 20.1–26.4 mm) differs from that of large-sized species of the genus, especially A. glauciae (male SVL = 27.6–30.4 mm) and A. lutzi (male SVL = 27.5–33.5 mm). Adenomera guarani has a broad mid-dorsal stripe, whereas A. diptyx, A. martinezi, and A. saci have a vertebral pin stripe. Additionally, A. guarani is distinguished from A. diptyx by a mask-like pattern in the interorbital region (an interorbital bar in A. diptyx). Adenomera guarani has toe tips unexpanded with a tapered point (character state A), whereas the following 14 species have moderately to fully expanded toe tips (states C–D, i.e., swollen, knob-shaped toe tips and toe discs, respectively): A. ajurauna, A. amicorum, A. andreae, A. chicomendesi, A. engelsi, A. gridipappi, A. guarayo, A. heyeri, A. inopinata, A. lutzi, A. marmorata, A. nana, A. simonstuarti, and A. tapajonica. Adenomera guarani differs from A. amicorum, A. aurantiaca, A. cotuba, A. glauciae, A. gridipappi, A. inopinata, A. kayapo, A. lutzi, A. phonotriccus, and A. tapajonica by the absence of an antebrachial tubercle. The exotrophic larva of A. guarani distinguishes the new species from almost all congeners, except A. saci and A. thomei (Almeida & Angulo 2006; Carvalho & Giaretta 2013b), as well as A. diptyx and A. martinezi (assumed based on calling habitat, but their tadpoles remain unknown; Carvalho & Giaretta 2013b; T.R. Carvalho, field obs.). The tadpole of A. guarani has a labial tooth row formula (LTRF): 2(2)/3(1), whereas that of A. thomei has a LTRF: 2(2)/3 (Almeida & Angulo 2006).

Adenomera guarani sp. nov. can also be distinguished from congeners in advertisement call traits. The single-note call of A. guarani differs from the multi-note calls of A. amicorum, A. aurantiaca, A. cotuba, A. glauciae, A. gridipappi, A. inopinata, and A. simonstuarti. Among Adenomera with single-note calls, call notes of A. guarani are formed by incomplete pulses, whereas those of A. guarayo and A. phonotriccus are formed by complete pulses, and those of A. ajurauna, A. bokermanni, A. engelsi, A. kweti, A. lutzi, A. marmorata, A. nana, and A. saci are nonpulsed. From congeners also having single-note calls formed by incomplete pulses, A. guarani differs from A. andreae (24–68 per minute), A. araucaria (23–46 per minute), A. chicomendesi (5–29 per minute), A. heyeri (22–27 per minute), A. juikitam (30–52 per minute), A. kayapo (23–33 per minute), A. tapajonica (52–59 per minute), and A. thomei (10–23 per minute) by a higher note repetition rate (73–147 per minute; Table 3), and by a lower note rate than that of A. diptyx (176–299 per minute; Table 3). Adenomera guarani differs from A. coca (10–15; Angulo & Reichle 2008) and A. martinezi (15–21; Carvalho & Giaretta, 2013a) by a lower pulse number per note (4–9; Table 3). Adenomera guarani cannot be consistently distinguished from the allopatric A. hylaedactyla in any of the analyzed call traits (Carvalho et al. 2019a). Still, these two species are segregated by distinct breeding habitats and reproductive modes. Adenomera guarani, endemic to the Humid Chaco and Pantanal Wetlands, has exotrophic larvae, whereas the Amazonian A. hylaedactyla has endotrophic larvae (Kokubum & Souza 2008; Carvalho et al. 2019a). This is the most reliable character in the discrimination of the two species, in addition to their phylogenetic relationships not sharing an immediate common ancestor (Fig. 2). Adenomera guarani is the sister taxon of A. diptyx, from which the new species is distinguished by morphological and acoustic traits.

