Difference between revisions of "Polystichum munitum"

(Kaulfuss) C. Presl

Tent. Pterid. 83. 1836.

Common names: Common sword fern
Illustrated
Basionym: Aspidium munitum Kaulfuss Enum. Filic., 236. 1824
Treatment appears in FNA Volume 2.
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|common_names=Common sword fern
 
|common_names=Common sword fern
|basionyms={{Treatment/ID/Synonym
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|special_status={{Treatment/ID/Special_status
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|code=F
 +
|label=Illustrated
 +
}}
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|basionyms={{Treatment/ID/Basionym
 
|name=Aspidium munitum
 
|name=Aspidium munitum
 
|authority=Kaulfuss
 
|authority=Kaulfuss
 +
|rank=species
 +
|publication_title=Enum. Filic.,
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|publication_place=236. 1824
 
}}
 
}}
 
|synonyms=
 
|synonyms=
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}}<!--
 
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--><span class="statement" id="st-d0_s0" data-properties="stem orientation;stem orientation"><b>Stems </b>erect or ascending.</span> <span class="statement" id="st-d0_s1" data-properties="leaf orientation;leaf some measurement"><b>Leaves </b>arching, 5–18 dm;</span> <span class="statement" id="st-d0_s2" data-properties="bulblet count">bulblets absent.</span> <span class="statement" id="st-d0_s3" data-properties="petiole length;petiole architecture or pubescence"><b>Petiole </b>1/8–1/4 length of leaf, densely scaly;</span> <span class="statement" id="st-d0_s4" data-properties="scale coloration;scale coloration;scale coloration;scale coloration;scale size">scales redbrown to dark-brown or nearly black, gradually diminishing in size distally.</span> <span class="statement" id="st-d0_s5" data-properties="blade shape;blade architecture or shape;base shape"><b>Blade </b>linear-lanceolate, 1-pinnate, base slightly narrowed.</span> <span class="statement" id="st-d0_s6" data-properties="pinna shape;pinna course;pinna shape;pinna arrangement;pinna architecture;pinna arrangement or shape;pinna some measurement;plant habitat;plant habitat"><b>Pinnae </b>narrowly lanceolate, straight to falcate, not overlapping, pinnae of shade-growing plants in 1 plane, those of sun-growing plants twisted or contorted, 1–15 cm;</span> <span class="statement" id="st-d0_s7" data-properties="base shape;auricle development">base ± cuneate, auricles well developed;</span> <span class="statement" id="st-d0_s8" data-properties="margin architecture or shape;tooth orientation">margins serrulate-spiny with teeth ascending;</span> <span class="statement" id="st-d0_s9" data-properties="apex shape">apex acuminate with subapical teeth same size as apical tooth;</span> <span class="statement" id="st-d0_s10" data-properties="microscale shape;microscale shape;microscale shape;microscale density;projection arrangement or shape">microscales ovatelanceolate to linear-lanceolate, with contorted projections, dense, on abaxial surface only.</span> <span class="statement" id="st-d0_s11" data-properties="indusium architecture or pubescence or shape"><b>Indusia </b>ciliate.</span> <span class="statement" id="st-d0_s12" data-properties=""><b>Spores </b>light yellow.</span> <span class="statement" id="st-d0_s13" data-properties="spore coloration;2n chromosome count">2n = 82.</span><!--
+
--><span class="statement" id="st-undefined" data-properties=""><b>Stems </b>erect or ascending. <b>Leaves</b> arching, 5–18 dm; bulblets absent. <b>Petiole</b> 1/8–1/4 length of leaf, densely scaly; scales red-brown to dark brown or nearly black, gradually diminishing in size distally. <b>Blade</b> linear-lanceolate, 1-pinnate, base slightly narrowed. <b>Pinnae</b> narrowly lanceolate, straight to falcate, not overlapping, pinnae of shade-growing plants in 1 plane, those of sun-growing plants twisted or contorted, 1–15 cm; base ± cuneate, auricles well developed; margins serrulate-spiny with teeth ascending; apex acuminate with subapical teeth same size as apical tooth; microscales ovate-lanceolate to linear-lanceolate, with contorted projections, dense, on abaxial surface only. <b>Indusia</b> ciliate. <b>Spores</b> light yellow. <b>2n</b> = 82.</span><!--
  
 
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|elevation=0–2200 m
 
|elevation=0–2200 m
 
|distribution=B.C.;Calif.;Idaho;Mont.;Oreg.;S.Dak.;Wash.;Mexico on Guadalupe Island;naturalized in Europe.
 
