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1

OTA, Y., and N. YONEKURA. "Coral Reef Terraces, Huon Peninsula, Papua New Guinea." Journal of Geography (Chigaku Zasshi) 98, no. 2 (1989): Plate3—Plate4. http://dx.doi.org/10.5026/jgeography.98.2_plate3.

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NAKAMORI, Toru, Colin R. CAMPBELL, and Eugene WALLENSKY. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Living Hermatypic Coral Assemblages at Huon Peninsula, Papua New Guinea." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 743–57. http://dx.doi.org/10.5026/jgeography.104.5_743.

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3

Crandall-Stotler, Barbara, Robert E. Magill, T. Koponen, and D. H. Norris. "Bryophyte Flora of the Huon Peninsula, Papua New Guinea." Bryologist 92, no. 1 (1989): 151. http://dx.doi.org/10.2307/3244035.

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4

Davies, H. L., J. Lock, D. L. Tiffin, et al. "Convergent tectonics in the Huon Peninsula region, Papua New Guinea." Geo-Marine Letters 7, no. 3 (1987): 143–52. http://dx.doi.org/10.1007/bf02238044.

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5

OTA, Yoko, Nobuyuki YONEKURA, and Eiji MATSUMOTO. "Notes on the Coral Reef Terraces, Huon Peninsula, Papua New Guinea." Journal of Geography (Chigaku Zasshi) 98, no. 2 (1989): 177–82. http://dx.doi.org/10.5026/jgeography.98.2_177.

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6

Chappell, John, Yoko Ota, and Kelvin Berryman. "Late quaternary coseismic uplift history of Huon Peninsula, Papua New Guinea." Quaternary Science Reviews 15, no. 1 (1996): 7–22. http://dx.doi.org/10.1016/0277-3791(95)00062-3.

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7

OTA, Yoko, John CHAPPELL, Kelvin R. BERRYMAN, and Akio OMURA. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Late Quaternary Coseismic Uplift, Analysed by Coral Terraces of the Huon Peninsula, Papua New Guinea." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 665–83. http://dx.doi.org/10.5026/jgeography.104.5_665.

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8

Kraus, Fred, Hinrich Kaiser, and Mark O’Shea. "Hidden diversity in semi-fossorial Melanesian forest snakes: A revision of the Toxicocalamus loriae complex (Squamata, Elapidae) from New Guinea." Vertebrate Zoology 72 (November 10, 2022): 997–1034. http://dx.doi.org/10.3897/vz.72.e89647.

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With its conservative set of scalation characters, Toxicocalamus loriae is a morphologically confusing species to which a wide array of phenotypes has been assigned. Careful analysis of 224 museum specimens reveals that multiple distinct species remain hidden under the name T. loriae and that diagnostic, species-level differences are more nuanced in this group of snakes than among other members of the genus. Our taxonomic reassessment leads us to resurrect the species T. lamingtonicomb. nov., T. loennbergiicomb. nov., and T. nymanicomb. nov. from synonymy with T. loriae, retain only T. pratti as a synonym, and describe three new species. As a consequence, T. loriae is no longer recognized as ranging throughout the entire island of New Guinea but is instead restricted to the southern versant of the Papuan Peninsula, and T. lamingtoni and T. spilorhynchussp. nov. are species restricted to that same peninsula’s northern versant. Toxicocalamus loennbergii is known only from the type series taken on the Onin Peninsula in West Papua, Indonesia, Toxicocalamus atratussp. nov. is a high-elevation (800–2200 m) Central Highlands endemic, and T. vertebralissp. nov. ranges from the Central Highlands of Papua New Guinea eastward into the Wau area of Morobe Province. Toxicocalamus nymani inhabits a geologically more heterogenous region, occurring from the Central Highlands eastward to the Huon Peninsula, including Karkar Island, and adjacent areas of Madang Province as well as the northernmost reaches of the Papuan Peninsula. We expect that denser geographic sampling across New Guinea and focussed specimen collection of a few known populations will result in the recognition of additional species in this complex.
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9

Richards, Stephen J., and Paul M. Oliver. "A new species ofHylophorbus (Anura, Microhylidae) from the Huon Peninsula, Papua New Guinea." Mitteilungen aus dem Museum für Naturkunde in Berlin – Zoologische Reihe 83, S1 (2007): 83–89. http://dx.doi.org/10.1002/mmnz.200600030.

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10

Norris, Daniel H., Timo Koponen, and William R. Buck. "Bryophyte Flora of the Huon Peninsula, Papua New Guinea. LXXIMerrilliobryum(Myriniaceae, Musci)." Annales Botanici Fennici 45, no. 4 (2008): 269–76. http://dx.doi.org/10.5735/085.045.0403.

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11

Chappell, John, Yoko Ota, and Colin Campbell. "Decoupling post-glacial tectonism and eustasy at Huon Peninsula, Papua New Guinea." Geological Society, London, Special Publications 146, no. 1 (1999): 31–40. http://dx.doi.org/10.1144/gsl.sp.1999.146.01.02.

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12

MATSUDA, Shinya. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Quaternary Limestones on Huon Peninsula, Papua New Guinea with Special Refernce to Nonarticulated Coralline Algae(Rhodophyta, corallinacear)." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 706–18. http://dx.doi.org/10.5026/jgeography.104.5_706.

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13

RICHARDS, STEPHEN J. "A new species of treefrog (Anura: Hylidae: Litoria) from the Huon Peninsula, Papua New Guinea." Zootaxa 1052, no. 1 (2005): 29. http://dx.doi.org/10.11646/zootaxa.1052.1.3.