Variation (Figs 10–12)

Measurements of males and females are shown in Table 2. Most specimens show small, white-tipped tubercles on the dorsal surface of the shank, heel, and the sole of the foot, but absent on the dorsal surface of thigh; tubercle density is variable and usually visible under magnification. The supratympanic fold in some specimens is barely visible (may be due to preservation methods). Paracloacal glands generally developed well, but sometimes only a colored spot. Axillary glands are conspicuous in recently fixed specimens (Fig. 12B). Postcommissural gland is variable in size and form. Inner metacarpal tubercle is ⅓ to ⅔ smaller than the outer. Palmar tubercles are variable in number (one or two by finger), varying even between the hands of the same specimen. Dorsal and lateral glandular rows have varying degrees of development (i.e., the number of individual glands and their extent along the body length). When well-developed (as observed in most specimens), the dorsal row extends from behind the eye and the lateral row runs from the posterodorsal region of the tympanum, almost overlapping with the supratympanic fold. Some specimens also have additional small glands posteriorly, sometimes a pair highlighting as a lumbar gland, variable in size and dark colored (Fig. 12A).

A great variation of color patterns is exhibited in living Adenomera guarani sp. nov. (Figs 10–11). Dorsal coloration is variable in shades of light to dark brown; even in the same individual exposed to different conditions of luminosity. Sometimes the broad mid-dorsal stripe is poorly evident (Figs 10C, F–G, 11M) and the mask pattern on the interorbital region is easier to distinguish in preserved specimens. Dark marks on the posterior surface of the dorsum variable in shape and number. The coloration of the glandular rows is homogeneous (dorsal row dark and lateral row light). The medial region of the paracloacal gland is always light-colored, but its borders bear dispersed dark-colored marks of variable size and shape. Color pattern on legs is variable from well-defined cross-bands to a splash of small and dark marks. In life, the ventral surface is usually whitish, but one individual (UNNEC 8357) showed a ventral coloration with black stains.

Sexual dimorphism is evident. The snout of males in lateral view is shovel-shaped, with a well-developed, fleshy white ridge; in females, the snout is rounded and without ridges (Fig. 12C–D). Aside from the snout shape, nostrils are closer to the tip of the snout in females than in males. Only males have axillary glands. Paracloacal glands are more well-developed in males than in females (smaller or represented only by a pair of pale, small spots (Fig. 12E–F). Vocal sac in males with dark lateral sides (Fig. 12E). In life, the gular region of females is white (Fig. 12H).

Advertisement call (Fig. 7, Table 3)

We characterized the advertisement call of A. guarani sp. nov. based on 23 males from Argentina and Brazil (N = 399 quantified calls and 2423 quantified pulses; see Appendix 2 for locality data and voucher specimens). The call consists of single notes given at a repetition rate of 73 to 147 per minute (102± 18). Note duration varies from 45 to 98 (66± 11) ms, and the rise time is 1 to 59 % of note duration (10 ± 12). Notes are formed by 4 to 9 (6 ±1) incomplete pulses (i.e., not separated by silent gaps) emitted at a repetition rate of 60 to 146 per second (106 ± 16). The dominant frequency coincides with the second harmonic, ranging from 3984 to 4974 (4329 ± 165) Hz. Notes can have a modest or pronounced frequency modulation, either positive or negative, ranging from -345 to 603 (150± 112) Hz.

Natural history

Data about reproductive aspects from Brazilian and Argentinean populations were published by Zaracho & Kokubum (2017) under the name A. diptyx. In summary, Adenomera guarani sp. nov. lay eggs in a foam nest inside an underground chamber with the entrance partially closed, constructed by males near temporary pools and seasonally flooded areas. When the breeding microhabitat is flooded, embryos/tadpoles are washed out of the underground chamber and complete their development in the water. The larvae have functional mouthparts and a labial tooth row LTRF: 2(2)/3(1) (Zaracho & Kokubum 2017: fig. 2C). Diet and parasitism from Argentinean populations were provided also by Zaracho & Lamas (2008) and Zaracho et al. (2012a), both under the name A. diptyx.

Chromosome number

The chromosome number 2n = 26 of A. guarani sp. nov. from Argentinean populations was reported by Zaracho & Hernando (2011) under the name of Adenomera diptyx.

Geographic distribution and habitat (Fig. 1)

Adenomera guarani sp. nov. occurs in Argentina, Paraguay, and Brazil, associated mainly with the Paraguay and Paraná river basins, and the Pantanal wetlands. All known populations of Adenomera from the Argentinean Humid Chaco belong to A. guarani.

