Organohalogen concentrations and a gross and histologic ...
Organohalogen concentrations and a gross and histologic ...
Organohalogen concentrations and a gross and histologic ...
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Table 4<br />
Range in the levels (ng/g l.w. or w.w.) of organohalogene compounds associated with osteoporosis <strong>and</strong> dysosteogenesis in wildlife <strong>and</strong><br />
laboratory mammals compared to levels measured in the adipose tissue of polar bears in the present study as well as their prey (blubber<br />
of ringed seal) <strong>and</strong> thereby intake. Data from: Bergman et al. 1992 1 , Lind et al. 2003 2 , Blomkvist et al. 1992 3 , Mortensen et al.<br />
1992 4 , Sch<strong>and</strong>orff 1997a 5 , Lind et al. (2004) 6 , Beard <strong>and</strong> Jong 2000 7 , Glynn et al. (2000) 8 , Guo et al. (1994) 9 , Alveblom et al. (2003) 10 ,<br />
Lind et al. (1999) 11 , Riget et al. (In press) 12 , Johansen et al. (2004) 13 , Lind et al. 2000a, b 14, 15 . ND: below dectection limit.<br />
Study Compound n Concentration Concentration in adipose tissue<br />
(a) <strong>and</strong> food (f) of<br />
East Greenl<strong>and</strong> polar bears<br />
Wildlife:<br />
1, 2<br />
Grey seal<br />
1, 2<br />
Grey seal<br />
4, 5<br />
Harbour seal<br />
4, 5<br />
Harbour seal<br />
Alligator 6<br />
Humans:<br />
Woman 7<br />
Men 8<br />
Men 8<br />
Men 8<br />
Men 8<br />
Women 9<br />
Women (<strong>and</strong> Men) 10<br />
Laboratory studies:<br />
Rats 11<br />
Rats 14<br />
Rats 15<br />
∑-DDTs 38 11000-1600000 ng/g l.w. (blubber) 3<br />
74-1112 ng/g l.w. (a)<br />
∑-PCBs 37 32000-5300000 ng/g l.w. (blubber) 3<br />
898-20407 ng/g l.w. (a)<br />
∑-DDTs 38 2000-13000 ng/g l.w. (blubber) 3<br />
74-1113 ng/g l.w. (a)<br />
∑-PCBs 37 6000-110000 ng/g l.w. (blubber) 3<br />
898-20407 ng/g l.w. (a)<br />
∑-DDTs 16 ? 74-1112 ng/g l.w. (a)<br />
4,4’-DDE 68 ND-45 ng/g w.w. (serum) 66-1019 ng/g l.w. (a)<br />
Oxychlordane 115 4-36 ng/g w.w. (serum) 171-6022 ng/g l.w. (a)<br />
4,4’-DDE 115 25-4030 ng/g w.w. (serum) 66-1019 ng/g l.w. (a)<br />
∑-DDTs 115 >25-4140 ng/g w.w. (serum) 74-1113 ng/g l.w. (a)<br />
∑-PCBs 115 >110-1805 ng/g w.w. (serum) 898-20407 ng/g l.w. (a)<br />
∑-PCBs 25 10 ng/g w.w. (serum) 898-20407 ng/g l.w. (a)<br />
∑-PCBs 82 2000 ng/g w.w. (serum) 898-20407 ng/g l.w. (a)<br />
PCB-126 20 7 ng/g body wgt./day (i.p.) 0.003 ng/g body wgt./day 12, 13 (f)<br />
PCB-126 20 7 ng/g body wgt./day (i.p.) 0.003 ng/g body wgt./day 12, 13 (f)<br />
PCB-126 20 5 ng/g body wgt./day (i.p.) 0.003 ng/g body wgt./day 12, 13 (f)<br />
In our study, we cannot prove whether the negative correlation between<br />
organohalogens <strong>and</strong> BMD is true cause-effect relations. This would require a<br />
case-control, dose-effect study on polar bears or another Arctic relevant top<br />
predator. However, such controlled studies are in progress on domestic<br />
Greenl<strong>and</strong> sledge dogs (Canis familiaris) <strong>and</strong> Svalbard Arctic fox (Alopex lagopus)<br />
in cooperation with Norwegian research groups.<br />
Macroscopic anatomy <strong>and</strong> BMD of bacula<br />
Beside the analysis of skull BMD from the period 1892 to 2002, the baculum<br />
from a sub-set of 52 East Greenl<strong>and</strong> male polar bears (n=52) sampled during<br />
1999-2002 was investigated macroscopically <strong>and</strong> analysed by DXA-scanning.<br />
The statistical analysis applied to the bacula data followed those described<br />
in Paper III.<br />
The polar bear penis <strong>and</strong> bacula were similar to carnivorous in general <strong>and</strong><br />
all were morphologically normal without any sign of malformation or asymmetry.<br />
The BMD in the baculum increased with age, similar to skull BMD,<br />
<strong>and</strong> was significantly positively correlated to BMD in skull (r=0.85; p0.05; n=41). This<br />
could probably be due to the lower metabolic activity of cortical bone tissue,<br />
compared to trabecular bone tissue, in this specific site of the skeletal system<br />
which make it less susceptible to endocrine disruption from organohalogens<br />
(e.g. Kanis 1997).<br />
39