Journal articles on the topic 'Champassak (Laos)'

AbstractAlthough biographical and life history approaches are potentially important tools for historical geographers, biographical methodologies have rarely been used to specifically investigate borderland dynamics. In this article, I argue that biography can be useful for understanding the ways in which borders have been recognised and negotiated historically. As a case study, I examine the life of Chao Sone Bouttarobol, a member of the Champassak Royal House, who was born in 1895 and died in 1979. As his life story illustrates, the emergence of new national borders had a significant impact on Sone, although family ties and relationships allowed him to cross the national administrative borders that now exist between Thailand, Laos, and Cambodia, often with relative ease. Studying one individual makes it possible to explore the ways in which he interacted and negotiated with borders that cut across the Champassak Royal House's traditional space of influence.

Two new Zodariidae species, collected from the natural forest of Pakse City, Champasak Province, Laos, are described as Asceua adunca sp. nov. (male, female) and Mallinella renaria sp. nov. (male, female). Asceua torquata (Simon, 1909) and A. piperata Ono, 2004 are newly recorded from Laos, and the male of A. piperata is described and illustrated for the first time.

Two new species of the gekkonid lizard genus Hemiphyllodactylus are described based on specimens collected from Champasak Province in southern Laos and Houaphanh Province in northern Laos. Phylogenetic analyses recover H. indosobrinus sp. nov. from Champasak Province as the sister lineage to the Thai endemic H. flaviventris. Hemiphyllodactylus indosobrinus sp. nov. can be diagnosed by having 15 supralabial scales, eight chin scales, 4‑5‑5‑4 subdigital lamellae on Fingers II–V, 4‑5‑5‑5 subdigital lamellae on Toes II–V, and 18 continuous precloacofemoral pores. Phylogenetic analyses recover H. serpispecus sp. nov. from Houaphanh Province to be most closely related to the Vietnamese endemic H. banaensis. Hemiphyllodactylus serpispecus sp. nov. differs from congeners by having seven chin scales; 3‑4‑4‑4 subdigital lamellae on Fingers II–V; 3‑4‑4‑5 subdigital lamellae on Toes II–V; and 11 continuous precloacofemoral pores. The recognition of these two new species doubles the number of Hemiphyllodactylus known from Laos.

Specimens of the spider family Ctenidae from South, East and Southeast Asia were examined. Thirteen new species aredescribed: Anahita jinsi spec. nov. (male, female; China, Sichuan); Ctenus martensi spec. nov. (male; Nepal), Ctenuscladarus spec. nov. (male; Burma), Ctenus theodorianum spec. nov. (male, female; Laos, Oudomxai), Ctenus lishuqiangspec. nov. (female; China, Sichuan), Ctenus holthoffi spec. nov. (male, female; Laos, Champasak), Ctenus bayeri spec.nov. (male; Laos, Champasak); Amauropelma beyersdorfi spec. nov. (male; India, Himachal Pradesh), Amauropelmastaschi spec. nov. (male; India, Uttar Pradesh), Amauropelma ekeftys spec. nov. (male, ?female; India, Meghalaya),Amauropelma hoffmanni spec. nov. (male, female; Laos, Luang Nam Tha), Amauropelma jagelkii spec. nov. (male,female; Laos, Luang Prabang), Amauropelma annegretae spec. nov. (male, female; Laos, Luang Prabang). Ctenus simplexThorell 1897 (Luang Prabang, Vientiane) and C. robustus Thorell 1897 (Luang Nam Tha, Luang Prabang) are recordedfor the first time from Laos, and the female of C. simplex is described for the first time. Ctenus ramosus Thorell 1887, C.robustus and C. palembangensis Strand 1906 as well as internal copulatory structures of Anahita fauna Karsch 1879 areillustrated for the first time. Anahita feai (F.O. Pickard-Cambridge 1902) comb. nov., A. jucunda (Thorell 1897) comb.nov., A. denticulata (Simon 1884) comb. nov., A. smythiesi (Simon 1897) comb. nov. and Amauropelma fungifer (Thorell1890) comb. nov. are transferred from the genus Ctenus. The nomina nova “Ctenus karschi” and “Ctenus tamerlani” proposed by Roewer (1951) are recognised as unavailable and thus invalid names.

The spider family Anapidae is reported from Laos for the first time. One new species is described: Pseudanapis namkhan n. sp. from Nam Khan Valley, Luang Prabang Province. Another species is recorded for the first time from Champasak Province, Laos and the following new synonymy is proposed: Sinanapis thaleri Ono 2009 = Sinanapis crassitarsus Wunderlich & Song 1995 n. syn. Morphological descriptions, diagnoses and comparative illustrations are provided for the two species.

Three new species of the spider genus Olios Walckenaer, 1837 are described from Laos: Olios diao spec. nov. (male) from Bolikhamsay Province, Nam Kading National Protected Area, Olios jaenicke spec. nov. (male) from Champasak Province, Pakse, and Olios suung spec. nov. (male) from Luang Prabang Province, Phou Khoun.

