347,744 research outputs found
Niti Raja Sasana
No full textNaskah Niti .Raja Sasana yang menjadi sumber kajian dan analisis ini merupakan salah satu naskah kuno yang menguraikan tentang kepemimpinan. Naskah aslinya ditulis pada daun tal (rontal) dengan aksara Bali dan berbahasa Jawa Tengahan serta disajikan dalam bentuk tembang
Analisis Sosio-Historis terhadap Peran Batsyeba dalam Pemilihan Salomo sebagai Raja dalam 1 Raja-Raja 1
No full textPenelitian ini merupakan upaya untuk mendeskripsikan prinsip-prinsip peran Batsyeba, yang dilihat dari kitab 1 Raja-raja 1 dalam konteks sosio-historisnya, serta mendeskripsikan latar belakang yang terjadi dalam pengangkatan Salomo menjadi raja. Penelitian mengenai peran Batsyeba dalam 1 Raja-raja 1, dikaji melalui analisis sosio-historis. Secara sosio-historis, Batsyeba adalah karakter perempuan dalam 1 Raja-raja 1 yang dibangun dalam kerangka berpikir Deuteronomis yang menekankan pada urusan pemerintahan, politik, dan agama, serta sistem politik monarki yang menjunjung tinggi nilai-nilai patriarki. Salah satu contohnya adalah untuk menjadi raja dan mempertahankan pemerintahan yang stabil, seseorang harus mendapat persetujuan dari para pemimpin suku, dan dia harus ditunjuk oleh seorang nabi. Dia juga membutuhkan imamat yang mendukung, disebabkan oleh para imam, nabi, dan pemimpin suku yang semuanya diwakili oleh para laki-laki. Jika dilihat dari sisi demikian, tentu saja peran dari seorang perempuan, yaitu Batsyeba sangat terbebani dan kesulitan untuk muncul sebagai aktor penting dalam kitab 1 Raja-raja 1. Namun, di sinilah tulisan ini menjadi penting, yaitu bagaimana Batsyeba hadir dengan berani menghadap raja Daud dan bersumpah atas nama YHWH, bahwa seharushnya yang menjadi raja selanjutnya adalah Salomo bukan Adonia
O suočavanju s prošlošću – razgovor s Louise L. Lambrichs
No full textHrvatska povjesničarka Nada Kisić Kolanović razgovarala je s Louise L. Lambrichs, francuskom spisateljicom i filozofkinjom koja se u većem broju svojih djela bavila temama iz hrvatske suvremene povijesti
Kisah raja-raja Gowa
No full textBuku yang berjudul Kisah
Raja-Raja Gowa ini adalah ajakan kepada setiap orang
untuk kembali melihat sejarah salah satu kerajaan
maritim terbesar yang pernah ada di Nusantara.
Mempelajari bagaimana Kerajaan Gowa menjadi besar
hingga akhirnya harus kalah menjadi semacam seruan
kepada generasi terbaik Indonesia agar menyiapkan
diri menjadi pemimpin yang jujur, berani, dan cerdas di
masa yang akan datang
Image of Nada Coussmaker on the guest cabin porch (2 of 6)
No full textNada Coussmaker on the porch of her guest cabin, called Matt�s Cabin after Matt Turner, on Triangle X Ranch, Grand Teton National Park
Kontribusi Hermeneutis 1 Raja-Raja 21 terhadap Konflik Agraria di Indonesia
No full textAgrarian conflict is a very classic discussion in Indonesia. It affects humanity and environmental issues. As many discriminations happens toward marginalized society, it’s needed to be a concern. The author will dialogue this issue with text 1 Kings 21. This event is almost the same with the text 1 Kings 21, about the seizure of land between King Ahab and Naboth. To investigate and review the meaning of 1 Kings 21, the author uses critical history method. In conclusion, greed is the cause, so there was a land seizure between King Ahab and Nabot which resulted in the killing of Nabot as a weaker person. However, God declared justice for His people, and declared judgment on King Ahab. The event like this also often occurred in Indonesian society, due to economic interests and the legitimacy of national development. However, it is unfortunate that the prophetic voice from the church could not be heard. AbstrakKonflik agraria merupakan persoalan yang sangat klasik di Indonesia. Konflik tersebut berdampak pada kemanusiaan, bahkan pada masalah lingkungan. Dengan banyaknya terjadi diskriminasi terhadap orang-orang marginal (tak berdaya) tentunya