- Open Access
The effect of parental rearing conditions on offspring life history in Anopheles stephensi
© Grech et al; licensee BioMed Central Ltd. 2007
Received: 07 March 2007
Accepted: 24 September 2007
Published: 24 September 2007
The environmental conditions experienced by parents are increasingly recognized to impact the success of offspring. Little is known on the presence of such parental effects in Anopheles. If present, parental effects could influence mosquito breeding programmes, some malaria control measures and have epidemiological and evolutionary consequences.
The presence of parental effects on offspring emergence time, size, survival, blood meal size and fecundity in laboratory reared An. stephensi were tested.
Parental rearing conditions did not influence the time taken for offspring to emerge, or their size or survival as adults. However, parental effects were influential in determining the fecundity of daughters. Counter-intuitively, daughters of parents reared in low food conditions produced larger egg clutches than daughters of parents reared in high food conditions. Offspring reared in low food conditions took larger blood meals if their parents had also experienced a low food environment.
So far as we are aware, this is the first evidence of parental effects on progeny in Anopheles.
The reproductive success of an individual is dependent on genetic background, environmental conditions, and interactions between these. One factor which is increasingly recognized to have a profound impact on individual success is the environmental conditions experienced by their parents [1–4] Parental effects have been demonstrated in a wide range of taxa [e.g. [5–18]]. Some of these effects arise from environmental constraints where, for instance, nutrient deprivation in mothers results in less well-provisioned and hence smaller offspring. Parental effects can also be adaptive if parents can perceive cues in their environment and adjust per offspring investment so as to optimize offspring fitness. For instance, in the freshwater crustacean Daphnia, mothers kept in poor conditions alter offspring size, survival, fecundity or resistance to parasites [e.g. [16, 19, 20]]. Here, mothers in poor environments increase per offspring investment in the few offspring they can produce. Thus, there are various routes by which maternal effects can affect important offspring traits such as development time, survival and fecundity.
Anopheline mosquitoes (Diptera: Culicidae) are medically important vectors, responsible for the transmission of many diseases including malaria, filariasis and several arboviral diseases. The distribution of Anopheles mosquitoes is an important factor in determining the prevalence of Plasmodium infections and is influenced by the presence of suitable blood-meal hosts and oviposition sites. Female preference studies indicate that fecund mosquitoes choose oviposition sites based on many factors including the presence/absence of conspecific instars (which may indicate high food levels), food sources, moisture content and the presence/absence of potential predators [e.g. [21–25]]. Such behaviour indicates that female mosquitoes have the ability to alter their offspring fitness through behaviour and raises the question of whether Anopheles parents may also alter investment in their offspring in response to their own condition, or the environmental conditions their offspring might experience.
Despite the hope for large scale rearing and release of sterile males and genetically modified mosquitoes for malaria control, little is known about the effect of Anopheles larval parental rearing experience on offspring success. Yet, central to the success of any breeding and release strategy is the production of large numbers of laboratory-reared mosquitoes, and the fitness of released mosquitoes [26, 27]. Moreover, many larval control programmes are aimed at actively degrading larval habitats, with unknown effects on the fitness of survivors and their progeny.
To begin the study of non-behavioural parental effects on Anopheles life-history, a laboratory study was conducted where Anopheles larvae experienced either the same or different rearing conditions to that experienced by their parents (high or low food availability). After varying the parental environment, the offspring fitness components of emergence time, size, survival, blood meal size and fecundity were measured. As genetic and phenotypic variance is often greater in stressful environments, particular attention is paid to parental effects in offspring reared in low food environments[5, 28, 29]. This study shows that parental rearing conditions can influence offspring life history.
On emergence, the mosquitoes were pooled into three mesh cages (30 × 30 × 30 cm) per treatments groups and provided with 10% glucose solution ad libitum (Figure 1b). Approximately one week after emergence, one anaesthetized mouse was placed on each cage from which the mosquitoes were allowed to feed for 20 minutes. One day later bowls of water were introduced into the cage for oviposition.
