Pseudoromicia kityoi, 2020
publication ID |
https://doi.org/ 10.1093/zoolinnean/zlaa087 |
DOI |
https://doi.org/10.5281/zenodo.4451452 |
persistent identifier |
https://treatment.plazi.org/id/25458781-FFA1-E41C-50D7-FB91FBCE544C |
treatment provided by |
Admin |
scientific name |
Pseudoromicia kityoi |
status |
sp. nov. |
PSEUDOROMICIA KITYOI MONADJEM, KERBIS PETERHANS, NALIKKA, WASWA, DEMOS & PATTERSON View in CoL SP. NOV.
KITYO’ S SEROTINE
LSID: http://zoobank.org/ urn:lsid:zoobank.org:pub:71737F08-2938-4403-8385-5438B2E5EABE
Holotype: FMNH 223211 , field number JCK 7436 . This specimen was collected by Betty Nalikka and Sadic Waswa Babyesiza during a field training exercise with Julian Kerbis Peterhans. It is an adult male preserved in ethanol, with skull extracted and cleaned, and tissue taken from breast muscle and preserved in dimethyl sulfoxide. Type locality: Mabira Forest Reserve, 0.79 km northeast of Nagojje Station , Mukono District of the Central Region , Uganda; geographical coordinates: 0.4451°N, 32.88876°E ( Fig. 1 View Figure 1 ). The type specimen was netted on 19 October 2012 in cultivated gardens directly adjacent (for a photograph of the type locality, see Fig. S2 View Figure 2 ) to Mabira forest at an elevation of 1130 m above sea level GoogleMaps .
Paratype: One other male ( FMNH 223555 ) was netted at the same location and on the same night as the holotype, and closely resembles it genetically ( Fig. 3B View Figure 3 ) and morphologically ( Tables 5–7) and can therefore be considered a paratype.
Etymology: This species is named in honour of Dr. Robert M. Kityo, mammalogist, mentor and longserving curator at the Museum of Zoology, Makerere University, in recognition of his valuable contributions to bats and small mammal research in the region. His welcoming nature, curiosity, hospitality and support have facilitated numerous and diverse research agendas over the decades for both national and international researchers.
Diagnosis: This is the largest member of the genus Pseudoromicia , with forearm length of 37 and 38 mm ( Table 5) and greatest skull length of 14.70 and 14.99 mm for the two known specimens ( Table 6). In comparison, the maximum greatest skull length in Pse. roseveari (which is the second largest member of the genus) is 14.5 mm ( Table 6). Pseudoromicia brunnea is smaller in forearm length and in most craniodental measurements. Therefore, this species is readily diagnosable by size alone. It can easily be distinguished from the white-winged members of this genus ( Pse. rendalli , Pse. isabella and Pse. tenuipinnis ) by its dark wings.
Description: External characters: Pseudoromicia kityoi is a large-sized pipistrelle-like bat, similar in size to the largest members of the Nycticeinops group, specifically Nyc. macrocephalus and Nyc. happoldorum , which were both described in the genus Paraphypsugo ( Hutterer & Kerbis Peterhans, 2019; Hutterer et al., 2019). Despite its large size, this species is similar in external features to other black-winged members of Pseudoromicia . The pelage is medium brown above and slightly paler below. The individual hairs are unicoloured on the upper parts and bicoloured on the under parts, with the proximal half darker than the distal half. Like Pse. brunnea and Pse. roseveari , the patagium and uropatagium are both dark in colour. The ears are short and rounded, and the tragus has a curved outer margin as is typical of the genus ( Monadjem et al., 2013).
Craniodental characters: The skull is robust for a Pseudoromicia , even more so than in Pse. roseveari . The rostrum has a shallow depression, and the brain case is moderately inflated as in other members of the genus. There is no occipital ‘helmet’ as seen in the cranium of Lae. capensis ( Monadjem et al., 2020b) . The sagittal and lambdoidal crests are visible, and the zygomatic arches are robust for a pipistrelle-like bat ( Fig. 9 View Figure 9 ). The dentition in Pse. kityoi is typical of the genus, with I 2/3, C 1/1, P 1/3, M2/3. In the upper tooth row, I 1 is unicuspid and I 2 is tiny, extending slightly beyond the cingulum of I 1. The P 1 is absent, putting C in contact with P 2. The m 3 is myotodont sensu Van Cakenberghe & Happold (2013).