ini perlu menjadi perhatian. Penulis akan mencoba melihat impikasi dari teks 1 raja-raja 21 terhadap konteks saat ini. Peristiwa diskriminasi tersebut tentunya hampir sama terjadi dalam teks 1 Raja-raja 2, tentang perebutan tanah antara raja Ahab dan Nabot. Dalam menyelidiki dan mengkaji makna dari 1 Raja-raja 21, penulis mengunakan metode penafsiran kritik sejarah (historis). Kesimpulannya, keserakahan yang menjadi penyebab, sehingga terjadi perebutan tanah antara Raja Ahab dan Nabot yang mengakibatkan terbunuhnya Nabot sebagai yang lemah. Namun, Tuhan tetap menyatakan keadilannya bagi umat-Nya, dan menyatakan penghakiman kepada raja Ahab. Peristiwa tersebut juga sering terjadi dalam masyarakat Indonesia, dikarenakan kepentingan ekonomi dan legitimasi pembangunan nasional. Namun, sangat disayangkan gaungan suara kenabian dari gereja tak begitu terdengar
<i>Raja</i> Linnaeus 1758
No full textIdentification guide to Raja (rays), and the geographical distribution of that species. Produced by R. S. Clark, 1931. Includes 1 figure.</p
The return of the red bourgeoisie: an interview with Nada Prlja
No full textHeavily influenced by the Black Wave or dissident Yugoslav cinema of her childhood, artist Nada Prlja considers its unique balancing act between iconoclasm and idealism, individualism and communism to be exemplary. In an interview with Stefan Szczelkun, Prlja talks about the cultural context of communist Yugoslavia and its mutation into a consumer culture - a shift that her artwork pivots on
Myocardial protection in adult patients. In: “Raja S., Cardiac Surgery: A Complete Guide”.
No full textPygoluciola dunguna Nada & Ballantyne 2018
No full textPygoluciola dunguna Nada sp nov. Figs 2̄37 Type. Holotype male. MALAYSIA. Terengganu: Dungun, Jengai Forest Reserve, Compartment 40, lat. 4.610939, long. 103.158919 19.vii.2016, B. Nada. (FRIM). Paratypes. MALAYSIA Perak: Tanjung Malim, Gunung Liang, 3.80205 N, 101.590969 E, 350 m a.s.l, 21.vi.2015, B. Nada, female (GL350) (FRIM). Selangor: Gombak x.4.1965, J. Buck, male (ANIC); 30.i.2015, W. Jusoh & Thary, male (MZUM). Kepong, Forest Research Institute Malaysia, 3.233139 N, 101.630403 E, 14.vi.2011, Rover Track, 171 m a.s.l., O. Khirul-Faizal, male (ADULT8); 27.vi.2011, Canopy Walkway Trail, C.N. Nafaruding, male (ADULTCNPY2); 6.vii.2011, Waterfall Trail, 139 m a.s.l, M.S. Salman, male (ADULTWFALL4) (FRIM). Kuala Kubu Bharu, Bukit Kutu, 3.55395 N, 101.734211 E, 26.v. 2015, 400 m a.s.l. and 600 m a.s.l., B. Nada, male, female (BK400) (BK600) (FRIM). Terengganu: Dungun, Besul Forest Reserve, Compartment 10, l 4.693225 N, 103.167175 E, 10.v.2016, S. Muhammad-Jafni, 2 males, female (B10); Compartment 19, lat.4.63415, long. 103.200553, 8.viii.2016, Z.A. Saiful-Azhari, 4 males, 3 females (B19) (FRIM). Jengai Forest Reserve, Compartment 52, 4.548261 N, 102.979878 E, 30.vi.2016, M.S. Asraf, 2 males (JI52); Compartment 40, 4.610939 N, 103.158919 E, 19.vii.2016, R.S. Raja-Ahmad-Bazli, female (JI40) (FRIM). Jerangau Forest Reserve, Compartment 100, 4.8699 N, 103.046725 E, 20.vii.2016, M.S. Asraf, female (JU100); Compartment 99, 4.862742 N, 103.048636 E, 17.viii.2016, S. Mohd-Fadhlullah, 4 males, female (JU99) (FRIM). Pasir Raja Barat Forest Reserve, Compartment 87, 4.858047 N, 103.009394 E, 2.viii.2016, S. Muhammad-Jafni, 6 males, 2 females, 22.viii.2016, Z.A. Saiful-Azhari, 1 female (PB87) (FRIM). Hulu Terengganu Tambahan Forest Reserve, Compartment 27, 4.984031 N, 102.932167 E, 30.viii.2016, Z.A. Saiful-Azhari, 4 males, female (UTT27) (FRIM). All but two specimens (in ANIC and MZUM) are preserved in 70% ethanol. Diagnosis. Dorsally pale yellowish brown with diffuse pale brown pronotal markings; ventral abdomen yellow except for white LO in V6, 7, with narrow black posterior margin of V5; 9.1¯10.6 mm long. The only species of Pygoluciola having a broad apically truncate MPP which inclines without any bend slightly upwards to engage