Schulze W, Schulze E D, Pate J S, Gillison A N
Plant Ecology, University Bayreuth, D-95440 Bayreuth, Germany, , , , , , DE.
Dept. of Botany, University of Western Australia, Nedlands WA 6009 Australia, , , , , , AU.
Oecologia. 1997 Nov;112(4):464-471. doi: 10.1007/s004420050333.
This study investigated the nitrogen (N) acquisition from soil and insect capture during the growth of three species of pitcher plants, Nepenthes mirabilis, Cephalotus follicularis and Darlingtonia californica. N/N natural abundance ratios (δN) of plants and pitchers of different age, non-carnivorous reference plants, and insect prey were used to estimate proportional contributions of insects to the N content of leaves and whole plants. Young Nepenthes leaves (phyllodes) carrying closed pitchers comprised major sinks for N and developed mainly from insect N captured elsewhere on the plant. Their δN values of up to 7.2‰ were higher than the average δN value of captured insects (mean δN value = 5.3‰). In leaves carrying old pitchers that are acting as a N source, the δN decreased to 3.0‰ indicating either an increasing contribution of soil N to those plant parts which in fact captured the insects or N gain from N fixation by microorganisms which may exist in old pitchers. The δN value of N in water collected from old pitchers was 1.2‰ and contained free amino acids. The fraction of insect N in young and old pitchers and their associated leaves decreased from 1.0 to 0.3 mg g. This fraction decreased further with the size of the investigated tiller. Nepenthes contained on average 61.5 ± 7.6% (mean ± SD, range 50-71%) insect N based on the N content of a whole tiller. In the absence of suitable non-carnivorous reference plants for Cephalotus, δN values were assessed across a developmental sequence from young plants lacking pitchers to large adults with up to 38 pitchers. The data indicated dependence on soil N until 4 pitchers had opened. Beyond that stage, plant size increased with the number of catching pitchers but the fraction of soil N remained high. Large Cephalotus plants were estimated to derive 26 ± 5.9% (mean ± SD of the three largest plants; range: 19-30%) of the N from insects. In Cephalotus we observed an increased δN value in sink versus source pitchers of about 1.2‰ on average. Source and sink pitchers of Darlingtonia had a similar δN value, but plant N in this species showed δN signals closer to that of insect N than in either Cephalotus or Nepenthes. Insect N contributed 76.4 ± 8.4% (range 57-90%) to total pitcher N content. The data suggest complex patterns of partitioning of insect and soil-derived N between source and sink regions in pitcher plants and possibly higher dependence on insect N than recorded elsewhere for Drosera species.
本研究调查了三种猪笼草(奇异猪笼草、澳大利亚瓶子草和加州瓶子草)生长过程中从土壤获取氮以及捕获昆虫的情况。利用不同年龄的植物和捕虫笼、非食虫参考植物以及昆虫猎物的氮/氮自然丰度比(δN)来估算昆虫对叶片和整株植物氮含量的贡献率。带有闭合捕虫笼的奇异猪笼草幼叶(叶状柄)是氮的主要储存部位,主要由植物其他部位捕获的昆虫氮发育而来。其高达7.2‰的δN值高于捕获昆虫的平均δN值(平均δN值 = 5.3‰)。在作为氮源的带有老捕虫笼的叶片中,δN降至3.0‰,这表明要么土壤氮对实际捕获昆虫的那些植物部位的贡献增加,要么是老捕虫笼中可能存在的微生物通过固氮作用获得了氮。从老捕虫笼收集的水中氮的δN值为1.2‰,且含有游离氨基酸。幼嫩和老捕虫笼及其相关叶片中昆虫氮的比例从1.0降至0.3毫克/克。随着所研究分蘖的大小增加,这一比例进一步降低。基于整个分蘖的氮含量,奇异猪笼草平均含有61.5±7.6%(平均值±标准差,范围50 - 71%)的昆虫氮。由于没有适合澳大利亚瓶子草的非食虫参考植物,所以对从没有捕虫笼的幼苗到有多达38个捕虫笼的大型成株的发育序列进行了δN值评估。数据表明,在4个捕虫笼开放之前依赖土壤氮。在那个阶段之后,植株大小随着捕虫笼数量增加,但土壤氮的比例仍然很高。估计大型澳大利亚瓶子草植株从昆虫获取的氮占总氮的26±5.9%(三个最大植株的平均值±标准差;范围:19 - 30%)。在澳大利亚瓶子草中,我们观察到储存部位捕虫笼与供应部位捕虫笼的δN值平均增加约1.2‰。加州瓶子草的供应部位和储存部位捕虫笼具有相似δN值,但该物种的植物氮δN信号比澳大利亚瓶子草或奇异猪笼草更接近昆虫氮。昆虫氮对捕虫笼总氮含量的贡献为76.4±8.4%(范围57 - 90%)。数据表明猪笼草中昆虫源氮和土壤源氮在供应部位和储存部位之间的分配模式复杂,并且可能比其他地方记录的茅膏菜属植物对昆虫氮的依赖性更高。