identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
5F37DB1E8207EC20FED9FD84FA0EFD49.text	5F37DB1E8207EC20FED9FD84FA0EFD49.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Nolina MICHX	<div><p>NOLINA MICHX</p><p>Plants dioecious, arborescent or acaulescent plants with leaf rosettes at the apices of stems and branches. Leaves linear, flat or concave, green or glaucous green, with leaf margins microdenticulate or fibrous. Inflorescences a panicle with a scape and branches subtended by deltoid or triangular to linear bracts. Second order branches or branchlets subtended by triangular to linear papery bracts. Flowers campanulate, in fascicles or secondarily solitary, surrounded by laciniate or dentate membranaceous bracteoles; tepals 6 in two series, whitish, the midvein apparent, trichomes at the apex; staminate flowers with six stamens, anthers introrse, sagittate, ovary not developed and functioning as a nectary, tepals reflexed at maturity; pistillate flowers with a 3-carpelar ovary, rounded; stigmas sessile, 3-branched or 3-lobed; staminodes 6, septal nectaries present; ovules basal, two per carpel, sometimes subtended by a shelf-like or a small protruding structure. Fruits 3-lobed, dry, indehiscent, with an apical notch that bears the persistent stigmas; tepals persistent, all reflexed or at least the external ones. Seeds round, 1–2(–3) per fruit, in any case, one per locule or none if ovules abortive, exposed at maturity or not; testa smooth, microreticulate or reticulate, brown or gray.</p></div>	https://treatment.plazi.org/id/5F37DB1E8207EC20FED9FD84FA0EFD49	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Hernández-Sandoval, Luis;Rebman, Jon P.	Hernández-Sandoval, Luis, Rebman, Jon P. (2018): The Genus Nolina (Asparagaceae) of the Baja California Peninsula, and the Recognition of a New Species Combination. Systematic Botany (Basel, Switzerland) 43 (3): 717-733, DOI: 10.1600/036364418X697436, URL: https://doi.org/10.1600/036364418x697436
5F37DB1E8207EC27FF29FBBCFEFAFC6F.text	5F37DB1E8207EC27FF29FBBCFEFAFC6F.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Nolina beldingii Brandegee, Zoe	<div><p>NOLINA BELDINGII Brandegee, Zoe 1: 305. 1890. TYPE: MEXICO: Baja California Sur, La Chuparrosa, 17 Oct. 1893, T. S. Brandegee s. n. (lectotype UC! (accession number: 142652); isolectotypes: BM!, GH!, KEW!, and the fragment at MO labeled as October 17, 1893)  .</p><p>Plants arborescent, 3 to 7 m high, trunk 50 cm diam, bark fissured forming rectangular blocks 10 to 25 cm long with ridges 5 cm deep, gray to maroon with age; branched with 1 to 26 apical leaf rosettes, 2 to 3 m diam, leaving persistent old leaves on at least half the size of the branches and trunk or even more. Leaves long linear, 0.75–1.15 m long, 1.4–2.0 cm wide at the middle, sometimes narrower or with a constriction above up the base, flat in cross section, smooth, dark green, sometimes reddish at the back; base long triangular, (4.5–) 7 to 9 cm long, (3.5–) 4 to 5 cm wide at the inferior part, 1.4 cm wide at the superior part; leaf apex entire; leaf margin denticulate, with very small teeth or denticles ca. 0.2 mm long, yellowish. Inflorescence paniculate, largely ovoid, 2 to 3(–3.5) m long, 20 to 70 cm diam, rachis undulate; scape 1 m, smooth, bracts linear, decreasing in size towards the apex from 60 to 40 cm; branches lax, curved to undulate, perpendicular to slightly ascending, 23 cm long, decreasing in size towards the apex to 15 cm, with two weak basal branchlets (ca. 1/5 the size of the branches), subtended by largely triangular papery bracts, 18 cm long, decreasing in size towards the apex to 3 cm, bract base blotched with red or purple; branchlets lax, 8 cm long, decreasing in size towards the apex to 2 cm long. Staminate flowers 2(–3) per node, campanulate, 4 to 6 mm diam on pedicels 2.5 to 3 mm long, articulated at or above the middle, surrounded by membranaceous bracteoles 2 to 3 mm long with laciniate margins; tepals ovate to lanceolate, 3–4 mm long, 1.5–2 mm wide, the external ones with apiculate apices, all reflexed from the middle part at maturity; filaments 2–2.5 mm long; anthers 1–1.5 mm long. Pistillate flowers 2 per node, campanulate, on pedicels 4 to 8 mm long articulated near the base, surrounded by two membranaceous bracteoles 2 to 4 mm long, margins laciniate; tepals lanceolate, 3 to 3.5 mm long, 1.5 mm wide, light yellow to cream with the midvein reddish to purple; ovary 3-lobed, 2–4 mm diam; style 0.2–0.4 mm long; stigmas 3-lobed. Fruits 1(22) per node, depressed, 0.9 cm long, 1.4 to 1.5 cm wide, with persistent tepals, reflexed at maturity; peduncles 9.5 to 11.5 mm, articulated near the base. Seed 1 per fruit, 4.5 mm long, 3 mm wide, ovoid, not exposed, and green to brown, grayish at maturity, hilum yellow. Figure 1.</p><p>Ecology and Distribution —This species occurs on steep slopes and cliffs at the highest areas in the Sierra de La Laguna, in the state of Baja California Sur, Mexico, in oak forests ( Quercus species) with  Quercus tuberculata Liebm.,  Q. devia Goldman,  Q. arizonica Sarg.,  Arbutus peninsularis Rose &amp; Goldman,  Sideroxylon peninsulare (Brandegee) T. D. Pennington,  Buddleja crotonoides A. Gray,  Randia capitata DC., Muhlenbergia spp.,  Opuntia spp.,  Croton sp., from 1000 to 1800 m in elevation, on granite outcrops (Fig. 2). This species flowers from May to June and fruits from June to August.