北大西洋的新产量源于地表叶绿素的季节模式

Janet W. Campbell , Thorkild Aarup
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引用次数: 104

摘要

利用1979年至1983年海岸带彩色扫描仪(CZCS)的数据估计了北大西洋冬季硝酸盐每年的新产量。基于CZCS数据的5年平均值,利用12个月平均地表叶绿素图像识别出3个不同季节模式的区域。在面积为7 × 106 km2的中纬度地区,春季出现水华,整个夏季地表呈现贫营养状态。春季开花后地表叶绿素的下降被认为表明混合层中的冬季硝酸盐已经耗尽,并且在深处形成了硝酸碱。根据Strass和Woods (Deep-Sea Research, 38,35 - 56, 1991)在北大西洋的观测,我们估计硝酸碱以每月10米的速度加深,从混合层的底部开始。通过从卫星数据中确定少营养条件发生的时间,我们可以估计夏末硝酸线上方硝酸盐耗尽水的体积。这与生长季节开始时硝酸盐浓度的估计相结合,得出新的产量。初始硝酸盐浓度的模型是基于Glover和Brewer (Deep-Sea Research, 35,1525 - 1546, 1988)的冬季硝酸盐与春季开花结束时最大叶绿素之间的经验关系。在这个中纬度过渡带,新产量为24 g C m−2 y−1 (4.2 g N m−2 y−1)。将同样的方法应用于面积大致相等的亚热带地区,估计新产量为18 g C m−2 y−1 (3.1 g N m−2 y−1);两个区域的面积加权平均值为21 g cm−2 y−1 (3.7 g N m−2 y−1)。在亚热带地区,叶绿素在冬季最高,夏末最低,表明全年的生产都受到营养限制。第三个较小的区域(2.5 × 106 km2)位于北部的亚极地地区,该区域的地表叶绿素在冬季最低,在夏末最高。假设到夏季结束时,该区域水柱上部40米内的所有冬季硝酸盐都已被同化,则新产量估计为43 g C m−2 y−1 (7.6 g N m−2 y−1)。我们的结果低估了新产量,因为它们仅仅基于浮游植物在冬季和夏末之间吸收的冬季硝酸盐。然而,这些数值在量级上可与以前对少营养化海洋区域总生产力的估计相比较(Koblentz-Mishkeet等人,《南太平洋的科学探索》,W.S. Wooster,编辑,第183-193页,1970年)。
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New production in the North Atlantic derived from seasonal patterns of surface chlorophyll

Annual new production resulting from winter nitrate has been estimated for the North Atlantic using data from the Coastal Zone Color Scanner (CZCS) between 1979 and 1983. Twelve monthly mean surface chlorophyll images, based on 5-year averages of CZCS data, were used to identify three zones with distinct seasonal patterns. A mid-latitude zone, with an area of 7 × 106 km2, exhibited a spring bloom followed by oligotrophic conditions at the surface throughout the summer. The decline in surface chlorophyll following the spring bloom was assumed to indicate that winter nitrate in the mixed layer was exhausted and that a nitracline had formed at depth. Based on observations by Strass and Woods (Deep-Sea Research, 38, 35–56, 1991) in the North Atlantic, we estimate that the nitracline deepened at a rate of 10 m per month, starting at the base of the mixed layer. By determining the timing of the onset of oligotrophic conditions from the satellite data, we can estimate the volume of nitrate-depleted water lying above the nitracline in late summer. This was combined with an estimate of the nitrate concentration at the start of the growing season to derive new production. The model for the initial nitrate concentration is based on an empirical relationship between winter nitrate from Glover and Brewer (Deep-Sea Research, 35, 1525–1546, 1988) and the maximum chlorophyll at the end of the spring bloom.

The resulting new production was 24 g C m−2 y−1 (4.2 g N m−2 y−1) in this mid-latitude transitional zone. Applying the same method to subtropical zone of approximately equal area yields an estimate of new production of 18 g C m−2 y−1 (3.1 g N m−2 y−1); the area-weighted average for both zones was 21 g C m−2 y−1 (3.7 g N m−2 y−1). In the subtropical zone, the maximum chlorophyll occurred in the winter and the minimum in late summer, suggesting that production was nutrient-limited throughout the year. The third smaller zone (2.5 × 106 km2) was located in subpolar regions to the north, where surface chlorophyll was minimum in winter and maximum in late summer. Assuming that all winter nitrate had been assimilated by the end of the summer within the upper 40 m of the water column in this zone, new production is estimated to be 43 g C m−2 y−1 (7.6 g N m−2 y−1). Our results underestimate new production because they are based solely on winter nitrate assimilated by phytoplankton between winter and late summer. Nevertheless, the values are comparable in magnitude to previous estimates of total productivity in oligotrophic oceanic regions (Koblentz-Mishkeet al., in Scientific exploration of the South Pacific, W.S. Wooster, editor, pp 183–193, 1970).

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