Zootaxa 4273 (3): 407–422 ISSN 1175-5326 (print edition) Article ZOOTAXA http://www.mapress.com/j/zt/ Copyright © 2017 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4273.3.5 http://zoobank.org/urn:lsid:zoobank.org:pub:775B7652-3A6E-49A6-A297-C69B411D64DD A new species of iguana Brachylophus Cuvier 1829 (Sauria: Iguania: Iguanidae) from Gau Island, Fiji Islands ROBERT N. FISHER1,5, JONE NIUKULA2, DICK WATLING3 & PETER S. HARLOW4 1U.S. Geological Survey, Western Ecological Research Center, San Diego Field Station, 4165 Spruance Road, Suite 200, San Diego, CA 92101-0812, USA. E-mail: [email protected] 2 The National Trust of Fiji, PO Box 2089, Government Buildings, Suva, FIJI ISLANDS. E-mail: [email protected] 3NatureFiji-MareqetiViti, P.O. Box 2041, Government Buildings, Suva, FIJI ISLANDS. E-mail: [email protected] 4Taronga Conservation Society Australia, PO Box 20, Mosman, NSW, AUSTRALIA. E-mail: [email protected] 5Corresponding author. E-mail: Robert Fisher [email protected] Abstract The south Pacific iguanas (Brachylophus) currently have three recognized living species in Fiji. Recent surveys have un- covered more specific variation (morphological and genetic) within the genus and have better defined the geographic rang- es of the named species. One of these recent discoveries is a strikingly different iguana from all other island populations in Fiji which is restricted to Gau Island of the Lomaiviti Province. Gau is the fifth largest island in Fiji and maintains excellent upland forests in the higher elevations. We describe this population from Gau Island as a new species, Brachy- lophus gau sp. nov., in recognition of its type locality. Key words: Pacific islands, endemism, conservation, Iguanian, Brachylophus, Gau Island Introduction The genus Brachylophus currently consists of three living (B. bulabula, B. fasciatus, and B. vitiensis) and one extinct (B. gibbonsi) species of iguanas from Fiji and Tonga in the South Pacific (Pregill & Steadman 2004; Keogh et al. 2008). Additionally the extinct monotypic iguana genus Lapitiguana was also known only from Fiji and was twice the length of the largest living Brachylophus (Pregill & Worthy 2003). Iguanas have had a deep history in the South Pacific and these three extant species are the only true iguanidae remaining in the South Pacific. These iguanas have possibly been present there for 40 million years and their closest relatives occur in the New World in the North American southwest deserts (Townsend et al. 2011). Keogh et al. (2008) recently reviewed Brachylophus using the available genetic and morphological data, resulting in the author’s description of the new species Brachylophus bulabula. All three living species were restricted taxonomically to only the islands where either of these data sets was available in that study. This avoided the issue of over predicting the range of these species from islands where no actual data was collected. This was a conservative approach as the various Fijian iguanas have been mapped as occurring on many more islands in various papers (Gibbons 1981, 1985; Gibbons & Watkins 1982; Zug 1991; Morrison 2003) but since there are no vouchers from most of these islands they were left as species uncertain in this recent taxonomic treatise (see Figure 1 in Keogh et al. 2008). Since 2009, we have been visiting many of the islands where iguanas or their habitat are still known, but from which no tissue samples, morphological measurements, or specimens exist. Our goal is to better