KR0151504B1 - Disease control agent for useful gramineous plants and control method - Google Patents

Abstract

In the pest control method of rice family plants containing microorganisms belonging to the genus Exerohirum which has a disease control function against rice plants and plants, and the pest control method of rice plants used to treat this pesticides plants It is about.

Description

[Name of invention]

Disease Control and Control Methods of Rice Plants

Technical Field of the Invention

The present invention relates to a pest control agent and a method for controlling rice plants using the microorganism belonging to the genus Exerohirum.

Background of the Invention

Since the blast is a very frequent and susceptible disease, one to three or four sprays of fungicide are required every year.

However, recently, due to the problem of environmental pollution caused by chemical pesticides, the development of a control agent for crop pests that is not chemical pesticides and the method of using the same are desired.

So, it was conceived to control crop diseases using microorganisms, but the means can be divided into two.

The first method is to induce rice disease resistance by inoculating rice cultivars that show incompatibility with rice varieties to control rice blasts. Such methods include, for example, the method described in Dofu-ku Agricultural Test Extension Report No. 75, pages 27 to 39 (1987), and the Japanese Society of Plant Pathology, Vol. 56, No. 2, pages 273 to 275 (1990). Another method is to induce rice disease resistance by inoculating rice isolates with weak pathogenicity against rice and to control blast diseases.

For example, the method for writing Nihon Pest Research Bulletin No. 30, pages 53 to 55 (1979).

Another method is to control microorganisms that exhibit antagonistic action against septic bacteria.

Such methods include, for example, the method described in Japanese Society of Plant Pathology, Vol. 58, No. 3, pages 380-385 (1992), Japanese Laid-Open Patent Publication No. 2-35076, Japanese Laid-Open Patent Publication No. 5-65209. .

[Problems that the invention tries to solve]

However, there is a problem in the method of inducing disease resistance by the above-mentioned non-affinity heat germ. In other words, since the affinity property is a relative property between a race of a pathogen and a variety of crops, some races may show affinity for other varieties even if they are not affinity for some varieties. For this reason, the method of spreading rice fever bacteria on rice field has a risk of developing fever in varieties showing affinity. Among them, where a variety of different varieties are cultivated, the presence of affinity rice varieties increases the likelihood of blast disease. Moreover, since non-affinity may change into affinity, there exists a danger that the bacteria which show affinity may mix in the bacterium which shows spreading affinity.

Helminthos Porium or Yzae (Bipolaris oryzae) exhibits a very high control effect of bleeding disease by inducing disease resistance by the bacteria isolated from rice.

In general, a method of using a microorganism that exhibits an antagonistic action against the heat-resistant bacterium is often low in control effect. For example, in the method described in Japanese Society of Plant Pathology Vol. 58, No. 3, the control effect on the blast disease is only about 50%. In addition, the microorganisms used in this method are often pathogens of useful plants and there is a risk of harm to other useful crops. For example, Japanese Patent Application Laid-Open No. 2-35076 uses Gradiolas soft bacteria, and Japanese Patent Application Laid-open No. 5-65209 uses rice seedlings.

For the above reasons, the method of controlling crop diseases using microorganisms is rarely used despite the high social demand.

It is an object of the present invention to provide a means for controlling crop diseases, including thermal diseases, without affecting the growth of useful plants in view of such a phenomenon.

[Initiation of invention]

According to the present invention, as a result of repeated studies on weed pathogens that did not affect the growth of useful plants, strains belonging to the genus Exerohilum SPP, which is a wild-blood pathogen, have a high control effect against rice plants. The present invention was found by completing the description.

In other words, the first of the present invention is a pest control plant of rice plants and plants, characterized in that it contains microorganisms belonging to the genus Serohirum having a disease control ability against rice plants and plants as an active ingredient. The microorganisms belonging to the genus Exerohirum include Exserohilum monoceras, and the preferred strains are Exerohirum monoceras B026 strain, Exerohirum monoceras B276 strain, Exerohirum monoceras strain. B232 shares, 263 shares of excellence room, Monoceras, Ex2 accompaniment room, Monoceras B267 share, Excellence rooms, Monoceras JTB-159 share, Exoces room, Monoceras JTB-215 share, Exocera room Monoceras JTB -240 shares, Exero Hirum Monoceras JTB-264, Exero Hirum Monoceras JTB-277, Exero Hirum Monoceras JTB-281, Exero Hirum Monoceras JTB-673, Exero Hirum monoceras JTB-674 share, exerohirum monoceras JTB-675 share, exerohirum monoceras JTB-676 share, exerohirum monoceras JTB-677 share, exerohirum monoceras JTB- There are 678 shares, Exerohirum Monoceras JTB-679, Exerohirum Monoceras JTB-680.

