FNA: Orobanche vs. Orobanche ramosa

Phenology

Flowering Feb–Apr, Jul–Sep.

Habitat

Roadsides, crop fields, lawns, disturbed areas, greenhouses.

Elevation

0–300 m. (0–1000 ft.)

Distribution

North America; Mexico; Central America; South America; Europe; Asia; n Africa [Introduced widely]

[BONAP county map]

CA; IL; KY; NJ; TX; VA; Eurasia; Africa [Introduced in North America]

Discussion

Species ca. 150 (17 in the flora).

As noted by J. W. Thieret (1971), systematists have generally accepted the classification by G. Beck (1930) of a broadly circumscribed Orobanche comprising four sections, all of which are represented in the flora area. However, J. Holub (1990) and some other authors have questioned whether this classification accurately reflects the phylogeny and taxonomic complexity of the group and have proposed recognizing the sections of Beck as separate genera. More recently, cytological and molecular phylogenetic studies have added new data to the discussion but have not resulted in a well-supported, revised classification. G. M. Schneeweiss et al. (2004b) reviewed a large series of new and earlier chromosome counts and concluded that sect. Orobanche has a base number of x = 19, whereas members of the other sections are characterized by x = 24. As summarized by J. M. Park et al. (2008), molecular data have resulted in discordant phylogenies, depending on taxon sampling and whether plastid or nuclear markers were sequenced, but have suggested that five lineages should be recognized within the traditional Orobanche. The fifth lineage has been segregated by some authors as the monospecific Boulardia latisquama F. W. Schultz [O. latisquama (F. W. Schultz) Battandier], native to the Iberian Peninsula and Morocco. The molecular data support the group as monophyletic whether treated as one genus or several. Although the authors retain Orobanche in the broad sense, it seems inevitable that Orobanche will be split into three or more genera once the number of well-supported segregates is resolved. Most recently, A. C. Schneider (2016) has made a case for splitting all of the species native to the New World [sect. Gymnocaulis Nuttall and sect. Nothaphyllon (A. Gray) Heckard] into two sections of a single generic segregate, Aphyllon Mitchell, and has published new combinations for the constituent taxa.

As outlined in the key to species below, the two Old World sections present as adventives in our region are notable for their usually four-lobed or -toothed calyces and spicate inflorescences. Members of the two New World sections have five-lobed calyces and a variety of inflorescence types. Section Orobanche includes 120 to 130 species and is widespread in Europe, Asia, and Africa. The flowers lack bracteoles, the calyces are deeply two-parted with one or both halves toothed or lobed, and the corollas are usually yellow, red, or brown. The 12 to 16 species of sect. Trionychon Wallroth (Phelipanche Pomel) are most diverse in the Mediterranean region; their flowers have a small pair of bracteoles adnate to the calyx bases, the calyces are four-toothed or -lobed, and the corollas are usually purple or blue.

In the New World, the small sect. Gymnocaulis [sect. Euanoplon (Endlicher ex Walpers) Thieret; Aphyllon] comprises two or more species widespread in the flora area and is notable for its condensed inflorescence axes shorter than the elongate pedicels, flowers lacking bracteoles, and calyces shallowly to moderately lobed. About 15 members of sect. Nothaphyllon [sect. Myzorrhiza (R. A. Philippi) Beck-Mannagetta; Myzorrhiza R. A. Philippi] are widespread from temperate North America south to Guatemala, with a few disjunct species in western South America. They are characterized by usually elongate inflorescence axes usually much longer than the pedicels, flowers with a pair of bracteoles, and deeply five-lobed calyces.

Several of the Old World species are introduced widely, including the species treated below. They parasitize various crop plants, principally tomatoes (Solanum lycopersicum), tobacco (Nicotiana tabacum), clovers (Trifolium spp.), and hemp (Cannabis sativa) in the United States and are considered agricultural pests. In response, the Federal Government has placed all of the non-native taxa of Orobanche on the United States Department of Agriculture’s noxious weed list (http://www.aphis.usda.gov/plant_health/plant_pest_info/weeds/downloads/weedlist.pdf), which regulates their movement into, out of, and within the United States. Several states also regulate various non-native broomrapes as noxious weeds.

