Know Your Natives – Sweet Coneflower

Sweet Coneflower (Rudbeckia subtomentosa) of the Aster family (Asteraceae) grows to 3-5 feet tall and has entire to lobed leaves. The genus name honors “Olof Rudbeck the Younger”, a Swedish botanist*. The specific epithet is Latin for “somewhat hairy” to denote its leaf pubescence. Sweet Coneflower occurs in a broad area extending from western Louisiana to southern Wisconsin and from eastern Kansas to western Indiana. In Arkansas, it occurs primarily in the Ouachita Mountains, Arkansas Valley and Ozark Plateaus along with several counties at the southeast corner of the state. It grows in prairies, open woodlands, stream banks, and roadsides in dry to moist sites with various soils. Sweet Coneflower prefers mostly to partially sunny areas. Other common names are Fragrant Coneflower and Sweet Black-Eyed Susan because the crushed flowerheads having an anise scent.

This erect herbaceous perennial develops multiple stems from a compact rootstock producing stubby, rhizomatous roots encircled by growth rings. Single composite flowerheads, on long peduncles, terminate stems and short branches along with additional peduncles growing directly from uppermost leaf axils. A stem and its branches may bear 12+ flowerheads. Width of the terete stems, to about ¼ inch at their bases, gradually reduce to 1/16 inch at flowerheads. Stems have slight, closely spaced ribs extending from their bases to the flowerheads. The straight stems, branches, and peduncles are erect to spreading. Very short, spreading to ascending, hirsute pubescence extends from stem base to the flowerheads – decreasing distally with age.

Photo 1: Stubby rhizomes grow from bases of old stems and directly from the rootstock. Remnants of an old stem of this 3-year old plant can be seen at center of the rootstock. Growth rings encircle rhizomes. Photo – September 27.
Photo 2: Mature plants have multiple stems. Stems, along their lower portion, have large, ascending, lobed leaves. Slight ridges extend from stem base to the flowerheads. Photo – May 12.
Photo 3: Straight stems and branches bear composite flowerheads on long, straight peduncles. Stem on right is 3¾ feet tall. Photo – August 13.

Petiolate leaves, with compound and simple shapes, have a medium green adaxial surface and pale green abaxial surface with whitish principal veins. Well-spaced secondary veins are recessed above and strongly expressed below. Adaxially, the blade surface between minor veins is puckered. Adaxial leaf surface and leaf margins have minute, hirsute pubescence while abaxial surface has dense slightly longer hirsute to short-pilose pubescence, especially on principal veins. Expanded bases of petioles are clasping – more so on lower leaves.

Photo 4: This unbranched stem (shown in 3 segments) has composite flowerheads on long peduncles. Large, petiolate leaves have compound and simple shapes. Peduncle of right flowerhead is 4¾ inches long. Photo – September 11.
Photo 5: Abaxial side of leaves is pale green (left) while adaxial side is medium green (right) with whitish principal veins. Veins are well spaced. Photo – July 6.
Photo 6: Adaxial side of leaves has short hirsute pubescence. Veins are recessed. Photo – July 6.
Photo 7: Abaxial side of leaves bears appressed hirsute pubescence on blade fabric and spreading pilose pubescence along principal veins. Veins are strongly expressed. In photo, leaf tip is toward top of photo. Photo – July 6.

Ascending lower leaves are variously lobed with three primary lobes – a lateral pair of deeply cut lobes and a larger deeply cut terminal lobe. Leaf size is to 9 inches long (including a 3-inch petiole) and to 4½ inches wide. Secondary lobes, ascending in plane of a leaf, are elliptic to broadly elliptic with a tapering base and acuminate tips. Tertiary lobes, spreading in the plane of a leaf, tend to be finger-like. Primary lobes may be cut close to leaf rachis so that the rachis becomes winged – wing width tapers proximally. Leaf margins vary from entire (mostly on rachis side of lobes) to shallowly toothed to shallowly crenulated. Secondary venation varies from arcuate for broad lobes to parallel-arcuate for finger-like lobes. Secondary veins trend toward tips of leaves and lobes. Lowermost leaves drop-off with development of the upper stalk, especially with drying soil.

Ascending upper leaves are unlobed with elliptic to ovate shapes and with rounded bases and acuminate tips. A few leaves between lower-lobed and upper-unlobed leaves may have a single lateral lobe. For the unlobed leaves, leaves are to 3½ inches long (including a ¼-inch petiole) and 1½ inches wide while uppermost leaves are about 2¼ inches long (including a 1¼ inch petiole) and 1⅛ inches wide. Uppermost leaves of a flowering stem subtend either a branch (with leaves and 1+ flowerheads) or a peduncle. Peduncles, to 8 inches long, may bear 1+ leafy, sessile, lanceolate bracts as small as ⅜ inch long and 1/16 inch wide. All lobed and unlobed leaves are alternate and have the same color, margination and vein pattern.

Photo 8: With this stem’s inflorescence at bud-stage (hidden in photo), unlobed upper leaves continue to grow. Lobed leaf on left is 4¼ inches long and 2½ inches wide. Slight ribs can be seen along stem. Photo – June 27.
Photo 9: At flowering, these elliptic to ovate upper leaves are firm with a puckered surface between minor veins. Two peduncles extend off the photo. Photo – September 24.
Photo 10: Lower leaves (3 on left) have 3 primary lobes with the largest leaf having secondary and tertiary lobes. Leaf second from right has a single lateral lobe while the leaf on the right is entire. Leaves are positioned proximal to distal (left to right). Petioles have clasping bases. Photo – July 26.
Photo 11: This stem has three peduncles of which the central peduncle terminates the stem while the other two are axillary. Peduncles may bear one to several small sessile leaves (bracts). Photo – September 11.

The inflorescence develops in mid-July with flowerheads in bloom from late July into late September. Flowerheads, to 3 inches wide, have a purplish brown central disk composed of numerous tightly packed, fertile, tubular florets surrounded by 16± sterile yellow ray florets. When in bud, the rounded tops of disk florets are closed by 5 stubby, triangular lobes. Florets reach anthesis successionally from the outer edge of the central disk to the center in circular fashion as lobes spread wide. Florets, about ⅛-inch long and 1/16 inch wide, have 5 stamens (filament + anther) and a pistil (fertile ovary + style +stigma). Florets have purplish brown upper portion and pale green hidden portion. Stamens and style/stigma are purplish brown. Stamens, adnate at base of corolla tube, have connate anthers which form an elongate ring which rises above the corolla. Yellow pollen is released inside the anther ring. As the style/stigma pushes through the anther ring, pollen is pushed outside and anthers shrink as the stigma bifurcates to expose an opposite pair of elongate stigmatic surfaces which recurve just above the corolla. Each disk floret is subtended, on the exterior-side of the central disk, by a thin, lanceolate green bract. These bracts remain shorter than the florets.

Ray florets have strap-like ligules (aka laminae) that first appear as a green finger extending from the margin of the central disk. Becoming bright yellow, ligules are oblanceolate with a pinched base forming several pleats extending to a rounded apex. Abaxial side of ligules bears sparse to dense minute pubescence. Rays, in a single series, attach to infertile ovaries.

Photo 12: Flowerheads are at various stages of development. Disk florets reach anthesis inward from outer edge of the disk in circular fashion. Green finger-like ligules of ray florets become bright yellow. Photo – July 30.
Photo 13: Flowerheads are on long peduncles that terminate stems and branches or grow directly from uppermost leaf axils. Photo – August 5.
Photo 14: Exserted anther rings of disk florets can be seen extending above the disk along with yellow pollen pushed out by the emerging stigmas. Emerged, recurved stigmas can be seen. Photo – July 30.

Flowerheads have a conic receptacle and a flat-bottomed involucre of closely spaced to overlapping lanceolate to broad-lanceolate bracts (phyllaries) in 2 to 3 series – those in upper series spreading while those of lower series down-turned. The firm bracts (to ⅜ inch long and ⅛ inch wide) are pale green with dense, appressed, minute pubescence on their exterior and margins with the pubescence extending onto the peduncles. When disk florets have passed anthesis, the central disk becomes dark brown before ray florets whither and head dries while remainder of plant remains viable.

Fertilized disk florets produce ⅛-long dark brown, 4-sided, narrow, conic achenes (aka cypselae in Aster family) with a truncate top rimmed with minute bristles (pappus). In the dense dry head, the bracts subtending disk florets becomes chaff that remains while the achenes drop from the head.

Photo 15: The involucre has a flattened bottom bearing pointed bracts in 2 to 3 series. This flowerhead, including the pleated ligules, is 2 inches wide. Photo – August 21.
Photo 16: Tightly packed disk florets attach to a conic receptacle. As shown, disk florets have passed anthesis. Ligules, ovules removed, were detached from the disk. Photo – September 3.
Photo 17: Ray florets are shown with their infertile ovules. Disk florets, subtended by a green lanceolate bracts, have a purplish brown upper portion and whitish lower portion above white fertile ovules. Photo – September 11.
Photo 18: With disk florets having completed anthesis, the now-spherical central disks become dark brown. Photo – September 24.
Photo 19: Crushed flowerheads separate into dried corollas of disk florets, achenes (see arrow) and other parts. Crushed dried flowerheads have an anise scent. Photo – September 26.

Sweet Coneflower is a good choice for most garden styles where the site is mostly sunny with well-drained soil. With its modest size, this perennial has interesting leaf shapes and showy composite flowerheads with bright yellow ligules. Flowerheads persist for a month or more in mid to late summer. The number of stems increases from year to year but plants are not aggressive invaders. Plants provide pollen and nectar to insects and seed for birds and small mammals.

In addition to Sweet Coneflower, 9 additional species of the genus occur in Arkansas – all with yellow composite flowerheads. Only 2 of the 9 species have lobed leaves; namely, Brown-Eyed Susan (Rudbeckia triloba var. triloba) and Cut Leaf Coneflower (Rudbeckia laciniata var laciniata). Sweet Coneflower can be identified by its perennial nature and larger flowerheads as compared to the annual much-branched Brown-Eyed Susan with small flowerheads, and by its compact clumping habit and pubescence as compared to the clonal perennial Cut Leaf Coneflower with glabrous stems and leaves and which favors significantly moister habitats.

*The genus name, established by Carl Linnaeus (who developed the binomial nomenclature in the 18th century) to commemorate his professor “Olof Rudbeck the Younger”. “Olof Rudbeck the Younger” is the son of Olaus Rudbeck (aka “Olof Rudbeck the Elder”), both prominent Swedish scientists and botanists. For a summation of their accomplishments see: Olaus Rudbeck – Wikipedia and Olof Rudbeck the Younger – Wikipedia.

