We report the discovery of a new species of Lophostoma from Panama, which we name L. kalkoae. This new species resembles L. carrikeri and L. yasuni in possessing a white venter, but is distinguishable from both by external and cranial characteristics. The new species is similar in size to L. carrikeri and L. schulzi. Lophostoma sp. nov. can be most easily recognized by its combination of white venter, postauricular patches connected by a thin line of pale hair to the white fur on the chest, elongated clitoris and swollen labia, less strongly developed lateral projection of mastoid processes, well-marked indentation on the lingual cingulum of the upper canine, well-developed P3, well-developed posterior lingual cusp on the cingulum of P4, and parastyle absent on Ml and M2. We present a dichotomous key for the genus Lophostoma and a map showing all the localities where white-bellied Lophostoma have been recorded.
Map of southern Central America and northern South America, showing the type localities of Lophostoma kalkoae sp. nov. (star) and L. yasuni (square), and all reported localities for L. carrikeri (triangles).
Herein, we describe a new species of white-ventered Lophostoma from Panama. We analyzed morphometric and morphological data to distinguished this new taxon from other species of the genus, and provide a map (Fig. 1) of all the localities where white-ventered Lophostoma have been collected.
For the morphometric analyses, we examined 288 specimens of adult Lophostoma (152 males and 136 females) representing all known species of Lophostoma (see Appendix I). We used a digital caliper to take 8 external and 16 craniodental measurements to the nearest 0.01 mm on each specimen (Fig. 2). Descriptive statistics (mean and range) were calculated for all samples for selected measurements. Definitions for craniodental, mandibular, and external measurements are listed in Table 1.
Dorsal and ventral views of the cranium and lateral view of the cranium and mandible illustrating most of the measurements used in the morphometric analyses. For definitions of abbreviations see Table 1.
Definition of craniodental, mandibular, and external measurements used in the present study.
Forearm length (FA)
Distance from the elbow (tip of the olecranon process) to the wrist (including the carpals). This
measurement is made with the wing at least partially folded.
Metacarpal III length (MET-III)
Distance from the joint of the wrist (carpal bones) with the 3rd metacarpal to the metacarpophalangeal
joint of 3rd digit.
Metacarpal IV length (MET-IV)
Distance from the joint of the wrist (carpal bones) with the 4th metacarpal to the metacarpophalangeal
joint of 4th digit.
Metacarpal V length (MET-V)
Distance from the joint of the wrist (carpal bones) with the 5th metacarpal to the metacarpophalangeal
joint of 5th digit.
Tail length (TL)
Distance from dorsal flexure at base of the tail to the tip of the last caudal vertebra.
Hind-foot length (HF)
From the proximal edge of the base of the calcar to the tip of the claw of the longest toe.
Tibia length (TiL)
From the proximal end of the tibia to the distal base of the calcar.
Calcar length (CL)
From the joint with the ankle to the calcar tip.
Greatest length of skull (GLS)
Greatest distance from the occiput to the anteriormost point on the premaxilla (including the incisors).
Condyloincisive length (CIL)
Distance between a line connecting the posteriormost margins of the occipital condyles and the
anteriormost point on the upper incisors.
Condylocanine length (CCL)
Distance between a line connecting the posteriormost margins of the occipital condyles and a line
connecting the anteriormost surfaces of the upper canines.
Braincase breadth (BB)
Greatest breadth of the globular part of the braincase, excluding mastoid and paraoccipital processes.
Zygomatic breadth (ZB)
Greatest breadth across the zygomatic arches.
Postorbital breadth (PB)
Least breadth at the postorbital constriction.
Palatal width at canines (C-C)
Least width across palate between lingual margins of the alveoli of upper canines.
Mastoid width (MSTW)
Least breadth across skull immediately behind jugal base of zygomatic arches.
Mastoid process width (MPW)
Greatest breadth across skull, including mastoid processes.
Palatal length (PL)
Distance from the posterior palatal notch to the anteriormost border of the incisive alveoli.
