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Ed.Note: Captain René Pita is a professor at the Spanish Military NBC Defense School and a toxicologist with the Joint Assessment Team (JAT) - NATO Multinational CBRN Defense Battalion (NRF-5). Al-Qa`ida and the Chemical ThreatRené Pita, Ph.D. After the 11 September 2001 (9/11) terrorist attacks in the US there has been a perception that the risk of possible attacks with chemical or biological weapons, especially by groups associated with the al-Qa`ida terrorist network, is high. Surprisingly, the risk perception was higher than after the 1994 and 1995 sarin attacks in Japan, when a chemical warfare agent caused a large number of casualties. However, the mailing of letters containing anthrax spores, accompanied by images of the attacks on the World Trade Center towers, have increased the concern about chemical and biological attacks. This paper aims to analyze information from open sources about the possible use of chemical weapons by groups affiliated with or linked to the al-Qa`ida terrorist network
Pre-9/11 Incidents • The first incident, interestingly, comes from the February 1993 bombing of the World Trade Center as it is sometimes claimed that cyanide was incorporated in the bomb. The mastermind of the attack was Ramzi Yousef, who fought in Afghanistan against the former Soviet Union and was arrested on 7 February 1995 in Peshawar (Pakistan) while staying at an Usama bin Ladin guest house [1]. Although the terrorists had cyanide salt in their possession, cyanide was never detected in the attack. A detailed study of this incident also leads to the conclusion that the agent was not used [2]. Post-9/11 Incidents • Four Moroccans, members of the Salafist Group for Preaching and Fighting, were arrested in Rome on 19 February 2002. They had about 4 kg of potassium ferrocyanide that they intended to use to contaminate the water supplies in the area where the US Embassy is located [9]. However, that particular substance is widely used as a food additive (E 536), and because of its toxicological properties was probably not the best choice to use in a chemical attack [10]. It seems that the terrorists may have been attracted but misled by the “cyano” group in its chemical structure.
• On 12 December 2002 The Washington Post reported that Islamic extremists affiliated to al-Qa`ida had acquired VX from Iraq and had smuggled it overland through Turkey [13]. Nevertheless, this article notes that “like most intelligence, the reported chemical weapon transfer is not backed by definitive evidence.” • Jordanian authorities made public in April 2004 that they had broken up an al-Qa`ida plot to employ large quantities of toxic industrial chemicals (TICs), such as sulfuric acid, cyanide salts and insecticides, against the US Embassy, the Jordanian prime minister’s office, and the headquarters of Jordanian intelligence [25]. In a confession shown on state-run television, the cell’s ringleader stated that the mastermind of the alleged plot was Abu Mus`ab al-Zarqawi, al-Qa`ida’s “amir” in Iraq.
• In November 2004 US forces discovered “cookbooks” on how to make hydrogen cyanide and a “chemical laboratory” in a house in Fallujah that was allegedly used by terrorists linked to Abu Mus`ab al-Zarqawi [28]. However, the images of the “chemical laboratory” released to the media remind one of those seen in some homemade “amateur terrorist” videos, and are far from what a laboratory capable of making chemical warfare agents would look like. Threat Analysis Since 9/11 the number of reports in open sources about incidents with chemical weapons and radical Islamist terrorism has increased. This may be a consequence of a real increase in the number of incidents, the high risk perception of possible attacks with chemical weapons, or a combination of both. Some of these reports have presented inaccurate or incorrect information that may contribute to creating an amplified and distorted risk perception, which may in turn serve to inspire terrorists or increase the psychological effects of a future chemical attack. Indeed, one of the objectives of using chemical or biological weapons in a military scenario is not only to cause physical casualties, but also to demoralize troops. Similarly, in a terrorist attack on civilians, one of the primary goals is to create a general sense of panic and fear.