In 2014, an infestation of Orobanche aegyptiaca Persoon [Phelipanche aegyptiaca (Persoon) Pomel] was discovered in a tomato field in Solano County, California, the first report of this taxon from the flora area. Egyptian broomrape is native to the Middle East and adjacent portions of Europe and Asia but is a widely distributed weed in Europe, Asia, and Africa, and has also been reported from Cuba (R. Oviedo Prieto et al. 2012). Its principal negative economic impact is to crop species in the Solanaceae (tomatoes, potatoes, tobacco), but, like O. ramosa, it has a broad host range, including a variety of other crops. Although the appearance of the species in North America is not unexpected, a full treatment is not provided here, because there is no certainty that it will become established. Vigorous efforts have been undertaken to eradicate plants at the sole known location. Orobanche aegyptiaca is similar to O. ramosa in its branched, glandular-pubescent stems and general floral morphology, but it differs from that species in its usually more robust habit (stems to 40 cm), with larger corollas (20–35 mm) that are often darker purple, and by having densely villous versus glabrous anthers.

Plants of Orobanche hederae Duby (ivy broomrape), another Eurasian species in sect. Orobanche, have been documented since 2000 parasitizing planted Hedera (Araliaceae) in Alameda County, California, on the campus of the University of California-Berkeley. It can be difficult to distinguish from the morphologically variable O. minor, differing in its often slightly more lax inflorescences and corollas with a constriction on the abaxial side just behind the throat. For recognition, most botanists focus on the difference in hosts, as O. hederae parasitizes species of Hedera. The taxon is excluded from the flora for the present, because its host specificity has limited its ability to spread beyond the immediate vicinity of the initial infection site.

The native North American species have had a negligible impact on agriculture. Orobanche cooperi and O. riparia (as O. ludoviciana) have been reported on cultivated tomato crops in southern California and on tobacco crops in the Ohio River Valley, respectively, with O. cooperi having required control measures (G. H. Starr 1943; S. Wilhelm et al. 1958).

Some of the western North American taxa were recorded as a minor, but apparently widely utilized, food source for western American Indians and were also used medicinally, mainly for treating colds and other pulmonary ailments (D. E. Moerman 1998).

The North American Orobanche species are more host-specific than has been reported previously (A. C. Schneider et al. 2016b), and understanding of host relationships continues to be refined. Many collectors merely note the nearest living plant as the host species or have neglected to note host species entirely, thus perpetuating imprecise knowledge of host relationships in this group. In this treatment, a host species is noted as a primary host when it has been confirmed multiple times by excavation and is frequently reported as the host. Less frequent, but reliable, reports of other hosts are noted as occasional hosts. Localized shifts in host preference in Orobanche species may reflect an indication of lineage divergence.

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

The identity of the sole historical collection of Orobanche ramosa from North Carolina (Roan Mtn., J. Ball s.n., 17 September 1884, E) remains tentative (L. J. Musselman 1984). Many other historic infestations of this weedy species in the region have been eradicated. However, in recent decades the species appears to be spreading in central and eastern Texas using disturbed roadsides as avenues for dispersal.

This destructive agricultural weed has a large host range. L. J. Musselman and K. C. Nixon (1981) documented plants within a single population in Texas attached to the roots of ten different hosts in eight angiosperm families: Apiaceae, Asteraceae, Caryophyllaceae, Fabaceae, Geraniaceae, Malvaceae, Onagraceae, and Verbenaceae. Other voucher specimens have recorded an even more diverse assemblage of hosts, mainly eudicots and occasionally even monocots. Historically, the principal crop species affected in the region have been hemp, tobacco, and tomato, but an infestation in a commercial greenhouse in New York impacted coleus (Plectranthus) production in the 1920s. Currently, the main negative economic impact of Orobanche ramosa is in tomato fields in California.