Maxillary toothrow length (MTRL)
Distance from the anteriormost surface of the upper canine to the posteriormost surface of the crown of M3.
Molariform toothrow length (MLTRL)
Distance from the anteriormost surface of P3 to the posteriormost surface of the crown of M3.
Width at M2 (M2-M2)
Greatest width of palate across labial margins of the alveoli of M2s.
Dentary length (DENL)
Distance from midpoint of condyle to the anteriormost point of the dentary.
Mandibular toothrow length (MANDL)
Distance from the anteriormost surface of the lower canine to the posteriormost surface of m3.
Coronoid height (COH)
Perpendicular height from the ventral margin of mandible to the tip of coronoid process.
All craniodental and 2 external (FA and MET-III) measurements were log-transformed to achieve normalization for statistical analyses. We evaluated differences among morphological groups by principal component analysis using a covariance matrix. Principal component (PC) scores were plotted to show relationships between species groups in morphospace. Principal component analysis was performed using IBM SPSS Statistics for Windows, version 19 (IBM, Armonk, New York). We constructed a dichotomous identification key for all recognized species of Lophostoma.
Photographs of the holotype and paratype of Lophostoma sp. nov. (32 images: M54224-M54255) and of the female genitalia of L. schulzi (AMNH 257128 [M54312 and M54313]; AMNH 267420 [M54314 and M54315]; and AMNH 267421 [M54316]) are available at Morphobank (http://morphobank.org/permalink/7P421). We reference some of these images throughout our description (the image reference numbers begin with the letter M).
We examined specimens from the following institutional collections: American Museum of Natural History, New York (AMNH); Carnegie Museum of Natural History, Pittsburgh (CM); Field Museum of Natural History, Chicago (FMNH); Instituto de Ciencias Naturales, Universidad Nacional de Colombia, Bogotá (ICN); Instituto Nacional de Pesquisas da Amazônia, Manaus (INPA); Museum of Natural Science, Louisiana State University, Baton Rouge (LSUMZ); Museu Paraense Emílio Goeldi, Beiérn+ (MPEG); Museo de Historia Natural de la Universidad Nacional Mayor de San Marcos, Lima (MUSM); Museo de Vertebrados de la Universidad de Panama, Panama (MVUP); Museo de Zoología, Pontificia Universidad Católica del Ecuador, Quito (QCAZ); Royal Ontario Museum, Toronto (ROM); Museum of Texas Tech University, Lubbock (TTU); National Museum of Natural History, Smithsonian Institution, Washington (USNM).
Dorsal and ventral views of the cranium and lateral view of the cranium and mandible of Lophostoma kalkoae sp. nov. (USNM 582249, holotype). See Table 2 for measurements.
Holotype.—An adult male (USNM 582249; Fig. 3, M54237-54246) caught on Pipeline Road, near the former Limbo Hunt Club (9°9′50″N, 79°45′10″W), Soberania National Park, Colón Province, Panamá, by Elisabeth K. V. Kalko (field number EKVK 118) on 11 October 1998. The holotype is preserved in alcohol with the skull removed and cleaned. The upper and lower dentition lost some of the enamel during initial preservation in unbuffered formalin.
Paratype.—An adult pregnant female (EKVK 119 to be deposited in the MVUP, M54224-M54236, M54247-M54255) caught at the type locality by Elisabeth K. V. Kalko (original field number EKVK 119) on 11 October 1998. The paratype is preserved in alcohol with the skull removed and cleaned. As with the holotype, the dentition has lost some enamel due to decalcification in unbuffered formalin.
Distribution.—The new species is currently known only from the type locality (Fig. 1).
Etymology.—The name kalkoae is in honor of our late friend Dr. Elisabeth K. V. Kalko, a remarkable scientist who collected both specimens and who has contributed in significant ways to the understanding of bat behavior and ecology worldwide.
Measurements.—External and craniodental measurements are presented in Table 2.