</p><p>At the time of the original species description (Brandegee 1890), Brandegee did not assign an actual type specimen, and did not mention any herbaria where specimens might be deposited. Even though he had his own herbarium, it seems that some vouchers were not deposited into others or at least at UC where the largest portion of Brandegee´s herbarium collection is currently housed. He dedicated the specific epithet to Mr. L. Belding, but apparently did not see his specimen collection (Belding 6 at GH, which represents a small individual), and just said that he “was the first to notice it in his ornithological expeditions to the Sierra la Laguna, several years ago, and gave me directions as to the route by which I was enable to find it.” The best specimen collection for  N. beldingii is at UC is from La Chuparrosa (“Chuparosa” spelling variant), dated 17 October 1893, with duplicates at GH, BM, KEW, and MO. However, the voucher at MO is a mixed sheet with  N. brandegeei from San Julio, 19–20 April 1889). There are also older specimens from the Sierra de San Francisquito, labeled as Brandegee 583 but with different dates, the one at GH is from March 29, 1890 and the one at UC is from March 29, 1892. In the paper on Brandegee´s itineraries, Moran (1952) considers the last date (1892) as the correct one, and it is the one accepted here. A voucher with a collection date after the original publication date cannot be considered an inferred type specimen, but since Brandegee did not mention any specimen in his original publication, and since Belding´s specimen and the collection from the Sierra de San Francisquito are not complete, and also labeled with different dates, it seems best to assign the specimen from La Chuparrosa at UC as the lectotype, and the vouchers at BM, GH, KEW, and the fragment at MO labeled as October 17, 1893 as isolectotypes.</p><p>Nolina beldingii is an endemic species to the southern part of the Baja California peninsula which occurs only in the Sierra de La Laguna. Taxonomically, this species is close to  N. brandegeei . They can be readily distinguished because  N. beldingii has longer leaves (ca. 1 m) usually narrowing or with a constriction above the base, entire leaf apices, and larger fruits and pedicels.  Nolina beldingii is locally known as “sotol” or “palmilla” and its leaves have been used for thatching (Fig. 1).</p><p>Representative Specimens Examined —   Mexico. — BAJA CALIFORNIA SUR:  Laguna. L. Belding 6, 3 Feb s/y (GH) ;   Sierra de San Francisquito, 29 Mar. 1892, T. S. Brandegee 583 (GH as 29 Mar. 1890, UC) ;  La Chuparosa, 17 Oct. 1893, T. S. Brandegee s/n (GH);  La Laguna, Sierra de la Laguna, 21 Jan. 1906. E. Nelson &amp; E. Goldman 7465 (US);   La Laguna,  Sierra La Laguna, 24 Mar. 1939, H. S. Gentry 4424 (CAS, GH, KEW, MO) ;   Valle de la Laguna, 23 Aug. 1944, M. Mart´ınez s/n (MEXU) ;   Along trail to La Laguna,  Sierra de La Laguna, E of Todos Santos, 28 Dec. 1947, A. Carter 2439 (US) ;   Rancho Laguna and vicinity, Sierra Laguna,  Cape District, 3 Oct. 1951, H. S. Gentry 11216 (MEXU) ;   From San Jorge to San Francisquito and La Chuparrosa,  East of Sierra de la Victoria, 12 Apr. 1955, A. Carter 3331 (GH, MEXU, MO, SD, US) ;   Cape Region, Potrero de Almenta near head of S fork canyon  San Pedro, 9 May 1959, R. Moran 7369, 7369 A (GH, MEXU, SD) ;   Cape Region about La Laguna, 16 May 1959, R. Moran 7428 &amp; 7428 A (GH, MEXU, SD) ;   La Laguna, Sierra de la Laguna,  Huerigo Canyon, 24 Aug. 1959, C. H. Lowe 3064 &amp; R. L. Turner 59–159 (MEXU, MO) ;   At end trail La Burrera - La Laguna,  Cape District, 21 Aug. 1972, A. J. Gilmartin 1840 (MEXU) ;   Sierra de La Laguna, trail to La Laguna, ridge above tributary of  Canón ~ la Burrera, just west of la Laguna, about 30 km (air) northeast of  Todos Santos, 19 Mar. 1998, M. Fishbein 3167 (MEXU) ;   Sierra de La Victoria, arriba de la zona del chalet de Cano, 7 Dec. 2007, J. L. de la Luz 7073 (HCIB, SD) ;   Sierra de La Victoria, arriba de la caba~ na de Cano, 17 Apr. 2008, J. L. de la Luz 8075 (HCIB, MEXU, SD) ;   Cerrito El Encino frente al cerro el Picacho, zona núcleo de la  Reserva de la Biósfera la Sierra de La Laguna, 17 Jun. 2009, A. Garc´ ıa- Mendoza 9268 (MEXU)  .</p></div>	https://treatment.plazi.org/id/5F37DB1E8207EC27FF29FBBCFEFAFC6F	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Hernández-Sandoval, Luis;Rebman, Jon P.	Hernández-Sandoval, Luis, Rebman, Jon P. (2018): The Genus Nolina (Asparagaceae) of the Baja California Peninsula, and the Recognition of a New Species Combination. Systematic Botany (Basel, Switzerland) 43 (3): 717-733, DOI: 10.1600/036364418X697436, URL: https://doi.org/10.1600/036364418x697436