These eggs were then pooled and hatched in six plastic trays for each treatment and 400 individual larvae (200 from each parental treatment group) transferred to a standard vials as above (Figure 1c). The larvae were allocated to either the high or low food treatment groups (as above) and monitored daily for pupation. When individuals pupated, they were transferred to a vial that was covered with fine nylon gauze and maintained without food for survival analysis (Figure 1d). On death, mosquitoes were transferred to a 1 ml tube and refrigerated until the end of the experiment. At the end of the experiment the wings of each mosquito were dissected and measured from the distal to dorsal points using microscopy.
This experiment was repeated eight weeks later. In the repeat experiment, offspring were separated into two groups for either survival analysis as in the previous experiment, or for fecundity analysis after a blood meal (Figure 1d and 1e). Fecundity analysis involved transferring both male and female offspring into mating cages (30 × 30 × 30 cm), with four mating cages per offspring group. Five days after emergence, anaesthetized mice were placed on each of the 16 mating cages and the mosquitoes allowed feed for 20 minutes. These mice had all been infected 14 days before the feed with Plasmodium chabaudi, as the original intention was to determine whether vectorial capacity was affected by parental environmental conditions. However, most unexpectedly on the day of the blood-meal, neither asexual nor sexual parasites were present in any of the mice and on dissection of the female mosquitoes after egg-laying, no transmission had occurred. As all infected mice were parasite negative on the day of the feed and were randomly assigned treatment groups which were replicated, any treatment effect should be unrelated to any effect of infection. Immediately after the feed, each female mosquito was transferred to a clean vial covered with fine nylon gauze for three days to allow all haematin (a by-product of decomposition of haemoglobin) to be excreted (Figure 1e), from which blood meal size was estimated . Excreted haematin collected in the bottom of the vial was dissolved in 1 ml of 1% LiC03 solution. The absorbance of the resulting mixture was read at 387 nm in a spectrophotometer using LiC03 solution as a blank and compared with a standard curve made with porcine serum haematin (Sigma Aldrich). Solutions that were within the error range of the LiC03 blanks (absorbance < 0.01) were eliminated from the analysis and classified as non-feeders. After the 3-day haematin collection period, mosquitoes were moved to new 30 ml tubes containing 3 mls of water to allow oviposition (Figure 1f).
The fitness components of emergence time, survival, adult size, blood meal size and fecundity were measured. Both emergence time and survival were measured as the number of days required for either a) the larvae to emerge as an adult, post hatching, or b) taken to die post emergence. As an indicator of size, the length of one wing per mosquito from the distal to dorsal points using microscopy was measured. Haematin mass was used as an indicator of blood meal size, while fecundity was determined by counting the number of eggs laid over the three days following the blood meal.
The life history traits of emergence time and survival were analysed using Proportional Hazards (JMP in 5.1). Adult size, blood meal size and fecundity were analysed using General Linear Models. The explanatory variables were parental food (two levels), offspring food (two levels), gender (two levels) and where relevant, experimental block (two levels). For all models, a maximal model including all two and three-way interactions was fitted first. Models were then minimized by removing non-significant terms beginning with the highest-level interaction. In no cases were any of the three-way block*parent*offspring condition interactions significant and these are therefore not reported. Significant block*parent or block*offspring interactions did occur, but as they only reflected differences in magnitude between blocks, they are not reported. For the blood meal analysis as well as the fecundity analysis, the average blood meal size per replicate cage and the average number of eggs per replicate cage were used as response variables (n = 16), with average adult size as a covariate. This is a conservative approach to deal with the issue of pseudoreplication of treatments arising from mosquitoes fed on the same mouse. The statistical significance of the main effect of mouse and of the interactions between mouse and the covariates (adult size and blood meal size) was also tested. For both of the response variables of blood meal size and fecundity, the main effect of mouse and the interactions were non-significant.
In experiment 1, two hundred larvae were split into either a high food group or low food group, to form the parental generation. Once adults, these parents were mated within groups (three per treatment) and 400 eggs from the parental high food generation and 400 eggs from the parental low food generation were used for the offspring experiments. Of these, complete records of the emergence time, survival, gender and size were noted for 460 mosquitoes which were included in the analysis. In the repeat experiment, 120 larvae formed the parental generation, from which, 400 eggs from the parental high food generation and 400 eggs from the parental low food generation were used for the offspring analysis. Of these, emergence time was noted for 478 mosquitoes, with 140 of used in the survival trial and 287 used for blood meal and fecundity analysis. Altogether, 149 females were included the fecundity trials in which 19,844 eggs were counted.
