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21 results for “Anastrepha ludens”

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zenodo40/100

Fig. 2 in Evaluation of field dispersal and survival capacity of the genetic sexing strain Tapachula-7 of Anastrepha ludens (Diptera: Tephritidae)

Fig. 2. General displacement of Anastrepha ludens SMR strain (solid line) and Tap-7 strain (broken line) in a Cartesian plane.

opencc-by-4.0Mar 2015View details →
zenodo40/100

Fig. 1 in Evaluation of field dispersal and survival capacity of the genetic sexing strain Tapachula-7 of Anastrepha ludens (Diptera: Tephritidae)

Fig. 1. Contours of displacement of the SMR strain (lef) and Tap-7 strain (right) of Anastrepha ludens inside the field plot. The density of the flies at each contour is indicated by the number.

opencc-by-4.0Mar 2015View details →
zenodo40/100

Fig. 1 in Infection of Anastrepha ludens (Diptera: Tephritidae) adults during emergence from soil treated with Beauveria bassiana under various texture, humidity, and temperature conditions

Fig. 1. Adult mortality of Anastrepha ludens infected with different concentrations of Beauveria bassiana conidia, afer emerging from treated soil. Different letters indicate significant differences among treatments based on 1-way ANOVA followed by the Tukey Honest Significant Difference test, P <0.05).

opencc-by-4.0Sep 2017View details →
zenodo40/100

Fig. 1 in Timing of irradiation and male mating history effects on female remating in Anastrepha ludens (Diptera: Tephritidae)

Fig. 1. Interaction between age of pupal irradiation (24, 48, or 72 h before emergence) and male previous sexual experience (virgin, once mated, or twice mated) of the GSS strain of A. ludens (Tapachula-7) males on wild female likelihood to remate (N = 945).

opencc-by-4.0Sep 2017View details →
zenodo40/100

Impact of larval high density on the performance of Anastrepha ludens: competition or feeding facilitation?

<p>A critical point in diet management is maximizing density as a strategy for reducing costs. Artificial diets elaborated with large particle sizes have increased volume, possess high porosity and aeration capacity, are more penetrable and facilitate the movement of larvae, and increase the bioavailability of nutrients. The present experiment consisted in demonstrating that the bulking agent facilitates feeding and could have more capacity to support a high density of larvae with a minimal effect of competition on the life-history traits of <em>Anastrepha ludens</em>. The results indicate that density affected larval and pupal weight, but not pupation at 24 h, adult emergence, and flier percentage, which remained unchanged. However, there was an increase in yield and bioconversion. Larvae in high density conditions aggregated to increase the effect of regurgitation of amylases and proteases as a strategy to metabolize the food prior to ingestion through enzymes secreted in the saliva, contributing thus to feeding facilitation and the uptake of ingested food, which decreased the negative impact of competition in high density conditions. High density leads to an increase in food consumption and a consequent increase in digestive enzyme activity, contributing to the bioavailability of macronutrients ─ proteins, carbohydrates, and lipids ─ in the diet.</p> <p>Identifying the properties of bulking agents and other ingredients and their interaction under high-density conditions is essential to develop novel artificial diets and improve the mass-rearing strategies for the SIT.</p> <p>&nbsp;</p>

opencc-by-4.0Dec 2022View details →
dryad36/100

Nuclear genetic diversity and structure of Anastrepha ludens wild populations evidenced by microsatellite markers

<p class="MsoNormal"><span>The Mexican fruit fly, <em>Anastrepha ludens </em>is an important pest that causes widespread damage to a number of fruit crops in Mexico. The Sterile Insect Technique (SIT) is commonly used for its control. However, the existence of natural barriers can give rise to a population structure in neutral loci and possibly behavioral or adaptive traits that interfere with SIT. For this reason, it is important to understand the genetic diversity and structure of<em> A. ludens </em>populations and to better understand the evolutionary ecology and population processes in view of possible expansions and possible host shifts due to climate change. We genotyped nine nuclear DNA (nDNA) microsatellite loci among fruit fly populations collected from five biogeographic areas within Mexico, Mexican Plateau, the Northeastern Coastal Plain, the Pacific Coast, the Gulf Coast of Mexico, the Soconusco and a laboratory strain. The nuclear genetic diversity was moderate (from <em>H</em>e = 0.34 to <em>H</em>e = 0.39) within the wild mexfly population. We found that populations were clustered in three genetic groups (<em>K</em>=3). The diversity and genetic structure of <em>A. ludens</em> are produced by environmental and geological conditions as well as local conditions like anthropogenic perturbation which would produce population expansion and the existence of possible predators that would affect the population density. Gene flow showed recent migration among populations. The laboratory strain showed less diversity than the wild samples. Large values of current and ancestral population size suggest high resistance to climatic changes, probably due to biological attributes, such as its polyphagous, multivoltine and high dispersal characteristics. In particular ecosystem fragmentation and perturbation as well as the existence of new plant hosts all of which would probably increase the abundance of flies.</span></p>

opencc-zeroJul 2022View details →
zenodo36/100

Fig. 3 in Evaluation of field dispersal and survival capacity of the genetic sexing strain Tapachula-7 of Anastrepha ludens (Diptera: Tephritidae)