5F37DB1E8200EC27FF3DFAFFFC45F944.text	5F37DB1E8200EC27FF3DFAFFFC45F944.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Nolina beldingii var. deserticola Trelease., Proc. Amer. Philos. Soc.	<div><p>Nolina beldingii Brandegee var. deserticola Trelease., Proc. Amer. Philos. Soc. 50:424. 1911.</p><p>Plants shrubby, with trunks or branches 1 to 3 m tall, branching from the base; rosettes with erect leaves, reflexed when old, persistent. Leaves linear, 0.8 to 1.2 m long, 1.5 to 3.5 cm wide, flat in cross section, green to glaucous green, if the latter then cerose, scabrid, papillate trichomes might be apparent; leaf margins smooth when young, fibrose with age, brown to grayish. Inflorescence ovoid, 1.5 to 2.5 m long; scape 0.9 to 1.5 m long; branches at the base of the inflorescence 30 to 35 cm long with a peduncle 4 to 7 cm long, the rest of the branches 20 cm long, decreasing in size towards the apex to 7 cm, subtended by linear bracts 40 to 43 cm long, sometimes with fibrous margins; branchlets 4 to 5 mm long, subtended by largely triangular bracts 10 cm long, decreasing in size towards the apex to 4 cm, 1 to 2 cm wide at the base, papery. Staminate flowers 2 to 3(–4) per node, campanulate, 2 mm long, 3 mm wide, on pedicels 2 mm long, articulated at the middle, surrounded by membranaceous bracteoles, 1.5–2 mm long, persistent, margins laciniate; tepals oblong to lanceolate, 3 mm long, 1 mm wide, reflexed from the middle at maturity, midbase thickened. Pistillate flowers 2 per node, campanulate 3.5 to 4.0 mm diam, on pedicels 2.5–3.5 mm long, articulate above the</p><p>middle, surrounded by membranaceous bracteoles, the external one 3 to 4 mm long, the internal ones 2.0– 2.5 mm long, persistent, margins laciniate; tepals oblong lanceolate, 2.5–3 mm long, 1 mm wide, apex short apiculate, reflexed from the base at maturity; ovules basal, supported by a small, round or shelf-like structure; stigmas sessile, 3-branched. Fruits 1(–2) per node, orbicular to oblongate, 6–7 mm long, 7 to 9(–10) mm wide, on peduncles 3.5 to 5 mm long, articulate above or at the middle; fruit lobes with margins, apically accrescent; stigmas persistent; tepals persistent. Seed 1(–2) per fruit, oblongate to ellipsoid, 3.5–4.5 mm long, 2–2.5 mm wide, not exposed at maturity, grayish to glaucous green, rarely reddish, reticulate. Figures 3, 4.</p><p>Ecology and Distribution —Plants of  Nolina bigelovii grow on steep slopes in forests and chaparrals at 540 to 1250 m elevation on granite outcrops of the sierras of the state of Baja California, such as at La Rumorosa in the Sierra de Juárez, Sierra de San Pedro Mártir, Catavi~ ná, Sierra de San Borja, and Isla Angel de la Guarda (Fig. 4). This species is also found in Sonora, Mexico, and in California and Arizona in the USA. It is locally known as “palma.” Flowers are present May to June and fruits from June to November.</p><p>Representative Specimens Examined —  Mexico.— BAJA CALIFORNIA: Ca ~ nón Cantillas, Jun., 1 Jul. 1884, C. Orcutt s/n (MEXU);   Tule Mountains, Mexican boundary line, 11 Feb.1894, E. A. Mearns 2797 (MO, US) ;   Jaraguay, about  50 km SE of San Fernando, 9 Sept. 1905, E. W. Nelson &amp; A. Goldman, 7130 (US); (J)  Yaraguay, 16 Jul. 1941, Harbison C. 310 (SD);   East end of Sierra  San Luis;   26–30 mi north of  Punta Prieta, 3 Apr. 1950, H. S. Gentry 8971 (MEXU, SD) ;  Cantillas (Tantillas) Canyon, 8 Sept. 1952, C. Harbison s/n (SD);   Summit of Cerro Quemazón, Sierra  San Borja, 26 Mar. 1960, R. Moran 8074 (CAS, SD) ;   Canyon above El Terminal, Sierra  San Borja, 7 June 1962, R. Moran 9732 (CAS, SD, US) ;  Arroyo de la mina de Santa Marta, 9 June 1962, R. Moran 9763 (SD);   Cantu Grade, about  4 mi E of La Rumorosa, near Tecate-Mexicali road, 30 Junio 1962, I. Wiggins 438 (CAS, MEXU, US) ;   Yubay, 10 Oct. 1962, C. Harbison s/n (SD) ;   NW of Cerro San Luis, 2 Mar. 1963, R. Moran 10278 (CAS, SD) ;   Peak ca. 4 miles SE of Refugio Bay,  Isla Angel de la Guarda, 22 Mar. 1963, R. Moran 10479 (CAS, SD, US) ;   Rancho La Suerte,  San Pedro Mártir, 4 June 1963, R. Moran 11163 (BCMEX, CAS, SD) ;   NE of Yubay, 30 Apr. 1964, C. Harbison s/d (SD) ;  Just above trail down into Cantillas Canyon. El Progreso, Sierra Juárez, 11 Sept. 1965, C. Harbison 392 (SD);   Cantillas Canyon, 11 Sept. 1965,  Howe D. F. 4132 (SD) ;   6.9 km (by road) south of  La Virgen, 15 Oct. 1966,  Hastings J. R. 66–131a (SD) ;   Mouth of Diablo Canyon,  Sierra de San Pedro Mártir, 10 Mar. 1971, R. Moran 18313 (BCMEX, SD) ;   ca.  15 mi W of San Felipe, along road to Valle Trinidad, 15 June 1973, H. S. Gentry 23291 (ASU, MEXU) ;  6 May 1978, R. Moran s/n (BCMEX);  Ca ~ nón del Diablo, Sierra San Pedro Mártir, 6 May 1978 R. Moran 25657 (BCMEX, SD);   9 km NW of Rancho Santa Inés, 18 June 1979, W. H. Clark 3160 (BCMEX, CAS, MEXU) ;   Sierra ca.  2 km NE of San Luis, 15 Nov. 1981, R. Moran 29900 (SD) ;   Arroyo El Palmarito ca.  4.5 km NW of Catavi ~ ná, 6 June 1984, J.  Dice 467 (MEXU, SD) ;   Arroyo El Palmarito ca.  4.5 km NW of Catavi ~ ná, 6 June 1984, J.  Dice 466 (SD) ;   La Rumorosa grade, 23 Feb. 1986, E. Jonsson 1327 (SD) ;   Canón ~ de Guadalupe, along canyon above resort area. 23 Mar. 1986, R.  Thorne s/n (BCMEX) ;   Arroyo Yubay. Ca.  0.4 km West of Tinajas of Yubay and ca. 2.3 km ENE of abandoned mine at El Desenga ~ no, 22, June 1986, J.  Dice 669 (SD) ;   Sierra La Asamblea: southwest foot of the range near the W edge of Mesa Yubay and the SSW side of  Mesa Cuerno de Borrego;  ca. 7.0 road miles NNE of the abandoned site of El Desenga ~ no, 3 May 1993, T. S. Ross 7088 (SD);  Canón ~ El Cajón, west of main dirt road providing access to Ca ~ nón de Guadalupe, 15 Mar. 1995, J. Rebman 8730 (SD);   Km 52 de la carr.  La Rumorosa - Tecate, Nov. 2004, O. Ram´ ırez s/n (QMEX) ;   La Rumorosa, Nov. 2004, O. Ram´ ırez s/n (QMEX) ; W. Hodgson 2656 (MEXU).</p></div>	https://treatment.plazi.org/id/5F37DB1E8200EC27FF3DFAFFFC45F944	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Hernández-Sandoval, Luis;Rebman, Jon P.	Hernández-Sandoval, Luis, Rebman, Jon P. (2018): The Genus Nolina (Asparagaceae) of the Baja California Peninsula, and the Recognition of a New Species Combination. Systematic Botany (Basel, Switzerland) 43 (3): 717-733, DOI: 10.1600/036364418X697436, URL: https://doi.org/10.1600/036364418x697436