Adenomera guarani sp. nov. inhabits open areas that can easily be flooded by rainwater during the wet season. The species is abundant in partially urbanized areas, such as roadsides or gardens. Males call amidst grasses, outside water, during the dusk and early in the night. They can easily be detected by their vocalizations, but due to their small size and secretive habits, are very difficult to observe.

At Parque Nacional Cerro Corá (Amambay Department, Paraguay), populations of A. guarani sp. nov. and A. diptyx were found at two sites less than 1 km from each other. Two males of A. guarani were found calling at dusk at the margins of a pond inside the forest, near Aquidabán stream, and A. diptyx males were calling on roadsides amidst grasses and at the margin of a stream inside the forest. Other species calling syntopically with A. guarani were Scinax fuscovarius (Lutz, 1925), S. berthae (Barrio, 1962), Pithecopus azureus (Cope, 1862), Dendropsophus nanus (Boulenger, 1889), D. minutus (Peters, 1872), Leptodactylus elenae Heyer, 1978, Rhinella diptycha (Cope, 1862), and Physalaemus nattereri (Steindachner, 1863). In Argentina, A. guarani was also found on roadsides associated with Copernicia alba Morong palms and Ludwigia sp. grassland, syntopically with S. acuminatus (Cope, 1862), P. azureus, D. nanus and Boana raniceps (Cope, 1862), and in banana plantations, under fallen leaves.

Conservation

In Paraguay, Adenomera guarani sp. nov. occurs in two national parks: Cerro Corá and Ybicuy. In Argentina, it was found in the Parque Nacional Mburucuyá (Corrientes Province), Parque Nacional Chaco (Chaco Province), and on the outskirts of Parque Nacional Río Pilcomayo (Formosa). Recently, Argentinean populations, under the name of Leptodactylus diptyx, were categorized at national level as “No Amenazada” (= Least Concern according to IUCN) since the finding of several new populations. Apparently, A. guarani reproduces in urbanized areas in the Argentinean Humid Chaco (Zaracho et al. 2012b).

Adenomera guarani sp. nov.

ARGENTINA – Corrientes • 3 ♀♀; Corrientes city (type locality); 27°28′04′′ S, 58°46′53″ W; UNNEC 9000, 9001, 11967 • 10 ♂♂; same collection data as for preceding; UNNEC 8974, 9606, 9704, 11961 to 11962, 11965, 11968 to 11970, 13611 • 2 ♂♂; same collection data as for preceding; MNHNP 12907, 12908 • 1 spec. (sex no determined); same collection data as for preceding; UNNEC 13607 • 1 ♀; Corrientes city; 27°29′26″ S, 58°50′13″ W; UNNEC 8362 • 6 ♂♂; same collection data as for preceding; UNNEC 8293 to 8295, 8354, 8363, 8505 • 1 ♂; Ituzaingó; 27°29′50″ S, 56°42′12″ W; UNNEC 12331 • 2 ♂♂; San Cayetano; 27°33′04″ S, 58°40′37″ W; MNHNP 12909, 12910 • 6 ♀♀; same collection data as for preceding; UNNEC 11974, 11976, 11980 to 11982, 13608 • 2 ♂♂; same collection data as for preceding; UNNEC 13609, 13610 • 1 ♀; Parque Nacional Mburucuyá; 28°02′09″ S, 58°05′45″ W; UNNEC 5260 • 3 ♂♂; same collection data as for preceding; UNNEC 8356, 8357, 8506 • 1 ♀; Paso de la Patria; 27°19′27″ S, 58°34′05″ W; UNNEC 9076 • 2 ♂♂; same collection data as for preceding; UNNEC 9002, 9075. Chaco • 1 ♀; San Martín; 26°08′28″ S, 59°35′43″ W; UNNEC 8261 • 1 ♂; La Leonesa; 27°05′48″ S, 58°44′42″ W; UNNEC 13612. Formosa • 2 ♂♂; Comandante Fontana; 25°20′19″ S, 59°41′19″ W; UNNEC 8800, 9727 • 3 ♀♀; Laguna Naick Neck; 25°10′58″ S, 58°07′29″ W; UNNEC 9725, 9726, 9863 • 11 ♂♂; same collection data as for preceding; UNNEC 9717 to 9724, 9859, 9865, 9870 • 3 juvs; same collection data as for preceding; UNNEC 9860 to 9862 • 5 sub-adult (sex no determined); same collection data as for preceding; UNNEC 9864, 9866 to 9868, 9871.

