Ameerega Ameerega A new species of poison-dart frog (Anura: Dendrobatidae) from Manu province, Amazon region of southeastern Peru, with notes on its natural history, bioacoustics, phylogenetics, and recommended conservation status Serrano-Rojas, Shirley J. Whitworth, Andrew Villacampa, Jaime May, Rudolf Von Gutiérrez, Roberto C. Padial, José M. Chaparro, Juan C. Zootaxa 2017 4221 1 71 94 CQ7D [151,412,1738,1764] Amphibia Dendrobatidae Ameerega Animalia Anura 2 73 Chordata species shihuemoy sp. nov.     Cryptophyllobatessp: Chaparro & Ochoa 2005 p.7 (  MHNC4779collected on 0  7 December 2004by J. C. Chaparro& J. A. Ochoaat Erika Lodge, Departamento Madre de Dios).    Ameeregagr. pictus: Chaparro et al.2016 p. 2 (from Amarakaeri Communal Reserve, Departamento Madre de Dios).  Ameeregasp1: Whitworth & Villacampa 2014 p. 3 (from Manu Learning Centre, Departamento Madre de Dios).     Holotype.  MHNC15488( Fig. 1), an adult female, from near Cupudnoe river,  440 melevation, Peru(Coordinates: 12°47'26.70" S, 70°58'21.30" W), Distrito Madre de Dios, Provincia Manu, Departamento Madre de Dios, collected on  25 April 2010by R. C. Gutiérrez.  Paratopotypes.Seven specimens: Five adult females (MUSA 3178, MUSA 3180–3182, MHNC 12988), and two immature females (MUSA 3177, MUSA 3 179), collected with the holotype by R. C. Gutiérrez.     Paratypes. Fifteenspecimens, all from Provincia Manu, Departamento Madre de Dios, Peru. Twoadult females (  MHNC10406–10407), and one adult male (  MHNC10408), from the Reserva Comunal Amarakaeri, 32 kmeast of Huepetuhe, near the headwaters of Coloradoriver,   846 melevation, (Coordinates: 12°59'59.25'' S, 70°50'31.32'' W), collected on 0  7 November 2010by J. Delgadoand J. G. Estrada. Twoadult females (  MHNC10525–10526), and two adult males (  MHNC10536,  MHNC10542), from the Reserva Comunal Amarakaeri, 21.5 kmsouthwest of Shintuya, near Azul river,   480 melevation, (Coordinates: 12°48'50.8'' S, 71°06'07.8'' W), collected on  23 May 2011by J. Delgado. Anadult male (  MHNC15863), from the Reserva Comunal Amarakaeri, Pad A, Lote76, near Dahuene river,   530 melevation, (Coordinates: 12°58'38.47'' S, 71°01'30.73'' W), collected on  20 July 2016by R. Coroneland G. Valencia. Two immature specimens (  MHNC10806,  MHNC10811), from 3.5 kmsouth of Shintuya, near Serjali river,   450 melevation, (Coordinates: 12°42'49.02'' S, 71°15'17.51'' W), collected on  20 January 2011by J. G. Estrada. Twoimmature specimens (  MHNC10816,  MHNC10826), from 10 kmsouthwest of Itahuania, near Shilive river,   450 melevation, (Coordinates: 12°43'02.93'' S, 71°09'07.56'' W), collected on  26 January 2011by J. G. Estrada. Animmature female (  MHNC14561; Figs. 2A, B), from the Reserva Comunal Amarakaeri, Pad A, Lote76, near Coloradoriver,   825 melevation, (Coordinates: 12°59'17.97'' S, 71°0'52.67'' W), collected on 0  4 February 2015by T. Gregory. Anadult specimen (  MHNC5012), from Aguas Calientes, 2.75 kmeast (downstream) from Shintuya, (Coordinates: 12°40'7.27" S, 71°16'12.20'' W), collected on 0  9 July 2014by S. J. Serrano. Animmature specimen (  MHNC4779; Figs. 2C, D), from Erika Lodge, 500 melevation, (Coordinates: 12°45'23.53" S, 71°22'48.68" W), collected on 0 7 December 2004by J. C. Chaparro and J. A. Ochoa.   Referred specimens.Five specimens: MUSM31611, MUSM31664, MUSM31691, MUSM31692 and MUSM31730, from Manu Learning Centre Research Station, 460 melevation, Peru, (Coordinates: 12°47'21.849" S, 71°23'28.06" W), Distrito Manu, Provincia Manu, Departamento Madre de Dios, Peru, collected on 12 February, 0 5 July, 21July, and 25 July 2012, and on 0 3 February 2013, respectively, by A. Whitworth.   Etymology.The specific name  shihuemoy(English pronunciation: shee-way-moy) corresponds to the Harakmbut word for "poison dart frog". The Amarakaeri are aboriginals from Amazonian Peruand their language belongs to the Harakmbut linguistic group. They coexist with the new species.   