New species of the genus Laena Latreille, 1829 (Tenebrionidae: Lagriinae) are described from the Malayan Peninsula (Laena kenyirica n. sp., Laena schulzi n. sp.), Burma (Laena kurbatovi n. sp.), Thailand (Laena inthanonica n. sp., Laena khaolaka n. sp., Laena rolandi n. sp.), Laos (Laena champasaka n. sp., Laena jocheni n. sp., Laena kiyoshii n. sp.) and Vietnam (Laena gialaica n. sp., Laena moguntia n. sp.). A check-list of all species of the genus Laena from the Malayan Peninsula (13), Myanmar/Burma (2), Thailand (13), Laos (3) and Vietnam (9) is added.

A new subgenus, 19 new species and two new subspecies are described from Vietnam, Laos and China: Tamdaotettix (Tamdaotettix) aculeatus sp. nov., T. (T.) flexus sp. nov., T. (T.) laocai sp. nov., T. (Laotettix subgen. nov.) tarasovi sp. nov., T. (L.) curvatus sp. nov., T. (L.) minutus sp. nov., T. (L.) inflatus sp. nov., T. (L.) sympatricus sp. nov., T. (?) robustus sp. nov., Gigantettix laosensis sp. nov., G. maximus auster subsp. nov., Diestramima hainanensis sp. nov., D. bispinosa sp. nov., D. hamata sp. nov., D. propria sp. nov., D. yunnanensis sp. nov., D. champasak sp. nov., Adiestramima adunca sp. nov., A. bella sp. nov., A. elongata sp. nov., A. perfecta hue subsp. nov. Previously unknown male of G. maximus maximus Gorochov, 1998 and imago of D. palpata (Rehn, 1906) are described on the base of a new material. New distributional data for some species are given.

Quantification and characterization of municipal solid waste are vital information for a proper solid waste management. However, these are under-investigated and scarcely implemented in Laos PDR, especially the local communities. This work, therefore, aimed to quantify and characterize municipal solid waste generated from Beung Kiat Ngong Ramsar Site and to recommend possible integrated solid waste management strategies for a sustainable waste management. The average daily waste generation was estimated to be 3.6 kg/day and 2.6 kg/day in Thabou village and Kiat Ngong village, respectively. Organic waste appeared to be the biggest component (28%) for Thabou village, while packaging’s dominated waste composition in Kiat Ngong village. Interestingly, high percentage of golden apple shells waste were mismanaged. These had the potential to convert into value-added products such as calcium carbonate (CaCO3). It was found that fresh golden apple shells contained only 24.16±0.48 g/l as CaCO3, while incineration method increased higher CaCO3 products. The result showed that incineration at the temperature of 400 oC gave the highest amount of CaCO3 with the values of 1207.67±9.45 g/l as CaCO3. Based on the resources and the strength of the Ramsar site, the production of value added material from bio-waste could be integrated into waste management strategies along with 3Rs policies implementation.

Objectives: The elimination of key breeding sites of dengue vector is applied worldwide to control the vector density under the critical epidemic threshold. This study aimed to identify key breeding sites of Aedes mosquitos and associated factors in Huaylau village, Pakse city, Champasack province in Laos in 2019. Methods: This was a cross-sectional study, combining of immature stage survey of Aedes mosquitoes in all water and discarded containers and the community’s knowledge and practices on the prevention of dengue fever in all 240 households in Huaylau village. Multivariate logistic regression was applied to identify factors associated with the absence of Aedes larvae and pupae in the village. Statistical significance was set at a p-value less than 0.05. Results: Among the 720 water and discarded containers surveyed, the study found 654 Aedes larvae and pupae; of which 94.6% were immature Aedes aegypti. Key breeding sites of Aedes aegypti included water jars (34.2%), plastic drums (30.7%), tanks < 500 litter (14.7%), and discarded containers (12.6%), while that of all Aedes albopictus was discarded containers. The community’s better practices on the prevention of dengue fever contributed to the increased odds of the absence of Aedes larvae ad pupae by 1.612 (95%CI: 1.218-2.134, p<0.01), and the cleanliness of the house were associated with the