Article and photographs by ANPS member Sid Vogelpohl

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Know Your Natives – Common Evening Primrose

Common Evening Primrose (Oenothera biennis) of the Evening Primrose (Onagraceae) family is a large edible plant noted for its historic and current-day medicinal uses. The genus name is believed to be based on Greek words for “wine” (oinos) and “seeker” (thera). The specific epithet refers to the plant’s typical biennial life cycle, but plants may also be winter-annuals. Occurrence is widespread across the eastern half of the U.S. along with scattered occurrences across the remainder of the U.S. Native to eastern North America, it has been introduced into many temperate and subtropical areas around the world. In Arkansas, occurrence is statewide. Preferred habitats are sunny sites with dry to mesic sandy soils in prairies, glades, rights-of-way and disturbed land.

Photo 1: These winter-annuals grow in a sunny glade on a rocky, south-facing slope. Photo – August 8.

Winter-annual plants have branched taproots while biennial plants have carrot-like taproots*. Early in their first growth-year, biennials and winter-annual plants, have a rosette of basal leaves. Basal leaves, to 4-8 inches long and 2 inches wide, have off-set pinnate venation. Basal leaves, all with short to long petioles, are medium green to reddish (in cold temperatures) with white midribs. Tapering leaf bases extend onto petioles. Margins are mostly entire but, later, may show marginal features of stem (cauline) leaves – – see below. The elliptic basal leaves of winter-annuals drop off with stem growth. Early basal leaves of biennial plants are also elliptic but become long-spatulate to long-lanceolate during the first growth-year and remain until stem growth in the following spring.

Photo 2: Winter annuals have branched taproots. This plant had a height of 4 feet 10 inches (central root bent for photo – see arrow). Base of stem is ½ inch wide. Photo – August 11.
Photo 3: Germinating over winter, these winter annuals developed into the flowering plants shown in Photo 1. Basal leaves drop off with stem growth. Photo – February 12.

Cauline leaves, oblanceolate to lanceolate, are to 5¼ inches long (including ½ inch petiole) and 1¼ inches wide. Leaves are arranged spirally on a terete stem. Firm leaf blades, fabric fairly flat to rumpled, are slightly ascending and slightly up-folded along midrib. To varying degree, tapering blade-bases extend onto petioles. Off-set pinnate veins, rather obscure above and prominent below, extend to near leaf margin where they align with one another and continue toward leaf apex. Upper and lower leaf surfaces have puberulent pubescence with that of the underside being denser. Upper sides of leaves are medium green while lower sides are a fuzzy-looking light green with midribs and petioles being a pale green. Margins of smaller leaves are entire while those of larger leaves are shallowly toothed to undulating with the teeth being blunt. Axillary buds that do not develop into branches often appear as very short stems with a few miniature leaves. With drying soils, lower cauline leaves drop off and upper leaves wilt until revived with renewed moisture.

Photo 4: With stem growth, leaves become oblanceolate to lanceolate and basal leaves drop off. Secondary veins are off-set pinnate. Leaf blades taper onto petioles. A winter annual shown. Photo – April 13.
Photo 5: Lower pair of leaves is from below inflorescence. Upper pair of leaves subtended a branch. Upper and lower sides shown. Leaves were removed from the 2⅛-inch stem segment. Parts from a winter annual. Photo – August 12.
Photo 6: At this stage, branches have not developed. Ascending leaves are slightly up-folded along midribs. A winter annual shown. Photo – May 12.
Photo 7: Leaves, arranged spirally, have margins varying from entire to shallowly toothed to undulating. Some leaves have been nibbled by insects. A winter annual shown. Photo – August 27.
Photo 8: Axillary buds that do not develop into branches often appear as very short stems with a few miniature leaves. A winter annual shown. Photo – August 27.

Stems, 3-6 feet tall with a base diameter of ½+ inches, may lack branches or, for more robust plants, have several to a half-dozen lower to mid-stem “primary branches” that are to 3+ feet long. Additionally, shorter branches, to 1 foot long, may occur along the distal portions of stems and primary branches. The terete, straight, solid-core, rigid stems and strongly ascending primary branches are initially pale green, becoming reddish-purple. Lower portions of stems and primary branches become tan to brown with the epidermis of more proximal portions splitting and exfoliating to varying degrees. Stems and branches are variously hairy with a dense mix of long hairs, hairs with reddish glandular bases (pustules) and short appressed hairs.

Photo 9: Primary branches are straight and ascending. Stems and branches become reddish-purple in the plant’s preferred sunny habitat. A winter annual shown. Photo – June 23.
Photo 10: This still-growing plant is 4 feet tall with branches that are to 3½ feet long. Shorter branches develop along distal portions of the stem and larger branches. A winter annual shown. Photo – August 14.
Photo 11: Stems are variously hairy with a dense mix of long hairs, hairs with reddish glandular bases and short appressed hairs. Also, see stem pubescence in Photo 5. Photo – August 12.
Photo 12: With maturity, epidermis along lower portions of stems and larger branches splits and exfoliates. Lower leaves drop off as the season progresses, especially with drying soils. A winter annual shown. Photo – August 27.

The inflorescence consists of stout, erect, terminal spikes of axillary yellow flowers – – 1 flower per leaf axil. Flowers of biennial plants are in bloom in early spring of their second growth-year while those of annual plants are in bloom in mid-summer of their first (and only) growth-year. Flowering proceeds up-spike, with several flowers of a stem or branch in bloom at the same time so that bloom period extends for a month or more. The sessile flowers, arranged spirally, are longer than the internode separation (⅛ to ½ inch apart).

The erect flowers have 4 sepals, 4 petals, 8 stamens (filaments + anthers), a pistil (ovary + style + stigma) and a slender floral tube to 2¼ inches long. Sepals, ½ to 1¼ inches long, are lanceolate with free-standing, blunt tips. With anthesis, sepals spread open along their sides while remaining connected at their apexes before strongly reflexing against the floral tube. Often, several sepals remain connected at their apices. Greenish yellow sepals rim the greenish yellow floral tube. Bowl-shaped petals are broadly cordate with a slightly notched apex and a broadened, tapering base. Petals attach to the tube at the base of the sepals. Flowers, 1-2 inches in diameter, have faint (to humans) nectar guides and a slight lemon scent. The sturdy yellow filaments (⅞ inch long), undulating in uniform fashion to either side of the style/stigma, bear an elongate 2-lobed anther divided across tips of filaments; filaments also attached to the rim of the floral tube. The pistil consists of an exposed elongate ovary, a very long style (to 2¾ inches) and a stigma with 4 wide-spread cylindric lobes, each lobe to ¼ inch long. Exteriors (undersides) of lobes are covered by stigmatic surfaces and feel sticky. Light yellow pollen grains are loosely connected by strands of viscin – aiding pollen transfer by insects. Stamens and stigma do not extend beyond the rim of the corolla but, with the bowl-shaped corolla, are easily accessible to insects. Depending on and varying with weather conditions, the bright yellow flowers usually open in the evening and close the next morning.

While the corolla, stamens and pistils are glabrous; the floral tube and sepals have pubescence. Exterior of the floral tube has a mix of short appressed hairs and scattered longer, ascending hairs while the interior has dense, short pubescence. Exteriors of sepals are densely covered with appressed, equal length, puberulent pubescence while the interiors are glabrous.

Photo 13: With this branch’s terminal growth continuing, developing seed capsules can be seen along with 2 flowers that have closed and 1 that is poised to open. Floral tube of flower at left is 2⅛ inches long. A winter annual shown. Photo – August 12.
Photo 14: This biennial plant, with rumpled leaves, shows vigorous stem growth in early spring. Site of this photo and next photo same as site shown in Photo 1. Photo March 27.
Photo 15: Flowering of this biennial plant occurred in mid-spring. Photo – April 28.
Photo 16: Inside of petals are shown on left, outside on right. The 2¾-inch style/stigma was removed from the floral tube (see red arrows) and separated from ovary. Each sepal has a free-standing, blunt tip (see white arrow). Photo – August 13.
Photo 17: Sepals reflex against the floral tube. Several sepals often remain connected at their tips. Exteriors of sepals have minute appressed pubescence while interiors are glabrous. Photo – August 15.
Photo 18: Stigmatic surfaces are on the outside of the 4 stigma-lobes while the inside (as seen from above) is smooth. Pollen grains are connected by viscin strands. Photo – August 15.
Photo 19: Petals and sepals, removed for photo, attach to rim of the floral tube. The firm stamens, with elongate anthers divided across their tips, undulate in uniform fashion. Entire length of flower-part in photo is 1⅛ inches. Photo – August 13.
Photo 20: With part of the floral tube removed, attachment of 4 filaments can be seen at lower right. Exterior and interior of tube are pubescent. Style extends upward. Photo – August 13.
Photo 21: With floral tube extending to lower right, the hollow style can be seen extending into the ovary. Ovaries have four locules with 2 rows of aligned ovules. Nectar at base of floral tube. Photo – August 15.

Flowers are fertilized by nectar-seeking moths with long proboscises and small bees and other insects gathering pollen. With the dropping of flowers, the 4-locule ovaries enlarge to become hardened green capsules (to 1+ inch long and 3/16 inch wide). The terete capsules, initially broader at their rounded base, are composed of 4 compartments marked on the exterior by prominent grooves and 2 small-stubby apical knobs. When dry, the now straight-sided capsules split across their apices and separate along their side-margins while remaining attached at their bases. Spikes of uniformly shaped capsules are densely spaced with individual spikes 1+foot long; those of a full plant having a candelabra structure. Seeds are tightly stacked in two rows per compartment so that each capsule may have several hundred seeds. Dead plants and their capsules remain upright so that seeds are gradually dispersed over several months, aided by strong wind. The brown, irregularly shaped seeds have a greatest dimension of about 1/16 inch.

Photo 22: Capsules, densely pubescent, are composed of 4 longitudinal compartments separated by a prominent grove and terminating with 2 rounded, small-stubby lobes. Upper capsule is ¾ inch long and ¼ inch wide. Photo – August 12.
Photo 23: Dried capsules split at their apices and along side-margins of the compartments. The style persists within gaping capsules. Pubescence is lost. Photo – December 3.
Photo 24: The brown angular seeds, tightly stacked within capsules, drop out over several months. Squares equal ¼ inch. Photo – Nov 19.

In considering its suitability for a garden, Common Evening Primrose with its large size and bold branching structure, would certainly stand out. Due to its propensity to self-seed, for a more formal or small garden, removal of fruited spikes may be necessary. Probably best suited for naturalizing larger spaces. Plants provide pollen, nectar and foliage for moths and insects and seed for birds. Dead fruited spikes work well in dry arrangements. Historically, plants have been used for medicinal and/or food uses, and the species is commercially cultivated for seed oil for medical uses and research. Food uses include boiled roots of biennial plants and foliage and flowers for salads.

