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Donatus Dahang
"This study concerns the conservation of Indonesian tarsiers, specifically the interface between field and captive studies. There are two problems that are central to field and captive conservation studies, behavior and taxonomy. In this thesis I address to two research questions:
1. Do Indonesian tarsiers have differences in locomotor behavior that warrant different cage designs?
2. Can tarsier taxa, many of which have been identified with expensive and labor intensive techniques including DNA and acoustic analysis, also be identified by a simple, low-cost technique involving the morphology of the tail tuft?
There are three species groups of tarsiers, Philippine Tarsiers, Western Tarsiers, and Eastern Tarsiers. Hill (1955) classified these as Tarsius syrichta, Tarsius bancanus, and Tarsius spectrum, respectively, but Brandon-Jones et al. (2004) revised Tarsius spectrum to include five distinct species: Tarsius tarsier (= Tarsius spectrum), Tarsius sangirensis, Tarsius pumilus, Tarsius pelengensis, and Tarsius dianae (probably a junior synonym of dentatus). Of these, two species groups are endemic to Indonesia, Western and Eastern Tarsiers. Hill (1955) indicates that these two species groups can be distinguished by their tail tufts (see figure II-5), the tuft of Western Tarsiers being less extensive than that of Eastern Tarsiers. These two species groups also have clear-cut social differences (Sussman 1999), and Niemitz (1979) hypothesized locomotor differences based on the limb anatomy.
I studied one male-female pair each of Tarsius bancanus and Tarsius tarsier in side-by-side cages at Captivity of Mammals Centre of Biological Research, Indonesian Institute of Sciences, Cibinong Bogor, over a three-month study,
I collected 546 hours of observation on Tarsius bancanus and 574 hours on Tarsius tarsier. Results from this study show statistically significant differences in locomotor behavior that support Niemitiz’s hypothesis, and which imply that Western and Eastern Tarsiers require different cage designs. In a second study of tail tuft morphology, I collected 13 measurements on the tail and tail tuft of 23 Western Tarsiers and 20 Eastern Tarsiers in the collection of the Museum Zoologicum Bogoriense. My results demonstrate that Western and Eastern Tarsiers can be easily and confidently classified by using a multivariate discriminant function analysis of the tail tuft.
The results of these two studies show clearly that Western and Eastern Tarsiers can be identified by a multivariate analysis of the tail tuft morphology, and that these two species groups have significant differences in locomotor behavior, but the greater significance of this study lies in the implications for cryptic species within species groups. Results from the discriminant function analysis indicate three populations of Eastern Tarsiers, those from Sulawesi, Sangihe, and Peleng Islands, can be confidently identified by multivariate analysis of tail tuft morphology, a result that Hill (1955) did not arrive at. Brandon-Jones et al. (2004) identified 16 populations of Eastern Tarsiers that might be taxonomically separable and warrant further studies. Thus, future studies should use this method to see if it is applicable to all of the populations identified by Brandon-Jones et al. (2004), not merely the three populations that I had access to. At present there are no hypotheses of significant locomotor differences within species groups. Further research is also needed to find out whether or not there are any differences of locomotor behavior among population of tarsiers, particularly those that had been identified by Brandon-Jones et al. (2004).
All living tarsiers are small, nocturnal, vertical clinging and leaping, faunivorous animal and ecological distinctive with regard to other primate (Sussman 1999). About 90% of their food consist of Arthropoda such as crickets, grasshoppers, cockroaches, beetles, butterflies, moths, termites, spiders; and 10% others consist of vertebrate such as small birds, lizards, geckoes, and small snakes (Niemitz 1984, Haring & Wright 1989, Sussman 1999, Supriatna & Wahyono 2000, Gursky 2000).
