Classification
 Nomenclature
Scientific Name:
Rhynchostegium laxatum (Mitt.) Paris, Index. Bryol. 1131 (1898) – as luxatum
Synonymy:
  • Hypnum laxatum Mitt., Hooker's J. Bot. Kew Gard. Misc. 8: 264 (1856)
Lectoype: Victoria, Gipps Land, Dr. Mueller 120, NY-Mitten 267964! (Designated by Hedenäs, 1996)
  • = Hypnum elusum Mitt. in Hooker, Handb. New Zealand Fl. 478 (1867)
Holotype: N.Z., Otago, N.E. Valley, 1862, Hector, NY-Mitten 267968!
  • = Rhynchostegium peracuminatum Dixon & Sainsbury in Sainsbury, Trans. & Proc. Roy. Soc. New Zealand 75: 185 (1945)
Isotype: N.Z., on damp log, Ohakune, 20 Aug. 1926, R. Mundy s.n., (herb. Sainsbury 728a), WELT M005804! CHR 570188A!, 570188B!
Etymology:
The epithet laxatum means wide or loose. It was used by Mitten in his protologue in reference to the relatively wide laminal cells in the present species compared to the European R. confertum.
 Description

Plants small to medium-sized, yellow‑green or occasionally bright green, weakly lustrous. Stems irregularly to subpinnately branched, c. 20–50 mm long, decumbent, in cross‑section with 3–5 layers of thick-walled outer cells and a distinct central strand. Branches ascendant and short (mostly 6–8 mm). Stem and branch leaves differentiated by shape, when dry ± striolate and erect, erect-spreading and not or weakly striolate when moist. Stem leaves broadly ovate to oblong-ovate, abruptly tapered to a narrowly acuminate or filiform apex (acumen mostly 0.45–0.6 mm and up to c. 0 4 the total leaf length), weakly concave, narrowed to the insertion, erect to spreading, weakly decurrent, 1.4–1.9 × 0.6–1.0 mm (including acumen), entire or denticulate above; mid laminal cells linear-rhombic, smooth, firm-walled, mostly 54–90 × 7–9 µm; cells of the acumen not differentiated; cells at insertion shorter, thicker-walled and porose in several rows; alar cells slightly inflated or subquadrate in a poorly differentiated group. Branch leaves ovate-acuminate, the acumen usually narrow and ± piliferous, mostly 1.2–1.6(–1.8) × 0.4–0.55(–0.65) mm, erect-spreading when moist, erect and striolate when dry; mid laminal cells linear-rhombic, firm-walled, mostly 45–60(–90) × 7–9 µm, becoming longer in lower leaf and shorter and broader at insertion; alar cells subquadrate and mostly weakly inflated, forming a medium-sized but poorly defined group. Costa variable in length, single or rarely slightly forked, (⅓–)½–⅔ the leaf length, terminal spine lacking or rarely rudimentary.

Perichaetia c. 2.0 mm long, the inner leaves acuminate from an oblong base and erect. Perigonia scattered on stems and branches, c. 0.6–0.8 mm, paraphyses not seen. Setae flexuose, sinistrorse, 12–15 mm, red-brown, smooth; capsules oblong-cylindric, red-brown, constricted below the mouth when dry, 1.4–1.8 mm; exothecial cells oblong, firm-walled, distinctly or weakly collenchymatous; annulus adhering to the operculum; operculum c. 1 mm, curved and distinctly shorter than the theca. Exostome teeth as genus, c. 450 µm; endostomal segments perforate, cilia single or paired, nodose. Spores 13–15 µm, green.

 Recognition

Many herbarium specimens of R. muriculatum are misnamed as R. laxatum. When sterile, the most useful character for distinguishing the two species is the width of the stem leaves, which are c. 0.6–1.0 mm wide in R. laxatum and mostly 0.4–0.5 wide in R. muriculatum. The smooth setae of R. laxatum will readily distinguish fertile material.

 Distribution

NI: N Auckland, S Auckland, Gisborne, Hawke’s Bay, Taranaki, Wellington; SI: Nelson, Marlborough, Canterbury, Westland, Otago, Southland; St; Ch; Sol; Sn; A. Reported from C by Vitt (1974).

Australasian. Tasmania*, mainland Australia*. Hedenäs (2002) has detailed the occurrence of this species in Australia.