Diagnosis and comparisons with other species.Following Grant et al. (2006), the new species is assigned to the genus  Ameeregaon the basis of the following characters: dorsal skin finely granular; Finger I> Finger II when adpressed; toe and finger webbing absent; presence of bright flash marks and absence of ventrolateral line. This is a medium species of  Ameeregawith an adult SVL of 23.3 ± 2.7 ( 19.3–30.4 mm, N = 25). Vocal slits present; snout subacuminated, short and protruding. The head and dorsal surfaces are blackish with bronze-brown shades. The flanks are black with metallic bluish-green blotches, with a distinct bright orange or coral stripe extending from groin to above the eye and forward along the canthus rostralis to join around the snout. A flash spot is observed on the hip and upper surface of thighs, and a pale orange spot is located on the anterodorsal base of the thighs. It lacks concealed axillary and calf spots. The ventral surfaces have black reticulations with blue. The maxillary arch has teeth and the dentigerous process of vomers is lacking. The choanae are partly concealed by the palatal shelf of maxilla. The finger discs are weakly to moderately expanded, and when adpressed the first finger is slightly longer than second, and the fourth is shorter than first and second fingers, while the third is longer than all others. The finger discs are weakly to moderately expanded. The finger disc of the third finger of adults is about 1.2 times wider than the immediately adjacent part of the finger. The third finger shows no sexual dimorphism. Basal webbing is present on toes II–IV. Morphologically, divergence of  A. shihuemoyfrom other species is supported by a unique combination of characters: the lack of the conspicuous axillary, thigh and calf flash marks, characteristics of many other species of  Ameerega; black granular dorsum with cream to light orange dorsolateral lines, metallic blue venter and underside of extremities with black reticulations and spots. Within  Ameerega, it shows the general appearance of  A. altamazonica Twomey & Brown 2008,  A. boliviana( Boulenger 1902),  A. hahneli( Boulenger 1883),  A. ignipedis Brown & Twomey 2009,  A. petersi( Silverstone 1976),  A. picta( Bibron 1838),  A. pongoensis( Schulte 1999),  A. pulchripecta( Silverstone 1976),  A. simulans( Myers, Rodriguez & Icochea 1998),  A. smaragdina( Silverstone 1976), and  A. yungicola( Lötters, Schmitz & Reichle 2005), with which it shares a granular black to brown dorsum, a light labial bar, a conspicuous dorsolateral line running from the snout to the groin, and a metallic blue belly and underside of arms and hind limbs. From all these species it can be distinguished by lacking flash marks on the axillae, thighs, and calves (absent only in  A. boliviana,  A. simulans,  A. smaragdina, most  A. petersi,and some  A. pongoensis), by having bright cream to orange dorsolateral stripes (white, pale yellowish-green, intense yellow, or green in all other species but  A. picta), and by its blue belly reticulated with black (bluish white and black in  A. boliviana, green and blue with black marbling in  A. petersi,and green and blue lacking black marbling in  A. smaragdina).   Measurements (in mm) of the holotype.The female holotype( Fig. 1) has SVL, 25.7; TL, 12.3; GBW, 8.2; HW, 7.9; HL, 8.0; ED, 5.2; IOD, 3.0; TSCN, 2.0; NED, 2.6; IND, 2.9; EL, 3.3; HDT, 2.0; MTD, 0.8; HaL, 7.0; WTFD, 0.7; WTF, 0.5; WTTD, 0.8; WTT, 0.4; WFTD, 0.9; WFT, 0.4.  Description of the typeseries.External morphology: A small to medium-size  Ameerega, with adult males attaining approximately 19.2–21.8 mmSVL and adult females approximately 21.5–25.7 mmSVL (measurements and proportions summarized in Table 1). Dorsal skin of head, body, shank, thigh, and hind limbs coarsely and conspicuously granular; skin smooth or nearly smooth on forelimbs, and smooth on sides of head, body and on ventral surfaces. Head slightly wider between jaw articulations than between outer edges of upper eyelids; head usually narrower than body or about as wide. Head width between jaws 29–33% of SVL. Snout sloping, bluntly pointed or rounded in profile, truncate to rounded (usually) or bluntly pointed in dorsal and ventral view. Nares situated near tip of snout, directed slightly posterolaterally; nares visible from front and from below but not from above. Canthus rostralis short, protruding; loreal region nearly vertical, slightly concave to flat. Interorbital distance wider than upper eyelid. Eye shorter than snout length; distance from center of naris to eye 60–87% of eye length. Tympanum 35–65% of eye size. Hand ( Fig. 1F) moderately large, its length 23–28% of SVL and 74–90% of head width between angles of jaws. Relative lengths of adpressed fingers IV> I> II> III; fingers I, II, and IV approximately similar in size when adpressed, with overlapping discs; adpressed first finger varies from slightly shorter to slightly longer than second. Finger discs weakly to moderately expanded; third finger disc 1.2–1.8 times wider than distal