The length of adult tarsier is only around 12-13 centimeters and its weight is 100-140 grams, and its infant weight 25-33% of the mother’s weight at birth (Sussman, 1999). The length of its tail is two times longer than its body and its hind limb is longer than its up limb. Tarsiers also has huge eyes and ears which are relatively bigger compared to their heads, lacking a reflecting tapetum lucidum and their heads can make a 1800 spin without moving their bodies (Supriatna & Wahyono 2000, Shekelle & Leksono 2004)
Social unit of tarsiers are different among species. Supriatna & Wahyono (2000) pointed out that commonly 80% of Tarsius tarsier (=Tarsius spectrum) live in pairs (monogamous) and only about 20% is multimale-multifemale. There are 2-6 individuals within a group. Their gestation period is about 180-190 days and they can live for 12 years. Unlike Tarsius tarsier, Tarsius bancanus is more solitary or living in pairs to create their home range. However, social systems of other species need further study.
Like many others endemic primate, tarsiers are threatened by human activities, particularly when the forests where they are habitat of are converted into plantations and transmigration settlements. Forest clearance, illegal logging, and burnings are some other hazards that also bring negative impact to the tarsiers. These activities can change the natural habitat of tarsiers into isolated, degradated, or fragmented ones. Merker et al. (2005) reported that in Lore Lindu National Park, Central Sulawesi the population of Tarsius dianae in a highly-disturbed habitat occupied by 45 individuals per km2 was smaller than the one in a low-disturbed habitat occupied by 268 individuals per km2. In a short term, impact of human activities might reduce the population of tarsiers, but in a long term, may lead to the extinction (Merker & Muhlenberg 2000). This fact is worsening by unsuccessful tarsiers breeding in captivity even in countries that have good facilities (Haring & Wright 1989). Therefore, a conservation to save the unique animal is a priority. Conservation of tarsiers is both in-situ and ex-situ. Captive breeding is one form of ex-situ conservation.
Tohari (1987) pointed out that an animal should be captivated if from time to time their field population decreases and is likely to extinct. One of the benefits of captivity is to reduce human reliance to nature population of wildlife (Alikodra 2002). The most important and beneficial reason for maintaining animal in captivity is to educate the public (Larson & Schulze 2001). Shekelle & Leksono (2004) noted that besides breeding, tarsier captivity is useful for researching, training, and establishing public awareness, and mainly changing the false belief of the local community about tarsiers. Moreover, if tarsiers in captivity die naturally, they may be used as a type specimen in museum.
Information about the number of species, distribution, taxonomy, and social system of tarsiers is needed to assist the conservation program of Indonesia tarsiers. Thus, an identification of the species and the habitat of wildlife is one of the conservation objectives. The identification result presented a description of wildlife species and the regions that significant for the conservation. In addition, the result identification can provide a recommendation for new species naming or for identification of new conservation region (Trainor & Lesmana 2000). Shekelle & Leksono (2004) has recommended using tarsiers as flagship species to promote and designed a new conservation area in Sulawesi and its surrounding small islands. Besides, the vocalization analyses showed that there are 11 populations of tarsiers in the region that are possibly new species. For identification purposes, one efficient method is collecting taxonomic information from tarsier’s tail tuft using multivariate technique. This technique can be applied to both living and non-living animals, including specimen which is collected in museum. The method is also applicable for local people in one region who has no modern equipment for conducting a research.
Conservation of tarsiers has faced some problems, some of which are limited population of tarsiers which have not yet been identified, human destruction of their habitat, expensive research for identification, and unsuccessful tarsiers breeding in captivity. Efforts to find inexpensive method for identification and to design suitable captive breeding are very important and urgent to carry out now. The results of this research might be useful for conservation of tarsiers."
