taxonID	type	description	language	source
03A3CA13FFC5FFCFFF369260FBC2E5FC.taxon	materials_examined	Holotype (Fig. 1). Adult male, CAS 262983 collected from Lang Cave, Mulu National Park, Sarawak, East Malaysia. (04 ° 1 ' 34.34 " N; 114 ° 49 ' 26.77 " E; 155 m; WGS 1984), collected by Izneil Nashriq and Hayden Davis on July 21, 2017 at 20: 00 – 22: 00 hrs.	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFC5FFCFFF369260FBC2E5FC.taxon	diagnosis	Diagnosis. Cyrtodactylus muluensis sp. nov. can be differentiated from all other species of Cyrtodactylus by the combination of the following characters: maximum SVL of at least 88 mm; 10 – 13 supralabials; 8 – 11 infralabials; weak tuberculation on body; no tubercles on ventral surface of forelimbs, gular region, or ventrolateral folds; 33 – 54 paravertebral tubercles; 13 – 15 longitudinal tubercle rows; 33 – 42 ventral scales; 19 – 22 subdigital lamellae on fourth toe; 5 femoro-precloacal pores; enlarged median row of transverse scales; shallow precloacal groove in males; 5 – 8 dark dorsal body bands; body bands as wide as or slightly wider than interspaces; no rostral chevron; no white line edging the body bands and nuchal loop; banding pattern on dorsal side of body; no scattered white tubercles on dorsum; and nine dark caudal bands on original tail. These characters are scored across all currently described Bornean Cyrtodactylus species in Table 3.	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFC5FFCFFF369260FBC2E5FC.taxon	description	Description of holotype. Adult male; 75.3 mm SVL; 98.6 mm TL; head large, moderate in length (HL / SVL 0.29), wide (HW / HL 0.62), slightly flattened (HD / HL 0.38), distinct from neck, triangular in dorsal profile; loreal scales slightly concave posteriorly, flat anteriorly; frontal and prefrontal regions concave; canthus rostralis rounded; snout elongate (ES / HL 0.44), rounded in dorsal profile, laterally constricted; eye large (ED / HL 0.25); ear opening elliptical, moderate in size (EL / HL 0.08), obliquely oriented; eye to ear distance greater than diameter of eye; rostral scale rectangular, divided dorsally by an inverted Y-shaped furrow, no postnasal scale, one medial postrostralis (internasal), bordered laterally by first supralabials; external nares bordered anteriorly by rostral, ventrally by first supralabial; 12 (L / R) rectangular supralabials extending to the upturn of the labial margin, tapering abruptly directly below midpoint of eye; first supralabial largest; 12 (L / R) infralabials extending to the upturn of the labial margin, tapering abruptly directly below midpoint of eye; rostral and loreal scales weakly raised, same size as scales on top of head, occiput, and canthus rostralis; no tubercles on occiput or interorbital region; bony ridge bordering the orbital rim; transverse frontoparietal ridge; 36 / 38 (L / R) supracilliary scales, elongate, smooth, largest anteriorly; mental triangular, bordered laterally by first infralabials and posteriorly by left and right rectangular postmentals which contact medially for approximately 40 % of their length, forming a Yshape; single row of slightly enlarged, elongate chinshields extending posteriorly to sixth infralabial scale; small, flat gular scales gradually grading posteriorly into larger, flat, smooth pectoral and ventral scales. Body with distinct, non-tuberculate ventrolateral folds; dorsal scales small, granular interspersed with low, regularly arranged keeled tubercles; small intervening tubercles occasionally present; tubercles extend from top of head to caudal constriction, and onto anterior one-fifth of tail; tubercles on occiput and nape small, those on posterior portion of body largest; approximately 15 longitudinal rows of tubercles slightly posterior of midbody; 43 paravertebral tubercles; 37 flat imbricate ventral scales between ventrolateral body folds; ventral scales larger than dorsal scales; precloacal scales smooth, slightly larger than ventral scales; moderately deep precloacal groove. Forelimbs relatively short (FL / SVL 0.16); scales on preaxial surface of forelimbs small, tubercles absent; scales on postaxial surface flat, subimbricate, tubercles absent; palmar scales weakly rounded; digits well developed, inflected at basal interphalangeal joints; 19 / 18 (L / R) subdigital lamellae on fourth finger, rectangular, broadly expanded proximal to joint inflection, slightly expanded immediately distal to joint becoming gradually more expanded near the claw; claws well-developed, relatively short; hind limbs more robust than forelimbs, moderate in length (TBL / SVL 0.20); postaxial thigh scales flat, smooth, slightly larger than dorsal