文章
Miss Chen
2018年08月19日
One of the first, and best known, re-blooming daylilies is the cultivar "Stella de Oro" (Hemerocallis "Stella de Oro"), which is hardy in U.S. Department of Agriculture plant hardiness zones 4 through 11. It first appeared in 1975, and 10 years later won the Stout Silver Medal. This is the highest award a daylily cultivar can receive from the American Hemerocallis Society. Like most daylilies, "Stella de Oro" benefits from division every few years.
How Often Should I Divide?
"Stella de Oro" is a dwarf daylily with foliage that only grows 12 inches tall. It tends to form tidy clumps that work well planted in rows, as individual clumps in perennial borders or massed as a groundcover. As the clumps grow, the individual daylily fans become crowded. Regular division reinvigorates daylilies, and gives you more plants for your garden or to pass along to other gardeners. Divide "Stella de Oro" every two to three years, when you notice a decrease in the number of blooms.
What Time of Year Is Best?
Daylilies are remarkably resilient plants, and can be divided any time during the spring, summer or fall growing seasons. Spring is the best season for division, however, since daylilies are actively growing. You want to divide plants when the new foliage is just starting to grow. This gives the daylilies time to put out new growth before blooming in the summer. Plants that were divided in the early spring will still flower, and may even produce more flowers than plants that were not divided.
If you miss dividing in the early spring, the second best time to divide plants is in the early fall. Daylilies put out another flush of growth after blooming. For "Stella de Oro," this doesn't happen until the weather starts to cool. You might have to cut off some late bloom stalks in order to divide the plants in early fall.
How Do I Divide Daylilies?
If you divide in the late spring, summer or fall, cut back the foliage to 8 inches tall with a pair of hedge shears and remove any flower stalks before dividing. For early spring division, you can skip this step. Make sure you disinfect shears and other cutting tools before use. Do this by soaking the tools in a mixture of 1 part bleach to 3 parts water for at least 5 minutes. Rinse tools in clean water, then let them air dry.
Use a gardening fork to lift the entire daylily clump from the soil. Separate the clump into smaller clumps using the gardening fork or a large, sharp knife. Each fan-shaped plant can grow on its own, but it is best to leave at least four fans together in each clump when you're dividing daylilies.
What Comes After Division?
Before replanting the daylily divisions, amend the soil with 2 to 3 inches of well-rotted compost worked in to a depth of 6 to 8 inches. This will provide a slow-release form of nitrogen and loosen the soil for new roots.
Re-plant each division at the same depth the plant was originally growing and space clumps 18 to 24 inches apart. Water each daylily clump thoroughly, and continue watering enough to keep the soil moist throughout the spring, summer and early fall. "Stella de Oro" needs little supplemental water after this first year.
How Often Should I Divide?
"Stella de Oro" is a dwarf daylily with foliage that only grows 12 inches tall. It tends to form tidy clumps that work well planted in rows, as individual clumps in perennial borders or massed as a groundcover. As the clumps grow, the individual daylily fans become crowded. Regular division reinvigorates daylilies, and gives you more plants for your garden or to pass along to other gardeners. Divide "Stella de Oro" every two to three years, when you notice a decrease in the number of blooms.
What Time of Year Is Best?
Daylilies are remarkably resilient plants, and can be divided any time during the spring, summer or fall growing seasons. Spring is the best season for division, however, since daylilies are actively growing. You want to divide plants when the new foliage is just starting to grow. This gives the daylilies time to put out new growth before blooming in the summer. Plants that were divided in the early spring will still flower, and may even produce more flowers than plants that were not divided.
If you miss dividing in the early spring, the second best time to divide plants is in the early fall. Daylilies put out another flush of growth after blooming. For "Stella de Oro," this doesn't happen until the weather starts to cool. You might have to cut off some late bloom stalks in order to divide the plants in early fall.
How Do I Divide Daylilies?
If you divide in the late spring, summer or fall, cut back the foliage to 8 inches tall with a pair of hedge shears and remove any flower stalks before dividing. For early spring division, you can skip this step. Make sure you disinfect shears and other cutting tools before use. Do this by soaking the tools in a mixture of 1 part bleach to 3 parts water for at least 5 minutes. Rinse tools in clean water, then let them air dry.
Use a gardening fork to lift the entire daylily clump from the soil. Separate the clump into smaller clumps using the gardening fork or a large, sharp knife. Each fan-shaped plant can grow on its own, but it is best to leave at least four fans together in each clump when you're dividing daylilies.
What Comes After Division?
Before replanting the daylily divisions, amend the soil with 2 to 3 inches of well-rotted compost worked in to a depth of 6 to 8 inches. This will provide a slow-release form of nitrogen and loosen the soil for new roots.
Re-plant each division at the same depth the plant was originally growing and space clumps 18 to 24 inches apart. Water each daylily clump thoroughly, and continue watering enough to keep the soil moist throughout the spring, summer and early fall. "Stella de Oro" needs little supplemental water after this first year.
0
0
文章
Miss Chen
2018年08月09日
Description: This plant is a perennial in areas with mild winters, otherwise it is an annual. It is about 2-4' tall and branches frequently. The smooth stems are greyish green and finely pubescent (canescent). The alternate leaves are up to 6" long and 4" across. They are ovate or cordate-ovate, smooth or slightly undulate along the margins, and finely pubescent on the underside (young leaves are finely pubescent on on the upperside as well). Each leaf is usually asymmetric at the base (oblique).
Individual flowers develop on short pedicels where the upper stems branch dichotomously. Each white flower is about 5-7" long and 3-4" across. The corolla has 5 shallow lobes that are barely perceptible; there is a short point between each pair of lobes along the rim of the corolla. Five white stamens are exerted from the center of the corolla. The base of the flower consists of a tubular calyx that has 5 broad teeth along its upper rim; this calyx extends to about ½ the length of the flower, and it lacks conspicuous ridges or wings. The blooming period occurs from mid-summer to fall and lasts about 1-2 months. The flowers often bloom during the day. Each flower is replaced by a prickly seed capsule about 1" across. Each capsule contains several seeds that are large and angular. The root system consists of a taproot. This plant reproduces by reseeding itself.
Cultivation: The preference is full sun, mesic conditions, and fertile loamy soil, preferably at a site that is not too windy. Flea beetles and other insects may chew tiny holes in the leaves.