Depok: [Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia;Universitas Indonesia, Universitas Indonesia], 2006
T39493-pdf
UI - Tesis Membership  Universitas Indonesia Library
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Akbar Ahya Putra
"Telah dilakukan penelitian yang bertujuan untuk mengamati perilaku makan nokturnal serta membandingkan preferensi pakan dan waktu makan setelah matahari terbenam dan menjelang matahari terbit Tarsius fuscus di Pusat Studi Satwa Primata (PSSP). Pengambilan data perilaku makan T. fuscus menggunakan metode scan animal sampling dan ad libitum sampling selama 26 hari dengan total waktu pengamatan 6240 menit. Waktu pengamatan terbagi atas dua fase, yaitu pada sore hari pukul 17.00--21.00 WIB dan pagi hari pukul 03.00--07.00 WIB. Perilaku makan T. fuscus di penangkaran menunjukkan masih mempertahankan aktivitas makan crepuscular nokturnalnya dengan adanya beberapa titik puncak waktu makan pada preferensi waktu makan yaitu sore hari setelah matahari terbenam dan pagi hari menjelang matahari terbit. Preferensi spot atau tempat makan T. fuscus yaitu jantan dan betina pada kemiringan 10o--80o serta anak pada kemiringan 0o--10o. Preferensi jenis pakan T. fuscus yang teramati yaitu ulat pada jantan serta jangkrik pada betina dan anak.

A research that aims to observe the nocturnal and crepuscular feeding behavior of Tarsius fuscus that also compares their feed and feeding preferences was carried out at Primate Research Center. The data for feeding behavior of T. fuscus is collected using the focal animal sampling and ad libitum sampling methods for 26 days with a total observation time of 6240 minutes. The tarsier?s were observe at different time periods, during evening (05.00--09.00 pm western time) and morning (03.00--07.00 am western time). The feeding behavior of T. fuscus in captivity shows they still maintain their crepuscular nocturnal feeding activity which has peak feeding times with preferred feeding time during after sunset and before sunrise. The preferred eating spot/position of male and female T. fuscus is at a slop 10o--80o and at a slope 0o--10o for infant. The feed preferences T. fuscus is caterpillar on males and crickets on females and infant."
Depok: Universitas Indonesia, 2016
S64143
UI - Skripsi Membership  Universitas Indonesia Library
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Zuliyanto Zakaria
"Penelitian ini bertujuan untuk memvalidasi batas-batas fauna pada tarsius di semenanjung utara Sulawesi serta mengukur dampak perubahan habitat khususnya aktivas perkebunan skala kecil dalam beberapa tahun terakhir terhadap keberlangsungan hidup tarsius. Studi dibagi menjadi tiga makalah yakni: 1) Analisis Kuantitatif Duet call Tarsius dari Survei Lapangan Mengungkap Bentuk Akustik Baru di Gorontalo (Indonesia); 2) Kerapatan Relatif Tarsius supriatnai pada Habitat Perkebunan dan Hutan Sekunder Bentang Alam Popayato-Paguat (Gorontalo, Indonesia); dan 3) Preferensi Habitat dan Site Fidelity Tarsius supriatnai di Area Perkebunan dan Hutan Sekunder Bentang Alam Popayato-Paguat (Gorontalo, Indonesia). Hasil analisis makalah pertama menemukan empat kelompok akustik yakni: Manado (Tarsius spectrumgurskyae), Gorontalo (T. supriatnai), Tinombo (T. wallacei) dan kelompok yang sebelumnya tidak diketahui tersebar di antara Manado dan Gorontalo, yang dinamakan Labanu. Hasil analisis menunjukkan batas fauna di sepanjang pantai selatan yakni Sungai Bone (antara bentuk akustik Manado dan Labanu), Sungai Paguyaman (antara bentuk Labanu dan Gorontalo), Sungai Palasa (antara bentuk Gorontalo dan Tinombo). Di sepanjang pantai utara ditemukan zona kontak melalui identifikasi kelompok sosial heterospesifik dalam satu spektogram. Hasil makalah kedua menunjukkan bahwa kerapatan relatif di habitat perkebunan adalah 0,38 kelompok/ha dan 0,70 kelompok/ha di hutan sekunder, kepadatan substrat pergerakan, NDSI dan ACI tertinggi ditemukan di hutan sekunder, sedangkan kelimpahan serangga paling banyak ditemukan di habitat perkebunan. Hasil makalah kedua menunjukkan bahwa Tarsius supriatnai dapat beradaptasi dengan habitat perkebunan dengan kepadatan yang jauh lebih rendah. Hasil makalah ketiga menunjukkan bahwa pada habitat perkebunan, tumbuhan dengan INP tertinggi bukan merupakan pohon sarang. Sementara pada hutan sekunder, tumbuhan dengan INP tertinggi pada tipe pertumbuhan pohon (Ficus virens) adalah pohon sarang. Hasil penelitian juga menunjukkan bahwa T. supriatnai sebagian besar menggunakan pohon sarang Bambusa vulgaris (26,32%) di areal perkebunan dan Schizostachyum lima dan Calamus zollingeri (28,57%) di hutan sekunder. Hasil survei juga menemukan bahwa 42,9% pohon sarang yang ditemukan pada tahun 2018 masih terus digunakan oleh T. supriatnai dalam lima tahun terakhir.