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Litoria singadanae sp. nov. is described from lower montane rainforest on the Huon Peninsula, Papua New Guinea. It is a moderately small green frog (two males 29.0–29.1 mm, a female 34.6 mm SV) with long limbs (TL/SV 0.55–0.60), extensively webbed fingers, and a large and prominent tympanum. The new species is unique among Australopapuan hylid frogs in possessing a transparent tympanic membrane. It is known only from the type locality at an altitude of 1280 m asl.
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14

OTA, Yoko, John CHAPPELL, Kelvin R. BERRYMAN, and Yuki OKAMOTO. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Distribution and Genesis of Large-scale Late Quaternary Landslides Disrupting Coral Terraces at Huon Peninsula, Papua New Guinea." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 684–705. http://dx.doi.org/10.5026/jgeography.104.5_684.

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15

Enroth, Johannes. "Altitudinal zonation of Bryophytes on the Huon Peninsula, Papua New Guinea. A floristic approach, with phytogeographic considerations." Bryophyte Diversity and Evolution 2, no. 1 (1990): 61–90. http://dx.doi.org/10.11646/bde.2.1.6.

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The study is based on the major part of the bryophyte material collected during the Koponen-Norris expedition on the Huon Peninsula, Papua New Guinea, in 1981. Only taxa which were collected at least twice are included. Five altitudinal zones, the boundaries of which are indicated by discontinuities in the bryophyte flora, are distinguished: 0 - 300 m, 300 - 1200 m, 1200 - 2200(-2300) m, 2200(-2300) - 2800(- 2900) m, and 2800(-2900) -3400 m. These zones, each characterized by a typical species assemblage, are well in accordance with some earlier New Guinean zonation schemes based on the phanerogamic flora and vegetation. The most obvious correlations between bryophytes’ altitudinal ranges on the Huon Peninsula and their general phytogeography are: New Guinean or Western Melanesian endemics, as well as Malesian endemics, are concentrated at relatively high altitudes (zones III-V); Asian - Oceanian and Asian - Oceanian - Australian taxa, notably mosses, are relatively strongly represented at low to moderate altitudes (zones I-III); species which have their main distribution in the northern hemisphere occur at high altitudes; ‘cosmopolitan’ species either have wide vertical ranges or are restricted to high altitudes.
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16

Ghasemi, Hadi, Phil Cummins, Graeme Weatherill, Chris McKee, Martyn Hazelwood, and Trevor Allen. "Seismotectonic model and probabilistic seismic hazard assessment for Papua New Guinea." Bulletin of Earthquake Engineering 18, no. 15 (2020): 6571–605. http://dx.doi.org/10.1007/s10518-020-00966-1.

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Abstract Papua New Guinea (PNG) lies in a belt of intense tectonic activity that experiences high levels of seismicity. Although this seismicity poses significant risks to society, the Building Code of PNG and its underpinning seismic loading requirements have not been revised since 1982. This study aims to partially address this gap by updating the seismic zoning map on which the earthquake loading component of the building code is based. We performed a new probabilistic seismic hazard assessment for PNG using the OpenQuake software developed by the Global Earthquake Model Foundation (Pagani et al. in Seism Res Lett 85(3):692–702, 2014). Among other enhancements, for the first time together with background sources, individual fault sources are implemented to represent active major and microplate boundaries in the region to better constrain the earthquake-rate and seismic-source models. The seismic-source model also models intraslab, Wadati–Benioff zone seismicity in a more realistic way using a continuous slab volume to constrain the finite ruptures of such events. The results suggest a high level of hazard in the coastal areas of the Huon Peninsula and the New Britain–Bougainville region, and a relatively low level of hazard in the southwestern part of mainland PNG. In comparison with the seismic zonation map in the current design standard, it can be noted that the spatial distribution of seismic hazard used for building design does not match the bedrock hazard distribution of this study. In particular, the high seismic hazard of the Huon Peninsula in the revised assessment is not captured in the current building code of PNG.
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17

Groube, Les, John Chappell, John Muke, and David Price. "A 40,000 year-old human occupation site at Huon Peninsula, Papua New Guinea." Nature 324, no. 6096 (1986): 453–55. http://dx.doi.org/10.1038/324453a0.

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18

Ota, Yoko, John Chappell, Kelvin Berryman, and Yuki Okamoto. "Late Quaternary paleolandslides on the coral terraces of Huon Peninsula, Papua New Guinea." Geomorphology 19, no. 1-2 (1997): 55–76. http://dx.doi.org/10.1016/s0169-555x(96)00041-4.

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19

Ota, Y., J. Chappell, R. Kelley, et al. "Holocene Coral Reef Terraces and Coseismic Uplift of Huon Peninsula, Papua New Guinea." Quaternary Research 40, no. 2 (1993): 177–88. http://dx.doi.org/10.1006/qres.1993.1070.

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AbstractAs many as six levels of emerged Holocene coral terraces occur along 40 km of coastline on the Huon Peninsula, Papua New Guinea, recording uplift history since culmination of the postglacial transgression. The Holocene reef crest, ca. 6000 yr B.P., is tilted down to the northwest, parallel to the coast and concordant with the deformation of the last interglacial coral reef terrace, and descends from 23 to 12 m in the study area. The pattern and rate of deformation have been uniform in the late Quaternary because average uplift rates have remained the same since the last interglaciation. The Holocene terraces described here are erosional features with regressive encrusting corals, developed upon the Holocene transgressive reef. The multiple levels represent episodic, probably coseismic uplift, which has occurred repeatedly in the last ca. 6000 yr. Significant longshore variation in the age of the lowest terrace, from 1700 to 2500 yr B.P., suggests independent coseismic uplift on different sectors of the coast. This is supported by age-height relationships of the higher Holocene terraces. Nonlinear uplift during the Holocene, with recurrence intervals increasing toward the present, is clearly recorded by the regressive terraces in each subregion. Some of the Holocene regressive terraces grade laterally into fluvial terraces capped with debris-flow deposits, probably reflecting seismically triggered mass movement.
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20

Liu, Keyu, Keith A. W. Crook, John Hughes Clarke, and Greg P. Whitmore. "Submarine features of modern open-sea fan deltas, Huon Peninsula, Papua New Guinea." Sedimentary Geology 98, no. 1-4 (1995): 63–77. http://dx.doi.org/10.1016/0037-0738(95)00027-6.

