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11.
鱿鱼内脏的营养及其开发利用   总被引:2,自引:2,他引:2  
按照国标方法,对鱿鱼内脏的营养成分进行检测。结果表明,鱿鱼内脏营养丰富,每100 g鱿鱼内脏中含脂肪21.15 g,蛋白质21.24 g,钙51.46 mg,铁609.07μg和磷95.88μg。此外,鱿鱼内脏消化液中还含有18种氨基酸(包括全部人体必需氨基酸),鱿鱼内脏油脂脂肪酸中含有10.58%的EPA和15.23%的DHA,非常值得研究开发与利用。  相似文献   
12.
As a renovation envelope, double-skin facade has the characteristics of environmental function and unique aesthetic effect. In this paper, the composition and functional characteristics of double skin facade is introduced briefly, its development history and a detailed typologic analysis combined with typical cases is reviewed. It is pointed out that the double skin facade has a bright future in 21~(st) century and the function and aesthetics are the footstone for its typologic research.  相似文献   
13.
为了确定细胞学检查在犬皮肤肥大细胞瘤诊断中的诊断意义,采取细胞学检查和病理组织学检查相结合的方法对2例犬皮肤肥大细胞瘤临床病例进行诊断.结果显示:细胞学检查结果与病理组织学检查结果相符.由此可以得出,在犬皮肤肥大细胞瘤的诊断中,细胞学检查具有一定的诊断价值,为肿瘤的性质及分化程度分级提供参考,为该病临床诊断提供了一种新...  相似文献   
14.
Varietal differences in the total phenolic content and astringency in the skin and flesh were determined among the cultivars and local collections of hardy kiwifruit with a ploidy variance found in Japan. The average values of the total phenolic content in the skin and flesh were 2.66 and 0.18 g 100 g−1 FW, respectively. There were large varietal differences in the total phenolic content in the skin in the range of 1.3–5.0 g 100 g−1 FW. Kochi (tetraploid), while Gassan and ‘Mitsuko’ (hexaploid) contained a larger amount of total phenolics. High astringency was found in Gassan, ‘Mitsuko’ and ‘Hoko’ (hexaploids) and Kochi. HPLC analysis showed that the major components of phenolics in the flesh were (+)-catechin, chlorogenic acid, rutin, (−)-epicatechin and quercetin.  相似文献   
15.
A single‐factor experiment was conducted to investigate the effects of dietary astaxanthin concentration on the skin colour of snapper. Snapper (mean weight=129 g) were held in white cages and fed one of seven dietary levels of unesterified astaxanthin (0, 13, 26, 39, 52, 65 or 78 mg astaxanthin kg?1) for 63 days. Treatments comprised four replicate cages, each containing five fish. The skin colour of all fish was quantified using the CIE L*, a*, b* colour scale after 21, 42 and 63 days. In addition, total carotenoid concentrations of the skin of two fish cage?1 were determined after 63 days. Supplementing diets with astaxanthin strongly affected redness (a*) and yellowness (b*) values of the skin at all sampling times. After 21 days, the a* values increased linearly as the dietary astaxanthin concentration was increased before a plateau was attained between 39 and 78 mg kg?1. The b* values similarly increased above basal levels in all astaxanthin diets. By 42 days, a* and b* values increased in magnitude while a plateau remained between 39 and 78 mg kg?1. After 63 days, there were no further increases in measured colour values, suggesting that maximum pigmentation was imparted in the skin of snapper fed diets >39 mg kg?1 after 42 days. Similarly, there were no differences in total carotenoid concentrations of the skin of snapper fed diets >39 mg kg?1 after 63 days. The plateaus that occurred in a* and b* values, while still increasing in magnitude between 21 and 42 days, indicate that the rate of astaxanthin deposition in snapper is limited and astaxanthin in diets containing >39 mg astaxanthin kg?1 is not efficiently utilized. Astaxanthin retention after 63 days was greatest from the 13 mg kg?1 diet; however, skin pigmentation was not adequate. An astaxanthin concentration of 39 mg kg?1 provided the second greatest retention in the skin while obtaining maximum pigmentation. To efficiently maximize skin pigmentation, snapper growers should commence feeding diets containing a minimum of 39 mg unesterified astaxanthin kg?1 at least 42 days before sale.  相似文献   
16.
