41
capacity. No correlation was seen. The explana-

tion for the higher B,, levels is not apparentat this

time.

Studies of Genetically Inherited Traits

Blood Groups.
The laboratory analysis of
blood groups was conducted by Dr. L.N. Sussman
and colleagues and reportedas follows. The results
of the 1958 and 1959 studies were combined,
making a total of 310 individual bloods. Care was

taken to avoid duplication. The results of this
broader sampling, comparedto findings of Simmonset al. for the same area*® and for the Polynesians’® are presented in Tables 27, 28, and 29.
Data on all individuals tested are given in Appendix 6. The findings may be summarized as

follows.
"
1. ABO system, The high frequency of the B gene
is again demonstrated, in contrast to the absence
of B genes in the Polynesians. The absence of A,
genein this area has been noted repeatedly.*® In
the presentseries a single individual of group A.B

was confirmed. The x° value in this system is 5.18

(p=0.15). The excess of AB persons (expected 8,
observed 14) contributes the major part of the x’
deviation.
2. MN system. The extremely low frequency of M
gene has been noted in manystudies of this population andarea,in contrastto its high frequency
in Polynesians. The x’ value in this system is 23.7
(£=0.001), whichis statistically invalid. The error

lies in the finding of 25 M persons whereas only
11.6 could be expected. Thus it appears that the
N gene in the heterozygote escapes detection.If

to the Amerindians, Mongolians, and Eskimos,**
among whom some Diego positive people are
found.
The following blood group characteristics of 310
Marshallese represent significant differences from
those of their eastern neighbors (Polynesians) and
suggest a relationship with Southeast Asians and
Indonesians.
1. A relatively high B gene frequency.
2. A high N gene frequency.
3. Extremely high R'‘ gene frequency.

4, Total absence of Kell and Diegofactors.
Haptoglobins and Transferrins.

124 individuals in which the families included, at

most, parents and one child. Thedistribution of
the haptoglobin types in this group did not differ
significantly from that in the total group. In each
case, agreement with the Hardy-Weinberg predictions was good, suggesting that the population

was homogeneousfor this trait. Omitting the two
sera with no haptoglobins, the frequencyof the
Hp' geneis 0.58 and ofthe Hp? gene 0.42. The
frequency of the Hp' geneis higher thanin the
West European populationsso fartested.
Four Rongelapese had no detectable haptoglobin either in 1957 or 1959. In addition, in
manysera only very small amounts of haptoglobin

this were corrected for, the result would be an

even greater frequency of N gene.
3. Rh-Hr system. The marked frequency of the R'
gene is again demonstrated, higher than reported
in any other study. Thefailure to demonstrate any

Table 29
Rh-Hr Frequency Among Marshallese and Polynesians
Marshallese

rh negative persons suggests that the probable

genotype of the heterozygous Rh, people is R'R°.
This is further supported bythe finding of two
persons of phenotype Rh,. The x’ value in this
system is 13.7. Again thestatistical value is diminished because 2 Rh, people were found whereas
0.26 were expected. It can be seen that a major
change in x” value can be causedbya single individualof “unusual” grouping.
4. Other systems. The failure to find in this group

of 310 a single person with a Diego or Kell factor
is noteworthy. The Marshallese, Maoris,?! and

Polynesiansare similarin this respect, in contrast

The distribu-

tion of the haptoglobin types in the 176 Rongelapese tested is shown in Table 30, Data on all individuals tested may be found in Appendix 6. This
sample included some families with two or more
offspring; in these, all siblings but one wereremoved by random selection to give a sample of

Present
report
Phenotype percent
Rh,Rh,
90.9
Rh,rh
4.2
Rh, Rh,
3.9
Rh,
0.3
Rh,
0.6
Genefrequency
R}
R?
R°

0.950
.020
030

Simmons
et al.”*

°

Polynesian
Simmons
and Graydon*®

90.6
0.7
8.0
0.3
0.12
0.951
04
.006

19.6
0.7
50.0
29.7

_

0.449
943
007

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