Please use this identifier to cite or link to this item: https://repositori.uma.ac.id/handle/123456789/557
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dc.contributor.authorMarpaung, Octo Pransisco-
dc.date.accessioned2017-08-01T08:15:12Z-
dc.date.available2017-08-01T08:15:12Z-
dc.date.issued2016-
dc.identifier.urihttps://repositori.uma.ac.id/123456789/557-
dc.descriptionPenelitian ini dilaksanakan di Laboratorium Universitas Medan Area (untuk uji invitro) dan untuk uji lapangan dilaksanakan di desa Durin Tonggal Ujung Bandar, Kec. Pancur Batu. Kab. Deli Serdang mulai bulan April sampai bulan Juli 2016. Penelitian di Laboratorium menggunakan Rancangan Acak Lengkap (RAL) secara Non Faktorial dengan 6 Perlakuan dan 4 Ulangan. Pada penelitian di Lapangan menggunakan Rancangan Acak Kelompok (RAK) Secara Non Faktorial dengan 6 Perlakuan dan 4 Ulangan. Pada Penelitian di Laboratorium Perlakuan Trichoderma sp ( kontrol positif ), Tanpa Trichoderma sp dan asap cair (kontrol negatif ) dan Berbagai Konsentrasi Asap Cair ( 0,5%, 1%, 1,5%, 2% per liter air). Pada penelitian di Lapangan Perlakuan Trichoderma sp ( kontrol positif ), Tanpa Trichoderma sp dan asap cair ( kontrol negatif ) dan Berbagai Konsentrasi Asap Cair ( 5ml, 10ml, 15ml, 20ml per liter air). Hasil penelitian di Laboratorium menunjukkan bahwa aplikasi asap cair tempurung kelapa dengan konsentrasi 1,5% dan 2% / liter air, memiliki kemampuan menekan pertumbuhan koloni jamur akar putih (Rigidoporus microporus) yang paling efektif. Hasil penelitian di Lapangan menunjukkan bahwa perlakuan asap cair tempurung kelapa dengan konsentrasi 15 ml dan 20 ml per liter air memiliki kemampuan meningkatkan pertumbuhan tinggi bibit karet, jumlah daun bibit karet, menekan volume akar terinfeksi dan menekan intensitas serangan pada 28 hari setelah aplikasi asap cair.en_US
dc.description.abstractThis research was conducted in Universitas Medan Area Laboratory (for invitro test) and for field test was conducted at Durin Tonggal Village Ujung Bandar, Sub-district. Pancur Batu, District. Deli Serdang from April to July 2016. Research Laboratory using Completely Randomized Design (CRD) Non Factorial with 6 treatments and 4 replications. In the field using Randomized Block Design (RBD) Non factorial with 6 treatments and 4 replications. On research in the Laboratory the treatment of the Trichoderma sp (control positive), Without the Trichoderma sp and liquid smoke (control negative) and various concentrations of the liquid smoke (0,5%, 1%, 1,5%, 2% per water liter). On researh in field the treatment of the Trichoderma sp(control positive), without the Trichoderma sp and liquid smoke (control negative) and various concentrations of the liquid smoke ( 5ml, 10 ml, 15ml, 20ml, per water liter). The results of laboratory research showed that the application of the liquid smoke of coconut shell with concentrate 1,5% and 2% of water, have the ability to suppress the growth of colonies the white root mushroom (Rigidoporus microporus) most effectively. The results of research in the field indicate that treatment of liquid smoke of coconut shell with concentrate 15 ml and 20 ml per water liter have ability to raise the high growth of rubber seeds, the amount of rubber seeds, to reduce the volume of infected root and supress the intensity of the attacks on 28th day after the application of liquid smoke.en_US
dc.language.isootheren_US
dc.publisherUniversitas Medan Areaen_US
dc.subjectasap cairen_US
dc.subjecttempurung kelapaen_US
dc.subjectrigidoporus microporusen_US
dc.subjecthevea brasiliensisen_US
dc.subjectthe liquid smokeen_US
dc.subjectcoconut shellen_US
dc.titleAplikasi Asap Cair Limbah Tempurung Kelapa untuk Menekan Pertumbuhan dan Perkembangan Jamur Akar Putih (Rigidoporus microporus) pada Okulasi Bibit Karet (Hevea brasiliensis)en_US
dc.typeThesisen_US
Appears in Collections:SP - Agricultural Technology

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128210061_file1.pdfCover163.8 kBAdobe PDFView/Open
128210061_file2.pdfAbstract133.01 kBAdobe PDFView/Open
128210061_file3.pdfIntroduction209.75 kBAdobe PDFView/Open
128210061_file4.pdfChapter I135.14 kBAdobe PDFView/Open
128210061_file5.pdfChapter II225.87 kBAdobe PDFView/Open
128210061_file6.pdfChapter III248.32 kBAdobe PDFView/Open
128210061_file8.pdfReference615.65 kBAdobe PDFView/Open


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