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Open Access PDF - Sven Kullander

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as tubed scales, may thus be influenced by misalignment<br />

or small size. The smallest specimens<br />

recorded with a continuous lateral line are 45.5<br />

(C. temensis), 50.0 (C. ocellaris), and 62.1 mm SL<br />

(C. jariina).<br />

The total number of dorsal fin spines and rays<br />

(Table 6) is modally 32 in all species except<br />

C. jariina with 31. All species have modal count<br />

XV.17 except C. jariina (XV.16), C. vazzoleri (XV.16),<br />

and C. nigromaculata (XVI.16). Also C. pinima and<br />

C. thyrorus have a high frequency of XV.16. The<br />

frequency distribution of anal fin rays (Table 7)<br />

shows little variation, with 11 rays modal for the<br />

genus and all species. The pectoral fin count<br />

(Table 8) varies between 14 and 15, with occasional<br />

13 or 16. Higher numbers occur principally<br />

in the more elongate species, viz. C. pinima,<br />

C. vazzoleri, C. temensis, and C. intermedia, but also<br />

in C. jariina.<br />

Vertebral counts (Table 9) separate species<br />

into two groups, those with modally 36 vertebrae<br />

(18+18 or 19+17), and those with 35 (almost exclusively<br />

18+17), and C. jariina exceptional with<br />

34 vertebrae.<br />

Gill rakers (Table 10) were counted as distinguishable<br />

units, and since the anteriormost gill<br />

rakers become flat and contiguous in large specimens,<br />

the variation in counts to some extent reflects<br />

the length of the specimens in the sample.<br />

Our only conclusion is that gill-raker counts are<br />

generally between 13 and 15, with juveniles having<br />

up to 20. The higher numbers in C. temensis<br />

may reflect a later transformation as well as a<br />

higher average.<br />

Morphometric information is available from<br />

304 specimens 29.3-414 mm SL (Tables 12-26). In<br />

a principal component analysis of morphometric<br />

distance data (Fig. 3, Table 11), there are only<br />

traces of allometry, except in the orbital diameter,<br />

and shearing factor 2 did not alter the scatter.<br />

Species with complete or abbreviated juvenile<br />

lateral band tend to cluster apart on factor 2, but<br />

show considerable overlap. Variation mainly<br />

refers to body depth, which tends to be less in<br />

several species with complete juvenile lateral band<br />

(particularly C. intermedia, C. jariina, C. pinima,<br />

C. temensis, and C. vazzoleri) compared to species<br />

with abbreviated juvenile band (C. kelberi, C. monoculus,<br />

C. ocellaris, C. orinocensis, C. pleiozona, and<br />

probably C. nigromaculata), and caudal peduncle<br />

length, which tends to be correspondingly longer.<br />

Cichla piquiti and C. thyrorus cluster in the<br />

midrange, and C. mirianae and C. melaniae span<br />

Ichthyol. Explor. Freshwaters, Vol. 17, No. 4<br />

387<br />

both major clusters. In comparing similar species,<br />

there are no trenchant morphometric differences.<br />

Proportional measurements for each species are<br />

summarized in Tables 12-26. Whereas some species<br />

of there is variation between extremes the<br />

overlap prevents use of proportional characters<br />

to identify specimens to species. Figure 4 illustrates<br />

the gradual variation in body depth expressed<br />

as per cent of SL, with species with abbreviated<br />

juvenile lateral band having body<br />

depths up to 31.5-34.6 % SL, the more deep-bodied<br />

species of species with complete lateral band<br />

up to 30.7-32.8 % SL, and the slender species<br />

(particularly C. intermedia, C. jariina, C. pinima,<br />

C. temensis, and C. vazzoleri) maximum body<br />

depths 27.3-30.7 % SL, with C. temensis at the<br />

extreme with a variation 21.3-27.3 % SL (Tables<br />

12-26). A comparison including only large specimens<br />

(> 199 mm SL; graph not shown) produces<br />

the same general graphic pattern, but with less<br />

confidence and excluding C. intermedia of which<br />

no large specimens were available.<br />

In the morphologically diverse South American<br />

cichlid genus Crenicichla body depth varies<br />

from 12.5 % SL in small, elongate species, to 32.4 %<br />

(N = 590) (pers. obs.). In genera representing a<br />

“normal” South American cichlid body plan, and<br />

with very little interspecific differences, the<br />

variation is 37-45 % of SL (N = 475) in Aequidens,<br />

and 34-45 % SL (N = 322) in Satanoperca (pers. obs.).<br />

The magnitude of variation in Cichla is thus comparable<br />

with Aequidens and Satanoperca albeit<br />

values are contained within the upper range of<br />

Crenicichla.<br />

Juvenile colour pattern. Comparatively little is<br />

known about larval and juvenile cichlid colour<br />

pattern ontogeny, although it is potentially phylogenetically<br />

informative. Cichla and Crenicichla<br />

are the only genera of South American cichlids<br />

with a juvenile colour pattern including a horizontal<br />

midlateral stripe (Figs. 37, 49, 50-51, 55, 60,<br />

64-66, 72, 74, 76-77, 81-85, 88, 90-91), and some<br />

species of Cichla are unique in the possession of<br />

an abbreviated lateral band extending only between<br />

the posterior lateral blotch and the caudal<br />

fin base (Figs. 5, 10-13, 24, 28-30).<br />

Species with a complete lateral band include<br />

C. intermedia, C. jariina, C. melaniae, C. mirianae,<br />

C. pinima, C. piquiti, C. temensis, C. thyrorus, and<br />

C. vazzoleri. In these species, the lateral band remains<br />

to at least 100-150 mm SL, in C. mirianae<br />

and C. intermedia it remains as an irregular stripe

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