define the taxonomic diversity within the genus and identify manageable conservation units. Iguanas have been known from Gau Island for decades but there had been no specimens previously identified in museum collections for analysis (Watling 1986). Recent conservation work on Gau for the Fiji Petrel has brought renewed field surveys, which have included several detections of these iguanas from around the island. This area of Fiji is poorly collected and poorly known herpetologically (Zug 1991), so it is not surprising that this population of Brachylophus might exhibit some distinctive characteristics. These characteristics uniquely Accepted by L. Avila: 15 May. 2017; published: 6 Jun. 2017 407 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 distinguish it from the other three described species and we describe this population as a new species. Additionally we revisited historic museum specimens to determine if any match this new species as recent reassessments of historical specimens have found specimens of systematic significance (Ineich & Fisher 2016). FIGURE 1. Map showing location of Gau Island, the only known location for this iguana species. No further details mapped due to sensitive nature of the records. Materials and Methods Morphological measurements and color pattern descriptions are based on six different live specimens, five preserved specimens (some of which were also observed in life), and photos of seven additional individuals collected on Gau Island. All recent preserved specimens are housed at the University of South Pacific Herpetology Collection, Suva, Fiji (SUVA H). A total of 232 specimens of other species, including possible undescribed species, of Brachylophus were examined for comparison representing 38 other island populations. Few voucher specimens of Brachylophus exist in museums, and most of these have no specific locality information, but we searched for any that might represent this new species. Previously the majority of these museum vouchers were studied resulting, in part, in the description of Brachylophus bulabula (Keogh et al. 2008) and the rediscovery of the type of B. fasciatus (Ineich & Fisher 2016). In this study most of the new Brachylophus specimens analyzed were captured live and measured in the field, and photographs were taken to document additional color pattern characteristics. These live photos are critical as the color and color patterns typically fade rapidly in preservative. 408 · Zootaxa 4273 (3) © 2017 Magnolia Press FISHER ET AL. The following list provides the character names and definitions, some of which are straightforward. Previously in Keogh et al. (2008), many of these were utilized but not necessarily defined in the text. Some changes in how they were recorded then have occurred recently as we discovered a greater phenotypic diversity in Fijian iguana populations, and thus many new characters were added. Not all characters are discussed in the text as they were not found to vary much within our current Brachylophus dataset but might be found variable later as we add more island populations. Expanded definitions of all characters are presented in Appendix 1. Measurements: Width at widest point of body bands; width at dorsal crest of bands; dorsal crest spine maximum height; dorsal crest spine maximum width; ear diameter; eye diameter; forearm length; head height; head length; head width; internaral distance; crus knee to heel; naris-eye length; width of nuchal band; width of pelvic band; tail