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Gadau, J., Brady, S.G. & Ward, P.S. 1999. Systematics Gadau, J., Brady, S.G. & Ward, P.S. 1999. Systematics, distribution, and ecology of an endemic California Camponotus quercicola. Annals of the Entomological Society of America 92: 514-522. Gaige, S.M. 1914. Description of a new subspecies of Pogonomyrmex occidentalis Cresson from Nevada. Proceedings of the Biological Society of Washington 27: 93-96. [11.v.1914.] Galkowski, C., Aubert, C. & Blatrix, R. 2019. Aphaenogaster ichnusa Santschi, 1925, bona species, and redescription of Aphaenogaster subterranea (Latreille, 1798). Sociobiology 66 (3): 420-425. Galkowski, C. & Cagniant, H. 2017. Contribution à la connaissance des fourmis du groupe angustulus dans le genre Temnothorax. Revue de l’Association Roussillonnaise d’Entomologie 26 (4): 180-191. Galkowski, C., Casevitz-Weulersse, J. & Cagniant, H. 2010. Redescription de Solenopsis fugax (Latreille, 1798) et notes sur les Solenopsis de France. Revue française d’Entomologie (NS) 32 (3-4): 151-163. Galkowski, C. & Lebas, C. 2016. Temnothorax conatensis nov. sp., décrite des Pyrénées-Orientales (France). Revue de l’Association Roussillonnaise d’Entomologie 25: 80-87. Galkowski, C., Lebas, C., Wegnez, P., Lenoir, A. & Blatrix, R. 2017. Redescription of Proformica nasuta (Nylander, 1856) using an integrative approach. European Journal of Taxonomy 290: 1-40. Gallardo, A. 1915. Observaciones sobre algunas hormigas de la República Argentina. Anales del Museo Nacional de Historia Natural de Buenos Aires 27: 1-35. [3.vi.1915.] Gallardo, A. 1916a. Las hormigas de la República Argentina. Subfamilia dolicoderinas. Anales del Museo Nacional de Historia Natural de Buenos Aires 28: 1-130. [Pp. 1-128 dated 18.v.1916; pp. 129-130 dated 13.vi.1916.] Gallardo, A. 1916b. Notas acerca de la hormiga Trachymyrmex pruinosus Emery. Anales del Museo Nacional de Historia Natural de Buenos Aires 28: 241-252. [4.ix.1916.] Gallardo, A. 1916c. Notas complementarias sobre las dolicoderinas argentinas. Anales del Museo Nacional de Historia Natural de Buenos Aires 28: 257-261. [4.ix.1916.] Gallardo, A. 1916d. Notes systématiques et éthologiques sur les fourmis attines de la République Argentine. Anales del Museo Nacional de Historia Natural de Buenos Aires 28: 317-344. [25.ix.1916.] Gallardo, A. 1917. Notes critiques sur les "Formicides sud-américains nouveaux ou peu connus du Docteur Santschi." Physis. Revista de la Sociedad Argentina de Ciencias Naturales 3: 48- 51. [17.iii.1917.] Gallardo, A. 1918a. Hormigas dolicoderinas de los Andes de Mendoza. Physis. Revista de la Sociedad Argentina de Ciencias Naturales 4: 28-31. [15.v.1918.] Gallardo, A. 1918b. Las hormigas de la República Argentina. Subfamilia Ponerinas. Anales del Museo Nacional de Historia Natural de Buenos Aires 30: 1-112. [15.xii.1918.] Gallardo, A. 1919a. Una nueva prodorilina Acanthostichus afflictus. Anales del Museo Nacional de Historia Natural de Buenos Aires 30: 237-242. [22.vii.1919.] Gallardo, A. 1919b. Hormigas del Neuquén y Rio Negro. Anales del Museo Nacional de Historia Natural de Buenos Aires 30: 243-254. [2.viii.1919.] Gallardo, A. 1920. Las hormigas de la República Argentina. Subfamilia dorilinas. Anales del Museo Nacional de Historia Natural de Buenos Aires 30: 281-410. [Pp. 281-408 dated 28.ii.1920; pp. 409-410 dated 13.iv.1920.] Gallardo, A. 1929. Note sur les moeurs de la fourmi Pseudoatta argentina. Revista de la Sociedad