At this time it does not seem likely that terrorist groups linked to al-Qa`ida have the skills and technical proficiency needed to make a “classical” chemical warfare agent or to disseminate it in an effective manner. The absence of successful Islamist chemical attacks up to this point seems to confirm these facts. However, their potential future capability should not be underestimated. The biggest worry, based on the information analyzed here, is that they are both interested in chemical weapons and actively trying to obtain them. As far back as 1998 Usama bin Ladin had stated that it was a “sacred duty” for Muslims to obtain weapons of mass destruction [35]. Acquiring these agents from black market smugglers or sponsoring states may be options that ultimately yield better results than adopting the crude procedures in the aforementioned manuals. For example, it is known that al-Qa`ida’s elite 055 Brigade was in contact with the Ukrainian and Russian mafia [36] and that, more recently, common Portuguese and Spanish criminals tried to sell two fake “mercury bombs” from the former Soviet Union [37], perhaps knowing of the interest of Islamist terrorists in “red mercury,” [38] a bogus substance allegedly used in fusion nuclear weapons [39]. Another concern is that terrorists will increasingly try to acquire chemicals that are not strictly classified as “classical” chemical weapons, but which could be equally effective. An attack against a chemical plant or transport vehicle may also result in the release of TICs, with potentially catastrophic consequences similar to the accidental release of methyl isocyanate in Bhopal (India) in 1984. Intelligence services and security measures are critical in the prevention and countering of chemical attacks, and, in case they do occur, governments must develop the capabilities to detect and minimize both their physical consequences and their psychological impact. Acknowledgement. The author wishes to thank Dr. Jeffrey M. Bale (Senior Research Associate, WMD Terrorism Research Program, Center for Nonproliferation Studies, Monterey Institute of International Studies, USA) for his critical review of this manuscript. Notes and References [1] Venzke, B. and Ibrahim, A., The al-Qaeda threat: An analytical guide to al-Qaeda’s tactics & targets, Tempest Publishing, Alexandria, 2003, p. 216. [5] Bamber, D., Hastings, C. and Syal, R., “Bin Laden British cell planned gas attack on European Parliament,” Daily Telegraph, 16 September 2001. [6] Hastings, C. and Bamber, D., “Police foil terror plot to use sarin gas in London,” Daily Telegraph, 18 February 2001. [7] Venzke and Ibrahim, op. cit., no. 1 above, pp. 32-33. [8] Ibid., p. 30. [9] “«Cyanide attack» foiled in Italy,” BBC News, 20 February 2002. [10] Because of the strong chemical bond between iron and the cyanide groups, potassium ferrocyanide has low toxicity. For information on the toxicology of potassium ferrocyanide, see Joint FAO/WHO Expert Committee on Food Additives, Toxicological evaluation of some food additives including anticaking agents, antimicrobials, antioxidants, emulsifiers and thickening agents, FAO Nutrition Meetings Report Series, no. 53, WHO Food Additives Series, no. 5, 1974. [11] Rohde, D. and Chivers, C. J., “Qaeda’s grocery lists and manuals of killing,” New York Times, 17 March 2002; and Chivers, C. J. and Rohde, D., “Turning out guerrillas and terrorists to wage a holy war,” New York Times, 18 March 2002. [12] “Three on London terror charges,” BBC News, 17 November 2002. [13] Gellman, B., “U.S. suspects Al Qaeda got nerve agent from Iraqis. Analysts: chemical may be VX, and was smuggled via Turkey,” Washington Post, 12 December 2002. [14] Warrick, J., “An Al Qaeda «chemist» and the quest for ricin,” Washington Post, 5 May 2004. [15] Bale, J. M., Bhattacharjee, A., Croddy, E., et al., “Ricin found in London: An al-Qa`ida connection?” Center for Nonproliferation Studies (Monterey Institute of International