granular scales; postaxial tibial scales flat, smooth; expanded femoral scales absent; 3 / 2 (L / R) pore-bearing precloacal scales; precloacal scales expanded forming an inverted T bearing a moderately deep precloacal groove in which porebearing scales are absent; plantar scales slightly raised; digits well developed, inflected at basal, interphalangeal joints; 20 (L / R) subdigital lamellae on fourth toe rectangular, broadly expanded proximal to joint inflection, slightly expanded immediately distal to joint becoming gradually more expanded near the claw. Tail original, 98.6 mm long, 5.9 mm wide at base, tapering to a point distally; dorsal scales flat, squarish; subcaudal region bearing enlarged median row of transverse scales; no caudal furrow; base of tail forming hemipenal swelling; and 4 / 6 cloacal spurs on left / right of hemipenal swelling, respectively, one tubercle substantially larger than the others on both sides. Coloration in life. Dorsum of head, body, limbs, and tail greyish-brown; no V-shaped line on rostrum; wide dark-brown nuchal loop that extends to the tip of the snout, edged by white line; seven dark-brown bands between nuchal loop and the posterior portion of the hindlimb insertion, each edged anteriorly and posteriorly by thin darkbrown lines; body bands wider than interspaces; limbs with light-brown band / blotch pattern; ventral portion of body bearing uniform light cream color; tail bearing nine dark bands separated by nine, narrower grey bands dorsally, uniform beige coloration ventrally. Variation (Fig. 1 & 2). The paratypes are very similar to the holotype in coloration and pattern. In life, the coloration varied due to apparent substrate matching with those on karst bearing a light grey coloration with dark banding, and those on wood and vines bearing a light brown coloration with dark banding. Preserved, CAS 262985 displays lighter coloration than the holotype, with less well-defined banding, and little to no dark coloration on the top of the head; CAS 262985 displays darker coloration than the holotype. The juvenile specimen (CAS 262995) has white bands separating the dark bands on the tail, and tan coloration on the ventral surface of the body.	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFC5FFCFFF369260FBC2E5FC.taxon	distribution	Distribution. Cyrtodactylus muluensis sp. nov. is known from the Clearwater Cave, Long Cave, and Lang Cave within Mulu National Park, Sarawak, East Malaysia. The Clearwater Cave and Long Cave are on the same karst peak ~ 1 km apart. The Mulu area has a high concentration of limestone karst formations, most of which were not surveyed over the course of our work (Fig. 3).	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFC5FFCFFF369260FBC2E5FC.taxon	etymology	Etymology. The specific epithet muluensis is in reference to the type locality, Gunung Mulu National Park. As this is the first endemic gekkonid described from Gunung Mulu, the name muluensis is fitting. Natural history. All specimens of Cyrtodactylus muluensis sp. nov. were collected between 1900 and 2200 hours on karst surfaces and thin vines and branches (Fig. 4). Lizards were found on both vegetation and karst walls, however, there was higher concentration near the cave openings, indicating that the species may find refuge inside of the caves during the daylight hours. All specimens were collected within 5 m of a karst structure. Only one specimen was collected from the inside of a cave; the specimen was approximately 10 m inside the cave entrance and 4 m up from the ground in the grooves of a stalagmite at Lang Cave. No female specimens were gravid; however, one hatchling was collected. The expansive primary forest at Mulu National Park contains a high concentration of karst massifs. Gua Lang is located ~ 1 km from the Melinau Paku River. Clearwater Cave and Long Cave are on the river with the openings of each cave roughly 100 m from the riverbank. The lizards were relatively common, especially on wooden walkways leading to the caves. They were quick to react when approached, and two of the specimens of the type series have regenerated tails. They occur sympatrically with Cyrtodactylus consobrinus (Peters) and C. cf. pubisulcus, however, C. consobrinus was seen almost exclusively on large tree trunks and C. cf. pubisulcus was almost exclusively on low-lying vegetation, indicating that they may not be syntopic with one another. Comparison. Cyrtodactylus muluensis sp. nov. differs from all its Bornean congeners by one or more morphological characteristics. The new species is distinguished from C. baluensis (Mocquard) by having a precloacal groove as opposed to a precloacal