Measurements of type series of Lophostoma kalkoaesp. nov. (in mm).
Holotype, USNM 582249 ♂
Paratype, EKVK 119 ♀
Greatest length of skull
Palatal width at canines
Mastoid process width
Maxillary toothrow length
Molariform toothrow length
Width at M2
Mandibular toothrow length
Metacarpal III length
Metacarpal IV length
Metacarpal V length
Diagnosis.—Postauricular patches connected by a thin line of pale hairs to the white fur on the chest; ventrally the proximal one-third of the forearm covered with long white hair; the clitoris elongated and labia swollen (M54253-M54255); hairs on rim of pinna are whitish; lateral projection of mastoid region of the skull less developed that in other Lophostoma; lingual cingulum of the upper canine strongly indented; P3 well developed; posterior lingual cusp on the cingulum of P4 well developed; Ml parastyle absent; Ml hypocone absent or weakly developed; Ml lingual cingulum present; M2 parastyle absent; M2 hypocone absent or weakly developed; M2 lingual cingulum present.
Description and comparisons.—A medium-sized Lophostoma (FA 44.6-45.8 mm; GLS 23.2-23.8 mm; CCL 19.2-19.6 mm; Table 2). All linear measurements of L. kalkoae show overlap with those of L. carrikeri and L. schulzi; L. kalkoae is larger than L. brasiliense, and smaller than L. evotis, L. occidentalism L. silvicolum, and L. yasuni (Table 3). Dorsal pelage in all species of Lophostoma is dark brown and long; individual hairs tricolored with a short, white base (approximately 15% of the length of each hair), a long, dark brown subterminal band (approximately 80% of each hair), and a very short, pale to whitish terminal band. Gular fur is dark brown in L. kalkoae, L. brasiliense, L. evotis, L. schulzi, and L. silvicolum, but pale to whitish in L. carrikeri, L. occidentalis, and L. yasuni. L. kalkoae, L. occidentalis, and L. evotis have white to pale gray postauricular patches (absent in L. brasiliense, L. carrikeri, L. schulzi, L. silvicolum, and L. yasuni) that are connected by a thin line of pale hairs to the white fur on the chest in L. kalkoae (pale line also present in L. evotis, which has a dark venter). The ventral fur is white across the chest, but restricted laterally over the abdomen by the pale brown fur of the sides of the body in L. kalkoae, L. carrikeri, and L. yasuni (venter pale brown in L. brasiliense, L. occidentalis, and L. schulzi; pale to dark brown chest in L. evotis, and L. silvicolum). Abdominal fur is white in L. kalkoae, L. carrikeri, and L. yasuni (pale brown in L. occidentalis, L. brasiliense, and L. schulzi; dark brown in L. evotis and L. silvicolum). Pinnae are sparsely haired and have a whitish rim; folds in the pinna are well marked; a band of skin across the head connects the internal bases of the pinnae. Uropatagium is essentially naked. The dorsal surface of the forearm appears naked in L. kalkoae, L. occidentalis, L. schulzi, and L. silvicolum (the proximal one-third is conspicuously covered with sparse, short hair in L. brasiliense, L. carrikeri, L. evotis, and L. yasuni); ventrally the proximal one-third of the forearm is covered with long, white hair in L. kalkoae (long, pale brown hair in L. brasiliense, L. carrikeri, L. evotis, and L. occidentalis; short, pale brown hair in L. schulzi and L. silvicolum). The dorsal surface of the forearm, digits, legs, and sagittal midline of nose leaf lack wartlike granulations in L. kalkoae, L. brasiliense, L. carrikeri, L. occidentalis, L. evotis, and L. silvicolum (present in L. schulzi). Dorsal surfaces of the feet are covered with short hair. Females have an elongated clitoris and swollen labia (dark red in the live specimen) in L. kalkoae and L. carrikeri (the clitoris is remarkably elongated and resembles the penis of males in L. schulzi; clitoris elongated but labia not swollen in L. brasiliense, L. occidentalis, and L. silvicolum). As is characteristic of other Lophostoma, metacarpal III is shorter than metacarpal V; there are 2 genal vibrissae, along with approximately 10 submental vibrissae on each side of the chin, and 2 interramal vibrissae implanted in a basal bulb.