Range & Habitat: Angel's Trumpet has naturalized in scattered counties across Illinois, although it rarely persists (see Distribution Map). Habitats include areas adjacent to gardens, areas along roads and railroads, and waste areas. This plant is occasionally cultivated in flower gardens, from which it occasionally escapes. Angel's Trumpet was introduced from central America and/or southwestern United States.
Faunal Associations: Little is known about floral-faunal relations for this species. The flowers are pollinated by hummingbirds and Sphinx moths. The foliage contains stramonium (a narcotic) and probably other toxic chemicals, therefore it is unlikely to be bothered by deer and other mammalian herbivores.
Photographic Location: An herb garden at Meadowbrook Park in Urbana, Illinois.
Comments: The flowers are extremely large and showy. The only other member of this genus that has naturalized in Illinois is Datura stramonium (Jimsonweed), which is common and weedy. Like Angel's Trumpet, Jimsonweed is a bushy herbaceous plant with large leaves and funnelform flowers. However, the flowers of Jimsonweed are smaller and less showy (up to 5" long and 2½" across), and they are less likely to bloom during the day. The foliage of Jimsonweed is largely hairless, while Angel's Trumpet has stems and leaf undersides that are finely pubescent. The leaf margins of Jimsonweed are lobed or undulate, while the leaf margins of Angel's Trumpet are smooth or slightly undulate. Another scientific name for Angel's Trumpet is Datura inoxia. Another common name for this species is Ghost Flower.
Individual flowers develop on short pedicels where the upper stems branch dichotomously. Each white flower is about 5-7" long and 3-4" across. The corolla has 5 shallow lobes that are barely perceptible; there is a short point between each pair of lobes along the rim of the corolla. Five white stamens are exerted from the center of the corolla. The base of the flower consists of a tubular calyx that has 5 broad teeth along its upper rim; this calyx extends to about ½ the length of the flower, and it lacks conspicuous ridges or wings. The blooming period occurs from mid-summer to fall and lasts about 1-2 months. The flowers often bloom during the day. Each flower is replaced by a prickly seed capsule about 1" across. Each capsule contains several seeds that are large and angular. The root system consists of a taproot. This plant reproduces by reseeding itself.
Cultivation: The preference is full sun, mesic conditions, and fertile loamy soil, preferably at a site that is not too windy. Flea beetles and other insects may chew tiny holes in the leaves.
Range & Habitat: Angel's Trumpet has naturalized in scattered counties across Illinois, although it rarely persists (see Distribution Map). Habitats include areas adjacent to gardens, areas along roads and railroads, and waste areas. This plant is occasionally cultivated in flower gardens, from which it occasionally escapes. Angel's Trumpet was introduced from central America and/or southwestern United States.
Faunal Associations: Little is known about floral-faunal relations for this species. The flowers are pollinated by hummingbirds and Sphinx moths. The foliage contains stramonium (a narcotic) and probably other toxic chemicals, therefore it is unlikely to be bothered by deer and other mammalian herbivores.
Photographic Location: An herb garden at Meadowbrook Park in Urbana, Illinois.
Comments: The flowers are extremely large and showy. The only other member of this genus that has naturalized in Illinois is Datura stramonium (Jimsonweed), which is common and weedy. Like Angel's Trumpet, Jimsonweed is a bushy herbaceous plant with large leaves and funnelform flowers. However, the flowers of Jimsonweed are smaller and less showy (up to 5" long and 2½" across), and they are less likely to bloom during the day. The foliage of Jimsonweed is largely hairless, while Angel's Trumpet has stems and leaf undersides that are finely pubescent. The leaf margins of Jimsonweed are lobed or undulate, while the leaf margins of Angel's Trumpet are smooth or slightly undulate. Another scientific name for Angel's Trumpet is Datura inoxia. Another common name for this species is Ghost Flower.
0
0
文章
Miss Chen
2018年08月09日
Description: This herbaceous plant is a winter or summer annual about 4-18" tall and similarly across; it branches dichotomously. Initially, a few basal leaves develop during the autumn or spring, but during late spring this plant bolts The stems of bolting plants are medium green, terete, and glabrous. Alternate leaves occur along the entire length of these stems, becoming smaller in size as they ascend. They vary in size from ½–3½" long and similarly across. The leaves are medium green, glabrous, and bipinnatifid or tripinnatifid in structure; they branch dichotomously and somewhat irregularly, forming narrowly linear to filiform lobes. These lobes are up to ¾" (20 mm.) long and about 0.5–1 mm. across. The narrow petioles of the leaves are nearly zero to 2" long; they are mostly green and glabrous, although the bases of these petioles have sheaths with white- to brown-membranous margins.
Both axillary and terminal umbels of flowers are produced in abundance. These umbels are usually compound, consisting of 2-3 umbellets (rarely with 4 umbellets), although sometimes they are simple. The compound umbels span about ¾–1¼" (20-32 mm.) across; their peduncles (basal stalks) are ¼–1" (6-24 mm.) long. The rays (basal stalklets) of the umbellets are ascending and divergent; they are ¼–¾" (6-20 mm.) in length. Individual umbellets span ¼–½" (6-12 mm.) across, consisting of 5-15 flowers; their pedicels are nearly zero to ¼" long. The peduncles, rays, and pedicels of each compound umbel are medium green, glabrous, and straight. Both the umbels and umbellets lack floral bracts. Individual flowers are only 1-2 mm. across when they are fully open. Each flower consists of 5 white petals, a toothless green calyx, 5 stamens, and a 2-celled ovary with a pair of short styles. The blooming period occurs during the summer and autumn, lasting about 2-3 months. Only a few flowers are in bloom at the same time.
Afterwards, the flowers are replaced by dry fruits (schizocarps); immature fruits are light green, while mature fruits turn brown; the latter soon fall to the ground. Each schizocarp consists of 2 hairless seeds. Individual seeds are 1.0–1.5 mm. long and asymmetrically ellipsoid in shape; one side of each seed is flat to slightly concave, while the other side is convex and conspicuously ribbed (3 ribs that are separated by 2 furrows). The root system consists of a slender taproot. This plant reproduces by reseeding itself.
Cultivation: The preference is full sun and moist conditions; a variety of soil types are tolerated. This plant will colonize drier ground, but it is vulnerable to hot dry weather. In some situations, this plant can spread aggressively, although this has not been a problem (thus far) in Illinois.