height; tail length; trunk length, between limbs; snout length, edge of eye to end of snout; snout- vent length; mass for live specimens. Scalation: Femoral pores, total of left and right side, exuding only; number of points on third digit combs; toe combs with fused scales; postmental paired; total postmentals; mental single or divided; parietal eye size; head scale size, shape; labial-nasal contact; rostral-nasal contact; nasal color and intensity; number of scales encircling nasals, including labials; postnasal enlarged and bordering entire posterior portion of nasal; internasals total; number of scales encircling rostral, including labials; size of postnasal/preocular scales; dorsal crest spines; nostril placement; nostril shape; number combs digit three; number combs digit two. Coloration: number dorsal bands; eye color; nuchal pattern. Additionally notes are taken on throat patterns and color, nuchal pattern, tail color and banding. Brachylophus gau sp. nov. Gau Iguana (pronounced Ngau) Figs. 2–7 Brachylophus fasciatus Gibbons 1984 (first map showing island record); Zug 1991; Morrison 2003 (on maps as literature record). Brachylophus bulabula Fisher, Harlow, Edwards, and Keogh 2008. Holotype. SUVA H 0264; collected in forest patch 1 km behind Nukuloa Village, Gau Island, Republic of Fiji (18°2'46.68"S; 179°18'11.41"E, datum WGS84); 243 meters in elevation; collected by Robert Fisher, Peter Harlow, Tuverea Tuamotu, Joeli Vadada, Maleli Biciloa, Mark O’Brien, Poasa Qalo, 1 July 2013. Paratypes. SUVA H 0265 female collected same date, collectors, and locality as holotype (Figure 1). SUVA H 0266–0267 were collected at Nalaqere Creek (18°2'25.91"S; 179°17'12.05"E) on 2 July 2013, by the same collectors as the type. SUVA H 0273 was collected at Waitabua Hill (18°2'S; 179°18'E, WGS84), Gau Island, 439 meters in elevation, on 10 July 2013 by Mark Fraser and Poasa Qalo. BMNH 55.8.16.1-2 collected at Sawaieke (17°59'14"S; 179°15'12"E), Gau Island, between 12 and 27 September 1854 by John MacGillivray. Diagnosis. This species has a unique combination of color pattern characters that distinguish it from all other species of described Brachylophus (Figures 2–7, Table 1). It also does not match any museum specimens we have previously seen in collections, except two from the BMNH that previously lacked specific locality info. These specimens are included in the type series as we were able to determine their provenance as Gau Island (see below in Provenance of Historic Specimens section). Although added to the type series, their measurements are left out of comparisons, but included in Table 2. We found that there are no locality specific museum vouchers that could represent extinct island populations of this species. Otherwise, this species differs from B. vitiensis by having sexually dichromatism, with banded males and females that are either unicolor or with small spots, and a maximum snout vent length for both sexes of 153 mm, versus 255 mm for B. vitiensis. It differs from B. bulabula and fasciatus in that males and females have green throats, whereas in these species males have white solid or white with green/grey spots or blotches, as do the females in most populations. Although in certain populations the females in B. bulabula and fasciatus the throat will be unicolor green, but never the males. It differs from the other three species by having a primarily green colored nasal scale. The mean snout vent length is 149.2 and max size for B. gau is 153 mm (n = 7), versus