Fig. 3. Survival of SMR and Tap-7 strains of Anastrepha ludens afer aerial release.

opencc-by-4.0Mar 2015View details →
zenodo36/100

Anastrepha ludens ̶ Pest Report and Datasheet to support ranking of EU candidate priority pests

<p>These two files are part of the outputs produced under the mandate&nbsp;<a href="http://registerofquestions.efsa.europa.eu/roqFrontend/wicket/page?1-1.ILinkListener-contentPane-listContainer-pageable-21-mandateNumberLnk">M-2017-0056</a>&nbsp;of the European Commission requesting EFSA for technical assistance in the field of quarantine pests qualifying as priority pests as by Article 6(2) of the Regulation (EU) 2016/2031 <em>on protective measures against pests of plants</em>.</p> <p>Under the mandate EFSA produced: i) 1 methodology report (DOI available at the field &quot;Related/alternate identifiers&quot;), ii) 28 datasheets, one for each of the 28 candidate pests, and iii) 28 pest reports supporting the information provided in the datasheets.</p> <p>EFSA wishes to acknowledge the contribution of Elma Bali, Josep Anton Jaques Miret, Nikolaos Papadopoulos, Stella Papanastassiou to the EKE and the review conducted by Dirkjan van der Gaag.</p>

opencc-by-4.0Jun 2019View details →
zenodo36/100

Improving the mating competitiveness of male Anastrepha ludens (Diptera: Tephritidae) fruit flies by adding two juvenile hormone analogues

<p>Improving the mating competitiveness and survival of sterile males are direct means to increasing the effectiveness of the Sterile Insect Technique (SIT). Some insecticide growth regulators, such as the juvenile hormone analogue (JHA) Methoprene, have been used to improve the mating competitiveness of male tephritid flies by reducing their sexual maturation period. However, a decrease in the period of sexual maturation induces a reduction in survival. Here, we compared the effects of methoprene and Pyriproxyfen (PPF), another JHA, in <em>Anastrepha</em> <em>ludens</em> males. Pyriproxyfen is an insect growth regulator that exhibits higher disruption on insects&rsquo; methamorphosis than methoprene or than natural JH. . Both compounds were administered at two doses (0.05 and 0.1%) via the male diet immediately after emergence. Our results show that both Pyriproxyfen and methoprene reduced male sexual maturation. However, PPF-treated males exhibited a shorter maturation period and obtained more matings at a given age than methoprene-treated males . No significant differences were observed between the two PPF doses tested (0.05 and 0.10 %). Male survival was equally accelerated by the two compounds. Our results demonstrate that PPF can be used as a tool to improve the mating performance of sterile males.</p>

opencc-by-4.0Aug 2023View details →
dryad36/100

Nuclear genetic diversity and structure of Anastrepha ludens wild populations evidenced by microsatellite markers

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publicAug 2022View details →
dryad32/100

FASTA file of sequences of identified proteins in Anastrepha ludens reproductive tissues

<p>Seminal fluid proteins (Sfps) modify female phenotypes and have wide-ranging evolutionary implications on fitness in many insects. However, in the Mexican fruit fly, <em>Anastrepha ludens</em>, a highly destructive agricultural pest, the functions of Sfps are still largely unknown. To gain insights into female phenotypes regulated by Sfps, we used nano liquid chromatography mass spectrometry to conduct a proteomic analysis of the soluble proteins from reproductive organs of <em>A. ludens</em>. The proteins predicted to be transferred from males to females during copulation were 100 proteins from the accessory glands, 69 from the testes, and 20 from the ejaculatory bulb, resulting in 141 unique proteins after accounting for redundancies from multiple tissues. These 141 included orthologs to <em>Drosophila melanogaster</em> proteins involved mainly in oogenesis, spermatogenesis, immune response, lifespan, and fecundity. In particular, we found one protein associated with female olfactory response to repellent stimuli (Scribble), and two related to memory formation (aPKC, Shibire). Together, these results raise the possibility that <em>A. ludens</em> Sfps could play a role in regulating female olfactory responses and memory formation and could be indicative of novel evolutionary functions in this important agricultural pest.</p>

opencc-zeroJun 2022View details →
dryad32/100

Data from: Directional selection to improve the sterile insect technique (SIT): survival and sexual performance of desiccation resistant Anastrepha ludens strains

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publicJun 2017View details →
dryad32/100

FASTA file of sequences of identified proteins in Anastrepha ludens reproductive tissues

