Asplenium Pinnatifidum

''Asplenium pinnatifidum'', commonly known as the lobed spleenwort or pinnatifid spleenwort, is a small fern found principally in the Appalachian Mountains and the Shawnee Hills, growing in rock crevices in moderately acid to subacid strata. Originally identified as a variety of walking fern (''Asplenium rhizophyllum''), it was classified as a separate species by Thomas Nuttall in 1818. It is believed to have originated by chromosome doubling in a hybrid between walking fern and mountain spleenwort (''Asplenium montanum''), producing a fertile tetraploid, a phenomenon known as alloploidy; however, the hypothesized parental hybrid has never been located. It is intermediate in morphology between the parent species: while its leaf blades are long and tapering like that of walking fern, the influence of mountain spleenwort means that the blades are lobed, rather than whole. ''A. pinnatifidum'' can itself form sterile hybrids with several other spleenworts.

Description

''Asplenium pinnatifidum'' is a small fern with bright green, wrinkled, pinnatifid (lobed) fronds. These form evergreen, perennial tufts. Notable characteristics are the shiny stipe (leaf stalk), dark only at the base, and the long-tapering, variably lobed leaf blades. The fronds are monomorphic, the sterile and fertile fronds appearing the same size and shape.

The roots of ''A. pinnatifidum'' are not proliferous, so it appears as clusters of leaves springing from a single rhizome. The leaves are closely spaced on the rhizome, which is frequently branched. The rhizome is about in diameter, covered with narrowly deltate (triangular) scales which are dark reddish-brown or blackish in color, and strongly clathrate (bearing a lattice-like pattern). The scales are long and 0.3 to 0.5 millimeters wide, with entire (untoothed) edges. The stipe is shiny and dark reddish brown at the base. This color fades to green in the upper one-third to one-half of the stipe. It is covered in scales similar to those of the rhizome at the base, which diminish into hairs in the upper part of the stipe. It may show narrow wings from the base of the leaf to near the base of the stipe. The stipe is long, and may be from one-tenth to one and one-half times the length of the blade.

The overall shape of the blade is narrowly deltate or lanceolate, sometimes with an irregular outline. The blade tapers to a long point, the length and degree of taper varying among specimens from merely acute to acuminate or attenuate. The blades are generally curled with downward-pointing tips. The tip of the blade sometimes develops a swelling which may differentiate into a proliferous bud and, very rarely, into a plantlet, as in walking ferns. Adventitious sporangia may appear around the buds when they form, even, unusually, on the upper surface of the leaf. The base of the blade may be squared off or notched to a varying extent along the rachis (central axis of the leaf). The blade ranges from long, rarely to , and in width, rarely to , and is thick and somewhat leathery. Blades are either entirely pinnatifid (lobed but not completely cut), or cut to form a single pair of pinnae at the base. When they exist, the pinnae are roughly oval or triangle-shaped, sometimes narrow, and are from long, rarely to , and 0.4 to 1 millimeters in width (rarely to 1.2 millimeters). The base of the pinnae may be squared off or taper to a point, while the edges are wrinkled to toothed. The tip can vary from rounded to pointed. The lobes of the blade gradually diminish towards the tip, sometimes becoming simply wavy. The rachis is green, sometimes turning tan when dry. The underside of the rachis and blade have a few scattered, small hairs. Overall, the blades are quite morphologically variable; in younger blades, the edges may be not at all lobed or may be wavy. The veins are free and forking, only rarely anastomosing (rejoining one another to form nets).

Each segment (pinna or lobe) of a fertile frond has one to six sori, sometimes more than forty in extreme cases. The sori usually fuse with one another as they age. These are long. They are covered with thin, whitish indusia with untoothed edges, which are persistent. Each sporangium holds 64 spores. The species has a chromosome number of 144 in the sporophyte, indicating an allotetraploid origin.

Variation

While no named varieties or forms of ''A. pinnatifidum'' have been described, an unusual population was described from Giant City State Park in southern Illinois in 1956. In it, the leaf blade was highly reduced, barely exceeding the rachis, except for a series of stubby projections under which the sori were borne. Individual plants have also been known on occasion to develop forked leaves, which appears to be a developmental accident rather than a stable genetically-controlled trait.

