Gymnosporangium juniperi-virginianae | |
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Galls of cedar-apple rust on eastern red cedar | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Basidiomycota |
Class: | Pucciniomycetes |
Order: | Pucciniales |
Family: | Gymnosporangiaceae |
Genus: | Gymnosporangium |
Species: | G. juniperi-virginianae |
Binomial name | |
Gymnosporangium juniperi-virginianae Schwein. (1822) | |
Gymnosporangium juniperi-virginianae is a plant pathogen that causes cedar-apple rust. [1] In virtually any location where apples or crabapples ( Malus ) and eastern red cedar ( Juniperus virginiana ) coexist, cedar apple rust can be a destructive or disfiguring disease on both the apples and cedars. Apples, crabapples, and eastern red cedar are the most common hosts for this disease. [2] Similar diseases can be found on quince and hawthorn [3] and many species of juniper can substitute for the eastern red cedars. [2]
On the apple tree, the infections occur on leaves, fruit and young twigs. [4] The brightly colored spots produced on the leaves make it easy to identify. Small, yellow-orange spots appear on the upper surfaces of the leaves, anytime from April to June. [5] These spots gradually enlarge and turn orange or red and may show concentric rings of color. Drops of orange liquid may be visible on the spots. Later in the season, black dots appear on the orange spots on the upper leaf surface. In late summer, tube-like structures develop on the undersurface of the apple leaf. Infected leaves sometimes drop prematurely, particularly during drought conditions or when the tree is under additional stress. Infections on fruit are usually near the blossom end and are somewhat similar to the leaf lesions.
On the eastern red cedar host, the fungus produces reddish-brown galls from 1⁄4 to 2 inches (6 to 50 mm). [3] [6] After reaching a diameter of about 1⁄2 inch (13 mm), the galls show many small circular depressions. In the center of each depression is a small, pimple-like structure. In the spring these structures absorb water during rainy periods and elongate into orange gelatinous telial horns that are 10–20 mm long. [3] The wind carries the microscopic spores to infect apple leaves, blossoms, fruit and young twigs on trees within a radius of several miles of the infected tree.
On other species of juniper more common in landscaping and bonsai, the sizes of the infections are reduced. Early in the infection, the galls are small bumps on the woody portions of the plant. They maintain the orange gelatinous form after the first warm rains of spring but generally on a greatly reduced scale.
Cedar apple rust is caused by the fungi Gymnosporangium or more specifically Gymnosporangium juniperi-virginianae that spend part of their life cycles on Eastern Red Cedars growing near orchards. The complex disease cycle of cedar apple rust, alternating between two host plants, was first delineated by Anders Sandøe Ørsted. [7]
When exposed to the first warm rain of spring, the small bumps on the galls absorb water, swell, and produce telial horns –gelatinous masses that produce teliospores. [3] When swollen, teliospores will germinate and produce basidiospores which are forcibly discharged and travel along air currents to infect apple trees and other alternate hosts. [8] The telial horns will dry out once the rain passes and will lose their gelatinous appearance, instead resembling dark brown threads. [8] When the rain returns, the horns will swell again. This process can repeat eight to ten times during the spring. [8] It can take as little as four hours for basidiospores to form inside the telial horns under optimal conditions. [8]
Wind [3] carries the spores to apple leaves at about the time that apple buds are in the pink or early blossom stage. [5] Upon reaching apple buds or leaves covered by films of water, [8] the spores attach themselves to the young leaves, germinate, and enter the leaf or fruit tissues. Light infection can take place in as little as two hours under favorable conditions. [8] Heavy infections take at least four hours to develop. [8] Lower temperatures delay infection. [8] Yellow-orange lesions develop on the upper sides of leaves or on fruit one to two weeks following infection. These lesions contain pycnia and pycniospores. [8] These lesions will produce a sticky honeydew like substance to attract insects that assist in the transport of the pycniospores to different lesions, allowing for sexual recombination. [9]
One to two months later, in July and August, orange-yellow aecia are produced in concentric rings on the bottom of the apple leaves or surrounding the pycnia on the fruit. [3] The aecia produce aeciospores. The wind carries the spores back to eastern red cedars, completing the infectious cycle. The spores land on cedar needle bases or in cracks or crevices of twigs. There, they germinate and produce small, green-brown swellings about the size of a pea. Galls do not produce spores until the second spring. However, mature galls usually are present every year. This fungus produces four out of five of the spores known to be produced by the class Urediniomycetes during its life cycle. (These include teliospores, basidiospores, spermatia (also called pycniospores, and aeciospores. The type of spore it does not produce is urediniospores.) Rust fungi have a complicated life-cycle with up to five types of spores (each borne on a different type of structure) in its life cycle and often an alternate host, and an "alternate alternate host" as well. Basidiomycetes that have all 5 spore stages and those with less are said to be "macrocyclic" or "microcyclic" respectively.