increased odds of 4.072 of the absent Aedes larvae and pupae in the participated households (95%CI: 1.589-10.434, p<0.01). Conclusions: Aedes aegypti mosquitoes in the Huaylau village laid their eggs in various breeding sites, including water containers and discarded containers while discarded containers were the only key breeding site of Aedes albopictus. Better practices on dengue prevention and better hygiene conditions of the houses contributed to the absence of Aedes larvae and pupae. Special attention should be paid to the clearance of all discarded containers and education of the community people to cover water containers in the village. Keywords: key breeding sites, Aedes, mosquito, pupae, larvae, Champasack province, Lao PDR

The genus Olios Walckenaer, 1837 is revised, a generic diagnosis is given and an identification key to eight species groups is provided. Olios in its revised sense includes 87 species and is distributed in Africa, southern Europe and Asia. Three species groups are revised in this first part, an identification key to species for each group is provided, five new species are described and all included species are illustrated. The Olios argelasius-group includes O. argelasius Walckenaer, 1806, O. canariensis (Lucas, 1838), O. pictus (Simon, 1885), O. fasciculatus Simon, 1880 and O. kunzi spec. nov. (male, female; Namibia, Zambia, South Africa); it is distributed in the Mediterranean region, northern Africa including Canary Islands, in the Middle East, South Sudan, East Africa, and southern Africa. The Olios coenobitus-group includes O. angolensis spec. nov. (male; Angola), O. coenobitus Fage, 1926, O. denticulus spec. nov. (male; Java), O. erraticus Fage, 1926, O. gambiensis spec. nov. (male, female; Gambia), O. milleti (Pocock, 1901b), O. mordax (O. Pickard-Cambridge, 1899) and O. pusillus Simon, 1880; it is distributed in Africa (Gambia, Angola, Tanzania, Madagascar) and Asia (India, Sri Lanka, Indonesia: Java). The Olios auricomis-group includes only O. auricomis (Simon, 1880), distributed in Africa south of 10°N. Other species groups are introduced briefly and will be revised in forthcoming revisions. The Olios correvoni-group includes currently O. claviger (Pocock, 1901a), O. correvoni Lessert, 1921, O. correvoni choupangensis Lessert, 1936, O. darlingi (Pocock, 1901a), O. faesi Lessert, 1933, O. freyi Lessert, 1929, O. kassenjicola Strand, 1916b, O. kruegeri (Simon, 1897a), O. quadrispilotus (Simon, 1880) comb. nov., O. lucieni comb. nov. nom. nov., O. sjostedti Lessert, 1921 and O. triarmatus Lessert, 1936; it is distributed in Africa (Zimbabwe, Tanzania incl. Zanzibar, Angola, Congo, Central Africa, South Africa, Botswana; O. darlingi was recorded from Zimbabwe and Botswana and not from South Africa). The Olios rossettii-group includes: O. baulnyi (Simon, 1874), O. bhattacharjeei (Saha & Raychaudhuri, 2007), O. brachycephalus Lawrence, 1938, O. floweri Lessert, 1921, O. jaldaparaensis Saha & Raychaudhuri, 2007, O. japonicus Jäger & Ono, 2000, O. kolosvaryi (Caporiacco, 1947b) comb. nov., O. longipes (Simon, 1884b), O. lutescens (Thorell, 1894), O. mahabangkawitus Barrion & Litsinger, 1995, O. obesulus (Pocock, 1901b), O. rossettii (Leardi, 1901), O. rotundiceps (Pocock, 1901b), O. sericeus (Kroneberg, 1875), O. sherwoodi Lessert, 1929, O. suavis (O. Pickard-Cambridge, 1876), O. tarandus (Simon, 1897d), O. tener (Thorell, 1891) and O. tiantongensis (Zhang & Kim, 1996); it is distributed in the Mediterranean region, in Africa (especially eastern half) and Asia (Middle East and Central Asia to Japan, Philippines and Java). The Olios nentwigi-group includes O. diao Jäger, 2012, O. digitatus Sun, Li & Zhang, 2011, O. jaenicke Jäger, 2012, O. muang Jäger, 2012, O. nanningensis (Hu & Ru, 1988), O. nentwigi spec. nov. (male, female; Indonesia: Krakatau), O. perezi Barrion & Litsinger, 1995, O. scalptor Jäger & Ono, 2001 and O. suung Jäger, 2012; it is distributed in Asia (Thailand, Laos, Vietnam, Cambodia, China, Taiwan, Indonesia, Philippines), Papua New Guinea and Mariana Islands. Olios diao is newly recorded from Cambodia and Champasak Province in Laos. The Olios stimulator-group includes O. admiratus (Pocock, 1901b), O. hampsoni (Pocock, 1901b), O. lamarcki (Latreille, 1806) and O. stimulator Simon, 1897c; it is distributed in Africa (Madagascar, Seychelles), Middle East and South Asia (United Arab Emirates, Iraq, Afghanistan, Pakistan, India, Maldives, Sri Lanka). The Olios hirtus-group includes O. bungarensis Strand, 1913b, O. debalae (Biswas & Roy, 2005), O. ferox (Thorell, 1892), O. hirtus (Karsch, 1879a), O. igraya (Barrion & Litsinger, 1995) comb. nov., O. menghaiensis (Wang & Zhang, 1990), O. nigrifrons (Simon, 1897b), O. punctipes Simon, 1884a, O. punctipes sordidatus (Thorell, 1895), O. pyrozonis (Pocock, 1901b), O. sungaya (Barrion & Litsinger, 1995) comb. nov., O. taprobanicus Strand, 1913b and O. tikaderi Kundu et al., 1999; it is distributed in South, East and Southeast Asia (Sri Lanka, India, Nepal, Bangladesh, Myanmar, China, Laos, Thailand, Cambodia, Vietnam, Malaysia, Indonesia, Philippines). Nineteen synonyms are recognised: Nisueta Simon, 1880, Nonianus Simon, 1885, both = Olios syn. nov.; O. spenceri Pocock, 1896, O. werneri (Simon, 1906a), O. albertius Strand, 1913a, O. banananus Strand, 1916a, O. aristophanei Lessert, 1936, all = O. fasciculatus; O. subpusillus Strand, 1907c = O. pusillus; O. schonlandi (Pocock, 1900b), O. rufilatus Pocock, 1900c, O. chiracanthiformis Strand, 1906, O. ituricus Strand, 1913a, O. isongonis Strand, 1915, O. flavescens Caporiacco, 1941 comb. nov., O. pacifer Lessert, 1921, all = O. auricomis; Olios sanguinifrons (Simon, 1906b) = O. rossettii Leardi, 1901; O. phipsoni (Pocock, 1899), Sparassus iranii (Pocock, 1901b), both = O. stimulator; O. fuligineus (Pocock, 1901b) = O. hampsoni. Nine species are transferred to Olios: O. gaujoni (Simon, 1897b) comb. nov., O. pictus comb. nov., O. unilateralis (Strand, 1908b) comb. nov. (all three from Nonianus), O. affinis (Strand, 1906) comb. nov., O. flavescens Caporiacco, 1941 comb. nov., O. quadrispilotus comb. nov., O. similis (Berland, 1922) comb. nov. (all four from Nisueta), O. sungaya (Barrion & Litsinger, 1995) comb. nov., O. igraya (Barrion & Litsinger, 1995) comb. nov. (both from Isopeda L. Koch 1875). Olios lucieni nom. nov. comb. nov. is proposed for Nisueta similis Berland, 1922, which becomes a secondary homonym. The male of O. quadrispilotus comb. nov. is described for the first time. Sixteen species are currently without affiliation to one of the eight species groups: O. acolastus (Thorell, 1890), O. alluaudi Simon, 1887a, O. batesi (Pocock, 1900c), O. bhavnagarensis Sethi & Tikader, 1988, O. croseiceps (Pocock, 1898b), O. durlaviae Biswas & Raychaudhuri, 2005, O. gentilis (Karsch, 1879b), O. gravelyi Sethi & Tikader, 1988, O. greeni (Pocock, 1901b), O. inaequipes (Simon 1890), O. punjabensis Dyal, 1935, O. ruwenzoricus Strand, 1913a, O. senilis Simon, 1880, O. somalicus Caporiacco, 1940, O. wroughtoni (Simon, 1897c) and O. zulu Simon, 1880. Five of these species are illustrated in order to allow identification of the opposite (male) sex and to settle their systematic placement. Thirty-seven species are considered nomina dubia, mostly because they were described from immatures, three of them are illustrated: O. abnormis (Blackwall, 1866), O. affinis (Strand, 1906) comb. nov., O. africanus (Karsch, 1878), O. amanensis Strand, 1907a, O. annandalei (Simon, 1901), O. bivittatus Roewer, 1951, O. ceylonicus (Leardi, 1902), O. conspersipes (Thorell, 1899), Palystes derasus (C.L. Koch, 1845) comb. nov., O. detritus (C.L. Koch, 1845), O. digitalis Eydoux & Souleyet, 1842, O. exterritorialis Strand, 1907b, O. flavovittatus (Caporiacco, 1935), O. fugax (O. Pickard-Cambridge, 1885), O. guineibius Strand, 1911c, O. guttipes (Simon, 1897a), O. kiranae Sethi & Tikader, 1988, O. longespinus Caporiacco, 1947b, O. maculinotatus Strand, 1909, O. morbillosus (MacLeay, 1827), O. occidentalis (Karsch, 1879b), O. ornatus (Thorell, 1877), O. pagurus Walckenaer, 1837, O. patagiatus (Simon, 1897b), O. praecinctus (L. Koch, 1865), O. provocator Walckenaer, 1837, O. quesitio Moradmand, 2013, O. quinquelineatus Taczanowski, 1872, O. sexpunctatus Caporiacco, 1947a, Heteropoda similaris (Rainbow, 1898) comb. rev., O. socotranus (Pocock, 1903), O. striatus (Blackwall, 1867), O. timidus (O. Pickard-Cambridge, 1885), Remmius variatus (Thorell, 1899) comb. nov., O. vittifemur Strand, 1916b, O. wolfi Strand, 1911a and O. zebra (Thorell, 1881). Eighty-nine species are misplaced in Olios but cannot be affiliated to any of the known genera. They belong to the subfamilies Deleninae Hogg, 1903, Sparassinae Bertkau, 1872 and Palystinae Simon, 1897a, nineteen of them are illustrated: O. acostae Schenkel, 1953, O. actaeon (Pocock, 1898c), O. artemis Hogg, 1915, O. atomarius Simon, 1880, O. attractus Petrunkevitch, 1911, O. auranticus Mello-Leitão, 1918, O. benitensis (Pocock, 1900c), O. berlandi Roewer, 1951, O. biarmatus Lessert, 1925, O. canalae Berland, 1924, O. caprinus Mello-Leitão, 1918, O. chelifer Lawrence, 1937, O. chubbi Lessert, 1923, O. clarus (Keyserling, 1880), O. coccineiventris (Simon, 1880), O. corallinus Schmidt, 1971, O. crassus Banks, 1909, O. debilipes Mello-Leitão, 1945, O. discolorichelis Caporiacco, 1947a, O. erroneus O. Pickard-Cambridge, 1890, O. extensus Berland, 1924, O. fasciiventris Simon, 1880 , O. feldmanni Strand, 1915, O. fimbriatus Chrysanthus, 1965, O. flavens Nicolet, 1849, O. fonticola (Pocock, 1902), O. formosus Banks, 1929, O. francoisi (Simon, 1898a), O. fulvithorax Berland, 1924, O. galapagoensis Banks, 1902, O. gaujoni (Simon, 1897b) comb. nov., O. giganteus Keyserling, 1884, O. hoplites Caporiacco, 1941, O. humboldtianus Berland, 1924, O. insignifer Chrysanthus, 1965, O. insulanus (Thorell, 1881), O. keyserlingi (Simon, 1880), O. lacticolor Lawrence, 1952, O. lepidus Vellard, 1924, O. longipedatus Roewer, 1951, O. machadoi Lawrence, 1952, O. macroepigynus Soares, 1944, O. maculatus Blackwall, 1862, O. marshalli (Pocock, 1898a), O. mathani (Simon, 1880), O. minensis Mello-Leitão, 1917, O. monticola Berland, 1924, O. mutabilis Mello-Leitão, 1917, O. mygalinus Doleschall, 1857, O. mygalinus cinctipes Merian, 1911, O. mygalinus nirgripalpis Merian, 1911, O. neocaledonicus Berland, 1924, O. nigristernis (Simon, 1880), O. nigriventris Taczanowski, 1872, O. oberzelleri Kritscher, 1966, O. obscurus (Keyserling, 1880), O. obtusus F.O. Pickard-Cambridge, 1900, O. orchiticus Mello-Leitão, 1930, O. oubatchensis Berland, 1924, O. paraensis (Keyserling, 1880), O. pellucidus (Keyserling, 1880), O. peruvianus Roewer, 1951, O. pictitarsis Simon, 1880, O. plumipes Mello-Leitão, 1937, O. princeps Hogg, 1914, O. pulchripes (Thorell, 1899), O. puniceus (Simon, 1880), O. roeweri Caporiacco, 1955a, O. rubripes Taczanowski, 1872, O. rubriventris (Thorell, 1881), O. rufus Keyserling, 1880, O. sanctivincenti (Simon, 1898b), O. similis (O. Pickard-Cambridge, 1890), O. simoni (O. Pickard-Cambridge, 1890), O. skwarrae Roewer, 1933, O. spinipalpis (Pocock, 1901a), O. stictopus (Pocock, 1898a), O. strandi Kolosváry, 1934, O. subadultus Mello-Leitão, 1930, O. sulphuratus (Thorell, 1899), O. sylvaticus (Blackwall, 1862), O. tamerlani Roewer, 1951, O. tigrinus (Keyserling, 1880), O. trifurcatus (Pocock, 1900c), O. trinitatis Strand, 1916a, O. velox (Simon, 1880), O. ventrosus Nicolet, 1849, O. vitiosus Vellard, 1924 and O. yucatanus Chamberlin, 1925. Seventeen taxa are transferred from Olios to other genera within Sparassidae, eight of them are illustrated: Adcatomus luteus (Keyserling, 1880) comb. nov., Eusparassus flavidus (O. Pickard-Cambridge, 1885) comb. nov., Palystes derasus (C.L. Koch, 1845) comb. nov., Heteropoda similaris (Rainbow, 1898) comb. rev., Remmius variatus (Thorell, 1899) comb. nov., Nolavia audax (Banks, 1909) comb. nov., Nolavia antiguensis (Keyserling, 1880) comb. nov., Nolavia antiguensis columbiensis (Schmidt, 1971) comb. nov., Nolavia fuhrmanni (Strand, 1914) comb. nov., Nolavia helva (Keyserling, 1880) comb. nov., Nolavia stylifer (F.O. Pickard-Cambridge, 1900) comb. nov., Nolavia valenciae (Strand, 1916a) comb. nov., Nungara cayana (Taczanowski, 1872) comb. nov., Polybetes bombilius (F.O. Pickard-Cambridge, 1899) comb. nov., Polybetes fasciatus (Keyserling, 1880) comb. nov., Polybetes hyeroglyphicus (Mello-Leitão, 1918) comb. nov. and Prychia paalonga (Barrion & Litsinger, 1995) comb. nov. One species is transferred from Olios to the family Clubionidae Wagner, 1887: Clubiona paenuliformis (Strand, 1916a) comb. nov.