against the under surface of the very narrow T8, and a yellow ventral abdomen with narrow black posterior margin of V5. Female macropterous and observed in flight; bursa plates in form of two elongated slender hooks which incline anteriorly and posteriorly. Description of male. 9.1 – 10.6 mm long. Colour (Figs 2̄9, 14, 16̄18, 25, 26): creamy yellow semitransparent pronotum with single median, and paired reddish markings along the posterior margin, all of which often coincide with retraction of fat body beneath the cuticle (Figs 2, 4, 6¯9); retraction of fat body along anterior margin of pronotum in ethanol preserved specimens allows black head to be visible from beneath and gives the erroneous impression of a dark marking along the pronotum (e.g. Fig. 9); MN and MS brown; elytra semitransparent, very light brown with lateral margins slightly paler (underlying body outline confuses interpretation of elytral colour especially in ethanol preserved specimens where the elytral punctures are dark brown at their bases) (Figs 2, 6); one of the two pinned Gombak males (Fig. 4) pale creamy yellow dorsally, pronotum with faint traces of median ginger brown markings (single median mark and paired areas along posterior margin); head antennae and palpi black (Figs 17, 18); venter of thorax pale yellow (Figs 3, 6); legs 1, 2 pale brown with black tibiae and tarsi; legs 3 light brown with slightly darker tibiae and black tarsi (BK600 single male with brown tints in middle area of coxae; B19 (1) II has tibiae 3 pale yellow); abdominal ventrites yellow with posterior margin of V5 narrowly black (Figs 3, 6, 14, 25, 26); LO in V7 white, retracted from sides and posterior margin, with white areas at side and area behind LO semitransparent with white fat body visible beneath cuticle (Figs 3, 6, 10, 14), and narrow longitudinal median line on MPP which is brown in the MZUM specimen (Fig. 6); abdominal tergites pale yellowish, semitransparent, T6 slightly darker than rest, T7, 8 slightly paler than preceding tergites (Fig. 16 shows one of two pinned males). Pronotum (Figs 2, 4, 5, 7¯9): width subequal to humeral width; median anterior margin broadly rounded and barely produced in front of the broadly rounded anterolateral corners; lateral margins strongly divergent along anterior 2/3 and posterolateral corners rounded and not projecting beyond median posterior margin; surface along posterior margin coinciding with the brown markings may appear elevated (only clearly visible in pinned specimens Figs 7, 8). Elytron (Figs 2, 4, 5): slightly convex sided; interstitial lines not well defined. Head: (Figs 3, 6, 17, 18, 25, 26) GHW 7 x SIW; ASD 2 x GHW but not attaining 3 x GHW; scape clavate, all other segments elongate slender about 7 x as long as wide. Abdomen (Figs 3, 6, 10̄16): posterior margin of V7 with elongate apically truncate MPP which curves gently upwards with the apex engaging against the underside of T8 (Fig. 12); dorsally reflexed margins of V7 well defined and anterior margin to either side of MPP produced into short rounded pieces (arrowed in Fig. 11); reflexed margin in two parts on dorsal surface of MPP where the narrow margin between left and right side is visible from beneath as a line in the middle of the MPP (Figs 10, 11, 13); much darker markings observed in pinned male (Fig. 13) may be due to age and appear to be accumulated material. T8 with narrow triangular posterior margin, lateral wing like projections and elongate slender anterolateral prolongations that diverge (Fig. 15). Aedeagal sheath (Figs 22 ̄24): basal ¾ of sheath sternite with narrow sclerotized margins which expand in apical ¼ where they are terminated by a slightly curved, transverse narrow strip of cuticle; to the sides of the apical ¼ (coinciding with the area of expansion of the median strip) there are wider more membranous portions (Fig. 22); tip of sternite terminates in paired narrowed hairy membranous