adult B. fasciatus with a mean 154.5 mm SVL and a maximum 176 mm SVL (n = 57) and B. bulabula with a mean 156.6 mm and a maximum 195 mm SVL (n = 23) (Table 1). FISHER NEW FIJI IGUANA Zootaxa 4273 (3) © 2017 Magnolia Press · 409 (cid:2)(cid:3)(cid:4)(cid:5)(cid:6)(cid:7)(cid:8)(cid:2)(cid:3)(cid:4)(cid:5)(cid:6)(cid:6)(cid:7)(cid:8)(cid:9)(cid:3)(cid:10)(cid:11)(cid:3)(cid:12)(cid:13)(cid:14)(cid:3)(cid:15)(cid:16)(cid:17)(cid:12)(cid:16)(cid:18)(cid:19)(cid:5)(cid:16)(cid:17)(cid:13)(cid:16)(cid:18)(cid:19)(cid:3)(cid:20)(cid:13)(cid:7)(cid:8)(cid:7)(cid:20)(cid:12)(cid:14)(cid:8)(cid:17)(cid:3)(cid:21)(cid:14)(cid:12)(cid:22)(cid:14)(cid:14)(cid:18)(cid:3)(cid:12)(cid:13)(cid:14)(cid:3)(cid:11)(cid:10)(cid:5)(cid:8)(cid:3)Brachylophus(cid:3)(cid:17)(cid:23)(cid:14)(cid:20)(cid:16)(cid:14)(cid:17)(cid:2)(cid:3) B. gau B. vitiensis B. bulabula B. fasciatus (cid:4)(cid:14)(cid:24)(cid:5)(cid:7)(cid:25)(cid:3)(cid:20)(cid:10)(cid:25)(cid:10)(cid:8)(cid:3)(cid:23)(cid:7)(cid:12)(cid:12)(cid:14)(cid:8)(cid:18)(cid:3)dichromatism + - + + (cid:26)(cid:5)(cid:20)(cid:13)(cid:7)(cid:25)(cid:3)(cid:21)(cid:7)(cid:18)(cid:15)(cid:3)(cid:23)(cid:8)(cid:14)(cid:17)(cid:14)(cid:18)(cid:12)(cid:3)(cid:16)(cid:18)(cid:3)(cid:6)(cid:7)(cid:25)(cid:14)(cid:17) (cid:23)(cid:7)(cid:8)(cid:12)(cid:16)(cid:7)(cid:25) (cid:27) (cid:27) (cid:28) (cid:29)(cid:14)(cid:6)(cid:7)(cid:25)(cid:14)(cid:17)(cid:3)(cid:22)(cid:16)(cid:12)(cid:13)(cid:3)(cid:15)(cid:10)(cid:8)(cid:17)(cid:7)(cid:25)(cid:3)(cid:21)(cid:7)(cid:18)(cid:15)(cid:17) (cid:28) (cid:27) (cid:28) (cid:28) (cid:30)(cid:7)(cid:25)(cid:14)(cid:17)(cid:3)(cid:22)(cid:16)(cid:12)(cid:13)(cid:3)(cid:22)(cid:16)(cid:15)(cid:14)(cid:3)(cid:15)(cid:10)(cid:8)(cid:17)(cid:7)(cid:25)(cid:3)(cid:21)(cid:7)(cid:18)(cid:15)(cid:17) (cid:27) (cid:28) (cid:27) (cid:28) (cid:30)(cid:7)(cid:24)(cid:3)(cid:17)(cid:16)(cid:31)(cid:14)(cid:3)!(cid:3)"#$(cid:3)(cid:6)(cid:6) (cid:27) (cid:28) (cid:28) (cid:28) %(cid:13)(cid:8)(cid:10)(cid:7)(cid:12)(cid:3)(cid:22)(cid:13)(cid:16)(cid:12)(cid:14)(cid:3)(cid:10)(cid:8)(cid:3)(cid:22)(cid:13)(cid:16)(cid:12)(cid:14)(cid:3)(cid:22)(cid:16)(cid:12)(cid:13)(cid:3)(cid:17)(cid:23)(cid:10)(cid:12)(cid:17) (cid:28) (cid:28) (cid:27) (cid:27) &(cid:9)(cid:14)(cid:3)(cid:20)(cid:10)(cid:25)(cid:10)(cid:8)(cid:3)(cid:16)(cid:18)(cid:3)(cid:25)(cid:16)(cid:11)(cid:14) (cid:20)(cid:10)(cid:23)(cid:23)(cid:14)(cid:8)(cid:9) (cid:12)(cid:7)(cid:18)(cid:28)(cid:19)(cid:10)(cid:25)(cid:15) (cid:8)(cid:14)(cid:15) (cid:19)(cid:10)(cid:25)(cid:15) (cid:19)(cid:8)(cid:14)(cid:14)(cid:18)/(cid:3)(cid:17)(cid:16)(cid:6)(cid:16)(cid:25)(cid:7)(cid:8)(cid:3)(cid:12)(cid:10)(cid:3) (cid:7)(cid:15)0(cid:7)(cid:20)(cid:14)(cid:18)(cid:12)(cid:3)(cid:17)(cid:20)(cid:7)(cid:25)(cid:14)(cid:17)/(cid:3)(cid:25)(cid:16)(cid:19)(cid:13)(cid:12)(cid:3) (cid:9)(cid:14)(cid:25)(cid:25)(cid:10)(cid:22)(cid:28)(cid:10)(cid:8)(cid:7)(cid:18)(cid:19)(cid:14)(cid:3)(cid:14)(cid:18)(cid:12)(cid:16)(cid:8)(cid:14)(cid:3) (cid:26)(cid:7)(cid:17)(cid:7)(cid:25)(cid:3)(cid:17)(cid:20)(cid:7)(cid:25)(cid:14)(cid:3)(cid:20)(cid:10)(cid:25)(cid:10)(cid:8)(cid:3)(cid:7)(cid:18)(cid:15)(cid:3)(cid:16)(cid:18)(cid:12)(cid:14)n(cid:17)(cid:16)(cid:12)(cid:9)(cid:3)’(cid:17)(cid:14)(cid:14)(cid:3) (cid:10)(cid:8)(cid:7)(cid:18)(cid:19)(cid:14)(cid:3)(cid:16)(cid:18)(cid:17)(cid:16)(cid:15)(cid:14)(cid:3)(cid:8)(cid:16)(cid:6)(cid:3) (cid:18)(cid:7)(cid:17)(cid:7)(cid:25)(cid:3)(cid:7)(cid:18)(cid:15)(cid:3)(cid:14)(cid:24)(cid:12)(cid:14)(cid:18)(cid:15)(cid:16)(cid:18)(cid:19)(cid:3) (cid:9)(cid:14)(cid:25)(cid:25)(cid:10)(cid:22)(cid:3)(cid:11)(cid:10)(cid:8)(cid:3)(cid:14)(cid:18)(cid:12)(cid:16)(cid:8)(cid:14)(cid:3) (cid:10)(cid:8)(cid:7)(cid:18)(cid:19)(cid:14)(cid:3)(cid:21)(cid:5)(cid:12)(cid:3)(cid:10)(cid:18)(cid:25)(cid:9)(cid:3) (cid:29)(cid:16)(cid:19)(cid:5)(cid:8)(cid:14)(cid:3)$(cid:3)(cid:16)(cid:18)(cid:3)((cid:14)(cid:10)(cid:19)(cid:13)(cid:3)et al.