Decapod crustaceans used as food by the Yanomami Indians of the Balawa-ú village, State of Amazonas, Brazil

The Yanomami are a group of South American Indians that live in the rainforest along the borderlands of Brazil and Venezuela. They depend on hunting, gardening and wild food for survival; crustaceans are a highly prized food item in their diet. Taxonomical and ethnozoological aspects of the Yanomami Indians of the Balawa-ú village, state of Amazonas, Brazil, related to the crustaceans are described. Information and specimens were obtained from August to December, 2003. Interviews were conducted with residents of the village and focused on questions about species exploited, indigenous names, modes of capture and use of the species. One shrimp species of the family Palaemonidae (Macrobrachium brasiliense) and two crab species of Trichodactylidae (Sylviocarcinus pictus, Valdivia serrata) as well as two of Pseudothelphusidae (Fredius fittkaui, F. platyacanthus) were recorded. The indigenous names applied to these species are: shuhu, for shrimp, oko and peimatherimi for each of the two pseudothelphusid crabs, and hesiki tôtôrema for both trichodactylid crabs.

Estoque de nutrientes sob diferentes sistemas de uso do solo de Colorado do Oeste-RO

A substituição da floresta por outro tipo de uso do solo pode levar a perdas significativas na matéria orgânica do solo, alterando sua dinâmica e como consequência alterando as entradas e saídas de nutrientes do sistema. Neste trabalho o objetivo foi avaliar o estoque de nutrientes em diferentes sistemas de uso de solo em Colorado do Oeste-RO. Os sistemas avaliados foram o agroflorestal (teca e cacau), florestal (teca com cinco anos), teca com oito anos, agrossilvopastoril (teca, cacau e pasto) e pastagem tendo a mata nativa como referência. Em cada sistema foram abertas três minitrincheiras, nas quais foram coletadas amostras deformadas e indeformadas nas profundidades de 0 a 5, 5 a 10, 10 a 20 e 20 a 30 cm. Nessas amostras foram determinados os nutrientes: N, P, K, Ca e Mg, a matéria orgânica, a densidade do solo e os teores de argila. Observaram-se diferenças nos estoques de nutrientes no solo entre os sistemas de uso e em profundidade. A concentração de nutrientes foi influenciada pelo sistema de uso do solo. O nutriente mais estocado em todos os sistemas de uso é o Ca, os valores variaram entre 5188,48 e 2912,86 kg ha-1 e o menos estocado o K, com estoques entre 46,22 e 17,33 kg ha-1. O sistema teca com cinco anos foi o sistema que mais se aproximou da mata, quanto ao armazenamento de nutrientes.

The Yanomami indians in the INTERSALT study

OBJECTIVE: To study the distribution and inter-relationship among constitutional and biochemical variables with blood pressure (BP) in an population of Yanomami indians. To compare these findings with those of other populations. METHODS: The Yanomami indians were part of the INTERSALT, a study comprising 10,079 males and females, aged from 20 to 59 years, belonging to 52 populations in 32 countries in Africa, the Americas, Asia, and Europe. Each of the 52 centers was required to accrue 200 individuals, 25 participants in each age group. The variables analyzed were as follows: age, sex, arterial BP, urinary sodium and potassium excretion (24-hour urine), body mass index, and alcohol ingestion. RESULTS: The findings in the Yanomami population were as follows: a very low urinary sodium excretion (0.9 mmol/24h); mean systolic and diastolic BP levels of 95.4 mmHg and 61.4 mmHg, respectively; no cases of hypertension or obesity; and they have no knowledge of alcoholic beverages. Their BP levels do not elevate with age. The urinary sodium excretion relates positively and the urinary potassium excretion relates negatively to systolic BP. This correlation was maintained even when controlled for age and body mass index. CONCLUSION: A positive relation between salt intake and blood pressure was detected in the analysis of a set of diverse populations participating in the INTERSALT Study, including populations such as the Yanomami Indians. The qualitative observation of their lifestyle provided additional information.