pit, and a distinct banding pattern as opposed to bands and blotches; it is distinguished from C. cavernicolus by having a lower number of ventral scales (31 – 38 versus 51 – 58), fewer subdigital lamellae on the fourth toe (19 – 22 versus 22 – 26), and distinct dorsal bands as opposed to dorsal bands and blotches; it is distinguished from C. consobrinus by having a smaller adult maximum SVL (88 mm versus 125 mm), and no white reticulated pattern on occiput; it is distinguished from C. ingeri Hikida by having a precloacal groove as opposed to no depression, and a distinct banding pattern as opposed to bands and blotches; it is distinguished from C. malayanus (de Rooij) by having a lower number of ventral scales (33 – 42 versus 58 – 62), and no tubercles on the upper arm; it is distinguished from C. matsuii Hikida by having a lower maximum SVL (88 mm versus 105 mm), enlarged subcaudals, and a lower number of ventral scales (33 – 42 versus 48 – 51); it is distinguished from C. pubisulcus Inger by having a larger maximum SVL (88 mm versus 74 mm), and a distinct banding pattern as opposed to primarily blotches; and it is distinguished from C. yoshii Hikida by having fewer subdigital lamellae (19 – 22 versus 25 – 30), enlarged subcaudals, and a lower number of ventral scales (33 – 42 versus 50 – 58).	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFCDFFD5FF36967AFF41E15F.taxon	materials_examined	Holotype (Fig. 5). Adult male, CAS 262848 collected near Kampung Tubih Mawang, Serian, Sarawak, East Malaysia. (01 ° 17 ' 47.62 " N; 110 ° 26 ' 33.00 " E; 88 m; WGS 1984) by Izneil Nashriq and Hayden Davis on August 06, 2017 at 20: 00 – 22: 00 hrs (Fig. 1). Paratypes. Paratypes (CAS 262846; CAS 262847; and CAS 262849) (Fig. 5) have the same collection data as the holotype.	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFCDFFD5FF36967AFF41E15F.taxon	diagnosis	Diagnosis. Cyrtodactylus limajalur sp. nov. can be differentiated from all other species of Cyrtodactylus by the combination of the following characters: maximum SVL of at least 94 mm; 10 – 12 supralabials; 9 – 11 infralabials; weak tuberculation on body; no tubercles on ventral surface of forelimbs, gular region, or ventrolateral folds; 34 – 38 paravertebral tubercles; 11 – 13 longitudinal tubercle rows; 33 – 42 ventral scales; 19 – 22 subdigital lamellae on fourth toe; 5 – 6 enlarged femoral scales; no femoral pores; 7 – 8 precloacal pores; precloacal pit in males; enlarged median row of transverse scales; 5 dark dorsal body bands; body bands more than two times the width of interspaces; rostral chevron just posterior to orbitals; no white line edging the body bands and nuchal loop; and no scattered white tubercles on dorsum. These characters are scored across all currently recorded Bornean Cyrtodactylus species in Table 3.	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFCDFFD5FF36967AFF41E15F.taxon	description	Description of holotype. Adult male; 90.8 mm SVL; head large, moderate in length (HL / SVL 0.28), relatively narrow (HW / HL 0.46), moderately flattened (HD / HL 0.36), distinct from neck, triangular in dorsal profile; loreal scales slightly concave posteriorly, flat anteriorly; frontal and prefrontal regions concave; canthus rostralis rounded; snout elongate (ES / HL 0.44), rounded in dorsal profile, laterally constricted; eye large (ED / HL 0.27); ear opening elliptical, moderate in size (EL / HL 0.10), obliquely oriented; eye to ear distance less than diameter of eye; rostral scale rectangular, partially divided dorsally by line extending from the posteriormost portion of the rostral scale to approximately half the distance anteriorly, two postnasal scales, one medial postrostralis (internasal), bordered laterally by first supralabials; external nares bordered anteriorly by rostral, ventrally by first supralabial; 12 / 10 (L / R) rectangular supralabials extending to the upturn of the labial margin, tapering abruptly directly below midpoint of eye; first supralabial largest; 9 / 11 (L / R) infralabials extending to the upturn of the labial margin, tapering abruptly directly below midpoint of eye; loreal scales weakly raised, same size as scales on top of head, occiput, and canthus rostralis; no tubercles on occiput or interorbital region; bony ridge bordering the orbital rim; transverse frontoparietal ridge; 38 / 34 (L / R) supracilliary scales, elongate, smooth, largest anteriorly; mental triangular, bordered laterally by first infralabials and posteriorly by left and right rectangular postmentals which contact medially for 40 % of their length, forming a Y-shape; single row of slightly enlarged, elongate chinshields extending