(cid:3))**,. 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(cid:4)(cid:14)(cid:24) (cid:30) (cid:29) (cid:29) (cid:30) (cid:30) (cid:30) (cid:29) (cid:30) (cid:29) (cid:4);< "#* ")) "#8 "*, "#) "#8 "$# ""8 ")9 %< (cid:8)(cid:14)(cid:19)(cid:14)(cid:18)(cid:14)(cid:8)(cid:7)(cid:12)(cid:14)(cid:15) 89* $$* 8)# $,8 #"* $"$ 8)* $") (cid:30)(cid:7)(cid:17)(cid:17)(cid:3)’(cid:19)(cid:6). ,* ## "", 87 =) (cid:28) (cid:28) (cid:28) (cid:28) %(cid:10)(cid:12)(cid:7)(cid:25)(cid:3)(cid:23)(cid:10)(cid:8)(cid:14)(cid:17) 8" )7 8* 8" ), $* ), )8 )= 3(cid:10)(cid:8)(cid:17)(cid:7)(cid:25)(cid:3)>(cid:8)(cid:14)(cid:17)(cid:12)(cid:3)(cid:17)(cid:23)(cid:16)(cid:18)(cid:14)(cid:17) 79 9" 99 7, 79 ,) 9" ,7 98 (cid:30)(cid:7)(cid:24)(cid:3)(cid:17)(cid:23)(cid:16)(cid:18)(cid:14)(cid:3)(cid:13)(cid:16)(cid:19)(cid:13)(cid:12) "(cid:2)7 "(cid:2)7 "(cid:2)9 "(cid:2)7 "(cid:2)# "(cid:2), "(cid:2)8 "(cid:2)" "(cid:2)= (cid:11)(cid:5)(cid:17)(cid:14)(cid:15)(cid:3)(cid:10)(cid:18)(cid:3)(cid:10)(cid:18)(cid:14)(cid:3) (cid:17)(cid:16)(cid:15)(cid:14)/(cid:3)(cid:14)(cid:18)(cid:25)(cid:7)(cid:8)(cid:19)(cid:14)(cid:15)(cid:3) (cid:11)(cid:5)(cid:17)(cid:14)(cid:15)(cid:3)(cid:10)(cid:18)(cid:3)(cid:21)(cid:10)(cid:12)(cid:13)(cid:3) (cid:11)(cid:5)(cid:17)(cid:14)(cid:15)(cid:3)(cid:10)(cid:18)(cid:3)(cid:21)(cid:10)(cid:12)(cid:13)(cid:3) (cid:11)(cid:5)(cid:17)(cid:14)(cid:15)(cid:3)(cid:10)(cid:18)(cid:3)(cid:21)(cid:10)(cid:12)(cid:13)(cid:3) (cid:14)(cid:18)(cid:25)(cid:7)(cid:8)(cid:19)(cid:14)(cid:15)(cid:3)(cid:10)(cid:18)(cid:3) (cid:4)(cid:5)(cid:21)(cid:10)(cid:20)(cid:5)(cid:25)(cid:7)(cid:8)(cid:3)(cid:17)(cid:20)(cid:7)(cid:25)(cid:14)(cid:17) (cid:10)(cid:18)(cid:3)(cid:10)(cid:12)(cid:13)(cid:14)(cid:8) (cid:17)(cid:16)(cid:15)(cid:14)(cid:17) (cid:28) (cid:28) (cid:17)(cid:16)(cid:15)(cid:14)(cid:17) (cid:17)(cid:16)(cid:15)(cid:14)(cid:17) (cid:21)(cid:10)(cid:12)(cid:13)(cid:3)(cid:17)(cid:16)(cid:15)(cid:14)(cid:17) (cid:28) (cid:28) 12 "=(cid:2)8 "#(cid:2)) "9(cid:2)= "#(cid:2)" "=(cid:2)$ )*(cid:2)" "=(cid:2)7 "7 "= 1< 8"(cid:2)$ )7 8"(cid:2)# )$(cid:2)8 8)(cid:2)) 8)(cid:2)$ )=(cid:2)= )#(cid:2)= 8* 11 ",(cid:2)" "$(cid:2)9 "9(cid:2)$ "8(cid:2)7 )* "=(cid:2)$ ",(cid:2)9 "7(cid:2)7 "=(cid:2)7 %(cid:8)(cid:5)(cid:18)?(cid:3)(cid:25)(cid:14)(cid:18)(cid:19)(cid:12)(cid:13) 7)(cid:2)# 7#(cid:2), 9$ $,(cid:2)$ 9*(cid:2)9 99(cid:2)# ," #= 7, (cid:29)(cid:10)(cid:8)(cid:14)(cid:7)(cid:8)(cid:6)(cid:3)(cid:25)(cid:14)(cid:18)(cid:19)(cid:12)(cid:13) )$(cid:2)9 )$(cid:2)# )9(cid:2)# ", )9(cid:2)9 )7(cid:2), )=(cid:2)) )"(cid:2)9 )7(cid:2)) >(cid:8)(cid:5)(cid:17)(cid:28)?