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Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

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curt-tars AND 121cc msr-zcrs 375<br />

("Make (1966) found, from light trap records between 1953 to 1964 in the<br />

Hoku<strong>ri</strong>ku dist<strong>ri</strong>ct, that unusually‘ small annual catches <strong>of</strong> 1V. cincficeps were in<br />

most cases preceded by‘ heavy snowfall. though he did not consider that snowfall<br />

was the only factor limiting population. Koshihara (1972) also analyzed<br />

light-trap records in nine localities in Tohoku dist<strong>ri</strong>ct for over 2O years. <strong>and</strong><br />

found that seasonal fluctuations <strong>of</strong> leathopper density‘ showed good synchronization<br />

among va<strong>ri</strong>ous localities. Particularly high densities in summer were preceded<br />

by a moderate winter from December to March. Temperature du<strong>ri</strong>ng<br />

June <strong>and</strong> July showed no correlation with the density <strong>of</strong> summer generations<br />

which cause feeding injury‘ to <strong>ri</strong>ce. These two reports reveal the important role<br />

<strong>of</strong> winter climate in determining the density <strong>of</strong> the sp<strong>ri</strong>ng generation in the<br />

boundary population. But in a warm region such as Kyushu. Kuno (1968) found<br />

that the density <strong>of</strong> 1N’. cinc<strong>ri</strong>ceps in the third generation. the highest density.<br />

showed smaller annual fluctuations than that <strong>of</strong> the tiveru-‘inte<strong>ri</strong>ng generation.<br />

He concluded that a kind <strong>of</strong> equilib<strong>ri</strong>um state was attained at the third generation,<br />

<strong>and</strong> density-dependent factor(s) control the equilib<strong>ri</strong>um density regardless<br />

<strong>of</strong> the density <strong>of</strong> the tivervviiite<strong>ri</strong>ng generation.<br />

Nezara vi<strong>ri</strong>dula adults migrate into hibemaeula from late September to Januva<strong>ri</strong>ous<br />

hibemaeula from 1961 to 1967. In 1962 <strong>and</strong> 1963. temperatures from<br />

Januaryi to March were extremely‘ love, <strong>and</strong> winter mortality <strong>of</strong> adult bugs<br />

showed a high value, 97.5 %. In the other years no clear va<strong>ri</strong>ation <strong>of</strong> temperature<br />

<strong>and</strong> mortality tvas shtiwn. mostly 3S to 56% mortality-n Winter mortality,<br />

obtained by recording the number <strong>of</strong> dead <strong>and</strong> living bugs found in late March<br />

in hibernacula before emigration. showed va<strong>ri</strong>ation according to the kind <strong>of</strong><br />

hibemaculum. The highest mortality occurred in Chinese juniper, <strong>and</strong> the lowest<br />

in Cryprome<strong>ri</strong>a which had a dense crown <strong>and</strong> was favorable for bugs hibernating<br />

deep inside. Innate conditions such as sex, body size, <strong>and</strong> hibernating coloration<br />

modified the winter mortality. Du<strong>ri</strong>ng the growing season, density-dependent<br />

factors such as egg parasites. density’ effect du<strong>ri</strong>ng nyunphal development. <strong>and</strong><br />

interference among females in egg lay<strong>ri</strong>ng are suggested instead as controlling<br />

the density‘ (Ki<strong>ri</strong>tani. 1971).<br />

The smaller <strong>ri</strong>ce leaf miner. Iiyzirellia g<strong>ri</strong>seola Fallen, is widely’ dist<strong>ri</strong>buted in<br />

the northem hemisphere from Tanegashirna to Finl<strong>and</strong> <strong>and</strong> Norwayn It nomially<br />

infests graminaceous weeds. but intermittently se<strong>ri</strong>ous outbreaks occur on <strong>ri</strong>ce.<br />

Outbreaks usually end within 1 or 2 years. It completes six or seven generations<br />

a year even in Hokkaido. The developmental zero <strong>and</strong> the total effective temperature<br />

were calculated as 10.1°C <strong>and</strong> 32.2 dayrdegrees. respectively. for eggs,<br />

60°C <strong>and</strong> 142.8 day-degrees for larvae, <strong>and</strong> 8.0°C <strong>and</strong> 111.1 dayfdegrees for<br />

pupae (Tomioka. 1955). Kuwayama (1955) found climatic factors to be the main<br />

cause <strong>of</strong> the outbreak in 1954 cove<strong>ri</strong>ng the whole <strong>of</strong> northern Japan. Summer<br />

temperatures in July <strong>and</strong> August in the preceding year tended to be low, favor~<br />

ing surv<strong>ri</strong>val <strong>of</strong> larvae. Winter temperatures in the outbreak year were high, but<br />

it was cool in May <strong>and</strong> Julie. These climatic characte<strong>ri</strong>stics were also seen in the

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