Difference between revisions of "Cheilanthes bonariensis"

(Willdenow) Proctor

Bull. Inst. Jamaica, Sci. Ser. 5(1): 15. 1953.

Common names: Bonaire lip fern
Basionym: Acrostichum bonariense Willdenow Sp. Pl. 5: 114. 1810
Synonyms: Notholaena aurea (Poiret) Desvaux
Treatment appears in FNA Volume 2.
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|common_names=Bonaire lip fern
 
|common_names=Bonaire lip fern
|basionyms={{Treatment/ID/Synonym
+
|basionyms={{Treatment/ID/Basionym
 
|name=Acrostichum bonariense
 
|name=Acrostichum bonariense
 
|authority=Willdenow
 
|authority=Willdenow
 +
|rank=species
 +
|publication_title=Sp. Pl.
 +
|publication_place=5: 114. 1810
 
}}
 
}}
 
|synonyms={{Treatment/ID/Synonym
 
|synonyms={{Treatment/ID/Synonym
 
|name=Notholaena aurea
 
|name=Notholaena aurea
 
|authority=(Poiret) Desvaux
 
|authority=(Poiret) Desvaux
 +
|rank=species
 
}}
 
}}
 
|hierarchy=Pteridaceae;Cheilanthes;Cheilanthes bonariensis
 
|hierarchy=Pteridaceae;Cheilanthes;Cheilanthes bonariensis
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}}<!--
 
}}<!--
  
--><span class="statement" id="st-d0_s0" data-properties="stem growth form or orientation;stem architecture or arrangement;stem diameter"><b>Stems </b>short-creeping to compact, usually 4–8 mm diam.;</span> <span class="statement" id="st-d0_s1" data-properties="scale coloration;scale size or width;central stripe width;central stripe prominence;central stripe coloration;margin coloration;margin shape;margin arrangement or shape;margin fixation or orientation;margin duration">scales bicolored, with broad, well-defined, dark, central stripe and narrow, light-brown margins, narrowly lanceolate, slightly contorted, strongly appressed, persistent.</span> <span class="statement" id="st-d0_s2" data-properties=""><b>Leaves </b>clustered, 10–60 cm;</span> <span class="statement" id="st-d0_s3" data-properties="leaf arrangement or growth form;leaf some measurement">vernation noncircinate.</span> <span class="statement" id="st-d0_s4" data-properties="petiole coloration;petiole shape"><b>Petiole </b>dark-brown, rounded adaxially.</span> <span class="statement" id="st-d0_s5" data-properties="blade arrangement or course or shape;blade shape;blade width"><b>Blade </b>linear, pinnate-pinnatifid throughout, 1–4 cm wide;</span> <span class="statement" id="st-d0_s6" data-properties="rachis shape;scale count">rachis rounded adaxially, lacking scales, with dense monomorphic pubescence.</span> <span class="statement" id="st-d0_s7" data-properties="pinna architecture;node shape;node pubescence;basal pinna size;basal pinna architecture or shape;basal pinna pubescence"><b>Pinnae </b>articulate at swollen, hirsute nodes, basal pair slightly smaller than adjacent pair, ± equilateral, appearing hirsute adaxially.</span> <span class="statement" id="st-d0_s8" data-properties="costa count"><b>Costae </b>absent.</span> <span class="statement" id="st-d0_s9" data-properties="ultimate segment shape;ultimate segment shape;ultimate segment shape;ultimate segment shape;ultimate segment size;ultimate segment some measurement;ultimate segment pubescence;ultimate segment pubescence"><b>Ultimate </b>segments elongate-deltate to ovate, not especially beadlike, the largest 1–7 mm, abaxially densely tomentose, adaxially hirsute.</span> <span class="statement" id="st-d0_s10" data-properties="false indusium position;false indusium variability;false indusium width"><b>False </b>indusia marginal, weakly differentiated, 0.05–0.25 mm wide.</span> <span class="statement" id="st-d0_s11" data-properties="sorus architecture"><b>Sori </b>± continuous around segment margins.</span> <span class="statement" id="st-d0_s12" data-properties="spore count"><b>Sporangia </b>containing 32 spores.</span> <span class="statement" id="st-d0_s13" data-properties="n=2n chromosome count">n = 2n = 90, apogamous.</span><!--
+
--><span class="statement" id="st-undefined" data-properties=""><b>Stems </b>short-creeping to compact, usually 4–8 mm diam.; scales bicolored, with broad, well-defined, dark, central stripe and narrow, light brown margins, narrowly lanceolate, slightly contorted, strongly appressed, persistent. <b>Leaves</b> clustered, 10–60 cm; vernation noncircinate. <b>Petiole</b> dark brown, rounded adaxially. <b>Blade</b> linear, pinnate-pinnatifid throughout, 1–4 cm wide; rachis rounded adaxially, lacking scales, with dense monomorphic pubescence. <b>Pinnae</b> articulate at swollen, hirsute nodes, basal pair slightly smaller than adjacent pair, ± equilateral, appearing hirsute adaxially. <b>Costae</b> absent. <b>Ultimate</b> segments elongate-deltate to ovate, not especially beadlike, the largest 1–7 mm, abaxially densely tomentose, adaxially hirsute. <b>False</b> indusia marginal, weakly differentiated, 0.05–0.25 mm wide. <b>Sori</b> ± continuous around segment margins. <b>Sporangia</b> containing 32 spores. n = 2n = 90, apogamous.</span><!--
  