Time taken to emerge
The effects of parent food level, offspring food level and an interaction between them on the fitness components of emergence time, adult size, survival, blood meal size and fecundity. * = <0.05, ** = <0.01, *** = <0.001, **** = <0.0001
Emergence time (days)
χ2 = 2.7
χ2 = 699.7
χ2 = 41.4
χ2 = 1.2
Size (wing length)
F1,593 = 1.2
F1,594 = 2567
F1,594 = 900
F1,592 = 0.7
χ2 = 1.1
χ2 = 96.7
χ2 = 1.9
χ2 = 1.1
controlling for offspring adult size
χ2 = 0.8
χ2 = 62.9
χ2 = 1.6
χ2 = 1.6
Blood meal size (haematin)
F1,13 = 3.29
F1,14 = 7.3
F1,12 = 0.8
controlling for offspring adult size
F1,12 = 3.1
F1,13 = 6.9
F1,11 = 0.9
Fecundity (egg number)
F1,14 = 6.7
F1,13 = 3.2
F1,12 = 2.5
controlling for offspring adult size
F1,13 = 5.9
F1,12 = 3.0
F1,11 = 2.4
controlling for daughters blood meal size
F1,11 = 16.7
F1,11 = 8.0
F1,11 = 5.6
Offspring larval food level was also the main factor influencing the size of offspring once they reached adulthood (Fig 2b, Table 1-2). Larvae emerging from high food conditions were on average 16% larger than those emerging from low food conditions. Gender was also an important determinant of offspring size, with females being 7% larger than males (Figure 2b, table 1-2). The larval food levels of the parental generation did not influence offspring adult size (Figure 2b, Table 1-2).
The food level experienced by the offspring was again the only factor found to be influencing adult survival (Figure 2c, Table 1-3a). As expected, offspring reared in high food conditions survived for longer than offspring reared in low food conditions. Survival did not differ between the males and the females and was unaffected by parental rearing conditions (Figure 2c, Table 1-3a). Larger offspring survived for longer than smaller offspring (χ2 = 148, df = 1, p = <0.0001), but offspring food level was still a major determinant of survival even when controlling for offspring size (Figure 2c, Table 1-3c).
Nineteen out of the 149 females that were given access to a blood meal were classified as non feeders. No effect of parental food level, offspring food level or an interaction between the two influenced female propensity to fed (parent: χ2 = 2.8, df = 1, p = 0.09; offspring: χ2 = 2.7, df = 1, p = 0.1; parent*offspring: χ2 = 2.5, df = 1, p = 0.1, respectively).
Parental effects influenced offspring fecundity. Offspring of parents reared in low food conditions produced more eggs than the offspring from parents reared in high food conditions (Figure 3b, Table 1-5a). Parental food level influenced offspring egg number, even when controlling for offspring size (Figure 3b, Table 1-5b). Considering the offspring reared on low food only, the fecundity of low food daughters was influenced by the larval food level of their parents, even when controlled for adult size (F1,6 = 13.6, p = 0.01, F1,5 = 12.3, p = 0.017, respectively).
Blood meal size and egg number were positively correlated, with larger blood meal sizes resulting in increased egg production (F1,14 = 34.1, p < 0.0001). The number of eggs produced for a given blood meal size was influenced by offspring as well as parental larval food level (Figure 3b, Table 1-5c). Parental effects influenced the fecundity of daughters reared at low food conditions but not of daughters reared at high food (F1,5 = 16.1, p = 0.01, F1,5 = 4.5, p = 0.09, respectively). For the same size blood meal, the daughters reared at low food conditions were 20% more fecund if their parents had also been reared at low food levels.
This study sought to establish the potential for parental effects to influence offspring reproduction in Anopheles. It was found that parental environment had variable effects on mosquito life history traits. Parental effects did not influence the time taken for offspring to emerge, offspring size or survival. These traits were influenced by current offspring food levels only. However, there was a parental effect on blood meal size, but only in offspring reared in the low food environment. Daughters raised in the low food environment took larger blood meals if their parents had also experienced low food than if their parents had experienced high food. It is tempting to think that the enlarged blood meals were to compensate for poor maternal provisioning and resource acquisition during larval development.