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21

OMURAI, Akio, John CHAPPELL, Arthur L. BLOOM, et al. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Re-evaluation of .ALPHA.-spectrometric 230Th/234U Ages for Late Pleistocene Coral Reef Terraces of Huon Peninsula, Papua New Guinea." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 758–76. http://dx.doi.org/10.5026/jgeography.104.5_758.

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22

OTA, Yoko, and Kelvin R. BERRYMAN. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Outlines of Tectonic Setting, Seismicity and Tectonic Landforms of the Huon Peninsula, Papua New Guinea. Background for the study of coral terraces." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 646–64. http://dx.doi.org/10.5026/jgeography.104.5_646.

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23

NAKAMORI, Toru, Shinya MATSUDA, Akio OMURA, and Yoko OTA. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Depositional Environments of the Pleistocene Reef Limestones at Huon Peninsul a, Papua New Guinea on the Basis of Hermatypic Coral Assemblages." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 725–42. http://dx.doi.org/10.5026/jgeography.104.5_725.

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24

MATSUDA, Shinya, Colin R. CAMPBELL, and Eugene WALLENSKY. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Nonarticulated Coralline Algal Flora of Present-day Coral Reefs on Huon Peninsula." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 719–24. http://dx.doi.org/10.5026/jgeography.104.5_719.

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25

RICHARDS, STEPHEN J., and PAUL M. OLIVER. "Two new species of large green canopy-dwelling frogs (Anura: Hylidae: Litoria) from Papua New Guinea." Zootaxa 1295, no. 1 (2006): 41. http://dx.doi.org/10.11646/zootaxa.1295.1.3.

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Litoria graminea is a large green canopy-dwelling frog originally described from a single specimen from an unknown locality in Papua New Guinea. We demonstrate that this species as currently recognised contains at least three distinct taxa. We restrict the name L. graminea to a population of animals occurring south of New Guinea’s main cordillera and describe two new species of large green arboreal frogs, one from the Kikori River Basin (Southern Highlands and Gulf Province) and one from the Huon Peninsula (Morobe Province). The two new species can be distinguished from each other by differences in iris and sclera colouration, and both can be distinguished from L. graminea by their narrower heads, different iris colouration and by their small round (vs elongate) nuptial pads.
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26

Piippo, Sinikka. "On the bryogeography of Western Melanesian Lejeuneaceae, with comments on their epiphyllous occurrence." Bryophyte Diversity and Evolution 9, no. 1 (1994): 43–57. http://dx.doi.org/10.11646/bde.9.1.8.

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The phytogeography of Western Melanesian (Papua New Guinea, West Irian and the Solomon Islands) Lejeuneaceae was studied on the basis of previous literature and the Huon Peninsula material from the Koponen-Norris expedition. The largest portion of the Lejeuneaceae belong to Western Melanesian and Malaysian endemics. The number of Western Melanesian endemic Lejeuneaceae (20.5 %) is, however, somewhat lower than generally in hepatics (38.2 %). This is apparently due to the large number of epiphyllous taxa in the Lejeuneaceae, a group especially widespread in lowland rainforests.
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27

Chappell, John, and Henry Polach. "Post-glacial sea-level rise from a coral record at Huon Peninsula, Papua New Guinea." Nature 349, no. 6305 (1991): 147–49. http://dx.doi.org/10.1038/349147a0.

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28

Burr, G. S., Chrystie Galang, F. W. Taylor, et al. "Radiocarbon Results from a 13-Kyr BP Coral from the Huon Peninsula, Papua New Guinea." Radiocarbon 46, no. 3 (2004): 1211–24. http://dx.doi.org/10.1017/s0033822200033105.

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This paper presents radiocarbon results from a single Goniastrea favulus coral from Papua New Guinea which lived continuously between 13.0 and 13.1 kyr BP. The specimen was collected from a drill core on the Huon Peninsula and has been independently dated with 230Th. A site-specific reservoir correction has been applied to the results, and coral growth bands were used to calibrate individual growth years. Alternating density bands, which are the result of seasonal growth variations, were subsampled to provide 2 integrated 6-month 14C measurements per year. This allows for 20 independent measurements to be averaged for each decadal value of the 14C calibration, making these results the highest resolution data set available for this brief time range. The finestructure of the data set exhibits 14C oscillations with frequencies on the order of 4 to 10 yr, similar to those observed in modern coral 14C records.
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29

Oliver, Paul M., and Stephen J. Richards. "A New Species of Small Bent-Toed Gecko (Cyrtodactylus: Gekkonidae) from the Huon Peninsula, Papua New Guinea." Journal of Herpetology 46, no. 4 (2012): 488–93. http://dx.doi.org/10.1670/11-101.

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30

Pandolfi, John M., Mairi M. R. Best, and Stephen P. Murray. "Coseismic event of May 15, 1992, Huon Peninsula, Papua New Guinea: Comparison with Quaternary tectonic history." Geology 22, no. 3 (1994): 239. http://dx.doi.org/10.1130/0091-7613(1994)022<0239:ceomhp>2.3.co;2.