In addition, the second aspect of the present invention is a pest control method of rice plants and plants, characterized in that the microorganisms belonging to the genus Exserohilum having a pest control ability against rice plants and plants is treated with rice plants. In addition, the third of the present invention is exercerorum monoceras B026, exercerorum monoceras B276 strains, exocerium monoceras B232 strains, exercerorum monoceras 263 strains, exerohirum monoceras B267 Note, excellorum monoceras JTB-159 note, exocrome room monoceras JTB-215 note, exocerum room monoceras JTB-240 note, exocerum room monoceras JTB-264 note, exerohirum Monoceras JTB-277 shares, Exerohirum monoceras JTB-281 shares, Exerohirum monoceras JTB-673 shares, Exerohirum monoceras JTB-674 shares, Exerohirum monoceras JTB-675 shares , Vertical room monoceras JTB-676 share, excello room monoceras JTB-677 share, excellerum room monoceras JTB-678 share, exocerome room monoceras JTB-679 share, exerohirum monoceras JTB-680 strain was selected from the bacterium.

Hereinafter, the present invention will be described in detail.

The microorganism used in the present invention is not particularly limited as long as it is a microorganism belonging to the genus Exerohirum. Preferably, the microorganism belonging to Exerohirum monoceras is used. Moreover, as a preferable strain, Exerohirum Monoceras B026 strain, Exerohirum Monoceras B276 strain, Exerohirum monoceras B232 strain, Exerohirum monoceras 263 strain, Exerohirum monoceras B267 strain, Ex Vertical room monoceras JTB-159 share, excello room monoceras JTB-215 share, excellerum room monoceras JTB-240 share, exocerome room monoceras JTB-264 share, exerohirum monoceras JTB -277 shares, Exero Hirum Monoceras JTB-281 shares, Exero Hirum Monoceras JTB-673 shares, Exero Hirum Monoceras JTB-667 shares, Exero Hirum Monoceras JTB-675 shares, Exero Hirum Monoceras JTB-675 shares Hirum monoceras JTB-676 shares, exerohirum monoceras JTB-677 shares, exerohirum monoceras JTB-678 shares, exerohirum monoceras JTB-679 shares, exerohirum monoceras JTB- 680 etc. can be mentioned.

These strains are deposited in the numbers as shown below, respectively, at the Japan Institute of Industrial Technology and Biotechnology Industrial Technology Research Institute. Exerohirum Monoceras B026 Note: FERM BP-4215 (March 5, Year of Declaration) Exerohirum Monoceras B276 Note: FERM BP-4220 (Mar. 5 Year of Declaration, May 5) Exerohirum Monoceras B232 Note: FERM BP-4217 (March 5, Year of Declaration) Exerohirum Monoceras 263 Note: FERM BP-4218 (Mar. 5 Year of Declaration) Exerorum and Monoceras B267 Note: FERM BP-4219 (March 5, year 5) Exerorum and Monoceras JTB-159 Note: FERM BP-4812 (October 6, October 3, 6) Exerohirum Monoceras JTB-215 Note: FERM BP-4813 (October 3, June 6, Expository Room) Monoceras JTB-240 Note: FERM BP-4814 October 3, 2013) Exero Hirum Monoceras JTB-264 Note: FERM BP-4815 (October 3, 6, June 6) Exero Hirum Monoceras JTB-277 Note: FERM BP-4816 Deposition day, October 3, 6) Exerorum and Monoceras JTB-281 Note: FERM BP-4817 ( Deposition day, October 3, 6 years) Exerorum and Monoceras JTB-673 Note: FERM BP-4915 (December 8, year 6) Exerorium and Monoceras JTB-674 Note: FERM BP -4916 (December 8, December 8) Exerohirum Monoceras JTB-675 Note: FERM BP-4917 (Dec 8, August 6) Exerohirum Monoceras JTB-676 Note: FERM BP-4918 (December 8, December 8) Exerorium / Monoceras JTB-677Note: FERM BP-4919 (Dec 8, December 6) CERA JTB-678 Note: FERM BP-4920 (December 8, June 8) Exerohirum Monoceras JTB-679 Note: FERM BP-4921 (Dec 8, December 6) Cerro Hirum Monoceras JTB-680: FERM BP-4922 (December 8, 6, June, 6).