end of adjacent phalanx. A large outer metacarpal (= palmar) tubercle on the base of the palm and a smaller inner metacarpal tubercle on the base of first finger, these being relatively small, with rounded surfaces. One subarticular tubercle on fingers I & II, and two subarticular tubercles on fingers III & IV; subarticular tubercles well developed and prominently raised, although distal one on finger III and both in IV sometimes weaker; supernumerary tubercles, finger keels, and outer metacarpal fold absent; tibia length 47–54% of SVL; relative lengths of adpressed toes, IV> III> V> II> I; first toe usually reaching base of subarticular tubercle of second toe; basal webbing on toes II–IV; toe fringes absent; outer metatarsal fold absent; a large inner metatarsal fold located on the distal half of tarsus and extended near the inner metatarsal tubercle ( Fig. 1G); ventrolateral side of tarsus relatively smooth, not especially rugose or tubercular; toes with moderately expanded discs, wider than finger discs ( Fig. 1G); one to three moderately raised subarticular tubercles (one each on toes I & II, two each on III & V, and three on IV); two large metatarsal tubercles with low, rounded surfaces; inner metatarsal tubercle slightly larger than outer metatarsal tubercle; supernumerary tubercles absent.  Color pattern in life.(Based on living specimens and photographs; Figs. 2, 3). The noticeably granular body is blackish with bronze shades middorsally, turning black and blue dorsolaterally. The flanks are mostly black with metallic bluish green, with a distinct bright orange, coral, or cream stripe extending obliquely from groin to above the eye, and forward along the canthus rostralis to join around the snout. A pale whitish-bronze labial stripe commences between naris and eye, and extends posteriorly under the eye and tympanum to the base of the upper arm. A bright orange to coral spot is present on the hip and upper thigh; there is no calf spot and no pale markings in axilla or groin. The limbs are bronze-brown with shades of green and black. The ventral surfaces are overall blue with variable black reticulation, while in some individuals the ventral surfaces are overall black with blue reticulation.  Color in preservative( Fig. 1). The bright orange and coral colors fade to pale grey; the blue ventral surfaces fade to grey in a dark reticulum of variable distinctiveness.   TABLE 1.Measurements (in mm) of  Ameerega shihuemoytype series.     MHNC 15448  MUSA 3181  MUSA 3178  MHNC 10525  MHNC 12988  MHNC 10526  MHNC 10406  MHNC 10407  MUSA 3180  MUSA 3182  MHNC 10408  MHNC 10536  MHNC 10542   SEX Female Female Female Female Female Female Female Female Female Female Male Male Male   SVL 25.7 25.2 25.1 24.4 24.0 23.5 23.2 23.1 22.8 21.5 21.8 21.6 19.2   TL 12.3 12.9 11.4 11.8 12.2 11.2 11.5 11.2 11.6 11.7 11.0 10.9 9.0   HaL 7.0 6.8 6.3 6.3 6.5 6.0 6.2 6.0 6.1 5.5 6.1 5.8 4.5   HL 8.0 7.2 7.9 7.8 7.5 7.7 8.2 8.3 6.7 6.9 6.8 7.9 7.4   HW 7.9 7.6 7.8 7.4 7.6 6.8 7.3 7.4 6.8 7.2 6.8 6.7 6.0   GBW 8.2 8.4 7.9 8.5 7.2 7.6 8.3 7.4 6.8 6.7 7.9 7.6 7.6   IOD 3.0 3.1 3.0 2.3 2.7 2.1 2.3 2.3 2.8 2.3 2.1 2.3 2.1   ED 5.2 5.2 5.1 5.0 5.1 5.1 4.7 5.1 4.9 4.8 4.5 4.7 4.3   HDT 2.0 1.9 1.5 1.4 1.5 1.3 1.5 1.4 1.5 1.1 1.4 1.1 1.0   EL 3.3 3.0 3.3 3.1 3.1 3.1 2.9 2.9 3.1 3.0 2.7 2.7 2.9   TSCN 2.0 1.6 1.8 1.3 1.6 1.5 1.2 1.5 1.8 1.8 1.0 1.1 1.1   NED 2.6 2.6 2.3 2.2 2.1 2.0 1.9 2.1 2.1 1.8 2.3 1.8 2.0   IND 2.9 2.7 2.9 2.9 2.9 2.5 2.3 2.8 2.6 2.8 2.7 2.6 2.2   MTD 0.8 0.8 0.9 0.7 0.9 0.7 0.7 0.5 0.7 0.6 0.8 0.6 0.7   W3FD 0.7 0.8 0.6 0.7 0.8 0.7 0.6 0.7 0.7 0.5 0.6 0.5 0.7   W3F 0.5 0.5 0.3 0.4 0.4 0.4 0.3 0.4 0.4 0.3 0.4 0.4 0.4   W4TD 0.9 0.9 0.8 0.7 0.8 0.7 0.5 0.7 0.7 0.5 0.6 0.7 0.6   W4T 0.4 0.4 0.4 0.3 0.3 0.4 0.3 0.4 0.3 0.3 0.4 0.5 0.4   W3TD 0.8 0.8 0.7 0.7 0.7 0.5 0.7 0.7 0.7 0.6 0.4 0.6 0.6   W3T 0.4 0.5 0.4 0.4 0.4 0.4 0.3 0.4 0.3 0.3 0.3 0.4 0.3  Vocalization.Recordings of three  A. shihuemoymales were taken at the Manu Learning Centre reserve. The advertisement call of this new species can be characterized as a series of chirp-like, pulsed notes. Notes are repeated at a rate of 0.8–1.0 notes per second (0.9 ± 0.1), duration of individual notes range from 84–109 ms (98.4 ± 6.8 ms), spaced 969–1196 ms apart (1042.5 ± 186.6 ms), with eight pulses (8.2 ± 0.8) per note. Dominant frequency ranges from 4478.9–4909.6 Hz (4672.72 ± 251.0 Hz) and is not frequency-modulated. Calling activity happens most frequently in the early mornings between 05:00 to 09:00 and late afternoon between 16:00 to 18:00. We also recorded a second call in  A. shihuemoyconsisting of three notes in quick succession (within 174.9 ± 16.6 ms of each other), repeated once every four to five seconds. The three notes in this call have different duration; the first note (87.2 ± 2.5 ms) typically has a longer duration than the second (69.4 ± 2.6 ms) and the third note (72.8 ± 2.8 ms). This three-note call seems to function as an aggressive or territorial call.  