Identification

''A. pinnatifidum'' is somewhat similar to its parent species ''A. rhizophyllum''. In comparison, however, ''A. pinnatifidum'' is distinctly lobed when mature, tends to have longer stipes in proportion to its leaf size, and has a more upright habit. It might be confused with Countess Dalhousie's spleenwort ( ''A. dalhousiae''), of Asia and the American Southeast, but the latter has short, dull stipes with larger, toothed scales. ''A. pinnatifidum'' closely resembles the hybrid Scott's spleenwort ( ''A. × ebenoides'') (including the fertile Tutwiler's spleenwort, ''A. tutwilerae''), but those species have a wholly dark stipe, with the dark color extending into the rachis, and longer lobes on the blade.

Among the hybrid species of which it is a parent, ''A. pinnatifidum'' is most similar to Graves' spleenwort ( ''A. × gravesii''), a hybrid with Bradley's spleenwort ( ''A. bradleyi''), and to a lesser extent, to Trudell's spleenwort ( ''A. × trudellii'') and Kentucky spleenwort ( ''A. × kentuckiense''). In ''A. × gravesii'', the dark color of the stipe extends to the base of the leaf blade, the blades often have more than one pair of pinnae, and their edges are shallowly wrinkled or toothed. In addition, the basal pinnae, which may themselves be pinnatifid, lack a stalk, the leaf blade is pointed at the tip but not drawn out at length, and there are generally fewer fronds. Its sori are dark brown, rather than cinnamon brown. ''A. trudellii'' is fully pinnate in the lower half of the blade, and its pinnae are toothed. ''A. × kentuckiense'' is also fully pinnate towards the base of the blade, with four to six pairs of pinnae, and the brown color of its stipe extends up into the basal part of the rachis.

Taxonomy

Lobed spleenwort was first recognized by Henry Muhlenberg in 1813, who considered it a variety of ''Asplenium rhizophyllum'', although he did not provide a description distinguishing the variety. In 1818, Thomas Nuttall observed that it was always distinguishable from ''A. rhizophyllum'', and described it as a species under the name of ''Asplenium pinnatifidum''. Alphonso Wood used the name ''Camptosorus pinnatifidus'' for the species in 1870, but this was not widely accepted.

Oliver A. Farwell, observing an unusual specimen of ''A. pinnatifidum'', was led to suggest that the species might be a hybrid between American walking fern, ''Camptosorus rhizophyllus'' (now ''A. rhizophyllum''), and ebony spleenwort ( ''A. platyneuron''). Such a hybrid, Scott's spleenwort ( ''A. × ebenoides'') was already known, but Farwell thought it bore a greater affinity to ''A. platyneuron'' while ''A. pinnatifidum'' had a greater affinity to ''A. rhizophyllum.'' He was correct in viewing ''A. pinnatifidum'' as a hybrid descendant of ''A. rhizophyllum'', but incorrect in identifying the other parent, and his suggestion was not widely taken up in the literature. Nor did his later attempt at subdividing ''Asplenium'', moving ''A. pinnatifidum'' to a new genus as ''Chamaefilix pinnatifida'' in 1931, meet with much favor.

As a member of the "Appalachian ''Asplenium'' complex", ''A. pinnatifidum'' readily acts as the progenitor of hybrids, as well. ''A. × gravesii'' was recognized as a hybrid of ''A. pinnatifidum'' and ''A. bradleyi'' by W. R. Maxon in 1918. Edgar T. Wherry noted the similarities between ''A. montanum'', ''A. pinnatifidum'', and ''A. × trudellii'' in 1925, and in 1936 concluded that Trudell's spleenwort was a hybrid between the first two. That same year, ''A. kentuckiense'' was described by Thomas McCoy; Wherry identified it as a hybrid between ''A. pinnatifidum'' and ''A. platyneuron''. In 1951, Herb Wagner, while reviewing Irene Manton's ''Problems of Cytology and Evolution in the Pteridophyta'', suggested in passing that ''A. pinnatifidum'' itself might represent a hybrid between ''A. montanum'' and ''A. rhizophyllum''.

In 1953, he made chromosome counts of ''A. × trudellii'', which had been classified by some simply as a variety of ''A. pinnatifidum''. As ''A. pinnatifidum'' proved to be a tetraploid while ''A. montanum'' was a diploid, a hybrid between them would be a triploid, and Wagner showed that this was in fact the case for ''A. × trudellii''. His further experiments, published the following year, strongly suggested that ''A. pinnatifidum'' is an allotetraploid, the product of hybridization between ''A. montanum'' and ''A. rhizophyllum'' to form a sterile diploid, followed by chromosome doubling that restored fertility. However, the hypothesized sterile diploid has never been found. Partial pairing of homologous chromosomes in ''A. × gravesii'' and ''A. × trudellii'' confirmed ''A. montanum'' parentage for ''A. pinnatifidum'', while an artificial hybrid between ''A. pinnatifidum'' and Tutwiler's spleenwort ( ''A. tutwilerae'') helped confirm their shared ''A. rhizophyllum'' parentage.