Selected measurements (in mm) of Lophostomaspecies. Summary statistics (mean and standard deviation [1st line], observed range and sample size [2nd line]) of measurements are given for each species (see Appendix I for a list of specimens measured and Table 1 for definitions of measurement abbreviations). All measurements are in millimeters.
X̄ ± SD Range (n)
20.0 ± 0.9 18.6-21.8 (70)
24.3 ± 0.8 23.0-25.3 (13)
25.3 ± 0.3 24.9-25.5 (3)
26.6 ± 0.7 25.5-28.7 (32)
23.2 ± 0.3 22.8-23.6 (4)
27.6 ± 1.1 25.4-30.5 (163)
X̄ ± SD Range (n)
17.6 ± 0.8 16.4-19.3 (70)
21.0 ± 0.5 20.2-21.9 (13)
21.9 ± 0.2 21.6-22.0 (3)
23.1 ± 0.6 22.1-24.4 (32)
20.1 ± 0.4 19.8-20.6 (4)
24.1 ± 0.9 22.4-26.2 (163)
X̄ ± SD Range (n)
17.1 ± 0.8 15.9-18.8 (70)
20.4 ± 0.5 19.5-21.3 (13)
21.1 ± 0.2 20.9-21.3 (3)
22.3 ± 0.5 21.5-23.7 (32)
19.5 ± 0.4 19.0-20.0 (4)
23.3 ± 0.8 21.6-25.5 (163)
X̄ ± SD Range (n)
8.1 ± 0.2 7.5-8.6 (70)
9.6 ± 0.3 9.1-10.3 (13)
10.0 ± 0.3 9.7-10.2 (3)
10.3 ± 0.3 9.8-11.2 (32)
9.5 ± 0.2 9.3-9.8 (4)
10.6 ± 0.3 10.0-11.7 (163)
ZB X̄ ± SD Range (n)
9.5 ± 0.5 8.5-10.6 (70)
11.2 ± 0.4 10.2-12.1 (13)
12.0 ± 0.3 11.6-12.3 (3)
12.7 ± 0.3 12.1-13.4 (32)
11.4 ± 0.3 11.0-11.8 (4)
13.4 ± 0.5 12.4-14.7 (163)
PB X̄ ± SD Range (n)
3.2 ± 0.1 2.8-3.4 (70)
3.8 ± 0.2 3.3—4.1 (13)
4.0 ± 0.2 3.8-4.2 (3)
4.1 ± 0.1 3.9-4.4 (32)
3.8 ± 0.2 3.7-4.1 (4)
4.1 ± 0.2 3.7-4.5 (163)
X̄ ± SD Range (n)
8.4 ± 0.4 7.5-9.5 (70)
9.7 ± 0.3 9.0-10.1 (13)
10.3 ± 0.2 10.1-10.5 (3)
10.5 ± 0.3 10.1-11.3 (32)
9.7 ± 0.2 9.5-10.0 (4)
11.0 ± 0.4 10.0-12.2 (163)
X̄ ± SD Range (n)
9.3 ± 0.4 8.6-10.2 (70)
11.6 ± 0.6 10.8-12.8 (13)
12.3 ± 0.0 12.3-12.3 (3)
12.8 ± 0.5 11.9-13.8 (32)
11.9 ± 0.2 11.6-12.1 (4)
13.5 ± 0.5 12.4-15.0 (163)
PL X̄ ± SD Range (n)
8.9 ± 0.4 8.2-10.0 (70)
10.7 ± 0.4 10.0-11.1 (13)
11.4 ± 0.2 11.3-11.6 (3)
12.2 ± 0.3 11.6-13.0 (32)