As many as 20 microspecies have been described as segregates from Orobanche ramosa (F. J. Rumsey and S. L. Jury 1991). However, A. O. Chater and D. A. Webb (1972), who chose to circumscribe O. ramosa broadly as a single species with three subspecies, noted that the characters used to discriminate among these taxa exhibit nearly continuous variation and are often quite variable within populations. In their treatment, subsp. ramosa is the widespread weedy taxon that has emigrated to the New World, and the other two infrataxa [subsp. mutelii (F. J. Schultz) Coutinho and subsp. nana (Reuter) Coutinho] are uncommon, non-weedy taxa endemic to southern Europe that differ from subsp. ramosa in perianth details. Further studies are needed before an infraspecific classification can be supported.

As noted by H. J. Scoggan (1978–1979), Orobanche purpurea Jacquin (yarrow broomrape), was collected in Huron County, Ontario, in 1895 by Jasi A. Morton but has not been rediscovered in the flora area since the initial collection. The voucher specimens lack habitat data, but in its native range the species parasitizes mainly open grassland and woodland taxa of Achillea and Artemisia (Asteraceae). The species resembles O. ramosa, differing in its usually simple stems, longer corollas (18–25 mm), and calyces with slightly longer, more narrowly triangular lobes. Although its native distribution in Europe, Asia, and northern Africa is broad, C. A. J. Kreutz (1995) noted that it is rare in much of the range, and F. J. Rumsey and S. L. Jury (1991) were alarmed at its historical decline in Great Britain.