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31

Zhu, Z., J. F. Marshall, and J. Chappell. "Effects of differential tectonic uplift on Late Quaternary coral reef diagenesis, Huon Peninsula, Papua New Guinea." Australian Journal of Earth Sciences 41, no. 5 (1994): 463–74. http://dx.doi.org/10.1080/08120099408728156.

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32

Yokoyama, Yusuke, Tezer M. Esat, and Kurt Lambeck. "Last glacial sea-level change deduced from uplifted coral terraces of Huon Peninsula, Papua New Guinea." Quaternary International 83-85 (September 2001): 275–83. http://dx.doi.org/10.1016/s1040-6182(01)00045-3.

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33

Reymond, Claire E., Michael Bode, Willem Renema, and John M. Pandolfi. "Ecological incumbency impedes stochastic community assembly in Holocene foraminifera from the Huon Peninsula, Papua New Guinea." Paleobiology 37, no. 4 (2011): 670–85. http://dx.doi.org/10.1666/09087.1.

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Persistence in the structure of ecological communities can be predicted both by deterministic and by stochastic theory. Evaluating ecological patterns against the neutral theory of biodiversity provides an appropriate methodology for differentiating between these alternatives. We traced the history of benthic foraminiferal communities from the Huon Peninsula, Papua New Guinea. From the well-preserved uplifted reef terrace at Bonah River we reconstructed the benthic foraminiferal communities during a 2200-year period (9000–6800 yr B.P.) of reef building during the Holocene transgressive sea-level rise. We found that the similarity of foraminiferal communities was consistently above 60%, even when comparing communities on either side of a massive volcanic eruption that smothered the existing reef system with ash. Similarly, species diversity and rank dominance were unchanged through time. However, similarity dropped dramatically in the final stages of reef growth, when accommodation space was reduced as sea-level rise slowed. We compared the community inertia index (CII) computed from the observed species abundances with that predicted from neutral theory. Despite the differences in foraminiferal community composition in the younger part of the reef sequence, we found an overall greater degree of community inertia with less variance in observed communities than was predicted from neutral theory, regardless of foraminiferal community size or species migration rate. Thus, persistent species assemblages could not be ascribed to neutral predictions. Ecological incumbency of established foraminiferal species likely prevented stochastic increases in both migrant and rare taxa at the Bonah River site. Regardless of the structuring mechanisms, our reconstruction of Holocene foraminiferal assemblages provides historical context for the management and potential restoration of degraded species assemblages.
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34

Flannery, T. F. "Taxonomic revision of the Thylogale brunii complex (Macropodidae: Marsupialia) in Melanesia, with description of a new spcies." Australian Mammalogy 15, no. 1 (1992): 7. http://dx.doi.org/10.1071/am92002.

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Three species are recognised among material previously referred to as Thylogale brunii. Thylogale brunii as newly defined here is distributed at low elevations in sourhern New Guinea, and inhabits areas with a marked dry season and a savannah-forest ecotone. Thylogate browni includes two subspecies: T. b. lanatus from subalpine grasslands above 3000 m on the Huon Peninsula, and T. b. browni from the Bismarck Archipelago and central-eastern New Guinea, where it occurs from the Cyclops Mountains in the West to the Bulolo area in the east at altitudes up to 2000 m. lt prefers disturbed habitats. Thylogale calobyi n. sp. is restricted to subalpine grasslands along the Central Cordillera at above 3000 m in Papua New Guinea. All three species seem to be sensitive to hunting pressure, with local extinctions being recorded for T. brunii and T. browni in historic times, and a prehistoric extinction for a population of uncertain status from subalpine grasslands in Irian Jaya.
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35

Ota, Yoko, and John Chappell. "Late Quaternary coseismic uplift events on the Huon Peninsula, Papua New Guinea, deduced from coral terrace data." Journal of Geophysical Research: Solid Earth 101, B3 (1996): 6071–82. http://dx.doi.org/10.1029/95jb02245.

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36

Ayling, Bridget F., John Chappell, Michael K. Gagan, and Malcolm T. McCulloch. "ENSO variability during MIS 11 (424–374 ka) from Tridacna gigas at Huon Peninsula, Papua New Guinea." Earth and Planetary Science Letters 431 (December 2015): 236–46. http://dx.doi.org/10.1016/j.epsl.2015.09.037.

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37

Hughes Clarke, John E., Keith A. W. Crook, Donald R. Montgomery, Keyu Liu, Gregory P. Whitmore, and David P. Johnson. "Combining AIRSAR data of Huon peninsula and Hawaii MR1 data of Huon Gulf, Papua New Guinea, for studies of tectonic and sedimentary processes." Marine Geodesy 21, no. 2 (1998): 111–28. http://dx.doi.org/10.1080/01490419809388128.

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38

Pandolfi, John M. "Limited membership in Pleistocene reef coral assemblages from the Huon Peninsula, Papua New Guinea: constancy during global change." Paleobiology 22, no. 2 (1996): 152–76. http://dx.doi.org/10.1017/s0094837300016158.