5F37DB1E8200EC29FCF0F8AAFE6FF8D5.text	5F37DB1E8200EC29FCF0F8AAFE6FF8D5.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Nolina palmeri var. brandegeei Trelease Proceedings	<div><p>Nolina palmeri S. Watson. var. brandegeei Trelease Proceedings of the American Philosophical Society 50:209. 1911.</p><p>This taxon was previously recognized as an infraspecies</p><p>(Trelease 1911) and as a synonym of  N. palmeri, a species considered by Hochstätter (2010) and Thiede (2012) within the section  Microcarpae with acaulescent plants, and narrow leaves with coiled tips, but our study found enough morphological differences to elevate in taxonomic rank to the species level.</p><p>Nolina brandegeei is quite different from  N. palmeri because it is an arborescent plant with linear leaves that have no narrowing or constriction above the base, leaf margins with erect and forked denticles, leaf tips shredded, fruits 0.6 cm long, 0.9 to 1 cm wide, fruit peduncles 6–12 mm long and articulated near the base, and flowers present in summer with fruits mature in fall, seeds exposed at maturity. This taxon resembles  N. beldingii, but that species has leaves with a constriction above the base, leaf margin with curved and nonforking denticles (Fig. 5), leaf apices entire, fruits 1 cm in diameter or more, flowers produced in spring with fruits maturing in summer and seeds not exposed in mature fruits.</p><p>Arborescent plant, 2 to 6 m high, trunks 20–30 cm diam, usually branched with apical rosettes, old specimens much branched; branches separate from each other at 30° to 40°; bark gray, fissured, forming small rectangles. Rosettes massive ca. 1.5 m in diam, with erect leaves, reflexed at maturity, persistent and covering the branches, but not the trunk. Leaves linear, not narrowing or constricted above the base, 95 to 120 cm long, 1.0– 1.5 cm wide at the middle, flat in cross section, green to glaucous green; leaf bases triangular, 4.5–7 cm long, 5.0 at the base, and 1.3–1.7 at the top; margins denticulate; teeth 0.2 mm, erect to curved, forked or branched, sometimes fused. Inflorescence 1 to 3.5 m long, 30 cm wide, ovoid; scape 15 to 70 cm long, 1.5–2.0 cm diam; bracts linear to long triangulate, 47 cm long decreasing apically in size to 20 cm; inflorescence branches perpendicular to ascending, up curved below the middle, 43 cm long, decreasing apically in size to 10 cm, subtended by bracts 17 to 6 cm long; branchlets 14 to 3 cm long, the final branchlets 5 to 8 cm long. Staminate flowers campanulate, 2.5 mm diam, 2 to 3 per node on pedicels 2 to 3.5 mm articulated below the middle, surrounded by wide lanceolate membranaceous bracteoles, 1.5 to 3 mm long, persistent, whitish to yellowish, margins laciniate; tepals oblong to oblong-lanceolate, 2.5 mm long, 1 mm wide, reflexed at maturity, apex with a glandular pilose area 0.1 mm long; filaments 1.5 mm long, anthers 1 to 1.2 mm long. Pistillate flowers campanulate, 2.5 mm diam, 1 to 2 per node, on pedicels 3 to 3.5 mm long, articulate below the middle, surrounded by lanceolate membranaceous bracteoles 1.5 to 3 mm long, persistent, yellowish, margins laciniate; tepals lanceolate, 2 mm long, 1.5 mm wide, thickened at the middle of the base, style very short, stigmas 3-branched; nectaries septal, at the base of the ovary. Fruits depressed, 1(–2) per node, 6 mm long, 10 mm wide, on peduncles 6 to 12 mm long, articulate near the base, tepals persistent, the internal adpressed covering the nectaries, the external reflex. Seed 1(2 or 3) per fruit, ovoid to ellipsoid, ca. 3.5 mm long, 2.5 to 3 mm wide, exposed at maturity, maroon. Figure 6; Table 1.</p><p>Ecology and Distribution —This species occurs on northfacing slopes, on steep hills and in canyons with alkaline igneous rocks in the sierras de La Giganta, San Francisco, Guadalupe, Las Palmas, and San Bruno in the state of Baja California Sur (Fig. 7). The plants grow mostly in  Quercus forests and desert scrub with  Brahea brandegeei (Purpus) H. E. Moore,  Fouquieria columnaris (Kellogg) Curran,  Ebenopsis confinis (Standl.) Barneby &amp; J. W. Grimes,  Prosopis sp., and  Croton sp., from 700 to 1900 m altitude on volcanic rocks. The plants flower from June to September, and set fruits from October to December.