Range & Habitat: The non-native Fir-leaved Celery is a rare weed in Illinois. So far, it has occurred only in Champaign County (see Distribution Map). It is probably native to subtropical areas of Central and South America. However, it has spread to both subtropical and temperate areas throughout the world. Illinois appears to lie along the northern range-limit of this species; it is more common in southeastern and southwestern United States. In Illinois, Fir-leaved Celery was growing in low shrubbery near a parking lot in downtown Champaign, Illinois. It also occurred nearby in weedy turf grass along a roadside. In general, habitats of this plant include cropland, abandoned fields, roadside ditches, areas along railroads, gardens, neglected lawns, and areas around landscape shrubs. Fire and regular mowing are not tolerated. Nonetheless, this plant prefers habitats with a history of disturbance.
Faunal Associations: Floral-faunal relationships for Fir-leaved Celery are not well-understood for North America. Occasionally, White-tailed Deer browse on the foliage (Everitt et al., 1999). Livestock, including dairy cattle, sometimes browse on the foliage of this plant, as there have been some concerns about whether or not it can taint the flavor of milk.
Photographic Location: Low shrubbery and weedy turfgrass in downtown Champaign, Illinois, where this plant has persisted for several years. One of the photographs was taken indoors.
Comments: Sometimes the scientific name of Fir-leaved Celery is spelled Ciclospermum leptophyllum, and another scientific name of this plant is Apium leptophyllum. It also has other common names, including Marsh Parsley and Slender Celery. Fir-leaved Celery is remarkable for its narrowly lobed leaves and abundant umbels of tiny flowers. It is possible to confuse this plant with two other groups of annual plants in the Carrot family, viz. species of Mock Bishop-weed (Ptilimnium spp.) and Scaleseed (Spermolepis spp.), as they also have leaves with very narrow lobes and small white flowers. Species of Mock Bishop-weed differ by having larger compound umbels of flowers with more umbellets and the presence of floral bracts at the bases of their compound umbels. Species of Scaleseed can be distinguished by the bractlets at the bases of their umbellets and the presence of tubercles or bristles on their seeds. In contrast, Fir-leaved Celery lacks both floral bracts and bractlets and its seeds lack tubercles or bristles.
Both axillary and terminal umbels of flowers are produced in abundance. These umbels are usually compound, consisting of 2-3 umbellets (rarely with 4 umbellets), although sometimes they are simple. The compound umbels span about ¾–1¼" (20-32 mm.) across; their peduncles (basal stalks) are ¼–1" (6-24 mm.) long. The rays (basal stalklets) of the umbellets are ascending and divergent; they are ¼–¾" (6-20 mm.) in length. Individual umbellets span ¼–½" (6-12 mm.) across, consisting of 5-15 flowers; their pedicels are nearly zero to ¼" long. The peduncles, rays, and pedicels of each compound umbel are medium green, glabrous, and straight. Both the umbels and umbellets lack floral bracts. Individual flowers are only 1-2 mm. across when they are fully open. Each flower consists of 5 white petals, a toothless green calyx, 5 stamens, and a 2-celled ovary with a pair of short styles. The blooming period occurs during the summer and autumn, lasting about 2-3 months. Only a few flowers are in bloom at the same time.
Afterwards, the flowers are replaced by dry fruits (schizocarps); immature fruits are light green, while mature fruits turn brown; the latter soon fall to the ground. Each schizocarp consists of 2 hairless seeds. Individual seeds are 1.0–1.5 mm. long and asymmetrically ellipsoid in shape; one side of each seed is flat to slightly concave, while the other side is convex and conspicuously ribbed (3 ribs that are separated by 2 furrows). The root system consists of a slender taproot. This plant reproduces by reseeding itself.
Cultivation: The preference is full sun and moist conditions; a variety of soil types are tolerated. This plant will colonize drier ground, but it is vulnerable to hot dry weather. In some situations, this plant can spread aggressively, although this has not been a problem (thus far) in Illinois.
Range & Habitat: The non-native Fir-leaved Celery is a rare weed in Illinois. So far, it has occurred only in Champaign County (see Distribution Map). It is probably native to subtropical areas of Central and South America. However, it has spread to both subtropical and temperate areas throughout the world. Illinois appears to lie along the northern range-limit of this species; it is more common in southeastern and southwestern United States. In Illinois, Fir-leaved Celery was growing in low shrubbery near a parking lot in downtown Champaign, Illinois. It also occurred nearby in weedy turf grass along a roadside. In general, habitats of this plant include cropland, abandoned fields, roadside ditches, areas along railroads, gardens, neglected lawns, and areas around landscape shrubs. Fire and regular mowing are not tolerated. Nonetheless, this plant prefers habitats with a history of disturbance.
Faunal Associations: Floral-faunal relationships for Fir-leaved Celery are not well-understood for North America. Occasionally, White-tailed Deer browse on the foliage (Everitt et al., 1999). Livestock, including dairy cattle, sometimes browse on the foliage of this plant, as there have been some concerns about whether or not it can taint the flavor of milk.
Photographic Location: Low shrubbery and weedy turfgrass in downtown Champaign, Illinois, where this plant has persisted for several years. One of the photographs was taken indoors.
Comments: Sometimes the scientific name of Fir-leaved Celery is spelled Ciclospermum leptophyllum, and another scientific name of this plant is Apium leptophyllum. It also has other common names, including Marsh Parsley and Slender Celery. Fir-leaved Celery is remarkable for its narrowly lobed leaves and abundant umbels of tiny flowers. It is possible to confuse this plant with two other groups of annual plants in the Carrot family, viz. species of Mock Bishop-weed (Ptilimnium spp.) and Scaleseed (Spermolepis spp.), as they also have leaves with very narrow lobes and small white flowers. Species of Mock Bishop-weed differ by having larger compound umbels of flowers with more umbellets and the presence of floral bracts at the bases of their compound umbels. Species of Scaleseed can be distinguished by the bractlets at the bases of their umbellets and the presence of tubercles or bristles on their seeds. In contrast, Fir-leaved Celery lacks both floral bracts and bractlets and its seeds lack tubercles or bristles.