Estudos experimentais sôbre a origem do milho

1) It may seem rather strange that, in spite of the efforts of a considerable number of scientists, the problem of the origin of indian corn or maize still has remained an open question. There are no fossil remains or archaeological relics except those which are quite identical with types still existing. (Fig. 1). The main difficulty in finding the wild ancestor- which may still exist - results from the fact that it has been somewhat difficult to decide what it should be like and also where to look for it. 2) There is no need to discuss the literature since an excellent review has recently been published by MANGELSDORF and REEVES (1939). It may be sufficient to state that there are basically two hypotheses, that of ST. HILAIRE (1829) who considered Brazilian pod corn as the nearest relative of wild corn still existing, and that of ASCHERSON (1875) who considered Euchlaena from Central America as the wild ancestor of corn. Later hypotheses represent or variants of these two hypotheses or of other concepts, howewer generally with neither disproving their predecessors nor showing why the new hypotheses were better than the older ones. Since nearly all possible combinations of ideas have thus been put forward, it har- dly seems possible to find something theoretically new, while it is essential first to produce new facts. 3) The studies about the origin of maize received a new impulse from MANGELSDORF and REEVES'S experimental work on both Zea-Tripsacum and Zea-Euchlaena hybrids. Independently I started experiments in 1937 with the hope that new results might be obtained when using South American material. Having lost priority in some respects I decided to withold publication untill now, when I can put forward more concise ideas about the origin of maize, based on a new experimental reconstruction of the "wild type". 4) The two main aspects of MANGELSDORF and REEVES hypothesis are discussed. We agree with the authors that ST. HILAIRE's theory is probably correct in so far as the tunicata gene is a wild type relic gene, but cannot accept the reconstruction of wild corn as a homozygous pod corn with a hermaphroditic tassel. As shown experimentally (Fig. 2-3) these tassels have their central spike transformed into a terminal, many rowed ear with a flexible rachis, while possessing at the same time the lateral ear. Thus no explanation is given of the origin of the corn ear, which is the main feature of cultivated corn (BRIEGER, 1943). The second part of the hypothesis referring to the origin of Euchlaena from corn, inverting thus ASCHERSON's theory, cannot be accepted for several reasons, stated in some detail. The data at hand justify only the conclusion that both genera, Euchlaena and Zea, are related, and there is as little proof for considering the former as ancestor of the latter as there is for the new inverse theory. 5) The analysis of indigenous corn, which will be published in detail by BRIEGER and CUTLER, showed several very primitive characters, but no type was found which was in all characters sufficiently primitive. A genetical analysis of Paulista Pod Corn showed that it contains the same gene as other tunicates, in the IV chromosome, the segregation being complicated by a new gametophyte factor Ga3. The full results of this analysis shall be published elsewhere. (BRIEGER). Selection experiments with Paulista Pod Corn showed that no approximation to a wild ancestor may be obtained when limiting the studies to pure corn. Thus it seemed necessary to substitute "domesticated" by "wild type" modifiers, and the only means for achieving this substitution are hybridizations with Euchlaena. These hybrids have now been analysed init fourth generation, including backcrosses, and, again, the full data will be published elsewhere, by BRIEGER and ADDISON. In one present publication three forms obtained will be described only, which represent an approximation to wild type corn. 6) Before entering howewer into detail, some arguments against ST. HILAIRE's theory must be mentioned. The premendelian argument, referring to the instability of this character, is explained by the fact that all fertile pod corn plants are heterozygous for the dominant Tu factor. But the sterility of the homozygous TuTu, which phenotypically cannot be identified, is still unexplained. The most important argument against the acceptance of the Tunicata faetor as wild type relic gene was removed recently by CUTLER (not yet published) who showed that this type has been preserved for centuries by the Bolivian indians as a mystical "medicine". 7) The main botanical requirements for transforming the corn ear into a wild type structure are stated, and alternative solutions given. One series of these characters are found in Tripsacum and Euchlaena : 2 rows on opposite sides of the rachis, protection of the grains by scales, fragility of the rachis. There remains the other alternative : 4 rows, possibly forming double rows of female and male spikelets, protection of kernels by their glumes, separation of grains at their base from the cob which is thin and flexible. 