</p><p>To assess the identity of the proposed taxon, a set of problems was found within the herbarium collections concerning the probability that this taxon could be either part of  N. palmeri or of  N. bigelovii . According to Brandegee (1889), he collected one specimen of an unknown  Nolina at San Julio on April 19–20 of the same year. He stated that the plant has “leaves only of an arborescent branching species, 15 feet high with light green narrow leaves 3–4 feet long.” These details, and the fact that he also cited a young specimen of  N. bigelovii from Ubi (Yubay), show evidence that he knew the species, and that it was a different taxonomical entity (Table 1). Recently, Hochstätter (2010) presented an article on  Nolina, considering  N. palmeri var. brandegeei as a synonym for  N. palmeri . But, the paper appears to be mainly a bibliographic revision and not a detailed taxonomic treatment. However, though  N. brandegeei has similarities with  N. palmeri, including the exposed seeds at maturity, it differs greatly in its arborescent habit, larger and flat leaves, leaf margin denticles forked, shredded and not coiled leaf tips, and larger fruits (Fig. 4). In addition, the type specimen of  Nolina brandegeei (Trelease) L. Hern. comb nov. deposited at MO should be relabeled as collected at San Julio, Baja California Sur, on April 19–20, 1889.</p><p>Representative Specimens Examined —   Mexico. — BAJA CALIFORNIA SUR:  San Julio, 11 Apr. 1889, Brandegee s/n (UC) ;   Ubi,  Agua Bonita, 8 May. 1889, Brandegee s/n (UC) ;   Sierra La Giganta, above  Los Encinos, 1 Mar. 1939, H. S. Gentry 4292 (GH, MO) ;   Ridge northwest of main peak,  Cerro de La Giganta, 23 Nov. 1947, A. Carter 2038 (LL, MEXU, US) ;   North slope of Cerro  San Juan, 4 Feb.1964, R. Moran 11584 (SD) ;   Summit of Volcán las  Tres V´ırgenes, 12 Feb. 1964, R. Moran 11691 (SD, US) ;   North slope, summit of Cerro de la Higuera, Sierra  San Francisco, 21 Feb. 1964, R. Moran 11723 (SD) ;   Summit, Cerro Natividad, Sierra  San Francisco, 24 Feb. 1964, R. Moran 11751 (SD) ;   At pass ca. 3 miles west of ex-mission Guadalupe on trail to  San Pedro, 11 Mar. 1964, R. Moran 11790 (CAS, SD) ;   North slope at summit of  Cerro Azufre, 20 Oct. 1971, R. Moran 18736 (SD, US) ;   North slope of Cerro Barranco,  Sierra de Guadalupe, 23 Oct.1971, R. Moran 18822 (SD) ;   Sierra de La Giganta,  Cerro Mechudo, the southernmost peak of the Sierra, 2 Nov. 1971, R. Moran 18892 (BM, MEXU, SD) ;   N slopes of NE side of  Volcán Tres V´ırgenes, 12 Apr. 1973, J. Henrickson 8993 (SD) ;   Sierra de Las Palmas, W de San Bruno (31 miles), 20 jun. 1973, H. S. Gentry 23319 (AZ, DES, CAS, MEXU, US) ;   Rancho La Laguna, Sierra  San Francisco, 23 Nov. 1976, R. Moran 23824 (SD) ;   Sierra San Francisco, Mesa  San Jorge, ca. 7–7.5 km W of San Francisco &amp; 16 km MW of Santa Marta, 9 jun. 1984, J.  Dice 512, 515, 516 (CAS, MEXU, SD) ;   Sierra de San Francisco, Mesa de San Jorge, ca. 4.21 km (by road) WSW of the  Village of San Francisco de la Sierra, 23 Jun. 1986, C.  Dice, 675 (GH, SD) ;   Sierra de San Francisco, west of the town of  San Francisco de La Sierra, along road to Rancho Sorpresa, 24 Apr. 1994, W. Hogdson 8185 A (DES, SD) ;   Sierra de San Francisco, west of the town of  San Francisco de La Sierra, on the road to Rancho Sorpresa, 24 Apr. 1994, J. Rebman 2627 (BCMEX, SD) ;   Sierra San Francisco,  Cerro Bola, 3 Sept. 1995, W. Hogdson 9582, 9589a (DES; SD) ;  San Francisco de la Sierra, 23 Oct 1997, J. Rebman s/n (HCIB, SD);   West of Mulegé;   cumbre de  San Pedro ;   between the Ex-mision Guadalupe and San Juan de las  Pilas, 29 Oct.1997, J. León de la Luz s/n (BCMEX) ;   Sierra de Guadalupe:  West of Mulegé: cumbre de San Pedro between ex-mission Guadalupe and San Juan de las Pilas, 29 Oct. 1997, J. Rebman 4716 (HCIB, SD) ;   Sierra de San Francisco, 1.5 km al NW de Santa Ana, Nov. 2004, O. Baltasar s/n, (QMEX) ;   Sierra de la Giganta,  Campamento de la Sabanilla del Mechudo, 11 Nov. 2007, J. L. León de la Luz 10539 (HCIB, SD) ;   Hernández 2007 (QMEX).  NOLINA INTERRATA H. S. Gentry Madro ~ no 8:181. 1946  . TYPE:</p><p>USA: California, San Diego Co. Slope west of Dehesa</p><p>School, 5 Aug. 1945, H. S. Gentry 7330 (Holotype SD,</p><p>isotypes: AZ, CAL, MICH).</p><p>Plant rhizomatous, subterranean stems growing in a horseshoe shape by branching always to the same side; bark reticulate forming pentagonal pyramids 0.5 cm deep, 1 cm wide. Leaf rosettes subsessile, 40 to 90 cm diam, 15 to 25 leaves per rosette. Leaves linear, 48 to 109 cm long, 0.7–1 cm wide, helicoidal, glaucous green, scabrid; leaf margins with two sizes of denticles, the larger ones separated ca. 0.5 mm; leaf bases triangular to long deltate, 6–7 cm long, 3–3.5 cm wide in the inferior part, 1.2–1.5 cm wide in the superior part, yellow straw to dark brown with age, persistent, recurved; leaf apex entire. Inflorescences paniculate, largely ovoid to largely ellipsoid, 0.8 to 2 m long, 40 to 42 cm wide; scapes 35 to 45 long, 0.8 to 1.3 cm diam at the base; scape bracts linear, 15 to 30 cm long, separated among them by 10 to 15 cm; inflorescence branches compound, 37 cm long, decreasing apically in size to 9 cm, pedunculated, with 2 branchlets at the base, all subtended by papery linearlanceolate bracts, 14 cm long, decreasing apically in size to 1 cm; branchlets 3 to 8 cm long, the apical ones 8 to 15 cm long, all subtended by amplexicaule papery bracts, 7 to 10 mm long. Staminate flowers 2 to 3(–4) per node, 3 to 3.5 mm diam, on pedicels 4 to 5 mm long, wider in the apex, articulate above the middle, surrounded by membranaceous bracteoles, 2 to 3 mm long, margins dentate; tepals lanceolate, 2 to 3 mm long, 1.5 mm wide, reflexed from the middle at maturity, white to creamy, the midvein yellow green; filament 1 to 1.2 mm long, anthers 0.8 to 1 mm long; ovary undeveloped, on a small stipe. Pistillate flowers 2 per node, 