At least 17 species or subspecies of the genus (in narrow circumscription; not including members of Gaura and Stenosiphon which are sometimes included) are reported in Arkansas. Other than Showy Evening Primrose (O. speciosa), all other species in the state (again, under narrow circumscription) have yellow flowers. Of the tall, yellow-flowered species, Common Evening Primrose has size and leaf-shape similar to the native Hairy Evening Primrose (O. villosa subp. villosa). Common Evening Primrose can be distinguished by being variously hairy with a dense mix of long hairs, hairs with reddish glandular bases and minute appressed hairs, as well as by green or yellowish sepals. Hairy Evening Primrose is densely and uniformly pubescent with minute appressed hairs and has red striped or flushed red sepals. A non-native, tall species of similar appearance, reported from Pulaski County, is Garden Evening (aka Large Flower and Red Sepal) Primrose (O. glazioviana) – distinguished by its distinctly red sepals and larger flowers.

Photo 25: Garden Evening Primrose has a height of up to 5 feet. (Photo taken outside of Arkansas.) Photo – July 17.

Another member of the genus that has been previously addressed in this series of articles is Sundrops (O. fruticosa).

*The branched taproot of a winter-annual is shown in Photo 2. For images of the carrot-like taproots of biennials, query “Oenothera biennis + roots + images”.

Article and photographs by ANPS member Sid Vogelpohl

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ANPS Fall 2023 Meeting

Dates: September 29 – October 1

Location: Little Rock, Arkansas

Everybody is welcome to attend! Meeting registration is only $10 with no pre-registration required. Registration will begin at 5:00 PM on Friday, September 29th.

Meeting Location:

Little Rock Audubon Center

4500 Springer Boulevard

Little Rock, Arkansas 72206

Hotel:

Hampton Inn West Little Rock  

1301 S. Shackleford Rd.

Little Rock, AR 72204

Phone: (501) 537-3000

15 king rooms have been reserved at the reduced rate of $109.00 plus tax per night. Reservations must be received by September 8, 2023 to guarantee the reduced rate. Be sure to mention that you are with the Arkansas Native Plant Society when making your reservation. Rate includes free parking and free breakfast. Individuals are responsible for their own room and tax.  All cancellations must be made 42 hours prior to arrival.

Dining Options: We will have a Potluck meal Friday and Saturday evenings. Bring a dish or just come and eat! There are also many dining options in the Little Rock areas near the hotel.

Field trips: Several field trips to local areas of top botanical interest will be scheduled for Saturday 8:30AM-5:00PM and Sunday 8:30AM-12:00PM:

We will offer something for everybody, whether you want to take it slow and easy or something more vigorous. You must sign up for field trips on Friday evening to allow for adequate logistical planning.

For complete and up-to-date details, go to www.anps.org or contact Eric Fuselier, anps.programs@gmail.com, (501) 231-7455.

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Know Your Natives – White-Leaf Mountain Mint

White-Leaf Mountain Mint (Pycnanthemum albescens) of the Mint (Lamiaceae) family is a tall, upright perennial forb with a strong minty scent and has an open, gangly structure. The genus name is based on Greek words for dense (pyknos) and flower (anthos) in reference to its flower clusters. The specific epithet is from a Latin word (albescentem) for “becoming white” in reference to the uppermost leaves and bracts. Its primary area of occurrence extends from the Florida panhandle, across southwestern Alabama, Mississippi (excluding the lowlands), Louisiana (excluding the lowlands), east Texas, east Oklahoma, south Missouri and Arkansas. In Arkansas, it occurs statewide except for some portions of the Mississippi Alluvial Plain. Habitats are variable from partial shade in open woods, to full sun in prairies, from pinelands to oak woodlands and from mesic to dry soils that may be sandy to rocky to clayey.

During summer months, new rhizomes grow from the sides of rhizomes that developed the previous growth year, near the current year’s stem. These smooth, white rhizomes have decussate nodes bearing rudimentary buds that do not develop unless the rhizome is damaged. In early winter, the growing tip appears as a new stem, old stems having died and began decaying. With growth of a new stem, the “umbilical” rhizome dies and a separate clonal plant with a retained portion of rhizome which becomes and develops wiry, fibrous roots. Colonies tend to be somewhat open and isolated one from another. The new year’s stem growth has purplish stems and ovate, petiolate, early-deciduous, purplish-green leaves; basal leaves are absent.

Photo 1: Red arrow indicates stump of the living rhizome. Previous year’s dying rhizomes are indicated by white arrows. Yellow arrow indicates current year’s 3½ foot stem. Green arrows indicate previous year’s dead stems on a dead portion of the rhizome. Plant has 6 new, white rhizomes. Photo – July 30.
Photo 2: Springtime stems are purplish with ovate, entire (margins uncut) leaves. Note the squareness of stems. Photo – March 19.

Mature stems are square in cross-section with distinct corners and flat sides. The erect stems have widely spaced, opposite leaves with internode lengths to 4 inches that are fairly equal, decreasing nearing stem apex. Stem leaves subtend ascending to wide-spreading branches that may be from near-zero-inch long (only a pair of leaves is seen) to 8 inches long; lengths quickly shortening near stem apex. A 4-foot stem, with a base-width of ⅛+ inch, may have up to 8 axillary branch pairs (primary branches) along its upper portion. Primary branches, square along their proximal portions, have base-widths less than half that of stems. Primary branches have one to several opposite leaf pairs with axillary buds which may develop into very short secondary branches bearing a single leaf pair. Leaves along primary branches orient toward sunlight and become aligned along sides of the branches. Stems and branches are covered by soft, dense, spreading pubescence which decreases with age. Lower primary branches typically terminate with a leaf-pair while upper primary branches often terminate with flower clusters. Leaves, branches, and flower clusters at the same node tend to be about the same size. At the end of the growing season, the hollow stems die back to the rhizome and readily break off and mostly decay by late spring.

Photo 3: Axillary branches are already present. With further internode growth, these branches will be positioned about the middle of mature stems. Photo – March 19.
Photo 4: Plants have an open, gangly structure. This isolated group of stems, source of the plant in Photo 1, are probably all clonal. Site is an open woods alongside a creek. Tallest stems are 4 feet. Photo – July 27.

The simple leaves of a mature stem are lanceolate to broadly lanceolate and to 3¾ inches long (including a ½ inch petiole) and ⅞ inch wide. Leaves of the branches are usually half that size. Leaf blades may taper onto petioles. The smallest leaves have entire margins while larger leaves’ smooth margins are interrupted on their upper half to two-thirds by 4-8 shallow teeth as blade width decreases to acuminate apices. Pinnate venation, recessed above and expressed below, is well spaced. Secondary veins, mostly opposite but may be alternate, extend from the mid-rib at about 45⁰ and become parallel to leaf margins as they fade. The lower end of secondary veins may trend along midrib, toward petiole. Leaves near the inflorescences (floral leaves, herein) are strongly whitened above and below while other leaves (green leaves, herein) are olive-green above and whitish green below, with midribs of floral and green leaves a lighter shade. Floral leaves have dense, white, appressed, matted puberulent pubescence on both surfaces. Green leaves have short hirsute pubescence above and minute, short-matted pubescence below along with relatively long marginal (ciliate) pubescence. Leaf pubescence extends onto the petioles where it transitions to the longer, spreading pubescence of the stem or branch.

Photo 5: Larger leaves have smooth margins that are interrupted by shallow teeth. These “green leaves” have an olive green upper surface and whitish green lower surface. Photo – July 5.
Photo 6: Upper leaf surface has short hirsute pubescence and longer, spreading pubescence on leaf margins and axis of this stem. The small leaf pair at right-center is on a very short axillary secondary branch. Photo – July 5.
Photo 7: Underside of branch shown in Photo 6. Opposite to alternate, pinnate, secondary veins roughly parallel leaf margins. Lower end of some secondary veins trend along the midrib. Leaf blades may extend partway along petioles. Photo – July 5.

From July into September, the inflorescence consists of terminal and lateral clusters on stems and branches. Single clusters, to ⅞ by ⅝ inch, are axillary to pairs of opposite leaves so that an opposite pair of single clusters, often, visually merge into a double cluster. Each single cluster is on a stalk that is ⅛ to ¼ inch long. Clusters (single and double) are broadly rounded when viewed from above and disk-like with a flat bottom and slightly convex top when viewed from the side. A single cluster is composed of 2-3 cymes consisting of one to several pedicellate flowers positioned between a lateral pair of opposing “arms” bearing multiple pedunculate flowers along a curved stalk. A final opposite whitish leaf pair subtends a double cluster with further divisions of arms and cymes being subtended by increasingly small leaf-like, spade-shaped, whitish bracts followed by linear to filiform whitish bracts which occur along and at the terminus of the cymes. Thus, double clusters are ringed by whitish leaves, leaf-like bracts, and bracts and clusters have a spiky appearance. Blooming flowers are seemingly randomly scattered across a cluster because pedicellate flowers bloom first, followed sequentially by the pedunculate flowers.

Photo 8: Lower in photo, a pair of opposite leaves are on a very short secondary branch from each axil of opposing leaves. At top of photo, the developing inflorescence is on the side of the branch with a tiny terminal bud in between the clusters. Photo – July 6.
Photo 9: The 2 largest leaves subtend the developing inflorescence (an opposite pair of cymes) while the 4 smaller leafy bracts are part of the inflorescence; two bracts subtending each cyme. Photo – July 21.
Photo 10: Other than the flowers themselves, all parts of the inflorescence including calyx bracts, along with the subtending leaf pair, have appressed puberulent pubescence. This cluster (excluding ring of leaves and bracts) is 3/8 inch by 5/16 inch. Photo – July 6.
Photo 11: Opposite pairs of cymes seemingly merge into a single cluster. With the numerous bracts extending from each cluster, clusters have a spiky appearance. Photo – July 26.
Photo 12: This divided cluster consisted of 3 cymes of which only 2 are shown. Red arrows indicate flowers on pedicels (left flower has died) and yellow arrows indicate flowers on peduncles. Calyxes are 2 lipped with 5 triangular lobes (see calyx above right pedicel). Photo – July 27.
Photo 13: Divided cluster: #1 = ½ of cluster , #2 = ¼ of cluster and #3 = ⅛ of cluster. Bracts change from spatulate to filiform along and at the end of the arms. Photo – August 10.
Photo 14: A close-up to show the similar “texture” of the puberulent pubescence that covers various parts of a cyme. The number of bracts within an inflorescence varies from cluster to cluster. Photo shows two pedicellate flowers on the backside. Photo – July 27.