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One of the most intriguing questions in community ecology remains unanswered: Are ecological communities open assemblages with each species reacting individually to environmental change, or are they integrated units consisting of multispecies assemblages acting in concert? I address this question for marine organisms by examining the taxonomic composition and diversity of Indo-Pacific reef coral communities that have undergone repeated global change between 125 and 30 Ka (thousand years before present).Investigation of community constancy through time relies on two critical questions: (1) Are there significant differences in taxonomic composition among communities from different times? and if not, (2) Are the observed patterns in temporal similarity significantly different from expected patterns resulting from a random sampling of the available within-habitat species pool?Constancy in taxonomic composition and species richness of Pleistocene reef coral assemblages is maintained through a 95-k.y. interval in the raised reef terraces of the Huon Peninsula, Papua New Guinea. Fossil reef coral assemblages show limited membership in species composition despite repeated exposure to marked fluctuations in sea level (up to 120 m) and sea-surface temperatures (up to 6°). During the 95-k.y. interval, the reefs experienced nine cycles of perturbation and subsequent reassembly with similar species composition. Spatial differences in reef coral species composition were greater among the three study sites than among reefs of different ages. Thus local environmental parameters associated with riverine and terrestrial sources had a greater influence on reef coral composition than global climate and sea level changes.The ecological dynamics of reef communities from Papua New Guinea are in marked contrast to those of Quaternary terrestrial and level bottom marine communities which appear to show unlimited community membership on both larger and smaller time scales. Differences in community assembly among ecosystems mean either that coral reefs are fundamentally different or that different ecological patterns and processes are occurring at different temporal scales.
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39

McGreevy, Thomas J., Lisa Dabek, and Thomas P. Husband. "Comparative mtDNA analyses of three sympatric macropodids from a conservation area on the Huon Peninsula, Papua New Guinea." Mitochondrial DNA Part A 27, no. 4 (2015): 2673–78. http://dx.doi.org/10.3109/19401736.2015.1022761.

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40

Ota, Yoko, and John Chappell. "Holocene sea-level rise and coral reef growth on a tectonically rising coast, Huon Peninsula, Papua New Guinea." Quaternary International 55, no. 1 (1999): 51–59. http://dx.doi.org/10.1016/s1040-6182(98)00024-x.

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41

Yokoyama, Yusuke, Tezer M. Esat, Kurt Lambeck, and L. Keith Fifield. "Last Ice Age Millennial Scale Climate Changes Recorded in Huon Peninsula Corals." Radiocarbon 42, no. 3 (2000): 383–401. http://dx.doi.org/10.1017/s0033822200030320.

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Uranium series and radiocarbon ages were measured in corals from the uplifted coral terraces of Huon Peninsula (HP), Papua New Guinea, to provide a calibration for the 14C time scale beyond 30 ka (kilo annum). Improved analytical procedures, and quantitative criteria for sample selection, helped discriminate diagenetically altered samples. The base-line of the calibration curve follows the trend of increasing divergence from calendar ages, as established by previous studies. Superimposed on this trend, four well-defined peaks of excess atmospheric radiocarbon were found ranging in magnitude from 100% to 700%, relative to current levels. They are related to episodes of sea-level rise and reef growth at HP. These peaks appear to be synchronous with Heinrich Events and concentrations of ice-rafted debris found in North Atlantic deep-sea cores. Relative timing of sea-level rise and atmospheric 14C excess imply the following sequence of events: An initial sea-level high is followed by a large increase in atmospheric 14C as the sea-level subsides. Over about 1800 years, the atmospheric radiocarbon drops to below present ambient levels. This cycle bears a close resemblance to ice-calving episodes of Dansgaard-Oeschger and Bond cycles and the slow-down or complete interruption of the North Atlantic thermohaline circulation. The increases in the atmospheric 14C levels are attributed to the cessation of the North Atlantic circulation.
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42

CHAPPELL, John, Akio OMURA, Tezar ESAT, et al. "Coral Terraces on the Huon Peninsula, North Eastern Papua New Guinea. Reconciliation of Late Quaternary Sea Levels Derived from Coral Terraces at Huon Peninsula with Deep Sea Oxygen Records." Journal of Geography (Chigaku Zasshi) 104, no. 5 (1995): 777–84. http://dx.doi.org/10.5026/jgeography.104.5_777.

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43

Koponen, Timo. "Finnish–Hungarian Cooperation in Bryology; Memories from Excursions, Congresses and Research with Professor Tamás Pócs." Polish Botanical Journal 58, no. 1 (2013): 31–38. http://dx.doi.org/10.2478/pbj-2013-0002.

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Abstract The paper describes Professor Tamás Pócs’ cooperation with Finnish bryologists and other cryptogam taxonomists. Cooperation began with exchange of reprints in 1966 and identification of African bryophyte specimens in 1973. In 1976, Timo Koponen visited Budapest and Eger, and joint work continued during a University of Helsinki Department of Botany student excursion to Tanzania in 1988. Tamás Pócs, then a professor at Sokoine Agricultural University, arranged the logistics for the preparatory visit of four teachers as well as for the excursion itself. Later, Pócs participated in the Congress of Eastern Asiatic Bryology, the EU-funded ‘Advanced instruction in bryology and lichenology’ (Large Scale Facility) program and the ‘Bryophyte Flora of the Huon Peninsula, Papua New Guinea’ project organized in Helsinki. He was elected a corresponding member of the Finnish Bryological Society in 2009.
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44

OTA, Yoko. "A Note on Future International Joint Work, Based on the Study of Coral Terraces at Huon Peninsula, Papua New Guinea." Geographical Review of Japa,. Ser. A, Chirigaku Hyoron 70, no. 12 (1997): 813–17. http://dx.doi.org/10.4157/grj1984a.70.12_813.

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45

Ayling, Bridget F., Stephen Eggins, Malcolm T. McCulloch, John Chappell, Rainer Grün, and Graham Mortimer. "Uranium uptake history, open-system behaviour and uranium-series ages of fossil Tridacna gigas from Huon Peninsula, Papua New Guinea." Geochimica et Cosmochimica Acta 213 (September 2017): 475–501. http://dx.doi.org/10.1016/j.gca.2017.06.037.