|distribution=B.C.;Calif.;Idaho;Mont.;Oreg.;S.Dak.;Wash.;Mexico on Guadalupe Island;naturalized in Europe.
|discussion=<p>One of the most abundant ferns in the western flora (rivaled only by Pteridium), Polystichum munitum also is of significant economic importance. Enormous quantities of leaves are gathered for backgrounds in funeral wreaths and other floral displays; the evergreen leaves keep well in cold storage and are exported to Europe. It is extensively used in landscaping, the trade being mainly in wild-collected plants.</p><!--
+
|discussion=<p>One of the most abundant ferns in the western flora (rivaled only by <i>Pteridium</i>), <i>Polystichum munitum</i> also is of significant economic importance. Enormous quantities of leaves are gathered for backgrounds in funeral wreaths and other floral displays; the evergreen leaves keep well in cold storage and are exported to Europe. It is extensively used in landscaping, the trade being mainly in wild-collected plants.</p><!--
--><p>Polystichum munitum appears to be most closely related to P. imbricans based on morphologic (D. H. Wagner 1979) and electrophoretic (P. S. Soltis et al. 1990) analyses. The chloroplast DNA of P. imbricans, however, is divergent (G. Yatskievych et al. 1988), suggesting a chloroplast origin independent of the nuclear genome. That Polystichum munitum is related to P. acrostichoides is supported by data from chloroplast DNA analysis (G. Yatskievych et al. 1988) but contradicted by data from electrophoretic studies (P. S. Soltis et al. 1990).</p><!--
+
--><p><i>Polystichum munitum</i> appears to be most closely related to <i>P. imbricans</i> based on morphologic (D. H. Wagner 1979) and electrophoretic (P. S. Soltis et al. 1990) analyses. The chloroplast DNA of <i>P. imbricans</i>, however, is divergent (G. Yatskievych et al. 1988), suggesting a chloroplast origin independent of the nuclear genome. That <i>Polystichum munitum</i> is related to <i>P. acrostichoides</i> is supported by data from chloroplast DNA analysis (G. Yatskievych et al. 1988) but contradicted by data from electrophoretic studies (P. S. Soltis et al. 1990).</p><!--
--><p>Polystichum munitum can be distinguished from P. imbricans by its persistent, wide (the largest wider than 1 mm) distal petiolar scales; such scales of P. imbricans are less than 1 mm wide and fall off early.</p><!--
+
--><p><i>Polystichum munitum</i> can be distinguished from <i>P. imbricans</i> by its persistent, wide (the largest wider than 1 mm) distal petiolar scales; such scales of <i>P. imbricans</i> are less than 1 mm wide and fall off early.</p><!--
--><p>From an evolutionary standpoint, Polystichum munitum is a diploid progenitor of P. andersonii, P. californicum, P. setigerum, and, perhaps, P. scopulinum. Hybrids with all except P. setigerum have been reported, all triploid, attesting to its parental role in the tetraploids (see discussion under each). Hybrids with P. braunii (A. Sleep and T. Reichstein 1967), P. kruckebergii (P. S. Soltis et al. 1987), P. dudleyi (W. H. Wagner Jr. 1973), and P. lemmonii (P. S. Soltis et al. 1989) also have been reported.</p><!--
+
--><p>From an evolutionary standpoint, <i>Polystichum munitum</i> is a diploid progenitor of <i>P. andersonii</i>, <i>P. californicum</i>, <i>P. setigerum</i>, and, perhaps, <i>P. scopulinum</i>. Hybrids with all except <i>P. setigerum</i> have been reported, all triploid, attesting to its parental role in the tetraploids (see discussion under each). Hybrids with <i>P. braunii</i> (A. Sleep and T. Reichstein 1967), <i>P. kruckebergii</i> (P. S. Soltis et al. 1987), <i>P. dudleyi</i> (W. H. Wagner Jr. 1973), and <i>P. lemmonii</i> (P. S. Soltis et al. 1989) also have been reported.</p><!--
--><p>The population on Guadalupe Island has been called Polystichum solitarium Maxon.</p>
+
--><p>The population on Guadalupe Island has been called <i>Polystichum</i> solitarium Maxon.</p>
 
|tables=
 
|tables=
 
|references=
 
|references=
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-->{{#Taxon:
 
-->{{#Taxon:
 
name=Polystichum munitum
 
name=Polystichum munitum
|author=
 
 
|authority=(Kaulfuss) C. Presl
 
|authority=(Kaulfuss) C. Presl
 
|rank=species
 
|rank=species
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|publication title=Tent. Pterid.
 
|publication title=Tent. Pterid.
 