Flowers have a white, wide-flared corolla consisting of a lower lip with a broad central lobe and 2 elongate lateral lobes and an upper lip with a single lobe. Purple spots are scattered across the lower lip with the greatest concentration being across the cupped central lobe. From the front, corollas are about ¼ inch tall and ⅛ inch wide across the lower lobe while the upper lip is about ⅛ inch long and 1/32 inch wide. Flowers are glabrous on the outside while throat is pubescent. Upper lip is positioned along a straight-line with the axis of the calyx while lower lip lobes curve downward sharply. Lips unite to form a tube that is inserted into a pale green, terete calyx with a widened top and pinched base. Calyces are 3/16 inch long and 1/16 inch wide. Calyces (see Photo 12) have 2 lips; an upper lip that is 2-lobed and a lower lip that is 3-lobed; sometimes all lips and/or lobes cannot be seen. Lobes are stubby-triangular. Calyces (as are pedicels, peduncles and adjoining stalks) are densely covered with white, appressed, puberulent pubescence.

Flowers have 4 stamens (filament + anther) and a pistil (ovary + style + stigma). The white filaments (adnate to the sides of the throat) and style are fine-thread-like. The elongate 2-lobed anthers, balanced at the filaments’ tips, are exerted from the corolla. The strongly exserted anthers change from white, to orange (with pollen release) to brown. The style, as anthers dry, extends slightly beyond the anthers and unequally divides slightly at its tip to expose 2 unequal stigmatic surfaces. The tiny green ovaries (too small to photograph) have 4 ovules which mature to 4 wheat-shaped, brown nutlets in the fall.

Photo 15: Flowers have a 3-lobe lower lip and a 1-lobe upper lip. As shown, anthers change from white, to orange to brown. A divided stigma is silhouetted at upper left. Photo – September 13.
Photo 16: Throats are filled with dense pubescence. Calyx lobes are stubby-triangular. Photo – August 10.
Photo 17: As clusters dry, numerous nutlets are easily shaken from calyces. Photo – November 20.
Photo 18: Tiny brown nutlets are wheat-shaped. Squares = ¼ inch. Photo – November 20.

In regards to gardening, considering its gangly appearance during most of the growing season, White-Leaf Mountain Mint may be best suited for a naturalistic garden. The near-inch-wide flower clusters have numerous tiny flowers which appear delicate when viewed up-close. White leaves and bracts associated with the inflorescence causes clusters to be showy. Plants do not seem to be aggressive spreaders, either by root or seed, but is easily propagated by rooted rhizomes. It has a fine minty scent when touched and provides nectar and pollen to insects for a month or more. White-Leaf Mountain Mint is not a preferred food by deer.

Photo 19: Flowers provide nectar to butterflies, including this Northern Metalmark (Calephelis borealis). Photo – August 4.

Other species of Pycnanthemum that occur in Arkansas are: Short-Tooth or Clustered Mountain Mint (P. muticum), Hairy Mountain Mint (P. pilosum), Slender or Narrow-Leaf Mountain Mint (P. tenuifolium) and Virginia Mountain Mint (P. viginianum). White-Leaf Mountain Mint is most similar to Clustered Mountain Mint, but White-Leaf Mountain Mint can be distinguished by its lanceolate to broadly lanceolate leaves and flower clusters that are more loosely arranged with noticeable, interspersed bracts. Additionally, bloom period of Clustered Mountain Mint is about a month earlier.

Photo 20: Photo shows the inflorescence of Clustered Mountain Mint (P. muticum). Photo – June 24.

Article and photographs by ANPS member Sid Vogelpohl

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Know Your Natives – White Wand Beardtongue

White Wand Beardtongue (Penstemon tubiflorus; also sometimes spelled P. tubaeflorus) of the Plantain (Plantaginaceae) family, formerly of the Figwort (Scrophulariaceae) family, has sparsely leafed, erect stems bearing an elongate inflorescence of white tubular flowers. There is some disagreement on the exact etymology of the genus name. It may be based on words meaning five (“penta”) and stamen (“stemon”) in reference to 5 stamens (4 fertile and one sterile staminode) or based on words meaning nearly/almost (“pen” or “paene”) and thread (“stemon”) possibly in reference to the thread-like staminode which is not a functional stamen. The specific epithet, regardless of spelling, alludes to the tube- or trumpet-shaped flower. It is native to the central U.S. where it is most concentrated in eastern Oklahoma, southeast Kansas, southwest Missouri and a large portion of Arkansas. Outside this area, scattered occurrences are known in surrounding states along with an area from Pennsylvania to Maine where it is considered introduced. In Arkansas, it occurs in the Arkansas Valley, Boston Mountains, Mississippi Valley Loess Plains (Crowley’s Ridge), Ouachita Mountains, and Ozark Highlands Ecoregions, mostly absent from lower portions of the Gulf Coastal and Mississippi Alluvial Plains. Habitats include areas with well-drained soils where full to partial sunlight is available, such as prairies, rights-of-way, open woodlands and woodland margins. Other common names include Tubed Penstemon and Trumpet Penstemon.

This perennial plant has a small caudex supported, during the growing season, by spreading white ropy roots. Individual mature plants have one to several erect flowering stems surrounded by basal leaves. Stems lack branches and grow to 3 feet tall. They die at the end of the growing season but may remain standing into the next growing season. The medium-green stems (lower portion may be purplish in sunny sites) are terete, smooth and glabrous with naked internodes. Diameter of the slender stems, about ¼ inch at their bases, gradually and uniformly decreases to the apex of the inflorescence. Individual plants may be clumped together.

Photo 1: This clump includes 2 plants each with 1 current year’s stem and 1 dead stem from the previous year, along with a non-flowering plant (in front). Seed capsules persist on dead stems. Stem with flowers is 21 inches. Diameter of the slender stems reduce gradually and uniformly. Photo – May 20.
Photo 2: Roots of this 3-plant clump (see also in Photo 1) are white, spreading and ropy.

Flowering plants have basal and cauline leaves, while non-flowerig plants have only basal leaves. Some basal leaves, to 4 inches long and ½ inch wide, may remain over winter months with renewed leaf-growth in late winter. Basal leaves vary from obovate to oblong-lanceolate with rounded to bluntly pointed apexes and long-tapered bases. Upper surface is medium green and lower surface is a slightly lighter green; both surfaces are typically glabrous. Margins of the slightly leathery leaves are usually entire but may have minute teeth. Widely spaced secondary pinnate veins extend from the midvein at 45⁰ angles, but gradually curve until they become parallel to leaf margin.

Cauline leaves occur in opposite pairs with 6+ pairs below the inflorescence. Pairs, widely spaced, are rotated one from another at varying degrees. The lowermost spatulate leaves, with long-tapering bases, are smaller than leaves immediately above – – those being to 5 inches long and 2 inches wide. Above the spatulate leaves, oblong-lanceolate leaves are sessile with rounded to slightly cordate to clasping bases and apexes change from rounded to acuminate to acute. Above the oblong-lanceolate leaves, leaf size decreases sharply to the base of the inflorescence where leaves become deltate-ovate. Internode lengths between the opposite pairs increases noticeably such that lower lengths of a mature 32-inch stem may be 1½-2½ inches, while lengths of upper internodes may be 6-8 inches. Leaf color, margins and venation of cauline leaves are about the same as for basal leaves with the blade surface of larger leaves in more favorable sites being undulating to “rumpled”. Within the inflorescence, the opposite bract-like leaves become lanceolate and increasingly small to the point of being minute at the most distal portions of the inflorescence.

Photo 3: In late winter this plant has basal and cauline leaves – – arrow indicating a lowermost cauline leaf. A previous-year stem (in background) persists. Larger leaves are slightly leathery with an undulating surface. Photo – March 18.
Photo 4: These ascending stems will become erect and harden as stems mature. Leaves and stems are all about the same medium green. Arrow indicates lowermost cauline leaf. Photo – April 18.
Photo 5: This clump (see also in Photo 1), from a sunny site, has purplish stems. Non-flowering plant in front has basal leaves and cauline leaves on a stubby stem.
Photo 6: Basal leaf (at bottom) is 4¾ inches long. The cauline leaves (other leaves) are from stem-base to just below the inflorescence (left to right). All leaves have their adaxial sides shown except upper-center leaf is shown with its abaxial side. Photo – May 20.

Flowers bloom for several weeks in mid-spring. The free-standing terminal inflorescences, from 6-18 inches long and ½-1+ inch wide, are in stout panicles with 4-8 pairs of opposite, strongly ascending cymes. Flowers of a well-formed panicle are arranged with a “primary flower” centered above the panicle’s stalk with a second flower behind the first flower, along with an opposite pair of cymes; one at both sides of the primary flower. A well-formed panicle may have 12+ flowers. When floral internodes are closely spaced, inflorescences tend to have a tight, cylindrical form while inflorescences with more widely spaced internodes tend to have a tiered-cylindrical form. Although variable, often the dense short glandular pubescence covering peduncles (stalks bearing multiple flowers) and pedicels (stalks bearing a single flower – – first flowers to reach anthesis) extends a short way down the main axis (rachis) of the inflorescence. In the inflorescence, the increasingly small leaf-pairs subtend the opposite cyme-pairs to the ultimate cyme at axis apex. The uppermost cyme-pairs, becoming increasingly small, also become increasingly compact as peduncles and pedicels become less stout.

Photo 7: Panicles are composed of 4-8 pairs of opposite cymes (1 cyme shown) on a stalk. A bract-like leaf pair subtends the cyme. A left and right peduncle, with about 6 flowers each, are positioned above each leaf with 2 pedicles between the peduncles. Photo – May 31.
Photo 8: With this cylindrical inflorescence, 2 lower-cauline leaves are displayed to show upper and lower sides of the slightly leathery leaves. Upper cauline leaves can also be seen. Photo – May 14.
Photo 9: When paired cymes are more widely spaced, the inflorescence has a tiered-cylindrical appearance. Also shown in background, Milkweed Vine and Downy Ragged Goldenrod. Photo – May 15.

The white tubular flowers (to ¾+ inch long) have a 2-lobed upper lip and a 3-lobed lower lip; lobes are uniformly spreading from a flared throat. All lobes, with rounded apexes, are about the same shape with those of the lower lip being larger and projecting farther. All lobes are smoothly textured and typically lack noticeable nectar guides. Lips unite at the throat to form a smoothly narrowing, funnel shaped tube set in a pale green calyx. The calyx (to 3/16 inch long) consist of 5 ascending, triangular to lanceolate lobes that join to form a very short cup. With calyxes horizontally oriented and the corolla tube descending, faces of flowers are down-cast. Typically, dense short glandular pubescence covers exterior of the corolla and the interior throat – – pubescence often extending onto the calyx. (Flowers may have faint purplish nectar guides and bases of flowers may be slightly purplish.)