The unnaturally dark pigmentation of cultured Australian snapper Pagrus auratus can be improved through dietary astaxanthin supplementation and by holding fish in tanks with a white background. The practical application of these laboratory‐based findings was examined with two experiments to establish if the advantages of transferring fish to light coloured tanks before harvest could be achieved on‐farm using white cages and to determine the effects of fish density on skin colour. For the first experiment, snapper (mean TL=29.7 cm) were transferred from a commercial snapper sea cage to black or white netted cages and fed diets supplemented with unesterified astaxanthin (supplied as Lucantin® Pink, BASF) at 0 or 39 mg kg?1 for 42 days. Skin colour was measured using the CIE (black–white), (green–red), (blue–yellow) colour scale. Snapper held in white netting cages became significantly lighter (higher ) than snapper held in black cages; however, values were not as high as previous laboratory‐based studies in which snapper were held in white plastic‐lined cages. Snapper fed astaxanthin displayed significantly greater and values, and total carotenoid concentrations after 42 days. In addition, total carotenoids were higher in fish from black than white cages. The second experiment was designed to investigate whether density reduced the improvements in skin colour achieved by holding fish in white coloured cages and whether cage colour affected stress. Snapper (mean weight=435 g) were acclimated to black cages and fed 39 mg kg?1 astaxanthin for 44 days before transferring to black or white plastic‐lined cages at 14 (low), 29 (mid) or 45 (high) kg m?3 for 7 days after which time skin colour, plasma cortisol and plasma glucose concentrations were measured. Skin lightness () was greater in snapper transferred to white plastic‐lined cages with the lightest coloured fish obtained from the lowest density after 7 days. Density had no effect on plasma cortisol or glucose levels after 7 days, although plasma cortisol was elevated in snapper from black cages. For improved skin colouration we recommend feeding unesterified astaxanthin at 39 mg kg?1 for approximately 6 weeks and transferring snapper to white plastic‐lined cages or similar at low densities for short periods before harvest rather than producing fish in white netting sea cages subject to biofouling.  相似文献   
17.
18.
‘小红玫瑰’葡萄是源自于‘小白玫瑰’的突变品种,二者都是优良的酿酒葡萄品种,但其果实颜色变异的分子机理尚不清楚。用12对SSR(Simple sequence repeats)荧光标记特征引物对两品种进行分析,结果表明这些位点在二者之间无差别。对色泽变异决定基因Vvmyb A1的基因型进行分析,‘小白玫瑰’仅检测到含有插入逆转座子Gret1(grapevine retrotransposon 1)的VvmybA1a,说明其为VvmybA1a/VvmybA1a纯合体;而‘小红玫瑰’检测到了Vvmyb A1a和残留Gret1 3′-LTR(long terminal repeat)的VvmybA1b,说明其为VvmybA1a/VvmybA1b的杂合体。花色苷合成相关基因的表达分析表明,VvmybA1、UFGT、F3′5′H、CHS、GST和OMT在‘小红玫瑰’及有色对照品种‘黑比诺’中大量表达,而在‘小白玫瑰’和无色对照品种‘白比诺’中几乎不表达。通过HPLC–ESI–MS/MS对花色苷主要成分进行测定,结果表明矢车菊素3–O–葡萄糖苷(CyG)、矢车菊素3,5–O–双葡萄糖苷(Cy2G)、飞燕草素3–O–葡萄糖苷(DpG)、锦葵色素3–O–葡萄糖苷(MvG)、芍药色素3–O–葡萄糖苷(PnG)和矮牵牛色素3–O–葡萄糖苷(PtG)等6种花色苷在有色品种‘小红玫瑰’和‘黑比诺’果皮中的含量均显著高于无色品种,花葵素3–O–葡萄糖苷(Pg G)、花葵素3,5–O–双葡萄糖苷(Pg2G)在有色/无色品种间无显著差异,且含量很低。说明‘小红玫瑰’的着色是由于转录因子基因Vvmyb A1及其调控结构基因的表达引起的,而无功能的VvmybA1a等位基因突变为有功能的VvmybA1b等位基因是其果皮颜色变异的遗传学原因。  相似文献   
19.
探究中药对兔子大面积皮肤缺损的治疗效果。本研究对1例流浪兔子腰荐部皮肤大面积缺损,在不借助抗生素控制感染的情况下,仅通过中药白芨膏外敷治疗,简便包扎,通过6~7周的精细护理,完全痊愈。结果显示,此方法操作简便,疗效确实,中药对该病治疗具有一定的优势,这为临床应用中药治疗此类疾病提供了科学依据。  相似文献   
20.
番茄裂果与果皮结构的关系及其杂种优势表现   总被引:3,自引:0,他引:3  
以4份抗裂番茄为母本,3份易裂番茄和1份抗裂番茄为父本,按照不完全双列杂交设计配制4×4的杂交组合,研究8个亲本和16个F1的裂果特性与果皮结构的关系,分析它们的杂种优势表现.结果表明,易裂基因型的果皮较薄,抗裂基因型的果皮普遍较厚,但也有果皮薄而抗裂能力强的基因型.裂果特性有明显的杂种优势,优势的方向在不同组合间有很大的差异.亲本的一般配合力对杂种后代的抗裂时间发挥了决定性作用.对利用结构特征改良番茄抗裂能力的潜力进行了讨论.  相似文献   
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