2 mm in diam, on pedicels 1.8 to 2 mm long, articulate around the middle, surrounded by membranaceous bracteoles 2 to 4 mm long, margins dentate; tepals lanceolate, 2 to 2.5 mm long, 1 to 1.5 mm wide, white to creamy with purple dots or blotches around the midvein; staminoids 1 mm long; ovary 1.5 to 2 mm diam, stigmas sessile, 3-lobulate. Fruits slightly depressed, 0.8 to 1 cm long, 1 to 1.2 cm wide, on peduncles 6 to 7 mm long, articulate below the middle; fruit lobes papery, brown with purple reddish spots at the middle, with weak margins; apical notch 2.5 to 3 mm deep; tepals persistent, the external ones reflexed. Seeds ovoid, asymmetrical, 4 to 4.5 mm long, 2 to 2.5 cm wide, grayish green to brown at maturity, microreticulate, punctate, and sometimes with papillate trichomes, hilum suprabasal with a conic caruncle. Figure 8.</p><p>Ecology and Distribution —This species grows in sandy to deep soils on slopes with gabbro outcrops, 340 to 460 m in elevation, in chaparral vegetation with  Adenostoma fasciculatum Hook. &amp; Arn.,  Arctostaphylos sp.,  Rhus ovata S. Watson and  Ceanothus sp. The individuals of  N. interrata can withstand periodic wildfires.</p><p>It is an endemic and endangered species of San Diego County, California and the northwestern part of Baja California, Mexico (Fig. 2). The plants flower from April to August, and set fruits from August to October.</p><p>Representative Specimens Examined —   Mexico. — BAJA CALIFORNIA: Rancho de la Cruz, 6 Km ENE of  San Antonio de Las Minas, 12 Aug. 1981 R. Moran 29794 (CAS, MO, TEX) ;   Rancho de la Cruz, 6 Km ENE of  San Antonio de Las Minas, 12 Aug. 1981 R. Moran 29795 (MEXU, MO, SD, UC) ;  1 km NW of ranch house, Rancho de la Cruz, 6 Sept. 1981, R. Moran 29836</p><p>(SD);   Upper Canyon Arce, 2 km SW of Rancho de la Cruz, 6 Sept. 1981, R. Moran 29841 (SD) ;   3 km SSW of Rancho La Cruz, 6 Sept. 1981, R. Moran 29845 (SD) ;   Upper portion of  Ca ~ nón Arce, ca. 2.1 km of Rancho de la Cruz, ca. 10 km N of Ensenada, J.  Dice 621 (CAS) ;   ca. 1 km of  Rancho La Cruz, 13 km N of Ensenada, J.  Dice 700 (SD)  .</p></div>	https://treatment.plazi.org/id/5F37DB1E8200EC29FCF0F8AAFE6FF8D5	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Hernández-Sandoval, Luis;Rebman, Jon P.	Hernández-Sandoval, Luis, Rebman, Jon P. (2018): The Genus Nolina (Asparagaceae) of the Baja California Peninsula, and the Recognition of a New Species Combination. Systematic Botany (Basel, Switzerland) 43 (3): 717-733, DOI: 10.1600/036364418X697436, URL: https://doi.org/10.1600/036364418x697436
5F37DB1E820EEC2FFCF0F8D2FC5EF939.text	5F37DB1E820EEC2FFCF0F8D2FC5EF939.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Nolina palmeri var. palmeri Trelease Proceedings	<div><p>Nolina palmeri var. palmeri Trelease Proceedings of the American Philosophical Society 50:420. 1911.</p><p>Plants cespitose forming clumps 3.5 m wide, acaulescent or with trunks 10 to 60(–100) cm high, 10 cm diam; bark forming polygonal pyramids 1 to 1.5 cm deep, 1 to 2(–2.5) cm wide. Rosettes 12. Leaves linear, 90 to 116 cm long, 4 to 8 mm wide at the middle, concave in cross section; leaf base triangular, (5–) 9 to 11 cm long, (2–) 4 to 7.5 cm wide below, (0.8–) 1 to 1.6 cm wide above; leaf margin with translucent to brown denticles with the epidermis up growing in the middle; leaf tips coiled, becoming dry with a yellow straw color. Inflorescence 0.96 to 3 m cm high, 8 cm wide; scape 10 to 0.35 to 1 m long, 1 to 4 cm diam at the base with linear bracts, 8 to 50 cm long; the first 15 to 30 cm of the inflorescence bear the loose and thin branches 5 to 8 cm long; the rest of the branches stiff, erect to curved, ascending, 24 to 17 cm long, decreasing in size to 6 to 4 cm at the apex branch, subtended by linear to long triangular bracts, shorter than the branches, from 16 cm long, decreasing to the apex to 2 cm, papery, the larger ones with tips coiled; branchlets 1–8 cm long, last part of branches beyond the last branching (4–) 6 to 11 cm long. Staminate flowers 1(–2) per node, campanulate, 2.5 to 3.5 mm long, 4 to 5 mm wide, on pedicels to 1 mm long, articulated at the very base, surrounded by 2 widely lanceolate bracteoles, the external one 2 to 3 mm long, the internal one 1.5 to 2 mm long, white, membranaceous, margins laciniate to denticulate; tepals oblong to oblong-lanceolate, 2.5–3 mm long, 1–1.5 mm wide, white, reflexed from the middle at maturity; filaments 1 to 1.2 mm long, anthers 1–1.1 mm long. Pistillate flowers 1 to 2(–3) per node, campanulate, 2–3.5 mm long, 3–4 mm wide, on pedicels up to 2 mm long, articulated above the middle, surrounded by lanceolate bracteoles, the external ones 2–4 mm long, the internal ones 1.5–2 mm long, white, membranaceous, margins long laciniate to denticulate; tepals lanceolate, 2.2–2.5 mm long, 1–1.5 mm wide, white with the base thick, greenish, midvein reddish to brown; ovary round, 3 mm diameter, 3- lobed; ovules basal, subtended by a small, round or shelf-like protruding structure, which is flattened by the fertilized ovule growth; stigmas sessile, 3 branched. Fruit depressed to orbicular, 4–5 mm long, 5–7 mm wide, on peduncles 3 to 4 mm long, articulated at or below the middle, green to brown; lobes with margins. Seeds 1 to 2 per fruit, rounded, 3.5–4 mm in diam, exposed at maturity, testa microreticulate, light to dark brown. Figure 9.