Flowers have a pistil (ovary + style + stigma), four fertile stamens (filaments + anthers) and an infertile stamen, referred to as a staminode or the beardtongue. Fertile stamens, adnate to lower side of the corolla tube, occur as a longer pair and a shorter pair, each with 2-lobed dark purple anthers separated across the tips of the white filaments. The paired-filaments, distally following the contours of the throat, curve away from each other and then recurve so that paired-anthers face each other at the mouth. Anthers of the shorter filaments are positioned just below those of the longer filaments; all visible below the upper lip. The white, terete style (⅜ inch long) extends from its slightly widened base to a flat apex topped with the stigmatic surface. The white staminode, adnate to the upper side of the corolla tube, curves down so that it is positioned on the lower lip and extends farther out than the anthers and style. The staminode’s flattened, up-facing distal portion is covered with relatively long, sparse, yellowish hairs. The stigma is well hidden among the stamens with the staminode extending well beyond the anthers. The glabrous, green ovary (less than 1/16 inch long), set within the very small cup, has an onion-shape topped with the style. At anthesis, anther lobes dehisce to release white pollen. Style and filaments are glabrous.

Photo 10: Flowers have a flared face with lobes about the same shape and a smoothly narrowing, funnel-shaped tube. Calyxes are oriented horizontally while corolla tubes are descending. The staminode, adnate to the upper side of the throat, rests on the lower lip. Photo – May 3.
Photo 11: Dense glandular pubescence covers exterior of flowers and calyxes. The final opposite, lanceolate, bract-like leaf-pairs subtend peduncles/pedicels (arrow indicates a final pair). Photo – May 20.
Photo 12: Flowers have purplish anthers, a bearded staminode and a straight and terete style. Lower portion of corolla, showing interior pubescence, and calyx are positioned at left. Calyx of this flower is glabrous. Photo – May 17.
Photo 13: An enlarged portion of Photo 12 showing lobed anthers divided across tips of filaments, cylindrical style ending with the stigmatic surface and distinctive yellowish pubescence of staminode.

The 2 locular ovaries of fertilized flowers develop into green, tear-drop-shaped hardened capsules that grow to be twice as long as the ⅜ inch calyx. With seed maturity, the entire inflorescence becomes a bronzy-brown and pubescence is lost. Capsules, to 5/16 inch long and 3/16 inch wide with a sharp apex (style remnant), split at their apexes into 2 chambers. Capsules divide near the top part-way down their sides so that the tiny seeds can be shaken out. The irregularly shaped, squarish, angular brown seeds are less than 1/32 inch wide. Stems with capsules still set in their calyxes may persist through the next growth-year, becoming dull brown.

Photo 14: Ovaries of fertilized flowers developed into tear-drop-shaped, green capsules that grow to be twice as long as the calyx. This 1¼ inch segment, from the top of an inflorescence, terminates an ultimate, reduced-size cyme. Photo – June 19.
Photo 15: With ripening of seeds, other parts of panicles become a bronzy brown. Capsules split at their apexes and part-way down their sides. The brown seeds are irregularly shaped and angular. Squares are ¼ inch. Photo – September 27.

White Wand Beardtongue is an excellent plant for any garden style where conditions are mostly sunny and soils are well-drained. This small, erect perennial is noticeable throughout the growing season and especially showy when the elevated inflorescence bears its pure-white flowers. It provides nectar and pollen to various bees, swallowtails and hummingbirds.

In addition to White Wand Beardtongue, eight other beardtongues occur in Arkansas. Five have white or whitish flowers (some with pinkish or purplish color or more noticeable colored nectar guides): Arkansas Beardtongue (P. arkansanus), Foxglove Beardtongue (P. digitalis), Lowland Beardtongue (P. alluviorum), Nodding Beardtongue (P. laxiflorus) and Pale Beardtongue (P. pallidus). White Wand Beardtongue can be distinguished by its smaller size, an inflorescence that is usually dense above a near-naked upper stem, corollas with similarly shaped flaring lobes (actinomorphic flowers), and corolla lobes that unite to form a smoothly narrowing, funnel-shaped tube. The other three non-white beardtongues in Arkansas are Scarlet Beardtongue (Penstemon murrayanus), Prairie or Showy Beardtongue (Penstemon cobaea), and Sharp-Sepal Beardtongue (Penstemon tenuis).

Article and photographs by ANPS member Sid Vogelpohl

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Know Your Natives – Clasping Venus’ Looking Glass

Clasping Venus’ Looking Glass (Triodanis perfoliata; formerly, Specularia perfoliata) of the Bellflower (Campanulaceae) family is an erect to reclined annual forb with clasping, ovate to orbicular leaves and both non-opening (cleistogamous – CL) flowers and opening (chasmogamous – CH) flowers. The genus name, based on Greek words for “three” and “tooth”, refers the typical number (3) of calyx lobes of CL flowers. The specific epithet, based on Latin, refers to the clasping bases of the sessile leaves which are seemingly perforated by the stem. The common name is a reference to a similar-looking European species [Venus’ Looking Glass (Legousia speculum)] which has relatively large, shiny seeds said to resemble a mirrored looking-glass. In the U.S., other than Nevada, this species occurs within all 48 contiguous states and extends into Canada and Mexico and into South America, including Argentina. In Arkansas, it occurs statewide. Habitats include sunny to partially sunny sites with various, well-drained sandy to rocky soils where soils are sufficiently exposed to allow the tiny seeds to germinate; including, such sites in prairies, glades, woodland openings, rocky outcrops, trails and old fields. Plants have a spreading, branching, rather stubby, white taproot system.

This herbaceous winter annual germinates in autumn and in winter has a basal rosette of broadly ovate, petiolate leaves with hispid pubescence. In late spring, a single main stem appears, which eventually reaches a height of 4-18 inches; however, in sunny habitats, main stems may grow to 30+ inches. Bases of main stems are to 3/16 inch wide. When mature plants remain small, they only have the single stem, but larger plants may have several to a half dozen secondary stems growing from lower leaf axils of the main stem (one stem per node). Secondary stems are ascending to widely spreading and have lengths from near 0 (see Photo 14) to 16+ inches. Secondary stems, which do not grow tertiary stems, remain shorter than main stems and are less stout. The light green stems have 5 straight ridges, with long hispid hairs, extending from stem-base to stem-apex. Main and secondary stems typically terminate with CH flowers, often a central flower and a pair of lateral flowers. Flowers develop in leaf axils of even the smallest plants with most or all of these being of the CL type. When stems grow without support, they become reclined and twisty. Stems and leaves produce a small quantity of milky sap.

Photo 1: This ¾ inch-wide plant has round, petiolate leaves with hispid pubescence. Photo – February 5.
Photo 2: Secondary stems are beginning to grow from the main stem of these plants. Plants in sunny, open sites typically develop secondary stems. Photo – March 13.
Photo 3: CH flowers are at various states of anthesis along upper portions of main and secondary stems. Capsules of lower CL flowers (tan) are already drying. Also shown, Woolly Lipfern (Cheilanthes tomentosa) and Hairy Lipfern (Cheilanthes lanosa). Photo – May 12.
Photo 4: This 32-inch plant (including its 1½ inch root) has side stems to 19 inches long. At the end of the growth-year, stems typically terminate with CH flowers. Upper portion of main stem cut and shifted to right (see connecting arrows). Photo – May 12.

Stems have regularly spaced ovate to orbicular leaves from stem base to apex, with leaf size decreasing distally. Each leaf is rotated about 70⁰ from the next so that the straight ridges connect to the base of every-other leaf. The leafy stems have a columnar appearance when younger. All leaf axils bear axillary buds of which, typically, the lowermost buds remain dormant, followed by buds that develop into secondary stems (if any), followed by axils with 1-3+ buds that develop into CL, followed by axils that produce one to several CH flowers. CL and CH flowers generally occur in separate leaf axils, but in the transitional zone between the two types, both may occur in the same axils. When multiple flowers occur in an axil, flowers reach anthesis successionally. Small plants and those growing in shade may have CL flowers only. Plants bearing CH flowers may revert to producing CL flower if growing conditions deteriorate.

Photo 5: Leaves are rotated about 70⁰ from one to the next. Five straight ridges with hispid pubescence extend from stem base to apex. Ridges connect with leaf bases. Photo – April 19.
Photo 6: Uniform leaf spacing and size give stems of younger plants a columnar appearance. Stems and leaves are the same light green color. Photo – April 10.
Photo 7: Flowers are axillary with the CL flowers sited below CH flowers; as shown. Any secondary stems are located below CL flowers. Photo – April 30.

Cauline leaves are light green. Lowermost cauline leaves are elongate-ovate with short petioles, with more distal leaves becoming ovate to ovate-cordate, sessile and strongly clasping. Largest leaves, to an inch long and wide, are just above stem-base with size gradually decreasing to stem apex. Blades of clasping leaves are ascending away from the midrib and sunken toward their bases so that blades are cupped. While leaf margins of weaker plants are entire, those of more robust plants have mostly smooth margins with four or so broad, very short teeth. Blades may be wavy to ruffled. Apexes of larger leaves are rounded to acuminate. Palmate venation, more pronounced on leaves from sunny sites, is recessed above (adaxially) and expressed below (abaxially) with the 3-6 secondary veins terminating at the base of marginal teeth. Leaves may be glabrous on the upper surface or may be minutely pubescent while the lower surface has short hairs (especially on veins), and leaf edges are ciliate. All except basal and lowermost cauline leaves remain viable until plants reach senescence in late spring at which time the entire plant becomes scraggly and soon dies. Cauline leaves of small plants are not clasping.

Both CL and CH flowers have elongate, fluted, glabrous, light green calyxes rimmed with prominent, spreading, narrowly triangular lobes. Calyxes of CL flowers have 3-4+ lobes while CH flowers typically have 5 lobes. CH calyxes are 2-3 times larger than CL calyxes. The tiny, closed CL flowers (with minute sepals and stamens) are barely visible to the naked eye. Calyx lobes of CH flowers alternate with corolla lobes. The colorful CH flowers have a corolla, ½ to ¾ inch wide, with 5 petal-like spreading corolla lobes (united at their bases), 5 stamens (filaments + anthers) and a pistil (ovaries + style + stigma). The lavender to violet corollas, marked with longitudinal dark lines (insect guides) have white throats, stigmatic surfaces and stamens. The elongate, slim, ivory anthers are set sleeve-like on short white filaments. The stout style protrudes well above the anthers at anthesis and is white along its lower portion and lavender to violet along its upper portion. The lavender to brown stigma is club-like with a roughened surface when closed but, when recurved, reveals 3 white stigmatic surfaces.