 Habitat

Mostly on soil, rotten logs, and tree bases, but also occurring on rock (especially basalt and limestone) and epiphytic on a variety of trees and shrubs, including Coprosma grandifolia, Hoheria sp., Melicytus ramiflorus, Metrosideros excelsa, and Myoporum laetum. Occurring in a range of indigenous forest, shrubland, and grassland types. Also occurring in disturbed habitats, and either under, or epiphytic on, a range of exotic trees (including Eucalyptus, Pinus, Populus, Quercus, Salix, and Sambucus), including those in plantations. On the North I. ranging from near sea level (near Foxton, Wellington L.D.) to at least 900 m (near Blyth Track, Wellington L.D.), and on the South I. to c. 1230 m (Mt Mytton, Nelson L.D.). Relatively few records are from above 1000 m, and these all come from limestone or marble ledges in Nelson L.D.

Occurring with a wide range of terrestrial, epilithic and epiphytic species, including Alleniella hymenodonta, Eurhynchium asperipes, Orthorrhynchium elegans, Racopilum strumiferum, Rhaphidorrhynchium amoenum, Rhynchostegium muriculatum, R. tenuifolium, and Weymouthia cochlearifolia. Mixtures of Rhynchostegium spp. are common and often confusing.

 Biostatus
Indigenous (Non-endemic)
 Notes

Representative material of R. laxatum is easily recognisable. The distinctly striolate (when dry) and non-complanate branch leaves, which are abruptly and usually narrowly acuminate, give this species a distinctive facies. Given its autoicous sexuality, at least some sporophytes are usually observable; the smooth seta and relatively short operculum help to differentiate this species from its congeners. Differences in habit are as reliable as the length of laminal cells to differentiate the present species from R. tenuifolium, despite considerable variability related to habitat conditions.

In the lectotype specimen of this species the upper laminal cells (in branch leaves) are mostly 54–75 µm long; mid to lower laminal cells have similar dimensions, and the leaves are mostly c. 1.2 mm long. These measurements are all near the lower end of the continuous variation for the species.

Although well-developed and representative material is easily recognised, this is a highly variable species and not all material can be named with confidence.

After initial uncertainty, I concur with Sainsbury (1955, p. 443) that R. peracuminatum Dixon & Sainsbury is referable here. The type specimen (three isotypes seen) has branch leaves at the upper end of continuous variation for this species (to c. 1.8 × 0.5 mm) and the specimen is brighter yellow and more lustrous than usual for R. laxatum; most mid laminal cells (branch leaves) are c. 75–90 µm long and the dry leaves are striolate. Like Sainsbury, I consider these specimens to represent an extreme form of R. laxatum.

 Bibliography
Fife, A.J. 2020: Brachytheciaceae. In: Smissen, R.; Wilton, A.D. (ed.) Flora of New Zealand – Mosses. Fascicle 46. Manaaki Whenua Press, Lincoln.
Hedenäs, L. 1996: Taxonomic and nomenclatural notes on Australian Brachytheciaceae (Musci). Nova Hedwigia 62(3-4): 451–465.
Hedenäs, L. 2002: An overview of the family Brachytheciaceae (Bryophyta) in Australia. Journal of the Hattori Botanical Laboratory 92: 51–90.
Hooker, J.D. 1867: Handbook of the New Zealand Flora: a systematic description of the native plants of New Zealand and the Chatham, Kermadec's, Lord Auckland's, Campbell's, and Macquarrie's Islands. Part II. Reeve, London.
Mitten, W. 1856: A list of the Musci and Hepaticae collected in Victoria, Australia, by Dr. F. Mueller. Hooker's Journal of Botany and Kew Garden Miscellany 8: 257–266.
Paris, E.G. 1894–1898: Index Bryologicus sive enumeratio muscorum hucusque cognitorum adjunctis synonymia distributioneque geographica locupletissimis. Klincksieck, Bordeaux.
Sainsbury, G.O.K. 1945: New and critical species of New Zealand mosses. Transactions and Proceedings of the Royal Society of New Zealand 75: 169–186.
Sainsbury, G.O.K. 1955: A handbook of the New Zealand mosses. Bulletin of the Royal Society of New Zealand 5: 1–490.
Vitt, D.H. 1974: A key and synopsis of the mosses of Campbell Island, New Zealand. New Zealand Journal of Botany 12: 185–210.