This paper seeks to explore environmental, social and governance issues arising from investment in special economic zones (SEZs) in the mainland Southeast Asian region through a mixture of thick analytical description and multiple case study approach. All the states studied here have embraced the SEZ approach as it offers rapid economic development without any implications for the political settlement, which is considered beneficial by current administrations. Particular emphasis is placed on environmental, social and governance issues in the region covered and some complex issues that have emerged. It is shown that the situation is complex and continually evolving and that there are limited constraints on the actions of corporations. Consequently, there is an opportunity for investors to set precedents and protocols on a progressive basis. Keywords Economic development; environmental, social and governance issues; mainland Southeast Asia; special economic zones References [1] Anderson, Benedict, “Murder and Progress in Modern Siam,” New Left Review. 181 (1990) 33-48.[2] Ando, “About Ando”. www.ando-kyo.co.jp/english/about/history.html/, 2016.[3] Apisitniran, Lamonphet, “Latest SEZ Land Proposal Fizzles out,” Bangkok Post, Business B2, June 19th, 2015.[4] Aung, Noe Noe, “Workers Strike over Wage Demands”, Myanmar Times. http:// www.mmtimes.com/national-news/yangon/7150-thousands-of-workers-protest-in-hlaing-tharyar.html/, November 12th, 2017. [5] Baissac, Claude, “Brief History of SEZs and Overview of Policy Debates,” in Thomas Farole, ed., Special Economic Zones in Africa: Company Performance and Learning from Global Experience (Washington, DC: World Bank. http://openknowledge.worldbank.org/bitstream/handle/10986/2341/638440PUB0Exto00Box0361527B0PUBLIC0.pdf/, 2011. [6] Beerlao, “Lao Brewery” (n.d.). http://www.beerlao.la/products/.[7] Champasak Province, “Investment Opportunities in Laos: Champasak Province”. http://www.poweringprogress.org/new/images/PDF/Champassak_10/Champassak_10.pdf/, 2009.[8] Chang, Ha-Joon, Ilene Grabel, Reclaiming Development: An Alternative Economic Policy Manual, London: Zedbooks, 2014.[9] Chintraruck, Alin and John Walsh, “Bangkok and the Floods of 2011: Urban Governance and the Struggle for Democratisation,” in Miller, M. and M. Douglass (eds.), Disaster Governance in Urbanising Asia, Singapore: Springer, 2016, pp.195-209.[10] David, Sen, “Garment Factory Employees Protest Short-Term Contracts,” Phnom Penh Post. http:// www.phnompenhpost.com/national/garment-factory-employees-protest-short-term-contracts/, 2016.[11] Embassy of Japan in the Lao PDR, “Remarks by H.E. Hiroyuki Kishino, Ambassador of Japan to the Lao PDR, at the Inauguration Ceremony of the New Ando Factory in Pakse. http://www.la.emb-japan.go.jp/content_japan_laos_relations/ambassador_speech/Ando.html/, 2013 (Champasak Province on 03 December, 2013”). [12] M. Eisenbruch, “Mass Fainting in Garment Factories in Cambodia”, Transcultural Psychiatry. 54 (2017) 155-78.[13] Gopalakrishnan, Raju, “China-Vietnam Dispute: “More than 20 Killed” in Anti-China Riots,” Independent. http:// www.independent.co.uk/news/world/asia/china-vietnam-dispute-more-than-20-killed-in-anti-china-riots-9375887.html/, 2014 (May 15th, 2014). [14] Guardian Staff, Agencies, “Aung San Suu Kyi Denies Ethnic Cleansing of Rohingya Muslims in Myanmar,” The Guardian. http:// www.theguardia.com/world/2017/apr/05/myanmar-aung-san-suu-kyi-ethnic-cleansing/, 2017 (April 5th, 2017). [15] Hance, Jeremy, “High-End Laos Resort Serves up Illegal Wildlife for Chinese Tourists”, The Guardian.http://www.theguardian.com/environment/radical-conservation/2015/mar/19/high-end-laos-resort-serves-up-illegal-wildlife-for-chinese-tourists/, 2015 (March 19th, 2015). [16] HKTDC, “Myanmar Rising: Industrial and Special Economic Zones”. http://economists-pick-research.hktdc.com/business-news/article/Research-Articles/Myanmar-Rising-Industrial-and-Special-Economic-Zones/rp/en/1/1X000000/1X0A72FF.htm/, 2016. [17] Inclusive Development International, “Cambodia: Boeung Kak Lake Evictions” (n.d.). http:// www.inclusivedevelopment.net/campaign/cambodia-boeung-kak-lake-evictions/. [18] International Rivers, “The World Bank and Dams”. http://www.internationalrivers.org/sites/default/files/attached-files/world-bank-and-dams-fact-sheet.pdf/, 2015 (April, 2015). [19] Jacobsen, Trudy, Lost Goddesses: The Denial of Female Power in Cambodian History (Copenhagen: NIAS Press, 2008).