We compared the call of the following species with  Ameerega shihuemoy: two recordings of  A. simulans(74 advertisement calls) by J. M. Padialfrom Marcapata, Quispicanchis Province, Department Cusco, Peru, were obtained from Fonoteca Zoologica ( Museo Nacional de Ciencias Naturales2016); two recordings of  A. boliviana(45 advertisement calls) by J. Bosch& I. De la Rivafrom Correo-Apolo,  La Paz, Bolivia; one recording of  A. yungicola(30 advertisement calls) by M. Pacheco-Suarezfrom Caranavi, Yungas, Boliviaobtained from “Guía fotográfica de los anfibios de la region de las yungas Bolivia” ( Pacheco-Suarez 2015); two recordings of  A. hahneli(46 advertisement calls) by J. Serrano-Rojasfrom Shintuya,  Madre de Dios, Peru; two recordings of  A. picta(63 advertisement calls) by J. M. Padialfrom Madidi National Park, Northern Boliviaand from Paractito,  Cochabamba Department, Central West Boliviadeposited at Fonoteca Zoologica ( Museo Nacional de Ciencias Naturales2016); two recordings of  A. macero(55 advertisement calls) by J. Serrano-Rojasfrom Manu Learning Centre,  Madre de Dios, Peru. The advertisement call of  A. shihuemoyis easily distinguished ( Fig. 4) from the morphologically similar  Ameeregaspecies of the  Ameerega pictagroup (for measurable call parameters and intra- and interspecific variation see Table 2).   TABLE 2.Summary of numerical parameters of vocalizations of  Ameerega shihuemoyand morphologically similar  Ameeregaspecies. Parameters  A. shihuemoy A. simulans A. picta A. hahneli Mean SD Mean SD Mean SD Mean SD Calls/N° of individuals 80/3 - 74/2 - 63/2 - 46/2 - Notes/min 52.8 5.4 79.2 3.6 130.2 6.0 511.8 4.2 Notes/s 0.9 0.1 1.3 0.1 2.2 0.1 8.5 0.1 Duration of the note (ms) 98.4 6.8 104.9 10.2 45.8 2.4 13.4 2.8 Break between calls (ms) 1042.5 186.6 691.4 162.7 429.9 44.6 107.4 12.6 Fundamental frequency (Hz) 4237.0 281.9 4060.9 74.6 3770.7 76.7 2516.8 83.7 Dominant frequency (Hz) 4672.7 251.0 4460.3 157.7 4044.2 94.7 4550.0 49.1 continued. Parameters  A. boliviana A. yungicola A. macero Mean SD Mean SD Mean SD Calls/N° of individuals 45/ 2 - 30 - 55/2 - Notes/min 72.0 4.2 313.2 0.0 519.4 2.2 Notes/s 1.2 0.1 5.2 0.0 8.7 0.0 Duration of the note (ms) 80.9 8.6 47.8 4.7 37.6 1.3 Break between calls (ms) 783.2 88.6 148.1 7.3 76.1 2.7 Fundamental frequency (Hz) 3416.1 68.2 3475.7 43.5 3353.7 38.1 Dominant frequency (Hz) 3846.0 46.3 3703.7 0.0 3617.6 0.0 The note duration of the new species (84–109 ms) is longer than  A. hahneli(11–18 ms),  A. macero(36–40 ms),  A. picta(41–52 ms) and  A. yungicola(40–57 ms), but similar to  A. boliviana(75–94 ms) and  A. simulans(91–118 ms). The space between calls in  A. shihuemoyis longer than in the other six species. The number of notes per second in the advertisement call of  A. shihuemoyis lower than the other six species. The call of the new species has a higher fundamental frequency than all other species but similar to  A. simulans,and a higher dominant frequency than all other species but similar to  A. hahneliand  A. simulans, except the latter species has pronounced upward frequency-modulated notes by about 950 Hz ( Fig. 5). It is important to take into consideration that this comparison was performed on recordings from three individuals of  A. shihuemoyfrom a single location.  Tadpoles.Ontogenetic variation of 11 characteristics measured for 16 tadpoles in stages 24–46 ( Gosner 1960) are summarized in Table 3. The tadpole of  A. shihuemoy sp. nov.belongs to the exotrophic ecomorphological guild, benthic typeas defined by Altig & Johnson (1989). This description is based on a tadpole (MHNC lot 12987) at developmental Stage 25 ( Gosner 1960; Figs. 3A, C) and measuring a total length 17.2 mm; body length 6.2 mm; maximum width 4.1 mm; depth 3.0 mm; internarial distance 0.6 mm; eye to nares distance 0.5 mm; eye diameter 0.6 mm; interorbital distance 1.0 mm, oral disc width 1.2 mm; tail length 11.0 mm. The body is globular, compressed in lateral view, and ovoid in dorsal view. The snout