Photo 8: CL flowers are axillary and successional with 1-3+ flowers per axil. Calyxes of CL flowers, smaller than those of CH flowers, have 3-4+ lobes. Photo – April 30.

Buds of CH flowers first become apparent as white, heavily ribbed “footballs” set atop calyxes – – ribs fitting between calyx lobes. With approaching anthesis, buds become lavender. Late in the bud-stage, the vertically positioned anthers are pressed tightly against upper portion of the style – – below the closed stigma-head. Anthers dehisce so that pollen is available for transfer to the hair-lined style as it elongates. The depleted anthers spread away from the style-stigma and shrivel. With corolla lobes spread wide, insects collect pollen from the style and, with sufficient insect activity, style-hairs retract. Later, the stigma-head opens and recurves so that three, elongate stigmatic surfaces are well exposed for pollination (preferably by pollen from other plants). Flowers have 2-3 chambered ovaries.

Photo 9: CH flowers have a 5-lobed corolla (mostly removed in photo), 5 stamens with short filaments and elongate anthers and a protruding style/stigma. As shown, the 3 stigmatic surfaces have spread for pollination. Photo – April 28.
Photo 10: In upper right flower, anthers are pressed tightly against the style. As the style continues to elongate through the anther-ring, hairs along the style collect pollen from the anthers as they dehisce. Hairs can be seen along midrib of corolla lobes. Photo – April 10.
Photo 11: After pollen has been collected by the style-hairs (as shown), stamens spread away from the style and shrivel. Stigma head has not yet opened. Stems, leaves and calyxes are all light green. Photo – May 18.
Photo 12: Flowers reach anthesis sequentially from leaf-to-leaf, toward stem apex. Multiple flowers in a leaf axil open successionally. Stems are initially erect. Photo – April 30.
Photo 13: White centers and dark lines serve as insect guides. Corolla lobes are positioned between the calyx lobes. Rarely, flowers may be white (see inset). These flowers are 5/16 inch wide. Photo – May 5.

Calyxes (on capsules) dry shortly after anthesis. The oblong-cylindric capsules have 2-3 flaps at mid-capsule that roll-up to expose oval pores. With slight movement, tiny, dull to slightly shiny, dark brown, ovoid seeds fall from capsules. The larger CH capsules may contain 150+ seed. Capsules of earlier flowers are dropping seeds as stems continue to grow and produce additional flowers. Along with seed dispersal by water run-off, the tiny seeds are probably also dispersed by wind. Both CL and CH flowers produce viable seed.

Photo 14: Arrow points to a leaf subtending a CH capsule. The capsule is growing from a leaf axil on a very short secondary stem. Beyond the same arrow, darker tan tear-drop shape is the pore-flap still covering the pore. (Black shapes are misplaced seeds.) Photo – May 12.
Photo 15: On a dry capsule, a flap of tissue has rolled up to expose the pore. Several seeds can be seen. Part of subtending leaf was removed to better expose capsules. Photo – May 8.
Photo 16: CH capsules are shown on left (leaf removed; 5 calyx lobes) and CL capsules (3-4 calyx lobes) on right. Arrows indicate pores. Left stem is ¾ inch long. Upper leaf surface (right) is minutely pubescent. Photo – May 8.

In regard to native plant gardening, this wide-spread winter annual may not be a good choice in a formal garden. In a natural setting, it may already be established. It is an interesting winter annual. Its small showy CH flowers provide color and supports various bees, flies and small butterflies. Seeds are probably too small for birds or small mammals. Large plants are rather scraggly with senescence but should disappear by summer. Should it be too aggressive, removal of some plants would be necessary in early spring.

Three additional species of the genus have been recorded in Arkansas. In comparison to T. perfoliata, these are:

1) Slim-Pod Venus’ Looking Glass (T. lamprosperma): Most similar. Has clasping leaves with flowers and similar calyxes except pores are just below lobes. Seeds are twice as large and shiny.

2) Prairie Venus’ Looking Glass (T. leptocarpa): Leaves are linear to oblanceolate and calyxes have long, slim lobes.

3) Small Venus’ Looking Glass (T. biflora, sometimes treated as a variety or subspecies of T. perfoliata): Has narrower, mostly non-clasping leaves. Leaves have acute tips with entire to scalloped margins. Elongate capsules have pores just below the calyx lobes.

Photo 17: Seeds of T. perfoliata (#1) and T. lamprosperma (#2) have a similar shape but those of T. lamprosperma are about twice as large and with shinier surfaces. Squares = ¼ inch. Photo – May 13.

Article and photographs by ANPS member Sid Vogelpohl

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Know Your Natives – Wild Strawberry

Wild Strawberry (Fragaria virginiana) is an evergreen plant which produces scarlet strawberries* with achenes embedded in pits. The genus name derives from the Latin word “fragum” in reference to the fragrance of mature strawberries. The specific epithet refers to the state from which the species was originally collected and described. The common name probably originates from the word “strew” in reference to the tangle of ground-hugging stems. In the eastern U.S., Wild Strawberry occurs in a large area roughly bounded by a line from North Dakota to Maine (extending into Alberta and Newfoundland, Canada), along the Atlantic Coast to the Florida Panhandle, across to eastern Texas and back to North Dakota. Also, it occurs in large disjunct areas of western U.S. In Arkansas, it occurs in the Ozark Plateaus, River Valley and Ouachita Mountains, along with widely scattered occurrences in the Gulf Coastal and Mississippi Alluvial Plains. Other common names include Common Strawberry, Scarlet Strawberry and Virginia Strawberry. Habitats include dry to mesic soils in sunny to partially shaded sites such as prairies, woodland borders, glades and rights-of-way. Some authorities have divided this species into various subspecies or varieties.**

Related to the cultivated strawberry***, Wild Strawberry is a low-growing, herbaceous, colonial species with stoloniferous stems. Stems appear at the same time as the inflorescence in mid-spring and continue to grow into late-spring. The several, ground-hugging stems of a mature plant radiate from the parent plant as they maneuver through their surroundings, often lodging in crevices. The slender, rather limp (but tough) stems (to 3 feet long) have widely spaced nodes bearing bracts, leafy bracts and leaves – – stems otherwise naked. Stems, terete along their internodes, have dense spreading (set at 90⁰ to stem) pubescence. The first node (which may be 1+ foot from the parent plant) may produce a secondary stem which may develop in the same manner as a primary stem. As stems elongate to their second node (then at stem tip), the node is bent down to the soil. New leaves rise at the node and roots anchor a new plantlet. As the stem lengthens with additional nodes, those nodes that may produce a secondary stem alternate with nodes that bear plantlets. The internode segments between two “plantlet nodes” arch above the soil so that any secondary stems are elevated and the next plantlet-node is again positioned at the soil level. In sunlight, young stems change from pale green to reddish. Stems remain viable into early winter, remaining persistent into spring.

Photo 1: As shown, stem is 12 inches long with an additional 7½ inches cut-off at lower right (at white asterisk; black arrows show former attachment of this stem segment). First node bears a 2-leaflet leaf and second node bears a plantlet. A third node (leaf-bearing) and growing stem terminus is at upper left. Photo – April 27.
Photo 2: As this plantlet produced roots, the lower stem continued to grow toward the left. A secondary stem, can be seen on the upper stem (arrow), also growing to the left. The stem to right of plantlet is arched. Photo – April 24.
Photo 3: These several plants were plantlets during the previous spring. Their originating stems, now dead, can be seen. Photo – March 3.

Plants that are several years old develop a stubby, vertical rhizome with an apical crown composed of several growth-points of varying sizes. Each growth-point produces a tight cluster of leaves with larger leaf clusters potentially including a stem and/or flower stalk, just off-center. Upper portion of older rhizomes is covered by bases of current year’s leaves while the lower portion is covered by persistent leaf bases from earlier leaves and remnants of old stems. Two-year-old plants seem to be most productive of stems and flower stalks; plants seeming to deteriorate after their third year. Thick clonal colonies may form. With summertime soil drying and heat, plants often become dormant.

Photo 4: Over winter, plants develop new roots along previous year’s rhizome-growth. Plant at left is approaching its first spring. Plant at right has an inch-long rhizome with 4-inch roots. Newly developing leaves can be seen on right. Photo – February 7.

At mid-spring, a mature plant may have a dozen basal leaves of varying sizes. The reddish overwintering basal leaves are relatively small, flat on the ground and fade as springtime leaves appear. Ascending springtime leaves are considerably larger and with largest leaves being present during flowering and fruiting. Largest leaves may reach 13 inches long (including a 9-inch petiole) with a compound blade that is 4 inches long and 3¾ inches wide. Leaflets are to 3¾ inch long and 2½ inch wide on short petiolules. Springtime leaves have a shiny, medium green upper surface and a dull, pale green lower surface.

Photo 5: Rhizomes are stubby and vertical. Crown of this plant, with two growth points, produced two floral stalks and two stems. Overwintering leaves die as springtime leaves develop. Photo – April 24.

Basal leaves are trifoliate compound. The terminal leaflet and the lateral pair of leaflets, all three of similar size and shape, are obovate to elliptic with wedge-shaped (cuneate) bases and broad rounded apices. Bases of lateral leaflets are oblique. Well-spaced, prominent pinnate secondary veins (set at 30⁰ off midrib) are finely recessed above and expressed below. Secondary veins, evenly spaced and parallel, extend to mucronate tips of prominent triangular teeth along the side margins. The midvein terminates in an apical tooth which is half as wide and smaller than the marginal teeth. Although widely variable, upper and lower blade surfaces generally have spreading to appressed pubescence; that of the lower surface being denser and longer, especially along veins. The slender, long to very long, straight petioles and stubby petiolules are densely pubescent with spreading hairs. Petioles, terete along most of their lengths, have winged bases that serve to position and protect subsequently emerging leaves. The winged bases have pinkish, free-standing, lanceolate apices. These bases are to about 1¼ inches long, of which about ¾ inch is free-standing above the soil.

Photo 6: Female plants are shown. Floral / fruiting stems are positioned below tall basal leaves. Photo – May 16.
Photo 7: Functionally male plants are shown (see Photo 15 for related information). Photo – April 13.
Photo 8: Pubescent petioles of overwintering basal leaves are short as compared to petioles of springtime leaves. The free-standing lanceolate apices of the basal leaves’ winged bases can be seen (pink). This male plant is past bloom stage. Photo – March 22.
Photo 9: This overwintering basal leaf has retained its pubescence. Hairs along petioles are spreading and those of the upper leaf surface are appressed. Photo – February 12.
Photo 10: Pubescence on upper surface of this springtime leaflet is not apparent. Note parallel-pinnate venation, mucronate marginal teeth and smaller tooth terminating midvein. Color is a shiny, medium green. Venation is recessed. Photo – April 16.
Photo 11: Pubescence on lower surface of this springtime leaflet is spreading along the petiolule while that on the blade is appressed. Color is a dull, pale green. Venation is expressed. Photo – April 16.