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publicJun 2022View details →
dryad28/100

Data from: Reasons for success: rapid evolution for desiccation resistance and life-history changes in the polyphagous fly Anastrepha ludens

Species that exhibit broad ranges of distribution may successfully navigate environmental changes by modifying some of their life history traits. Environmental humidity imposes a critical stress that organisms may overcome by increasing their resistance to desiccation. We used experimental evolution to investigate adaptation to desiccation in the tephritid Anastrepha ludens, a species with high fecundity, late maturation and long lifespan. We measured morphological, physiological, developmental as well as demographic changes involved in the adaptation to desiccation. Notwithstanding a low heritability (h2 = 0.237), desiccation resistance evolved extremely rapidly and few negative trade-offs were detected. Selected flies exhibited correlated increases in longevity, body size, the amount of body lipids and bulk water content, and in the duration of the pupal stage. Females further delayed sexual maturation, decreased daily fecundity but retained high lifetime reproductive potential. No differences in male mating competitiveness were found. Selected and control lines differed in longevity but not in total female fecundity, demonstrating that A. ludens flies have the capability for fast adaptation to desiccation without loosing their reproductive capability. Thus, it seems that a rapid evolutionary response to desiccation in this polyphagous insect works as a buffer for environmental variation and reduces the strength of selection on reproductive traits.

opencc-zeroDec 2015View details →
zenodo28/100

Capture of non target arthropods in citrus agroecosystems using control methods against Anastrepha ludens

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opencc-by-4.0May 2024View details →
zenodo28/100

Figure 4 from: Ayala A, Pérez-Lachaud G, Toledo J, Liedo P, Montoya P (2018) Host acceptance by three native braconid parasitoid species attacking larvae of the Mexican fruit fly, Anastrepha ludens (Diptera, Tephritidae). Journal of Hymenoptera Research 63: 33-49. https://doi.org/10.3897/jhr.63.23724

Figure 4 Latency (average ± SE, in minutes) between ovipositions of three native opine parasitoids attacking non-parasitized and previously parasitized Anastrepha ludens larvae. Different capital letters indicate statistically significant difference between the bars. Different letters, indicate statistically significant difference between the bars. Different lower case letters, indicate statistically significant difference between species.

opencc-by-4.0May 2018View details →
zenodo28/100

Figure 2 from: Ayala A, Pérez-Lachaud G, Toledo J, Liedo P, Montoya P (2018) Host acceptance by three native braconid parasitoid species attacking larvae of the Mexican fruit fly, Anastrepha ludens (Diptera, Tephritidae). Journal of Hymenoptera Research 63: 33-49. https://doi.org/10.3897/jhr.63.23724

Figure 2 Ethogram of oviposition of females of Utetes anastrephae on non-parasitized larvae (a) and larvae previously parasitized by conspecifics (b) under laboratory conditions. The width of the arrow is proportional to the relative frequency of transition. The numbers associated with the arrows represent the observed frequencies of the successive behaviors of a complex sequence of behavior (proportions are indicated in parentheses).

opencc-by-4.0May 2018View details →
zenodo28/100

Figure 3 from: Ayala A, Pérez-Lachaud G, Toledo J, Liedo P, Montoya P (2018) Host acceptance by three native braconid parasitoid species attacking larvae of the Mexican fruit fly, Anastrepha ludens (Diptera, Tephritidae). Journal of Hymenoptera Research 63: 33-49. https://doi.org/10.3897/jhr.63.23724

Figure 3 Ethogram of oviposition of females of Opius hirtus on non-parasitized larvae (a) and larvae previously parasitized by conspecifics (b) under laboratory conditions. The width of the arrow is proportional to the relative frequency of transition. The numbers associated with the arrows represent the observed frequencies of the successive behaviors of a complex sequence of behavior (proportions are indicated in parentheses).

opencc-by-4.0May 2018View details →
zenodo28/100

Figure 1 from: Ayala A, Pérez-Lachaud G, Toledo J, Liedo P, Montoya P (2018) Host acceptance by three native braconid parasitoid species attacking larvae of the Mexican fruit fly, Anastrepha ludens (Diptera, Tephritidae). Journal of Hymenoptera Research 63: 33-49. https://doi.org/10.3897/jhr.63.23724

Figure 1 Ethogram of oviposition of females of Doryctobracon crawfordi on non-parasitized larvae (a) and larvae previously parasitized by conspecifics (b) under laboratory conditions. The width of the arrow is proportional to the relative frequency of transition. The numbers associated with the arrows represent the observed frequencies of the successive behaviors of a complex sequence of behavior (proportions are indicated in parentheses).

opencc-by-4.0May 2018View details →
dryad28/100

Data from: Reasons for success: rapid evolution for desiccation resistance and life-history changes in the polyphagous fly Anastrepha ludens

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publicSep 2016View details →

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