8) Three successive stages in the reconstruction of wild corn, obtained experimentally, are discussed and illustrated, all characterized by the presence of the Tu gene. a) The structure of the Fl hybrids has already been described in 1943. The main features of the Tunicata hybrids (Fig. -8), when compared with non-tunicate hybrids (Fig. 5-6), consist in the absence of scaly protections, the fragility of the rachis and finally the differentiation of the double rows into one male and one female spikelet. As has been pointed out, these characters represent new phenotypic effects of the tunicate factor which do not appear in the presence of pure maize modifiers. b) The next step was observed among the first backcross to teosinte (Fig. 9). As shown in the photography, Fig. 9D, the features are essencially those of the Fl plants, except that the rachis is more teosinte like, with longer internodes, irregular four-row-arrangement and a complete fragility on the nodes. c) In the next generation a completely new type appeared (Fig. 10) which resembles neither corn nor teosinte, mainly in consequence of one character: the rachis is thin and flexible and not fragile, while the grains have an abscission layer at the base, The medium sized, pointed, brownish and hard granis are protected by their well developed corneous glumes. This last form may not yet be the nearest approach to a wild grass, and I shall try in further experiments to introduce other changes such as an increase of fertile flowers per spikelet, the reduction of difference between terminal and lateral inflorescences, etc.. But the nature of the atavistic reversion is alveadwy such that it alters considerably our expectation when looking for a still existing wild ancestor of corn. 9) The next step in our deductions must now consist in an reversion of our question. We must now explain how we may obtain domesticated corn, starting from a hypothetical wild plant, similar to type c. Of the several changes which must have been necessary to attract the attention of the Indians, the following two seem to me the most important: the disappearance of all abscission layers and the reduction of the glumes. This may have been brought about by an accumulation of mutations. But it seems much more probable to assume that some crossing with a tripsacoid grass or even with Tripsacum australe may have been responsible. In such a cross, the two types of abscission layer would be counterbalanced as shown by the Flhybrids of corn, Tripsacum and Euchlaena. Furthermore in later generations a.tu-allele of Tripsacum may become homozygous and substitute the wild tunicate factor of corn. The hypothesis of a hybrid origin of cultivated corn is not completely new, but has been discussed already by HARSHBERGER and COLLINS. Our hypothesis differs from that of MANGELSDORF and REEVES who assume that crosses with Tripsacum are responsible only for some features of Central and North American corn. 10) The following arguments give indirects evidence in support of our hypothesis: a) Several characters have been observed in indigenous corn from the central region of South America, which may be interpreted as "tripsacoid". b) Equally "zeoid" characters seem to be present in Tripsacum australe of central South-America. c) A system of unbalanced factors, combined by the in-tergeneric cross, may be responsible for the sterility of the wild type tunicata factor when homozygous, a result of the action of modifiers, brought in from Tripsacum together with the tuallele. d) The hybrid theory may explain satisfactorily the presence of so many lethals and semilethals, responsible for the phenomenon of inbreeding in cultivated corn. It must be emphasized that corn does not possess any efficient mechanism to prevent crossing and which could explain the accumulation of these mutants during the evolutionary process. Teosinte which'has about the same mechanism of sexual reproduction has not accumulated such genes, nor self-sterile plants in spite of their pronounced preference for crossing. 11) The second most important step in domestication must have consisted in transforming a four rowed ear into an ear with many rows. The fusion theory, recently revived byLANGHAM is rejected. What happened evidently, just as in succulent pXants (Cactus) or in cones os Gymnosperms, is that there has been a change in phyllotaxy and a symmetry of longitudinal rows superimposed on the original spiral arrangement. 12) The geographical distribution of indigenous corn in South America has been discussed. So far, we may distinguish three zones. The most primitive corn appears in the central lowlands of what I call the Central Triangle of South America: east of the Andies, south of the Amazone-Basin, Northwest of a line formed by the rivers São Prancisco-Paraná and including the Paraguay-Basin. The uniformity of the types found in this extremely large zone is astonishing (BRIEGER and CUTLER). To the west, there is the well known Andian region, characterized by a large number of extremely diverse types from small pop corn to large Cuszco, from soft starch to modified sweet corn, from large cylindrical ears to small round ears, etc.. The third region extends along the atlantic coast in the east, from the Caribean Sea to the Argentine, and is characterized by Cateto, an orange hard flint corn. The Andean types must have been obtained very early, and undoubtedly are the result of the intense Inca agriculture. The Cateto type may be obtained easily by crosses, for instance, of "São Paulo Pointed Pop" to some orange soft corn of the central region. The relation of these three South American zones to Central and North America are not discussed, and it seems essential first to study the intermediate region of Ecuador, Colombia and Venezuela. The geograprical distribution of chromosome knobs is rapidly discussed; but it seems that no conclusions can be drawn before a large number of Tripsacum species has been analysed.