lobes arising at the sides of the transverse strip, and are not clearly visible in Fig. 22; anterior margin of tergite shallowly emarginated. Aedeagus (Figs 19 ̄21): 2.5 x as long as wide and evenly wide along its entire length; basal piece well defined and in two well cuticularised narrow parts; membranous apical section of LL having short apically acute hair bearing lobe at the outer margin just before origin of the more membranous portion (arrowed in Figs 19, 21); with dense line of long hairs originating at this lobe and continuing inside their lateral margins (Fig. 21); membranous portion of LL as wide at base as at apex with both lobes having apices irregularly inclined ventrally (assumed to be an artefact of preparation) (Figs 19 ¯21); ML tapering to a rounded narrow apex, much shorter than LL and extending a little beyond the posterior margin of the darker basal portion of the LL which is widely separated for slightly more than half its length in middorsal line; anterior margin of basal portion of LL asymmetrical, being produced on its left side and margin rounded (Fig. 20). FIGURES 2–9. (2, 3 J152 (1); 4 Gombak pinned male ANIC; 5, 6 Gombak pinned male MZUM; 9 B192)). 2‾6 habitus, 2, 4, 5 dorsal, 3, 6 ventral; 7‾9 pronota dorsal. Scale line is 1 mm. Female. ( Figs 25 ̄37). 9.2̄10.3 mm long. Macropterous and taken in flight. Coloured as for male except for white LO in V6 only and V7, 8 pale coloured; V7 may have narrow darker marking in anteromedian area and the darker anterior apodeme of V8 may be visible through the transparent cuticle (e.g. Figs 27, 30, 33). Abdomen: LO occupying all of V6 only. Reproductive system differs little from what has been described elsewhere. An elongate vagina leads into a muscular bursa which may or may not be expanded (Figs 36, 37 show muscular striations). Just behind the bursa is the median oviduct (no median oviduct plates were detected). The bursa bears at its anterior end a thinner walled digesting gland, and towards its posterior end a stalked spermatheca which has an expanded base (Figs 35, 36). In some cases these may attain similar size (possibly due to immersion in water during dissection) and it may be difficult to determine which is which e.g. Ballantyne & Lambkin (2006 fig. 37) indicated the spermatheca and digesting gland of essentially equal size. In this species a large spermatheca was observed but whether this was due to immersion in water or not is not clear. There are two long slender needle shaped bursa hooks projecting either forwards or backwards and lying free in the bursa cavity, with the point of attachment to the bursa wall at their junction (Figs 34 ̄37). Both curve slightly inwards at their apices but their exact method of functioning within the bursa, and how it relates to a spermatophore, is not entirely clear. The posterior ‘plates’ may ensure the spermatophore is held within the bursa. FIGURES 29–33. Females. (29, 30 PB87 (4); 31 JU100 (6); 32, 33 B19 (2-3)). 29, 31, 32 dorsal; 30 33 ventral. Scale line is 1 mm. Ecological information. Pygoluciola dunguna sp. nov. is present in forested areas where shallow streams flow. The streams were less than 30 cm deep and 3̄ 10 m wide. All the streams have small rocks and sandy edges (Fig. 38). They were found mainly flying among the undergrowth of the forest, 10̄15 meters above ground (Fig 39). On frequent occasions, the females were collected apparently resting on herbaceous plants. Pairs of P. dunguna sp. nov. were also collected while mating on stems or leaves of undergrowth.Published as part of Nada, B. & Ballantyne, L. A., 2018, A new species of Pygoluciola Wittmer with unusual abdominal configuration, from lowland dipterocarp forest in Peninsular Malaysia (Coleoptera: Lampyridae: Luciolinae), pp. 343-362 in Zootaxa 4455 (2) on pages 348-357, DOI: 10.11646/zootaxa.4455.2.5, http://zenodo.org/record/145728
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