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46

McGreevy, Thomas J., Lisa Dabek, and Thomas P. Husband. "Tree kangaroo molecular systematics based on partial cytochrome b sequences: are Matschie's tree kangaroo (Dendrolagus matschiei) and Goodfellow's tree kangaroo (D. goodfellowi buergersi) sister taxa?" Australian Mammalogy 34, no. 1 (2012): 18. http://dx.doi.org/10.1071/am10017.

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New Guinea tree kangaroos (Dendrolagus spp.) are unique arboreal macropodid marsupials mainly listed as critically endangered or endangered. The molecular systematics of Dendrolagus has not been fully resolved and is critical for the accurate identification of species and their evolutionary relationships. Matschie’s tree kangaroo (D. matschiei) and Goodfellow’s tree kangaroo (D. goodfellowi buergersi) share numerous morphological, physiological, and behavioural traits. We analysed the partial mitochondrial DNA cytochrome b gene for D. matschiei (n = 67), D. g. buergersi (n = 8), D. goodfellowi unidentified ssp. (n = 8), golden-mantled tree kangaroo (D. g. pulcherrimus; n = 1), and two additional New Guinea Dendrolagus taxa to determine whether D. matschiei and D. g. buergersi are sister taxa. D. matschiei and D. g. buergersi were not placed as sister taxa in our phylogenetic analyses; however, we were unable to analyse a known sample from a D. g. goodfellowi. We found initial genetic evidence that D. matschiei and the Lowland tree kangaroo (D. spadix) are sister taxa – they may have diverged after the formation of the Huon Peninsula of Papua New Guinea. Our results also support the elevation of D. g. pulcherrimus to a full species. An improved understanding of Dendrolagus molecular systematics will contribute substantially to their conservation.
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McGREEVY, T. J., L. DABEK, and T. P. HUSBAND. "A multiplex PCR assay to distinguish among three sympatric marsupial taxa from Huon Peninsula, Papua New Guinea, using the mitochondrial control region." Molecular Ecology Resources 10, no. 2 (2010): 397–400. http://dx.doi.org/10.1111/j.1755-0998.2009.02758.x.

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48

McGreevy, Thomas J., Lisa Dabek, Marta Gomez-Chiarri, and Thomas P. Husband. "Genetic diversity in captive and wild Matschie's tree kangaroo (Dendrolagus matschiei) from Huon Peninsula, Papua New Guinea, based on mtDNA control region sequences." Zoo Biology 28, no. 3 (2009): 183–96. http://dx.doi.org/10.1002/zoo.20222.

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49

Cutler, K. B., S. C. Gray, G. S. Burr, et al. "Radiocarbon Calibration and Comparison to 50 Kyr BP with Paired 14C and 230Th Dating of Corals from Vanuatu and Papua New Guinea." Radiocarbon 46, no. 3 (2004): 1127–60. http://dx.doi.org/10.1017/s0033822200033063.

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We calibrated portions of the radiocarbon time scale with combined 230Th, 231Pa, 14C measurements of corals collected from Espiritu Santo, Vanuatu and the Huon Peninsula, Papua New Guinea. The new data map 14C variations ranging from the current limit of the tree-ring calibration [11,900 calendar years before present (cal BP), Kromer and Spurk 1998, now updated to 12,400 cal B P, see Kromer et al., this issue], to the 14C-dating limit of 50,000 cal BP, with detailed structure between 14 to 16 cal kyr BP and 19 to 24 cal kyr BP. Samples older than 25,000 cal BP were analyzed with high-precision 231Pa dating methods (Pickett et al. 1994; Edwards et al. 1997) as a rigorous second check on the accuracy of the 230Th ages. These are the first coral calibration data to receive this additional check, adding confidence to the age data forming the older portion of the calibration. Our results, in general, show that the offset between calibrated and 14C ages generally increases with age until about 28,000 cal BP, when the recorded 14C age is nearly 6800 yr too young. The gap between ages before this time is less; at 50,000 cal BP, the recorded 14C age is 4600 yr too young. Two major 14C-age plateaus result from a 130 drop in Δ14C between 14–15 cal kyr BP and a 700 drop in Δ14C between 22–25 cal kyr BP. In addition, a large atmospheric Δ14C excursion to values over 1000 occurs at 28 cal kyr BP. Between 20 and 10 cal kyr BP, a component of atmospheric Δ14C anti-correlates with Greenland ice δ18O, indicating that some portion of the variability in atmospheric Δ14C is related to climate change, most likely through climate-related changes in the carbon cycle. Furthermore, the 28-kyr excursion occurs at about the time of significant climate shifts. Taken as a whole, our data indicate that in addition to a terrestrial magnetic field, factors related to climate change have affected the history of atmospheric 14C.
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PERKINS, PHILIP D. "New species (130) of the hyperdiverse aquatic beetle genus Hydraena Kugelann from Papua New Guinea, and a preliminary analysis of areas of endemism (Coleoptera: Hydraenidae)." Zootaxa 2944, no. 1 (2011): 1. http://dx.doi.org/10.11646/zootaxa.2944.1.1.

