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heath star moss

campylopus moss

Habit Plants 0.5–5 cm, in dense mats, yellowish to olive green, tomentum present or almost absent. Plants usually 3–10 cm, occasionally longer.
Stems

usually simple, not tomentose or with dense reddish or whitish tomentum.

Leaves

4–6 mm, erect-patent when wet, appressed when dry, lanceolate, straight, with entire margins;

alar cells absent or formed by thin-walled, hyaline to reddish, inflated cells;

basal laminal cells hyaline, rectangular, thin-walled, extending higher at margins and forming a V-shaped area;

distal laminal cells incrassate, shortly rectangular to oblique, chlorophyllose;

costa filling 1/2–3/4 of leaf width, excurrent in a hyaline hair tip, which is conspicuously 90° reflexed, in transverse section showing adaxial hyalocysts and abaxial stereids, shortly lamellose at back with ribs 1–2 cells high.

3–12 mm, erect-patent or appressed foliate, narrowly lanceolate, ending in a smooth or denticulate, straight or reflexed tip;

alar cells large, inflated, hyaline or reddish brown, or not differentiated;

basal laminal cells thin-walled, hyaline, or thick-walled, chlorophyllose, sometimes with pitted walls, rectangular to subquadrate;

distal laminal cell walls incrassate, quadrate to short-rectangular, oblique, or oval to elongate oval;

costa strong, filling 1/3–4/5 of leaf width, excurrent in a more or less long, chlorophyllose or hyaline awn, in transverse section showing a median band of deuters, an adaxial layer of hyalocysts, substereids or stereids, and abaxially layers of stereid or non-stereid cells, and an abaxial row of chlorocysts;

abaxial side of the costa smooth, ridged or lamellose.

Seta

7–12 mm, yellowish brown to brownish in age, often several sporophytes from the same plant, curved or sinuose.

5–10 mm, those of young sporophytes curved downward, pushing the immature capsule between the comal leaves and leaving the calyptra behind when the mature capsule curves upward, sinuose, twisted, cygneous when wet and performing uncoiling movements.

Sexual condition

dioicous.

Capsule

brown, 1.5 mm, slightly asymmetric and curved when empty.

erect and symmetric or curved and asymmetric, sometimes strumose, furrowed when empty;

annulus present but not dehiscent;

operculum rostrate, half as long as the capsule;

peristome teeth divided to the middle in two prongs, reddish or orange and horizontally striate proximally, hyaline and papillose distally.

Calyptra

ciliate at base.

cucullate, ciliate or entire at base.

Spores

12–14 µm.

ca. 13 µm, smooth or papillose.

Specialized

asexual reproduction occasionally by deciduous stem tips.

asexual reproduction by brood leaves, microphyllous branches, deciduous leaves or stem tips or rhizoidal tubers.

Perichaetia

terminal, often bud like, rarely pseudolateral;

perichaetial leaves with a broader, sheathing base and a long, narrow subula.

Campylopus introflexus

Campylopus

Habitat Soil along trails, base of trees, flat roofs of buildings, peat in bogs, sand
Elevation 0-200 m (0-700 ft)
Distribution
from FNA
CA; OR; WA; BC; South America (Argentina, Brazil, Chile); Europe; s Africa; Pacific Islands (New Caledonia, subantarctic Islands, New Zealand); Australia
[WildflowerSearch map]
North America; Mexico; Central America; South America; West Indies; Europe; Asia; Africa; Atlantic Islands; Pacific Islands; Australia
Discussion

Campylopus introflexus occurs in masses in sand dunes along the west coast of North America and throughout the Southern Hemisphere. The species was introduced in Great Britain in 1942, and since the beginning of the 1970s has been aggressively spreading through Europe. It now ranges from Iceland to Spain and from Ireland to Poland. The first record in North America dates from August, 1975, and was made on a gravel roof of a building of Humboldt University, Arcata, California. The species is undoubtedly introduced in North America and is spreading here as rapidly as in Europe. The name C. introflexus was used previously for C. pilifer, thus all old references for C. introflexus in North America have to be referred to that species. Also, specimens of C. surinamensis and C. oerstedianus from North America were named as C. introflexus. Campylopus introflexus is easily recognized by the reflexed hair points. Female plants have terminal perichaetial buds. Problems may rarely arise with forms from shaded habitats, in which the hairpoints are absent or so short that they are not reflexed.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Species ca. 180 (17 in the flora).

The North American species of Campylopus were revised by J.-P. Frahm (1980) based on a study of more than 1000 herbarium specimens. At that time, four species of Campylopus were recorded as new to North America and two species were placed into synonymy. The most recent checklist of the mosses of North America (L. E. Anderson et al. 1990) lists 18 species. Of these, the record of C. zygodonticarpus is based on a misidentification and C. paradoxus is a superfluous name for C. flexuosus, which is also included in the list. Since that time, C. japonicus has been newly recorded for North America, resulting in a total of 17 species, and new names have been introduced for C. aureus, C. japonicus, and C. schwarzii.

