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the excretory system of the stick insect, dixippus morosus

the excretory system of the stick insect, dixippus morosus

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188 J. A. RAMSAY<br />

<strong>the</strong>se granules is calcium carbonate. The egg shells <strong>of</strong> phasmids are hardened with<br />

calcium oxalate (Moscona, 1950). Since <strong>the</strong> inferior tubules with <strong>the</strong>ir dilatations<br />

and granules are absent in <strong>the</strong> nymph and poorly developed in <strong>the</strong> male, and since<br />

<strong>the</strong> granules appear to be reduced in quantity during fasting (egg production<br />

continuing), it seems likely that <strong>the</strong>y are a calcium reserve which can be drawn<br />

upon to provide material for <strong>the</strong> egg shells.<br />

(c) Appendices <strong>of</strong> <strong>the</strong> midgut. These tubules are narrower (c. 50/i) than <strong>the</strong> o<strong>the</strong>rs<br />

and are uniform throughout <strong>the</strong>ir length. There is a well-developed brush border<br />

and <strong>the</strong> inner margin can be brought to focus (Fig. 3 c). It is perhaps less sharply<br />

defined than <strong>the</strong> scalloped edge <strong>of</strong> <strong>the</strong> 'wabensaum' in Rhodnius (Wigglesworth,<br />

1931ft), but more definite than <strong>the</strong> edge <strong>of</strong> <strong>the</strong> border as seen at <strong>the</strong> tip <strong>of</strong> <strong>the</strong><br />

superior tubule (Fig. 3 a). No granules have been seen in <strong>the</strong>se tubules.<br />

Wigglesworth has reported that in Rhodnius <strong>the</strong> normal histological appearance<br />

<strong>of</strong> <strong>the</strong> tubules is not preserved in artificial media. The same is true <strong>of</strong> <strong>the</strong> tubules<br />

<strong>of</strong> <strong>the</strong> <strong>stick</strong> <strong>insect</strong> in all artificial media as yet tested. A Ringer solution approximating<br />

to haemolymph in composition has been prepared (Ramsay, 1955). Within<br />

an hour or two after being placed in Ringer <strong>the</strong> walls <strong>of</strong> <strong>the</strong> tubules begin to lose<br />

<strong>the</strong>ir characteristic bright appearance. The striations <strong>of</strong> <strong>the</strong> brush border become<br />

fainter and <strong>the</strong> border eventually disintegrates. The appearance <strong>of</strong> <strong>the</strong> nuclei<br />

changes with what appears to be <strong>the</strong> separation <strong>of</strong> a coagulum from a clear fluid<br />

within <strong>the</strong> nuclear membrane (Fig. 3d). A space appears between <strong>the</strong> cells and <strong>the</strong><br />

basement membrane which is clearly visible only under <strong>the</strong>se conditions, and after<br />

5 or 6 hr. a disintegrating mass <strong>of</strong> cells fills <strong>the</strong> lumen. The contraction <strong>of</strong> <strong>the</strong><br />

muscular elements in <strong>the</strong> walls continues for some time longer.<br />

Table 1. Relative quantities <strong>of</strong> mineral bases as percentage<br />

<strong>of</strong> toted mineral base expressed in equivalents<br />

Na<br />

K<br />

Ca<br />

Mg<br />

Privet<br />

leaves<br />

(1)<br />

13<br />

35<br />

46<br />

6<br />

100<br />

Nymph<br />

faeces<br />

(2)<br />

9<br />

33<br />

Si<br />

7<br />

100<br />

Adult<br />

faeces<br />

(3)<br />

EXCHANGE OF MINERAL BASES<br />

The <strong>insect</strong> takes in sodium, potassium, calcium and magnesium in <strong>the</strong> proportions<br />

in which <strong>the</strong>y are present in privet leaves (Table 1, col. 1), and should presumably<br />

eliminate <strong>the</strong>m in <strong>the</strong> same proportions. In <strong>the</strong> case <strong>of</strong> <strong>the</strong> nymph elimination is<br />

entirely by way <strong>of</strong> <strong>the</strong> faeces, and it is found that in <strong>the</strong> faeces <strong>of</strong> <strong>the</strong> nymph <strong>the</strong><br />

four bases are present in much <strong>the</strong> same proportions as in <strong>the</strong> leaves (Table 1,<br />

col. 2). In <strong>the</strong> case <strong>of</strong> <strong>the</strong> adult female <strong>the</strong> eggs constitute a second channel <strong>of</strong><br />

elimination. The rate <strong>of</strong> egg production is considerable and in terms <strong>of</strong> ash a somewhat<br />

greater weight is eliminated as eggs than as faeces. It is difficult, however, to<br />

11<br />

66 8<br />

15<br />

100<br />

Eggs<br />

(4)<br />

10<br />

5<br />

83 2<br />

100

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