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Research on the mosquitoes of Angola - Systematic Catalog of ...

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RIBEIRO, H. & RAMOS, H. Cunha -- <str<strong>on</strong>g>Research</str<strong>on</strong>g> <strong>on</strong> <strong>the</strong> <strong>mosquitoes</strong> <strong>of</strong> <strong>Angola</strong> -- X<br />

rock-pools. Ground water biotopes included ground pools (31), river margins<br />

(14), irrigati<strong>on</strong> drains (7), shallow earth-wells (6), pools in river beds<br />

(4), a p<strong>on</strong>d and a crabhole. Artificial c<strong>on</strong>tainers were represented by old<br />

rubber tyres (10), barrels (8), cement water-tanks (8) and drums (2). The<br />

nature <strong>of</strong> <strong>the</strong> breeding area <strong>of</strong> C. tigripes as shown by <strong>the</strong>se data, points<br />

to an appreciable man-dependance <strong>of</strong> this species for breending.<br />

The breeding water was ei<strong>the</strong>r limpid or turbid, sometimes even foul<br />

water with decaying vegetables (, sisal, fallen leaves, etc.).<br />

Living macroscopic aquatic vegetati<strong>on</strong> was ei<strong>the</strong>r present, sometimes<br />

even abundant, or completely absent. !n seYeral instances, <strong>the</strong> presence<br />

<strong>of</strong> filamentous algae was recorded. The pH <strong>of</strong> <strong>the</strong> breeding water measured<br />

in 50 different breending places, ranged from 5.0 to 8.0, though it<br />

became evident that C. tigripes shows a marked preference for acid<br />

waters, <strong>the</strong>se representing 88 per cent <strong>of</strong> <strong>the</strong> total. The salt c<strong>on</strong>tent<br />

(NaCl) <strong>of</strong> <strong>the</strong> water, deterre:reed in 16 biotopes, ranged from 0.1 to<br />

4.15 g/1 (mean 1.1 g/l), salinity being an important limiting factor for<br />

breeding <strong>of</strong> tigripes.<br />

Larvae <strong>of</strong> C. tigripes are voracious predators <strong>on</strong> o<strong>the</strong>r mosquito<br />

larvae and we observed a full grown tigripes larva devoring three third<br />

or fourth instar larvae <strong>of</strong> C. pipiens at intervals <strong>of</strong> about 15 minutes.<br />

It seems that, in fact, <strong>the</strong> presence <strong>of</strong> prey mosquito larvae is a decisive<br />

factor for breeding <strong>of</strong> tigripes.<br />

As to <strong>the</strong> associated <strong>mosquitoes</strong>, larvae <strong>of</strong> o<strong>the</strong>r species <strong>of</strong> Culex were<br />

present in 75 out <strong>of</strong> <strong>the</strong> 104 breeding places <strong>of</strong> tigripes, while Anopheles<br />

spp. occurred in 37 <strong>of</strong> <strong>the</strong>se, Uranotaenia spp. in 10, Aedes spp. in 6,<br />

Ficalbia (F. mimomyial'ormis) in 3, and Aedomyia (Aed. [ur/urea) in<br />

<strong>on</strong>ly <strong>on</strong>e. 52 species <strong>of</strong> associated <strong>mosquitoes</strong> were recorded from <strong>the</strong><br />

<strong>Angola</strong>n larval biotopes <strong>of</strong> tigripes, bel<strong>on</strong>ging to genera Culex (22 species),<br />

Anopheles (19), Aedes (5), Uranotaenia (4), Ficalbia (1) and Aedemyia<br />

(1). The species most frequently associated with larval tigripes were,<br />

by decreasing order <strong>of</strong> frequency: C. dutt<strong>on</strong>i and C. univittatus (each<br />

<strong>on</strong>e recorded from 20 larval biotopes), An. coustani (18), C. p. piplens<br />

(11), C. p. quinque/asciatus and C. decens (9), An. gambiae (7), An. demeill<strong>on</strong>i,<br />

An. maculipalpis, C. annulioris, C. simps<strong>on</strong>i and U. fusca (6),<br />

An. pharoensis, C antennatus and C. telesilla (5), An. cydippis, An. rhodesiensis,<br />

C. ethiopicus and C. poicilipes (4) and Ae. yangambiensis, An.<br />

r. rufipes, C. chorleyi, C. cinerellus, C. invidiosus, C. <strong>the</strong>ileri and F. mimomyiaformis<br />

(3).<br />

Estud., Errs. e Doc.- 134 53

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