Campylopus was formerly divided into three subgenera on the basis of morphology of the transverse section of the costa. Although this classification is no longer used, the anatomy of the costa is still an important character for identification. It is, however, not in all cases necessary to prepare cross sections. The presence of adaxial stereids or hyalocysts can also be observed under the microscope by surface view of the adaxial side of the costa. Since the perichaetial leaves vary in both form and by the presence of thin-walled cells walls in species that usually have thick-walled cells, the study of such characters should be avoided. Alar cells are generally also not a valuable character in Campylopus; they are little differentiated in plants growing in damp habitats but are well developed in plants in exposed habitats with water uptake from the underground. The same is true for the presence or absence of a tomentum. Identification is facilitated if the ranges of the species are considered. Many species are found only very locally.

Excluded Species:

Campylopus zygodonticarpus (Müller Hal.) Paris

L. E. Anderson et al. (1990) in their most recent checklist of the mosses of North America listed this species, based on a specimen (Anderson 26656, DUKE) collected in Mississippi in 1992, consisting of C. tallulensis.

Campylopus subporodictyon (Brotherus) B. H. Allen & Ireland

Known in North America only from British Columbia, this species has recently been transferred to Campylopus from Dicranoweisia.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Leaf tips ending in a hyaline hairpoint
→ 2
1. Leaf tips concolorous
→ 8
2. Hairpoints reflexed.
C. introflexus
2. Hairpoints straight
→ 3
3. Basal laminal cells thick-walled, chlorophyllose, subquadrate to short-rectangular (2:1)
→ 4
3. Basal laminal cells thin-walled, hyaline, long-rectangular (more than 4:1)
→ 5
4. Distal laminal cells vermicular.
C. atrovirens
4. Distal laminal cells rectangular.
C. sinensis
5. Abaxial side of costa lamellose with lamellae 3-4 cells high.
C. pilifer
5. Abaxial side of costa smooth or ridged
→ 6
6. Distal laminal cells oval to elongate oval.
C. schmidii
6. Distal laminal cells rectangular to obliquely rectangular
→ 7
7. Distal laminal cells 4-6:1, plants less than 1 cm, leaves 2.5-4 mm, transverse section of costa with adaxial stereids.
Campylopus carolinae
7. Distal laminal cells 1.5-2:1, plants to 3 cm, transverse section of costa with adaxial hyalocysts.
C. oerstedianus
8. Leaf tips cucullate.
C. atrovirens
8. Leaf tips plane
→ 9
9. Basal laminal cell walls thick-walled, chlorophyllose
→ 10
9. Basal laminal cells thin-walled, hyaline
→ 13
10. Basal laminal cells pitted; transverse section of costa showing adaxial stereids
C. arctocarpus
10. Basal laminal cells with smooth walls; transverse section of costa showing adaxial hyalocysts
→ 11
11. Distal laminal cells 6-10:1; plants distantly foliate with spreading leaves.
C. angustiretis
11. Distal laminal cells shorter; plants densely foliate with appressed leaves
→ 12
12. Distal laminal cells short, subquadrate to rhombic; plants equally foliate
C. flexuosus
12. Distal laminal cells short- to long-rectangular or oblique, 2-4(-6):1; plants in small rosettes or with appressed foliate leaves in a terminal comal tuft.
C. surinamensis
13. Costa occupying 3/5-4/5 of leaf width.
C. gracilis
13. Costa 1/2 of leaf width
→ 14
14. Distal laminal cells rectangular, ca. 4:1
→ 15
14. Distal laminal cells shorter
→ 16
15. Plants in small rosettes; leaves long-subulate.
C. pyriformis
15. Plants in dense cushions; leaves shortly pointed.
C. schimperi
16. Leaves widest below mid leaf; basal and distal laminal cells sharply differentiated; specialized asexual reproduction frequently by boomerang-shaped brood leaves.
C. fragilis
16. Leaves widest at leaf base; basal and distal laminal cells not sharply delimited; specialized asexual reproduction occasionally by deciduous stem tips
→ 17
17. Costa in transverse section without abaxial stereids.
C. subulatus
17. Costa in transverse section showing distinct groups of abaxial stereids.
C. tallulensis
Source FNA vol. 27, p. 371. FNA vol. 27, p. 366. Author: Jan-Peter Frahm.
Parent taxa Dicranaceae > Campylopus Dicranaceae
Sibling taxa
C. angustiretis, C. arctocarpus, C. atrovirens, C. carolinae, C. flexuosus, C. fragilis, C. gracilis, C. oerstedianus, C. pilifer, C. pyriformis, C. schimperi, C. schmidii, C. sinensis, C. subulatus, C. surinamensis, C. tallulensis
Subordinate taxa
C. angustiretis, C. arctocarpus, C. atrovirens, C. flexuosus, C. fragilis, C. gracilis, C. introflexus, C. oerstedianus, C. pilifer, C. pyriformis, C. schimperi, C. schmidii, C. sinensis, C. subulatus, C. surinamensis, C. tallulensis
Synonyms Dicranum introflexum
Name authority (Hedwig) Bridel: Muscol. Recent., suppl. 4: 72. (1818) Bridel: Muscol. Recent., suppl. 4: 71. 1818 ,
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