Entomológica Argentina 10: 197-202. [31.x.1929.] Gallardo, A. 1930. Sobre el género Dorymyrmex Mayr en la Argentina. Revista Chilena de Historia Natural 34: 143-148. [24.xii.1930.] Gallardo, A. 1931a. Deux nouvelles espèces de Pogonomyrmex de la Republique Argentine. Revista del Museo de la Plata 33: 185-188. [18.xi.1931.] Gallardo, A. 1931b. Algunas formas sexuales aun no descriptas de las hormigas del género Crematogaster de la Republica Argentina. Revista de la Sociedad Entomologica Argentina 17: 297-304. [25.xi.1931.] Gallardo, A. 1932a. Las hormigas de la República Argentina. Subfamilia mirmicinas, sección Promyrmicinae. Anales del Museo Nacional de Historia Natural "Bernadino Rivadavia" 37: 37-88. [21.v.1932.] Gallardo, A. 1932b. Las hormigas de la República Argentina. Subfamilia mirmicinas. Segunda sección Eumyrmicinae, género Pogonomyrmex Mayr. Anales del Museo Nacional de Historia Natural "Bernardino Rivadavia" 37: 89-169. [30.x.1932.] Gallardo, A. 1932c. El subgenero Elasmopheidole en la Argentina. Revista Chilena de Historia Natural 36: 178-182. [(31.xii).1932.] Gallardo, A. 1934. Las hormigas de la República Argentina. Subfamilia mirmicinas. Segunda sección Eumyrmicinae. Tribu Crematogastrini. Género Crematogaster Lund. Anales del Museo Nacional de Ciencias Naturales "Bernardino Rivadavia" 38: 1-84. [31.viii.1934.] Gallé, L., Csösz, S., Tartally, A. & Kovács, E. 1998. A check-list of Hungarian ants. Folia Entomologica Hungarica 59: 213-220. Galvis, J.P. & Fernández, F. 2009. Ants of Colombia X. Acanthognathus with the description of a new species. Revista Colombiana de Entomologia 35: 245-249. García-Avendaño, E.I. & Guerrero, R.J. 2018. Taxonomía y distribución de los hormigas del género Tapinoma en Colombia. Revista Colombiana de Entomología 44: 223-237. Geer, C.de: see under De Geer, C. Gené, G. 1841. Untitled contribution introduced by "Il Prof. Cav. Gené legge alcune sue osservazioni sulle abitudini di tre specie d'Imenotteri (pp. 398-400). In Adunanza del di 29 Settembre 1841 (pp. 391-413). Atti della Terza Riunione degli Scienziati Italiani, Firenze: 791 pp. [(31.xii).1841.] General, D.E.M. 2015. Aretidris, a new genus of ants from the mountains of Luzon Island, Philippines. Myrmecological News 21: 131-136. General, D.E.M. 2016a. A review of the ant genus Harpegnathos Jerdon, 1851 in the Philippines, with the description of two new species. Halteres 7: 99-105. General, D.E.M. 2016b. Romblonella longinoi, a new species and first record of the genus from Sabah, Malaysia, with a key to the species of Romblonella Wheeler, 1935. Halteres 7: 112- 119. General, D.E.M. 2018. Odontomachus ferminae, a new Philippine species of the infandus species group. Halteres 9: 157-162. General, D.E.M. & Alpert, G.D. 2012. A synoptic review of the ant genera of the Philippines. ZooKeys 200: 1-111. General, D.E.M. & Buenavente, P.A.C. 2015. A second species of the ant genus Romblonella from the Philippines. Halteres 6: 56-62. General, D.E.M. & Buenavente, P.A.C. 2018. Revision and redefinition of the crematogastrine ant genus Tetheamyrma Bolton, 1991, with the description of a new species and the first description of the dealate queen. Myrmecological News 28: 45-51. Geoffroy, E.L. 1785. In Fourcroy, A.F.de, Entomologia Parisiensis; sive catalogus insectorum quae in Agro Parisiensi reperiuntur 2: 233-544. Parisiis. [(31.xii).1785.] (Formicidae pp. 451- 453.) Germar, E.F. 1837. Fauna Insectorum Europae. Fasciculus 19. Insectorum protogaeae