Does the rattle of Crotalus durissus terrificus reveal its dietary history?

Background Environmental devastation threatens the survival of many species, including venomous snakes such as the South American rattlesnake Crotalus durissus terrificus. This observation is based on the decrease of snakes collected and donated to Brazilian research institutes. Nevertheless, some individuals have managed to survive and procreate. The question is how these snakes are adapting in these new environmental conditions.Methods To answer it, the carbon-13 level of rattlesnakes and their feed (either laboratory or wild mice) was evaluated by isotope-ratio mass spectrometry. Thus, rattle segments from 16 adults and 15 offspring of captive snakes, and of three wild newborn C. d. terrificus were evaluated as well as 17 Mus musculus mice captured in traps, four live feeder mice and the ration offered to mice at animal houses.Results The isotopic exchange time of the captive adult snakes (n = 16) varied between 33 and 37 months and of captive-born animals (n = 15), until reaching a plateau of equilibrium, varied from 18 to 24 months. Regarding the captured Mus musculus (n = 17), 88.23% (n = 15) were from a C4 environment. Of the six rattle rings from offspring of captured C. d. terrificus, five were from a C4environment, whereas of the 170 rattle rings studied, 60% originated from a C3 environment and 40% from a C4. The same carbon-13 values were found in captive snakes.Conclusions Based on the present results, it can be inferred that most C. d. terrificus snakes (60%) fed animals from a C3environment; birds consist of an alimentary alternative for snakes, as well as rodents, small reptiles and amphibians; different venom compositions among snakes from the same region may be related to the food type; the primary rattle of offspring reflects the maternal diet during gestation; and, finally, the different rattle rings indicate the alimentary history of these animals.(AU)

Does the rattle of Crotalus durissus terrificus reveal its dietary history?

Background Environmental devastation threatens the survival of many species, including venomous snakes such as the South American rattlesnake Crotalus durissus terrificus. This observation is based on the decrease of snakes collected and donated to Brazilian research institutes. Nevertheless, some individuals have managed to survive and procreate. The question is how these snakes are adapting in these new environmental conditions.Methods To answer it, the carbon-13 level of rattlesnakes and their feed (either laboratory or wild mice) was evaluated by isotope-ratio mass spectrometry. Thus, rattle segments from 16 adults and 15 offspring of captive snakes, and of three wild newborn C. d. terrificus were evaluated as well as 17 Mus musculus mice captured in traps, four live feeder mice and the ration offered to mice at animal houses.Results The isotopic exchange time of the captive adult snakes (n = 16) varied between 33 and 37 months and of captive-born animals (n = 15), until reaching a plateau of equilibrium, varied from 18 to 24 months. Regarding the captured Mus musculus (n = 17), 88.23% (n = 15) were from a C4 environment. Of the six rattle rings from offspring of captured C. d. terrificus, five were from a C4environment, whereas of the 170 rattle rings studied, 60% originated from a C3 environment and 40% from a C4. The same carbon-13 values were found in captive snakes.Conclusions Based on the present results, it can be inferred that most C. d. terrificus snakes (60%) fed animals from a C3environment; birds consist of an alimentary alternative for snakes, as well as rodents, small reptiles and amphibians; different venom compositions among snakes from the same region may be related to the food type; the primary rattle of offspring reflects the maternal diet during gestation; and, finally, the different rattle rings indicate the alimentary history of these animals.

Isotopic traceability in body tissues and in different breeding periods of broilers / Rastreabilidade isotópica em tecidos corporais e em diferentes períodos de criação de frangos de corte

The inclusion of poultry viscera meal (VM) in broiler diets to possibly replace it with strictly vegetable diet (VE) and vice-versa, using the technique of carbon and nitrogen stable isotopes in different tissues was traced. One hundred ninety-two one-day-old chicks that had been distributed randomly were used in twelve experimental treatments with four replications of four chicks each. The treatments consisted of vegetable diet (VG) for diets containing FV going after a certain age or the reverse, in which the birds began feeding VM on diet and then switched to VE diet. At 42 days of age, samples of pectoral muscle (Pectoralis major), keel and tibia were collected, with later determination of isotopic ratios (13C/12C and 15N/14N). The stable isotopes technique couldn't trace the use of VM in feeding broilers when this ingredient was part of broiler diets only in the first seven, 14 or 21 days of age. However, this technique can be applied to younger poultry that have been sampled before a possible change in diet, since they can have the isotopic signature of feeding stabilized around two weeks of age.

Rastrearam-se a inclusão de farinha de vísceras de aves (FV) em dietas de frangos por ocasião de eventual substituição de dieta contendo FV por dieta estritamente vegetal, e vice-versa, por isótopos estáveis de carbono e de nitrogênio. Foram distribuídos aleatoriamente 192 pintos de um dia de idade, em 12 tratamentos com quatro repetições de quatro aves. Os tratamentos constituíam-se de dieta de vegetais (VG) passando para dietas contendo FV, após certa idade, ou o inverso, em que as aves começaram se alimentando de dieta FV e depois passaram para dieta VG. Aos 42 dias de idade, foram coletadas amostras de músculo peitoral (Pectoralis major), quilha e tíbia, para determinação das razões isotópicas (13C/12C e 15N/14N). A técnica dos isótopos estáveis somente não foi capaz de rastrear a utilização de FV na alimentação de frangos de corte, quando esse ingrediente fez parte da dieta das aves apenas nos primeiros sete, 14 ou 21 dias de idade. Entretanto, há a possibilidade da aplicação dessa técnica em aves mais jovens, amostradas antes de eventual mudança de dieta, pois elas podem ter a assinatura isotópica da alimentação estabilizada em torno de duas semanas de idade.