</p><p>Ecology and Distribution —  Nolina palmeri grows in canyons, on east and west slopes, crevices, boulders, and dry hills, on volcanic and granitic rocks, and granitic alluvium soils, 1250 to 2830 m in elevation (Fig. 10). It is part of the chaparral, and the pine, juniper, and oak forests, along with  Adenostoma spp.,  Arctostaphylos pungens Kunth;  Artemisia sp.,  Brahea armata S. Watson,  Ceanothus sp.,  Celtis ehrenbergiana (Klotzsch) Liebm.,  Condalia brandegeei I. M. Johnst.,  Cylindropuntia cholla (F. A. C. Weber) F. M. Knuth,  Cylindropuntia alcahes (F. A. C. Weber) F. M. Knuth,  Dodonaea viscosa Jacq.,  Juniperus californica Carrière,  Pinus jeffreyi Grev. &amp; Balf.,  P. contorta Loudon subsp. murrayana (Grev. &amp; Balf.) Critchf.,  Populus tremuloides Michx.,  Prosopis articulata S. Watson,  Quercus spp.,  Salvia pachyphylla Munz, and  Yucca schidigera Ortgies. The flowers are visited by Hemiptera to lay eggs that hatch in June. The species flowers from April to June, and produces fruits from July to November.</p><p>Nolina palmeri is an endemic species to Baja California, and occurs sympatrically with  N. bigelovii in the Sierra de San Pedro Mártir and Sierra de Juárez in the northern portion of the state, and is distributed to the Sierra de La Libertad at its southern limit.</p><p>Representative Specimens Examined —   Mexico. — BAJA CALIFORNIA:  Cantillas Canyon, s/d, C. R. Orcutt s/n (US) ;   Pinon ~ District, Oct.1882, C. R.  Orcutt 713 (GH, MO) ;   Pi ~ non forest, 26 Jul. 1883, C. R. Orcutt s/n (US) ;   N  Lower California, 3 Jul. 1885, C. R. Orcutt 530 (MEXU -photo-, US) ;   Para´ıso, 1890,  Brandegee s/n (UC) ;   San Pedro Mártir, 16 May.1893  Brandegee s/n (UC) ;   San Mat´ıas pass, N end of San Pedro Mártir Mountains, 28 June 1905,  Goldman E. A 1183 (US) ;   Lower California, 1 Jan 1907,  Orcutt C. R. s/n (US) ;   Between Neji Rancho and town Alaska, 16 Sept. 1929,  Wiggins I. R. 4167 (CAS, GH, SD, US) ;   La Encantada, Sierra San Pedro Mártir, 20 Sept. 1930,  Wiggins I. R. 4962 (CAS, GH, SD, US) ;   Rancho Neji, Sept. 1930, H.  Bravo 21–665 (MEXU) ;   Summit of rim just N of Picacho de La Encantada,  Sierra San Pedro Mártir, 18 Oct. 1946,  Wiggins I. R. 11278 (CAS) ;   Head of Cantillas Canyon 22 Apr. 4 1951,  Harbison C. F. s/n (SD) ;   Head of Cantillas Canyon, 1 Sept. 1951,  Harbison C. F. s/n (CAS, SD) ;   Head of the trail into Tajo ( Cantillas)  Canyon, 1 June 1952,  Harbison C. F. s/n (CAS, SD) ;   Canyon del Diablo, to the North and West of  Picacho del Diablo ( Cerro La Encantada), eastern flank of  Sierra San Pedro Mártir, 17</p><p>June 1954, Chambers K. L. 630 (CAS, UC) ;   Sierra  San Borja, San Juan Mine, 24 Mar. 1960, R. MoranR. Moran 8017 (CAS, SD) ;   3 mi W of Santa Catarina, 64 miles SE of  Ensenada, 21 Aug. 1961, Broder R. E. 599 (BM, MEXU, US) ;   Sierra San Pedro Mártir, along trail on way to La Encantada to Rimrock, 5 Sept. 1961, Wiggins I. R. 16647 (CAS) ;   Mouth of Valley of San Juan, 25 Nov. 1961, R. Moran 8497 (CAS, SD) ;   El Topo, Sierra Juárez, 29 June 1962, R. Moran 9811 (CAS, SD, UC) ;   3 mi north of  El Topo, Sierra Juárez, 29 June 1962, R. Moran 9806 (CAS, SD, UC, US) ;   Portezuelo de Jamau, 9 May 1963, R. Moran 10978 (SD, UC, US) ;   Cerro Chato, 3 June 1963, R. Moran 11120 (CAS, SD, UC) ;   Summit Cerro La Sand´ıa, 21 Jan 1964, R. Moran 11536 (CAS, SD) ;   Sierra San Borja, summit of Cerro La Chona, 19 Mar. 1966, R. Moran 12792 (CAS, SD) ;   Sierra Juárez, 1.5 miles NW of Rancho Marcos, 4 Sept. 1966, R. Moran 13481 (SD) ;   Cerro La Encantada, 19 Aug. 1967, R. Moran 14358 (BCMEX, MEXU, SD, UC) ;   Santa Rosa. San Pedro Mártir, 20 Aug. 1967, R. Moran &amp;  Thorne R. F. 14426 (BCMEX, LL, UC) ;   Sierra San Pedro Mártir, rocky ridge north of Vallecitos, 6 Jul. 1968, R. Moran 15279 (SD) ;   East slope above Arroyo Copal, 25 Aug. 1968, R. Moran 15515 (BCMEX, MEXU SD) ;   Sierra San Pedro Mártir, near the settlement of Vallecitos, 21 Sept. 1968, Breedlove D. E. 16365 (CAS) ;   On slope above meadow at Vallecitos, Sierra San Pedro Mártir, 9 Aug. 1969, Witham H. V. 420 (BCMEX, SD) ;   West slope of Cerro Pinón ~, 3 km north of el Alamo, 30 May. 1970, R. Moran 17672 (MEXU, SD) ;   Sierra Juárez, 3 miles SW of San Pedro, 19 Sept. 1971, R. Moran 18517 (SD) ;   Sierra Juárez, 3 Oct. 1971, R. Moran 18665 (SD) ;   North slope at summit of Cerro Matom´ı, 3 May 1973, R. Moran 20742 (CAS, SD, UC) ;   North slope of Cerro Tarasizo, southernmost peak of range. Also on summit, 2 May 1976, R. Moran 23008 (SD) ;   Los Manzanos, 20 Aug. 1977, R. Moran s/n (BCMEX) ;   Sierra  San Pedro Mártir, 20 Aug. 1977, R. Moran 24543 (SD) ;   Steep rocky hillside, 1 km NW of Tres Pozos, 26 May 1979, R. Moran 23008 (CAS, SD) ;   Tres Pozos, Sierra de Juárez, 26 May1979, R. Moran 27402 (CAS) ;   On rocky slope 3.5 km SE of El Compadre, 14 Nov. 1981, R. Moran 29888 (SD) ;   Arroyo 3 km west of Cerro el Toro, 31 May 1982, R. Moran 30894 (SD) ;   Vallecitos 3 June 1982,  Dice J. s/n (BCMEX) ;   Vallecitos Open, road to Observatory and campground, 18 June 1985,  Thorne R. F. s/n (BCMEX) ;   Area del observatorio, San Pedro Mártir. 