These strains were isolated from two weeds, and their microbial properties are as follows.

Colonies are aerobic green or black on aerobic bacteria and lower lichen potatoes. You may also see white or gray donated mycelia. Conidia (dark conidia) are dark, multi-foam, with 2 ~ 8 partition walls, fusiform, very wide in the center, tapered to both sides. The navel is also protruding at the proximal end.

The size of conidia is about 40-150x10-25 micrometers.

`` GRAMINICOLOUS SPECIES OF BIPOLARIS.CURVULARIA, DRECHSLERA, EXSEROHILUM AND THEIR TELEOMORPHS '' by A.SIVANESAN (Mycological papers, No 158 P-211. Exerohirum monoceras of the above strains, for example, because of the same shape of the shape congeners of colonies, as investigated in the two documents of the scientific name of the bacterium group (Plant Protection Vol. 32, No. 32, No. 361-368,1978). (Exserohilum monoceras).

The genus of the genus Exerohirum is based on the classification of Ueyama, Tsuda, Nashihara and A.SIVANESAN. LUTTRELL (Revue de Mycologie 41, 271-279,1977) and ALCORN (Mycotaxon 8, 411-414, 1978) also support this taxonomy. Ellis (Dematioceous Hyphomycetes, CMI, Kew, 608 1971) includes the genus Draxra, which includes genera and bipolaris in Drechslera. However, there is no researcher other than ELLis who did not recognize the genus Exerohirum and Non-Polaris. Moreover, since it is known that the complete generation of the genus Exerohirum is the genus Setosphaeria, the microorganisms classified as genus cetospaeria are also included in the technical scope of the present invention.

It is not necessary to use a special method for culturing the strains of the genus Exerohirum, the same method as the known strain belonging to the genus Exerohirum can be used.

As the medium, any medium can be used as long as it is a medium containing a magnetizable carbon source, nitrogen source, inorganic matter and necessary growth promoting substances.

Examples of specific medium include auto milled agar medium, auto milled agar medium, agar medium per potato lower liquor, v-8 juice agar medium, tourpep agar agar medium, and the like. Preferably it is 15-28 degreeC, Preferably it is 20-25 degreeC, It is desirable to keep PH at 3-9, Preferably it is 5-8.

When cultured for about 7 to 14 days under the above conditions, a sufficient amount of conidia is formed on the surface of the medium.

When the strain is used for the control method, microbial cells (conidia, spores of the spores, mycelia, etc.) are used, but preferably the conidia produced by the strain are used. The conidia can be recovered by injecting sterile water into the flora and scraping the surface of the media with a pencil. By this method, 1 × 10 ⁷ -10 ⁸ conidia can be obtained per sheet of 9 cm diameter.

The pest control agent of the present invention may be used directly as a microorganism, but generally mixed with a solid carrier or a liquid carrier that can be used in agrochemicals, and adjusted to a formulation form such as a liquid, a hydrating agent, a powder, a granule, an emulsion and a capsule. .

As microorganisms, conidia are usually used. Conidia concentration party is when the liquid 10 ^{3-10 7} to / ㎖, it is advisable preferably to a 10 ⁴ ~10 ⁶ / ㎖.

In the case of treatment to the actual packaging, it is desired to treat such that the number of microorganisms of microorganisms per package 10 days is 10 ⁸ to 10 ¹² , preferably 10 ⁹ to 10 ¹¹ .

Examples of the disease to be controlled in the present invention include rice plant diseases such as rice fever, rice leaf disease, rice leaf disease, rice leaf disease, corn leaf disease, corn black water disease, corn's moon disease, and various black water bottles of barley.

EXAMPLE

Example 1

Selection of B026 shares B232 shares B263 shares B267 shares B276 shares

After weeding diseased weeds from all over Japan and separating pathogens from the lesions, we investigated the control effect against rice fever by the following method.

Weed pathogens were treated with healthy rice (cultivar Koshihikari) and inoculated with rice plants with affinity for this rice after a certain period of time in the greenhouse. About 1 month later, the disease index of blast disease was assessed in a more effective way, and the more effective wild blood pathogens (B026, B276, B232, B263, B267, JTB-159, JTB-215, JTB-240, JTB-264, JTB-277, JTB-676, JTB-673, JTB-678, JTB-675, JTB-281, JTB-677, JTB-674, JTB-679, JTB-680).

