利用地径建立林木材积估测模型的探讨

通过实测铁杉、红桦和湖北花楸的地径、胸径、树高和材积，我们建立了根据林木地径估测树木材积的数学模型，具有较高的相关系数，可以应用于森林资源管理和森林生态系统研究。     

桥头跳车原因与防治措施

本文从路在沉降、施工方法和结构体系上对桥头跳车病害进行原因分析,提出减少病害防治措施。     

三种观赏竹抗旱生理指标的研究及其综合评价

可控条件下研究了三种观赏竹铺地竹、平安竹、小佛肚竹在干旱胁迫下的生理指标变化,即叶片叶绿素、SOD、M DA、质膜透性的含量的变化。根据这些生理生化指标进行了抗旱性综合评价,结果为:平安竹>小佛肚竹>铺地竹。这一结果与三种观赏竹的实际表现是一致的。     

岷江干旱河谷几种乔木抗旱性研究

岷江上游干旱河谷地区是我国西部生态环境最恶劣的地区之一,也是我国最困难的造林地区之一。本试验以生理研究为基础,选择干旱河谷区造林地内具有相对较高成活率和保存率的针叶树种岷江柏(Cupressus chen-giana)、辐射松(Pinus radiata)和阔叶树种臭椿(Ailanthus altissima)、榆树(Ulmus pumilaL.)、刺槐(Robinia pseu-doacacia),分别采用主成分分析法和综合评价法对影响其抗旱性的主要生理指标和试验树种的抗旱性进行了分析研究。结果表明:①影响该地区试验树种抗旱性的主要生理指标为:可溶性糖含量、SOD活性、游离脯氨酸含量、水分饱和亏缺度、叶片含水量和24h失水率;②5个试验树种的抗旱性表现为岷江柏最高,其次榆树>刺槐>臭椿,辐射松的抗旱性最差。     

阿坝州干旱河谷区自然植被及生长调查

2005年7月20日至10月15日,对阿坝州6个县干旱河谷地区的自然植被进行了调查。结果表明:干旱河谷区主要植物物种有26种,以小叶羊蹄甲分布范围最广,其次是野花椒、虎榛子、三颗针、白刺花。同一区域不同树种的生长状况差异显著,即使是相同树种,在不同地区的生长差异也很明显。综合各项生长指标,金川县虎榛子是干旱河谷区同类树种中生长状况最优的,其植株平均高度、平均冠幅占有相同树种不同地区的绝对优势。同样,茂县的小叶羊踢甲、黑水县的三颗针等也是干旱河谷区同类树种的最优树。     

胸径、根径、轮尺径之间关系的研究

通过对胸径、根径、轮尺径之间关系的研究,提供一种更加简捷的计算木材蓄积的方法。     

不同贮藏方法对3种药用植物种子发芽率的影响

为了保存药材种子的生活力 ,进行了不同贮藏方法的研究。试验采用 3种处理、 3次重复。结果表明 ,黄芪、桔梗和黄芩 3种药材种子以低温贮藏效果最好 ,贮藏 9个月后发芽率分别为 70 %、 82 %和 54% ,仍具有较高的播种品质。     

辽西地区主要造林树种抗旱性的研究

辽西地区属于半干旱季风气候区,年平均温度为7.1—8.2℃,年降水量为400—600mm,年蒸发量为1600mm,为降水量的3—4倍。干燥是该区总的气候特点。该区的植物群落主要为旱生的森林灌丛或草本植物群落,针叶树建群种为油松,阔叶树为蒙古栎,元宝槭,黄榆;灌木主要为荆条和酸枣。土壤是在各种岩石风化物残积母质上,以及黄土、红土母质上发育的淋溶褐土和褐色性土,土壤干旱瘠薄。水分是这一地区限制造林树种成活及生长的主要因子,本文试图通过对树种抗旱性的测定和分析,确定树种的抗旱能力,从而为辽西地区的造林提供树种选择的依据。     

平原地区杨树人工林阳性冠幅与胸径关系的研究

通过对100株中林46杨树人工林的调查,研究了平原地区杨树人工林阳性冠幅与胸径之间的关系。结果表明:两者之间存在着相当紧密的线性相关关系,其相关线性模型为y=-2.254+0.432x,相关系数为0.9043。     

Effects of the interaction between drought and shade on water relations, gas exchange and morphological traits in cork oak (Quercus suber L.) seedlings

The combined effect of drought and light on different physiological and biochemical traits was assessed in cork oak (Quercus suber L.) seedlings grown under two levels of light availability and submitted to a long-standing drought. Watering was withdrawn after germination and seedlings were allowed to dry to a water content of ca. 50% of field capacity. At this point, water-stressed seedlings were grown under moderate drought and two light regimes: high light (HL—50%) and low light (LL—2%). Soil water in control plants was kept close to field capacity (90–100%) for both light environments. Water-relations parameters derived from P–V curves, gas exchange and water status at predawn (Ψ_pd) were evaluated at twice during the experiment. Nitrogen and chlorophyll contents were determined in the same leaves used for the gas exchange measurements. In addition, maximum rate of carboxylation (V_cmax) and electronic transport (J_max) were derived from A–C_i curves in well-watered seedlings.

The variation on moisture availability during the experiment was the same under both light environments. In control plants, Ψ_pd was over −0.3 MPa at the two harvests, while stressed seedlings decreased to −0.9 MPa, with no differences between light treatments. Water stress decreased osmotic potentials at full (Ψπ₁₀₀) and zero turgor (Ψπ₀). The regressions between both potentials and Ψ_pd showed a higher intercept in shade grown seedlings. This fact will point out the higher osmoregulation capacity in sun seedlings whatever water availability.

Nitrogen investment on a per leaf mass (N_mass), chlorophyll content (Chl_mass) and SLA tended to show a typical pattern of sun-shade acclimation. Thus, the three parameters increased with shade. Only for N_mass there was a significant effect of watering, since water stress increased N_mass.

LL plants showed a lower photosynthetic capacity in terms of maximum net photosynthesis at saturating light (A_max), which was related to a decrease in V_cmax and J_max. Both parameters varied with specific leaf area (SLA) in a similar way. The low-light environment brought about a higher nitrogen investment in chlorophyll, while under high-light environment the investment was higher in carboxylation (V_cmax) and electronic transport (F_max).

Stomatal conductance to water vapour (g_wv) and A_max were lower in low-light seedlings independently of watering. In addition, there was a trend to keep higher intrinsic water use efficiency (IWUE) under high light environment. The increase of IWUE under water stress was higher in HL seedlings. This was as consequence of the steeper decline in g_wv as Ψ_pd decreased. The decrease of A_max with Ψ_pd occurred in a similar way in LL and HL seedlings. Thus, the HL seedlings tended to sustain a higher ability to increase IWUE than LL seedlings when they were submitted to the same water stress.