Haematophagous insects suffer big changes in water needs under different levels of starvation. Rhodnius prolixus is the most important haematophagous vector of Chagas disease in the north of South America and a model organism in insect physiology. Although there have been some studies on patterns of gas exchange and metabolic rates, there is little information regarding water loss in R. prolixus. We investigated whether there is any modulation of water loss and metabolic rate under different requirements for saving water. We measured simultaneously CO 2 production, water emission and activity in individual insects in real time by open-flow respirometry at different temperatures (15, 25 and 35°C) and post-feeding days (0, 5, 13 and 29). We found: (1) a clear drop in metabolic rate between 5 and 13 days after feeding that cannot be explained by activity and (2) a decrease in water loss rate with increasing starvation level, by a decrease in cuticular water loss during the first 5 days after feeding and a drop in the respiratory component thereafter. We calculated the surface area of the insects and estimated cuticular permeability. In addition, we analysed the pattern of gas exchange; the change from a cyclic to a continuous pattern was affected by temperature and activity, but it was not affected by the level of starvation. Modulation of metabolic and water loss rates with temperature and starvation could help R. prolixus to be more flexible in tolerating different periods of starvation, which is adaptive in a changing environment with the uncertainty of finding a suitable host. KEY WORDS: Flow-through respirometry, Respiratory water loss, Cuticular permeability, CO 2 emission rate INTRODUCTIONDesiccation resistance is vital for survival and colonization of terrestrial habitats. In insects in particular, there must be a fine and efficient control of water loss because of their high surface area to volume ratio. Insects lose water through various pathways: transpiration through the cuticle, evaporation along open spiracles through the tracheal system, and excretion (Edney, 1977;Hadley, 1994). The contribution of each of these pathways to overall water loss is variable but cuticular water loss (CWL) generally accounts for a high proportion of the total water loss (Gibbs and Johnson, 2004;Hadley, 1994). The contribution of respiratory water loss (RWL) to dehydration has been analysed mostly in insects showing discontinuous gas exchange (DGE) (e.g. Chown and Davis, 2003;Lighton, 1992;Quinlan and Lighton, 1999 techniques that enable CWL and RWL to be distinguished in insects with continuous gas exchange: the regression method (Gibbs and Johnson, 2004) and the hyperoxic switch method . Using these techniques, it was observed that spiracular control under continuous gas exchange can modulate RWL as effectively as DGE (Schilman et al., 2005;Gray and Chown, 2008).Haematophagous insects that do not drink free water show big changes in water balance under different levels of starvation (Benoit and Denlinger, 2010)....
Current evidence suggests that sexual size dimorphism (SSD) reflects the male and female adaptation to their different reproductive roles. Belostoma and Lethocerus species, included in Belostomatidae, present different kinds of paternal care. Females of Belostoma Latreille species lay their eggs on the back of males. Males carry, aerate and protect the clutch until hatching, which is critical for offspring survival. Males of Lethocerus Mayr species exhibit some parental care behavior but do not carry the eggs. The genera are nearly related. We studied and compared the SSD patterns of B. oxyurum (Dufour), B. micantulum (Stål), B. elegans (Mayr), B. bifoveolatum Spinola, B. gestroi Montandon and Lethocerus annulipes (Herrich‐Schäffer) by means of a multivariate approach to distinguish selection targets in different components of size. Morphometric analysis revealed that SSD patterns vary among traits and that the arrangements are similar in Belostoma species, showing a common trend under resembling selective mechanisms. The widespread SSD trend in insects is that all components of body size are biased towards females, generally related to a fecundity advantage, a pattern now also detected in L. annulipes. We found in Belostoma species that the male has relatively longer middle and hind legs. We propose that SSD in hind legs biased towards males is a selective response for paternal care; they denote a brood‐adapted morphology. The middle leg enlargement may be an associated response to maintain effective locomotion.
Neotropical Entomology 37 (6):662-667 (2008) Estudio Longitudinal en Dos Especies de Belostoma Latreille (Heteroptera: Belostomatidae): Alometría y Ontogenia RESUMEN -Los patrones de crecimiento alométrico de los segmentos del rostro y de las patas de Belostoma elegans (Mayr) y B. cummingsi De Carlo son presentados y comparados por primera vez. Se emplearon datos longitudinales de todos los estadios ninfales en un contexto multivariado. Los segmentos de la pata media y posterior presentan coefi cientes alométricos con polaridad opuesta a los de la pata anterior. Estas diferencias observadas pueden deberse al diferente rol que presentan las patas. La función principal de la pata anterior es la captura de las presas, mientras que las patas media y posterior están adaptadas para la natación. El tamaño relativo de los segmentos del rostro es una característica taxonómica importante en Belostoma. En B. cummingsi el segmento proximal es más largo que el medio, mientras que en B. elegans son subiguales. Nuestro propósito es explicar estas diferencias a través del análisis de las trayectorias ontogéneticas en un intento de aclarar diferencias morfológicas entre especies desde una perspectiva del desarrrollo.PALABRAS-CLAVE: Ninfa, desarrollo postembrionario, insecto acuático, morfometría ABSTRACT -The multivariate allometric growth patterns from longitudinal data of leg and rostral segments of all instars of Belostoma elegans (Mayr) and B. cummingsi De Carlo are presented for the fi rst time, and the allometric coeffi cients are compared. The segments of the middle and hind legs present allometric coeffi cients with opposite polarity to those of forelegs. This discrepancy in the ontogenetic trajectories may be due to the different functions of the legs. The foreleg main function is to capture of the prey, while the middle and hind legs are adapted to swimming. The relative size of rostral segments is an important taxonomic character in Belostoma. In B. cummingsi, the proximal segment is longer than the middle one, while in B. elegans they are subequal. Our purpose is to explain these differences through the analysis of their ontogenetic trajectories in an attempt to illuminate the morphological differences among species from a developmental perspective.
The monotypic genus Chileotrecha Maury, 1987, includes Chileotrecha atacamensis Maury, 1987 from Atacama and Coquimbo regions in Chile. We describe Chileotrecha argentinensis n. sp., which is the first record of the genus from Argentina. Phylogenetic relationships of Chileotrecha with other genera of Ammotrechidae are discussed based on external morphology. We report for the first time the presence of blunt and clubbed setae in Ammotrechidae. We also report for the first time the presence of two pairs of microsetae in the posterior margin of genital plate and in the posterior margin of spiracular sternites I and II, and the presence of a single microseta on each side of postspiracular sternite I.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.