10.1 ± 0.4 9.7-10.6 (4)
13.0 ± 0.6 11.8-14.6 (163)
X̄ ± SD Range (n)
7.0 ± 0.3 6.4-7.7 (70)
8.2 ± 0.2 7.9-8.6 (13)
8.7 ± 0.1 8.6-8.8 (3)
9.5 ± 0.2 9.2-10.0(32)
7.9 ± 0.2 7.7-8.2 (4)
9.8 ± 0.4 9.0-10.6 (163)
X̄ ± SD Range (n)
5.8 ± 0.3 5.0-6.5 (70)
7.0 ± 0.2 6.6-7.3 (13)
7.2 ± 0.1 7.1-7.2 (3)
7.6 ± 0.3 7.0-8.1 (32)
6.4 ± 0.2 6.0-6.6 (4)
7.9 ± 0.4 7.0-9.9 (163)
X̄ ± SD Range (n)
6.3 ± 0.3 5.6-7.0 (70)
7.5 ± 0.2 7.1-7.9 (13)
7.9 ± 0.1 7.7-8.0 (3)
8.5 ± 0.2 8.2-9.0 (32)
7.4 ± 0.2 7.2-7.6 (4)
8.8 ± 0.4 8.0-9.7 (163)
X̄ ± SD Range (n)
12.6 ± 0.6 11.7-14.1 (70)
15.0 ± 0.5 13.8-15.9 (13)
15.8 ± 0.3 15.6-16.1 (3)
17.0 ± 0.4 16.1-18.4 (32)
14.6 ± 0.2 14.2-14.8 (4)
17.9 ± 0.7 16.4-19.9 (163)
X̄ ± SD Range (n)
7.7 ± 0.4 7.0-8.6 (70)
9.3 ± 0.3 8.8-9.7 (13)
9.9 ± 0.1 9.7-10.0 (3)
10.6 ± 0.3 10.1-11.2 (32)
9.1 ± 0.3 8.8-9.3 (4)
11.0 ± 0.4 10.1-12.1 (163)
X̄ ± SD Range (n)
35.3 ± 1.9 30.1-39.9 (70)
46.1 ± 1.1 44.1-47.7 (13)
49.7 ± 1.5 48.7-51.4 (3)
53.9 ± 1.4 51.2-56.8 (32)
43.0 ± 1.1 41.6-44.4 (4)
53.8 ± 2.7 45.4-59.5 (163)
The skull of L. kalkoae has a slender rostrum with an accentuated postorbital constriction resembling that of L. brasiliense, L. carrikeri, and L. occidentalis (rostrum is robust in L. evotis, L. schulzi, L. silvicolum, and L. yasuni). Sagittal crest well developed in the female (EKVK 119) and weakly developed in the male (USNM 582249). Lateral development of the mastoid region is less in L. kalkoae and L. brasiliense; moderate in L. carrikeri; strongly developed and projecting well beyond sides of braincase in L. evotis, L. occidentalis, L. schulzi, L. silvicolum, and L. yasuni. The basioccipital is narrow; basisphenoid pits shallow and the midline septum comparatively wide; whereas in L. carrikeri basisphenoid pits are deeper and the septum conspicuously narrower.