Example 2

Control Effects of Rice Fever in 19 Strains of Wild Blood Pathogens

Seeds of rice (breed Koshihikari) were seeded in a pot of 10000 grains, and grown in a greenhouse for about 4 weeks, and then a 1% aqueous yuan solution was given as a fertilizer. About one week later, the rice was left standing in the greenhouse and the six-leaf rice was used for the control effect test.

Nineteen strains of wild-blood pathogens shown in Table 2 were incubated at 25 ° C. for 2 weeks on auto-milled sucrose medium to form conidia. The conidia were suspended in an aqueous solution of 0.02% Tween 20, and then a suspension of 10 ⁵ or 10 ⁶ conidia / ml was prepared to be a treated solution. The conidia suspension was placed in a rice paddy using a sprayer for 1 ml per rice, and then placed in an inoculation phase kept at 25 ° C. and 100% humidity for 20 hours.

Each port was also treated with three ports.

After standing in the greenhouse for 2 days, spray inoculation (1 ml per port) of conidia suspension (10 ⁵ conidia / ml 0.02% Tween 20 solution) of Pyricularia oryzae race007 showing affinity for Koshihikari It was left for 20 hours in the inoculation phase held at 25 ° C and 100% humidity.

After one week of inoculation, the number of germ pathogens per leaf of the sixth leaf was examined, and the control value was calculated by the formula shown below.

As shown in Table 1, it was recognized that certain strains had a high heat control effect.

Example 3

Persistence of Control Effects of Rice Fever

Seeds of rice (breed Koshihikari) were sprinkled on a pot of 1/1000 eggs and grown in a greenhouse for about 3 weeks, and then a 1% aqueous solution was applied as a fertilizer. In addition, rice was allowed to stand at room temperature for about 1 week, and rice of 4 and 5 leaves was used for the control effect test.

B026 strains of wild-blood pathogens were cultured on oatmeal sucrose for two weeks and conidia formed.

The conidia were suspended in sterile water containing 0.02% Tween80 and then 10 Or 10 A conidia / ml suspension was prepared to obtain a treatment liquid. The conidia suspension was sprayed with rice 2 ml per pot using a nebulizer and placed in an incubation box kept at 25 ° C. and 100% humidity for 18 hours. Each port was treated with 2 ports. Conidia suspension of rice fever bacteria showing affinity for Koshihikari for 2, 3 or 9 days in a greenhouse (10 Conidia / ml, .02% Tween 80 aqueous solution) After spraying inoculation (1 ml per pot), the cells were placed in an incubation box kept at 25 ° C and 100% humidity for 18 hours.

About one month after the inoculation, the disease index of the blast disease was assessed by the evaluation of the disease score (healthy, with the complete test being 100, and the degree of growth of the plants, etc.) and the control value was calculated by the formula shown below.

Control Price (%) = (1-treated disease pest index / no-treated disease pest index) × 100

As shown in Table 2, a high control effect against rice fever was recognized in the test treated at any concentration or in the liver after treatment with wild blood pathogens.

Example 4

Control Effect of Rice Fever by Seedling Treatment.

Seeds of rice (breed Koshihikari) were sown on seedlings (12 × 12 × 3 cm), and then grown in greenhouses. JTB-277 Caution Conidia Suspension 10 Or 10 Conidia / ml (0.02% Tween20 aqueous solution) was sprayed on rice and left for 20 hours in the incubation phase maintained at 25 ° C. and 100% humidity. After standing in the greenhouse for seven days, five pieces were transplanted into a pot of 10000 eggs which had been put into the faucet state.

Bacteria showing affinity for Koshihikari, which reached about 5 leaf stages after 14 days of transplantation, were placed for 18 hours in the inoculation phase at 25 ° C and 100% humidity after inoculation. Seven days after the inoculation, the average number of lesions per leaf of the fifth leaf was examined, and control was calculated by the formula shown below. As a result, as shown in Table 3, the high control effect against rice fever was obtained by the seedling treatment of the disease control agent of this invention.