0
0
文章
Miss Chen
2018年08月06日
Description: This perennial plant is a herbaceous vine that produces stems 2-4' long. The stems are usually glabrous, but are sometimes hairy where new growth occurs. The alternate leaves are 1-2' long and half as much across. They are often sagittate (arrowhead-shaped), but are variable and can assume other forms as well. Their margins are smooth and occasionally slightly ciliate. Long slender petioles connect the leaves with the stems. A slender flowering stalk may develop from the base of a petiole. This stalk occasionally branches and can produce 1-3 flowers. The corolla of a flower is funnelform in shape and up to 1" across; it is usually white, sometimes with light pink patterns. The 5 lobes of the corolla are very shallow and barely perceptible. Toward the throat of the corolla is a patch of yellow and the reproductive parts, consisting of 5 stamens and a pistil with a divided style. These reproductive parts are usually white, although the anthers may be pink or light purple in flowers with pink corollas. At the base of the flower, there are 5 green sepals that are much smaller than the corolla. Up to 1" below the base of a flower, there are a pair of small green bracts on the flowering stalk.
The blooming period can occur from late spring to early fall, and can span several months, even though individual flowers persist for only a single day, usually opening during the morning and closing by late afternoon. A hairless and well-rounded seed capsule about ¼" long replaces each flower; each 2-celled capsule contains 4 seeds. These dark seeds are 3-angled and oblong, but tapering somewhat at the ends. Each seed usually has 2 flat sides and 1 convex side; it is about 1/8" long. The root system consists of a slender taproot that branches frequently; it can extend 20' into the ground. Rhizomes are also produced in abundance, so that this plant often forms vegetative colonies.
Cultivation: Field Bindweed prefers full sunlight and mesic to dry conditions. It has considerable drought tolerance, and flourishes in poor soil that contains sand, gravel, or hardpan clay. It will also grow in moist fertile soil, but dislikes competition from taller plants. Eradication of this plant is difficult, as mechanical cultivation often spreads the rhizomes around, producing new plants. Because of the deep root system, it has been known to survive bulldozer operations. It can also persist in lawns, notwithstanding regular lawn-mowing. The application of broadleaf herbicides can be an effective control measure, if it is repeated as needed.
Range & Habitat: Field Bindweed is a common plant that has been reported from most counties in Illinois (see Distribution Map); it is native to Eurasia. This plant continues to spread and probably occurs in every county of the state. Habitats include lawns, gardens, fields, clay banks, areas along roadsides and railroads (including ballast), vacant lots, and miscellaneous waste areas. This plant occurs primarily in disturbed areas.
Faunal Associations: Mostly long-tongued bees visit the flowers for nectar, including bumblebees and little carpenter bees (Ceratina spp.). In addition, specialist bees that are attracted to funnelform flowers also visit the flowers for nectar, including Melitoma taurea (Mallow Bee) and Cemolobus ipomoeae (Morning Glory Bee). The adults and larvae of several tortoise beetles are known to feed destructively on the foliage of Field Bindweed, including Charidotella sexpunctata (Golden Tortoise Beetle), Chelymorpha cassidea (Argus Tortoise Beetle), Deloyala guttata (Mottled Tortoise Beetle), and Jonthonota nigripes (Black-legged Tortoise Beetle). Other beetles that feed on this plant include Chaetocnema confinis (Sweet Potato Flea Beetle) and Typophorus nigritus (Sweet Potato Leaf Beetle); see Clark et al. (2004). The larvae of a sawfly, Sphacophilus cellularis, feed on the leaves of bindweeds (Convolvulus spp.), as do the larvae of several moths, including Bedellia somnulentella (Morning Glory Leafminer), Spragueia leo (Common Spragueia), Emmelina monodactyla (Morning Glory Plume Moth), and Agrius cingulatus (Pink-spotted Hawk Moth); see Smith (2006), Cranshaw (2004), Covell (1984/2005), and Wagner (2005). Field Bindweed is not a preferred food source for mammalian herbivores because the foliage is mildly toxic. Furthermore, there have been reports of the rootstocks poisoning swine.
Photographic Location: Along a railroad in Urbana, Illinois. This plant is very common in the area.
Comments: Field Bindweed is an attractive plant while it is in flower, but it can be very aggressive and persistent. The flowers are smaller in size than Calystegia sepium (Hedge Bindweed) and Ipomoea pandurata (Wild Sweet Potato). Its leaves are sagittate, while the leaves of Ipomoea pandurata (Wild Sweet Potato) and Ipomoea lacunosa (Small White Morning Glory) are cordate.
The blooming period can occur from late spring to early fall, and can span several months, even though individual flowers persist for only a single day, usually opening during the morning and closing by late afternoon. A hairless and well-rounded seed capsule about ¼" long replaces each flower; each 2-celled capsule contains 4 seeds. These dark seeds are 3-angled and oblong, but tapering somewhat at the ends. Each seed usually has 2 flat sides and 1 convex side; it is about 1/8" long. The root system consists of a slender taproot that branches frequently; it can extend 20' into the ground. Rhizomes are also produced in abundance, so that this plant often forms vegetative colonies.
Cultivation: Field Bindweed prefers full sunlight and mesic to dry conditions. It has considerable drought tolerance, and flourishes in poor soil that contains sand, gravel, or hardpan clay. It will also grow in moist fertile soil, but dislikes competition from taller plants. Eradication of this plant is difficult, as mechanical cultivation often spreads the rhizomes around, producing new plants. Because of the deep root system, it has been known to survive bulldozer operations. It can also persist in lawns, notwithstanding regular lawn-mowing. The application of broadleaf herbicides can be an effective control measure, if it is repeated as needed.
Range & Habitat: Field Bindweed is a common plant that has been reported from most counties in Illinois (see Distribution Map); it is native to Eurasia. This plant continues to spread and probably occurs in every county of the state. Habitats include lawns, gardens, fields, clay banks, areas along roadsides and railroads (including ballast), vacant lots, and miscellaneous waste areas. This plant occurs primarily in disturbed areas.