Upper central incisors (I1) are well developed and orthodont; outer upper incisors (I2) well developed and convergent in L. kalkoae (smaller in L. carrikeri). I2 is not displaced from occlusion toothrow. A deep indentation is present on the lingual cingulum of the upper canine in L. kalkoae and L. silvicolum (not as well marked in L. brasiliense, L. carrikeri, L. evotis, L. occidentalis, and L. schulzi). P3 is tall and well developed in L. kalkoae (shorter in L. carrikeri); labial cingulum of P3 weakly developed in L. kalkoae, L. carrikeri, L. evotis, L. occidentalis, L. schulzi, and L. silvicolum (absent in L. brasiliense). P4 is longer than wide in occlusal view in L. kalkoae, L. brasiliense, L. carrikeri, L. evotis, L. occidentalis, and L. silvicolum (length and width subequal in L. schulzi); posterior lingual cusp on the cingulum of P4 well developed in L. kalkoae (weakly developed in L. carrikeri). Metacone and paracone of Ml are subequal in height; postparacrista contacts premetacrista on labial aspect of Ml, hence the trigon is closed labially in L. kalkoae, L. brasiliense, L. carrikeri, and L. schulzi (postparacrista does not contact premetacrista; therefore, trigon open labially in L. evotis, L. occidentalis, and L. silvicolum). Ml parastyle is absent in L. kalkoae and L. carrikeri (present in L. brasiliense, L. evotis, L. occidentalis, L. schulzi, and L. silvicolum); Ml hypocone either absent or weakly developed in L. kalkoae, L. carrikeri, and L. evotis (moderately to well developed in L. brasiliense, L. occidentalis, L. schulzi, and L. silvicolum); Ml lingual cingulum present in L. kalkoae and L. occidentalis (absent in L. brasiliense, L. carrikeri, L. evotis, L. schulzi, and L. silvicolum). Metacone and paracone of M2 are subequal in height; postparacrista contacts premetacrista on labial aspect of M2 closing the trigon labially in L. kalkoae, L. brasiliense, L. carrikeri, and L. schulzi (postparacrista does not contact premetacrista, hence trigon open labially in L. evotis, L. occidentalis, and L. silvicolum); M2 without parastyle in L. kalkoae and L carrikeri (present in L. brasiliense, L. evotis, L. occidentalis, L. schulzi, and L. silvicolum); M2 hypocone either absent or weakly developed in L. kalkoae and L. carrikeri (moderately or well developed in L. brasiliense, L. evotis, L. occidentalis, L. schulzi, and L. silvicolum); M2 lingual cingulum present in L. kalkoae and L. occidentalis (absent in L. brasiliense, L. carrikeri, L. evotis, L. schulzi, and L silvicolum). M3 is compressed labiolingually.
Length and width of the crown of the lower inner incisors are subequal in L. kalkoae, L. brasiliense, L. carrikeri, and L. schulzi (crown longer than wide in L. evotis; width greater than length in L. occidentalis and L. silvicolum). The p3 is well developed in L. kalkoae, L. carrikeri, L. evotis, L. occidentalis, L. schulzi, and L. silvicolum (p3 minute in L. brasiliense); p3 aligned in toothrow (occlusal view) in L. kalkoae, L. carrikeri, L. occidentalis, L. schulzi, and L. silvicolum (p3 labially displaced, not in line with other teeth in L. brasiliense and L. evotis). Labial cingulid of p4 is undulate in L. kalkoae, L. brasiliense, L. carrikeri, and L. evotis (straight in L. occidentalis, L. silvicolum, and L. schulzi).
Multivariate analysis.—We compared the 2 specimens of Lophostoma kalkoae with 70 specimens of L. brasiliense, 13 of L. carrikeri, 3 of L. evotis, 32 of L. occidentalis, 4 of L. schulzi, 163 of L. silvicolum, and 1 of L. yasuni (Appendix I). The first 3 PCs accounted for 91% of the overall variation (Table 4). A plot of factor scores on the first 2 axes (Fig. 4) shows that L. kalkoae clustered with L. carrikeri and L. schulzi on PC1, which represents overall size. We did not plot factor scores for L. brasiliense in Fig. 4 because we wanted a better depiction of the spatial distribution of the other species with L. kalkoae. L. brasiliense is the smallest species in the genus, so its specimens would plot lower on PC1 than all other species of the genus. L. evotis, L. occidentalis, L. silvicolum, and L. yasuni plot higher than L. carrikeri, L. kalkoae, and L. schulzi on PC1, corresponding to their larger sizes (Fig. 4).