posteriorly to sixth infralabial scale; small, flat gular scales gradually grading posteriorly into larger, flat, smooth pectoral and ventral scales. Body with distinct, non-tuberculate ventrolateral folds; dorsal scales small, granular interspersed with low, regularly arranged smooth tubercles; small intervening tubercles occasionally present; tubercles extend from top of head to caudal constriction, and onto anterior one-fifth of tail; tubercles on occiput and nape small, those on posterior portion of body largest; approximately 13 longitudinal rows of tubercles slightly posterior of midbody; 38 paravertebral tubercles; 42 flat imbricate ventral scales between ventrolateral body folds; ventral scales larger than dorsal scales; precloacal scales with 5 / 3 (L / R) pores, slightly larger than ventral scales; shallow precloacal pit. Forelimbs relatively short (FL / SVL 0.17); scales on preaxial surface of forelimbs small, tubercles absent; scales on postaxial surface flat, tubercles absent; palmar scales weakly rounded; digits well developed, inflected at basal interphalangeal joints; 22 / 21 (L / R) subdigital lamellae on fourth toe rectangular, broadly expanded proximal to joint inflection, slightly expanded immediately distal to joint becoming gradually more expanded near the claw; claws well-developed, relatively short; hind limbs more robust than forelimbs, moderate in length (TBL / SVL 0.20); postaxial thigh scales flat, smooth, slightly larger than dorsal granular scales; ventral tibial scales flat, smooth; 8 / 6 (L / R) expanded femoral scales; expanded precloacal scales; 7 pore-bearing precloacal scales; precloacal scales expanded, forming pit; plantar scales slightly raised; digits well developed, inflected at basal, interphalangeal joints; 20 / 21 (L / R) subdigital lamellae on fourth toe rectangular, broadly expanded proximal to joint inflection, slightly expanded immediately distal to joint becoming gradually more expanded near the claw. Tail regenerated from base, 114.0 mm long, 6.6 mm wide at base, tapering to a point distally; dorsal scales flat, squarish; subcaudal region bearing enlarged median row of transverse scales; no caudal furrow; base of tail forming hemipenal swelling; and 3 / 2 (L / R) cloacal spurs. Coloration in life. Dorsum of head, body, limbs, and tail greyish-brown; V-shaped line on rostrum; wide darkbrown nuchal loop that extends to the tip of the snout, edged by white line; five dark-brown bands between nuchal loop and the posterior portion of the limb insertion, edged anteriorly and posteriorly by thin dark-brown lines; body bands at least two times wider than interspaces; front limbs with light-brown blotch pattern; hind limbs with two dark bands separated by white interspaces; ventral portion of body bearing uniform light cream color; tail regenerated bearing four white spots on the anterior half, light grey dorsal and ventral coloration. Variation. The paratypes are very similar to the holotype in coloration and pattern (Table 4). CAS 262846 and CAS 262847 displays reduced dorsal tuberculation, particularly on the anterior half of the body; CAS 262849 has one less precloacal pore with 4 / 3 (L / R), a less well-defined rostral V-pattern, and no chevron posterior to the orbitals (Figs. 5 & 6).	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFCDFFD5FF36967AFF41E15F.taxon	distribution	Distribution. Cyrtodactylus limajalur sp. nov. is only known from an isolated karst massif in the greater Serian area in southwestern Sarawak. The Serian area has a high concentration of large, isolated karst massifs (Wilford, 1964). Cyrtodactylus limajalur sp. nov. was collected from a karst massif approximately one kilometer from a main road. Surrounding formations were not sampled due to inaccessibility, indicating the possibility that this species inhabits other surrounding karst formations (Fig. 4).	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFCDFFD5FF36967AFF41E15F.taxon	etymology	Etymology. The specific epithet limajalur is in reference to the banding pattern of the species. “ Lima jalur ” loosely translated from Malay is five-banded. Cyrtodactylus limajalur sp. nov. has a very distinct banding pattern that is consistently comprised of five bands. This species is the first Bornean Cyrtodactylus species that displays a consistent banding pattern, without blotches or other markings. Natural history. All specimens of Cyrtodactylus limajalur sp. nov. were collected between 19: 00 and 22: 00 hours on large karst boulders at the base of a large limestone face. No female specimens were gravid. They occur sympatrically with Cyrtodactylus consobrinus and C. pubisulcus, however, C. consobrinus