Parental effects were also influential in determining the fecundity of their daughters. Daughters from parents reared in low food conditions produced more eggs than daughters from parents reared in high food. This increased fecundity may arise to compensate for expected decreased longevity in low food environments. Although studies showing condition-mediated life history shifts affecting clutch size are limited, shifts to earlier reproduction due to parasite and predator mediated effects have been previously observed in invertebrates [31, 32]. For the female mosquitoes in this study, a reduced adult lifespan of even a few days could dramatically decrease total lifetime fecundity. In an environment where numerous bouts of reproduction are not probable, the optimal strategy may be to shift resources into few larger reproductive efforts . If this explanation is correct, there must be costs of increased fecundity, possibly in terms of survival in benign environments or in terms of offspring quality.
Does the potential for adaptive parental provisioning exist in this system? For this to be the case (i) ecologically-relevant environmental variation would need to affect offspring fitness, (ii) parents would need be able to predict their offspring's environment through reliable cues, and (iii) parents would be able to adaptively adjust the phenotype of their offspring to the anticipated environment . Evidence for environmental variation influencing mosquito fitness is abundant. Temperature, humidity, parasitism, sugar feeding and plant extracts have all been found to influence fecundity [e.g. [34–38]]. The potential for prediction and life history adjustment are less clear. Oviposition preference indicates that mothers can assess the environment their larval offspring will inhabit. However, the frequently ephemeral oviposition sites of Anopheles may make it difficult for a female mosquito to predict the environment that her offspring will inhabit. With little direct evidence either way; there is much potential for work on adaptive parental effects in Anopheles.
The parental effects reported here may be relevant to control strategies against vector-borne diseases. The deliberate ecological manipulation of larval habitats is a mainstay of vector control against malaria [e.g. [39–44]]. Moreover, the large scale releases of captive raised genetically-modified or sterile Anopheles are being proposed as possible future malaria control strategies [e.g. [45–50]]. Where maximal fecundity is an aspiration of mass rearing programmes, our finding that fecundity is influenced by parental condition argues for further work to optimize the offspring and parent rearing conditions. Furthermore, if the fecundity effects arise because of adaptive life history provisioning, then there must be fitness costs to larger clutches (otherwise, it would be hard to explain why only the offspring of parents raised in poor conditions respond to poor conditions by increasing fecundity). It may be that maximizing fecundity in mosquito captive rearing programmes would be sub-optimal. In the rearing and release of hatchery salmon, for example, it has been suggested that selection for increased fecundity has resulted in decreased egg size, which was linked to decreased survival . By its nature, captive breeding selects for quantity over quality. It may be that large-scale rearing in benign environments may lead to their maladaptation to wild conditions. These considerations, together with the data reported here, point to the need for more work on parental effects in malaria vectors. Obvious next steps include the analyses of wild caught mosquitoes, of other Anopheles species, and of other feeding regimes.
We thank E. Cunningham, H. Ferguson, A. Graham, T. Little and S. Mitchell for discussions and useful comments on the manuscript; A. Sans Sebastian for technical assistance; and the Wellcome Trust for funding. The MS was finished while AR was at the Wissenschaftskolleg zu Berlin.