Nucleotídeos na dieta de frangos de corte e seus efeitos sobre taxa de turnover da mucosa intestinal antes e após lesões causadas por coccidiose / Nucleotides in broilers challenged diet and its effects on intestinal mucosa turnover rate before and after injuries caused by coccidiose

O objetivo deste trabalho foi avaliar o efeito da dieta suplementada com nucleotídeos sobre taxa de turnover da mucosa intestinal de frangos antes e após lesões causadas por coccidiose por meio de análise isotópica, utilizando a variação do carbono-13 em plantas C3 e C4. Foram utilizados 264 pintos submetidos a dois tratamentos: dieta controle e dieta suplementada com 0,07 por cento nucleotídeos. Os pintos possuíam sinais isotópicos em seus tecidos semelhantes ao de ditas C4. Após o alojamento, para avaliar taxa de turnover da mucosa, as aves receberam dietas predominantemente C3. Com 16 dias de idade, 50 por cento das aves de cada tratamento foram inoculadas com oocistos de Eimeria acervulina e, a partir de 21 dias, para avaliar a taxa de turnover após desafio, as aves passaram a receber dieta predominantemente C4. Amostras de mucosa foram analisadas isotopicamente por espectrometria de massa. Na fase inicial, a suplementação com nucleotídeos propiciou aceleração na troca do carbono na mucosa, com meia-vida de 1,06 e 1,01 dias para dieta controle e com nucleotídeos, respectivamente, acelerando o crescimento intestinal. Na fase de 21 a 42 dias de idade, para os grupos não desafiados com coccidiose, as meias-vidas do carbono foram 1,81 e 1,80 dias para dieta controle e com nucleotídeos, respectivamente, não havendo influência dos tratamentos. Porém, nos grupos desafiados, as meias-vidas foram 1,01 dias no grupo controle e 0,75 dias no que recebeu dieta com nucleotídeos, indicando maior turnover da mucosa nesse último grupo. A adição de nucleotídeos promove aceleração no processo de renovação da mucosa intestinal e na regeneração após danos causados por coccidiose.

The objective was to evaluate the effect of nucleotides supplementation diet on the intestinal mucosa turnover rate of broilers before and after injury caused by coccidiosis, through isotopic analysis, using the carbon-13 variation in C³ and C4 plants. It was used 264 chicks under two treatments: control diet and diet supplemented with 0.07 percent nucleotides. The chicks had isotopic signals in their tissues similar to C4 diet. After housing, to assess mucosal turnover rate, the birds were fed with a predominantly C3 diet. At 16 days of age, 50 percent of birds from each treatment were inoculated with Eimeria acervulina oocysts and starting from 21 days, to assess the mucosa turnover rate after challenge, the birds received predominantly C4 diet. Samples of intestinal mucosa were isotopically analyzed by mass spectrometry. In the initial phase, supplementation with nucleotides led acceleration in carbon trading in the mucosa, with half-lives of 1.06 and 1.01 days for control diet and with nucleotides, respectively, accelerating intestinal growth. During the 21 to 42 days of age, for not coccidiosis challenged groups, the carbon half-lives were 1.81 and 1.80 days for control diet and with nucleotides respectively, without any influence of the treatments. However, in the challenged groups, the half-lives were 1.01 days in control group and 0.75 days in group receiving nucleotides diet supplementetion, indicating a higher mucosa turnover rate in the latter group. The addition of nucleotides promotes acceleration in the cell renewal process of intestinal mucosa and in regeneration after damage caused by coccidiosis.

Estudo de adulteração em méis brasileiros através de razão isotópica do carbono / A study of adulteration in brazilian honeys by carbon isotope ratio

Neste trabalho, objetivou-se analisar isotopicamente méis comercializados nas regiões Sul e Sudeste do Brasil, para a detecção de fraude. Foram colhidas amostras comerciais com registro no Serviço de Inspeção Federal, Estadual ou Municipal. As amostras foram submetidas à combustão no Analisador Elementar EA 1108 CHN e analisadas no espectrômetro de massas de razão isotópica DELTA-S (Finningan Mat). Os valores isotópicos (δ13C) dos méis in natura foram comparados aos de suas respectivas proteínas (padrão interno). Foram consideradas adulteradas as amostras cuja diferença entre o valor isotópico da proteína e do mel foi igual ou inferior a -1‰. As amostras consideradas adulteradas pela análise isotópica foram submetidas a testes químicos qualitativos que não foram capazes de indicar adulteração para algumas delas. Das 61 amostras analisadas, 18,0 por cento encontram-se adulteradas, sendo 11,5 por cento na Região Sudeste e 6,5 por cento na Região Sul. Ao contrário dos testes químicos, a análise isotópica mostrou-se eficaz em identificar e quantificar a adulteração de méis comerciais.

The aim of this study was the isotopic evaluation of honey traded in the Southern and Southeastern Brazilian regions, to detect fraud. Commercial samples, registered in the municipal, State or Federal Inspection Service, were collected and submitted to combustion in the EA 1108 CHN Elemental Analyzer and analyzed in the DELTA-S (Finningan Mat.) isotope ratio mass spectrometer. The isotopic values (δ13C) of in natura honey were compared to their respective proteins (internal standard). Samples whose difference between the isotopic value of protein and honey was equal or inferior to -1‰ were considered adulterated. The samples considered adulterated were submitted to qualitative chemical tests which were unable to show adulteration for some of them. Among the 61 samples analyzed, 18.0 percent were adulterated; 11.5 percent in the Southeastern and 6.5 percent in the Southern region. Unlike chemical tests, isotopic analysis has shown to be efficient to identify and quantify adulteration in commercial honey.