Faunal Associations: Mostly long-tongued bees visit the flowers for nectar, including bumblebees and little carpenter bees (Ceratina spp.). In addition, specialist bees that are attracted to funnelform flowers also visit the flowers for nectar, including Melitoma taurea (Mallow Bee) and Cemolobus ipomoeae (Morning Glory Bee). The adults and larvae of several tortoise beetles are known to feed destructively on the foliage of Field Bindweed, including Charidotella sexpunctata (Golden Tortoise Beetle), Chelymorpha cassidea (Argus Tortoise Beetle), Deloyala guttata (Mottled Tortoise Beetle), and Jonthonota nigripes (Black-legged Tortoise Beetle). Other beetles that feed on this plant include Chaetocnema confinis (Sweet Potato Flea Beetle) and Typophorus nigritus (Sweet Potato Leaf Beetle); see Clark et al. (2004). The larvae of a sawfly, Sphacophilus cellularis, feed on the leaves of bindweeds (Convolvulus spp.), as do the larvae of several moths, including Bedellia somnulentella (Morning Glory Leafminer), Spragueia leo (Common Spragueia), Emmelina monodactyla (Morning Glory Plume Moth), and Agrius cingulatus (Pink-spotted Hawk Moth); see Smith (2006), Cranshaw (2004), Covell (1984/2005), and Wagner (2005). Field Bindweed is not a preferred food source for mammalian herbivores because the foliage is mildly toxic. Furthermore, there have been reports of the rootstocks poisoning swine.
Photographic Location: Along a railroad in Urbana, Illinois. This plant is very common in the area.
Comments: Field Bindweed is an attractive plant while it is in flower, but it can be very aggressive and persistent. The flowers are smaller in size than Calystegia sepium (Hedge Bindweed) and Ipomoea pandurata (Wild Sweet Potato). Its leaves are sagittate, while the leaves of Ipomoea pandurata (Wild Sweet Potato) and Ipomoea lacunosa (Small White Morning Glory) are cordate.
0
0
绝骨
2018年08月02日
18年8月2日，帝都，爆热。迎来了4位新成员：半球，果冻，冰玉，达摩。总之折腾了1个多小时，种上了。说实在的，这两天买还不如一个月前暴雨时候买，至少那会儿凉快啊！但是手欠啊！就买了哈哈哈。放在没直晒又通风的北窗台，晾着。听天由命。
1
0
文章
Miss Chen
2018年08月01日
Description: This perennial herbaceous plant consists of a tuft of decumbent leafy stems about 4-12" tall and similarly across. The stems are light green, terete, and more or less covered with short white-woolly hairs; they branch occasionally. Alternate leaves occur along these stems that are ½–2" long and ½–1" across; most of these leaves are located close to the ground where the lower stems sprawl. The leaves are deeply bipinnatifid or tripinnatifid and rather irregular in their branching patterns; their ultimate leaf segments are linear-filiform and short. The leaves are light-medium green and sparsely to moderately covered with very short white-woolly hairs. Solitary flowerheads about ½–1" across are produced from long peduncles up to 6" long. The peduncles are light green, terete, and more or less covered with short white-woolly hairs. Underneath the flowerheads, however, the peduncles become more swollen, slightly furrowed, and more densely covered with white-woolly hairs. Each flowerhead consists of 10-20 ray florets surrounding numerous disk florets; the disk florets are arranged together in a hemispheric head that has a solid interior. The ray florets are pistillate and fertile, while the disk florets are perfect and fertile. The petaloid rays of the flowerheads are white, broadly oblong-elliptic in shape, and widely spreading; their tips have 1-2 small notches.
The corollas of the disk florets are 2-3 mm. long, narrowly tubular in shape, and yellow; they have 5 spreading lobes at their apices. Between the corollas of the disk florets, there are chaffy scales; these scales are white-membranous along their margins and oblong in shape with rounded erose (somewhat frayed) tips. Around the base of each flowerhead, there are phyllaries (floral bracts) in several overlapping and appressed series that together form a shallow saucer-like shape. The phyllaries are lanceolate-oblong with blunt tips, light green with white-membranous margins, and more or less covered with short white-woolly hairs. The blooming period occurs during the summer and early autumn for 1½–3 months. Afterwards, fertile florets are replaced by small achenes about 1–1.5 mm. long. These achenes are oblongoid in shape, pale-colored, and slightly flattened or 3-angled; each achene has 3 filiform ribs on one side. The root system is fibrous, rhizomatous, and relatively shallow. This plant can spread by reseeding itself or by forming clonal offsets from the short rhizomes.
Cultivation: The preference is full or partial sun, moist to mesic conditions, and soil consisting of either loam or sandy loam. This plant is easy to cultivate and it occasionally spreads into adjacent areas.
Range & Habitat: Roman Chamomile has rarely naturalized in Illinois and thus far wild populations have been reported from only a few counties (see Distribution Map). Roman Chamomile is native to western Europe and it was introduced into North America as an ornamental and herbal plant for gardens. In North America, naturalized populations of this plant are found primarily in urban areas, including such habitats as areas near gardens, lawns, grassy roadsides, vacant lots, and construction sites. In Europe, it has been found in such habitats as grassy roadsides, sandy lawns in commons areas, and sandy pastures. Roman Chamomile is still cultivated in flower and herbal gardens, from where it occasionally escapes, but rarely persists. Areas with a history of disturbance are preferred.
Faunal Associations: The nectar and pollen of the flowerheads probably attract small bees and various flies; wasps and beetles may visit the flowerheads to a lesser extent. Two aphids, Macrosiphoniella tanacetaria and Macrosiphoniella tapuskae, are known to feed on Roman Chamomile (Blackman & Eastop, 2013). A polyphagous leafhopper, Empoasca erigeron, also feeds on this plant (Dmitriev & Dietrich, 2010). At the present time, information about this plant's relationships with granivorous birds and herbivorous mammals is unavailable.
Photographic Location: An ornamental garden at the Urbana Public Library of Urbana, Illinois.
Comments: There are several species of plants in the Aster family that have daisy-like flowerheads with white petaloid rays. Many of these species have been introduced into North America from Eurasia as garden plants, including Roman Chamomile (Chamaemelum nobile). Roman Chamomile can be distinguished from most of these species by its highly fragrant foliage and crushed flowerheads, which have an apple-pineapple scent. One other species in this group that has naturalized in Illinois, German Chamomile (Matricaria chamomile), also has foliage and crushed flowerheads with a similar fruity scent. German Chamomile can be readily distinguished by its glabrous foliage, more erect habit, the hollow interior of its flowerheads, and the lack of chaffy scales between the disk florets. This latter plant is also an annual, rather than a perennial. Both of these species have been used as ingredients in Chamomile tea, and the chemical constituents of their flowerheads are said to have relaxing and soothing properties. An alternative scientific name for Roman Chamomile is Anthemis nobilis, and it has other common names, including Low Chamomile, English Chamomile, and Garden Chamomile.
