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MEDICAL ENTOMOLOGY LABORATORY(FMEL) PUBLICATIONS 1-4,*
Compiled by:
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List of Florida mosquito and sandfly species studied in detail by FMEL faculty and staff from 1948 to 2002.
|
Family Culicidae |
894, 998 |
larva, 4th instar |
998 |
|
Adult, female |
998 |
|
|
|
distribution, new Florida records |
60 |
||
|
blood-engorged, behavior |
171, 218, 325, 339 |
nutrients vs. wing length |
688 |
|
establishment |
457 |
host blood |
279 |
|
egg |
nectar feeding |
314 |
|
|
fine structure |
756 |
ovarian stages and parity |
339 |
|
chorionic sculpturing |
756 |
sampling, adult |
|
|
flight |
bait traps |
325 |
|
|
activity |
157, 171, 218, 268, 325, 339 |
light traps |
157, 325 |
|
humidity and rain effects |
268, 325 |
power aspirator |
171, 218, 268, 314, 325 |
|
moon effect |
325, 338 |
sound trap |
157 |
|
paths, sites, orientation |
157, 218, 268, 338, 339, 448 |
suction trap |
157, 218, 268, 314, 325, 338, 339 |
|
rhythms, daily |
294 |
truck net |
157, 218, 325 |
|
temperature effects |
268, 325 |
visual attraction |
441 |
|
wind effect |
268 |
growth |
225, 226, 237 |
|
distribution |
894 |
||
|
Aedes (Stegomyia) aegypti |
462, 466 |
infection with Brugia sp. |
731 |
|
20-OH-ecdysone |
|
infection with D. immitis |
565, 673 |
|
activity |
27 |
infection with D. immitis |
673, 769 |
|
adult |
|
inhibits |
|
|
adult |
64, 69, 144 |
insemination |
462 |
|
after feeding |
329, 330, 334, 384 |
interspecific competition |
1014 |
|
assessment |
192 |
intracellular concretions |
769 |
|
at emergence |
226, 237 |
isozyme variation |
701 |
|
autogeny |
142 |
juvenile hormone (JH) |
649 |
|
binding to mosquito gut |
865 |
laboratory |
620 |
|
biosynthesis |
816, 821, 835, 881 |
larval marking |
462 |
|
biosynthesis |
625 |
larval, protein |
622 |
|
biosynthesis |
882 |
life table characteristics |
|
|
biosynthesis and distribution |
603, 650 |
lipids |
151, 261 |
|
biosynthesis in male accessory glands |
872 |
longevity, adults |
|
|
blood digestion |
243, 245 |
Malpighian tubules |
|
|
blood digestion |
674, 735, 908 |
mating without insemination |
179 |
|
blood digestion |
|
mechanism of coexistence |
1014 |
|
blood feeding |
462, 567, 874 |
metabolism |
816, 821 |
|
carbohydrates |
151, 312, 329, 330 |
metabolism |
846 |
|
characterization |
846 |
metabolism |
|
|
characterization |
625 |
methoprene |
603 |
|
characterization |
846 |
midgut proteolytic enzyme |
674, 735, 696, 736 |
|
colonized in bromeliads |
577 |
migration of microfilariae from midgut |
901 |
|
control |
459 |
nectar feeding |
462 |
|
decline vs Ae. albopictus |
906 |
nutritional factors in development of Brugia |
772 |
|
defecation |
925 |
nutritional reserves |
|
|
desiccation |
1014 |
oogenesis |
908 |
|
determination |
681, 695 |
oostatic factor |
749 |
|
digestion |
908 |
oostatic hormone (TMOF) |
594, 771, 823, 846, 967 |
|
dispersal |
462 |
ovarian development |
462 |
|
diuresis |
|
ovary-specific protein |
440 |
|
ecdysone, biosynthesis and distribution |
603 |
oviposition |
462, 482 |
|
ecdysteroids |
674 |
oviposition preference |
577 |
|
effect of adult age |
312 |
peptide hormone (TMOF) |
823, 846, 882 |
|
effect of age |
245 |
peritrophic membrane |
335 |
|
effect of copper liners |