Wagner's conclusions as to the parentage of ''A. pinnatifidum'' were supported by later chromatographic analyses, in which the chromatograms of ''A. pinnatifidum'' contained all the compounds detected in the chromatograms of both parents. In 1985, an allozyme analysis confirmed the hybrid parentage of the species, and revealed that ''A. pinnatifidum'' had probably originated independently through chromosome doubling at more than one locality.

In 1956, C. V. Morton pointed out that, as ''A. pinnatifidum'' had been shown to arise from hybridization between walking fern and mountain spleenwort, it would constitute an intergeneric hybrid if walking fern was placed in the genus ''Camptosorus'' (as ''Camptosorus rhizophyllus''). The hybrid genus ×''Asplenosorus'' had been published, but Morton noted that it lacked a Latin diagnosis and was therefore invalid under the International Code of Botanical Nomenclature; he preferred to continue recognizing ''Asplenium pinnatifidum'' in ''Asplenium''. The ICBN's rules were relaxed in 1972, and in 1974, John Mickel published ''Asplenosorus pinnatifidus'' as a new combination for the species to allow the continued recognition of ''Camptosorus''. Since then, phylogenetic studies have shown that ''Camptosorus'' nests within ''Asplenium'', and current treatments do not recognize it as a separate genus.

In addition to ''A. × gravesii'', ''A. × trudellii'', and ''A. × kentuckiense'', ''A. pinnatifidum'' is known to be the parent of several other hybrid species. A sterile triploid hybrid, formed by the crossing of ''A. pinnatifidum'' with a diploid cytotype of maidenhair spleenwort (''A. trichomanes'' ssp. ''trichomanes'') was discovered in 1969 and named ''A. × herb-wagneri'' in 1977. Finally, several unnamed hybrids have been grown in culture. The hybrid between ''A. pinnatifidum'' and ''A. tutwilerae'' showed a "nondescript" morphology intermediate between the two parents, with slightly narrower lobes and more dimorphic fronds than ''A. pinnatifidum'', overall resembling ''A. × kentuckiense'' but with more regular lobes. Another, between ''A. pinnatifidum'' and the tetraploid American hart's-tongue fern ( ''A. scolopendrium'' var. ''americanum'') yielded peculiar specimens with a long blade, similar in texture and doubled indusia to the hart's-tongue fern, but lengthened and tapering to a point, and not lobed except for two surprisingly large auricles at the base.

Distribution and habitat

Native to eastern North America, ''A. pinnatifidum'' occurs in the middle and southern Appalachian Mountains, from Pennsylvania and New Jersey southwest to Alabama and the northeastern corner of Mississippi. It is also found in the Shawnee Hills and to some extent in the Ozarks, with outlying occurrences in southeastern Oklahoma and in Iowa County, Wisconsin. Early reports from New England proved to be variants of Scott's spleenwort, ''Asplenium × ebenoides''.

''A. pinnatifidum'' can be found on acidic rocks, often in steep habitats, from altitudes of . Sandstone is its usual substrate. The soil formed when these rocks weather must be subacid ( pH 4.5–5.0) to (pH 3.5–4.0) to support ''A. pinnatifidum''.

Ecology and conservation

The species is considered apparently secure globally (G4), but is endangered in many parts of its range. NatureServe considers it to be extirpated in New York, where it was known from a single 1877 collection, critically imperiled (S1) in Illinois, Maryland, Mississippi, New Jersey, Oklahoma, South Carolina, and Wisconsin, imperiled (S2) in North Carolina, and vulnerable (S3) in Arkansas, Georgia, Pennsylvania, and Virginia. It is threatened by changes in land use, habitat fragmentation, and certain forest management practices.

Cultivation

''A. pinnatifidum'' can be cultivated in rock gardens and terraria. It prefers medium light and will grow on a moist soil or potting mixture. Some authorities recommend adding sandstone chips to the soil.

See also

* Asplenium hybrids

Notes and references

Notes

References

Works cited

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{{Taxonbar, from=Q4808138

pinnatifidum
Ferns of the United States
Hybrid plants
Plants described in 1818