Una nueva especie de Gnamptogenys (Hymenoptera: Formicidae) y comentarios sobre las especies del género en Colombia y Ecuador

The species of the predatory ant genus Gnamptogenys Roger, 1863 from Colombia (42 species) and Ecuador (25 species) are diagnosed and presented, including their known geographical distribution. Gnamptogenys enodis, new species from Colombia is described. Gnamptogenys stellae Lattke, 1995 is new record for Colombia.

Dos nuevas especies del grupo Drosophila onychophora (Diptera, Drosophilidae) en los bosques de Polylepis de Papallacta, Pichincha, Ecuador

A pesar de ser un país relativamente pequeño, Ecuador tiene una gran variedad de ecosistemas que han favorecido altos niveles de especiación. Uno de estos ecosistemas es el bosque de Polylepis. En estos bosques existe una gran diversidad de plantas, como las asteráceas (compuestas), cuyas flores hospedan una plétora de insectos, entre los que se encuentran las especies del grupo Drosophila onychophora. En este estudio, describimos dos nuevas especies de Drosophila recolectadas en un parche de bosque de Polylepis pauta en el Páramo de Papallacta a 4000 msnm. Ambas especies pertenecen al grupo D. onychophora: Drosophila yurag sp. nov. y Drosophila yuragshina sp. nov. Las dos especies presentan edeagos alargados, este carácter es propio de especies del grupo. Morfológicamente ambas especies son muy parecidas, la manera más fácil de distinguirlas consiste en la observación de las alas.

Cuatro nuevas especies del grupo Drosophila onychophora (Diptera, Drosophilidae) en el Parque Arqueológico Rumipamba, Pichincha, Ecuador

Las especies de los subgéneros Phloridosa y Drosophila (este último en relación con los grupos de especies: D. flavopilosa, D. onychophora y D. bromeliae) son especies de Drosophila que se desarrollan únicamente en flores. El grupo D. onychophora fue propuestopara agrupar a especies exclusivamente antófilas. El grupo D. onychophora está integrado por 18 especies, que se encuentran relacionadas con las flores de Asteraceae. En el Parque Arqueológico Rumipamba, provincia de Pichincha, Ecuador, se realizaron capturas de Drosophila, en los meses de febrero, mayo, julio, septiembre y diciembre del 2009. Las especies fueron recolectadas directamente en las flores con un aspirador entomológico. En total se capturaron 427 individuos de Drosophila y se identificaron 11 especies, de las cuales seis son nuevas especies del grupo D. onychophora y una es un nuevo registro para el Ecuador. En este trabajo se describen cuatro de las seis especies nuevas.

Descripción de tres especies nuevas del género Drosophila (Diptera, Drosophilidae) en el Ecuador

Se encontraron tres especies nuevas de Drosophila entre los individuos colectados en diferentes localidades del Ecuador. Una de las especies nuevas pertenecen al grupo Drosophila willistoni y otra al grupo Drosophila asiri, la tercera especie se encuentra sin agrupar. En todos los muestreos realizados se usaron trampas fabricadas con botellas de plástico agujereadas con cebo de banano y levadura. Las tres especies son: D. (Sophophora) neocapnoptera sp. nov., esta especie es similar a D. capnoptera Patterson & Mainland, 1944, sin embargo presentan algunas diferencias en el ala que permiten distinguirlas. Drosophila (Drosophila) neoasiri sp. nov., una especie similar a D. asiri Vela & Rafael, 2005, la diferencia más relevante entre las dos especies se observa a nivel del edeago y Drosophila (Drosophila) papallacta sp. nov. que por el momento no se encuentra relacionada a ningún grupo de especies del género Drosophila.

