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MATING BEHAVIOUR OF CROCIDOLOMIA PAVONANA F. Purwatiningsih Purwatiningsih; Mirza Devara
UNEJ e-Proceeding 2016: Proceeding The 1st International Basic Science Conference
Publisher : UPT Penerbitan Universitas Jember

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Abstract

The sequence and duration of mating behaviour Crocidolomia pavonana were observed and investigated by using ethogram time budgets. This research was conducted in the dark hours from 18:00 pm to 06.00 am. The results showed that C. pavonana mating behaviour consists of calling behaviour , courtship behaviour, copulation and oviposition behaviour. Behaviour of copulation was dominated among other behaviour. It took about 48% of on all mating steps behaviour. However, the frequency of the calling leaded by 70.8 times among other behaviour.
Distribusi dan Frekuensi Alel Golongan Darah Sistem ABO dan Rhesus pada Penduduk Pulau Gili Ketapang Probolinggo Kirana Eka Rezki; Rike Oktarianti; Hidayat Teguh Wiyono; Purwatiningsih Purwatiningsih
Jurnal Ilmiah Biosaintropis (Bioscience -Tropic) Vol 7 No 1 (2021): Agustus 2021
Publisher : Fakultas Matematika & Ilmu Pengetahuan Alam - Universitas Islam Malang

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (461.049 KB)

Abstract

Sistem penggolongan darah pada manusia yang banyak dikenal adalah sistem ABO dan rhesus. Tujuan penelitian ini adalah Mengetahui distribusi golongan darah sistem ABO dan rhesus serta frekuensi alel pada populasi penduduk pulau Gili Ketapang, kabupaten Probolinggo. Pengambilan sampel dilakukan secara acak dengan cara dilakukan pengundian jumlah sampel yang diambil sebanyak 384 jiwa. Identifikasi golongan darah sistem ABO pada penelitian ini dilakukan dengan metode slide dengan prinsip antigen (aglutinogen) yang direaksikan dengan antibodi (aglutinin). Hasil penelitian menunjukkan distribusi golongan darah sistem ABO dan Rhesus O+ (46,61%), B+ (24,22%), A+ (23,18%), dan AB+ (5,99%). Frekuensi alel IA(0,16), frekuensi alel IB (0,16), frekuensi alel i (0,68), dan frekuensi alel rhesus positif (Rh+) adalah 1
TOKSISITAS EKSTRAK EKSTRAKSI SERBUK GERGAJI KAYU SENGON LAUT (Albizia falcataria L. Forberg) TERHADAP MORTALITAS Hypothenemus hampei Ferr. (COLEOPTERA: SCOLITYDAE) Paramita Pratiwi; Rudju Winarsa; Purwatiningsih Purwatiningsih
Jurnal Pro-Life Vol. 6 No. 2 (2019): Juli
Publisher : Program Studi Pendidikan Biologi Fakultas Keguruan dan Ilmu Pendidikan

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33541/jpvol6Iss2pp102

Abstract

This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract This study was conducted to determine the toxicity of methanol extract SengonSengon SengonSengonSengon wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust wood sawdust againstagainstagainstagainst againstagainst Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different con Hypothenemus hampei. There were 6 different conHypothenemus hampei. There were 6 different concentration centrationcentration centrationcentration centrations of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of extract tested to insect by using contact method. Ten of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 of H. hampei were used for each concentration and replicated 10 times. Mortality insects was recorded 24, 48 and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te and 72 hours. The data was analyzed using GLM (General Linear Model) teand 72 hours. The data was analyzed using GLM (General Linear Model) te st and st and st and st and st and st and Duncan DuncanDuncanDuncanDuncan test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence test at 95% confidence level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of level. Results showed that methanol extract of SengonSengon SengonSengonSengon wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. wood sawdust had significant effect on the mortality of H. hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of hampei after 72 hours. It can be concluded that methanol extract of SengonSengon SengonSengonSengon wood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase thewood sawdust could increase the wood sawdust could increase the wood sawdust could increase thewood sawdust could increase the wood sawdust could increase thewood sawdust could increase the wood sawdust could increase the wood sawdust could increase the wood sawdust could increase thewood sawdust could increase the wood sawdust could increase the wood sawdust could increase the mortality of H. hampei. mortality of H. hampei.mortality of H. hampei. mortality of H. hampei. mortality of H. hampei. mortality of H. hampei.mortality of H. hampei.mortality of H. hampei.mortality of H. hampei.mortality of H. hampei. mortality of H. hampei.Keywords: Hipotenemus hampei, mortality, Sengon wood sawdust, toxcicity.
Keanekaragaman Jenis Nyamuk yang Berpotensi Sebagai Vektor Penyakit (Diptera: Culicidae) di Taman Nasional Baluran, Indonesia Purwatiningsih Purwatiningsih; Rike Oktarianti; Rendy Setiawan; Wahyu Tri Agustin; Aida Mursyidah
Al-Kauniyah: Jurnal Biologi Vol 14, No 2 (2021): AL-KAUNIYAH JURNAL BIOLOGI
Publisher : Department of Biology, Faculty of Science and Technology, Syarif Hidayatullah State Islami