(cid:18)(cid:14)(cid:14)(cid:3)(cid:12)(cid:10)(cid:3)(cid:13)(cid:14)(cid:14)(cid:25) )= )7 8*(cid:2)" ))(cid:2)8 8)(cid:2)" )=(cid:2), )=(cid:2)7 )#(cid:2)8 8*(cid:2)7 (cid:4)(cid:18)(cid:10)(cid:5)(cid:12)(cid:3)(cid:25)(cid:14)(cid:18)(cid:19)(cid:12)(cid:13) "$(cid:2)) ""(cid:2)= "8(cid:2)8 "*(cid:2)7 "$(cid:2)8 "8(cid:2)$ "8(cid:2)8 "" "8(cid:2)# 1<@(cid:4);<(cid:3)’A. )*(cid:2)=8 )"(cid:2)8" )*(cid:2)#= ))(cid:2)#* )"(cid:2)", )"(cid:2)", )*(cid:2)7) ))(cid:2)=) )8(cid:2)7) %<@(cid:4);< (cid:28) 8(cid:2)*88 )(cid:2),97 8(cid:2)**= 8(cid:2)"9, 8(cid:2)888 )(cid:2),## )(cid:2),8) 8(cid:2))$$ 12@1<(cid:3)’A. 7"(cid:2)$7# #,(cid:2)$7) #7(cid:2),)# 7)(cid:2)"$* 7*(cid:2))$, 7)(cid:2)*89 7#(cid:2)##) 7"(cid:2)997 78(cid:2)888 Description of holotype. Holotype is an adult male (Figure 2–3). Meristics are as follows: snout vent length 150 mm, tail length regenerated, live weight 80 gm, head length 31.4 mm, head width 19.3 mm, head height 18.1 mm, and jaw length 24.4 mm. It has 16 elongated/enlarged upper labials (9 left, 7 right) and 17 elongated/enlarged lower labials (8 left, 9 right). Rostral enlarged and triangular wide at base, apparently split on the left side and contacts with nasal scale only on the right side. Mental is incised half way anteriorly, with three postmental scales between the labial scales. Tympanum is translucent and unpigmented, vertical and oval in shape with less height (5 mm) then the eye is wide (6.4 mm). Nostril scale squarish with egg shaped opening raised dorsally within the scale, pale orange in color within the opening, fades to light-green over the rest of the scale. Parietal eye small and scale containing parietal eye similar in size to surrounding parietal. Supraocular head scales smallest, other head scales larger and polygonal shaped, a fused subocular scale on the right side, enlarged subocular scales on the left side. Dewlap is small in size, slightly rounded and unicolor with the throat. Poorly defined gular pouch covered with smaller scales. 410 · Zootaxa 4273 (3) © 2017 Magnolia Press FISHER ET AL. FIGURE 2. Illustration of the holotype (SUVA H 0264; left) and paratype female (SUVA H 0265; right) of Brachylophus gau sp. nov. The painting is from photographs of these specimens and others from life. Measurements to scale within illustration. The holotype is missing later 2/3 of tail, but tail drawn here based on photos from other males. Painting by Cindy Hitchcock. FISHER NEW FIJI IGUANA Zootaxa 4273 (3) © 2017 Magnolia Press · 411 FIGURE 3. Preserved holotype of Brachylophus gau sp. nov. (SUVA H 0264): A) dorsal view; and B) ventral view. Note distinctive striping on rear legs and diffuse banding on dorsal, and lack of differentiation in throat color from ventrum and no spotting, also tail lacking any distinctive ventral banding. Photo by Baravi Thaman. Two nuchal bands on right side, one originating at tympanum and continuing posteriorly, reaching nuchal crest, the other above shoulder, left side contains one band with some spotting; two dorsal body bands, both with a dorsal bifurcation leading to green infusion within the bands similar to a saddle at the dorsum, one axial band, and all bands not completely colored, with some background diffusion. Tail regenerated and three tail bands, banding 412 · Zootaxa 4273 (3) © 2017 Magnolia Press FISHER ET AL. fades posteriorly into background tail coloration. Nuchal crest poorly defined, 67 modified scales, up to 1.6 mm in height and 2.3 mm in width on the nuchal region. Dorsal scales small and conical shaped. Ventral scales much larger then dorsal ones, elongated and strongly keeled, with posterior ends pointed and elevated. FIGURE 4. Photo of a live male Brachylophus gau sp. nov., illustrating the green throat and diffusion within the dorsal bands. Photo by Joerg Kretzschmar. Limbs long and thin covered with keeled scales similar in size to ventral ones; forearm length 24.7 mm, crus- knee to heal 29 mm. Digits elongated, palms covered