[20] Kongkirati, Prajak, “Murder without Progress in Siam: From Hired Gunmen to Men in Uniform,” Kyoto University Center for Southeast Asia Studies. http://kyotoreview.org/issue-21/murder-without-progress-siam/, 2017. [21] Ku, Samuel, “China’s Expanding Influence in Laos,” East Asia Forum. http:// www.eastasiforum.org/2016/02/26/chinas-expanding-influence-in-laos/, 2016 (February 26th, 2016).[22] Kurlantzick, Joshua, “Cambodia Draws Closer to Outright Authoritarianism,” Council on Foreign Relations. http://www.cfr.org/blog/cambodia-draws-closer-outright-authoritarianism/, 2017 (October 10th, 2017). [23] Kyozuki, Tamaki, “Laos OKs Economic Zone for Smaller Japanese Companies,” Nikkei Asian Review. http://asia.nikkei.com/Politics-Economy/Economy/Laos-OKs-economic-zone-for-smaller-Japanese-companies/, 2015 (September 18th, 2015).[24] Larsson, Naomi, “Human Rights in Thailand: Andy Hall’s Legal Battle to Defend Migrant Workers,” The Guardian. http:// www.theguardian.com/global-development-professionals-network/2016/jan/22/human-rights-thailand-andy-hall-legal-battle-migrant-workers/, 2016 (January 22nd, 2016). [25] Le Coz, Clothilde, “Blood Sugar”. http://www.ruom.net/portfolio-item/blood-sugar/, 2013. [26] LNC, “Nishimatsu Capitalized on Pakse-Japan SME SEZ Development”. http://laonishimatsu.com/?lang=en&module=news&idz=7/, 2016.[27] T.G. McGee, The Southeast Asian City: a Social Geography of the Primate Cities of Southeast Asia (London: G. Bell and Sons, 1967), 1967.[28] McGrath, Cam, “Sihanoukville Zone Prospers on China Links,” The Phnom Penh Post. https:// www.phnompenhpost.com/business/sihanoukville-zone-prospers-china-links/, 2017 (June 12th, 2017). [29] Mills, Mary Beth, “From Nimble Fingers to Raised Fists: Women and Labor Activism in Globalizing Thailand,” Signs: Journal of Women in Culture and Society. 31 (2005) 117-44.[30] Minami, Ryoshin and Xinxin Ma, “The Lewis Turning Point of Chinese Economy: Comparison with Japanese Economy,” China Economic Journal. 3 (2010) 163-79.[31] Mingaladon Industrial Park, “Internal Infrastructure”. https://www.mingaladon.com/infrastructure-services.htm/, 2017a. [32] Mingaladon Industrial Park (2017b), “Investment Incentives,” http:// www.mingaladon.com/investment-incentives.htm.[33] Myanmar Industries, “Main Activities”. https:// myanmarindustries.org/index.php/main-activities-2/, 2017b. [34] Myanmar Industries, “Background”. https://myanmarindustries.org/index.php/background-2/, 2017a. [35] Nikon, “Establishment of a New Factory in Laos”. https://www.nikon.com/news/2013/0321_01.htm/,2013. [36] Nolintha, Vanthana, “Cities, SEZs and Connectivity in Major Provinces of Laos,” in Masami Ishida, ed., Intra- and Inter-City Connectivity in the Mekong Region, BRC Research Report No.6 (Bangkok: IDE-JETRO Bangkok Research Centre, 2011). http://www.ide.go.jp/library/English/Publish/Download/Brc/pdf/06_chapter4.pdf/, 2011.[37] Paing, Yan, “Chinese Developer to Invest US$390m in Mandalay Project,” Eleven Myanmar (13th, October, 2017), http://www.elevenmyanmar.com/local/11966/, 2017 (13th, October, 2017). [38] Phnom Penh SEZ, ‘Facilities and Services,’ Phnom Penh SEZ, available at: www.ppsez.com/en/the-zone/phnom-penh-sez/facilities/, 2017. [39] Pinyochatchinda, Supaporn and John Walsh, “Pollution Management and Industrial Estates: Perceptions of Residents in the Vicinity of Map Ta Phut Industrial Estate,” Information Management and Business Review. 6 (2014) 42-8.http://bua.rmutr.ac.th/wpcontent/uploads/2016/09/WY-13-56.pdf. [40] Poupon, Roland, The Thai Food Complex: From the Rice Fields to Industrial and Organic Foods (Bangkok: White Lotus Press, 2013), 2013.