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The Papua New Guinea (PNG) species of the water beetle genus Hydraena Kugelann, 1794, are revised, based on the study of 7,411 databased specimens. The two previously named species are redescribed, and 130 new species are described. The species are placed in 32 species groups. High resolution digital images of all primary types are presented (online version in color), scanning electron micrographs of representative species are given, and geographic distributions are mapped. Male genitalia, representative female terminal abdominal segments and representative spermathecae are illustrated. Papua New Guinea Hydraena species are typically found in sandy/gravelly stream margins, often in association with streamside litter; some species are primarily pond or swamp dwelling, and a few species are usually found in the hygropetric splash zone on stream boulders or on rocks at the margins of waterfalls. The geographic distributions of PNG Hydraena are compared with the Areas of Freshwater Endemism recently proposed by Polhemus and Allen (2007), and found to substantially support those areas. Only one species, H. impercepta Zwick, 1977 is known to be found in both Australia and Papua New Guinea. The probable Australian origins of the PNG hydraenid genera Gymnochthebius and Limnebius are discussed. The origins of just a few species of PNG Hydraena appear to clearly be Australia, and of comparatively recent origin, whereas the origins of the remainder remain problematic because of lack of knowledge of the Hydraena fauna in Papua Province, Indonesia, and islands large and small to the west of New Guinea. No endemic genera of Hydraenidae are currently known for New Guinea, whereas 98% of the known species are endemic. New species of Hydraena are: H. acumena (Eastern Highlands Province: Koma River, tributary of Fio River), H. adelbertensis (Madang Province: Adelbert Mts., below Keki), H. akameku (Madang Province: Akameku–Brahmin, Bismarck Range), H. altapapua (Southern Highlands Province: Sopulkul, 30–35 km NE Mendi), H. ambra (Eastern Highlands Province: Wanitabi Valley, nr. Okapa), H. ambripes (Madang Province: Finisterre Mts., Naho River Valley, Budemu), H. ambroides (Eastern Highlands Province: Wanitabi Valley, nr. Okapa), H. apertista (Madang Province: Finisterre Mts., Lower Naho Valley, Hinggia), H. apexa (Eastern Highlands Province: Okapa), H. aquila (Madang Province: Simbai area), H. aulaarta (Western Highlands Province: Kundum), H. austrobesa (Central Province: nr. Port Moresby, Sogeri Plateau, Musgrave River), H. bacchusi (Eastern Highlands Province: Wanitabi Valley, nr. Okapa), H. balkei (Eastern Highlands Province: Akameku–Brahmin, Bismarck Range), H. bicarinova (Eastern Highlands Province: Wanitabi Valley, nr. Okapa), H. bifunda (Morobe Province: c. 7 mi. Lae–Bulolo road), H. biundulata (Morobe Province: Lae–Bulolo road), H. brahman (Madang Province: Ramu Valley, 4.5 km N Brahman), H. bubulla (Madang Province: Akameku–Brahmin, Bismarck Range), H. buloba (Morobe Province: Herzog Mts., Wagau), H. buquintana (Western Highlands Province: Mt. Hagen town area), H. carinocisiva (Eastern Highlands Province: Aiyura), H. carmellita (Morobe Province: Herzog Mts., Wagau), H. cavifrons (Madang Province: Ramu Valley, 4.5 km N Brahman), H. cheesmanae (Central Province: Kokoda), H. clarinis (Madang Province: Sepik Ramu Basin, Kojé Creek), H. colorata (Morobe Province: 5 miles W of Lae, Buins Creek), H. confluenta (Eastern Highlands Province: Umg. [=environs of] Kainantu, Onerunka), H. copulata (Gulf Province: Marawaka, Mala), H. cunicula (Madang Province: Akameku–Brahmin, Bismarck Range), H. decepta (Eastern Highlands Province: Okapa), H. diadema (Eastern Highlands Province: Purosa Valley, nr. Okapa), H. dudgeoni (Madang Province: Sepik Ramu Basin, Kojé Creek), H. einsteini (Central Province: Port Moresby–Brown River road), H. essentia (Eastern Highlands Province: Sepik River Basin, stream beside milestone labelled G-99), H. exhalista (Gulf Province: Marawaka, Mala), H. fasciata (Morobe Province: Herzog Mts., Wagau), H. fascinata (Madang Province: Finisterre Mts., Naho River Valley, nr. Moro), H. fasciolata (Madang Province: Madang, Ohu Village), H. fasciopaca (Madang Province: Keki, Adelbert Mts.), H. fenestella (Morobe Province: Lae-Bulolo road), H. foliobba (Morobe Province: Herzog Mts., Wagau), H. formosopala (East Sepik Province: Prince Alexander Mts., Wewak), H. funda (Central Province: Moitaka, 7 miles N of Port Moresby), H. fundacta (Madang Province: Adelbert Mts., Sewan–Keki), H. fundapta (Central Province: Port Moresby–Brown River road), H. fundarca (Eastern Highlands Province: Okapa), H. fundextra (Morobe Province: Markham Valley, Gusap), H. galea (Eastern Highlands Province: Akameku–Brahmin, Bismarck Range, 700 m), H. herzogestella (Morobe Province: Herzog Mts., Bundun), H. hornabrooki (East Sepik Province: Sepik, main river), H. huonica (Madang Province: Kewensa, Finisterre Range, Yupna, Huon Peninsula), H. ibalimi (Sandaun Province: Mianmin), H. idema (Eastern Highlands Province: Umg. [=environs