with small keeled scales. Third digit of hind feet contains a denticulate comb on proximate phalynx with some fusion of scales. Toenails very long and not worn. Total of 28 enlarged exuding femoral pores (15 left; 13 right). Tail laterally compressed in cross section, weakly crested for first 30% then undifferentiated. Anterior dorsal scales on tail smaller than ventral ones. All tail scales keeled and posteriorly all scales become similar in size and larger. Color in life. Head is emerald green with a white stripe lining the lower jaw just at margin. No blue on face. Eye is copper or coppery brown, and a light orange rim around the interior of the nostril. Throat color is unicolor green but hints of some grey bars. No color break but a subtle transition between throat and venter. Dorsal body background color is an avocado green and transitions to a sulfurous green ventrally. There are two wide bands across the back of a blue/grey green color, but diffused with background color and head color via individual scales. The bands do not cross to the ventral side and break into saddles at dorsal crest. Tail with three bands colored as body, but the last two very faded, this is first third of tail then brown bands towards the anterior. The tail maintains a white lateral border. Hindlimbs with striking recurved bars colored as with body stripes. Forelimbs are unicolor. Dorsal crest scales are green and become less distinctive towards anterior. Color in alcohol. Overall dorsal color is greatly darkened with banding less distinctive but still present. Ventral maintains light-green to blue-grey coloration. Dewlap remains unicolor and not distinctive from ventral coloration. Striking leg banding is obscured. Nasal scale retains light orange color within rim. Parietal eye relatively obscure. Tympanum translucent. Tail becomes brownish and bands become less obvious towards tip. Variation. The diagnosis above describes some of the variability in this species for the main characteristics that distinguish it from the other living forms (Table 1). Variability in scalation and measurements for B. gau are reported in Table 2. Overall it’s a gracile species with long legs and tail. Additional variability in this species is described here and includes either fused or elongated subocular scales in all of the paratypes. Relatively high femoral pore counts. Short dorsal crest height, but high number of dorsal crest scales. Males with two wide dorsal bands, a pelvic band, and a partial nuchal band. Background color of males and females the same lime green. Females have small blue spots anteriorly when looked at closely. FISHER NEW FIJI IGUANA Zootaxa 4273 (3) © 2017 Magnolia Press · 413 FIGURE 5. Photos of two live female Brachylophus gau sp. nov., illustrating the overall green coloration and light spotting. Photos by Mark Fraser and Theo Blossom. 414 · Zootaxa 4273 (3) © 2017 Magnolia Press FISHER ET AL. FIGURE 6. Photo of preserved male paratype of Brachylophus gau sp. nov., (BMNH 55.8.16.2) collected during September 1854 by John MacGillivray on Gau Island. Photo by Sam Fisher. FIGURE 7. Photo of preserved female paratype of Brachylophus gau sp. nov., (BMNH 55.8.16.1) collected during September 1854 by John MacGillivray on Gau Island. Photo by Sam Fisher. Etymology. The specific epithet is for the only island where the species is known to occur, Gau. Comparisons. Table 1 reports the most important characters that distinguish between B. gau and the other three living Brachylophus