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25 results for “Tenebrio molitor”
dataset: The Effects of Density on the Growth and Temperature Production of Tenebrio molitor Larvae
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Figura 1 in Uso de Tenebrio molitor Linnaeus 1758 (Coleoptera: Tenebrionidae) como agente biológico para la limpieza de osamentas de pequeños vertebrados
Figura 1. Larvas de Tenebrio molitor, contenedor con sustrato y ejemplares procesados después de 3 meses. Larvas (a), cubeta con la crianza de las larvas y los ejemplares sobre el sustrato (b); ejemplares luego de tres meses de limpieza: cabeza de rata (c), cabeza de gallina (d), carcasa de pollo (e) y carcasa de diamante mandarÍn (f). / Tenebrio molitor larvae, container with substrate and specimens processed after 3 months. Larvae (a), bucket with the rearing of larvae and the specimens on the substrate (b); specimens after three months of cleaning: rat head (c), hen head (d), chicken carcass (e) and diamond Mandarin carcass (f).
Figura 2 in Uso de Tenebrio molitor Linnaeus 1758 (Coleoptera: Tenebrionidae) como agente biológico para la limpieza de osamentas de pequeños vertebrados
Figura 2. Daño producido por la acción de las larvas de Tenebrio molitor. Carcasa de diamante mandarÍn con esternón dañado (a), detalle del esternón de diamante mandarÍn con daño indicado por flechas (b), ausencia del anillo esclerótico del ojo por destrucción completa en cabeza de diamante mandarÍn (c) y cabeza de pollo (d). e = esternón. / Damage caused by the action of Tenebrio molitor larvae. Diamond Mandarin carcass with damaged sternum (a), detail of sternum of diamond Mandarin with damage indicated by arrows (b), absence of sclerotic ring of the eye due to complete destruction in diamond Mandarin head (c) and chicken head (d). e = sternum.
Fig. 3 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 3. Mean body weight of larvae (mg) fed 30,000 and 50,000 ppm of volcanic ash treated flour disks afer 15 d. Bars with the same letter are not significantly different α = 0.05. Bioassay endpoint = 15 d, n = 10, substrate = treated and control insect food (ANOVA: F = 93.67; df = 2; P <0.0001).
Fig. 1 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 1. Chemical composition of ash from Puyehue Cordon Caulle eruption collected in Collón Curá, Neuquén, Argentina (40.0400°S, 70.2405°W) 15 Jun 2011, determined by energy dispersive spectroscopy. Previously published in Buteler et al. (2011), Revista de la Sociedad Entomológica Argentina 70 (3–4), Figure 3, copyright RSEA, reproduced with permission.
Fig. 6 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 6. Molting rate of Tenebrio molitor larvae feed on flour disks treated with sub-lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash. Molting rate = number of molts per incubation period of 27 d.
Fig. 5 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 5. Larval body length (cm) of Tenebrio molitor larvae fed on flour disks treated with sub-lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash. Bars with the same letter are not significantly different α = 0.05. Bioassay endpoint = 27 d, n = 10, substrate = treated and control insect food (ANOVA: F = 95.15; df = 3; P <0.0001).
Fig. 4 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions
Fig. 4. Mean body weight of larvae (mg) fed on sub lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash treated flour disks. Bars with the same letter are not significantly different at α = 0.05. Bioassay endpoint = 27 d, n = 10, substrate = treated and control insect food (ANOVA: F = 133.97; df = 3; P <0.0001).