Plot of scores on 1st and 2nd axes from a principal component analysis of 18 variables from 13 Lophostoma carrikeri, 3 L. evotis, 2 L. kalkoae sp. nov., 32 L. occidentalis, 4 L. schulzi, 163 L. silvicolum, and 1 L. yasuni. pc = principal component.
Factor loadings for the first 3 factors extracted from a principal component (pc) analysis of 18 variables for Lophostoma brasiliense, L. carrikeri, L. evotis, L. kalkoaesp. nov., L. occidentalis, L. schulzi, L silvicolum,and L. yasuni.See Table 1 for definitions of abbreviations of variables.
Both bats were placed in a flight cage to record their echolocation calls and be photographed. During the photography session the bats where fed katydids, which they readily consumed (M54224-M54236). Both bats emitted echolocation calls that were typical for phyllostomid bats (Kalko 2004): steep frequency-modulated, multiharmonic calls with the main energy in the higher harmonics (mostly in the 2nd and 3rd or in the 3rd to the 4th, rather than the 1st).
In several species of mammals (e.g., Crocuta crocuta and Lemur catta), the appearance of female genitalia resembles those of the male. Such “masculinized” females may show elongation of the clitoris, increased overall size, and aggressively mediated social dominance over males (Drea 2009). This pattern is expressed to greater or lesser extent in some species of Lophostoma. Based on a specimen of L. schulzi (AMNH 257128 [M54312 and M54313]), McCarthy et al. (1989) reported that the clitoris is pendulous, resembling a penis. Simmons and Voss (1998) confirmed the observations of McCarthy et al. (1989), based on 3 specimens collected in French Guiana (AMNH 267105, 267420 [M54314 and M54315], and 267421 [M54316]). The clitoris of L. kalkoae (M54253-M54255) is similar to that of L. carrikeri in being elongated, although not to the same degree as in L. schulzi (M54312-M54316), and the labia are swollen (dark red in live L. kalkoae). Our observations indicate that the clitorides of L. brasiliense, L. occidentalis, and L. silvicolum are elongated like those of L. kalkoae and L. carrikeri, but the labia are not swollen. Further studies are needed in order to understand the significance of and the physiological mechanisms behind this pattern in some species of Lophostoma.
Although L. brasiliense and L. silvicolum are each currently regarded as species, we found considerable morphological and morphometric evidence suggesting that both taxa (Table 3) are composite and deserving of revisory studies (see Velazco and Cadenillas 2011). The morphological patterns found in these 2 species are similar to those of species with distributions in both Central and South America and that now, after analyses based on large sample sizes and a combination of molecular and morphological approaches, are found to be composites of 2 or more species (e.g., Artibeus jamaicensis [Larsen et al. 2010; MarchánRivadeneira et al. 2010], Platyrrhinus helleri [Velazco et al. 2010], and Vampyrodes caraccioli [Velazco and Simmons 2011]). L. kalkoae is the only species of white-bellied Lophostoma present in Central America (Fig. 1) and its recognition increases the number of known species in the genus to 8.