This study aims to validate the boundaries of the tarsier fauna on the northern peninsula of Sulawesi and measure the impact of changes in habitat, especially small-scale plantation activities in recent years, on the survival of tarsiers. The study is divided into three papers, namely: 1) Quantitative Analysis of Tarsier Duet Calls from Field Surveys Reveals a New Acoustic Form in Gorontalo (Indonesia; 2) Relative Density of Tarsius supriatnai in Agricultural Habitat and Secondary Forest in the Popayato-Paguat Landscape (Gorontalo, Indonesia); and 3) Habitat Preference and Site Fidelity of Tarsius supriatnai in Agricultural Areas and Secondary Forest in the Popayato-Paguat Landscape (Gorontalo, Indonesia). The results of the analysis in the first paper found four acoustic groups, namely: Manado (Tarsius spectrumgurskyae), Gorontalo (T. supriatnai), Tinombo (T. wallacei) and a previously unknown group spread between Manado and Gorontalo, called Labanu. The results of the analysis show that the faunal boundaries along the south coast are the Bone River (between the Manado and Labanu acoustic forms), the Paguyaman River (between the Labanu and Gorontalo forms), the Palasa River (between the Gorontalo and Tinombo forms). Along the north coast, contact zones were found through the identification of heterospecific social groups in one spectrogram. The results of the second paper show that the relative density in agricultural habitat is 0.38 groups per ha and 0.70 groups per ha in secondary forest; the highest density of substrate movement, NDSI and ACI is found in secondary forest, while the abundance of insects is most commonly found in agricultural habitat. The results of the second paper show that Tarsius supriatnai can adapt to agricultural habitats with much lower densities. The results of the third paper show that in agricultaral habitats, plants with the highest IVI are not nest trees. Whereas in secondary forest, the plants with the highest IVI for tree growth species (Ficus virens) were nest trees. The results also showed that T. supriatnai mostly used bamboo nest trees (26.32%) in plantation areas and Schizostachyum lima and Calamus zollingeri (28.57%) in secondary forests. The survey results also found that 42.9% of the nest trees found in 2018 were still used by T. supriatnai in the last five years."