BRAZIL – Mato Grosso do Sul • 10 ♂♂; Nhecolândia, Passo do Lontra; 19°34′00″ S, 57°00′00″ W; LHUFCG 173 to 179, 205 to 207.

PARAGUAY – San Pedro • 6 ♀♀; Lima; 23°53 09 S, 56°28 40 W; MNHNP 0419, 0422, 0434, 5696, 5701, 5702 • 8 ♂♂; same collection data as for preceding; MNHNP 0411, 0431, 0433, 0435, 5695, 5698 to 5700 • 1 ♂; same collection data as for preceding; UNNEC 13939 • 5 ♀♀; Villa del Rosario, Compañía Mbocayá; 24°26 18 S, 57°05 48 W; MNHNP 0412, 0424, 0425, 0441, 0442 • 1 ♂; Río Aguaray Guazú, 2 km NW of Lima; 23°52 28 S, 56°29 46 W; MNHNP 5332. Concepción • 1 ♀; Rancho Z; 22°58 24 S, 57°00 38 W; MNHNP 7045 • 2 ♂♂; 20 km NE of Concepción, about Route to Loreto; 23°17 45 S, 57°22 18 W; MNHNP 0432, 5703 • 1 ♀; 85 km NE of Concepción, Arroyo Capitigo; 22°46 30 S, 56°47 56 W; MNHNP 0430. Presidente Hayes • 1 ♀; Ea. La Golondrina; 24°57 02 S, 57°42 07 W; MNHNP 0428 • 1 ♀; 44 km W of Concepción, Riacho Negro; 23°27 48 S, 57°48 02 W; MNHNP 0426 • 1 ♂; same collection data as for preceding; MNHNP 0420. Caaguazú • 2 ♂♂; 24 km N of Coronel Oviedo; 25°17 19 S, 56°24 08 W; MNHNP 0414, 0440. – Central • 1 ♀; Villeta; 25°30 48 S, 57°33 30 W; MNHNP 1404. Cordillera • 1 ♂; Saltos de Piraretá; 25°29 55 S, 56°55 20 W; MNHNP 0423. Paraguari • 1 ♀; Parque Nacional Ybycuí, Fundición La Rosada; 26°01 05 S, 57°02 53 W; MNHNP 5391 • 15 ♂♂; same collection data as for preceding; MNHNP 0427, 0439, 4396, 4398, 4408, 4440, 4452, 4494, 4496, 5532, 5704 to 5708. Amambay • 2 ♀♀; Parque Nacional Cerro Corá, Administración; 22°39 56 S, 56°00 24 W; MNHNP 0443, 5710. Alto Paraguay • 1 ♀; Ea. Doña Julia, 5 km N of Bahía Negra; 20°15 34 S, 58°12 02 W; MNHNP 3699. Ñeembucú • 1 ♂; 26 km NE of Pilar; 26°39 27 S, 58°08 40 W; MNHNP 10062.

Adenomera guarani sp. nov.

BRAZIL – Mato Grosso do Sul • Nhecolândia, Passo do Lontra; 19°34′00′′ S, 57°00′00′′ W LHUFCG207 _canto078_parte 1_BEP: 29 Nov 2006, 20:47 h, air 30.0°C (LHUFCG 207).