dataset: Transporting Tenebrio molitor Eggs: The Effect of Temperature, Humidity and Time on the Hatch Rate
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Tenebrio molitor Physicochemical raw data - Insects MDPI 2023
<p><em>Tenebrio molitor</em>, one of the insect species evaluated and assessed its dead insect individual component, for its ammonification rate, based on physicochemical attributes. </p>
dataset: The Influence of Wet Feed pH on the Growth of Tenebrio molitor Larvae
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dataset: The Effects of Density on the Growth and Temperature Production of Tenebrio molitor Larvae
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The influence of wet feed distribution on the density, growth rate and growth variability of Tenebrio molitor
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Raw data for the submitted manuscript: Response of the terrestrial crustacean Porcellio scaber and the mealworm Tenebrio molitor to agricultural microplastics exposure: comparison of nondegradable and biodegradable fossil-based mulching films
<p>We uploaded two datasets on the response of terrestrial crustacean Porcellio scaber and the mealworm Tenebrio molitor to agricultural microplastics exposed in soil for 3 weeks and 4 weeks, respectively. </p> <p>a) <strong>Dataset</strong> "Response of the terrestrial crustacean Porcellio scaber to agricultural microplastics in soil" contains data on: electron transfer system activity, haemocyte viability, and share of hyalinocytes, semigranulocytes and granulocytes in haemolymph. </p> <p>b) <strong>Dataset</strong> "Response of the mealworm Tenebrio molitor to agricultural microplastics in soil" contains data on: larval moult and growth and animal survival </p> <p>These datasets are linked to publication entitled: Response of the terrestrial crustacean Porcellio scaber and the mealworm Tenebrio molitor to agricultural microplastics exposure: comparison of nondegradable and biodegradable fossil-based mulching films. Methods are described in detail in publication. Manuscript under review. </p>
Raw data for the submitted manuscript: Multigenerational effects of agricultural microplastics on the mealworm Tenebrio molitor
<p>Dataset "Multigenerational effects of agricultural microplastics on the mealworm Tenebrio molitor" contains data on the moult, growth. development and survival of mealworms exposed to microplastics in food over two generations. Datasets are part of publication entitled: Multigenerational effects of agricultural microplastics on the mealworm Tenebrio molitor which is currently under review. </p> <p> </p>
Survival of antimicrobial peptide resistant Staphylococcus aureus in mealworm beetles (Tenebrio molitor) with manipulated AMPexpression
<p><span>Antimicrobial peptides (AMP) are essential immune effectors of multicellular organisms. Bacteria can evolve resistance to AMPs. Surprisingly, when used to challenge the insect <em>Tenebrio molitor</em>, <em>Staphylococcus aureus</em> resistant to an abundant beetle AMP (tenecin 1) and also pleiotropically to phagocytosis did not increase host mortality or bacterial load compared to infections with wild-type <em>S. aureus</em>. A possible explanation is that antimicrobial resistance is costly due to collaterally increased sensitivity of AMP-resistant strains to other immune effectors. Here, we studied the sensitivity of a group of AMP-resistant <em>S. aureus</em> strains (which are either resistant to tenecin 1 or a combination of both tenecin 1 and tenecin 2) to other immune effectors such as phenoloxidase (PO) and other AMPs (specifically tenecin 1, tenecin 2 and tenecin 4) <em>in vivo</em>. Using RNAi-based knockdown (KD), we investigated <em>S. aureus in vivo</em> survival in insect hosts lacking particular immune effectors. We found that all except one AMP-resistant strain displayed collateral sensitivity toward phenoloxidase. Moreover, some AMP-resistant mutant strains showed sensitivity to one or more components of the beetle AMP defence cocktail. Our findings are consistent with the idea that resistance to AMPs and phagocytosis does not translate into changes in virulence because it is balanced by collaterally increased sensitivity to other host immune effectors. AMP resistance fails to provide a net survival advantage to <em>S. aureus</em> in a host environment that is dominated by AMPs because of the greater sensitivity to other immune effectors.</span></p>
Raw data for publication: "Effect of Probiotics on Tenebrio molitor Larval Development and Resistance against the Fungal Pathogen Metarhizium brunneum"
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Survival of antimicrobial peptide resistant Staphylococcus aureus in mealworm beetles (Tenebrio molitor) with manipulated AMPexpression
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Data from: Genetic and phenotypic relationships between immune defense, melanism and life history traits at different temperatures and sexes in Tenebrio molitor
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Data from: Social cues trigger differential immune investment strategies in a non-social insect, Tenebrio molitor
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