 
-->{{Treatment/Body
 
-->{{Treatment/Body
 +
|phenology=Sporulating summer–fall.
 
|habitat=Rocky slopes and ledges, found on a variety of substrates though rarely observed on limestone
 
|habitat=Rocky slopes and ledges, found on a variety of substrates though rarely observed on limestone
 
|elevation=1200–2400 m
 
|elevation=1200–2400 m
 
|distribution=Ariz.;N.Mex.;Tex.;Mexico;West Indies;Central America;South America.
 
|distribution=Ariz.;N.Mex.;Tex.;Mexico;West Indies;Central America;South America.
|discussion=<p>Cheilanthes bonariensis has been assigned to Notholaena in past treatments. It is distantly related (at best) to the species here included in Notholaena, however, and we concur with R. M. Tryon and A. F. Tryon (1982) that it should be transferred to Cheilanthes. Chromosomal studies (G. J. Gastony and M. D. Windham 1989) suggest that C. bonariensis is an apogamous triploid that arose through autopolyploidy. Further investigation is necessary to determine whether 64-spored, sexually reproducing populations of C. bonariensis are still extant.</p>
+
|discussion=<p><i>Cheilanthes bonariensis</i> has been assigned to <i>Notholaena</i> in past treatments. It is distantly related (at best) to the species here included in <i>Notholaena</i>, however, and we concur with R. M. Tryon and A. F. Tryon (1982) that it should be transferred to <i>Cheilanthes</i>. Chromosomal studies (G. J. Gastony and M. D. Windham 1989) suggest that <i>C. bonariensis</i> is an apogamous triploid that arose through autopolyploidy. Further investigation is necessary to determine whether 64-spored, sexually reproducing populations of <i>C. bonariensis</i> are still extant.</p>
 
|tables=
 
|tables=
 
|references=
 
|references=
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-->{{#Taxon:
 
-->{{#Taxon:
 
name=Cheilanthes bonariensis
 
name=Cheilanthes bonariensis
|author=
 
 
|authority=(Willdenow) Proctor
 
|authority=(Willdenow) Proctor
 
|rank=species
 
|rank=species
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|basionyms=Acrostichum bonariense
 
|basionyms=Acrostichum bonariense
 
|family=Pteridaceae
 
|family=Pteridaceae
 +
|phenology=Sporulating summer–fall.
 
|habitat=Rocky slopes and ledges, found on a variety of substrates though rarely observed on limestone
 
|habitat=Rocky slopes and ledges, found on a variety of substrates though rarely observed on limestone
 
|elevation=1200–2400 m
 
|elevation=1200–2400 m
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|publication year=1953
 
|publication year=1953
 
|special status=
 
|special status=
|source xml=https://jpend@bitbucket.org/aafc-mbb/fna-fine-grained-xml.git/src/287ef3db526bd807d435a3c7423ef2df1e951227/V2/V2_360.xml
+
|source xml=https://bitbucket.org/aafc-mbb/fna-data-curation/src/2e0870ddd59836b60bcf96646a41e87ea5a5943a/coarse_grained_fna_xml/V2/V2_360.xml
 