The April inflorescence develops at same time as when stems begin to grow. The inflorescence, originating just off-center of a current-year leaf cluster, consists of a floral stem bearing to 12+ flowers in a compound umbel. Of a 6-7-inch long inflorescence, about 4¾ inches would be the naked stalk. The stalk is topped by a two-bracted-node from which several small floral leaves and an umbel of 2-4 erect peduncles (to 1½ inches long) emerge. Peduncles, in turn, are topped by a smaller two-bracted-node from which several simple floral leaves and an umbel of 2-5 weak pedicels (to 1½ inches long) emerge. The bracts subtending the peduncle-umbel are obovate while those subtending pedicel-umbel are lanceolate. Additional small lanceolate bracts may occur at the base or along pedicels. The terete stems, peduncles and pedicels are light green and densely pubescent. Floral bracts are slightly pubescent on their exterior and glabrous on their interior. Floral stems of female and male plants have the same structure.

Floral leaves may be compound with 2 leaflets or simple with serrated margins or simple with entire margins. Leaf size and complexity decrease distally. Floral leaves have the same color, texture and pubescence as basal leaves. Smaller floral leaves become entire and lose marginal teeth. When a leaf is serrate, the apical tooth and marginal teeth are the same size. (See a floral stem in Photo 16.)

Photo 12: Floral leaves are mostly simple, becoming smaller and entire (lacking teeth) distally. Of the serrated floral leaflets or leaves, the apical tooth is equal to or larger than the marginal teeth. Color and texture are similar to that of basal leaves. (see Photo 16) Photo – April 21.

Flowers have 5 petals, 20+ stamens (filaments + anthers) and numerous pistils (ovary + style + stigma) covering a domed receptacle. Flowers are male (staminate), female (pistillate) or appear to be perfect (with stamens and pistils) but are functionally staminate. Flowers, ½ – ¾ inch across, have 5 broadly lanceolate sepals interspersed with 5 lanceolate sepal-like bracts united at their bases. In bud, sepals cling to the bud while bracts are ascending. At anthesis, the pale green sepals and bracts form a single layer that is calyx-like. Sepals are positioned between the overlapped petals and bracts. Sepals and bracts are slightly pubescent on both sides. The elongate yellow anthers stand upright on tips of lighter yellow filaments. Styles are tipped with slightly spreading stigmas, both the same color as the filaments. The white petals, which may slightly overlap or be separated, have an obovate upper portion that quickly reduce to a clawed base. The stamens and pistils rise slightly above the petals’ clawed bases with pistils being shorter.

Photo 13: This emerging inflorescence is atop a 4⅞-inch stalk (not shown). Sepals and interspersed floral bracts, united at their bases, can be seen at various stages of flower development. Flower is an inch wide. Photo – April 16.

Photo 14: Receptacles of female flowers are covered with numerous pistils. With weak pedicels, flowers dangle. Photo – April 10.
Photo 15: Flowers from this colony are perfect (with stamens and stigmas). However, the colony has not produced fruits although nearby female plants did (see Photo 17), indicating that flowers of this colony are functionally male. Photo – April 3.
Photo 16: This post-bloom male floral stem bears 2 peduncles (in umbel style), each topped with pedicels (in umbel style). Pedicels bear a single flower. Simple floral leaves and paired bracts can be seen at the base of umbels and along some pedicels. Photo – April 21.

Fertilized pistillate flowers produce fruits (achenes) that are embedded into strawberries maturing in May. Early whitish green strawberries mature to shiny scarlet with the exposed achenes. The ovoid to globoid strawberries are to ½ to ¾ inch long and wide. The calyx of sepals and bracts become appressed to the mature strawberry. Wild Strawberry is said to have a sweeter taste than cultivated strawberries. Year-to-year fruiting success is variable.

Photo 17: Early whitish green strawberries become scarlet with maturity. Fruits (achenes) are embedded. Fruiting success is variable from year-to-year depending on weather conditions. Photo – May 7.
Photo 18: Calyxes are appressed against the strawberries. The tasty strawberries are relished by small mammals (and humans). Squares = ¼ inch. Photo – May 12.

In a sunny to partially sunny garden with well drained mesic soils, Wild Strawberries would add textural variety and provide enjoyment while a person searches for the showy flowers and strawberries. It has active growth from late winter into mid-spring, but small basal leaves remain throughout the winter. Annual flowering can be expected but appearance of strawberries is affected by weather conditions. Being a cool-season plant, it can compete with taller herbaceous plants. A gardener needs to be aware of the plant’s reputation for clonal spreading; however, in a small area, timely removal of stems would restrict clonal spread. Excellent as a ground cover or for erosion control and suitable for naturalizing. Foliage, flowers and fruits are of high ecological value for insects, animals and birds. Fruits (achenes) are dispersed by animals and birds that consume the strawberries.

Wild Strawberry is the only wild species of the genus known in Arkansas. Other “strawberries” which might be encountered are 1) the non-native Indian-Strawberry (Duchesnea indica), whose common name refers to the country of India, and 2) Barren Strawberry (Waldsteinia fragarioides), a plant of conservation concern. Indian-Strawberry can be distinguished by its yellow flowers, having achenes that are not embedded in its scarlet strawberries and floral bracts that are 3-lobed. Barren Strawberry is a ground-cover plant with spreading, shallow, underground rhizomes, very short petioles, yellow flowers and heads of 2-6 dry seeds without an enlarged receptacle.

*Botanically, strawberries, which are not actual berries and not technically the fruit, are referred to as “aggregate accessory fruits”. Examples of true berries are dewberries and blackberries which have achenes immersed in pulp. The fruits of Wild Strawberry are the achenes which are embedded on the outside of the accessory fruit.

**This species has considerable variation in pubescence on petioles, peduncles, pedicels, and stems. Four subspecies/varieties are based on: 1) whether pubescence is ascending, appressed or appressed-ascending and 2) if hairs are visible to the naked eye. Other authorities (including Arkansas) treat these variations as a continuum within the species.

***In 1766, Antoine Nicolas Duchesne documented successful crossing of Wild Strawberry and Chilean/Coastal Strawberry (Fragaria chiloensis) to create the cultivated strawberry (Fragaria × ananassa) with its larger flowers and larger, sweet strawberries.

Article and photographs by ANPS member Sid Vogelpohl

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Know Your Natives – Old Field Cinquefoil

Old Field Cinquefoil (Potentilla simplex*) of the Rose (Rosaceae) family is a low-growing plant with short rhizomes and 5-petal, bright yellow flowers. The genus name is from the Latin word for “powerful” in reference to medicinal properties of some species of the genus. The specific epithet is Latin for “simple” in reference to the plant’s typically unbranched stems. “Cinquefoil” is French for “five leaves” in reference to the five (sometimes 7) leaflets. In the U.S., it occurs in an area bounded by a line from eastern Oklahoma into Minnesota, across to Maine, thence south along the Atlantic Coast to South Carolina, thence southwest to south Alabama and west to northeast Texas. It also extends into eastern Canada. In Arkansas, occurrence is statewide. It is also known as Five-Finger Cinquefoil and Common Cinquefoil. Habitats include moist to dry sunny sites with various well-drained soils of woodland edges, prairies, rights-of way, disturbed areas and abandoned fields.

Old Field Cinquefoil has palmate basal leaves tightly clustered around a stem. Nodes along stems produce palmate cauline leaves, leafy bracts and flowers. Early in their growth, stems are erect and green, becoming reddish with age. The string-like to cord-like ascending to prostrate stems, to 3+ feet long, have well-spaced nodes. Stems, typically not branched, have node-to-node segments from less than 1 inch to 6+ inches. Stem segments between the lowermost nodes are straight, while stem-segments along mid-stem are broadly arched and the most distal segments are straight. The distal trailing portion of stems is stoloniferous, with stem-tips that root to form clonal plantlets. At the end of their first growth year, new rhizomes are bulbous and smooth with irregular growth rings. Dead stems remain attached to new rhizomes for a year or so.

The shallow, horizontal rhizomes are segmented by growth-years with new growth elongating rhizomes from their distal tips. One to several new growth points may develop along the sides so that the original rhizomes may become branched so that a plant may have several growing tips. With each growing tip bearing several stems, in a favorable habitat, a dense mat of clonal plants may form. Stems bear palmate leaves (cauline leaves) and flowers at their proximal nodes, along with leafy bracts, while more distal nodes bear only leafy bracts. Bracts, to 1 inch long, have one to several lanceolate lobes which may be entire or divided. Diameter of stems and size of leaves and bracts gradually decrease toward the stems’ apices. The cauline leaves have broadened bases similar to those of basal leaves (see below).

Each growth year, a new segment is added to the distal end of rhizomes. This growth pattern results in rhizomes being segmented and roughened by remnants of leaf and stem bases (the first segment being smooth). Each growth year, long fibrous roots grow from the underside of the most recent rhizome segment. When a rhizome reaches its third to fourth year, the older segments begin to decay so that the viable portion of rhizomes is limited to several inches. The tough rhizomes (about ¼ inch in diameter) have a dense, white interior with a pinkish hue.

Photo 1: Active vegetative-growth ends in summer. Basal leaves and roots have been lost while dying stems persist. Plant at right may be 5 years old. Dead stem on rhizome at left grew from the rhizome of the parent plant (not shown). Photo – June 8.
Photo 2: Early basal leaves of the new growth-year appear overwinter. These leaves will die as additional basal leaves appear in spring. Lower left leaf is 1¼ inch wide. Photo – January 13.
Photo 3: From left to right: 1) current year clonal plantlet, 2) second year plant with new bulbous rhizome with irregular growth rings and 3) five-year plant with a branched rhizome (2 inches long) that has a decaying proximal segment. Early basal leaves of #2 and #3 are dying. Photo – March 28.

New basal leaves, appearing overwinter, encircle the growing tips of rhizomes. In spring, as rhizome growth continues, additional basal palmate leaves develop (as earlier leaves die) and long stems appear, also bearing palmate leaves. Basal leaves have 5 (sometimes 7) sessile leaflets while cauline leaves have 5-3 sessile leaflets. Leaflets of cauline leaves tend to be larger and more elongate. Leaflets of basal leaves tend to be obovate (with broadly rounded apices) while those of cauline leaves tend to be more elongate (with broadly tapered apices). All leaflets have wedge-shaped bases. Petioles are initially the same color as lower sides of leaves but become reddish over time. Petioles often have dense appressed pubescence. Bases of petioles, tightly pressed together in a flattened group, have V-shaped “wings” in cross-section (to ⅝ inch long) as a result of having clasped additional emerging leaves and encircled stems. The wings, often hidden in the litter layer, have free-standing, lanceolate apices with straight side-margins.