The corollas of the disk florets are 2-3 mm. long, narrowly tubular in shape, and yellow; they have 5 spreading lobes at their apices. Between the corollas of the disk florets, there are chaffy scales; these scales are white-membranous along their margins and oblong in shape with rounded erose (somewhat frayed) tips. Around the base of each flowerhead, there are phyllaries (floral bracts) in several overlapping and appressed series that together form a shallow saucer-like shape. The phyllaries are lanceolate-oblong with blunt tips, light green with white-membranous margins, and more or less covered with short white-woolly hairs. The blooming period occurs during the summer and early autumn for 1½–3 months. Afterwards, fertile florets are replaced by small achenes about 1–1.5 mm. long. These achenes are oblongoid in shape, pale-colored, and slightly flattened or 3-angled; each achene has 3 filiform ribs on one side. The root system is fibrous, rhizomatous, and relatively shallow. This plant can spread by reseeding itself or by forming clonal offsets from the short rhizomes.
Cultivation: The preference is full or partial sun, moist to mesic conditions, and soil consisting of either loam or sandy loam. This plant is easy to cultivate and it occasionally spreads into adjacent areas.
Range & Habitat: Roman Chamomile has rarely naturalized in Illinois and thus far wild populations have been reported from only a few counties (see Distribution Map). Roman Chamomile is native to western Europe and it was introduced into North America as an ornamental and herbal plant for gardens. In North America, naturalized populations of this plant are found primarily in urban areas, including such habitats as areas near gardens, lawns, grassy roadsides, vacant lots, and construction sites. In Europe, it has been found in such habitats as grassy roadsides, sandy lawns in commons areas, and sandy pastures. Roman Chamomile is still cultivated in flower and herbal gardens, from where it occasionally escapes, but rarely persists. Areas with a history of disturbance are preferred.
Faunal Associations: The nectar and pollen of the flowerheads probably attract small bees and various flies; wasps and beetles may visit the flowerheads to a lesser extent. Two aphids, Macrosiphoniella tanacetaria and Macrosiphoniella tapuskae, are known to feed on Roman Chamomile (Blackman & Eastop, 2013). A polyphagous leafhopper, Empoasca erigeron, also feeds on this plant (Dmitriev & Dietrich, 2010). At the present time, information about this plant's relationships with granivorous birds and herbivorous mammals is unavailable.
Photographic Location: An ornamental garden at the Urbana Public Library of Urbana, Illinois.
Comments: There are several species of plants in the Aster family that have daisy-like flowerheads with white petaloid rays. Many of these species have been introduced into North America from Eurasia as garden plants, including Roman Chamomile (Chamaemelum nobile). Roman Chamomile can be distinguished from most of these species by its highly fragrant foliage and crushed flowerheads, which have an apple-pineapple scent. One other species in this group that has naturalized in Illinois, German Chamomile (Matricaria chamomile), also has foliage and crushed flowerheads with a similar fruity scent. German Chamomile can be readily distinguished by its glabrous foliage, more erect habit, the hollow interior of its flowerheads, and the lack of chaffy scales between the disk florets. This latter plant is also an annual, rather than a perennial. Both of these species have been used as ingredients in Chamomile tea, and the chemical constituents of their flowerheads are said to have relaxing and soothing properties. An alternative scientific name for Roman Chamomile is Anthemis nobilis, and it has other common names, including Low Chamomile, English Chamomile, and Garden Chamomile.
0
0
文章
Miss Chen
2018年07月31日
Description: This herbaceous perennial plant is 1-4' tall and usually unbranched, except sometimes at the base. The central stem is light green, short-pubescent, and 4-angled with shallow vertical grooves. At intervals, there occurs pairs of opposite leaves that become slightly shorter and more narrow as they ascend the stem. Each pair of leaves rotates about 90° from the pair of leaves either immediately above or below. The leaf blades are 1-3" long, 1/3-1¼" (8-31 mm.) across, and flat; they are ovate to oblong-lanceolate in shape and their margins are dentate to sparsely crenate. The upper surface of each leaf blade is medium green and sparsely short-pubescent, while the lower surface is slightly more pale and pubescent (at least along the central veins). On each leaf blade, there are usually 2 lateral veins that run parallel to the central central and a few secondary veins that branch from the central vein along its length. The petioles of the leaves are ¼-¾" long. The lowest leaves, which are wider, are often withered by the time that flowering occurs.
The flowers occur in dense axillary clusters along the upper half of each stem; these floral clusters are whorled and sessile. Individual flowers are about ¼" (6 mm.) long and 1/8" (3 mm.) across, consisting of a 2-lipped tubular corolla with 4 lobes, a calyx with 5 teeth that have spine-like tips, 4 stamens, and a pistil with an ovary that is divided into 4 parts. The corolla is white to pink and softly short-hairy along the exterior of the upper lobe, which functions as a protective hood. There is also a rounded lower lobe and two smaller lateral lobes. A patch of red occurs within the throat of the corolla. The calyx is light green, sparsely canescent along its exterior, and 5-veined. The corolla of the flower is about the same length as the calyx (including the tips of its teeth) or a little longer. The blooming period occurs fromDistribution Map early summer to early fall for about 2-3 months. Usually, only a few flowers are in bloom at the same time across several floral clusters. Each flower is replaced by a cluster of 4 small nutlets during the fall. Individual nutlets are oblongoid and 3-sided. The root system is fibrous and rhizomatous. Clonal colonies of plants are often formed from the rhizomes.
Cultivation: The preference is full sun to light shade, moist to dry-mesic conditions, and loamy, rocky, or sandy soil that is calcareous. Depending on fertility of the soil, moisture levels, and time of year, individual plants can vary considerably in their height.
Range & Habitat: False Motherwort is uncommon to occasional in both central and NE Illinois, while in the rest of the state it is rare or absent. This plant is not native to Illinois; it was accidentally introduced into North America from Eurasia. Habitats include dolomite prairies, sandy savannas near Lake Michigan, riverbanks, roadsides, and pastures. This plant is usually found in disturbed areas, although it sometimes occurs in higher quality habitats.
Faunal Associations: Very little is known about floral-faunal relationships for this plant in North America, although they are probably similar to those for Motherwort (Leonurus cardiaca), which is closely related to False Motherwort and more common. The flowers are likely pollinated by various bees, including bumblebees, little carpenter bees (Ceratina spp.), and Halictid bees (Halictus spp., Lasioglossum spp.), which seek nectar or collect pollen from the flowers. Syrphid flies may also visit the flowers to feed on pollen, but they are less effective at cross-pollination. The Currant Aphid (Cryptomyzus ribis) uses Leonurus spp. (Motherworts) as summer hosts. Because of the bitter foliage, it is unlikely that mammalian herbivores browse on False Motherwort to any significant extent.