of] Onerunka, Ramu River), H. impala (Central Province: nr. Port Moresby, Sogeri Plateau, Musgrave River), H. incisiva (Morobe Province: Herzog Mts., Wagau), H. incista (Western Highlands Province: Simbai, Kairong River), H. infoveola (Gulf Province: Marawaka, Mala), H. inhalista (Madang Province: Finisterre Mts., Naho River Valley, Damanti), H. inplacopaca (Eastern Highlands Province: Waisa, nr. Okapa), H. insandalia (Eastern Highlands Province: Headwaters of Fio River, 0.5 km downstream of river crossing on Herowana/Oke Lookout path, ca. 4.5 km N of Herowana airstrip), H. intensa (Morobe Province: Lae–Bulolo road), H. johncoltranei (National Capital District, Varirata NP), H. jubilata (Madang Province: Finisterre Mts., Naho River Valley, Budemu), H. koje (Madang Province: Sepik Ramu Basin, Kojé Creek), H. koma (Eastern Highlands Province: Koma River, tributary of Fio River, 100 m downstream of rattan bridge crossing, ca. 3.8 km S by E of Herowana airstrip), H. labropaca (Central Province: nr. Port Moresby, Sogeri Plateau, Musgrave River), H. lassulipes (Morobe Province: Herzog Mts., Wagau), H. limbobesa (Gulf Province: Marawaka, near Ande), H. maculopala (Madang Province: Madang, Ohu Village), H. manulea (Morobe Province: Lae, Buins Creek), H. manuloides (Central Province: Port Moresby–Brown River road), H. marawaka (Gulf Province: Marawaka, Mala), H. mercuriala (Sandaun Province: May River), H. mianminica (Sandaun Province:May River), H. nanocolorata (Madang Province: Sepik Ramu Basin, Kojé Creek), H. nanopala (Madang Province: Sepik Ramu Basin, Kojé Creek), H. nitidimenta (Eastern Highlands Province: Koma River, tributary of Fio River, at rattan bridge crossing, ca. 2.6 km N by W of Herowana airstrip), H. okapa (Eastern Highlands Province: Wanitabi Valley, nr. Okapa), H. ollopa (Western Highlands Province: Kundum), H. otiarca (Morobe Province: Herzog Mts., Wagau, Snake River), H. owenobesa (Morobe Province: ca. 10 km S Garaina Saureri), H. pacificica (Morobe Province: Huon Pen., Kwapsanek), H. pala (Morobe Province: Lae–Bulolo road, Gurakor Creek), H. palamita (Central Province: nr. Port Moresby, Sogeri Plateau, Musgrave River), H. paxillipes (Morobe Province: Lae–Bulolo road, Patep Creek), H. pectenata (Madang Province: Finisterre Mts., Naho River Valley, Damanti), H. pegopyga (Madang Province: Ramu Valley, 3 km N Brahman), H. penultimata (Sandaun Province: May River), H. perpunctata (Madang Province: Sepik Ramu Basin, Kojé Creek), H. pertransversa (Eastern Highlands Province: Clear stream, summit of Kassem Pass at forest level), H. phainops (Morobe Province: Lae–Bulolo road, Patep Creek), H. photogenica (Eastern Highlands Province: Goroka, Mt. Gahavisuka), H. picula (Eastern Highlands Province: Goroka, Daulo Pass), H. pilulambra (Eastern Highlands Province: Clear stream, summit of Kassem Pass at forest level), H. pluralticola (Morobe Province: c. 7 miles Lae–Bulolo road), H. processa (Morobe Province: Herzog Mts., Wagau), H. quadriplumipes (Madang Province: Aiome area), H. quintana (Morobe Province: Markham Valley, Lae–Kainantu road, Erap R), H. ramuensis (Madang Province: Ramu Valley, 6 km N Brahman), H. ramuquintana (Madang Province: Ramu Valley, 6 km N Brahman), H. receptiva (Morobe Province: Lae–Bulolo road), H. remulipes (Morobe Province: Herzog Mts., Wagau), H. reticulobesa (Madang Province: Finisterre Mts., Naho River Valley, Moro), H. sagatai (Sandaun Province: Abau River), H. saluta (Madang Province: Finisterre Mts., Naho River Valley, Damanti), H. sepikramuensis (Madang Province: Ramu Valley, Sare River, 4 km N Brahman), H. sexarcuata (Eastern Highlands Province: Akameku–Brahmin, Bismarck Range), H. sexsuprema (Madang Province: Finisterre Mts., Naho River Valley, Damanti), H. spinobesa (Madang Province: Finisterre Mts., Naho River Valley, Budemu), H. striolata (Oro Province: Northern District, Tanbugal Afore village), H. supersexa (Eastern Highlands Province: Okapa), H. supina (Eastern Highlands Province: Wanitabi Valley, nr. Okapa), H. tarsotricha (Morobe Province: Herzog Mts., Wagau, Snake River), H. tetana (Eastern Highlands Province: Okapa), H. thola (Central Province: Port Moresby– Brown River road), H. tholasoris (Morobe Province: Markham Valley, Gusap, c. 90 miles NW of Lae), H. thumbelina (Madang Province: Finisterre Mts., Naho River Valley, Damanti), H. thumbelipes (Sandaun Province: Mianmin), H. tibiopaca (Morobe Province: ridge between Aseki–Menyamya), H. torosopala (Madang Province: Keki, Adelbert Mts.), H. torricellica (Morobe Province: Torricelli Mts., village below Sibilanga Stn.), H. transvallis (Madang Province: Finisterre Mts., Naho River Valley, Damanti), H. trichotarsa (Morobe Province: Lae–Bulolo road), H. tricosipes (Morobe Province: Herzog Mts., Wagau), H. tritropis (Madang Province: Sepik Ramu Basin, Kojé Creek), H. tritutela (Morobe Province: ca. 10 km S Garaina Saureri), H. ulna (Morobe Province: Herzog Mts., Wagau), H. variopaca (Eastern Highlands Province: Wanitabi Valley, nr. Okapa), H. velvetina (Eastern Highlands Province: Purosa Valley, nr. Okapa).
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