CA1064823A - Procede de traitement des graines - Google Patents

Procede de traitement des graines

Info

Publication number: CA1064823A
Authority: CA; Canada
Prior art keywords: active ingredient; composition according; compound; seed; formula
Prior art date: 1975-06-06
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA254,104A

Other languages

English (en)

Inventor

Asbjorn Baklien

Alexander Serban

Keith T. Alcock

Richard B. Warner

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Orica Ltd

Original Assignee

ICI Australia Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1975-06-06

Filing date

1976-06-04

Publication date

1979-10-23

1976-06-04 Application filed by ICI Australia Ltd filed Critical ICI Australia Ltd

1979-10-23 Application granted granted Critical

1979-10-23 Publication of CA1064823A publication Critical patent/CA1064823A/fr

Status Expired legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 14
239000000203 mixture Substances 0.000 claims abstract description 35
150000001875 compounds Chemical class 0.000 claims abstract description 33
125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
239000001257 hydrogen Substances 0.000 claims abstract description 7
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 5
238000009331 sowing Methods 0.000 claims abstract description 4
125000001246 bromo group Chemical group Br* 0.000 claims abstract description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 3
125000001153 fluoro group Chemical group F* 0.000 claims abstract description 3
125000001475 halogen functional group Chemical group 0.000 claims abstract description 3
125000002346 iodo group Chemical group I* 0.000 claims abstract description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 3
125000000217 alkyl group Chemical group 0.000 claims abstract 2
239000004480 active ingredient Substances 0.000 claims description 24
-1 bromo, iodo Chemical group 0.000 claims description 13
230000000855 fungicidal effect Effects 0.000 claims description 8
125000000547 substituted alkyl group Chemical group 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
150000002431 hydrogen Chemical group 0.000 claims 1
125000004435 hydrogen atom Chemical class [H]* 0.000 abstract description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 2
241000233866 Fungi Species 0.000 description 7
201000010099 disease Diseases 0.000 description 6
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
239000000843 powder Substances 0.000 description 6
235000013339 cereals Nutrition 0.000 description 5
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
241000209140 Triticum Species 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
229940042396 direct acting antivirals thiosemicarbazones Drugs 0.000 description 4
210000003254 palate Anatomy 0.000 description 4
238000011282 treatment Methods 0.000 description 4
235000021307 Triticum Nutrition 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
241000722133 Tilletia Species 0.000 description 2
241000031845 Tilletia laevis Species 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000009472 formulation Methods 0.000 description 2
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000007787 solid Substances 0.000 description 2
241000894007 species Species 0.000 description 2
239000000375 suspending agent Substances 0.000 description 2
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
RSZXXBTXZJGELH-UHFFFAOYSA-N 2,3,4-tri(propan-2-yl)naphthalene-1-sulfonic acid Chemical class C1=CC=CC2=C(C(C)C)C(C(C)C)=C(C(C)C)C(S(O)(=O)=O)=C21 RSZXXBTXZJGELH-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
CBQDTCDOVVBGMN-UHFFFAOYSA-N 2-methyl-3-octylphenol Chemical compound CCCCCCCCC1=CC=CC(O)=C1C CBQDTCDOVVBGMN-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
235000006491 Acacia senegal Nutrition 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000416162 Astragalus gummifer Species 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
240000002329 Inga feuillei Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
239000005949 Malathion Substances 0.000 description 1
239000005802 Mancozeb Substances 0.000 description 1
241000700159 Rattus Species 0.000 description 1
102400000830 Saposin-B Human genes 0.000 description 1
101800001697 Saposin-B Proteins 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000005843 Thiram Substances 0.000 description 1
241000722093 Tilletia caries Species 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
229920001938 Vegetable gum Polymers 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
125000001931 aliphatic group Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
PVTHIYCCXJJALA-UHFFFAOYSA-N aminoazanium;thiocyanate Chemical compound [NH3+]N.[S-]C#N PVTHIYCCXJJALA-UHFFFAOYSA-N 0.000 description 1
229920005550 ammonium lignosulfonate Polymers 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
238000000498 ball milling Methods 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
239000000969 carrier Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 description 1
201000006747 infectious mononucleosis Diseases 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
229960002809 lindane Drugs 0.000 description 1
239000007788 liquid Substances 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
229960000453 malathion Drugs 0.000 description 1
239000000463 material Substances 0.000 description 1
229940100892 mercury compound Drugs 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
244000052769 pathogen Species 0.000 description 1
239000000047 product Substances 0.000 description 1
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
238000004088 simulation Methods 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
150000003584 thiosemicarbazones Chemical class 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CA254,104A 1975-06-06 1976-06-04 Procede de traitement des graines Expired CA1064823A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
AUPC190875		1975-06-06
AUPC299275		1975-08-29