ARGENTINA – Corrientes • Corrientes city (type locality); 27°28′04′′ S, 58°46′53′′ W FZ-UNNE 0709: 08 Feb 2007, 18:55 h, air 26.8°C

FZ-UNNE 0711: 08 Feb 2007, 19:15 h, air 26.8°C

FZ-UNNE 0712: 08 Feb 2007, 19:38 h, air 25.4°C

FZ-UNNE 0713: 08 Feb 2007, 19:45 h, air 25.5°C

FZ-UNNE 0714: 08 Feb 2007, 19:56 h, air 24.5°C

FZ-UNNE 0715: 08 Feb 2007, 20:00 h, air 24.8°C

FZ-UNNE 0716: 08 Feb 2007, 20:05 h, air 25°C (UNNEC 9074)

FZ-UNNE 0096: 22 Nov 2011, 18:20 h, air 27.7°C

FZ-UNNE 0284: 14 Nov 2013, 20:28 h, air 24.5°C (UNNEC 13611)

FZ-UNNE 1013: 13 Dec 2013, 21:25 h, air 20.6°C

FZ-UNNE 1014: 16 Dec 2013, 21:53 h, air 27.9°C

FZ-UNNE 1016: 28 Nov 2013, 21:34 h, air 17.4°C

• Paso de la Patria FZ-UNNE 0706: 10 Feb 2007, 21:42 h, air 29.1°C

FZ-UNNE 0708: 11 Feb 2007, 21:18 h, air 22.2°C

– Formosa • Laguna Naick Neck FZ-UNNE 0010: 23 Nov 2007, 19:50 h, air 22.7°C (UNNEC 9722)

FZ-UNNE 0011: 23 Nov 2007, 20:00 h, air 22.3°C(UNNEC 9723)

FZ-UNNE 0013: 23 Nov 2007, 20:10 h, air 22°C (UNNEC 9724)

FZ-UNNE 0020: 29 Feb 2008, 20:00 h, air 28.7°C (UNNEC 9856)

FZ-UNNE 0023: 29 Feb 2008, 20:35 h, air 26°C (UNNEC 9859)

• Comandante Fontana FZ-UNNE 0014: 24 Nov 2007, 21:27 h, air 20.2°C (UNNEC 9727)

FZ-UNNE 0019: 25 Nov 2007, 18:37 h, air 23.7°C

• Clorinda FZ-UNNE 0081: 15 Nov 2010; 18:30 h; 25°C

Notes

Published as part of Zaracho, Víctor H., Lavilla, Esteban O., Carvalho, Thiago R., Motte, Martha & Basso, Néstor G., 2023, Redescription of Adenomera diptyx (Boettger, 1885) (Anura, Leptodactylidae) and description of a closely related new species, pp. 1-45 in European Journal of Taxonomy 888 (1) on pages 19-41, DOI: 10.5852/ejt.2023.888.2205, http://zenodo.org/record/8222476