Control value (%) = (average number of lesions in 1-treatment / average number of lesions in untreated) x 100

Example 5

Control effect of rice febrile fever by foliage treatment A total of 12 test zones of 4m2 and 3 repetitions (test zones I to IV) for 1 week 4㎡ and 3 repetitions were placed on a machine- transplanted package of rice seedlings (cultivar Koshihikari). Did together

Conidia concentration 10 Condenser / ml JTB-678 main suspension (0.02% Tween20 aqueous solution) was used in a pressurized compact sprayer at a rate of 100 liters per 10 tablets. Three spraying treatments were carried out in old III and four spraying treatments in test IV.

After the leaf was completely developed, the incidence rate of the foliar fever in each of the 24 test zones was examined, and the control value was calculated by the following formula. In addition, 2 weeks prior to harvesting, the incidence of all the wood fever in each of the eight test zones was examined by degree, and the control value was calculated by a commonly used formula shown below. As a result, as shown in Table 4, by the foliage treatment of the disease control agent of the present invention, a high control effect was obtained against leaf fever and neck fever.

Test Ⅰ: Treated with rice at 5-7 leaf

Test Ⅱ: Treatment of 5-7 leaf and 8-9 leaf

Test Ⅲ: Treatment of 5-7 leaf, 8-9 leaf and 10-11 leaf

Test IV: 5-7 leaf, 8-9 leaf, 10-11 leaf and 11-12 leaf

Example 6

The control effect of rice blight by rice ear treatment (cultivar Kori Kari) was set up in a 4 ㎡, 3 repeat test zone on a machine-grafted package, and cultivation management was carried out as usual. Conidia concentration 10 Conidia / ml JTB-159 strain suspension was sprayed once on the ear of rice and sprayed at a rate of 100 liters per 10 grains using a pressurized small atomizer. As in Example 5, the degree of incidence was calculated by investigating the incidence of all woody fever by 8 weeks before 2 weeks of harvesting, and the high control effect on woody fever by ear treatment of the pesticide of the present invention as shown in Example 5 Was obtained.

Example 7

Control Effect of Rice Leaf Disease

Seeds of rice (cultivar Koshihikari) were sown in one thousandth pot and grown in a greenhouse, and rice of 4 and 5 leaves was used for the control effect test. Conidia suspension of JTB-679 and JTB-680 strains (0.02% Tween20 aqueous solution) 10 Or 10 The conidia / ml were sprayed on rice and left for 20 hours in the inoculation phase kept at 25 ° C. and 100% humidity.

After standing in the greenhouse for 1 day, it was spray-inoculated with Bipolaris aryzae and left for 20 hours in the inoculation phase kept at 25 ° C. and 100% humidity. Seven days after the inoculation, the average number of leaves per leaf was examined and the control value was calculated by the formula shown in Example 4. As shown in Table 6, the disease control agent of the present invention controlled the occurrence of rice leaf disease.

[Example]

Preparation Example 1 (Liquid)

Conqueror (2 × 10) Dog) Tween 80 (4 g) was added to 20 L of sterile water and mixed to prepare a liquid. This liquid was sprayed into one paddy field in which heat generation was expected to occur.

Preparation Example 2 (Hydrating Agent)

Conidia per 1 ml of maltose 9%, cray 1%, water 90% (JTB-680) 10 Suspended the dog. After drying this, the dried product was mixed and ground to adjust the hydrating agent.

Preparation Example 3 (Hydrating)

Conidia per 1 ml of lactose 9%, zeolite 1%, water 90% (B263) 10 Suspended the dog. After air drying, the dried product was mixed and ground to adjust the hydrating agent.

Preparation Example 4 (Hydrating)

Conidia per 15 g of diatomaceous earth, 77% kaolin, 8% polyoxyethylene alkylphenyl ether (JTB-674) 10 Suspended the dog. After drying it, the dried product was mixed and ground to adjust the hydrating agent.

Preparation Example 5 (Hydrating)

Conidia per 33 ml of diatomaceous earth, 0.33% of carboxymethylcerose, 66.67% of water (JTB-159) 10 Suspended the dog. After air drying, the dried product was mixed and ground to adjust the hydrating agent.

Preparation Example 6 (powder)

Conidia per 1 g mixture of 14% Haridoxyprophyl-β-cyclodextrin, 12% white carbon, 74% cray (B-276 strain) 10 Mixed dogs. The powder was adjusted by grinding it uniformly after drying.

Preparation Example 7

Conidia per 1 g mixture of 15% β-cyclodextrin, 2% starch, 18% bentonite, 36% calcium carbonate and 29% water (JTB-281) After the addition of dogs, the granules were adjusted by assembling and drying the granulator.