is rounded in dorsal view ( Figs. 6A and C). The mouth is located anteroventrally and is surrounded by a small oral disc ( Figs. 6B and D). Papillae are laterally emarginated, simple and conical. Marginal papillae absent on anterior labium, present in one complete row on posterior labium. Anterior jaw sheath has a medial indentation with reduced serration, posterior jaw sheath Vshaped and has serration throughout. Lateral processes long, extending well past lower jaw. Labial Tooth Row Formula (LTRF) is 2(2)/3(1). A-1 complete, A-2 with medial gap, same width as A-1. P-1, P-2, and P-3 complete; P-1 and P-2 equal width, P-3 shorter. Nares are oval, small, without projections and inflexions, and are located dorsolaterally. Eyes are small and oriented dorsolaterally. The spiracle is single, sinistral, and located just before mid-body. Fins are concave and the posterior end is rounded, reaching their maximum height at the last third of the tail; the dorsal fin does not extend onto the body. The maximum tail height is reached at about the end length and is as high as body height. In preservative, the body is dark grey, the belly is translucent with intestines slightly visible; caudal musculature creamy white with small, irregular grey flecks and slightly translucent fins. In life, the body is dark brown with black spots, the belly is transparent but slightly pigmented posteriorly, intestines well visible through skin, caudal musculature poorly pigmented and transparent tail fin with melanophores in small and irregular clusters along the tail.   TABLE 3.Morphometric measurements (mean ± SD, in millimeters) of developmental stages of tadpoles of  Ameerega shihuemoy.Total length (TL), body length (BL), body height (BH), body width (BW), tail length (TAL), tail muscle height at the base of the tail (TMH), tail muscle width at the base of tail (TMW), eye-nares distance (END), internarial distance (IND), eye diameter (ED), interorbital distance (IOD), and oral disc width (OD). Gosner stages In addition, we described observations in the field following Gosner (1960). We found two clutches of eggs in small rocky cavities; they were monitored every two days in order to take notes about the development of eggs. The first set was found on 25 June 2013, with 22 eggsat stage 13; a stage in which the neural plate develops on the dorsal surface, and eggs were covered by a transparent orange mucilage. After nine days, eggs become tadpoles, where they reach stage 17 (tail bud). The same embryos were abandoned by the father after two days on 0 5 July 2013. The embryos were getting dirty and dry, and inside we could observe the larvae of an insect, which could likely prey upon the embryos.    Character 24 (N=1) 25 (N=3) 26 (N=2) 27 (N=1) 40 (N=2) 41 (N=2) 42 (N=1) 43 (N=1) 44 (N=1) 45 (N=1) 46 (N=1)  TL 17.8 16.9 ± 1.9 17 ± 2.8 18.3 22.6 ± 0.2 23.1 ± 0.6 16.6 14.5 12.1 10.5 10.4  BL BW 6.4 3.9 6 ± 0.9 3.6 ± 0.5 6.5 ± 0.8 3.9 ± 0.4 9.5 4.7 9.4 ± 0.1 5.3 ± 0 9.4 ± 0.4 6.8 ± 1.1 8.5 4.3 9.2 4.6 11.9 3.5 9.5 4.8 10.4 4.6  BH TAL TMW 2.2 11.4 1.1 2.6 ± 0.4 10.9 ± 1.1 1.5 ± 0.2 3 ± 0.2 10.5 ± 2 1.3 ± 0.1 3.5 11.8 2.0 3.8 ± 0.4 13.2 ± 0.1 2.2 ± 0.2 4.5 ± 0.1 13.7 ± 0.1 2.8 ± 0.1 3.2 8.1 2.2 4.2 5.3 2.7 3.3 0.2 1.4 2.4 1.0 1.9 2.4 _ _  TMH END IND 1.7 1.0 0.6 1.6 ± 0.2 0.6 ± 0.3 0.6 ± 0.1 2.1 ± 0.2 0.6 ± 0.2 0.9 ± 0.2 2.0 1.1 1.0 3.1 ± 0.2 0.9 ± 0.1 0.9 ± 0.2 3.5 ± 0.1 1 ± 0.3 1.2 ± 0.2 2.3 0.6 1.1 2.7 1.6 1.1 1.1 1.0 0.9 1.7 0.8 0.9 _ 1.8 0.8  ED IOD OD 0.6 0.8 1.1 0.6 ± 0.2 0.9 ± 0.2 1.1 ± 0.4 0.7 ± 0.1 1.2 ± 0 1.2 ± 0 1.0 1.7 1.2 1.3 ± 0 1.7 ± 0.4 2.15 ± 0.1 1.3 ± 0.1 2 ± 0.1 2.2 ± 0 1.4 2.0 2.3 1.3 2.5 1.8 1.5 2.1 2.6 1.4 2.3 3.2 1.5 2.4 3.9   FIGURE 4.Box plots representing the median (black horizontal line), interquartile range (box), range (whiskers) and outside values (circles) of call parameters comparison among  Ameerega shihuemoy,  A. boliviana,  A. hahneli,  A. picta, A. simulansand  A. yungicolawhere: a) note duration (ms), b) calling rate, c) fundamental frequency (Hz) and d) dominant frequency (Hz).   