Pine-pine gall rust, also known as western gall rust, is a fungal disease of pine trees. This plant disease is caused by Endocronartium harknessii (asexual name is Peridermium harknessii), an autoecious, endocyclic, rust fungus that grows in the vascular cambium of the host. Pine-pine gall rust is found on pine trees (Pinus spp.) with two or three needles such as ponderosa pine, jack pine, and scots pine. The disease 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. The hosts of the aecial stage of the fungus includes two and three needled Pinus spp. The most important aecial hosts include jack pine (P. banksiana), lodgepole pine (P. contorta), western yellow pine (P. ponderosa), and the European Scots pine (P. sylvestris). A variety of other pines, such as Pinus nigra, P. mugo, P. palustris, P. banksiana, P. muricata, and P. radiata have also been reported as hosts to pine-pine gall rust (E. harknessii), but these pine species are considered less valuable. Because E. harknessii is an autoecious short-cycle rust lacking telial a host, there is no alternative hosts. The pathogen can infect actively growing shoots of any age very quickly without infecting an alternative host, making the disease cycle more destructive that typical rust species that switch between hosts. This also prevents control of the fungus by management of the alternative host species. Symptoms of pine-pine gall rust can be quite conspicuous and are useful for diagnostic identification. The most prominent symptoms are hip cankers and swollen, spherical to oblong growths (galls) on the branches, stems, or main trunk of the host. The galls on small twigs of 1–2 years of age are often pear-shaped. Gall formation results from the overproduction of xylem tissue stimulated by the fungus. Witches brooming occasionally occurs along with galling. The bark on large galls will slough off over time, exposing the smooth wood beneath. Signs of pine-pine gall rust include the pale yellow aecia (1-8mm in diameter) formed on galls in spring as well as the yellow-orange aeciospores contained within. Immature galls are spindle-shaped. Infections usually occur on more succulent (thick) branches. When mature, galls can grow as large as a softball (30.5 cm circumference), but most are the size of a golf ball (4.2 cm). Before the production of spores, the needles on highly infected branches become chlorotic or red, eventually turning brown when the branch dies. Western gall rust can cause dwarfing to occur if leader stem of younger pines are infected. Early identification of the disease is important for treatment, but is often hard to diagnose due to the inconspicuous initial symptoms and a lack of galls until the second year. A red pigmentation may develop on the epidermal galls of P. contorta seedlings 14–28 days after infection, but this is not always a reliable indicator. Pine-pine gall rust has characteristically brown to yellow-orange sori visible on large globular galls on pines. Gall formation on trunks occurs over 2–4 years and is stimulated by the pathogen, which causes cells to grow and divide quickly at the site of initial infection. When mature, the gall splits open and the yellow-orange aeciospores are dispersed and carried to new hosts by wind. Because P. harknessii does not require an alternate host, the aeciospores can infect another pine directly. This typically occurs during moist conditions and rarely infects older shoots. Infection continues on the host shoots and needles until they have reached 90% of their elongation. Gall mortality is associated with squirrel feeding or invasion and inactivation by secondary organisms. The life cycle of E. Harknessii is different from other pine stem rust in that it is autoecious, making large stands of pines ideal hosts for survival and reproduction of the fungus. Wind carries teliospores to pines shoots that then germinate under cool humid conditions, producing germ tubes with up to three side branches that act as basidia. The basidium directly penetrate the cuticle and epidermis. Other pines rusts like Cronartium ribicola and C. comandrae infect through the stomata. After penetration and establishment of a intracellular infection structure, primary hyphae are produced, infecting the epidermis and cortex intercellularly. Haustoria extend through neighboring cells and the cortex to reach the vascular cambium before the host becomes dormant follow the first infection season. The cambium is invade inwardly through the phloem and cortex, as opposed to a vertical or peripheral hyphael growth. Initiation of gall formation is through exogenous stimulation of the cambium and pith rays, causing an increased production of ray parenchyma. The host reacts by hyperplasia (increased division) providing the resources needed for further hyphae proliferation in the cortex, phloem, and cambium until the galls death. The gall will enlarge for 2 years and sporulate on the third. Spermogonia ooze from infected bark in early spring, but they are non-functional since they do not form aecia (vestigial). Dikaryotization of the haploid mycelium that produce the teliospores takes place in the outer cortex, just beneath the first periderm. They are surrounded by a membrane called a peridium that bursts, releasing the spores. Stimulation of dikaryotization is not understood, though it is likely a combination of host sap flow and environmental cues. Damp surfaces on these pine trees provide an environment conducive to spore germination; these surfaces are usually found on very young tissue of the current season's growth. The proper conditions must persist for at least 24 hours after the spore lands on its host in order to allow enough time for germination, penetration of host defenses, and establishment of the fungus. Environmental conditions conducive to infection typically occur during spring and early summer when weather is consistently cool and moist. Because of the very specific conditions required for spore germination and infection, pine-pine gall rust may not be observed in consecutive years as it is unlikely that optimal weather conditions and susceptible host tissue are both present at the time of spore release. Furthermore, infection severity is not uniform year after year. Only minor infections occur in an ordinary year, however infection may be prolific in certain years if the proper conditions occur. These years of abundant infection are termed 'wave years' and are characterized by consistent cool, wet conditions and the increased local sporulation E. harknessii. Favorable conditions for large outbreaks of pine-pine gall rust do not occur often, but when they do they can affect areas as large as an entire state. Localized outbreaks are much more common, occurring in dense even-aged stands. Good cultural practices to prevent pine-pine gall rust include removal of dense patches of grasses, weeds, and brush near susceptible trees, as they may prevent good spray coverage of the lower whorl (spiraling pattern) of branches. Severely infected trees should be rogued and burned to prevent further spread of inoculum. It is often difficult to detect infection in trees before symptoms such as stunting, chlorosis, and witch's brooming are evident. Until all diseased trees in the area are diagnosed and destroyed it is suggested that a protectant fungicide be applied to all susceptible trees in the stand. Using a registered systemic fungicide such as Bayleton (50% Dry Flowable Fungicide, EPA Reg. No. 2135-32 ) registered in California can help control western gall rust, although it is not used on seeds or seedlings and may kill mycorrhizal fungi if advised application concentration is exceeded. If trees in a commercial stand are only lightly infected it is possible to prevent an increase in galling by applying a fungicidal spray, allowing the tree to reach cutting age so that it may be harvested. Copper-based and manganese-based fungicides have proven effective in the field but the sensitivity of P. harnknessii to these fungicides has not yet been researched in a laboratory setting. It has been demonstrated that development of the rust fungus is closely synchronized with Pinus sylvestris. Spore dissemination begins when needles start to emerge from the fascicle sheaths and has finished when the needles have grown to three-quarters of their final length. This provides a basis for the timing of the application of fungicides either before or during sporulation, depending on the chemicals mode of action.