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Get system time in Android’s service
I have an Android app (using different apps as the user has different roles) that needs to keep track of when certain system jobs have been completed. These jobs are fairly complicated, but the flow goes as follows:
The app runs a series of commands, using RxJava and the pipe operator, from within a Service. The Service is configured in the Manifest so it is always launched, but it only executes the commands every few minutes.
If the commands have completed successfully, the commands complete, the progress of the commands updates the UI, and the app closes.
If the commands fail for any reason, the commands are retried after some delay, and the app closes.
The progress of the commands is currently displayed by a CircularProgressIndicator, but I would like to implement a similar idea, but for the “time” of the execution of the commands.
To do this, I need to keep track of the “time” when the commands started. In my head this would be the time on the phone, since this is running in a service and not an Activity.
I’m running Android 5.0.1 and the phone is locked to the time on the device.
Since the phone is locked to the time on the device, and the app is in a service, I think that the only way to keep track of this time is through the Android system (running in the OS, not the app).
From what I’ve read, the System class in Java doesn’t seem to be able to do what I want, and the only way to get time from the OS is through the WakeLock. In other posts, I’ve read that the System class is no longer being used, but apparently it is still used in Android 5+ and the documentation still states that it is available.
The only way I can think of to get the time without setting a WakeLock would be to make the app stay awake all the time, which isn’t a good idea. I could also just use an IntentService (and stop the service whenever the app is closed, but I would want the service to start when the app starts).
Is what I’m trying to do even possible?
A:
This class might help you:
class
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Grape seeds are used in folk medicine as an anti-inflammatory agent. However, the mechanisms underlying these effects are unknown. Therefore, we investigated the estrogenic and antiestrogenic properties of grape seeds in estrogen receptor positive and negative breast cancer cells. For in vitro investigations, grape seeds were obtained after manual digestion from wild type (WT) and knockout (KO) mice for type I estrogen receptor (ER) and for β-estradiol (E2) binding (Elovl-2-KO and Elovl-2-WT). Grape seeds were extracted using a Soxhlet apparatus and the extract was then lyophilized. For in vivo studies, grape seeds were obtained from WT and KO female mice by manual digestion and the extract was lyophilized. After dispersion of grape seeds in dimethylsulfoxide, different concentrations were added to the culture medium for 24 h of treatment. For in vivo studies, mice were treated with grape seeds (1 mg/day per mouse) for three consecutive days. The cells were treated for 24 h and then assayed for gene expression by quantitative real-time polymerase chain reaction. In vitro studies revealed that grape seeds are able to activate ERα and downregulate ERβ (20 μg/mL) and consequently transactivate β-estradiol-stimulated response element (ERE) (12.5 μg/mL) and progesterone receptor (PGR)
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Q:
How to prove that the subset of $ \mathbb{Z} $ generated by $\mathbb{Z} \cup \{2\}$ is neither $ \mathbb{Z} $ nor $\mathbb{Q}$?
If I take the subset of $\mathbb{Z}$, i.e. the finite set of integers which contains the elements $0$ and $1$, and choose $2$ as an element. This means that $2$ has an inverse but all elements of this subset have an inverse. Hence the question becomes this: How to prove that the subset of $\mathbb{Z}$ generated by $\mathbb{Z} \cup \{2\}$ is neither $ \mathbb{Z} $ nor $ \mathbb{Q} $?
A:
We have $\mathbb{Q}\subseteq \{2\}$ and $\mathbb{Z}\subseteq \{0,1\}$, and the only such unions are $\mathbb{Z}\cup\{2\}$ and $\mathbb{Z}\cup\{0,1\}$.
A:
Hint: Consider the set $\{x\in\Bbb Z\;:\;x
eq 0\}\cup\{2\}$. What can you say about this set?
The effects of reserpine on 5-HT neurons projecting to the spinal cord in the rat.
The present study was undertaken to determine whether reserpine affects the activity of the spinal 5-HT neurons that are known to project to the spinal cord. Intraventricular injections of reserpine (50 mg/kg) caused a decrease of the threonine-resistant 5-HT uptake in the rat spinal cord. Reserpine also caused a significant decrease in the 5-HT content of the cervical and lumbar dorsal horns. Following a spinal transection at the level of the mid-thoracic vertebra, the effect of intrathecal injection of reserpine was followed for 2 weeks. During this period, the loss of the 5-HT innervation of the cervical and lumbar dorsal horns is relatively slow, returning to the control level after 2 weeks. A concomitant reduction of the 5-HT content occurred when the 5-HT axon terminals of the dorsal horns underwent degeneration. In
