鲈鱼人工配合饲料中豆饼替代部分鱼粉的适宜含量

本文根据实验探讨了在最适蛋白质含量下配合饲料不同的豆饼含量替代鱼粉对鲈鱼生长的影响。经４０ｄ的试验结果表明；用鲈鱼的相对增长率、体长相对增长率、饲料系数和饲料的蛋白质消化率来衡量，鲈鱼人工配合饮料中用１５％以内的豆饼含量替代鱼粉是适宜的。     

饵料对斑玉螺浮游幼虫存活与生长的影响

采用金藻、金藻和云微藻、云微藻三组饵料分别投喂斑玉螺浮游幼虫，每天测定壳宽和存活率.结果表明，10d后，投有金藻的两组存活率较高，生长较快，作者认为，金藻是斑玉螺浮游幼虫的适合饵料.     

环境因素对蜗牛Achatina fulica壳体碳酸盐δ13C 组成影响的实验研究

陆生蜗牛化石稳定同位素组成是一种良好的古环境信息载体,常被用于古环境古气候的重建。由于缺少古环境因子 对蜗牛壳体稳定同位素组成机理性的结论,因此越来越多的研究侧重于对现代蜗牛壳体的环境效应进行探讨。实验室蜗牛 饲养实验则可以通过控制环境因素来确定其对壳体碳酸盐稳定同位素组成的影响程度,从而得到较为确切的结果。该文在 前人的研究基础上,利用Achatina fulica 进行实验室饲养实验。结果表明,在相同的温、湿度下,同种食物喂养的蜗牛壳体 有非常稳定的分馏值,不同食物类型的结果有一定的差异,莴苣叶、玉米粉和饲料喂养的蜗牛壳体相对于食物的分馏值分 别为16.70‰±0.2‰,10.57‰±0.2‰和10.65‰±0.2‰;在20~30℃实验条件下,壳体δ13C并不受环境温度的影响,主要受食 物的影响,并得到两者之间的回归方程为δ13Cs=0.6665δ13Cv+6.2302（n=26）;无机碳酸盐对Achatina fulica 壳体文石δ13C值影 响很少;根据端元组分分析方法的统计结果显示,食物是Achatina fulica 壳体碳同位素组成的主要影响因素,贡献值约为 80％±5％,除此以外,大气CO2的贡献值约为20％±5％。     

不同饵料对管角螺生长、肝脏消化酶活性及软体部营养成分的影响

以缢蛏(Sinonovacula constricta)(A)、菲律宾蛤(Venerupis Philippinaram)仔(B)及自制配合饲料(C)作为饵料,分别研究了上述3种饵料对二龄管角螺(Hemifusus tuba Gmelin)生长、肝脏消化酶活性以及软体部营养成分的影响。结果表明：(1)鲜活饵料的投喂更有利于管角螺的生长和营养物质的累积,配合饲料的摄食效果较差,还需进一步的优化和完善;其特定生长率大小为：缢蛏组＞菲律宾蛤仔组＞配合饲料组,组间差异显著(P＜0.05);(2)不同饵料的投喂对其肝脏消化酶活性的影响差异显著,在整个实验区间的胰蛋白酶活力的大小为：缢蛏组＞菲律宾蛤仔组＞配合饲料组,组间差异显著(P＜0.05);配合饲料组的淀粉酶活力和脂肪酶活力先降后升,鲜活饵料组则较稳定;45 d 后配合饲料组的淀粉酶活力和脂肪酶活力皆显著高于鲜活饵料组的(P＜0.05);表明管角螺在饥饿时,消化酶可能存在补偿性分泌,优先利用糖原和脂肪作为能源物质;(3)不同饵料对管角螺软体部的灰分和水分没有显著影响(P＞0.05),鲜活饵料组的粗蛋白和粗脂肪含量皆显著高于配合饲料组(P＜0.05)。     

Agroecological measures and circular economy strategies to ensure sufficient nitrogen for sustainable farming

Sustainable food systems face trade-offs between demands of low environmental pressures per unit area and requirements of increasing production. Organic farming has lower yields than conventional agriculture and requires the introduction of nitrogen (N) fixing legumes in crop rotations. Here we perform an integrated assessment of the feasibility of future food systems in terms of land and N availability and the potential for reducing greenhouse gas (GHG) emissions. Results show that switching to 100% organic farming without additional measures results in N deficiency. Dietary change towards a reduced share of animal products can aggravate N limitations, which can be overcome through the implementation of a combination of agroecological, circular economy and decarbonization strategies. These measures help to recycle and transfer N from grassland. A vegan diet from fully decarbonized conventional production performs similarly as the optimized organic scenario. Sustainable food systems hence require measures beyond the agricultural sector.     

海洋鱼类育苗期配合饵料代替活饵的研究进展

综述了近年来在海水鱼类育苗中，利用配合词料代替活饵的研究状况，以及海水鱼类幼体消化酶与微胶囊饵科吸收和利用的关系；同时对海水鱼类幼体微粒子饵科的制备方法进行了探讨，以期为研制海洋鱼类育苗期的配合饵科提供参考。     

Dietary leucine requirement for juvenile large yellow croaker <Emphasis Type="Italic">Pseudosciaena crocea</Emphasis> (Richardson, 1846)

Dietary leucine requirement for juvenile large yellow croaker, Pseudosciaena crocea Richardson 1846 (initial body weight 6.0 g ± 0.1 g) was determined using dose-response method. Six isonitogenous (crude protein 43%) and isoenergetic (19 kJ g⁻¹) practical diets containing six levels of leucine (Diets 1–6) ranging from 1.23% to 4.80% (dry matter) were made at about 0.7% increment of leucine. Equal amino acid nitrogen was maintained by replacing leucine with glutamic acid. Triplicate groups of 60 individuals were fed to apparent satiation by hand twice daily (05:00 and 17:30). The water temperature was 26–32°C, salinity 26–30 and dissolved oxygen approximately 7 mg L⁻¹ during the experimental period. Final weight (FW) of large yellow croaker initially increased with increasing level of dietary leucine but then decreased at further higher level of leucine. The highest FW was obtained in fish fed diet with 3.30% Leucine (Diet 4). FW of fish fed the diet with 4.80% Leucine (Diet 6) was significantly lower than those fed Diet 4. However, no significant differences were observed between the other dietary treatments. Feed efficiency (FE) and whole body composition were independent of dietary leucine contents (P > 0.05). The results indicated that leucine was essential for growth of juvenile large yellow croaker. On the basis of FW, the optimum dietary leucine requirement for juvenile large yellow croaker was estimated to be 2.92% of dry matter (6.79% of dietary protein).