species. One important difference is that this species has fused or elongated subocular scales, and these scales are as long or longer as the eye, this condition is rare in Brachylophus, and absent in most populations. Dorsal crest scales average 53.2 with a range of 45–60 (n = 50) for B. vitiensis and for B. bulabula dorsal crest scales vary in number between 55–88 with an average of 66.2 (n = 14). B. gau has a greater count than these two species with an average of 71.8 and a range of 67–82 (n = 7), and a lower count than B. fasciatus which averages 74.6 with a range of 52–94 (n = 48). It also has the shortest dorsal crest scales of any species, with a maximum height of 1.8 mm (n = 7). So comparing it to B. vitiensis, it is much shorter, with longer legs and tail, thinner build with fewer dorsal crest spines. Its nasal is mostly the same color as the head with a slight orange tinge on the rim. It has unicolor females, versus the banded females of B. vitiensis. When compared to B. bulabula, this species is shorter by almost 25%, it has a uniform lime green throat, with few black spots, versus white throat in FISHER NEW FIJI IGUANA Zootaxa 4273 (3) © 2017 Magnolia Press · 415 males that may have grey/green or black barring. It lacks a strong nuchal band in males, and has very little orange on the nasal scale. Finally comparing B. gau to B. fasciatus, it has much wider dorsal bands in males, and a more coppery eye, versus the gold eye of B. fasciatus. It lacks the pastel light blue that B. fasciatus tends to have on the anterior of the face, and instead has unicolor lime green head color. Distribution. Brachylophus gau appears restricted to the large inland forest patches on Gau Island (Figure 1). Iguanas were reported from Gau by Watling (1986), but no specimens were collected or described. It continues to be widespread in high quality forest habitat in the interior of Gau Island (Figure 8), with some individuals also in degraded forest closer to the coast (Figure 9). Gau is about 136 sq. km. in size and is the fifth largest island in Fiji. FIGURE 8. Photo showing extensive intact patch of moist forest at higher elevations on Gau Island. Photo courtesy of NatureFiji-MareqetiViti. Provenance of historic specimens. The two specimens at the Natural History Museum, London (BMNH 55.8.16.1-2) were obviously Brachylophus gau based on morphology, but lacked specific locality information except that they were submitted by John MacGillivray, esq. and from H.M.S. Herald. A more complete log of the overall expedition of the Herald within Fiji is presented by David (1995). By examining his expedition notes we were able to determine that John MacGillivray directly discusses finding and collecting an iguana on Gau Island (as he spells it Ngau) on page 55, on line 4 (Figure 10; MacGillivray 1855): In the wood behind the beach I shot but lost a large parrot, and a singular chameleon—like green + variegated lizard with extremely long tail among the foliage of an ivi (Tahitian Chestnut) tree to which it closely assimilated in colour. Later he summarizes his reptile samples from Gau Island collected between September 12th and 27th, 1854, and highlights the Brachylophus, and accurately points out that as of this time there were no samples yet in the British Museum (MacGillivray 1855). Additionally he discusses/collected Gehyra vorax, Laticauda sp. and Candoia bibroni from Gau Island. This is from page 59 of his notes (Figure 11): 416 · Zootaxa 4273 (3) © 2017 Magnolia Press FISHER ET AL.