Una nueva especie del grupo Drosophila annulimana (Diptera, Drosophilidae) y un nuevo registro en las Provincias de Pichincha y Napo, Ecuador

En estudios realizados en el bosque nublado Intillacta, provincia de Pichincha, Ecuador, y en la Cordillera de los Guacamayos, provincia de Napo, Ecuador, se encontró una nueva especie de Drosophila. En base a estudios de la morfología de la genitalia masculina, se propone que, Drosophila intillacta sp. nov. pertenece al grupo Drosophila annulimana. Así mismo, se reporta Drosophila tarsata Schiner, 1868, capturada en la Cordillera de los Guacamayos, como un nuevo registro para el país.

Ommatius nanciae, a new species from Ecuador (Diptera, Asilidae, Ommatiinae)

ABSTRACT A new species of Ommatius Wiedemann, 1821 is described from Ecuador. The habitus, male and female terminalia are described and illustrated.

Descripción de cuatro especies nuevas del subgrupo Drosophila fasciola, gruporepleta (Diptera, Drosophilidae) en dos bosques nublados del Ecuador

RESUMEN En el presente trabajo se describen cuatro miembros nuevos del grupoDrosophila repleta capturados en dos bosques nublados del Ecuador. Las nuevas especies fueron agrupadas dentro del subgrupo D. fasciola basados en el patrón de pigmentación del tórax y la morfología de la genitalia masculina. Drosophila inti sp. nov.,D. nigua sp. nov. y D. yambe sp. nov. fueron capturadas con trampas de banano, mientras que D. carvalhoi sp. nov. fue recolectada en inflorescencias deAnthurium sp. La pigmentación del abdomen y la forma del edeago de D. nigua sp. nov., D. yambe sp. nov. y D. carvalhoi sp. nov. indicarían que están relacionadas entre ellas, mientras que D. inti sp. nov. sería más cercana aD. linearepleta Patterson & Wheeler, 1942.

Intestinal parasites in Iaualapiti indians from Xingu Park, Mato Grosso, Brazil

Brine flotation and gravity sedimentation coproscopical examinations were performed in stool samples from 69 of the 147 Iaualapiti Indians of the Xingu Park, Mato Grosso State, Brazil. Intestinal [arasites were present in 89.9% of the population examined. High rates of prevalence were found for some parasite species. Ancylostomidae, 82.6%; Enterobius vermicularis, 26.1%; Ascaris lumbricoides, 20.3%; and Entamoeba coli, 68.1%. Infection by Trichuris trichuria, Schistosoma mansoni, Taenia spp. and Hymenolepis nana was not detected. Helminth's prevalence in children aged one year or less was comparatively low (33.3%). Quantitative coproscopy was done in positive samples for Ascaris and Ancylostomidae and the results expressed in eggs per gram of feces (EPG). Quantitative results revealed that worm burdens are very low and overdispersed in this Indian tribe, a previously unreported fact.

New records of phlebotomine sand flies (Diptera: Psychodidae) from Ecuador

The plebotomine sand fly fauna of Ecuador was surveyed in two 3-month collecting trips made in 1988 and 1990. A total of 12 provinces were visited, including three (Bolivar, Loja and Morona Santiago) from wich no previous records to phlebotomines existed. Forty-six species were collected, 13 of wich, together with 1 subspecies and 1 genus (Warileya) represented new records for the country. This survey increases the known number of species in Ecuador to 60. The distribuition of Ecuadorian sand flies is discussed in the light of these new findings.

Description of Leishmania equatorensis sp. n. (Kinetoplastida: Trypanosomatidae), a new parasite infecting arboreal mammals in Ecuador

Characterization is given of a new parasite, Leishmania equatoriensis sp.n. wich was isolated from the viscera of a sloth (Choloepus hoffmanni) and a squirrel (Sciurus granatensis), captured in humid tropical forest onthe Pacific Coast of Ecuador. Data based on biological and molecular criteria, as well as numerical zymotaxonomical analysis, indicate that this parasite is a new species of the L. brasiliensis complex. L. equatoriensis is cleary distinguishable form all other known species within this complex, using the following molecular criteria: reactivity patterns with specific monoclonal antibodies, isoenzyme electrophoresis, and restriction-endonuclease fragment patterns of kinetoplast DNA (k-DNA).