- Bernardo J: Maternal effects in animal ecology. Am Zool. 1996, 36: 83-105.View ArticleGoogle Scholar
- Kirkpatrick M, Lande R: The evolution of maternal characters. Evolution. 1989, 43: 485-503. 10.2307/2409054.View ArticleGoogle Scholar
- Mousseau TA, Fox CW: The adaptive significance of maternal effects. Trends Ecol Evol. 1998, 13: 403-407. 10.1016/S0169-5347(98)01472-4.View ArticlePubMedGoogle Scholar
- Wolf JB, Brodie ED, Cheverud JM, Moore AJ, Wade MJ: Evolutionary consequences of indirect genetic effects. Trends Ecol Evol. 1998, 13: 64-69. 10.1016/S0169-5347(97)01233-0.View ArticlePubMedGoogle Scholar
- Andersen DH, Pertoldi C, Scali V, Loeschcke V: Heat stress and age induced maternal effects on wing size and shape in parthenogenetic Drosophila mercatorum. J Evolution Biol. 2005, 18: 884-892. 10.1111/j.1420-9101.2005.00955.x.View ArticleGoogle Scholar
- Rotem K, Agrawal AA, Kott L: Parental effects in Pieris rapae in response to variation in food quality: adaptive plasticity across generations?. Ecol Entomol. 2003, 28: 211-218. 10.1046/j.1365-2311.2003.00507.x.View ArticleGoogle Scholar
- Jones TM, Widemo F: Survival and reproduction when food is scarce: implications for a lekking Hawaiian Drosophila. Ecol Entomol. 2005, 30: 397-405. 10.1111/j.0307-6946.2005.00705.x.View ArticleGoogle Scholar
- Badyaev AV: Maternal inheritance and rapid evolution of sexual size dimorphism: Passive effects or active strategies?. Am Nat. 2005, 166: S17-S30. 10.1086/444601.View ArticlePubMedGoogle Scholar
- Bateson P, Barker D, Clutton-Brock T, Deb D, D'Udine B, Foley RA, Gluckman P, Godfrey K, Kirkwood T, Lahr MM: Developmental plasticity and human health. Nature. 2004, 430: 419-421. 10.1038/nature02725.View ArticlePubMedGoogle Scholar
- Benton TG, Plaistow SJ, Beckerman AP, Lapsley CT, Littlejohns S: Changes in maternal investment in eggs can affect population dynamics. Proc R Soc B-Biol Sci. 2005, 272: 1351-1356. 10.1098/rspb.2005.3081.View ArticleGoogle Scholar
- Fox CW, Czesak ME, Wallin WG: Complex genetic architecture of population differences in adult lifespan of a beetle: nonadditive inheritance, gender differences, body size and a large maternal effect. J of Evolution Biol. 2004, 17: 1007-1017. 10.1111/j.1420-9101.2004.00752.x.View ArticleGoogle Scholar
- Gilchrist GW, Huey RB: Parental and developmental temperature effects on the thermal dependence of fitness in Drosophila melanogaster. Evolution. 2001, 55: 209-214.View ArticlePubMedGoogle Scholar
- Laurila A, Karttunen S, Merila J: Adaptive phenotypic plasticity and genetics of larval life histories in two Rana temporaria populations. Evolution. 2002, 56: 617-627.View ArticlePubMedGoogle Scholar
- Marshall DJ, Cook CN, Emlet RB: Offspring size effects mediate competitive interactions in a colonial marine invertebrate. Ecology. 2006, 87: 214-225. 10.1890/05-0350.View ArticlePubMedGoogle Scholar
- Moret Y: Trans-generational immune priming: specific enhancement of the antimicrobial immune response in the mealworm beetle, Tenebrio molitor. Proc R Soc B-Biol Sci. 2006, 273: 1399-1405. 10.1098/rspb.2006.3465.View ArticleGoogle Scholar
- Pieters BJ, Liess M: Maternal nutritional state determines the sensitivity of Daphnia magna offspring to short-term Fenvalerate exposure. Aquat Toxicol. 2006, 76: 268-277. 10.1016/j.aquatox.2005.09.013.View ArticlePubMedGoogle Scholar
- Reinhold K: Maternal effects and the evolution of behavioral and morphological characters: A literature review indicates the importance of extended maternal care. J Hered. 2002, 93: 400-405. 10.1093/jhered/93.6.400.View ArticlePubMedGoogle Scholar
