Under AB 32, GHGs are reported pursuant to the Regulation for the Mandatory Reporting of Greenhouse Gas Emissions (MRR) California power plants must report facility-level emissions Electricity importers must report imports based on physical delivery of electricity by source Imported electricity is reported as either specified or unspecified Renewable, hydro, and nuclear energy is generally assigned a zero-emission factor 排放数据报告受MRR
• The fire was reported to Idaho Power at 5:20 a.m., Monday Oct. 2 • Idaho Power arrived on-site at 6:02 a.m. • Neighbors were encouraged to evacuate, hotels offered • Fire responders reported on-site, no action needed • Roads were closed to maintain a 200 ft perimeter • Regular updates to fire, city, and county throughout event • Industrial Hygiene Professionals arrived to begin air quality testing
6。measuring instruments: results in health, quality of life and experience reported by patients with DM2 ................................. 41
4.1 Overview ...............................................................................................................................................................5 4.2 Notational Definitions ...........................................................................................................................................6 4.3 Quality Control of Reported Data (Scope 1&2) .................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................................
在临床研究中参与合并症的受试者中观察到的Vaxigriptetra的安全性与在整体人群中观察到的受试者没有差异。此外,在肾移植患者中对Vaxigrip进行的研究,哮喘患者在这些人群中Vaxigrip的安全性方面没有显着差异。在南非和马里孕妇进行的临床研究中使用Vaxigrip进行的孕妇(请参阅第4.6和5.1节),在疫苗给药后7天内报道的本地和全身性征求反应的频率与vaxigrip进行临床研究期间成人人群报道的疫苗一致。 在南非的研究中,Vaxigrip组的局部反应比在HIV阴性和HIV阳性队列中的安慰剂组中更频繁。 在两个队列中,Vaxigrip和安慰剂组之间的征求反应没有其他显着差异。 In one clinical study conducted in pregnant women in Finland with VaxigripTetra (see sections 4.6 and 5.1), frequencies of local and systemic solicited reactions reported within 7 days following administration of VaxigripTetra were consistent with those reported for the adult population (with the exception of pregnant women) during clinical studies conducted with VaxigripTetra even though higher for some adverse reactions (injection site pain, malaise, shivering, headache,肌痛)。使用Vaxigrip进行的孕妇(请参阅第4.6和5.1节),在疫苗给药后7天内报道的本地和全身性征求反应的频率与vaxigrip进行临床研究期间成人人群报道的疫苗一致。在南非的研究中,Vaxigrip组的局部反应比在HIV阴性和HIV阳性队列中的安慰剂组中更频繁。 在两个队列中,Vaxigrip和安慰剂组之间的征求反应没有其他显着差异。 In one clinical study conducted in pregnant women in Finland with VaxigripTetra (see sections 4.6 and 5.1), frequencies of local and systemic solicited reactions reported within 7 days following administration of VaxigripTetra were consistent with those reported for the adult population (with the exception of pregnant women) during clinical studies conducted with VaxigripTetra even though higher for some adverse reactions (injection site pain, malaise, shivering, headache,肌痛)。在南非的研究中,Vaxigrip组的局部反应比在HIV阴性和HIV阳性队列中的安慰剂组中更频繁。在两个队列中,Vaxigrip和安慰剂组之间的征求反应没有其他显着差异。In one clinical study conducted in pregnant women in Finland with VaxigripTetra (see sections 4.6 and 5.1), frequencies of local and systemic solicited reactions reported within 7 days following administration of VaxigripTetra were consistent with those reported for the adult population (with the exception of pregnant women) during clinical studies conducted with VaxigripTetra even though higher for some adverse reactions (injection site pain, malaise, shivering, headache,肌痛)。
表1。In- and exclusion criteria .................................................................................................... 8 Table 2.Data charting form ............................................................................................................. 9 Table 3.研究中使用的结果和措施的类型................................................................................................................................................................................................................................................................................................................................................................................................. 14表4。Factors that were reported in studies as affecting implementation and adoption of exoskeletons ................................................................................................................................. 23 Table 5.Reported limitations from authors' perspectives ............................................................... 24
Special Notes ............................................................................................................................ 67 Account Information ............................................................................................................. 68 Contact Information .............................................................................................................. 68 Criteria Emissions Totals ......................................................................................................................................................................................................................................................................................................................................................................................................................................................................................... 69 Facility Information ................................................................................................................ 70 Control Device Information ................................................................................................. 75 Emission Point Information ................................................................................................. 75 Total Aggregate Annual Heat Input ................................................................................... 76 Emissions Factors ................................................................................................................... 76 Updating Reported Emissions ............................................................................................. 77
Acknowledgements 3 Quiet Sound's Leadership Committee 3 Project Funders 3 Executive Summary 4 Background 4 2023-24 Voluntary Vessel Slowdown Results 4 Acronyms 5 Background 6 About Quiet Sound 6 Underwater Noise Impacts on Southern Resident Killer Whales 7 Vessel Slowdowns Reduce Underwater Noise 8 Parameters of the 2023-24 Voluntary Vessel Slowdown 9 Geography of the Slowdown Area 10 Vessels 11 Slowdown Speeds 11 Other vessel interventions 12 Dates 12 Implementing the Slowdown 13 Communications and Engagement Plan 13 Tribal Engagement 13 Communications with Mariners 13 Participant and Supporter Recognition 14 Monitoring the Slowdown 14 Vessel Participation 14 Vessel speed participation calculated using AIS data 15 Vessel participation as reported by the Puget Sound Pilots 15 Underwater Noise 15 Whale Presence 16 Evaluation and Results 16 Industry Participation 16 Participation as Reported by the Puget Sound Pilots 16 Calculated Vessel Speed Through Water Participation 17 Recognition 19 Slowdown后参与者反馈19
4.1。If the Original Buyer wishes to make a warranty claim under this Limited Warranty, the warranty claim must be reported in writing to NINGBO DEYE ESS Partner (or, if the Original Buyer is unable to contact them, please report it to DEYE ESS Global Service Department), with the information specified in the table below, using the contact information specified below:
Side effects which have been reported following administration of FLUARIX TETRA include redness, swelling, a hard lump, soreness, bruising or itching around the injection site, pain at the injection site, fever, chills, shivering, sweating, dizziness, headache, a general feeling of being unwell, muscle aches and pain, joint pain, a loss of appetite, feeling sick, vomiting, diarrhoea, stomach pain, irritability,嗜睡,疲劳和皮疹。