specimen sistens insecta carbonum fossilium: pl.19, figs.1-25. Halae. [(31.xii).1837.] Gerstäcker, A. [Note: alternative spellings with and without the umlaut (Gerstäcker/Gerstaecker) occur in his titles. His publications are listed here with his name standardised as the former.] Gerstäcker, A. 1859. Hr. Peters berichtete über sein Reisewerk, von dem die Insecten bis zum 64., die Botanik bis zum 34. Bogen gedruckt sind und theilte den Schluss der Diagnosen der von Hrn. Dr. Gerstäcker bearbeiteten Hymenopteren mit. Monatsberichte der Königlichen Preuss. Akademie der Wissenschaften zu Berlin, April 1858: 261-264. [(31.xii).1859.] Gerstäcker, A. 1862. In Peters, W.C.H. Naturwissenschaftliche Reise nach Mossambique auf befehl seiner Majestät des Königs Friedrich Wilhelm IV in den Jahren 1842 bis 1848 ausgeführt. Zoologie 5. Insecten und Myriapoden. Hymenoptera Hautflügler: 439-526. Berlin. [(31.xii).1862.] (Formicidae pp. 497-518.) Gerstäcker, A. 1863. Ueber ein merkwürdiges neues Hymenopteren. Entomologische Zeitung herausgegeben von dem Entomologischen Vereine zu Stettin 24: 76-93. [(31).iii.1863.] Gerstäcker, A. 1871. Beitrag zur Insektenfauna von Zanzibar. Archiv für Naturgeschichte 37: 345- 363. [(31.xii).1871.] Gerstäcker, A. 1872. Hymenopterologische Beiträge. Entomologische Zeitung herausgegeben von dem Entomologischen Vereine zu Stettin 33: 250-308. [(31).vii.1872.] Ghosh, S.N., Sheela, S. & Kundu, B.G. 2005. Ants of Rabindra Sarovar, Kolkata. Records of the Zoological Survey of India, Occasional Papers 234: 1-40. Giebel, C.G. 1856. Fauna der Vorwelt mit steter Berucksichtigung der lebenden Thiere 2. Die Insecten und Spinnen der Vorwelt: 511 pp. Leipzig. [6.x.1856.] (Formicidae pp. 161-180.) Girard, M. 1879. Traité élémentaire d'entomology 2: 1028 pp. Paris [(31.xii).1879.] Gistel, J. 1856. Mysterien der europäischen Insectenwelt: 530 pp. Kempten. [(31.xii).1856.] Glaser, F., Lush, M.J. & Seifert, B. 2011. Rediscovered after 140 years at two localities: Myrmica myrmicoxena Forel, 1895. Myrmecological News 14: 107-111. Gmelin, J.F. 1790. In Linnaeus, C. Systema Naturae. Editio 13. 1 (part 5): 2225-3020. Lipsiae. [6.xii.1790.] (Formicidae pp. 2797-2805.) Godfrey, R. 1907. Notes on the animal life of the hothouses of the Royal Botanic Garden, Edinburgh. Notes from the Royal Botanic Garden, Edinburgh 17: 99-103. [(30).iv.1907.] Goetsch, W. 1933. Chilenische Wüsten-, Steppen- und Wald-Ameisen. Sitzungsberichte der Gesellschaft für Morphologie und Physiologie in München 42: 27-35. [13.vi.1933.] Goetsch, W. & Menozzi, C. 1935. Die Ameisen Chiles. Konowia 14: 94-102. [15.iii.1935.] Gómez, K. & Espadaler, X. 2005. Description of the queen caste in Messor marocanus Santschi, 1927. Myrmecologische Nachrichten 7: 25-29. Gómez, K. & Espadaler, X. 2006. Exotic ants in the Balearic Islands. Myrmecologische Nachrichten 8: 225-233. Gómez, K., Lorite, P., García, F., Tinaut, A., Espadaler, X., Palomeque, T., Sanllorente, O. & Trager, J. 2018. Differentiating Iberoformica and Formica (Serviformica) with description of the sexual castes of Formica (Serviformica) gerardi Bondroit, 1917 stat. rev. Sociobiology 65: 463-470. Gómez, K., Martínez, D. & Espadaler, X. 2018. Phylogeny of the ant genus Aphaenogaster in the Iberian Peninsula, with the description of a new species. Sociobiology 65: 215-224. Gonçalves, C.R. 1942. Contribuição para o conhecimento do gênero Atta Fabr., das formigas saúvas.
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