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2023
D-pdf
UI - Disertasi Membership  Universitas Indonesia Library
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Ditha Inawati Sam
"ABSTRAK
Telah dilakukan penelitian (nomor etik: IPB PRC-13-C014) pada Tarsius spectrum dan Tarsius bancanus di penangkaran PSSP. Tujuan dari penelitian yaitu untuk mengamati ada atau tidaknya pengaruh tekanan lingkungan terhadap Tarsius yang telah hidup di penangkaran selama ±6,5 tahun. Subjek penelitian meliputi kandang Ts1: satu Tarsius spectrum jantan dan satu Tarsius spectrum betina; kandang Ts2: satu Tarsius spectrum jantan, satu Tarsius spectrum betina dan satu Tarsius spectrum anak; kandang Tb1: satu Tarsius bancanus jantan; dan kandang Tb2: satu Tarsius bancanus jantan. Penelitian meliputi pengamatan aktivitas siang hari (diurnal) pada pukul 09.00-16.00 (GMT+7) dengan metode Scan Sampling interval 10 menit tanpa jeda selama 1680 menit dalam satu bulan, serta pengukuran kadar hormon kortisol feses dengan metode ELISA (Enzyme-linked Immunosorbent Assay) menggunakan Cusabio™ Monkey Cortisol ELISA kit. Konsentrasi hormon kortisol didapatkan melalui konversi nilai OD terhadap kurva standar y= -6,6535x+6,5962. Hasil penelitian menunjukkan aktivitas diurnal pada Tarsius spectrum dengan persentase rata-rata terbesar meliputi 30,95% moving, 29,1% resting dan 8,12% autogrooming serta aktivitas diurnal dengan persentase rata-rata terbesar pada Tarsius bancanus meliputi 66,02% resting, 18,42% sleeping, dan 7,86% moving. Kadar kortisol tertinggi (mean±SD) ditunjukkan kandang Tb2 (2,92 ±2,91 ng/ml) dan terendah kandang Tb1 (2,35 ±2,49 ng/ml).

ABSTRACT
Research on Tarsius spectrum and Tarsius bancanus (IPB PRC-13-C014) has conducted in Primate Research Center, Bogor. This research aims to examine the presence of environmental influence to Tarsius who have been living in captivity for ±6,5 years. Subject on four cages consist of Ts1: one male and one female of Tarsius spectrum; Ts2: one male and one female with an infant of Tarsius spectrum; Tb1: one single male of Tarsius bancanus; and Tb2: one single male of Tarsius bancanus. Behavioural observation during the day (diurnal) had been done at 09:00-16:00 (GMT +7) through Scan Sampling method with interval 10 minutes without pause for 1680 minutes in a month. Cortisol level had been done with the competitive-ELISA (Enzyme-linked Immunosorbent Assay) method. Cortisol level obtained through conversion of OD value with standard curve y = (-)6,6535x+6,5962. Results of the study showed diurnal activities with largest average percentage on Tarsius spectrum namely moving (30,95%), resting (29,1%), and autogrooming (8,12%). Activities with largest average percentage on Tarsius bancanus namely resting (66,02%), sleeping (18,42%), and moving (7,86). Highest cortisol level (mean±SD) shown by cage Tb2 (2,92 ±2,91ng/ml) and the lowest by cage Tb1 (2,35 ±2,49ng/ml)."
2015
S59647
UI - Skripsi Membership  Universitas Indonesia Library
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"Ramin (Gonystylus bancanus) is one of the major timber species that facing high exploitation in Indonesia. This species can only be found on a specific peat swamp habitat, thus it confines its distribution. Information on its current population and microhabitat characteristics is relatively limited. Here, we investigated natural population and microhabitat of ramin in a peat swamp area in Riau Province using random transects consist of 46 (100m2) sampling plots. Forty-eight individuals of ramin were found in which 46 of these belonged to G. bancanus, while the other two were different species. The estimated population density of ramin in this area was 7.18±2.75 individuals/ha i.e there were approximately seven individuals in each one-ha area of study. The population structure of ramin showed a J-shaped curve bearing many large old trees with few saplings without any seedlings. The microhabitat was investigated using the Discriminant Function Analysis (DFA) and Canonical Analysis, generating two significant variables that discriminated three groups of the population."