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FZ-UNNE , LGE , LHUFCG , MNHNP , UNNEC
Material sample ID
FZ-UNNE 0010, UNNEC 9722 , FZ-UNNE 0011, UNNEC 9723 , FZ-UNNE 0013, UNNEC 9724 , FZ-UNNE 0014, UNNEC 9727 , FZ-UNNE 0019 , FZ-UNNE 0020, UNNEC 9856 , FZ-UNNE 0023, UNNEC 9859 , FZ-UNNE 0081 , FZ-UNNE 0096 , FZ-UNNE 0284, UNNEC 13611 , FZ-UNNE 0706 , FZ-UNNE 0708 , FZ-UNNE 0709 , FZ-UNNE 0711 , FZ-UNNE 0712 , FZ-UNNE 0713 , FZ-UNNE 0714 , FZ-UNNE 0715 , FZ-UNNE 0716, UNNEC 9074 , FZ-UNNE 1013 , FZ-UNNE 1014 , FZ-UNNE 1016 , LGE 25740 , LGE 25741 , LHUFCG 173, LHUFCG 174, LHUFCG 175, LHUFCG 176, LHUFCG 177, LHUFCG 178, LHUFCG 179, LHUFCG 205, LHUFCG 206, LHUFCG 207 , LHUFCG207, LHUFCG 207 , MNHNP 0411, MNHNP 0431, MNHNP 0433, MNHNP 0435, MNHNP 5695, MNHNP 5698, MNHNP 5699, MNHNP 5700 , MNHNP 0412, MNHNP 0424, MNHNP 0425, MNHNP 0441, MNHNP 0442 , MNHNP 0413, MNHNP 0415, MNHNP 0421, MNHNP 0436 , MNHNP 0414, MNHNP 0440 , MNHNP 0417 , MNHNP 0419, MNHNP 0422, MNHNP 0434, MNHNP 5696, MNHNP 5701, MNHNP 5702 , MNHNP 0420 , MNHNP 0423 , MNHNP 0426 , MNHNP 0427, MNHNP 0439, MNHNP 4396, MNHNP 4398, MNHNP 4408, MNHNP 4440, MNHNP 4452, MNHNP 4494, MNHNP 4496, MNHNP 5532, MNHNP 5704, MNHNP 5705, MNHNP 5706, MNHNP 5707, MNHNP 5708 , MNHNP 0428 , MNHNP 0430 , MNHNP 0432, MNHNP 5703 , MNHNP 0443, MNHNP 5710 , MNHNP 0783 , MNHNP 0784, MNHNP 0785, MNHNP 0786 , MNHNP 10046 , MNHNP 10062 , MNHNP 11333 , MNHNP 12907, 12908 , MNHNP 12909, MNHNP 12910 , MNHNP 1404 , MNHNP 3699 , MNHNP 5332 , MNHNP 5391 , MNHNP 7045 , UNNEC 11964 , UNNEC 11974, UNNEC 11976, UNNEC 11980, UNNEC 11981, UNNEC 11982, UNNEC 13608 , UNNEC 11977, UNNEC 11978 , UNNEC 12331 , UNNEC 13607 , UNNEC 13609, UNNEC 13610 , UNNEC 13612 , UNNEC 13938 , UNNEC 13939 , UNNEC 5260 , UNNEC 8261 , UNNEC 8293, UNNEC 8294, UNNEC 8295, UNNEC 8354, UNNEC 8363, UNNEC 8505 , UNNEC 8356, UNNEC 8357, UNNEC 8506 , UNNEC 8362 , UNNEC 8365, UNNEC 8367 , UNNEC 8531 , UNNEC 8800, UNNEC 9727 , UNNEC 8974, UNNEC 9606, UNNEC 9704, UNNEC 11961, UNNEC 11962, UNNEC 11965, UNNEC 11968, UNNEC 11969, UNNEC 11970, UNNEC 13611 , UNNEC 8994 , UNNEC 9000, 9001, 11967 , UNNEC 9002, UNNEC 9075 , UNNEC 9003 , UNNEC 9074 , UNNEC 9076 , UNNEC 9551 , UNNEC 9717, UNNEC 9718, UNNEC 9719, UNNEC 9720, UNNEC 9721, UNNEC 9722, UNNEC 9723, UNNEC 9724, UNNEC 9859, UNNEC 9865, UNNEC 9870 , UNNEC 9725, UNNEC 9726, UNNEC 9863 , UNNEC 9728, UNNEC 9729 , UNNEC 9856, UNNEC 9857, UNNEC 9858 , UNNEC 9860, UNNEC 9861, UNNEC 9862 , UNNEC 9864, UNNEC 9866, UNNEC 9867, UNNEC 9868, UNNEC 9871
Event date
1981-11-11 , 1982-08-31 , 1982-09-09 , 1984-10-01 , 1996-02-20 , 2005-06-24 , 2005-12-13 , 2006-11-29 , 2006-12-02 , 2007-02-08 , 2007-02-10 , 2007-02-11 , 2007-07-29 , 2007-11-23 , 2007-11-24 , 2007-11-25 , 2008-02-29 , 2009-10-13 , 2009-10-15 , 2010-11-15 , 2011-03-18 , 2011-11-22 , 2013-11-14 , 2013-11-28 , 2013-12-13 , 2013-12-16 , 2016-11-08
Verbatim event date
1981-11-11 , 1982-08-31 , 1982-09-09 , 1984-10-01 , 1996-02-20 , 2005-06-24 , 2005-12-13 , 2006-11-29 , 2006-12-02 , 2007-02-08 , 2007-02-10 , 2007-02-11 , 2007-07-29 , 2007-11-23 , 2007-11-24 , 2007-11-25 , 2008-02-29 , 2009-10-13 , 2009-10-15 , 2010-11-15 , 2011-03-18 , 2011-11-22 , 2013-11-14 , 2013-11-28 , 2013-12-13 , 2013-12-16 , 2016-11-08
Scientific name authorship
Zaracho & Lavilla & Carvalho & Motte & Basso
Kingdom
Animalia
Phylum
Chordata
Order
Anura
Family
Leptodactylidae
Genus
Adenomera
Species
guarani
Taxon rank
species
Taxonomic status
sp. nov.
Type status
holotype , paratype
Taxonomic concept label
Adenomera guarani Zaracho, Lavilla, Carvalho, Motte & Basso, 2023