Key to the Species of Lophostoma
1. Fur of underparts entirely white, except on chin and sides of abdomen … 2
1′. Fur of underparts brown to gray, a pale patch on the chest can be present … 4
2. Forearm longer than 44 mm; greatest length of skull 25.5 mm or less… 3
2′. Forearm shorter than 44 mm; greatest length of skull 25.5 mm or more; known only from Ecuador … Lophostoma yasuni
3. Conspicuous pale to white postauricular patches; strong indentation on lingual cingulum of upper canine; known only from Panama … Lophostoma kalkoae
3′. Pale to white postauricular patches lacking; weak indentation on lingual cingulum of the upper canine; known only from South America … Lophostoma carrikeri
4. Forearm shorter than 45 mm; greatest length of skull 24 mm or less … 5
4′. Forearm longer than 45 mm; greatest length of skull 24 mm or more … 6
5. Forearm shorter than 40 mm; lacking small wartlike granulations on head, wings, and legs; greatest length of skull less than 22 mm … Lophostoma brasiliense
5′. Forearm longer than 40 mm; small wartlike granulations on dorsal surfaces of forearms, digits, legs, and nose leaf; greatest length of skull more than 22 mm … Lophostoma schulzi
6. Ml hypocone moderately to well developed; p3 aligned in toothrow when seen in occlusal view …7
6′. Ml hypocone absent; p3 displaced labially from toothrow, not in line with other teeth … Lophostoma evotis
7. Pale to white postauricular patches; indentation on the lingual cingulum of the upper canine either absent or weakly developed … Lophostoma occidentalis
7′. Postauricular patches lacking; strong indentation present on the lingual cingulum of the upper canine … Lophostoma silvicolum
The following curators and collection staff graciously provided access to specimens under their care: N. b.+ Simmons and e.+ Westwig, American Museum of Natural History, New York; B. D. Patterson and J. Phelps, Field Museum of Natural History, Chicago; M. S. Hafner, Museum of Natural Science, Louisiana State University, Baton Rouge; V. Pacheco, Museo de Historia Natural de la Universidad Nacional Mayor de San Marcos, Lima; S. Burneo, Museo de Zoología, Pontificia Universidad Católica del Ecuador, Quito; R. J. Baker, Museum of Texas Tech University, Lubbock; and S. C. Peurach, Patuxent Wildlife Research Center, United States Geological Survey. We thank P. J. Wynne for the illustration of Fig. 2, J. P. Carrera and C. M. Pinto for their measurements of the holotypes of Lophostoma aequatorialis+and L. yasuni, and D. von Staden for the live bat photographs. For critical comments on an early draft of this manuscript, we thank T. Chesser, K. Kline, R. Pine, N. Woodman, and 1 anonymous reviewer. Funding for this project was provided to PMV by the Gerstner and Roosevelt postdoctoral fellowships at the American Museum of Natural History.
1836. Mammifères. In Voyage dans l'Amérique méridionale (le Brésil, la République orientale de l'Uruguay, la République Argentine, la Patagonie, la République du Chili, la République de Bolivia, la République du Pérou), exécuté pendant les années 1826, 1827, 1828, 1829, 1830, 1831, 1832 et 1833 (A. d'Orbigny, ed.), plate 6. P. Bertrand Paris, Paris, France; V. Levrault, Strasbourg, France 4:1–32, 23 plates. [See Sherborn and Griffin 1934 for dates of publication.]
1827. A synopsis of the species of the class Mammalia. Pp. 1–296 in The animal kingdom arranged in conformity with its organization, by the Baron Cuvier, with additional descriptions of all the species hitherto named, and of many not before noticed, by Edward Griffith, F.L.S., A.S., and others (GriffithE., ed.). Geo. B. Whittaker, London, England5:1–392.
2004. Neotropical leaf-nosed bats (Phyllostomidae): ‘whispering’ bats as candidates for acoustic surveys? Pp. 63–69 in Bat echolocation research, tools, techniques and analysis (BrighamR. M., KalkoE. K. V., JonesG., ParsonsS., LimpensH. J. G. A., eds.). Bat Conservation International, Austin, Texas.
1867. Fernere Mittheilungen zur Kenntniss der Flederthiere, namentlich über Arten des Leidener und Britischen Museums. Monatsberichte der Königlich-Preussischen Akademie der Wissenschaften zu Berlin 1867:672–681.
. 2000. Phylogeny of phyllostomid bats (Mammalia: Chiroptera): data from diverse morphological systems, sex chromosomes, and restriction sites. Bulletin of the American Museum of Natural History 248:1–200.
. 2008. Subfamily Phyllostominae Gray, 1825. Pp. 255–300 in Mammals of South America, volume 1. Marsupials, xenarthrans, shrews, and bats (GardnerA. L., ed.). University of Chicago Press, Chicago, Illinois. [Copyright 2007; published March 2008.]