Classification
 Nomenclature
Scientific Name:
Camptochaete pulvinata (Hook.f. & Wilson) A.Jaeger, Ber. Thätigk. St. Gallischen Naturwiss. Ges. 1875–1876: 309 (1877)
Synonymy:
  • Isothecium pulvinatum Hook.f. & Wilson in Wilson, Bot. Antarct. Voy. II (Fl. Nov.-Zel.) Part II, 105 (1854)
  • Ptilocladus pulvinatus (Hook.f. & Wilson) Lindb. in Paris, Index. Bryol. 234 (1894) nom. inval.
  • Thamniella pulvinata (Hook.f. & Wilson) Besch. ex Paris, Index. Bryol. 234 (1894) nom. inval.
Lectotype: N.Z., North Island, Colenso "o", BM-Wilson 000850973! Isotype: BM-Hooker 000850977! (Lectotype designated by Tangney 1997b, p. 95).
  • = Camptochaete beckettii Broth., Öfvers. Finska Vetensk.-Soc. Förh. 42: 114 (1900)
Holotype: N.Z., S Auckland, Thames, D. Petrie, July 1896, H-Brotherus (not seen). Isotype: CHR 629483!
  • = Camptochaete falcifolia Broth., Bernice P. Bishop Mus. Bull. 40: 23 (1927)
Holotype: Hawaiʻi, Maui: without locality, Baldwin, D.D. s.n., H-Brotherus (ex. herb. Levier)!
  • = Stereodon maculosus Dixon, Bull. New Zealand Inst. 3: 337 (1929)
  • Camptochaete maculosa (Dixon) Sainsbury, Rev. Bryol. Lichénol., n.s. 21: 222 (1952)
Holotype: New Zealand, Great Barrier Island, Hutton & Kirk, 81, ex herb.-Mitten, BM 015671412 ! Isotypes: OTA 075721!, NY 00913352!, NY 00913353!
 Description

 Plants slender to robust, (10–) 15–25 (–40–50) mm, dark to pale, green or green-brown, or olive green. Stems ± erect to scrambling, moderately complanate, stipitate; in cross-section oval, 530 × 420 µm with an outer layer of 3–4 cells surrounding a parenchyma and an indistinct central strand. Stipes often weakly developed, 4–7 mm. Fronds loosely and ± irregularly (bi-) pinnate, complanate. Branches straight, distichous, moderately complanate. Frond axis leaves falcate-secund, not altered when dry, concave, oblong-ovate, acute to finely acuminate, entire, (1.4–) 1.6–2.0 × 0.5–0.6 mm, with alar cells forming an often extensive group 10 cells wide and extending c. 14 cells from the leaf base. Branch leaves smaller, sometimes denticulate to the lower margin, with a smaller alar group, 1.0–1.2 (–1.6) × 0.3–0.5 mm. Costa double and failing below mid leaf, faint, sometimes absent. Mid laminal cells not porose, (40–) 53–58 (–85) × 5 µm; becoming moderately porose below to form a weakly differentiated basal band, (18–) 30–50 × 8–10 µm; those above 32–40 × 5 µm, at the extreme apex c. 12–18 (–22) × 5–8 µm.

Dioicous or pseudautoicous. Setae 8–10 mm. Capsules inclined to horizontal, c. 2 mm long; exothecial cells mostly 28–48 × 20–28 µm. Operculum conic, blunt or apiculate, c. 0.7– 0.8 mm long. Exostome teeth c. 500 µm; endostome with a basal membrance ½ the exostome. Calyptra c. 2 mm. Spores 10–12 µm. 

 Recognition

C. pulvinata forms low often dense wefts on rocks and the lower bark of trees. It is easily distinguished by its falcate-secund leaves. It is sometimes difficult to separate from some forms of C. deflexa which may rarely have falcate leaves, but the latter usually lacks the numerous alar cells of C. pulvinata.

While the falcate-secund leaves are unusual in Camptochaete, the rigid stems, dendroid-stipitate growth form and the laminal cell pattern are typical. The sporophyte is that of the genus

C. pulvinata exhibits two forms: a larger (25–40 (–50+) mm) southern form with widely acute leaves and perichaetia and an often small (c. 5–7 × 5–7) group of alar cells, and a northern form which is smaller (10–15 (–20) mm), and has narrower leaf apices, aciculate perichaetia and numerous alar cells (often forming a group 14 × 10–12). However, because of variation within both forms, they are not well separated morphologically and are not here formally recognised. Beever (1986, 1990) has noted the variability of leaf and cell form in C. pulvinata and she treated C. maculosa (Dixon) Sainsbury as a synonym of the former. The features of C. maculosa are characteristic of the northern form.