was seen almost exclusively on large tree trunks and C. pubisulcus was only found on low-lying vegetation, indicating that they may not be syntopic with C. limajalur sp. nov. There were no noticeable cave entrances on the karst massif. All specimens were collected within approximately ~ 5 m 2 of each other, however, there did not appear to be anything different or significant about that specific location. All of the specimens comprising the type series had regenerated tails. However, the tails were all fully regenerated indicating that the species may experience higher rates of predation at earlier stages in life. Comparison. Cyrtodactylus limajalur sp. nov. differs from all its Bornean congeners by one or more morphological characteristics. The new species is distinguished from C. baluensis by having a distinct banding pattern as opposed to bands and blotches; it is distinguished from C. cavernicolus by having a lower number of ventral scales (33 – 42 versus 51 – 58), enlarged subcaudals, and a precloacal pit as opposed to a precloacal groove; it is distinguished from C. consobrinus by having a smaller adult maximum SVL (94 mm versus 125 mm), and no white reticulated pattern on occiput; it is distinguished from C. ingeri by having a precloacal pit as opposed to no depression, 5 – 6 enlarged femoral scales as opposed to none, and a distinct banding pattern as opposed to bands and blotches; it is distinguished from C. malayanus by having no tubercles on the upper arm, and a lower number of ventral scales (33 – 42 versus 58 – 62); it is distinguished from C. matsuii by having enlarged subcaudals, 5 – 6 enlarged femoral scales as opposed to none, and a smaller maximum SVL (94 mm versus 105 mm); it is distinguished from C. pubisulcus by having enlarged subcaudals, 5 – 6 enlarged femoral scales as opposed to none, and a precloacal pit as opposed to a precloacal groove; and it is distinguished from C. yoshii by having no tubercles on the upper arm, a lower number of ventral scales (33 – 42 versus 50 – 58), a lower number of subdigital lamellae (19 – 22 versus 25 – 30), and 5 – 6 enlarged femoral scales as opposed to none.	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
03A3CA13FFCDFFD5FF36967AFF41E15F.taxon	description	Phylogenetic analyses. The ML tree shown herein corroborates the morphological data distinguishing the two lineages as new species (Fig. 7). The ML analysis places both C. limajalur sp. nov. and C. muluensis sp. nov. in separate deeply divergent clades with both being distinct from C. cavernicolus sensu stricto, as previously suggested. Cyrtodactylus muluensis sp. nov. is well supported as the sister species to C. pubisulcus sensu stricto, another Bornean endemic. Furthermore, C. muluensis sp. nov. is embedded within the monophyletic group of primarily Philippine endemics, including C. philippinicus, C. redimiculus, C. jambangan, C. tautborum, and the C. agusanensis species complex. Nodal support is lacking for some of the noted relationships: C. pubisulcus and C. baluensis as outgroups to the monophyly containing C. muluensis sp. nov.; C. redimiculus as the nearest outgroup to the C. muluensis sp. nov., C. pubisulcus sensu stricto, C. aurensis, and C. cavernicolus monophyly; and the sister clade relationship between the C. muluensis sp. nov. group and the C. agusanensis clade; but there is strong support for the deepest node forming the Philippine clade. The phylogeny has strong support (92 / 1.00) for designating C. muluensis sp. nov. as a distinct lineage. The two subclades demonstrated within the C. muluensis sp. nov. clade correlate with the karst formation in which they were found in. The clade comprised of specimens CAS 262995 – 262997 originated from the karst formation around the Clearwater Cave, and the specimens in the other subclade were from the karst formation around the Lang Cave. No morphological differences were found between the individuals in the two subclades Cyrtodactylus limajalur sp. nov. forms a clade that is well supported (99 / 0.99) as the sister species to the C. consobrinus / malayanus group. While these latter two species are difficult to distinguish from one another morphologically (Hikida 1991; references therein), they are well-supported as phylogenetically distinct lineages based on the concatenated dataset. Regardless, C. limajalur sp. nov. has strong support for its designation as a new species.	en	Davis, Hayden R., Bauer, Aaron M., Jackman, Todd R., Nashriq, Izneil, Das, Indraneil (2019): Uncovering karst endemism within Borneo: two new Cyrtodactylus species from Sarawak, Malaysia. Zootaxa 4614 (2): 331-352, DOI: 10.11646/zootaxa.4614.2.4