Because apples are an economically important crop, control is usually focused there. Interruption of the disease cycle is the only effective method for control of the cedar apple rust. Removing as many cedar trees within close proximity of an apple orchard will reduce potential sources of inoculum. The closer the tree to the orchard the greater impact removal will have. Removing all junipers within the 4–5 miles (6.5–8 km) would provide complete control of the disease. [10] Additionally, pruning and disposing of galls from infected cedar trees would reduce sources of inoculum for infection of apple trees, however this would likely be time consuming and uneconomical. [6] For those doing bonsai, it is common to have the trees within feet of each other and on the central eastern seaboard of the United States, eastern red cedar is a common first-growth conifer along roadsides.
There are differences in the susceptibility of various apple varieties. 'Jonathan', 'Rome Beauty', 'Wealthy', 'Stayman', 'Jonafree' and 'York Imperial' are susceptible. [11] 'Grimes Golden', 'Red Delicious', 'Winesap', 'Redfree', 'McIntosh', 'Liberty', and 'Priscilla' are resistant. [11] Crabapples are generally more susceptible than apples. Resistant crabapples include 'Adams', 'Beverly', 'Candied Apple', 'Dolgo', 'Donald Wyman', 'Eleyi', 'Inglis', 'Indian Summer', 'Liset', 'Mt. Arbor', M. persicifolia, 'Red Jewel', 'Robinson', 'Robusta', 'Royalty', M. sargentii , 'Tina', 'Snowdrift', and 'Special Radiant'. Resistant Crataegus (Hawthorn) include C. crus-galli , series Intricatae, C. laevigata , 'Autumn Glory', C. phaenopyrum , C. pruinosa , C. viridis , and 'Winter King'. The resistant varieties are less susceptible to attack, but that does not mean that they are free from an aggressive attack.
Fungicide sprays applied in a timely manner are highly effective against the rust diseases during the apple cycle. [12] Most protective fungicide sprays are applied four times at 7- to 10-day intervals, starting with pink bud on crabapples. These applications are to protect the apples from spores being released from the cedar host in mid-spring. If cedar apple rust disease is diagnosed on apple fruits and leaves it is far too late to spray. Although curative fungicides also exist for cedar apple rust, they must still be applied before trees begin to develop symptoms. [13] Systemic fungicides are available as well, which require fewer sprays during the season. [14] However, there are no fungicides available to home gardeners that can be used on trees that produce fruit which will be eaten by people. [2]
Gymnosporangium is a genus of heteroecious plant-pathogenic fungi which alternately infect members of the family Cupressaceae, primarily species in the genus Juniperus (junipers), and members of the family Rosaceae in the subfamily Amygdaloideae. The common name cedar-apple rusts has been used for these fungi. According to the Dictionary of the Fungi, there was 57 species in the genus. In 2023, Species Fungorum lists up to 74 species.
Rusts are fungal plant pathogens of the order Pucciniales causing plant fungal diseases.
Teliospore is the thick-walled resting spore of some fungi, from which the basidium arises.
Gymnosporangium clavipes is a plant pathogen, a fungus that causes cedar-quince rust. Similar to Gymnosporangium juniperi-virginianae and Gymnosporangium globosum, the fungus infects a wide range of Rosaceae, such as apple, hawthorn and quince trees, and also requires an evergreen host such as eastern red cedar or a number of other juniper species to complete its life cycle.
Gymnosporangium globosum is a fungal plant pathogen that causes cedar-hawthorn rust.
Phragmidium violaceum is a plant pathogen native to Europe, Africa, and the Middle East. It primarily infects Rubus species.
Puccinia schedonnardii is a basidiomycete fungus that affects cotton. More commonly known as a “rust,” this pathogen typically affects cotton leaves, which can decrease the quality of the boll at time of harvest. As large percentages of cotton in the United States are resistant to various rust varieties, there is little economic importance to this disease. In places where rust is prevalent, however, growers could see up to a 50% reduction in yield due to rust infection.