|genus=Cheilanthes
 
|genus=Cheilanthes
 
|species=Cheilanthes bonariensis
 
|species=Cheilanthes bonariensis
|basal pinna architecture or shape=equilateral
 
|basal pinna pubescence=hirsute
 
|basal pinna size=slightly smaller than adjacent pair
 
|blade arrangement or course or shape=linear
 
|blade shape=pinnate-pinnatifid
 
|blade width=1cm;4cm
 
|central stripe coloration=dark
 
|central stripe prominence=well-defined
 
|central stripe width=broad
 
|costa count=absent
 
|false indusium position=marginal
 
|false indusium variability=differentiated
 
|false indusium width=0.05mm;0.25mm
 
|leaf arrangement or growth form=clustered
 
|leaf some measurement=10cm;60cm
 
|margin arrangement or shape=contorted
 
|margin coloration=light-brown
 
|margin duration=persistent
 
|margin fixation or orientation=appressed
 
|margin shape=lanceolate
 
|n=2n chromosome count=90
 
|node pubescence=hirsute
 
|node shape=swollen
 
|petiole coloration=dark-brown
 
|petiole shape=rounded
 
|pinna architecture=articulate
 
|rachis shape=rounded
 
|scale coloration=bicolored
 
|scale count=lacking
 
|scale size or width=narrow
 
|sorus architecture=continuous
 
|spore count=32
 
|stem architecture or arrangement=compact
 
|stem diameter=4mm;8mm
 
|stem growth form or orientation=short-creeping
 
|ultimate segment pubescence=hirsute;tomentose
 
|ultimate segment shape=beadlike;elongate-deltate;ovate
 
|ultimate segment size=largest
 
|ultimate segment some measurement=1mm;7mm
 
 
}}<!--
 
}}<!--
  
 
-->[[Category:Treatment]][[Category:Cheilanthes]]
 
-->[[Category:Treatment]][[Category:Cheilanthes]]

Latest revision as of 20:22, 5 November 2020

Stems short-creeping to compact, usually 4–8 mm diam.; scales bicolored, with broad, well-defined, dark, central stripe and narrow, light brown margins, narrowly lanceolate, slightly contorted, strongly appressed, persistent. Leaves clustered, 10–60 cm; vernation noncircinate. Petiole dark brown, rounded adaxially. Blade linear, pinnate-pinnatifid throughout, 1–4 cm wide; rachis rounded adaxially, lacking scales, with dense monomorphic pubescence. Pinnae articulate at swollen, hirsute nodes, basal pair slightly smaller than adjacent pair, ± equilateral, appearing hirsute adaxially. Costae absent. Ultimate segments elongate-deltate to ovate, not especially beadlike, the largest 1–7 mm, abaxially densely tomentose, adaxially hirsute. False indusia marginal, weakly differentiated, 0.05–0.25 mm wide. Sori ± continuous around segment margins. Sporangia containing 32 spores. n = 2n = 90, apogamous.


Phenology: Sporulating summer–fall.
Habitat: Rocky slopes and ledges, found on a variety of substrates though rarely observed on limestone
Elevation: 1200–2400 m

Distribution

V2 360-distribution-map.gif

Ariz., N.Mex., Tex., Mexico, West Indies, Central America, South America.

Discussion

Cheilanthes bonariensis has been assigned to Notholaena in past treatments. It is distantly related (at best) to the species here included in Notholaena, however, and we concur with R. M. Tryon and A. F. Tryon (1982) that it should be transferred to Cheilanthes. Chromosomal studies (G. J. Gastony and M. D. Windham 1989) suggest that C. bonariensis is an apogamous triploid that arose through autopolyploidy. Further investigation is necessary to determine whether 64-spored, sexually reproducing populations of C. bonariensis are still extant.

Selected References

None.

Lower Taxa

None.
... more about "Cheilanthes bonariensis"
Michael D. Windham +  and Eric W. Rabe +
(Willdenow) Proctor +
Acrostichum bonariense +
Bonaire lip fern +
Ariz. +, N.Mex. +, Tex. +, Mexico +, West Indies +, Central America +  and South America. +
1200–2400 m +
Rocky slopes and ledges, found on a variety of substrates though rarely observed on limestone +
Bull. Inst. Jamaica, Sci. Ser. +
Notholaena aurea +
Cheilanthes bonariensis +
Cheilanthes +
species +