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15408/kauniyah.v14i1.12918

Abstract

AbstrakNyamuk famili Culicidae berperan sebagai vektor penyakit malaria, demam berdarah, dan demam chikungunya. Resort Labuhan Merak memiliki potensi besar sebagai tempat perindukan berbagai jenis nyamuk, baik sebagai vektor penyakit atau bukan. Penelitian ini bertujuan untuk mengetahui jenis-jenis nyamuk yang berperan sebagai vektor penyakit di Resort Labuhan Merak Kawasan Taman Nasional Baluran berdasarkan karakteristik morfologi. Pengambilan koleksi nyamuk dewasa dilakukan dengan metode landing collection. Nyamuk ditangkap dengan cara koleksi aktif menggunakan aspirator. Lokasi koleksi pada beberapa titik yaitu di dalam dan luar rumah, di sekitar kandang, serta di rawa. Hasil identifikasi terdapat tujuh jenis nyamuk, yaitu Aedes aegypti, Ae. Albopictus, Ae. indonesiae, Culex quinquefasciatus, Cx. vishnui, Cx. mammilifer, dan Cx. sitiens. Nyamuk Ae. indonesiae paling banyak ditemukan (69,4 %). Sementara itu, jenis nyamuk Cx. vishnui, Cx. mammilifer, dan Cx. sitiens ditemukan sangat sedikit (2,92 %). Ae aegypti dan Ae. albopictus telah diketahui berperan sebagai vektor penyakit demam berdarah dengue (DBD) dan chikungunya, sedangkan Cx. quinquefasciatus sebagai vektor penyakit filariasis limfatik, dan Cx. vishnui maupun Cx. sitiens sebagai vektor penyakit japanese encephalitis. Hal yang menarik pada penelitian ini adalah belum diketahuinya peran Ae. indonesiae dan Cx. mammilifer sebagai vektor penyakit. Indeks keanekaragaman nyamuk termasuk dalam kategori sedang.Abstract The Culicidae family is one of the mosquito disease vectors such as malaria, dengue fever, and chikungunya fever. Labuhan Merak resort Baluran National Park has great potency for mosquito breeding sites. The research aimed to determine the species of mosquitoes based on morphological characteristics as a disease vector. Mosquitoes were collected by landing collection method and active collection with an aspirator. The collection has been done at several points at the house both inside and outside; around the cage, and at the swamp. The results obtained 7 species of mosquitoes, there were Aedes aegypti, Ae. albopictus, Ae. indonesiae, Culex quinquefasciatus, Cx vishnui, Cx. mammilifer, and Cx. sitiens. Mosquito of A. indonesiae was the most common (69.4 %), while Cx. vishnui, Cx. mammilifer, and Cx. Sitiens were found very few (2.92 %). Ae. aegypti and Ae. albopictus has been known as a vector of dengue hemorrhagic fever and chikungunya, while Cx. quinquefasciatus as a vector of lymphatic filariasis, and Cx. vishnui and Cx. sitiens as a vector of japanese encephalitis disease. The interesting finding from this study is that Ae. indonesiae and Cx. mammilifer are not yet known for their role as disease vectors. The diversity index of the mosquitos’ species showed moderate category.
Cellulase, Pectinase, and Xylanase Production by Listeria sp. ISH 16 using Coffee Pulp Waste Medium Ummi Wasilah; Kahar Muzakhar; Purwatiningsih Purwatiningsih
IPTEK Journal of Proceedings Series No 6 (2020): 6th International Seminar on Science and Technology 2020 (ISST 2020)
Publisher : Institut Teknologi Sepuluh Nopember

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.12962/j23546026.y2020i6.11122