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

Key

1. Calyces bilaterally symmetric, sometimes strongly so, 2- or 4-lobed (rarely with an additional vestigial abaxial lobe); inflorescences spikes or spikelike racemes; pedicels 0–1 mm (rarely to 30 mm in proximalmost flowers).	→ 2
2. Calyces deeply divided into 2 lateral lobes (rarely with an additional vestigial abaxial lobe), lobes entire or asymmetrically divided into 2 teeth or short lobes, these much shorter than tube; bracteoles 0 [sect. Orobanche].	O. minor
2. Calyces divided into 4 subequal lobes, lobes entire, slightly shorter to slightly longer than tube; bracteoles 2 [sect. Trionychon].	O. ramosa
1. Calyces ± radially symmetric or weakly bilaterally symmetric, 5-lobed; inflorescences fascicles, corymbs, panicles, or racemes, sometimes spikelike, or of solitary flowers; pedicels 1+ mm (except in distalmost flowers of a few species).	→ 3
3. Pedicels (8–)10–110(–170) mm, as long as or longer than plant axis, distal sometimes shorter (O. fasciculata); inflorescences of solitary flowers or fascicles, irregular corymbs, or short racemes of (1–)6–15(–20) flowers; bracteoles 0 [sect. Gymnocaulis].	→ 4
4. Flowers 1 or 2(–4); pedicels much longer than plant axis.	O. uniflora
4. Flowers (1–)6–15(–20); proximal pedicels as long as or ± longer than plant axis, distals.	O. fasciculata
3. Pedicels 0–30 mm (to 35 mm proximally), shorter than plant axis; inflorescences racemes, sometimes spikelike, corymbs, or panicles (flowers numerous, rarely 10 or fewer in depauperate plants); bracteoles 2 [sect. Nothaphyllon].	→ 5
5. Inflorescences corymbs or panicles, sometimes racemes.	→ 6
6. Inflorescences panicles, open or dense and pyramidal; anthers glabrous or sparsely pubescent; corollas less than 20 mm; palatal folds not prominent, pale or light yellow.	→ 7
7. Inflorescences dense, pyramidal, dark purple-brown, imbricately branched; calyces divided into 5 unequal lobes, cleft to base only on adaxial side, otherwise deeply lobed; filaments glabrous.	O. bulbosa
7. Inflorescences open, cylindric (axis visible between flowers), ochraceous, red-brown, purple or purple streaked, yellow, or cream-white, loosely branched, rarely simple; calyces divided into 5 subequal lobes (lobes slightly shorter than to ca. as long as tube); filaments with ring of hairs at base.	O. pinorum
6. Inflorescences corymbs, sometimes racemes; anthers woolly, tomentose, pubescent, or glabrous; corollas (8–)12–50(–55) mm; palatal folds prominent, yellow, sometimes cream to lemon or white.	→ 8
8. Pedicels 2–10 mm (to 35 mm proximally); corollas (8–)15–25(–30) mm, tubes white to cream, sometimes pale purplish tinged distally, sometimes with purple veins, adaxial lips 4–6(–9) mm; inflorescences compact, corymbs to subracemose.	O. robbinsii
8. Pedicels (0–)3–20(–40) mm; corollas (15–)18–50(–55) mm, tubes white to grayish white, cream, ± pink, ± purple, or pinkish to purplish tinged, rarely brick red, sometimes with darker veins, adaxial lips 5–15(–18) mm; inflorescences corymbs, subcorymbose, racemes, or subcapitate.	→ 9
9. Corollas (15–)18–34 mm, lips 5–9 mm, erect, sometimes spreading or reflexed; palatal folds glabrous (with blisterlike swellings); Great Basin.	O. corymbosa
9. Corollas 22–50(–55) mm, lips 8–15 mm, ± spreading; palatal folds glabrous (without blisterlike swellings), sometimes pubescent; w of Cascade and Sierra mountains.	O. californica
5. Inflorescences racemes or spikelike racemes.	→ 10
10. Abaxial corolla lobe apices rounded or obtuse.	→ 11
11. Corolla lips internally maroon or reddish purple, sometimes with maroon or reddish purple stripes, veins, or blotches; palatal folds glabrous; s California, Nevada, Oregon.	O. parishii
11. Corolla lips internally pink or purple, sometimes white with purple veins, rarely light yellow; palatal folds pubescent; absent in California, widespread to the n and e.	→ 12
12. Corollas 14–20 mm, lips 3–6 mm; anthers glabrous or with a few woolly hairs along sutures.	O. ludoviciana
12. Corollas 22–36 mm, lips 5–12 mm; anthers woolly.	O. multiflora
10. Abaxial corolla lobe apices acute, pointed, or with an apiculate tooth.	→ 13
13. Corollas 15–32(–33) mm, lips 4–9(–10) mm.	→ 14
14. Corolla tubes purple or lavender, rarely white, tinged with purple, lips dark purple to lavender, with darker purple veins, lobes often with apiculate teeth; anthers usually with inconspicuous stalked glands.	O. cooperi
14. Corolla tubes white or pale yellow to pale pink, lips white to pale pink, often with darker pink veins, lobes without apiculate teeth; anthers without stalked glands.	O. vallicola
13. Corollas 12–22 mm, lips 3–6 mm.	→ 15
15. Corollas 12–16(–18) mm, tubes dark purple, sometimes yellow to white abaxially, adaxial lips 3–5 mm.	O. valida
15. Corollas (13–)15–20(–22) mm, tubes white, distally sometimes tinged with purple or pink, or with dark purple veins, adaxial lips 4–6 mm.	→ 16
16. Corollas 15–20(–22) mm, tubes white, adaxial lips dark purple, sometimes lavender; Colorado Plateau and Great Basin Desert; host Gutierrezia.	O. arizonica
16. Corollas (13–)15–22 mm, tubes white, distally often tinged with purple or pink, or with dark purple veins, adaxial lips lavender or dark purple; riparian habitats; host Ambrosia, Dicoria, or Xanthium.	O. riparia