Photographic Location: A sandy oak savanna near Lake Michigan at the Indiana Dunes State Park in NW Indiana.
Comments: Across different populations, the leaf blades of False Motherwort can vary significantly in their width and in the abundance or size of the teeth along their margins. This plant is sometimes referred to as Leonurus marrubiastrum, but it differs from Leonurus spp. (Motherworts) by the lack of cleft lobes on its leaves. Like Motherwort (Leonurus cardiaca), False Motherwort can be distinguished from many other members of the Mint family by the spiny teeth of its calyces, the shape of its leaves, and other characteristics. Other common names of this plant are Lion's Tail and Horehound Motherwort.
The flowers occur in dense axillary clusters along the upper half of each stem; these floral clusters are whorled and sessile. Individual flowers are about ¼" (6 mm.) long and 1/8" (3 mm.) across, consisting of a 2-lipped tubular corolla with 4 lobes, a calyx with 5 teeth that have spine-like tips, 4 stamens, and a pistil with an ovary that is divided into 4 parts. The corolla is white to pink and softly short-hairy along the exterior of the upper lobe, which functions as a protective hood. There is also a rounded lower lobe and two smaller lateral lobes. A patch of red occurs within the throat of the corolla. The calyx is light green, sparsely canescent along its exterior, and 5-veined. The corolla of the flower is about the same length as the calyx (including the tips of its teeth) or a little longer. The blooming period occurs fromDistribution Map early summer to early fall for about 2-3 months. Usually, only a few flowers are in bloom at the same time across several floral clusters. Each flower is replaced by a cluster of 4 small nutlets during the fall. Individual nutlets are oblongoid and 3-sided. The root system is fibrous and rhizomatous. Clonal colonies of plants are often formed from the rhizomes.
Cultivation: The preference is full sun to light shade, moist to dry-mesic conditions, and loamy, rocky, or sandy soil that is calcareous. Depending on fertility of the soil, moisture levels, and time of year, individual plants can vary considerably in their height.
Range & Habitat: False Motherwort is uncommon to occasional in both central and NE Illinois, while in the rest of the state it is rare or absent. This plant is not native to Illinois; it was accidentally introduced into North America from Eurasia. Habitats include dolomite prairies, sandy savannas near Lake Michigan, riverbanks, roadsides, and pastures. This plant is usually found in disturbed areas, although it sometimes occurs in higher quality habitats.
Faunal Associations: Very little is known about floral-faunal relationships for this plant in North America, although they are probably similar to those for Motherwort (Leonurus cardiaca), which is closely related to False Motherwort and more common. The flowers are likely pollinated by various bees, including bumblebees, little carpenter bees (Ceratina spp.), and Halictid bees (Halictus spp., Lasioglossum spp.), which seek nectar or collect pollen from the flowers. Syrphid flies may also visit the flowers to feed on pollen, but they are less effective at cross-pollination. The Currant Aphid (Cryptomyzus ribis) uses Leonurus spp. (Motherworts) as summer hosts. Because of the bitter foliage, it is unlikely that mammalian herbivores browse on False Motherwort to any significant extent.
Photographic Location: A sandy oak savanna near Lake Michigan at the Indiana Dunes State Park in NW Indiana.
Comments: Across different populations, the leaf blades of False Motherwort can vary significantly in their width and in the abundance or size of the teeth along their margins. This plant is sometimes referred to as Leonurus marrubiastrum, but it differs from Leonurus spp. (Motherworts) by the lack of cleft lobes on its leaves. Like Motherwort (Leonurus cardiaca), False Motherwort can be distinguished from many other members of the Mint family by the spiny teeth of its calyces, the shape of its leaves, and other characteristics. Other common names of this plant are Lion's Tail and Horehound Motherwort.
0
0
文章
Miss Chen
2018年07月31日
Description: This plant is a winter or spring annual that becomes 4-16" tall, usually forming a tuft of leafy stems that are ascending to sprawling. These stems are branched at the base near the crown of the plant, otherwise they are unbranched. Individual stems are light green, terete, and glandular-hairy. Pairs of opposite leaves occur along these stems (typically at intervals of 1-2½"). These leaves are ¾-2" long, 5-9 mm. across, and elliptic, oblong-lanceolate, or oblong-oblanceolate in shape. The leaf margins are smooth (entire) and slightly ciliate. The leaf surfaces are medium green and either sparsely short-pubescent or hairless. Each leaf has a prominent central vein.
The upper stems terminate in either cymes or compound cymes of flowers (usually the latter); these cymes are dichotomously branched and variable in size. Each terminal branch of the inflorescence typically has 3 flowers with divergent slender pedicels up to 1¼" long. While the flower buds are nodding, the flowers are more erect. Similar to the stems, the branches and pedicels of each inflorescence are light green, terete, and glandular-pubescent. At the base of each pair of branches in an inflorescence, there is a pair of leafy bracts up to ¾" and 5 mm. across. These bracts are lanceolate in shape and they lack membranous margins. The flowers are up to ¼" across while they are in bloom. Each flower has 5 white petals with notched tips, 5 green sepals, an ovary with 5 styles, and 10 stamens (usually). The sepals are lanceolate in shape with membranous margins and short-pubescent; they are about 3-5 mm. long. The petals are the same length or a little longer than the sepals. The blooming period occurs from mid-spring to early summer, lasting about 1 month. Usually, only a few flowers are in bloom at the same time. Sometimes cleistogamous flowers that fail to open are produced.Distribution Map Afterwards, the flowers are replaced by cylindrical seed capsules that become 8-12 mm. long at maturity. Like the flowerbuds, they tend to nod downward. Mature seed capsules are membranous, light tan, longitudinally veined, and often slightly curved; they are more than twice as long as the sepals. Each seed capsule has an open rim at its apex with 10 tiny teeth. Each seed capsule contains several tiny seeds about 0.5 mm. in length. The seeds are obovoid, somewhat flattened, brownish, and minutely tuberculate (warty). The root system system consists of a shallow spreading taproot.
Cultivation: The preference is full sun to light shade and moist conditions. Nodding Chickweed is not particular about soil. Most growth and development occurs during the spring when the weather is cool and moist, after which the foliage dies down.