- Sadd BM, Kleinlogel Y, Schmid-Hempel R, Schmid-Hempel P: Trans-generational immune priming in a social insect. Biol Lett. 2005, DOI:10.1098/rsbl.2005.0369Google Scholar
- Lynch MER: Resource availability, maternal effects, and longevity. Exp Gerontol. 1983, 18: 147-165. 10.1016/0531-5565(83)90008-6.View ArticlePubMedGoogle Scholar
- Mitchell SE, Read AF: Poor maternal environment enhances offspring disease resistance in an invertebrate. Proc R Soc B-Biol Sci. 2005, 272: 2601-2607. 10.1098/rspb.2005.3253.View ArticleGoogle Scholar
- Bond JG, Arredondo-Jimenez JI, Rodriguez MH, Quiroz-Martinez H, Williams T: Oviposition habitat selection for a predator refuge and food source in a mosquito. Ecol Entomol. 2005, 30: 255-263. 10.1111/j.0307-6946.2005.00704.x.View ArticleGoogle Scholar
- Huang J, Walker ED, Giroux PY, Vulule J, Miller JR: Ovipositional site selection by Anopheles gambiae: influences of substrate moisture and texture. Med Vet Entomol. 2005, 19: 442-450. 10.1111/j.1365-2915.2005.00588.x.View ArticlePubMedGoogle Scholar
- Kiflawi M, Blaustein L, Mangel M: Oviposition habitat selection by the mosquito Culiseta longiareolata in response to risk of predation and conspecific larval density. Ecol Entomol. 2003, 28: 168-173. 10.1046/j.1365-2311.2003.00505.x.View ArticleGoogle Scholar
- Mokany A, Shine R: Oviposition site selection by mosquitoes is affected by cues from conspecific larvae and anuran tadpoles. Austral Ecol. 2003, 28: 33-37. 10.1046/j.1442-9993.2003.01239.x.View ArticleGoogle Scholar
- Pates H, Curtis C: Mosquito behavior and vector control. Annu Rev Entomol. 2005, 50: 53-70. 10.1146/annurev.ento.50.071803.130439.View ArticlePubMedGoogle Scholar
- Andreasen MH, Curtis CF: Optimal life stage for radiation sterilization of Anopheles males and their fitness for release. Med Vet Entomol. 2005, 19: 238-244. 10.1111/j.1365-2915.2005.00565.x.View ArticlePubMedGoogle Scholar
- Ferguson HM, John B, Ng'habi K, Knols BGJ: Redressing the sex imbalance in knowledge of vector biology. Trends Ecol Evol. 2005, 20: 202-209. 10.1016/j.tree.2005.02.003.View ArticlePubMedGoogle Scholar
- Danks HV: Key themes in the study of seasonal adaptations in insects II. Life-cycle patterns. Appl Entomol Zool. 2006, 41: 1-13. 10.1303/aez.2006.1.View ArticleGoogle Scholar
- Hoffmann AA, Merila J: Heritable variation and evolution under favourable and unfavourable conditions. Trends Ecol Evol. 1999, 14: 96-101. 10.1016/S0169-5347(99)01595-5.View ArticlePubMedGoogle Scholar
- Briegel H: Determination of uric acid and hematin in a single sample of excreta from blood fed insects. Experientia. 1980, 36: 1428-1428. 10.1007/BF01960142.View ArticleGoogle Scholar
- Chadwick W, Little TJ: A parasite-mediated life-history shift in Daphnia magna. Proc R Soc B-Biol Sci. 2005, 272: 505-509. 10.1098/rspb.2004.2959.View ArticleGoogle Scholar
- Wedekind C: Induced hatching to avoid infectious egg disease in whitefish. Curr Biol. 2002, 12: 69-71. 10.1016/S0960-9822(01)00627-3.View ArticlePubMedGoogle Scholar
- Stearns SC: The evolutionary significance of phenotypic plasticity. Bioscience. 1989, 39: 436-445. 10.2307/1311135.View ArticleGoogle Scholar
- Afrane YA, Zhou GF, Lawson BW, Githeko AK, Yan GY: Effects of microclimatic changes caused by deforestation on the survivorship and reproductive fitness of Anopheles gambiae in Western Kenya highlands. Am J Trop Med Hyg. 2006, 74: 772-778.PubMedGoogle Scholar
- Jahan N, Hurd H: The effects of infection with Plasmodium yoelii nigeriensis on the reproductive fitness of Anopheles stephensi. Ann Trop Med Parasit. 1997, 91: 365-369. 10.1080/00034989760987.View ArticlePubMedGoogle Scholar