Abstract

In this study, microbial utilization of coffee pulp waste to produce three carbohydrases (cellulase, pectinase, and xylanase) has been investigated. An isolate Listeria sp. ISH-16 which grown in liquid medium containing 0.5% coffee pulp alkali extract can grow well with density of reach 107 x 58.5 cell/mL. Further, the culture can optimum produced of pectinase after 72 hours incubation at 37oC, but for cellulase and xylanase longer 84 hours incubation needed. The harvested of crude pectinase, cellulase and xylanase had activity 0.15, 0.23, and 0.61 unit/ ml after dialysis, respectively. All enzymes stable at a range of pH 4-5.5, but they work optimum at different pH. Of each enzyme pectinase, cellulase, and xylanase work optimum at pH 5, 4.5, and 5.5. based on these results, it may be adopted as a strategy to produce enzymes with low cost so that further investigation such as large scale and purification enzyme is needed.
The Aplications Biological Control of the Pest Population ( Plutella xylostella Linn. And C. pavonana Zell.) and Their Natural Enemies in Cabbage Plants in the Village Kalibaru Kulon, District Banyuwangi Helmi Helmi; Didik Sulistyanto; Purwatiningsih Purwatiningsih
Jurnal ILMU DASAR Vol 16 No 2 (2015)
Publisher : Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (285.627 KB) | DOI: 10.19184/jid.v16i2.1352

Abstract

The aim of the research was to determine the effectiveness of biological control agens  to the population of pests  and their natural enemies in cabbage crops in agricultural land Kalibaru kulon Kab. Banyuwangi. The research was conducted by Randomized Complete Block Design with with five replications. The treatments were Control as P0, Heterorhabditis sp. as P1, Bacillus thuringiensis as P2, Profenofos as P3, Beauveria bassiana as P4, Red bacteria as P5. Data were obtained from observations of pest population and their natural enemies, as well as the percentage decrease in the population of pests and their natural enemies. Data were analyzed using ANOVA and LSD were tested further by 5%. The results showed that Heterorhabditis sp. was the most effective agents to control populations of Plutella xylostela Linn. and Crocidolomia pavonana Zell., this is also indicated by a decrease in pest population of Plutella xylostela by 54.66% and amounted to 47.9% Crocidolomia  pavonana. Aplication biological agens  was not  affect  the population of natural enemies Coccinela repanda, and Verania sp. Keywords : Cabbage, Biological Control, Pests, Natural enemies
Biological Control Entomopathogenic Nematodes Heterorhabditis sp. and Steinernema sp. Pest Control Termite Land As Coptotermes sp. and Microtermes sp. in The District Lumajang Qodiriyah Qodiriyah; Didik Sulistyanto; Purwatiningsih Purwatiningsih
Jurnal ILMU DASAR Vol 16 No 1 (2015)
Publisher : Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (187.051 KB) | DOI: 10.19184/jid.v16i1.1518

Abstract

This research aims to find out the most effective concentration (LC50) and the most effective time (LT50)  and  to select a biological agent netamoda of nematodes Steinernema sp. dan Heterorhabditis sp. as the environmentally friendly biological control agents on the ground termite Coptotermes sp. and   Microtermes sp. in Lumajang. All the data were analyzed by using the termite mortality percentage variance analysis. The LC50 and LT50 were tested by using the probit analysis. Therefore, the empirical probit values were obtained from the percentage of mortality after they were calculated by the Abbot formulation. The biological agents netamoda entomopathogenic Heterorhabditis sp. and Steinernema sp. had the high value on the pathogenicity of Coptotermes sp. and Microtermes sp., the LC50 values on Coptotermes sp. of nematodes Heterorhabditis sp. was 14.94 IJ/ml and Steinernema sp. was 15.22 IJ/ml., the LC50 values on Microtermes sp. of nematodes Heterorhabditis sp. was 16.54 IJ/ml and  Steinernema sp. was 20.39 IJ/ml., the LT50 values on Coptotermes sp. of nematodes Heterorhabditis sp. was 1.29 hours and Steinernema sp. was 1.35 hours, and the LT50 values on Microtermes sp. of nematodes Heterorhabditis sp. was 2.14 hours and Steinernema sp. was 1.82 hours. Through pathogenicity test, the entomopathogenic nematodes Heterorhabditis sp. is more effective to control subterranean termites compared with the nematode Steinernema sp. This happens because Heterorhabditis sp. are actively engaged and looking for a host so that there are a large number of possibilities of contacting them with a very large subterranean termites.Keywords: Entomopathogenic nematodes,   Heterorhabditis sp., Steinernema sp., LC50, LT50 
Antifeedant Activity from Leaves Extract of Aglaia ganggo Miq on Spodoptera litura Purwatiningsih Purwatiningsih; I Nyoman Adi Winata
Jurnal ILMU DASAR Vol 14 No 1 (2013)
Publisher : Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (175.851 KB) | DOI: 10.19184/jid.v14i1.475