Range & Habitat: The native Nodding Chickweed is occasional to locally common in most areas of Illinois. Habitats include floodplain woodlands, streambanks in wooded areas, ravines and ledges along streams, gravel bars along rivers, weedy meadows, nursery plots, and moist waste areas. Nodding Chickweed occurs in both natural areas and human-mediated environments. In natural areas, it tends to occur in places where there is some disturbance by the action of water (e.g., soil erosion or deposits of gravel).
Faunal Associations: The flowers are cross-pollinated by honeybees, Halictid bees (Halictus spp., Lasioglossum spp.), small butterflies, Syrphid flies, and other flies (Robertson, 1929). Both nectar and pollen are available as floral rewards. The caterpillars and cutworms of various moths are known to feed on chickweeds (Stellaria spp., Cerastium spp.). These moth species include Haematopis grataria (Chickweed Geometer), Lobocleta ossularia (Drab Brown Wave), Agrotis venerabilis (Venerable Dart), Hyles lineata (White-Lined Sphinx), Feltia jaculifera (Dingy Cutworm), Xestia badinodis (Spot-Sided Cutworm), and Xanthorhoe ferrugata (Red Twin-Spot). Vertebrate animals also feed on these plants to some extent. Various sparrows and other granivorous songbirds eat the seeds, while deer, rabbits, and domesticated farm animals (cattle, horses, sheep, & pigs) occasionally browse on the foliage.
Photographic Location: A gravel bar along a river in a wooded area of Pine Hills State Nature Preserve in west-central Indiana.
Comments: Notwithstanding its weedy appearance and habits, this is one of the native chickweeds in Illinois. It is a rather floppy plant with small white flowers. Nodding Chickweed can be distinguished from other chickweeds (Stellaria spp., Cerastium spp.) by the shape of its leaves, diffuse inflorescence, and structure of its flowers. In particular, the pedicels of its flowers are rather long (1" in length or more) and divergent, while its flowerbuds and seed capsules nod downward. Among the Mouse-Eared Chickweeds (Cerastium spp.), Nodding Chickweed has rather long and narrow leaves. Some authorities consider the more western Cerastium brachypodum to be a variety of Nodding Chickweed, or Cerastium nutans obtectum. This latter species (or variety) tends to have more hairy leaves and its pedicels are shorter (less than 1" in length).
The upper stems terminate in either cymes or compound cymes of flowers (usually the latter); these cymes are dichotomously branched and variable in size. Each terminal branch of the inflorescence typically has 3 flowers with divergent slender pedicels up to 1¼" long. While the flower buds are nodding, the flowers are more erect. Similar to the stems, the branches and pedicels of each inflorescence are light green, terete, and glandular-pubescent. At the base of each pair of branches in an inflorescence, there is a pair of leafy bracts up to ¾" and 5 mm. across. These bracts are lanceolate in shape and they lack membranous margins. The flowers are up to ¼" across while they are in bloom. Each flower has 5 white petals with notched tips, 5 green sepals, an ovary with 5 styles, and 10 stamens (usually). The sepals are lanceolate in shape with membranous margins and short-pubescent; they are about 3-5 mm. long. The petals are the same length or a little longer than the sepals. The blooming period occurs from mid-spring to early summer, lasting about 1 month. Usually, only a few flowers are in bloom at the same time. Sometimes cleistogamous flowers that fail to open are produced.Distribution Map Afterwards, the flowers are replaced by cylindrical seed capsules that become 8-12 mm. long at maturity. Like the flowerbuds, they tend to nod downward. Mature seed capsules are membranous, light tan, longitudinally veined, and often slightly curved; they are more than twice as long as the sepals. Each seed capsule has an open rim at its apex with 10 tiny teeth. Each seed capsule contains several tiny seeds about 0.5 mm. in length. The seeds are obovoid, somewhat flattened, brownish, and minutely tuberculate (warty). The root system system consists of a shallow spreading taproot.
Cultivation: The preference is full sun to light shade and moist conditions. Nodding Chickweed is not particular about soil. Most growth and development occurs during the spring when the weather is cool and moist, after which the foliage dies down.
Range & Habitat: The native Nodding Chickweed is occasional to locally common in most areas of Illinois. Habitats include floodplain woodlands, streambanks in wooded areas, ravines and ledges along streams, gravel bars along rivers, weedy meadows, nursery plots, and moist waste areas. Nodding Chickweed occurs in both natural areas and human-mediated environments. In natural areas, it tends to occur in places where there is some disturbance by the action of water (e.g., soil erosion or deposits of gravel).
Faunal Associations: The flowers are cross-pollinated by honeybees, Halictid bees (Halictus spp., Lasioglossum spp.), small butterflies, Syrphid flies, and other flies (Robertson, 1929). Both nectar and pollen are available as floral rewards. The caterpillars and cutworms of various moths are known to feed on chickweeds (Stellaria spp., Cerastium spp.). These moth species include Haematopis grataria (Chickweed Geometer), Lobocleta ossularia (Drab Brown Wave), Agrotis venerabilis (Venerable Dart), Hyles lineata (White-Lined Sphinx), Feltia jaculifera (Dingy Cutworm), Xestia badinodis (Spot-Sided Cutworm), and Xanthorhoe ferrugata (Red Twin-Spot). Vertebrate animals also feed on these plants to some extent. Various sparrows and other granivorous songbirds eat the seeds, while deer, rabbits, and domesticated farm animals (cattle, horses, sheep, & pigs) occasionally browse on the foliage.
Photographic Location: A gravel bar along a river in a wooded area of Pine Hills State Nature Preserve in west-central Indiana.
Comments: Notwithstanding its weedy appearance and habits, this is one of the native chickweeds in Illinois. It is a rather floppy plant with small white flowers. Nodding Chickweed can be distinguished from other chickweeds (Stellaria spp., Cerastium spp.) by the shape of its leaves, diffuse inflorescence, and structure of its flowers. In particular, the pedicels of its flowers are rather long (1" in length or more) and divergent, while its flowerbuds and seed capsules nod downward. Among the Mouse-Eared Chickweeds (Cerastium spp.), Nodding Chickweed has rather long and narrow leaves. Some authorities consider the more western Cerastium brachypodum to be a variety of Nodding Chickweed, or Cerastium nutans obtectum. This latter species (or variety) tends to have more hairy leaves and its pedicels are shorter (less than 1" in length).
0
0