|publication year=1836
 
|publication year=1836
|special status=
+
|special status=Illustrated
|source xml=https://jpend@bitbucket.org/aafc-mbb/fna-fine-grained-xml.git/src/287ef3db526bd807d435a3c7423ef2df1e951227/V2/V2_179.xml
+
|source xml=https://bitbucket.org/aafc-mbb/fna-data-curation/src/2e0870ddd59836b60bcf96646a41e87ea5a5943a/coarse_grained_fna_xml/V2/V2_179.xml
 
|genus=Polystichum
 
|genus=Polystichum
 
|species=Polystichum munitum
 
|species=Polystichum munitum
|2n chromosome count=82
 
|apex shape=acuminate
 
|auricle development=developed
 
|base shape=cuneate;narrowed
 
|blade architecture or shape=1-pinnate
 
|blade shape=linear-lanceolate
 
|bulblet count=absent
 
|indusium architecture or pubescence or shape=ciliate
 
|leaf orientation=arching
 
|leaf some measurement=5dm;18dm
 
|margin architecture or shape=serrulate-spiny
 
|microscale density=dense
 
|microscale shape=ovatelanceolate;linear-lanceolate
 
|petiole architecture or pubescence=scaly
 
|petiole length=1/8 length of leaf;1/4 length of leaf
 
|pinna architecture=twisted
 
|pinna arrangement=not overlapping
 
|pinna arrangement or shape=contorted
 
|pinna course=straight
 
|pinna shape=falcate;lanceolate
 
|pinna some measurement=1cm;15cm
 
|plant habitat=sun-growing;shade-growing
 
|projection arrangement or shape=contorted
 
|scale coloration=redbrown;dark-brown or nearly black
 
|scale size=diminishing
 
|spore coloration=light yellow
 
|stem orientation=ascending;erect
 
|tooth orientation=ascending
 
 
}}<!--
 
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-->[[Category:Treatment]][[Category:Polystichum]]
 
-->[[Category:Treatment]][[Category:Polystichum]]

Latest revision as of 20:21, 5 November 2020

Stems erect or ascending. Leaves arching, 5–18 dm; bulblets absent. Petiole 1/8–1/4 length of leaf, densely scaly; scales red-brown to dark brown or nearly black, gradually diminishing in size distally. Blade linear-lanceolate, 1-pinnate, base slightly narrowed. Pinnae narrowly lanceolate, straight to falcate, not overlapping, pinnae of shade-growing plants in 1 plane, those of sun-growing plants twisted or contorted, 1–15 cm; base ± cuneate, auricles well developed; margins serrulate-spiny with teeth ascending; apex acuminate with subapical teeth same size as apical tooth; microscales ovate-lanceolate to linear-lanceolate, with contorted projections, dense, on abaxial surface only. Indusia ciliate. Spores light yellow. 2n = 82.


Habitat: Terrestrial, forest floor, only occasionally on rock, in mesic coniferous to moist, mixed evergreen forests
Elevation: 0–2200 m

Distribution

V2 179-distribution-map.gif

B.C., Calif., Idaho, Mont., Oreg., S.Dak., Wash., Mexico on Guadalupe Island, naturalized in Europe.

Discussion

One of the most abundant ferns in the western flora (rivaled only by Pteridium), Polystichum munitum also is of significant economic importance. Enormous quantities of leaves are gathered for backgrounds in funeral wreaths and other floral displays; the evergreen leaves keep well in cold storage and are exported to Europe. It is extensively used in landscaping, the trade being mainly in wild-collected plants.

Polystichum munitum appears to be most closely related to P. imbricans based on morphologic (D. H. Wagner 1979) and electrophoretic (P. S. Soltis et al. 1990) analyses. The chloroplast DNA of P. imbricans, however, is divergent (G. Yatskievych et al. 1988), suggesting a chloroplast origin independent of the nuclear genome. That Polystichum munitum is related to P. acrostichoides is supported by data from chloroplast DNA analysis (G. Yatskievych et al. 1988) but contradicted by data from electrophoretic studies (P. S. Soltis et al. 1990).

Polystichum munitum can be distinguished from P. imbricans by its persistent, wide (the largest wider than 1 mm) distal petiolar scales; such scales of P. imbricans are less than 1 mm wide and fall off early.

From an evolutionary standpoint, Polystichum munitum is a diploid progenitor of P. andersonii, P. californicum, P. setigerum, and, perhaps, P. scopulinum. Hybrids with all except P. setigerum have been reported, all triploid, attesting to its parental role in the tetraploids (see discussion under each). Hybrids with P. braunii (A. Sleep and T. Reichstein 1967), P. kruckebergii (P. S. Soltis et al. 1987), P. dudleyi (W. H. Wagner Jr. 1973), and P. lemmonii (P. S. Soltis et al. 1989) also have been reported.

The population on Guadalupe Island has been called Polystichum solitarium Maxon.

Selected References

None.

Lower Taxa

None.
... more about "Polystichum munitum"
David H. Wagner +
(Kaulfuss) C. Presl +
Aspidium munitum +
Common sword fern +
B.C. +, Calif. +, Idaho +, Mont. +, Oreg. +, S.Dak. +, Wash. +, Mexico on Guadalupe Island +  and naturalized in Europe. +
0–2200 m +
Terrestrial, forest floor, only occasionally on rock, in mesic coniferous to moist, mixed evergreen forests +
Tent. Pterid. +
Polystichum munitum +
Polystichum +
species +