FIGURE 5.Spectrograms of advertisement calls of morphologically similar species of  Ameerega. A)  A. shihuemoy, recorded at Manu Learning Centre, Madre de Dios, Peru 12 June 2014 (temperature not noted). B)  A. boliviana,recorded from Correo- Apolo, La Paz, Bolivia. C)  A. simulansrecorded from Marcapata, Cusco, Peru. D)  A. pictarecorded from Madidi National Park, Bolivia. E)  A. yungicolarecorded from Caranavi, Yungas, Bolivia. F)  A. hahneli,recorded from Shintuya, Madre de Dios, Peru. G)  A. macero,recorded at Manu Learning Centre, Madre de Dios, Peru. The second set was found on 10 July 2013, containing 25 eggsin stage 13 covered by a transparent orange mucilage. After ten days, eggs were observed at stage 19 (heart beat), which is represented mainly by the development of the gills and tail. Seven days later tadpoles were at stage 21 (cornea transparent), in which the tail becomes increasingly transparent. Finally, three days later ( 30 July 2013) only five tadpoles were found at stage 22 (tail fin circulation); we assumed that the father was carrying the rest of tadpoles. One year later we found two other tadpoles at stage 26 (limb bud), on 11 June 2014. After four days, these reached stage 38 (toe development XIII). Another group of four tadpoles were found at stage 40 (cloacal tail piece XV–XVII), which changed to stage 42 (nose development XXI) after four days. Two more tadpoles were found at stage 42 (nose development XXI) on 15 June 2014; the stage 46 (metamorphosis complete) was reached after three days. In summary, we suggest that the development between stages 13–22 takes twenty days, stages 26–38, four days, and stages 40–46, seven days. However, the time of development of stages 22–26, and stages 36–40 remains unknown.  Phylogenetics.Our Maximum Likelihood (ML) tree was generally congruent with previous molecular phylogenies based on mitochondrial DNA ( Twomey & Brown 2008, Brown & Twomey 2009) and supported the distinctiveness of the  Ameerega shihuemoyfrom other closely related taxa. The new species was most closely related to  Ameerega macero,  A. altamazonica,  A. rubriventris( Lötters et al.1997), and two undescribed species—  Ameeregasp. from Porto Walter, Acre, Brazil, and  Ameeregasp. from Ivochote, Cusco, Peru( Fig. 7). In general, the topology we recovered is similar to the ones obtained by Twomey & Brown (2008)and Brown & Twomey (2009), although there were some differences. These differences were likely a result of using only one mitochondrial gene (our study) versus three mitochondrial genes. Nevertheless, in addition to determining the relationship between the new species and other closely related taxa, our analysis inferred three main cladesbassleri,  hahneliand  petersi—identified in these previous studies ( Twomey & Brown 2008, Brown & Twomey 2009). Our analysis also inferred several species pairs that were inferred to be closely related according to the previous analyses (e.g.,  A. pictaand  A. yungicola;  A. rubriventrisand  A. altamazonica).   Distribution and natural history.  Ameerega shihuemoyis distributed in southeastern Peruat the transition between the montane forest and the lowlands. Its altitudinal range spans from 340 to 850 mabove sea level. This species is known from nine localities; three in the buffer zone of the Manu Biosphere Reserve (The Manu Learning Centre, Erika lodge, and Aguas Calientes, Shintuya) and another six locations in the Amarakaeri Communal Reserve. The area is humid and hot: during the wet season, the average daily temperature is 24.78°C, the average humidity is 90.58% and the rainfall is 3098 mm; during the dry season the average temperature is 23.74°C, the average humidity is 84.89% and the average monthly rainfall is 1557 mm(climate information from Whitworth et al.2016b).   Ameerega shihuemoyis most commonly found in low disturbance forest. During the dry season it is frequently found amongst boulders along or near forest streams ( Fig. 8). During the rainy season it moves away from the streams into the forest interior. The activity patterns appear to be distinctly crepuscular, being most active in the early morning (05:30 to 09:00) or evening (16:00 to 18:00) when males call vigorously. Males typically call from exposed positions of rocks, leaf litter, or woody debris. Calling has been heard throughout the year. Crevices or holes made of boulders or roots are used as refuges. During the night, individuals rest on low vegetation between 0.1 to 0.5 mabove the ground. Reproduction takes place near both permanent and seasonal streams. On 25 June 2013and 10 July 2013two clutches of eggs were found inside of small shelters next to a stream. These clutches contained 22 and 25 eggsrespectively, and were guarded by males. On 30 July 2013, one uncollected male was observed transporting ten tadpoles along a slow moving stream. We detected free-living  A. shihuemoytadpoles and metamorphs co-occurring with