Photo 4: Close-up photo of plant #3 shown in Photo 3. Fibrous roots grow from most recent rhizome segment. A stem (on left – see arrow) emerges from center of a group of basal leaves – – a folded cauline leaf extends above and behind the stem. Note pubescence of stem. Photo – March 28.
Photo 5: The typical palmate (hand-like) basal leaves have 5 leaflets. Shapes of leaflets vary from obovate to oblanceolate with prominent teeth. These leaves are basal. Photo – March 20.

Basal and cauline palmate leaves are similar. Leaflets, narrowly obovate to broadly lanceolate, have a glossy green upper surface and a pale to silvery green lower surface. Central leaflets are largest, usually 2 or more times as long as wide, and the lower lateral pair is smallest. Leaves may have an “extra” small pair of lateral leaflets (for 7 leaflets) or may have only 3 leaflets. Upper one-half to three-fourths of a leaflet’s margins have 4 to 10 prominent teeth per side. Pinnate venation is finely depressed on the upper surface and finely expressed on the lower surface. Secondary veins terminate at the mucronate tips of the marginal teeth. The midvein terminates leaflets with a smaller tooth. Leaflets are symmetrical across the midvein except lateral leaflets have down-trending midveins. Leaf pubescence is variable in that either surface may be somewhat hairy to glabrous and the petiole, too, has variable pubescence. The pale green petioles, to 6 inches long, become reddish with age. Cauline leaves may be sessile.

Photo 6: Basal leaves at lower right have 7 leaflets. Short, dense pubescence can be seen on upper surface of leaf at lower right. Photo – March 20.
Photo 7: From this lower node of a stem, straight below, the stem continues with a down-arch (toward right foreground). This stem could grow for another 2½ feet. The long-stemmed flower bud (in background) is from the same node. Photo – March 28.
Photo 8: Upper sides (left) and lower sides (right) of leaves are shown. Bases of petioles are V-shaped in cross-section with lanceolate, free standing, basal “wings” at their apices. Blade at upper right is 1½ inch long and 1¼ inch wide.
Photo 9: These cauline leaves are larger than basal leaves (mostly hidden herein) and tend to have more elongate leaflets. Apices of stems are actively growing. Photo – April 17.

The blooming period begins in the early weeks of spring and continues for about a month. The inflorescence consist of a few single flowers per stem on long, very slender pedicels (to 3 inches long). There is one flower per palmate-leaf-bearing node. The lowermost flower is typically at the node with the second lowest cauline leaf.

Photo 10: As can be seen in the upper right corner, the clusters of leaves and leafy bracts grow from the upper side of stems. As shown, stems are still ascending but will become prostrate. Photo – April 27.
Photo 11: As shown, all palmate stem leaves have developed. White arrow points to a node that bears two palmate leaves and a flower bud. Note red stems. Photo – May 1.
Photo 12: Margins of leaflets are prominently toothed with those on the proximal side of lower leaflets extending farther down the leaflet. Secondary veins terminate at the teeth as mucronated tips. Apical tooth is shorter. A leafy bract is shown at lower left. Photo – April 25.

The yellow flowers (to ½ inch wide) have 5 petals, about 20 stamens (filaments + anthers) and 20-50 pistils (ovary + style + stigma); all the same bright yellow. The obovate petals have rounded apices with a shallow apical indention (retuse petals) and a clawed base. Stamens are in a single row encircling a short-elongate receptacle covered with straight, slender and terete styles/stigmas. The styles/stigmas flex from the receptacle in rather random fashion.

Flowers have a calyx of 5 broad-triangular sepals immediately above an epicalyx of 5 triangular-lanceolate floral bracts. Sepals and bracts extend straight-out from the pedicel. Sepals are positioned between the petals and bracts. The dark green, pubescent sepals are broadly triangular with short-acute apices while bracts are broadly lanceolate with acuminate apices. Sepals are shorter than bracts and bracts are about the same length as petals. The elongate anthers, with widened bases, stand upright on tips of filaments. Styles are tipped with tiny, poorly defined stigmas.

Photo 13: Five sepals enclose this bud immediately above five floral bracts. Photo – April 25.
Photo 14: Stamens, in a single row, encircle the head covered with pistils. Apices of petals tend to be retuse. As shown, interior surface of sepals is pubescent. Photo – May 1.

With maturity of fruiting heads, styles/stigmas drop off the receptacle while drying stamens persist as receptacle, sepals, bracts and pedicels remain green. Heads bear an aggregate of one-seeded indehiscent nutlets. The glabrous bean-shaped nutlets, about 1/32-inch long, are tan with a roughened surface. The seeds’ small size and weak attachment suggest that nutlets could be dispersed by strong wind and fallen nutlets could be transported by surface-water flow during heavy rains.

Photo 15: Fruiting heads are an aggregate of indehiscent bean-shaped nutlets. Nutlets have a glabrous, roughened surface. Squares are ¼ inch. Photo – June 21.

Regarding garden use, Old Field Cinquefoil has pleasing visual characteristics (palmate leaves, bright flowers). Flowers provide pollen and nectar for insects and foliage for deer, rabbits and marmots. With its stoloniferous stems, extending as far as 3 feet, it could expand quickly. Should be welcomed in natural areas. May provide a good groundcover to stabilize soil from erosion. Degree of self-seeding is not known.

Three additional species in the genus occur in Arkansas; namely, Dwarf or Five-Finger Cinquefoil** (Potentilla canadensis), Rough Cinquefoil (Potentilla norvegica) and Sulfur or Rough-Fruit Cinquefoil (Potentilla recta). Also, Mock or Indian-Strawberry (Duchesnea indica) is sometimes treated within the genus (as Potentilla indica). Of these species, Dwarf Cinquefoil is most similar. Dwarf Cinquefoil is a smaller plant with smaller and strongly obovate to oblanceolate leaflets, with fewer teeth. Flowers of Dwarf Cinquefoil usually occur from the first stem node and thinner stems are usually prostrate from the start of growth. Dwarf Cinquefoil has been reported from northeastern Arkansas.

*This species has considerable variation in leaf and stem pubescence, to the extent that some authorities have named three varieties. Other authorities (including Arkansas) treat these varieties as a continuum within the species.

**The common name “Five-Finger” is used for both P. simplex and P. canadensis.

Article and photographs by ANPS member Sid Vogelpohl

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New T-Shirts for 2023

We have 5 new T-Shirt designs available on Bonfire. These are made to order and different colors and styles are available for each design. Click on each photo to be taken to Bonfire to place your order.

ANPS receives a small portion of the sale of each shirt – so you’ll be helping support our grants and scholarships program while looking super cool at your next picnic!

Note – these shirts are ONLY available online. They will not be available for in-person purchase at our Spring and Fall meetings.

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2023 ANPS Spring Meeting Information

ANPS Spring 2023 Meeting
May 19-21 in Northwest Arkansas

Everyone is welcome to attend! Meeting registration is only $10 with no pre-registration required. Registration will begin at 5:00 p.m. on Friday, May 19 at the Illinois River Watershed Partnership Watershed Learning Center.

MEETING LOCATION
Illinois River Watershed Partnership Watershed Learning Center
221 S. Main St., Cave Springs, AR 72718
Website: irwp.org

HOTEL LOCATION
Holiday Inn Express and Suites Bentonville
2205 S.E. Walton Boulevard, Bentonville, AR
479-271-2222

We have reserved 10 king rooms at a rate of $109.00 plus tax per night and 10 double queen rooms at a rate of $119.00 plus tax per night. Reservations must be received by April 28, 2023 to guarantee these rates. 

Follow the link in the hotel’s name above to book your room, or if you prefer to call to make a reservation be sure to mention that you are with the Arkansas Native Plant Society.

DINING OPTIONS
We will have a potluck meal Friday and Saturday evenings. Bring a dish to share or just come and eat! The IRWP Watershed Learning Center has a refrigerator we can use to store food overnight. 

There are also many dining options near the hotel.

SILENT AUCTION
The silent auction will begin at 6:00 p.m. on Friday and close at the end of the program on Saturday evening. Proceeds from the auction support the ANPS small grants program, student research grants, and student scholarships! Bring any donations to you would like to include in the auction before 6:00. Auction sheets will be provided. If your item does not sell, you must take it back with you at the end of the meeting.

FIELD TRIPS
Several field trips to local areas of top botanical interest are scheduled for Saturday 8:30 a.m. – 5:00 p.m. and Sunday 8:30 a.m. – 12:00 p.m.

You must sign up for field trips on Friday evening to allow for adequate logistical planning. We will also provide directions to each site on Friday evening. 

We advise bringing a hat, sunscreen, water, snacks, and bug spray on field trips!

NOTE: Field trip locations may change due to inclement weather, so check the ANPS website and Facebook for the latest field trip locations in case of rain, as we will post alternative activities there.

EVENING PROGRAMS SCHEDULE – at the IRWP Watershed Learning Center


Friday, May 19
5:00 PMDoors to meeting room open and registration begins; silent auction setup
6:00 PMSilent Auction opens
7:00 PMEvening program begins
7:15 PMBrendan Kosnik, M.S. student in biology at Arkansas State University and 2022 ANPS Delzie Demaree Research Grant recipient, will speak on his research “Discovering the Rare Sedges of Eastern Arkansas”
8:00 PMVirginia McDaniel, Acting Forest Botanist for the Ouachita National Forest, will introduce the informative videos “Glade Restoration on the Ozark-St. Francis and Ouachita National Forests” and “Shortleaf Pine-Bluestem Restoration on the Ouachita National Forest” produced by Fauna Creative with funding from the US Forest Service and The Nature Conservancy
8:15 PMMarson Nance, Director of Land Stewardship and Research, Northwest Arkansas Land Trust, will speak on the topic “Restoration Ecology of Wilson Springs Preserve”
Saturday, May 20
5:30 PMDoors to meeting room open, registration continues
6:00 PMANPS Business Meeting
7:30 PMKeynote Speaker: Dr. Ray Fisher, Research Entomologist at Mississippi State University and adjunct Professor at the University of Arkansas, will speak on the topic “Girdlers, Gallers, and Get-togetherers: tales of plants and arthropods”
8:30 PMSilent Auction closes

Here is a map showing the location of the meeting along with all nearby parking options:

QUESTIONS?  Visit anps.org or contact Eric Fuselier at anps.programs@gmail.com.

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