827 |
phenoloxidase activity |
890 |
|
effect of D. immitis infection |
726 |
plant sugars in adults |
870 |
|
effect of D. immitis infection |
725 |
potential |
|
|
effect of larval crowding |
237, 294 |
protease |
674, 681 |
|
effect of mating |
245 |
proteins |
330, 399 |
|
effect of parity |
245 |
purification |
625 |
|
effect on adults |
226, 237 |
recycling of discarded tires |
459 |
|
effect on egg maturation |
127, 163, 205, 465, 589, 603 |
refractoriness to D. immitis |
565 |
|
effect on metabolism |
151 |
reproductive cycle |
470 |
|
effect on trypsin biosynthesis |
908 |
rhythm, daily |
294, 296 |
|
egg |
|
scanning electron microscopy |
719 |
|
egg development |
674, 735, 908 |
secretion |
892 |
|
egg development, neurosecretory hormone |
470, 471, 589, 603 |
size and weight |
237 |
|
encapsulation of Brugia malayi |
|
stimulus for vitellogenesis |
574 |
|
endocrines |
|
sugar feeding |
144, 329, 334, 874 |
|
energy reserves |
|
survival |
874 |
|
excretion |
925 |
susceptibility/refractoriness to D. immitis |
565, 673, 701 |
|
factors |
225 |
synthesis and degradation |
699 |
|
fecundity |
329, 330, 334, 384, 874 |
terminal abdominal ganglion |
925 |
|
fed |
264, 329, 330 |
thermal tolerance |
1014 |
|
field |
620 |
trypsin |
674 |
|
flight |
|
trypsin biosynthesis |
908 |
|
fuel utilization |
312 |
trypsin modulating oostatic hormone (TMOF) |
834, 842, 882, 967 |
|
genetics |
701 |
trypsinlike enzyme |
823 |
|
growth, larval |
|
unfed (potential) |
264 |
|
gut receptor |
865 |
uric acid |
925 |
|
gut transport |
|
vector of dog heartworm |
365 |
|
immunochemistry |
865, 882 |
vector of human filariasis |
536 |
|
in vitro development of Brugia spp. |
763, 779 |
vitellin and vitellogenin |
674 |
|
infection with Brugia patei |
561 |
vitellogenesis |
399, 437, 449, 452, 470, 570, 571, 574, 589, 603, 648 |
|
vitellogenin synthesis |
452, 471, 504, 570 |
||
| arboviruses | 632 | host of Dirofilaria immitis | 974 |
| Ascogregarina tawinanensis | 974 | interspecific competition | 1014 |
| bacterial abundance in larval habitats | 935 | invasion | 945 |
| control in waste tires | 932 | invasion of bromeliads | 916 |
| control possibilities | 945, 982 | invasion of cemeteries | 804, 811, 823, 935 |
| control with copper liners | 827, 935 | mechanism of coexistence | 1014 |
| desiccation | 1014 | scanning EM | 719 |
| distribution(spread) | 851, 906, 945, 982 | size vs. fecundity | 996 |
| egg | thermal tolerance | 1014 | |
| evaluation of larvicides | 898 | vector potential | 945 |
|
Coquillettidia (Coquillettidia) pertubans (Mansonia perturbans) |
|||
| abundance | 757 | humidity, rain, moon, temperature effects | 157 |
| activity | 157 | laboratory | 620 |
| bait traps | 157 | larval development | 181 |
| control, adult | 23, 138 | light trap | 23, 65, 157, 392 |
| distribution | 757 | nectar feeding | 314 |
| field | 620 | nutritional reserves | |
| flight | paths, sites and orientation | 157, 218, 268, 338 | |
| generations per year | 25, 181, 392 | plant association | 434, 516, 757 |
| growth | 181 | sampling, adult | |
| host, blood | 279 | swarming, male | 115 |
| larval identification, first instar larvae | 531 |
seasonal abundance |
477 |
| mosquito attractant, 1-Octenl-3-OL | 766 | ||
| distribution, new Florida records | |||