Studies), 23 January 2003. [16] Cowell, A., “Just one of 9 suspects convicted in 2003 British poison plot case,” New York Times, 14 April 2005. [17] Ross, B., “Poison plot: Ricin, cyanide found in Paris; U.S. facilities may have been targets,” ABC News, 20 March 2003. [18] “Ricin «linked to militants»,” BBC News, 21 March 2003. [19] “France: Testing shows Parisian ricin find was actually common grain,” NTI Global Security Newswire, 14 April 2003. [20] “On the street,” ASA Newsletter, no. 96, 20 June 2003, p. 15. [21] Arnuero, P., “El FBI cree que los salafistas iban a mezclar el napalm con gas sarín,” La Razón, 14 November 2003. [22] “Un lugarteniente de Al Zarqaui revela un plan para atacar con armas químicas la base de Rota,” ABC, 3 May 2005. [23] “U.S. Forces in Iraq find some cyanide,” ABC News, 7 February 2004. [24] Baker, M. and Kosal, M. E., “Osmium tetroxide - A new chemical terrorism weapon?” Center for Nonproliferation Studies (Monterey Institute of International Studies), 13 April 2004. [25] “Jordan says major al Qaeda plot disrupted,” CNN, 26 April 2004; and Lázaro, F., “El FBI alerta de que las nuevas bombas que prepara Al Qaeda producen gases mortíferos,” El Mundo, 1 May 2005. [26] “Islamist group claims Senate ricin attack,” NTI Global Security Newswire, 7 July 2004. [27] Comprehensive Report of the Special Advisor to the Director of Central Intelligence on Iraq’s Weapons of Mass Destruction, Volume III, 30 September 2004, pp. 93-95. [28] Gertz, B., “Iraqi bomb labs signal attacks in the works,” Washington Times, 30 November 2004. [29] “FSB says major terror attacks foiled,” Moscow Times, 6 May 2005. [30] Bale, Bhattacharjee and Croddy et al., op. cit., no. 15 above. [31] For more information on hydrogen cyanide use as a chemical weapon see Dr. Jan Medema’s excellent paper: Medema, J., “AC, HCN, Blausaure,” ASA Newsletter, no. 107, 22 April 2005, pp. 1, 22-23. [32] Pita, R., Anadón, A. and Martínez-Larrañaga, M. R., “Ricina: Una fitotoxina de uso potencial como arma,” Revista de Toxicología, vol. 21, no. 2-3, 2004, pp. 51-63. [33] Birstein, V. J., “Deadly science,” in The perversion of knowledge: The true story of Soviet science, Westview Press, Colorado, 2001, p. 110. [34] Pita, R., Domingo, J., Aizpurura, C. et al., “Extracción de ricina por procedimientos incluidos en publicaciones paramilitares y manuales relacionados con la red terrorista Al Qaeda,” Medicina Militar, vol. 60, no. 3, 2004, pp. 172-175. [35] Reinares, F., “¿Bombas del Apocalipsis?” in Terrorismo global, Taurus, Madrid, 2003, pp. 151-152. [36] De Arístegui, G., “El funcionamiento de Al-Qaeda y el FIM (Frente Islámico Mundial),” in El islamismo contra el islam, Ediciones B, Barcelona, 2004, p. 270. [37] “Un grupo de estafadores pretendía vender dos bombas de mercurio falsas,” ABC, 9 November 2004. [38] Velasco, F., “La «célula» de Barcelona buscaba material químico para atacar España o Marruecos,” La Razón, 28 December 2004. [39] Red mercury (RM) would be a constituent of a former Soviet Union “pure” fusion nuclear weapon of deuterium and tritium. When ignited, RM would not explode but produce enormous temperatures and pressures sufficient to enable the deuterium-tritium fusion. Although it is supposed to be a hoax substance used in smuggling swindles, some authors defend its existence and some even identify it as Hg2Sb2O7 with a small quantity of an actinide. See Barnaby, F., “Red mercury: Is there a pure-fusion bomb for sale?” Jane’s International Defense Review, vol. 27, no. 6, 1994, pp. 79-81; Hounam, P. and McQuillan, S., The mini-nuke conspiracy: Mandela’s nuclear nightmare, Viking Books, New York, 1995; Cohen, S. and Douglass, J., “The nuclear threat that doesn’t exist - Or does it?” Financial Sense Online, 11 March 2003; and Sleight, A. W., “New ternary oxides of mercury with the pyrochlore structure,” Inorganic Chemistry, vol. 7, no. 9, 1968, pp. 1704-1708.
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