Puccinia asparagi is the causative agent of asparagus rust. It is an autoecious fungus, meaning that all stages of its life cycle – pycniospores, aeciospores, and teliospores – all develop upon the same host plant . Rust diseases are among the most destructive plant diseases, known to cause famine following destruction of grains, vegetables, and legumes. Asparagus rust occurs wherever the plant is grown and attacks asparagus plants during and after the cutting season. Asparagus spears are usually harvested before extensive rust symptoms appear. Symptoms are first noticeable on the growing shoots in early summer as light green, oval lesions, followed by tan blister spots and black, protruding blisters later in the season. The lesions are symptoms of Puccinia asparagi during early spring, mid-summer and later summer to fall, respectively. Severe rust infections stunt or kill young asparagus shoots, causing foliage to fall prematurely, and reduce the ability of the plant to store food reserves. The Puccinia asparagi fungus accomplishes this by rust lowering the amounts of root storage metabolites. The infected plant has reduced plant vigor and yield, often leading to death in severe cases. Most rust diseases have several stages, some of which may occur on different hosts; however, in asparagus rust all the life stages occur on asparagus. Because of this, many observers mistake the different stages of the Puccinia asparagi life cycle as the presence of different diseases. The effects of Puccinia asparagi are present worldwide wherever asparagus is being grown. Asparagus rust is a serious threat to the asparagus industry.
Puccinia helianthi is a macrocyclic and autoecious fungal plant pathogen that causes rust on sunflower. It is also known as "common rust" and "red rust" of sunflower.
Uromyces viciae-fabae var. viciae-fabae is a plant pathogen commonly known as faba-bean rust. The rust is distinguished by the typical rust-like marks on the stem and leaves, causing defoliation and loss of photosynthetic surface along with reduction in yield. The disease is fungal and is autoecious meaning it has one plant host. The rust of faba beans is macrocyclic, or contains 5 spores during its life cycle.
Gymnosporangium sabinae is a species of rust fungus in the subdivision Pucciniomycotina. Known as pear rust, European pear rust, or pear trellis rust, it is a heteroecious plant pathogen with Juniperus sabina as the main primary (telial) host and Pyrus communis as the main secondary (aecial) host.
Puccinia horiana is a species of fungus that causes chrysanthemum white rust, is a disease of plant species of the genus Chrysanthemum.
This article summarizes different crops, what common fungal problems they have, and how fungicide should be used in order to mitigate damage and crop loss. This page also covers how specific fungal infections affect crops present in the United States.
Telium, plural telia, are structures produced by rust fungi as part of the reproductive cycle. They are typically yellow or orange drying to brown or black and are exclusively a mechanism for the release of teliospores which are released by wind or water to infect the alternate host in the rust life-cycle. The telial stage provides an overwintering strategy in the life cycle of a parasitic heteroecious fungus by producing teliospores; this occurs on cedar trees. A primary aecial stage is spent parasitizing a separate host plant which is a precursor in the life cycle of heteroecious fungi. Teliospores are released from the telia in the spring. The spores can spread many kilometers through the air, however most are spread near the host plant.
Gymnosporangium clavariiforme is a species of rust fungus which alternately infects Juniperus and hawthorns.
Pine-pine gall rust, also known as western gall rust, is a fungal disease of pine trees. It is caused by Endocronartium harknessii, an autoecious, endocyclic, rust fungus that grows in the vascular cambium of the host. The disease is found on pine trees with two or three needles, such as ponderosa pine, jack pine and scots pine. It is very similar to pine-oak gall rust, but its second host is another Pinus species. The fungal infection results in gall formation on branches or trunks of infected hosts. Gall formation is typically not detrimental to old trees, but has been known to kill younger, less stable saplings. Galls can vary from small growths on branch extremities to grapefruit-sized galls on trunks.
Chrysomyxa weirii, is a fungus that causes a disease, commonly known as Weir's cushion rust, of spruce trees. It is mostly a cosmetic problem, causing yellowish spotting and banding on spruce needles, but in some cases can cause severe premature defoliation. Weir’s cushion rust can also disfigure and reduce growth of spruce trees by targeting the tender needles of newly emerging shoots. This pathogen's spores are spread by wind and water splash and germinate to infect newly developing needles on the same spruce, or neighboring spruce trees. Unlike many other rust disease pathogens, C. weirii is autoecious, only infecting spruce trees. C. weirii is also microcyclic, producing only two of the five possible spore stages common in rust fungi. Trees affected by Weir's cushion rust usually have obvious symptoms, but if treated correctly, the disease can be managed.
Phakopsora euvitis is a rust fungus that causes disease of grape leaves. This rust fungus has been seen in regions including: Eastern Asia, Southern Asia, Southwestern Brazil, the Americas, and northern Australia. It is widely distributed in eastern and southern Asia but was first discovered on grapevines in Darwin, Australia in 2001 and was identified as Asian grapevine leaf rust by July 2007.
Puccinia sorghi, or common rust of maize, is a species of rust fungus that infects corn and species from the plant genus Oxalis.
Cronartium quercuum, also known as pine-oak gall rust is a fungal disease of pine and oak trees. Similar to pine-pine gall rust, this disease is found on pine trees but its second host is an oak tree rather than another pine.
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