580 BKR 16:1 (2013)
Artikel Jurnal  Universitas Indonesia Library
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Indra Yustian
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2001
T40118
UI - Tesis Membership  Universitas Indonesia Library
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Luluk Lely Soraya Ichwan
"ABSTRAK
Sebagai Iangkah awal untuk menjelaskan hubungan kekerabatan antar spesies Tarsius Storr, 1780, dilakukan studi fiogenetik menggunakan data sekuen DNA mitokondria daerah ND4—ND5. Pada analisis tersebut di akukan pendekatan maximum parsimony dengan ap ikasi komputer Phylogenetic Analysis Using Parsimony (PAUP). Hasil anal isis men unjukkan bahwa posisi genus Tarsius dalam ordo Primata perlu dipisahkan dan subordo Anthropoidea ataupun ordo Prosimii. Selain itu pada kelompok Tarsius di Filipina lebih berkerabat dengan kelompok Tarsius di P. Sulawesi, dibandingkan dengan kelompok Tarsius di P. Kalimantan dan P. Sumatra. Adapun kelompok-kelompok Tarsius yang diperbandingkan antara lain T. syrichta (Linnaeus, 1758) di Filipina; T. spectrum (Pallas, 1778) dan T. sangirensis Meyer, 1896 di P. Sulawesi; serta T. bancanus Horsfield, 1821 di P. Kalimantan dan P. Sumatra."
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 1998
S-Pdf
UI - Skripsi Membership  Universitas Indonesia Library
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Suganda Kusmana
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2006
S31346
UI - Skripsi Membership  Universitas Indonesia Library
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Bhisma Gusti Anugra
"ABSTRACT
Taman Nasional Baluran merupakan taman nasional yang terletak di Kabupaten Situbondo Jawa Timur dan merupakan habitat alami dari Jalak putih-punggung abu. Jalak putih-punggung abu (Acridotheres tricolor Horsfield, 1821) merupakan burung berukuran sedang (23 cm) dari famili sturnidae. Populasi jalak putih umum dijumpai di savana, namun belum ada catatan mengenai populasi burung tersebut di habitat lain selain savana. Penelitian ini bertujuan untuk mengetahui kelimpahan relatif dan penggunaan habitat dari populasi jalak putih-punggung abu pada beberapa habitat di Baluran. Kelimpahan relatif populasi jalak putih dihitung dengan menggunakan rumus encounter rates, sedangkan penggunaan habitat akan dianalisis dengan menggunakan PCA. Penelitian dilakukan pada bulan Oktober hingga November 2018 di 6 habitat berbeda yaitu savana padang rumput, savana hutan, savana restorasi, hutan musim, hutan akasia, dan hutan pantai. Berdasarkan hasil perhitungan encounter rates habitat savana padang rumput memiliki nilai encounter rates tertinggi sebesar 11,16; sedangkan habitat hutan pantai menjadi habitat dengan nilai encounter rates terendah sebesar 0. Hasil analisis PCA menunjukkan bahwa penggunaan habitat jalak putih-punggung abu cenderung ditentukan berdasarkan oleh struktur habitat dengan banyak Brachiaria reptans Acacia nilotica, gebang, (Corypha utan), terdapat batang pohon mati, dan pohon berdiameter besar, serta keberadaan pohon asam (Tamarindus indica) dan serasah yang sedikit.

ABSTRACT
Baluran National Park (TNB) is a national park located in Situbondo Regency, East Java one of the natural habitats of the Grey-Backed Myna. Grey-backed myna (Acridotheres tricolor Horsfield, 1821) is a medium-sized bird (23 cm) from the family sturnidae. The population of grey-backed myna is common in savannahs, but there is no record of these bird populations in habitats other than savanna. This study aims to determine the relative abundance and habitat use of grey-backed myna populations in several habitats in Baluran. The relative abundance of the grey-backed myna population is calculated using the encounter rates, while the habitat use will be analyzed using PCA. The study was conducted in October to November 2018 in 6 different habitats: grassland savannah, woodland savannah, restoration savannah, dry minsoon forest, acacia forest, and beach forest. The results showed that grassland savannah had the highest encounter rates with score 11,16; and the beach forest is a habitat with the lowest encounter rates with score 0. The results of PCA analysis show that the habitat use of grey-backed myna tends to be determined by habitat structure with the abundant of Brachiaria reptans, Acacia nilotica, gebang (Corypha utan), dead tree stem, and trees with large diameter, also a habitat with fewer tamarind trees (Tamarindus indica) and detritus."
2019
S-Pdf
UI - Skripsi Membership  Universitas Indonesia Library
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