13 Oct. 1985, Delgadillo J. s/n (BCMEX) ;   Observatorio  San Pedro Mártir, 29 Jul. 1986,  Salazar M. s/n (BCMEX) ;   San Pedro Mártir, 29 Jul. 1986, Passini &amp;  Salazar s/n (BCMEX) ;   San Pedro Mártir, 8 Aug. 1986, Passini &amp;  Salazar s/n (HCIB) ;  Northern Sierra San Pedro Mártir, SW corner of a small plateu on the western escarpment, 17 June 1988, Sanders A. C. 7940 (BCMEX, SD, UC);   Sierra Juárez, 3 miles East of Laguna Hanson, 26 Jul. 1994, Rebman J. 2840 (BCMEX, SD, UC) ;   Sierra San Pedro Mártir, ridgetop above and east of Vallecitos area, 25 June 1996, Rebman J. 3263 (BCMEX, SD) ;   Sierra  San Pedro Mártir: Rancho Picacho, norte de SPM, 5 May. 1998, Delgadillo J. s/n (BCMEX) ;  10 km al W de la Reserva de la Biósfera San Pedro Mártir, 11 Apr. 2004, Hernández L. 5274 (QMEX);  11 km al W de la Reserva de la Biósfera San Pedro Mártir, 11 Apr. 2004, Hernández L. 5275 (QMEX);   Carreteras entre Ensenada y San Felipe, 13 Apr. 2004, Hernández L. 5278 (QMEX) ;   Sierra La Libertad: vicinity of el Rodeo ;   along the trail  between Rancho Hierba Buena and Las Cuevitas, 25 Oct. 2009, Rebman J. 18666 (SD)  .</p><p>Species Possibly Present on the Baja California Peninsula —Two species,  Nolina cismontana and  N. parryi have not yet been discovered on the Baja California peninsula, but grow at a distance less than 50 miles north of it in San Diego County, California, USA (Hess 2002). It is very likely that either one of these species could occur in the Baja California region. We consider it important to include a small diagnosis of each as well as photographs for both species so that accurate identification can be made if encountered in the region.</p></div>	https://treatment.plazi.org/id/5F37DB1E820EEC2FFCF0F8D2FC5EF939	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Hernández-Sandoval, Luis;Rebman, Jon P.	Hernández-Sandoval, Luis, Rebman, Jon P. (2018): The Genus Nolina (Asparagaceae) of the Baja California Peninsula, and the Recognition of a New Species Combination. Systematic Botany (Basel, Switzerland) 43 (3): 717-733, DOI: 10.1600/036364418X697436, URL: https://doi.org/10.1600/036364418x697436
5F37DB1E8208EC2CFBA6F915FC3DF840.text	5F37DB1E8208EC2CFBA6F915FC3DF840.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Nolina cismontana DICE	<div><p>NOLINA CISMONTANA DICE</p><p>Plants caulescent; rosettes 3 to 7; stems 30–150 cm. Leaves 30 to 90 per rosette; blade wiry, 50–140 cm long, 12–30 mm wide, occasionally glaucous, margins denticulate, not filiferous; bases spoon-shaped, 30–85 mm long. Scape 40–150 cm, 14–35 mm diam at base. Inflorescences paniculate, 90–180 cm long, 10–40 cm wide; bracts persistent, conspicuous. Pistillate flowers 3 to 5 mm diam on pedicels erect, 3 to 5 mm long, articulate at or above the middle, surrounded by laciniate bractlets; tepals 2.5 to 5 mm long, staminoids 1–1.2 mm, anthers 0.4–0.6 mm; Staminate flowers 3 to 5 mm diam; filaments 2 to 4 mm long, anthers to 1.2 mm; Fruit 8.2–11.2 mm long, 9–12 mm wide, notched basally and apically. Seeds ovoid, 4 to 5 mm long, 3 to 4 mm wide, reddish brown, exposed at fruit maturity. Figure 11.</p><p>According to Hess (2002),  N. cismontana flowers in early to mid-spring, and grows on rocky hillsides in dry chaparral of coastal mountains from 200 to 1300 m in elevation.</p></div>	https://treatment.plazi.org/id/5F37DB1E8208EC2CFBA6F915FC3DF840	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Hernández-Sandoval, Luis;Rebman, Jon P.	Hernández-Sandoval, Luis, Rebman, Jon P. (2018): The Genus Nolina (Asparagaceae) of the Baja California Peninsula, and the Recognition of a New Species Combination. Systematic Botany (Basel, Switzerland) 43 (3): 717-733, DOI: 10.1600/036364418X697436, URL: https://doi.org/10.1600/036364418x697436
5F37DB1E820AEC32FEF2F8E2FDF6F840.text	5F37DB1E820AEC32FEF2F8E2FDF6F840.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Nolina parryi S. WATSON	<div><p>NOLINA PARRYI S. WATSON</p><p>Plants caulescent; rosettes from woody, branched caudices and forming small colonies. Stems 0.5 to 2.1 m. Leaves 65 to 220 per rosette; blade helicoidal, 50 to 140 cm long, 20 to 40 mm wide, rarely glaucous; bases spoon-shaped, 5–16.5 cm wide; margins denticulate. Scape 40–170 cm, 26–90 mm diam at base. Inflorescences 20 to 130 cm long, 9–18 cm wide; bracts persistent, 15 to 36 cm long, papery. Pistillate flowers 3 to 5.5 mm diam on pedicel erect, 3 to 4 mm long, articulated at or above the middle, surrounded by laciniate bractlets, to 10 mm, fragile; tepals 2.5 to 5 mm; staminoids 1–2.5 mm long, anthers 0.4 to 0.5 mm long. Staminate flowers 3–5.5 mm diam, stamens 3–4 mm, anthers 1.3–1.8 mm. Fruits 9 to 13 mm long, 8 to 11 mm wide, notched basally and apically. Seeds ovoid to oblong, 3–4 mm long, 2–3 mm wide, reddish brown, exposed at fruit maturity. Figure 11.</p><p>According to Hess (2002),  N. parryi flowers in early spring and grows on rocky slopes of desert and pinyon-juniper woodlands from 900 to 2100 m in elevation.</p></div>	https://treatment.plazi.org/id/5F37DB1E820AEC32FEF2F8E2FDF6F840	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Hernández-Sandoval, Luis;Rebman, Jon P.	Hernández-Sandoval, Luis, Rebman, Jon P. (2018): The Genus Nolina (Asparagaceae) of the Baja California Peninsula, and the Recognition of a New Species Combination. Systematic Botany (Basel, Switzerland) 43 (3): 717-733, DOI: 10.1600/036364418X697436, URL: https://doi.org/10.1600/036364418x697436