Preparation Example 8 (Emulsion)

Conidia per 1 g of a mixture of 18% polyoxyethylene nonylphenyl ether ammonium phosphate, 6% polyoxyethylene nonylphenyl ether, triethyl phosphate and 47% tributyl phosphate (JTB-675) 10 Dogs were added to uniformly suspend and adjust the emulsion.

Preparation Example 9 (Emulsion)

Conidia (JTB-277 strain) 10 ml in a mixed solution of 95% of Stindle oil, 4% castor oil, and 1% silicone oil. The dog was suspended to adjust the emulsion.

Preparation Example 10 (Dry Pro Able Product)

Conidia (JTB-215) 10 ml of alkynebenzenesulfonate 12%, polyethylene glycol ether 88% composition The dog was suspended to adjust the dry probable agent.

Preparation Example 11 (Capsules)

Sodium alginate 0.7%, kaolin 5%, glycerin 15%, water 79.3% Conidia in 1 ml mixed solution (JTB-679) 10 The dog was suspended and added dropwise into a 0.2 mol calcium acetate solution to obtain a capsule product. After this, the capsules were filtered and air dried to prepare a capsule.

Preparation Example 12 (Capsule)

Conidia (JTB-678) 10% in sodium alginate 0.7%, diatomaceous earth 5%, glycerine 15%, water 73.3% mixture The dog was suspended and added dropwise into a 0.2 mol calcium chloride solution to obtain a capsule product. After this, the capsules were filtered and air dried to prepare capsules.

[Effects of the Invention]

The present invention provides a novel disease control and control method of rice and useful plants. Since the control agent and the control method of the present invention use weed pathogens, there is no fear of environmental pollution, and there is no adverse effect on useful plants like conventional microbial control agents. In addition, the control agent of the present invention can control rice and useful plants by one treatment, and at the same time exhibited a control effect against diseases occurring in all growing stages of rice and useful plants. Therefore, it is extremely useful industrially.

Claims (5)

A pest control agent of rice and useful plants, which contains as a active ingredient a microorganism belonging to the genus Exscrohilum having a pest control ability against rice and useful plants The microorganism belonging to the genus Obedient plant according to claim 1, wherein the microorganism belonging to the genus Exserohilum, which has a pesticidal activity against the endemic plant, is Exerohilum monoceras. The Exerohilum monoceras according to claim 2 is composed of Exerohilum monoceras, B026 strains, Exerohirum monoceras B276 strains, Exerohirum monoceras B232 strains, Exerohirum monoceras strain 263 strains. , Excellent Room Monoceras B267, Excellent Room Monoceras JTB-159, Excellent Room Monoceras JTB-215, Excellent Room Monoceras JTB-240, Excellent Room Monoceras JTB -264 shares, Exo Hirum Monoceras JTB-277, Exo Hirum Monoceras JTB-281, Exo Hirum Monoceras JTB-673, Exo Hirum Monoceras JTB-674 Hiroom Monoceras JTB-676, Exocyrum Monoceras JTB-675, Exocyrum Monoceras JTB-677, Exocyrum Monoceras JTB-678, Exocyrum Monoceras JTB- A pesticide for rice and useful plants, characterized in that it is a monarch selected from the crowd consisting of 679 shares, Exerohirum monoceras JTB-680 shares. A method for controlling pests of rice and useful plants, characterized by treating microorganisms belonging to the genus Exserohilum, which has the ability to control pests against rice plants. Exo Hiro Room Monoceras B026, Exo Hiro Room Monoceras B276, Exo Hiro Room Monoceras B232, Exo Hiro Room Monoceras B267, Exo Hiro Room Monoceras B267, Exo Hiroroom Monono Cera JTB-159, Exocerum Monoceras JTB-215, Exocera Himonos JTB-240, Exocera Himonos JTB-264, Exocera Himonos JTB-277, Exerohirum Monoceras JTB-281, Exerohirum Monoceras JTB-673, Exerohirum Monoceras JTB-674, Exerohirum Monoceras JTB-675, Exerohirum Monoceras JTB-676 Week, Exocrome Room Monoceras JTB-677 Week, Exocrome Room Monoceras JTB-678 Week, Exocrome Room Monoceras JTB-679 Week, Exocrome Room Monoceras JTB-680 Share Monarch selected from