Biology: Owing to the paucity of specimens, almost nothing can be said about the biology of this species. The only two known specimens were captured within 200 m from the edge of Mabira Forest in a domestic garden (Supporting Information, Fig. S2 View Figure 2 ). However, considering that most members of this genus are restricted to tropical rainforest habitats, and that the two known specimens of this species were captured in a remnant patch of rainforest, its global distribution might be both fragmented and limited in extent. Urgent surveys are required to assess the status of this species at Mabira Forest Reserve, which has been steadily losing habitat to agriculture over the past few decades ( Boffa et al., 2008). We suggest that this species might be present in other Congo Basin forest patches in Uganda (e.g. Semliki, Kibale, Kashyoha-Kitomi) and Kenya (Kakamega), although extensive surveys at Kakamega forest have failed to locate this species there ( Webala et al., 2019). Owing to the limited information available on this species, we recommend that it be given the IUCN conservation status of ‘Data Deficient’, but we note that because of its presumed close association with rapidly disappearing forest habitat, this species is probably of conservation concern.
Its closest known relative is Pse. roseveari , recently described from Mount Nimba and with a limited distribution in the borderland zone between Liberia and Guinea ( Monadjem et al., 2013; Decher et al., 2015; Mamba et al., in press), some 4700 km to the west. Whether either species occurs in the vast tropical rainforests between these two sites is unknown and deserves investigation.
Specimen or taxon | Total length | Tail length | Hindfoot length | Ear length | Forearm length | Body mass |
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Pseudoromicia kityoi | 88 | 34 | 10 | 10 | 38.0 | 7.9 |
Holotype FMNH 223211 | ||||||
Pseudoromicia kityoi | 89 | 36 | 9 | 10 | 37.0 | 8.0 |
Paratype FMNH 223555 | ||||||
Pseudoromicia roseveari | 87.3 ± 2.95, 83–93, | 39.7 ± 2.65, 34–44, | 9.9 ± 1.10, 8–11, | 12.9 ± 0.64, 12–14, | 36.5 ± 1.54, 32.6–38.0, | 6.5 ± 0.50, 6.0–7.0, |
N = 10 | N = 9 | N = 10 | N = 8 | N = 10 | N = 10 | |
Pseudoromicia brunnea | 84.8 ± 3.14, 80–89, | 35.9 ± 1.55, 33–38, | 7.79 ± 0.97, 7–10, | 12.4 ± 0.83, 11–14, | 34.6 ± 1.06, 32.8–36.7, | 6.0 ± 1.04, 4.8–9.4, |
N = 15 | N = 15 | N = 14 | N = 15 | N = 15 | N = 15 | |
Pseudoromicia nyanza | 83 | 30 | 7 | 11 | 31.0 | 8.3 |
Holotype FMNH 215626 | ||||||
Pseudoromicia nyanza | 83.5 ± 2.73, 79–89, | 33.3 ± 2.29, 30–38, | 7.5 ± 0.66, 7–9, | 13.0 ± 0.64, 11–13, | 31.2 ± 1.24, 29.0– 33.0, | 6.1 ± 0.99, 4.8–8.3, |
(other specimens) | N = 13 | N = 13 | N = 13 | N = 13 | N = 13 | N = 13 |
Pseudoromicia rendalli | 88.5 ± 3.92, 82–95, | 37.0 ± 3.15, 32–42, | 7.5 ± 0.90, 6–9, | 11.3 ± 1.57, 9–13, | 34.8 ± 1.30, 33.4–37.0, | 5.8 ± 0.94, 4.0–6.8, |
N = 15 | N = 9 | N = 8 | N = 9 | N = 9 | N = 6 | |
Pseudoromicia isabella | 78.8 ± 2.73, 74–82, | 29.3 ± 4.23, 24–36, | 6.9 ± 1.18, 5–8, | 12.3 ± 1.37, 10–14, | 30.6 ± 1.47, 28.0– 31.9, | 4.7 ± 0.87, 4.0–6.0, |
N = 15 | N = 6 | N = 6 | N = 6 | N = 6 | N = 6 | |
Pseudoromicia tenuipinnis s.s. | 74.2 ± 2.17, 72–77, | 29.2 ± 0.84, 28–30, | 6.5 ± 0.80, 5–7, | 12.7 ± 0.91, 12–14, | 29.4 ± 1.18, 28.1– 32.0, | 4.0 ± 0.29, 3.5–4.4, |
(West Africa) | N = 5 | N = 5 | N = 7 | N = 7 | N = 6 | N = 6 |
Measurements are presented as the mean ± SD, range and sample size (N). Measurements are of the holotypes, other individuals of the two new species and other species of Pseudoromicia . The three species listed above the horizontal black line are dark winged, the four below are white winged (see main text for more details).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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