 Distribution

NI: N Auckland, including offshore islands (TK, HC, GB, LB, Whale I.), S Auckland, Gisborne, Taranaki (Taranaki Maunga), Wellington; SI: Nelson, Marlborough, Canterbury, Westland, Otago, Southland.
Endemic? Also recorded for Hawaiʻi *, see note below.

 Habitat

Common in lowland forests on rocks and the lower bark of trees, it also extends to mid elevations.  It occurs in a wide range of mostly shaded habitats from wet forest near streams in Fiordland to drier habitats such as rocks under coastal kanuka scrub. Altitudinal range: near sea level (Akatore Creek, Otago LD) to 940 m (Mt Cook National Park) and 1000 m on Mt Fyffe (Marborough LD) on the South I., and near sea level on Little Barrier Island, Great Barrier Island, and Raukokore River (Gisborne LD) to 1310 m (north end of Kaweka Range, Hawke’s Bay LD) on the North I.

 Biostatus
Indigenous (Non-endemic)
 Notes

Camptochaete falcifolia Broth. from Hawaiʻi is treated here as a synonym of C. pulvinata. Bartram (1933) compared the type of C. falcifolia with C. pulvinata and found it to be ‘almost in complete accord' with C. pulvinata, and both Hoe (1974) and Miller et al. (1978) followed Bartram in accepting the synonomy. Camptochaete falcifolia is apparently only known from the type specimen. This specimen is incomplete, lacking sufficient material to establish whether or not the plants are stipitate, but it is otherwise typical of C. pulvinata in its wiry pinnate fronds and falcate weakly costate leaves (Bartram 1933; Tangney 1997). Camptochaete pulvinata is otherwise known from N.Z. Camptochaete arbuscula is also present in Hawaiʻi, and Weymouthia mollis​​​​​​​ is shared with Tahiti (Allen & Magill 2003​​​​​​​).

 Bibliography
Allen, B.H.; Magill, R.E. 2003: A revision of Pilotrichella (Lembophyllaceae, Musci). Egri Tanarkepzo foiskola Tudomanyos kozlemenyei. Acta Academiae Paedagogicae Agriensis.Sectio Biologiae. n.s. 24: 43–83.
Bartram, E.B. 1933: Manual of Hawaiian Mosses. Bernice P. Bishop Museum Bulletin 101: 1–275.
Beever, J.E. 1986: Mosses of the Poor Knights Islands, northern New Zealand. Journal of the Royal Society of New Zealand 16: 259–273.
Beever, J.E. 1990: The mosses of Miner’s Cove, Great Barrier Island, northern New Zealand. Records of the Auckland Institute and Museum 27: 155–164.
Brotherus, V.F. 1900: Some new species of Australian mosses described, V. Öfversigt af Finska Vetenskaps-Societetens Förhandlingar 42: 91–128.
Brotherus, V.F. 1927: Hawaiian mosses. Bernice P. Bishop Museum Bulletin 40: 3–35.
Dixon, H.N. 1929: Studies in the bryology of New Zealand, with special reference to the herbarium of Robert Brown. Part VI. Bulletin, New Zealand Institute 3(6): 299–372.
Hoe, W.J. 1974: Annotated checklist of Hawaiian mosses. Lyonia 1: 1–45.
Jaeger, A. 1877: Genera et species muscorum systematice disposita seu adumbratio florae muscorum totius orbis terrarum (continuatio) [Pars VII]. Bericht über die Thätigkeit der St. Gallischen Naturwissenschaftlichen Gesellschaft 1875–1876: 201–371. [More commonly available as the “Separatabdruck” of the same title: 1870–1879: 2 vols.]
Miller, H.A.; Whittier, H.O.; Whittier, B.A. 1978: Prodromus florae muscorum Polynesiae: with a key to genera. Bryophytorum Bibliotheca 16: 1–334.
Paris, E.G. 1894–1898: Index Bryologicus sive enumeratio muscorum hucusque cognitorum adjunctis synonymia distributioneque geographica locupletissimis. Klincksieck, Bordeaux.
Sainsbury, G.O.K. 1952: Critical New Zealand mosses. Revue Bryologique et Lichénologique, n.s. 21: 213–225.
Tangney, R.S. 1997: A taxonomic revision of the genus Camptochaete Reichdt., Lembophyllaceae (Musci). Journal of the Hattori Botanical Laboratory 81: 53–121.
Tangney, R.S. 2026: Lembophyllaceae. In: Glenny, D. (ed.) Flora of New Zealand — Mosses. Fascicle 51. Manaaki Whenua Press, Lincoln.
Wilson, W. 1854 ("1855"): Musci. In: Hooker, J.D. The Botany of the Antarctic Voyage of H.M. Discovery Ships Erebus and Terror, in the years 1839–1843, under the command of Captain Sir James Clark Ross. II. Flora Novae-Zelandiae. Part II. Flowerless plants. Lovell Reeve, London. 57–125.