References

  • Almeida A. P. & Angulo A. 2006. A new species of Leptodactylus (Anura: Leptodactylidae) from the state of Espirito Santo, Brazil, with remarks on the systematics of associated populations. Zootaxa 1334 (1): 1 - 25. https: // doi. org / 10.11646 / zootaxa. 1334.1.1
  • Carvalho T. R. & Giaretta A. A. 2013 b. Bioacoustics reveals two new syntopic species of Adenomera Steindachner (Anura: Leptodactylidae: Leptodactylinae) in the Cerrado of central Brazil. Zootaxa 3731 (3): 533 - 551. https: // doi. org / 10.11646 / zootaxa. 3731.4.6
  • Angulo A. & Reichle S. 2008. Acoustic signal, species diagnosis, and species concepts: the case of a new cryptic species of Leptodactylus (Amphibia, Anura, Leptodactylidae) from the Chapare region, Bolivia. Zoological Journal of the Linnean Society 152 (1): 59 - 77. https: // doi. org / 10.1111 / j. 1096 - 3642.2007.00338. x
  • Carvalho T. R. & Giaretta A. A. 2013 a. Taxonomic circumscription of Adenomera martinezi (Bokermann, 1956) (Anura: Leptodactylidae: Leptodactylinae) with the recognition of a new cryptic taxon through a bioacoustic approach. Zootaxa 3701 (2): 207 - 237. https: // doi. org / 10.11646 / zootaxa. 3701.2.5
  • Carvalho T. R., Giaretta A. A., Maciel N. M., Barrera D. A., Aguilar-Puntriano C., Haddad C. F. B., Kokubum M. N. C., Menin M. & Angulo A. 2019 a. On the uncertain taxonomic identity of Adenomera hylaedactyla (Cope, 1868) and the composite type series of A. andreae (Muller, 1923) (Anura, Leptodactylidae). Copeia 107 (4): 708 - 723. https: // doi. org / 10.1643 / CH- 19 - 237
  • Zaracho V. H. & Kokubum M. N. C. 2017. Reproduction and larval morphology of Adenomera diptyx (Anura: Leptodactylidae) from the Argentinean humid Chaco and Brazilian pantanal. Salamandra 53: 1 - 9.
  • Zaracho V. H. & Lamas M. F. 2008. Leptodactylus diptyx. Endoparasites. Natural History Notes. Herpetological Review 39 (3): 337.
  • Zaracho V. H., Acosta J. L. & Lamas M. F. 2012 a. Dieta y parasitismo de Leptodactylus diptyx (Anura: Leptodactylidae) del nordeste argentino. Revista Mexicana de Biodiversidad 83: 1180 - 1186. https: // doi. org / 10.22201 / ib. 20078706 e. 2012.4.1016
  • Zaracho V. H. & Hernando A. B. 2011. The karyotype of Adenomera diptyx (Boettger 1885) (Anura, Leptodactylidae) from northeastern Argentina. Genetics and Molecular Biology 34 (1): 84 - 87. https: // doi. org / 10.1590 / S 1415 - 47572010005000116
  • Zaracho V. H., Schaefer E. & Dure M. 2012 b. Leptodactylus diptyx (Boettger, 1885). In: Categorizacion del Estado de Conservacion de la Herpetofauna de la Republica Argentina. Ficha de los Taxones. Anfibios. Cuadernos de Herpetologia 26 (S 1): 204.