- Jeyabalan D, Arul N, Thangamathi P: Studies on effects of Pelargonium citrosa leaf extracts on malarial vector,Anopheles stephensi liston. Bioresource Technol. 2003, 89: 185-189. 10.1016/S0960-8524(03)00036-1.View ArticleGoogle Scholar
- Mostowy WM, Foster WA: Antagonistic effects of energy status on meal size and egg-batch size of Aedes aegypti (Diptera : Culicidae). J Vector Ecol. 2004, 29: 84-93.PubMedGoogle Scholar
- Tripathi AK, Prajapati V, Ahmad A, Aggarwal KK, Khanuja SPS: Piperitenone oxide as toxic, repellent, and reproduction retardant toward malarial vector Anopheles stephensi (Diptera : Anophelinae). J Med Entomol. 2004, 41: 691-698.View ArticlePubMedGoogle Scholar
- Ault SK: Environmental management – a reemerging vector control strategy. American Journal of Tropical Medicine and Hygiene. 1994, 50: 35-49.PubMedGoogle Scholar
- Bond JG, Rojas JC, Arredondo-Jimenez JI, Quiroz-Martinez H, Valle J, Williams T: Population control of the malaria vector Anopheles pseudopunctipennis by habitat manipulation. Proceedings of the Royal Society of London Series B-Biological Sciences. 2004, 271: 2161-2169. 10.1098/rspb.2004.2826.View ArticleGoogle Scholar
- Utzinger J, Tozan Y, Singer BH: Efficacy and cost-effectiveness of environmental management for malaria control. Tropical Medicine & International Health. 2001, 6: 677-687. 10.1046/j.1365-3156.2001.00769.x.View ArticleGoogle Scholar
- Gu WD, Novak RJ: Habitat-based modeling of impacts of mosquito larval interventions on entomological inoculation rates, incidence, and prevalence of malaria. Am J Trop Med Hyg. 2005, 73: 546-552.PubMedGoogle Scholar
- Keiser J, Singer BH, Utzinger J: Reducing the burden of malaria in different eco-epidemiological settings with environmental management: a systematic review. Lancet Infect Dis. 2005, 5: 695-708. 10.1016/S1473-3099(05)70268-1.View ArticlePubMedGoogle Scholar
- Grieco JP, Vogtsberger RC, Achee NL, Vanzie E, Andre RG, Roberts DR, Rejmankova E: Evaluation of habitat management strategies for the reduction of malaria vectors in northern Belize. J Vector Ecol. 2005, 30: 235-243.PubMedGoogle Scholar
- Benedict MQ, Robinson AS: The first releases of transgenic mosquitoes: an argument for the sterile insect technique. Trends Parasitol. 2003, 19: 349-355. 10.1016/S1471-4922(03)00144-2.View ArticlePubMedGoogle Scholar
- Helinski MEH, Parker AG, Knols BGJ: Radiation-induced sterility for pupal and adult stages of the malaria mosquito Anopheles arabiensis. Malaria J. 2006, 5:Google Scholar
- Ito J, Ghosh A, Moreira LA, Wimmer EA, Jacobs-Lorena M: Transgenic anopheline mosquitoes impaired in transmission of a malaria parasite. Nature. 2002, 417: 452-455. 10.1038/417452a.View ArticlePubMedGoogle Scholar
- James AA: Engineering mosquito resistance to malaria parasites: the avian malaria model. Insect Biochem Molec. 2002, 32: 1317-1323. 10.1016/S0965-1748(02)00094-2.View ArticleGoogle Scholar
- Moreira LA, Ghosh AK, Abraham EG, Jacobs-Lorena M: Genetic transformation of mosquitoes: a quest for malaria control. Int J Parasitol. 2002, 32: 1599-1605. 10.1016/S0020-7519(02)00188-1.View ArticlePubMedGoogle Scholar
- Phillips RS: Current status of malaria and potential for control. Clin Microbiol Rev. 2001, 14: 208-226. 10.1128/CMR.14.1.208-226.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Heath DD, Heath JW, Bryden CA, Johnson RM, Fox CW: Rapid evolution of egg size in captive salmon. Science. 2003, 299: 1738-1740. 10.1126/science.1079707.View ArticlePubMedGoogle Scholar
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