Abstract

The different fraction extracts (viz methanol, dichlorometana, n-hexane, ethylacetate, and aceton) obtained from leaves of Aglaia ganggo Miq were investigated for antifeedant activity against Spodoptera litura. All extract fractions showed antifeedant activity with aceton fraction exhibited the highest antifeedant activity at 1 ppm concentration. Only hexane fraction showed a dose dependent concentration while the other fractions exhibited the opposite respond.Keywords : Antifeedant, Aglaia ganggo, extract, fraction
OVITRAP SEBAGAI UPAYA PENGENDALIAN NYAMUK (CULICIDAE) SECARA MANDIRI Husnatun Nihayah; Hurin Nur Laili; Purwatiningsih Purwatiningsih
JMM (Jurnal Masyarakat Mandiri) Vol 9, No 1 (2025): Februari
Publisher : Universitas Muhammadiyah Mataram

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31764/jmm.v9i1.28177

Abstract

Abstrak: Nyamuk (Famili Culicidae) merupakan insekta yang berperan sebagai vektor. Pemasangan ovitrap merupakan salah satu upaya pengendalian nyamuk vektor yang dapat dilakukan oleh Masyarakat. Tujuan pengabdian ini adalah untuk meningkatkan kemampuan masyarakat Kelurahan Tegalgede Kabupaten Jember dalam membuat, memanfaatkan serta mengontrol ovitrap sebagai upaya pengendalian nyamuk vektor penyakit. Metode yang dilakukan yaitu melalui sosialisasi dan pelatihan pembuatan ovitrap sederhana kepada Masyarakat. Selanjutnya ovitrap dipasang oleh masing-masing peserta dan dilakukan monitoring oleh tim pengabdian. Kegiatan diikuti oleh 24 orang dengan 3 diantaranya merupakan kader juru pemantau jentik Kelurahan Tegalgede. Pengisian kuesioner Pemberantasang Sarang Nyamuk (PSN) dilakukan pada awal kegiatan. Hasilnya menunjukkan bahwa 71,5% masyarakat telah melakukan kegiatan PSN. Kegiatan sosialisasi dan pelatihan pembuatan ovitrap diikuti dengan antusias. Masyarakat telah mampu membuat, memanfaatkan serta melakukan monitoring ovitrap sederhana secara mandiri. Hasil monitoring dan evaluasi ovitrap menunjukkan adanya penurunan secara signifikan terhadap populasi nyamuk yang terperangkap. nilai Ovitrap Index di kelurahan Tegalgede mencapai 79,17%.Abstract: Mosquitoes (Family Culicidae) are one of the insects that act as vectors. Installing ovitraps is one of the mosquito vector control efforts that can be carried out by the community. The aim of this community service is to improve the ability of the Tegalgede community to make, utilize and control ovitraps as an effort to control mosquito vectors of disease. The method used is through socialization and training in making simple ovitraps for the community. Furthermore, the ovitraps were installed by the community and monitored by the community service team. The activity was attended by 24 people, 3 of whom were cadres of mosquito larvae monitors in Tegalgede Village. The mosquito nest eradication questionnaire was filled out at the beginning of the activity. The results showed that 71.5% of the community had carried out mosquito nest eradication activities. The socialization and training activities for making ovitraps were followed enthusiastically. The community has been able to make, utilize and control simple ovitraps independently. The results of monitoring and evaluation showed a significant decrease in the number of mosquito populations trapped in ovitraps. The Ovitrap Index value in Tegalgede reached 79.17%.
Toksisitas Ekstrak n-heksana Serbuk Gergaji Kayu Sengon (Albizia falcataria l. Forberg) terhadap Mortalitas Serangga Penggerek Buah Kopi (Hypothenemus hampei ferr.) (Scolytidae: Coleoptera) Purwatiningsih Purwatiningsih; Firna Putri Mandasari; Susantin Fajariyah
Biotropic : The Journal of Tropical Biology Vol. 3 No. 1 (2019): Biotropic, Volume 3, Nomor 1, 2019
Publisher : Program Studi Biologi, Fakultas Sains dan Teknologi, Universitas Islam Negeri Sunan Ampel Surabaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.29080/biotropic.2019.3.1.39-48

Abstract

Research on the toxicity of n-hexane extract of Albizia falcataria sawdust against Hypothenemus hampei has been conducted. The method of research was contact method. The concentrations used in the experiment were control (aquadest); 0.25%; 0.5%; 1%; 2%; and 4%. Every concentration was sprayed on the female imago. Observations were performed 120 hours after treatment. The results showed that there was an effect of the length of observation time and concentration on the mortality of H. hampei (GLM Test α= 5%). The time of observation and concentration of A. falcataria sawdust n-hexane extract has positive correlation on H. hampei mortality. Therefore, the longer the treatment time, the more H. hampei mortality is increased. The mortality of H. hampei also increased with increasing concentration given. At a concentration of 4%, extract of A. falcataria sawdust has high toxicity which causes the highest mortality (> 92%).