Publications (1)

Publication Number	Publication Date
CA1064823A true CA1064823A (fr)	1979-10-23

Family

ID=25642087

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CA254,105A Expired CA1064824A (fr)	1975-06-06	1976-06-04	Procede de traitement des graines
CA254,104A Expired CA1064823A (fr)	1975-06-06	1976-06-04	Procede de traitement des graines

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
CA254,105A Expired CA1064824A (fr)	1975-06-06	1976-06-04	Procede de traitement des graines

Country Status (2)

Country	Link
CA (2)	CA1064824A (fr)
FR (1)	FR2312957A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN104351231A (zh) *	2014-10-11	2015-02-18	中国农业大学	4-氯肉桂醛缩氨基硫脲在防治植物病害中的应用

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN103694155A (zh) *	2012-09-27	2014-04-02	中国农业大学	新型取代苯丙(烯)醛缩氨基硫脲类化合物及其作为农用杀菌剂的应用

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE874904C (de) *	1944-07-14	1953-04-27	Bayer Ag	Verfahren zur Herstellung von Thiosemicarbazonen

1976
- 1976-06-04 CA CA254,105A patent/CA1064824A/fr not_active Expired
- 1976-06-04 CA CA254,104A patent/CA1064823A/fr not_active Expired
- 1976-06-04 FR FR7617154A patent/FR2312957A1/fr active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN104351231A (zh) *	2014-10-11	2015-02-18	中国农业大学	4-氯肉桂醛缩氨基硫脲在防治植物病害中的应用

Also Published As

Publication number	Publication date
FR2312957A1 (fr)	1976-12-31
CA1064824A (fr)	1979-10-23
FR2312957B1 (fr)	1980-08-29

Publication	Publication Date	Title
EP0236272B1 (fr)	1991-06-12	Utilisation comme fongicide d'un dérivé de cyanopyrolle
HU222444B1 (hu)	2003-07-28	Tiofénkarboxamid-származék és alkalmazása növények torzsgomba betegségének kezelésére
HU220370B (hu)	2002-01-28	Szinergetikus fungicid hatóanyag-kombinációk
RU2040900C1 (ru)	1995-08-09	Фунгицидное средство
JPH01151546A (ja)	1989-06-14	Ｎ−フェニルアルキルベンズアミド抗菌剤
US3034949A (en)	1962-05-15	Fungicidal composition comprising chlorophenol mercury sulfate and tetramethlthiuram isulfide
CA1064823A (fr)	1979-10-23	Procede de traitement des graines
JPH01157964A (ja)	1989-06-21	殺菌性ピリジルシクロプロパンカルボキサミジン
RU2058077C1 (ru)	1996-04-20	Фунгицидная композиция для защиты растений
JPH07277909A (ja)	1995-10-24	殺菌剤組成物
US4164582A (en)	1979-08-14	Synergistic fungicidal compositions
CH643537A5 (de)	1984-06-15	2-(propargyloxyimino)-1,7,7-trimethyl-bicyclo(2.2.1)heptan.
JP2916736B2 (ja)	1999-07-05	種子消毒剤
US6228883B1 (en)	2001-05-08	Seed treatment fungicides for control of plant diseases
US2758053A (en)	1956-08-07	Method of controlling fungi on plants and seeds with benzoyl phenyl hydrazines
JP3463976B2 (ja)	2003-11-05	殺菌・殺カビ性活性化合物の組み合わせ剤
EP3518673A1 (fr)	2019-08-07	Procédé de fabrication de compositions insecticides et compositions insecticides comprenant du chlorhydrate de thiocyclam
SU519109A3 (ru)	1976-06-25	Фунгицидное средство
US4000290A (en)	1976-12-28	Fungistatic composition for treating seeds using a mixture of a substituted benzimidazole and 2-(thiocyanomethylthio)-benzothiazole
US3328155A (en)	1967-06-27	1-nitro-3-nitrosobenzene and derivatives thereof as herbicides
US3272695A (en)	1966-09-13	Vinyl-sulphonic acid ester fungicides
SU849976A3 (ru)	1981-07-23	Фунгицидоинсектицидное средство
JPH05155718A (ja)	1993-06-22	種子消毒剤
US4301158A (en)	1981-11-17	N-(2-Propynyl)-2,6-dinitro-benzenamine derivatives
US2839444A (en)	1958-06-17	Fungicidal composition comprising 2, 4, dinitrofluorobenzene and methods of using same

CA1064823A - Procede de traitement des graines - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=25642087

Family Applications (2)

Family Applications Before (1)

Country Status (2)

Cited By (1)

Families Citing this family (1)

Family Cites Families (1)

Cited By (1)

Also Published As

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