metamorphs of  A. maceroin the same streams; with shallow, slow moving, clear water and bottoms of sand and dead leaves. Results of the GLM analysis in both forest types(CCR and SLR) showed that six environmental variables were the most important habitat features to explain the species presence near streams (frog presence ~ canopy cover + leaf litter cover + number of potential refuges + presence of large rocks + presence of a still body of water + stream flow; Table 4, Appendix IV). The best supported model explained 89.05% of the variation in the data. When we ran the same analysis just in streams where the frogs were found (SLR forest), the GLM analysis presents two top models with ∆AICc <2 ( Table 5, Appendix V). The best supported model explained 83.41% of the variation in the data. Model averaging was carried out in these two models. The relative importance for leaf litter cover, number of potential refuges, presence of large rocks, presence of a still body of water and stream flow were 1.0, signalling that they were important predictors. Canopy cover had some support (0.69), suggesting lower importance when comparing just within the SLR forest, and was therefore excluded from the top-preferred, and more parsimonious model (Appendix V). This top model suggests that a greater number of potential refuges (often created by the presence of a high quantity of large rocks), a great amount of leaf litter cover, the presence of still bodies of water, and a low stream flow (likely to benefit breeding strategy) are the most important predictors of the presence of  A. shihuemoynear streams.  Conservation status. Applying IUCN Red List criteria (IUCN Red List of Threatened Species, 2 0 0 1 Criteria & Categories (version 3.1.); http://www.iucnredlist.org/info/categories_criteria2001, accessed 20 February 2016), which indicates that if a species occurs in less than ten threat-defined locations and the extent of occurrence is less than 20,000 km2, it should be classified as Vulnerable or Endangered.  Ameerega shihuemoyis known from nine localities distributed in the buffer zone of the Manu Biosphere Reserve and the Amarakaeri Communal Reserve ( Fig. 9), with an estimated extent of occurrence of ca. 1,124 km2, as such, we suggest that this new species might be classified as Vulnerable. However, due to the lack of intensive sampling effort in the Amarakaeri Communal Reserve, which may host a greater number of locations, we propose that  A. shihuemoyshould likely be categorized as Near Threatened (NT).   TABLE 4. Model selection for environmental variables potentially explaining habitat selection of  Ameerega shihuemoybased on Akaike’s Information Criterion corrected for small sample size (AICc) showing the ten first candidates models and the null model: log likelihood (logLik), k (number of parameters), AICc values, AICc differences between the best model and each candidate model (∆AICc) and Akaike weights (ωi).    Model K AICc ∆AICc  ωi  frog presence~ A + B + C + D + E + F 6 39.015 0.000 0.395  frog presence~ A + B + C + D + E + F + G 7 41.169 2.154 0.135  frog presence~ A + B + C + D + E + F + H 7 41.210 2.194 0.132  frog presence~ B + C + D + E + F 5 41.567 2.552 0.110  frog presence~ B + C + D + E + F + G 6 43.303 4.288 0.046  frog presence~ A + B + C + D + E + F + G + H 8 43.388 4.372 0.044  frog presence~ B + C + D + E + F + H 6 43.593 4.578 0.040  frog presence~ A + B + C + D + F 5 45.232 6.217 0.018  frog presence~ B + C + D + E + F + G + H 7 45.414 6.399 0.016  frog presence~ B + C + D + F 4 46.134 7.118 0.011  frog presence~1 1 224.474 185.459 0.000 Predictor variables are canopy cover (A), leaf litter cover (B), number of potential refuges (C), percentage of large rocks (D), presence of a still body of water (E), stream flow (F), leaf litter depth (G) and Wood debris percent (H).   FIGURE 7.Maximum Likelihood (ML) phylogeny of  Ameeregabased on 16S ribosomal RNA gene. Numbers above nodes are bootstrap values.   FIGURE 8.Habitat at Manu Learning Centre, Manu, Madre de Dios, Peru, where several individuals of  Ameerega shihuemoywere observed calling on July 2015. Photos by Katie Lin.   TABLE 5.Model selection for environmental variables potentially explaining habitat selection of  Ameerega shihuemoy,on streams within the SLR forest, based on Akaike’s Information Criterion corrected for small sample size (AICc), showing the ten first candidates models and the null model: log likelihood (logLik), k (number of parameters), AICc values, AICc differences between the best model and each candidate model (∆AICc) and Akaike weights (ωi).    