[41] QTSP, “Who We Are”, available at: https://web.archive.org/web/20110501200030/http://www.quangtrungsoft.com.vn:80/index.php/en/about-qtsc/who-we-are?start=3/, 2011. [42] Rentsbuy, “Govt Approves New SEZ in Champasak”. https:// www.rentsbuy.com/project/economic-zone/pakxe-japan-sme-specific-economic-zone.html/, 2015 (August 10th, 2015).[43] Reporters without Borders, “2017 World Press Freedom Index”. https://rsf.org/en/ranking/, 2017.[44] Scott, C. James, Weapons of the Weak: Everyday Forms of Peasant Resistance, New Haven, CT: Yale University Press, 1985. [45] Sihanoukville SEZ, “Social Responsibility”. https:// ssez.com/en/social.asp#/, 2017. [46] Siu, Kaxton, “The Vietnam Strike Wave,” Asia Monitor Resource Centre. www.amrc.org.hk/content/vietnam-strike-wave/, 2011 (June 27th, 2011). [47] Stuart-Fox, Martin, “Historical and Cultural Constraints on Development in the Mekong Region,” paper prepared for the seminar “Accelerating Development in the Mekong Region: The Role of Economic Integration,” Siem Reap, Cambodia. http://www.imf.org/external/np/seminars/eng/2006/mekong/fox.pdf/, 2006 (June 26th-27th, 2006). [48] The Nation, “Laos-Japan Economic Zone to Benefit Local Community”. http://www.nationmultimedia.com/business/Laos-Japan-economic-zone-to-benefit-local-communit-30276007.html/, 2016 (January 2nd, 2016).[49] The Nation, “Foreigners to Be Allowed to Set up Universities in Special Economic Zones,” The Nation. http://www.nationmultimedia.com/news/breakingnews/30315506/, 2017 (May 17th, 2017). [50] Thongnoi, Jitsinee, “Open for Business, If Anyone Wants to Come,” Bangkok Post, April 5th, 2015, pp. 6-9.[51] Thul, Prak Chan, “Cambodian Forces Open Fire as Factory Strikes Turn Violent,” Reuters. http://www.reuters.com/article/us-cambodia-protest/cambodian-forces-open-fire-as-factory-strikes-turn-violent-idUSBREA0203H20140103/, 2014 (January 3rd, 2014).[52] Transparency International, “Country Analysis”. https://www.transparency.org/country/, 2016.[53] Trinh, Vo Thi Trung, Narumon Sriratanaviriyakul, Matthews Nkhoma and Hiep Pham, “Quang Trung Software City - The Largest Vietnamese Software Park,” Journal of Information Technology Education: Discussion Cases, Vol.2, Case No.6 (2013), http://www.jite.org/documents/DCVol02/v02-06-QuangTrung.pdf/, 2013. [54] UNCTAD, Investment and Enterprise Responsibility Review: Analysis of Investor and Enterprise Policies on Corporate Social Responsibility (New York, NY and Geneva: UNCTAD.http://unctad.org/en/Docs/diaeed20101_en.pdf/, 2011. [55] Vietnam Briefing, “IT Parks in Vietnam: Present and Future”. http://www.vietname-briefing.com/news/it-parks-in-vietnam-present-and-future7461.html/, 2017. [56] Vietnam.net, “More Software Parks to Go up”. https:// english.vietnamnet.vn/fms/science-it/116286/more-software-parks-to-go-up.html/, 2014 (November 13th, 2014a).[57] Vietnam Net, “China Attempts to Control Vietnam’s Mineral Industries”. https:// english.vietnamenet.vn/fms/business/94502/china-attempts-tocontrol-vietnam-s-mineral-industries.html/, 2014b (January 25th, 2014b). [58] Walsh, John, “Tesco Lotus Thailand: Managing Stakeholders in a Hostile Environment,” in B.S. Sahay, Tojo Thatchenkery and G.D. Sardana, Handbook on Management Cases (New Delhi: Allied Publishers Pvt. Ltd., 2008, pp. 447-51.[59] Walsh, John, “The Development of Dawei Special Economic Zone,” The Myanmar Journal. 2 (2015) 9-26, [60] Walsh, John and Nittana Southiseng, “Vientiane - A Failure to Exert Power?” City: Analysis of Urban Trends, Culture, Theory, Policy, Action. 13 (2009) 95-102.[61] Wancharoen, Supoj and Sirinya Wattanasukchai, “Urban Projects Gain Favour, Stoke Fury,” Bangkok Post (December 30th 2015), 2015. [62] Whitehead, Judith, “Intersectionality and Primary Accumulation: Caste and Gender in India under the Sign of Monopoly-finance Capital,” Monthly Review. 68 (2016) 37-52.[63] World Bank, “International Scorecard”. https://lpi.worldbank.org/international/scorecard/ 2016.[64] World Economic Forum (2016), Global Competitiveness Report, 2016, available at: reports.weforum.org/global-competititveness-report-2015-2016.[65] WTO, “Members and Observers”. https://www.wto.org/english/thewto_e/whatitis_e/tif_e/org6_3.htm/, 2016.