Model K AICc ∆AICc ωi  frog presence~ A + B + C + D + E + F frog presence~ B + C + D + E + F frog presence~ A + B + C + D + E + F + H 6 5 7 38.109 39.667 40.385 0.000 1.558 2.276 0.284 0.130 0.091  frog presence~ A + B + C + D + E + F + G frog presence~ A + B + C + D + F frog presence~ B + C + D + F 7 5 4 40.400 41.082 41.728 2.292 2.973 3.619 0.090 0.064 0.046  frog presence~ B + C + D + E + F + G frog presence~ B + C + D + E + F + H frog presence~ A + B + C + D + E + F + G + H 6 6 8 41.733 41.914 42.712 3.625 3.805 4.603 0.046 0.042 0.028  frog presence~ B + D + E + F frog presence~1 4 1 42.793 164.154 4.684 126.045 0.027 0.000 Predictor variables are canopy cover (A), leaf litter cover (B), number of potential refuges (C), percentage of large rocks (D), presence of a still body of water (E), stream flow (F), leaf litter depth (G) and Wood debris percent (H).   Remarks. The area that  Ameerega shihuemoyinhabits is threatened by human disturbance associated with activities such as logging, agriculture, and gold mining, especially within the Biosphere Reserve ( Finer et al.2015). Currently, these threats are increasing rapidly due to a draft law in favor of the construction of The Nuevo Eden– Boca Manu–Boca Coloradoroad that cuts through the buffer zones of the Amarakaeri Communal Reserve and Manu National Park ( Finer et al.2016). This road has already begun to be illegally constructed with the purpose of fuel transport for illegal mining and logging. The approval of this road will trigger increased human disturbance within the buffer zone, resulting in a potential new deforestation hotspot in the Madre de Dios region. Changes affecting the habitat surrounding the reserve could ultimately lead to degradation of habitat within the nearby protected areas ( Laurance et al.2012). This could therefore result in both a reduction of the number of known populations of  A. shihuemoyand reduce the overall area of occupancy of the species. The discovery of a new species in Manu Province underscores the need of continued habitat protection in Madre de Dios region( Jarvis et al.2015), which is home to more than 114 amphibian species, and is one of the most biodiverse regions on the planet for herpetofauna (von May et al. 2009; Catenazzi et al.2013) and a variety of other taxa. 1424728377 2004-12-07 MHNC J. C. Chaparro & J. A. Ochoa Departamento Madre de Dios 2 73 MHNC 4779 1 Departamento Madre de Dios 1424728379 2010-04-25 MHNC Distrito Madre de Dios & Provincia Manu & Departamento Madre de Dios & R. C. Gutierrez. Peru 440 3 74 -12.7907505 Cupudnoe river 1 -70.97259 2 73 MHNC 15488 1 Madre de Dios holotype 1424728367 MHNC Fifteen & Provincia Manu & Departamento Madre de Dios & Two Peru Huepetuhe Reserva Comunal Amarakaeri 4 75 MHNC 10406-10407, MHNC 10408 1 Madre de Dios paratype 1424728371 2010-11-07 MHNC J. Delgado & J. G. Estrada. Two Peru Reserva Comunal Amarakaeri 846 -12.999792 Azul river 1 -70.84203 Shintuya 4 75 MHNC 10525-10526, MHNC 10536, MHNC 10542 1 Madre de Dios paratype 1424728368 2011-05-23 MHNC J. Delgado. An & Pad A Peru Reserva Comunal Amarakaeri 480 -12.814112 Dahuene river 1 -71.102165 Lote 4 75 MHNC 15863 1 Madre de Dios paratype 1424728378 2016-07-20 MHNC R. Coronel Peru 530 5 76 -12.977352 Serjali river 1 -71.02521 Shintuya 4 75 MHNC 10806, MHNC 10811 1 Valencia paratype 1424728381 2011-01-20 MHNC J. G. Estrada. Two Peru 450 -12.713616 Shilive river 1 -71.25487 Itahuania 5 76 MHNC 10816, MHNC 10826 1 Valencia paratype 1424728370 2011-01-26 MHNC J. G. Estrada. An & Pad A Peru 450 -12.71748 Lote 1 -71.1521 Reserva Comunal Amarakaeri 5 76 MHNC 14561 1 Colorado paratype 1424728380 2014-07-09 2015-02-04 2014-07-09 MHNC T. Gregory. An & Aguas Calientes & Shintuya & S. J. Serrano. An Peru 825 -12.668687 Erika Lodge 1 -71.27006 5 76 MHNC 5012, MHNC 4779 1 Colorado paratype 1424728374 J. M. Padial & Museo Nacional de Ciencias Naturales & J. Bosch & I. De la Riva Peru Quispicanchis Province 8 79 1 Cusco 1424728373 [1014,1197,620,645] Bolivia La Paz 8 79 1 La Paz 1424728369 M. Pacheco-Suarez & J. Serrano-Rojas Bolivia Bolivia 8 79 1 1424728376 [840,1080,727,752] Peru Madre de Dios 8 79 1 Madre de Dios 1424728372 J. M. Padial Bolivia Bolivia 8 79 1 1424728366 Museo Nacional de Ciencias Naturales & J. Serrano-Rojas Bolivia Cochabamba Department 8 79 1 Cochabamba Department 1424728375 Peru Madre de Dios 8 79 1 Madre de Dios